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Limehouse Veterinary Clinic Of Holistic Medicine …

October 17th, 2018 2:40 am

Welcome toLimehouse Veterinary Clinic of Holistic Medicine

If you live in Glendale or the surrounding area in CA, then you have picked the perfect site to find a holistic veterinarian.Your pet's health and well being is very important to us and we will take every step to give your pet the best possible care.

At Limehouse Veterinary Clinic of Holistic Medicine,we offer acupuncture by veterinarians that are certified in veterinary acupuncture by the International Veterinary Acupuncture Society (IVAS), homeopathy, Chinese and Western herbal therapy, musculoskeletal manipulation (our doctors have been trained by the American Veterinary Chiropractic Association),nutritional counseling, as well as conventional veterinary care.

Because our doctors and staff are trained in both holistic and Western allopathic medicine, we are able to integrate these treatment methods as dictated by the needs of each pet; therefore,providing truly individualized treatment for each of our patients.

If you are like us, then you consider your pet to be a member of your family. We havegatheredseveral resourcesto help youlearn about how to take better care of your furry family members. Feel free to browsethrough our website which includeseducational articles and videos. We believe the best veterinary care for pets includes proper nutrition, wellness,and problem prevention. Call today with any questions you may have or to schedule an appointment818-761-0787. For your convenience,you may also contact uselectronically by filling out our on-line contact form. Our Glendale clinic is very easyto locate.Click onour Contact Us page forspecific directions.You can also subscribe to our newsletter which is created especially for Glendale pet owners. In between your veterinary visits, your pet will benefit from you reading these free informative articles.

At Limehouse Veterinary Clinic of Holistic Medicine, we treat your pets like the valued family members they are.

Glendale Veterinarian | Limehouse Veterinary Clinic of Holistic Medicine | 818-761-0787

1733 Victory Blvd.Glendale, CA 91201staff@limehousevetclinic.com

The Limehouse Clinic provides all customers with full and equal access to our services. Please identify the need for any disability accommodation or wheelchair access upon making your appointment.

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What are Tooth Stem Cells? | Dental Stem Cells | BioInformant

October 16th, 2018 10:41 am

Tooth stem cells (also called dental stem cells) are cells collected from the teeth and supporting oral structures.Dental pulp is the soft living tissue inside a tooth that contains a type of adult stem cell called a mesenchymal stem cell (MSC). The ideal time to harvest dental stem cells is when children lose their baby teeth through natural loss or extraction by a dentist.

In this article:

Tooth stem cells are defined as stem cells collected from the dental structures, including components of the developing tooth, as well as structures within the mature tooth and periodontal ligaments. Tooth stem cells are multipotent, meaning they can become a variety of cell types that could potentially be used for therapeutic applications.

The type of stem cell found within the dental pulp is called a mesenchymal stem cell (MSC). MSCs from a range of sources are being explored in more than 800 clinical trials worldwide, making teeth an interesting source of these cells.

While MSCs from teeth have not yet been approved for clinical use in humans, there is interesting potential for their use within regenerative medicine applications.

Tooth Stem Cell Cost

The cost of tooth stem cell storage has two parts, the Processing Fee and the Storage Fee. The Processing Fee is a one-time fee, while the Storage Fee is a reoccurring fee.

The Processing Fee covers the steps that the dental stem cell bank must take to prepare the valuable cells within a tooth for long-term storage. The Storage Fee covers the cost of preserving the tooth stem cells in frozen (cryogenic) conditions with proper backup systems and data protection.

For BioEden, the market leader in the U.S. and worldwide, its Processing Fee is$1,250. Its annual Storage Cost is $120 per year or $17.95 per month.

Alternatively, BioEden offers the option for a family to pay a lump sum fee to cover One Off Processing and 21 Years of Storage for $2930. Over a 21 year period, this options offers over $840 in savings as compared to paying annually at $120/year.

Click here to see BioEdens full pricing schedule for tooth stem cell storage.

Should I Store Tooth Stem Cells?

Whether or not to store tooth stem cells is a personal decisions, but stem cells from dental pulp do have differences in comparison to other types of stem cells. First, they are not limited to the quantity extracted from a tooth, because the cells can be expanded in number within a laboratory.

Second, they have the ability todifferentiate into range of other cell types, and in this regard, have a diverse range of potentialapplications.

Cellsharvested from baby teeth are also advantageous in that they have been harvested while the cells are young, healthy, and full offunctionality.

Finally, harvesting tooth stem cells is a non-invasive method of collecting stem cells. No medical or dental intervention is required, because a tooth can be exfoliatednaturally. In the case of tooth extraction, these procedures are necessary for other dental reasons and the ability to preserve tooth stem cells is a valuable byproduct.

Stem cells from teeth are of growing interest among parents, because these stem cells can be collected without the need for invasive procedures.

While tooth stem cell storageis a relatively new service, new competitors are entering the market on a global basis. The United States, UK, and India currently host the greatest number of dental stem cell storage companies.

The largest competitor within the tooth stem cell storage market is BioEden.BioEden became the worlds first company to collect, assess, and cryogenically store living stem cells from teeth when it began offering services in 2006.

BioEden now operates in 25 countries and has members in over 60 countries. It also has laboratories in the US (Texas), Europe (UK), and Asia (Thailand).

It is also one of the few tooth stem cell companies that storesallsamples in duplicate inseparate locations for thepurpose of creating additional security and safety. This can preserve the cells in the event of natural disaster or other emergency.

With this wide global reach and early entry into the field, BioEden is estimated to control morethan 50% of the dental stem cell storage market worldwide.To learn more, view our interview with Tony Veverka, the CEO of BioEden.

Interview with Tony Veverka, Chief Group Executive of BioEden How Dental Stem Cells Will Impact Our Future https://t.co/ubbG3TFa1M

BioInformant (@StemCellMarket) June 19, 2016

Types of Tooth Stem Cells

Five different types of tooth stem cells have been discovered, which are:

While the future is unknown, it is possible that tooth stem cells could be used in the future to restore tooth structure lost to decay or injury, as well astreat a range of acute and chronic diseases.

Up Next:Do You Know the 5 Types of Dental Stem Cells?

What are Tooth Stem Cells? | Dental Stem Cells

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Freed Vision Center – Secaucus, NJ – Yelp

October 14th, 2018 5:43 am

Specialties

Treatment of eye diseaseGlaucoma and Cataract ManagementContact LensesLasik ManagementSports visionGeriatricsInfants and ChildrenGeneral Eye Glasses

Established in 1900.

Welcome to Freed Vision Center, Where family eyecare is our most important concern. We are Therapeutic Optometrists so we perform Diabetic eye exams and treat many disease conditions including glaucoma and eye infections, in addition to prescribing eyeglasses and contact lenses. All our Doctors are certified to Co-Manage LASIK and Cataract Surgery. Our Doctors also have 20+ years of experience fitting specialty contact lenses for Keratoconus, Pellucid Marginal Dystrophy and other corneal conditions.

Our office has been located in Secaucus, New Jersey for over 50 years and we service all areas of Northern New Jersey, including North Bergen, Union City, Rutherford and Lyndhurst.

Dr. Randi Freed Graduated from Syracuse University and Fairleigh Dickenson University with a degree in Clinical Pathology. She received her Masters in Microbiology and Chemistry from Fairleigh Dickenson University. She received her Doctor of Optometry in 1993 from Pennsylvania College of Optometry.

Dr. Freed is credited with medical research and has published numerous medical articles. She taught Biology at William Paterson College and is an Adjunct Professor.

Dr. Freed is a member of The American Optometric Association, The New Jersey Society of Optometric Physicians, and The American Society of Clinical Pathologists.

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How Does Gene Therapy Work?

October 14th, 2018 5:43 am

Scientists have promised that gene therapy will be the next big leap for medicine. It's a term that's tossed about regularly, but what is it exactly? Trace shows us how scientists can change your very genetic code.

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How does gene therapy work?http://ghr.nlm.nih.gov/handbook/thera..."Gene therapy is designed to introduce genetic material into cells to compensate for abnormal genes or to make a beneficial protein. If a mutated gene causes a necessary protein to be faulty or missing, gene therapy may be able to introduce a normal copy of the gene to restore the function of the protein."

Gene therapy trial 'cures children'http://www.bbc.co.uk/news/health-2326..."A disease which robs children of the ability to walk and talk has been cured by pioneering gene therapy to correct errors in their DNA, say doctors."

Gene therapy cures diabetic dogshttp://www.newscientist.com/article/d..."Five diabetic beagles no longer needed insulin injections after being given two extra genes, with two of them still alive more than four years later."

Gene Therapy for Cancer: Questions and Answershttp://www.cancer.gov/cancertopics/fa..."Gene therapy is an experimental treatment that involves introducing genetic material into a person's cells to fight or prevent disease."

How does gene therapy work?http://www.scientificamerican.com/art..."Gene therapy is the addition of new genes to a patient's cells to replace missing or malfunctioning genes. Researchers typically do this using a virus to carry the genetic cargo into cells, because that's what viruses evolved to do with their own genetic material."

Gene therapy cures leukaemia in eight dayshttp://www.newscientist.com/article/m...eight-days.htmlWITHIN just eight days of starting a novel gene therapy, David Aponte's "incurable" leukaemia had vanished. For four other patients, the same happened within eight weeks, although one later died from a blood clot unrelated to the treatment, and another after relapsing.

Cell Therapy Shows Promise for Acute Type of Leukemiahttp://www.nytimes.com/2013/03/21/hea..."A treatment that genetically alters a patient's own immune cells to fight cancer has, for the first time, produced remissions in adults with an acute leukemia that is usually lethal, researchers are reporting."

Watch More:Tricking the Immune Systemhttp://www.youtube.com/watch?v=Kr_HRl...Babies with 3 Parents?!http://www.youtube.com/watch?v=jQxsW_...Pick Your Poison: Cyanidehttp://www.youtube.com/watch?v=JDBrdE...____________________

DNews is dedicated to satisfying your curiosity and to bringing you mind-bending stories & perspectives you won't find anywhere else! New videos twice daily.

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Maternalfetal medicine – Wikipedia

October 14th, 2018 5:42 am

Maternalfetal medicine (MFM) (also known as perinatology) is a branch of medicine that focuses on managing health concerns of the mother and fetus prior to, during, and shortly after pregnancy.

Maternalfetal medicine specialists are physicians who subspecialize within the field of obstetrics.[1] Their training typically includes a four-year residency in obstetrics and gynecology followed by a three-year fellowship. They may perform prenatal tests, provide treatments, and perform surgeries. They act both as a consultant during lower-risk pregnancies and as the primary obstetrician in especially high-risk pregnancies. After birth, they may work closely with pediatricians or neonatologists. For the mother, perinatologists assist with pre-existing health concerns, as well as complications caused by pregnancy.

Maternalfetal medicine began to emerge as a discipline in the 1960s. Advances in research and technology allowed physicians to diagnose and treat fetal complications in utero, whereas previously, obstetricians could only rely on heart rate monitoring and maternal reports of fetal movement. The development of amniocentesis in 1952, fetal blood sampling during labor in the early 1960s, more precise fetal heart monitoring in 1968, and real-time ultrasound in 1971 resulted in early intervention and lower mortality rates.[2] In 1963, Albert William Liley developed a course of intrauterine transfusions for Rh incompatibility at the National Women's Hospital in Australia, regarded as the first fetal treatment.[3] Other antenatal treatments, such as the administration of glucocorticoids to speed lung maturation in neonates at risk for respiratory distress syndrome, led to improved outcomes for premature infants.

Consequently, organizations were developed to focus on these emerging medical practices, and in 1991, the First International Congress of Perinatal Medicine was held, at which the World Association of Perinatal Medicine was founded.[2]

Today, maternal-fetal medicine specialists can be found in major hospitals internationally. They may work in privately owned clinics, or in larger, government-funded institutions.[4][5]

The field of maternal-fetal medicine is one of the most rapidly evolving fields in medicine, especially with respect to the fetus. Research is being carried on in the field of fetal gene and stem cell therapy in hope to provide early treatment for genetic disorders,[6] open fetal surgery for the correction of birth defects like congenital heart disease,[7] and the prevention of preeclampsia.

Maternalfetal medicine specialists attend to patients who fall within certain levels of maternal care. These levels correspond to health risks for the baby, mother, or both, during pregnancy.[8]

They take care of pregnant women who have chronic conditions (e.g. heart or kidney disease, hypertension, diabetes, and thrombophilia), pregnant women who are at risk for pregnancy-related complications (e.g. preterm labor, pre-eclampsia, and twin or triplet pregnancies), and pregnant women with fetuses at risk. Fetuses may be at risk due to chromosomal or congenital abnormalities, maternal disease, infections, genetic diseases and growth restriction.[9]

Expecting mothers with chronic conditions, such as high blood pressure, drug use during or before pregnancy, or a diagnosed medical condition may require a consult with a maternal-fetal specialist. In addition, women who experience difficulty conceiving may be referred to a maternal-fetal specialist for assistance.

During pregnancy, a variety of complications of pregnancy can arise. Depending on the severity of the complication, a maternal-fetal specialist may meet with the patient intermittently, or become the primary obstetrician for the length of the pregnancy. Post-partum, maternal-fetal specialists may follow up with a patient and monitor any medical complications that may arise.

The rates of maternal and infant mortality due to complications of pregnancy have decreased by over 23% since 1990, from 377,000 deaths to 293,000 deaths. Most deaths can be attributed to infection, maternal bleeding, and obstructed labor, and their incidence of mortality vary widely internationally.[10] The Society for Maternal-fetal Medicine (SMFM) strives to improve maternal and child outcomes by standards of prevention, diagnosis and treatment through research, education and training.[11]

Maternalfetal medicine specialists are obstetrician-gynecologists who undergo an additional 3 years of specialized training in the assessment and management of high-risk pregnancies. In the United States, such obstetrician-gynecologists are certified by the American Board of Obstetrician Gynecologists (ABOG) or the American Osteopathic Board of Obstetrics and Gynecology.

Maternalfetal medicine specialists have training in obstetric ultrasound, invasive prenatal diagnosis using amniocentesis and chorionic villus sampling, and the management of high-risk pregnancies. Some are further trained in the field of fetal diagnosis and prenatal therapy where they become competent in advanced procedures such as targeted fetal assessment using ultrasound and Doppler, fetal blood sampling and transfusion, fetoscopy, and open fetal surgery.[12][13]

For the ABOG, MFM subspecialists are required to do a minimum of 12 months in clinical rotation and 18-months in research activities. They are encouraged to use simulation and case-based learning incorporated in their training, a certification in advanced cardiac life support (ACLS) is required, they are required to develop in-service examination and expand leadership training. Obstetrical care and service has been improved to provide academic advancement for MFM in-patient directorships, improve skills in coding and reimbursement for maternal care, establish national, stratified system for levels of maternal care, develop specific, proscriptive guidelines on complications with highest maternal morbidity and mortality, and finally, increase departmental and divisional support for MFM subspecialists with maternal focus. As Maternalfetal medicine subspecialists improve their work ethics and knowledge of this advancing field, they are capable of reducing the rate of maternal mortality and maternal morbidity.[14]

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Supraspinatus Tendon Tear: Shoulder Pain PRP and Stem Cell …

October 14th, 2018 5:42 am

Supraspinatus Tendon Tear: Shoulder Pain Treated with PRP and Stem Cell Therapy

Tampa, Saint Petersburg and Clearwater, Fl

Platelet Rich Plasma (PRP) and Stem Cell Therapy are being used for a variety of shoulder problems. The rotator cuff is one of these shoulder problems that these regenerative therapies is used to treat by Dr. Dennis Lox. The rotator cuff is actually the tendinous insertion of 4 muscles muscles forming a cuff to protect the shoulder joint.

One of these muscles the Supraspinatus, is often injured and may develop tendonosis, partial tears, or unfortunately sometimes a complete tear. The Supraspinatus muscle may be treated with Platelet Rich Plasma (PRP) or Stem Cell Therapy. These regenerative therapies heal and repair by harnessing the bodies own natural healing properties and allowing them to repair in areas that cannot achieve this affect do to injury or poor blood supply. Blood supply is vital providing repair cells to regenerate and heal damaged tissue. Dr. Lox has great experience in treating these problems non-surgically. Improperly healing rotator cuff problems may lead to shoulder joint arthritis. Successful treatment and healing can help prevent degenerative arthritis of the shoulder. Surgery can lead to more shoulder joint trauma. Trauma has been shown to accelerate arthritis. Platelet Rich Plasma (PRP) and Stem Cell Therapy may be effective techniques to treat shoulder pain that wont go away.

Click Here for more ways (PRP) and Stemcells can help

Dr. Dennis Loxserves patients in the greater Tampa Bay area, including, Clearwater, St. Petersburg, Tampa, New Port Richey, Sarasota, and Spring Hill. He has been pleased to accommodate the needs of patients throughout Florida, the United States, the Western Hemisphere, and Europe, as well. Located in the 33765 and 33765 areas, our offices can be reached at (727) 462-5582 (Clearwater) and (727) 817-1909 (New Port Richey). Call to schedule your visit today.

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Vector (molecular biology) – Wikipedia

October 13th, 2018 1:41 am

In molecular cloning, a vector is a DNA molecule used as a vehicle to artificially carry foreign genetic material into another cell, where it can be replicated and/or expressed (e.g.- plasmid, cosmid, Lambda phages). A vector containing foreign DNA is termed recombinant DNA. The four major types of vectors are plasmids, viral vectors, cosmids, and artificial chromosomes. Of these, the most commonly used vectors are plasmids.[1] Common to all engineered vectors are an origin of replication, a multicloning site, and a selectable marker.

The vector itself is generally a DNA sequence that consists of an insert (transgene) and a larger sequence that serves as the "backbone" of the vector. The purpose of a vector which transfers genetic information to another cell is typically to isolate, multiply, or express the insert in the target cell. All vectors may be used for cloning and are therefore cloning vectors, but there are also vectors designed specially for cloning, while others may be designed specifically for other purposes, such as transcription and protein expression. Vectors designed specifically for the expression of the transgene in the target cell are called expression vectors, and generally have a promoter sequence that drives expression of the transgene. Simpler vectors called transcription vectors are only capable of being transcribed but not translated: they can be replicated in a target cell but not expressed, unlike expression vectors. Transcription vectors are used to amplify their insert.

The manipulation of DNA is normally conducted on E. coli vectors, which contain elements necessary for their maintenance in E. coli. However, vectors may also have elements that allow them to be maintained in another organism such as yeast, plant or mammalian cells, and these vectors are called shuttle vectors. Such vectors have bacterial or viral elements which may be transferred to the non-bacterial host organism, however other vectors termed intragenic vectors have also been developed to avoid the transfer of any genetic material from an alien species.[2]

Insertion of a vector into the target cell is usually called transformation for bacterial cells,[3] transfection for eukaryotic cells,[4] although insertion of a viral vector is often called transduction.[5]

Plasmids are double-stranded extra chromosomal and generally circular DNA sequences that are capable of replication using the host cell's replication machinery.[6] Plasmid vectors minimalistically consist of an origin of replication that allows for semi-independent replication of the plasmid in the host. Plasmids are found widely in many bacteria, for example in Escherichia coli, but may also be found in a few eukaryotes, for example in yeast such as Saccharomyces cerevisiae.[7] Bacterial plasmids may be conjugative/transmissible and non-conjugative:

Plasmids with specially-constructed features are commonly used in laboratory for cloning purposes. These plasmid are generally non-conjugative but may have many more features, notably a "multiple cloning site" where multiple restriction enzyme cleavage sites allow for the insertion of a transgene insert. The bacteria containing the plasmids can generate millions of copies of the vector within the bacteria in hours, and the amplified vectors can be extracted from the bacteria for further manipulation. Plasmids may be used specifically as transcription vectors and such plasmids may lack crucial sequences for protein expression. Plasmids used for protein expression, called expression vectors, would include elements for translation of protein, such as a ribosome binding site, start and stop codons.

Viral vectors are generally genetically engineered viruses carrying modified viral DNA or RNA that has been rendered noninfectious, but still contain viral promoters and also the transgene, thus allowing for translation of the transgene through a viral promoter. However, because viral vectors frequently are lacking infectious sequences, they require helper viruses or packaging lines for large-scale transfection. Viral vectors are often designed for permanent incorporation of the insert into the host genome, and thus leave distinct genetic markers in the host genome after incorporating the transgene. For example, retroviruses leave a characteristic retroviral integration pattern after insertion that is detectable and indicates that the viral vector has incorporated into the host genome.

Artificial chromosomes are manufactured chromosomes in the context of yeast artificial chromosomes (YACs), bacterial artificial chromosomes (BACs), or human artificial chromosomes (HACs). An artificial chromosome can carry a much larger DNA fragment than other vectors.[8] YACs and BACs can carry a DNA fragment up to 300,000 nucleotides long. Three structural necessities of an artificial chromosome include an origin of replication, a centromere, and telomeric end sequences.[9]

Transcription of the cloned gene is a necessary component of the vector when expression of the gene is required: one gene may be amplified through transcription to generate multiple copies of mRNAs, the template on which protein may be produced through translation.[10] A larger number of mRNAs would express a greater amount of protein, and how many copies of mRNA are generated depends on the promoter used in the vector.[11] The expression may be constitutive, meaning that the protein is produced constantly in the background, or it may be inducible whereby the protein is expressed only under certain condition, for example when a chemical inducer is added. These two different types of expression depend on the types of promoter and operator used.

Viral promoters are often used for constitutive expression in plasmids and in viral vectors because they normally force constant transcription in many cell lines and types reliably.[12] Inducible expression depends on promoters that respond to the induction conditions: for example, the murine mammary tumor virus promoter only initiates transcription after dexamethasone application and the Drosophilia heat shock promoter only initiates after high temperatures.

Some vectors are designed for transcription only, for example for in vitro mRNA production. These vectors are called transcription vectors. They may lack the sequences necessary for polyadenylation and termination, therefore may not be used for protein production.

Expression vectors produce proteins through the transcription of the vector's insert followed by translation of the mRNA produced, they therefore require more components than the simpler transcription-only vectors. Expression in different host organism would require different elements, although they share similar requirements, for example a promoter for initiation of transcription, a ribosomal binding site for translation initiation, and termination signals.

Eukaryote expression vectors require sequences that encode for:

Modern artificially-constructed vectors contain essential components found in all vectors, and may contain other additional features found only in some vectors:

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Sanford School of Medicine | USD

October 11th, 2018 1:41 pm

This workshop offers guidelines for creating the first draft of a scientific research paper, as well as addressing revision strategies. You'll also learn what distinguishes a strong research paper from a weak one. The workshop presenter is Jeff Wesner, Assistant Professor, Department of Biology. DISTANCE STUDENTS: to attend live online, log into D2L and select the Online Writing Center (if you don't see the link, email wcenter@usd.edu to be added). Under Communications, select Collaborate Ultra. Then, select the link for the current workshop.

Presenter: Angela Campbell, MD, MPH, FAAP, FPIDS, FIDSA, Medical Officer, Influenza Division, Center for Disease Control, Atlanta, GALocation: Sanford USD Medical Center, Schroeder Auditorium, Videoconferenced to registered videoconferencing sites.

Company representatives will be available to discuss their job and internship opportunities and answer your questions. All majors and years welcome.

"Systems Based Practice" - Michael Wilde, M.D., FACP, Vice President Medical Officer, Sanford, Sioux Falls

Stop by to learn about a variety of internship opportunities.

South Dakota middle school and high school students take part in several scientific events throughout the USD campus starting at 9:00 am. The opening ceremony will start at 8:30 am in Aalfs Auditorium, Slagle Hall. The awards ceremony will start at 5:00 pm in Aalfs Auditorium, Slagle Hall.South Dakota Science Olympiad605-658-5973sdscienceolympiad@usd.edu

IdeaFest is an annual campus event celebrating student research, creative scholarship and academic engagement. Undergraduate and graduate students in all disciplines present their work in oral and poster presentations, live performances, readings, exhibits and displays. Keynote speakers are invited to present their involvement in similar endeavors.

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7 Health Problems Eye Exams Can Detect – Your Sight Matters

October 10th, 2018 3:44 pm

Did you know that an eye exam can be as effective as a physical in determining your health? Unfortunately, many Americans put off going to the eye doctor if they feel like their vision has not changed. Comprehensive eye exams are important for many reasons. Your eyesight may change very gradually over time, and you may not even know that you need a stronger prescription. Your eye doctor will also perform several tests during the eye examination that will rule out eye disorders such as glaucoma, cataracts or retinal problems.

Along with eye-related concerns, eye doctors may even be able to detect other health issues during a comprehensive eye exam. In fact, you may even find yourself leaving the eye doctor with a referral to another specialist because of a specific test that your ophthalmologist performed during your comprehensive eye exam. Here are just a few health issues that may be discovered during an eye exam:

Comprehensive eye exams are recommended once every two years for optimum eye health and overall wellness. If you are not currently under the care of an eye doctor, you can locate a physician in your area using our physician locator tool.

Related Articles:

Comprehensive Eye Exams Can Help Identify Chronic Conditions

Preventative Eye Care: A Worthy Investment

Tags: cataracts, diabetes, eye exam, eye health, high cholesterol, hypertension, lupus, physical, thyroid, tumors

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Top 18 Biotechnology ETFs – ETFdb.com

October 8th, 2018 11:45 am

ETF Overview

This is a list of all Biotechnology ETFs traded in the USA which are currently tagged by ETF Database. Please note that the list may not contain newly issued ETFs. If youre looking for a more simplified way to browse and compare ETFs, you may want to visit our ETFdb.com Categories, which categorize every ETF in a single best fit category.

* Assets and Average Volume as of 2018-10-05 20:19 UTC

This page includes historical return information for all Biotechnology ETFs listed on U.S. exchanges that are currently tracked by ETF Database.

The table below includes fund flow data for all U.S. listed Biotechnology ETFs. Total fund flow is the capital inflow into an ETF minus the capital outflow from the ETF for a particular time period.

Fund Flows in millions of U.S. Dollars.

The following table includes expense data and other descriptive information for all Biotechnology ETFs listed on U.S. exchanges that are currently tracked by ETF Database. In addition to expense ratio and issuer information, this table displays platforms that offer commission-free trading for certain ETFs.

Clicking on any of the links in the table below will provide additional descriptive and quantitative information on Biotechnology ETFs.

The following table includes ESG Scores and other descriptive information for all Biotechnology ETFs listed on U.S. exchanges that are currently tracked by ETF Database. Easily browse and evaluate ETFs by visiting our ESG Investing themes section and find ETFs that map to various environmental, social, governance and morality themes.

This page includes historical dividend information for all Biotechnology ETFs listed on U.S. exchanges that are currently tracked by ETF Database. Note that certain ETPs may not make dividend payments, and as such some of the information below may not be meaningful.

The table below includes basic holdings data for all U.S. listed Biotechnology ETFs that are currently tagged by ETF Database. The table below includes the number of holdings for each ETF and the percentage of assets that the top ten assets make up, if applicable. For more detailed holdings information for any ETF, click on the link in the right column.

The following table includes certain tax information for all Biotechnology ETFs listed on U.S. exchanges that are currently tracked by ETF Database, including applicable short-term and long-term capital gains rates and the tax form on which gains or losses in each ETF will be reported.

This page contains certain technical information for all Biotechnology ETFs that are listed on U.S. exchanges and tracked by ETF Database. Note that the table below only includes limited technical indicators; click on the View link in the far right column for each ETF to see an expanded display of the products technicals.

This page provides links to various analysis for all Biotechnology ETFs that are listed on U.S. exchanges and tracked by ETF Database. The links in the table below will guide you to various analytical resources for the relevant ETF, including an X-ray of holdings, official fund fact sheet, or objective analyst report.

This page provides ETFdb Ratings for all Biotechnology ETFs that are listed on U.S. exchanges and tracked by ETF Database. The ETFdb Ratings are transparent, quant-based evaluations of ETFs relative to other products in the same ETFdb.com Category. As such, it should be noted that this page may include ETFs from multiple ETFdb.com Categories.

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Biotechnology Conferences | Biotechnology Congress | 2018 …

October 8th, 2018 11:45 am

About the conference

Biotechnology International Conferences invites all the participants from all over the world to attend 4thInternational Conference onAdvances in Biotechnology and Bioscience during November 15-17, 2018 in Berlin, Germany which includes prompt keynote presentations, Oral Talks, Poster Presentations, Exhibitions.

Biotechnologyis a field which interrelates biological sciences with engineering technologies to increase living organisms and biological systems to produce products . We bring together a diversity of disciplines that complement one another to unravel the complexity of biology. We incorporate the physical sciences, engineering, mathematics, computational and bioinformatics, and the social sciences, as appropriate, to problems we are addressing. We work with animals, plants and microorganisms and our research span the levels of the biological hierarchy from molecules to ecosystems.Bioscienceis defined as technologies that relate to therapeutic or diagnostic products or services, including medical devices and digital health technologies that improve human health. Also included in the state definition are technologies that rely on research to improve agricultural output. As name Bioscience reflects a belief that the study of biological systems is best approached by incorporating many perspectives.

Biotechnology International organizeconferences of 1000+ Global Events inclusive of 300+ Conferences, 500+ Upcoming and Previous Symposiums and Workshops in the USA, Europe & Asia with support from 1000 more scientificsocietiesand publishes 700+Open access journalswhich contains over 30000 eminent personalities, reputed scientists as editorial board members.

Why to attend???

This unique international conference provides a platform for researchers and decision makers in Biotechnology and Bioscience to present their latest findings and learn about all the important developments in Biotechnology and Bioscience. Many scientists and world's renowned experts will participate in the conference. Throughout the course of the two-day conference, you will have the opportunity to both networks and hear leaders from the international academic and corporate bioscience communities.

Target Audience:

The conference will attract a large group of scientists and researchers from around the globe. Delegates will have a valuable, informative and positive experience.

Track: Biotechnology

Biotechnologyis the usage of living systems and organisms to develop or make products, mark or modify products or processes for specific use". Science and innovation have in the past presumed an indispensable part in enhancing general wellbeing.Biotechnology has noteworthy applications in therapeutics, diagnostics, genetically modified crops for agriculture, processed food, bioremediation, waste treatment, and energy production. Biotechnology has likewise prompted to the advancement of anti-infection agents.

Related Biotechnology Conferences | Genetic Engineering Conferences | Pharmaceutical Chemistry Conferences | Biological Engineering Conferences | Bio economy Conferences | Biomedicine Conferences | Microbiology Conferences | Molecular Biology Conferences | Nano-Biotechnology Conferences | Biology Conferences | Embryology Conferences | Pharmacogenomics Conferences

21st European Biotechnology Congress, October 11-13, 2018 Moscow, Russia; 22nd Global Biotechnology Congress September 10-11, 2018 Stockholm, Sweden; 4th Synthetic Biology Conferences October 18-19, 2018 Rome, Italy; 4th Tissue Engineering Conferences; October 18-19, 2018 Rome, Italy; 11th Tissue Engineering Conferences October 18-20, 2018 Rome, Italy; 11th Regenerative Medicine Conferences October 18-20, 2018 at Rome, Italy; The 2nd edition of Biotech France 2018 International Conference and Exhibition June 27 -29, 2018 Paris, France; BIO World Congress on Industrial Biotechnology July 16 - 19, 2018 Philadelphia, Pennsylvania; World Biotechnology Conference June 25-27, 2018 Stockholm, Sweden; International Biotechnology and Research Conference April 25-27, 2018 Rome, Italy

Related Societies:

Europe: Spanish Society of Biotechnology, The Pharmaceutical Society of Ireland, Russian Medical Society, Society for Engineering in Agriculture, Society of Microbial Ecology and Disease, Manchester University Pharmaceutical Society, Italian Society of Biochemistry and Molecular Biology, European Society for Precision Engineering and Nanotechnology, Society for Chemical Engineering Biotechnology, Romanian Society of Medical Mycology and Mycotoxicology, New Zealand Plant Protection Society, International Society for Pharmaceutical Engineering, Pharmaceutical Society of Australia.

Related Societies:

Related Societies:

Related Societies:

Related Societies:

Related Societies:

Related Biotechnology Conferences | Genetic Engineering Conferences | Pharmaceutical Chemistry Conferences | Biological Engineering Conferences | Bio economy Conferences | Biomedicine Conferences | Microbiology Conferences | Molecular Biology Conferences | Nano-Biotechnology Conferences | Biology Conferences | Embryology Conferences | Pharmacogenomics Conferences

4th Glycobiology World Congress September 17-19, 2018 Rome, Italy; 13th Metabolomics Conferences October 11-12, 2018 Zurich, Switzerland; 13th Systems Biology Conferences October 11-12, 2018 Zurich, Switzerland; 14th Structural Biology Conferences September 24-26, 2018 Berlin, Germany; 12th Bioinformatics Conferences November 26-27, 2018 Dublin, Ireland; 12th Drug Discovery Conferences November 26-27, 2018 Dublin, Ireland; 12th Proteomics Expo November 26-28, 2018 Dublin, Ireland; 12th Molecular Medicine November 26-28, 2018 Dublin, Ireland; 5th Enzymology Conferences February 28-March 01, 2019 Berlin, Germany; Biomanufacturing Strategy Meeting June 11, 2018 Boston, United States; Biostimulants Summit 2018 June 27-28, 2018 Chicago, United States; European Microbiology and Research Conference July 04-06, 2018 Rome, Italy; Molecular Diagnostics July 09-10, 2018; London, UK; 18th International Biotechnology Symposium and Exhibition August 12-17, 2018 Montral, Canada; International Conference On Nanomedicine And Nanobiotechnology September26-28, 2018 Rome, Italy; Marine Biotechnology October 08-12, 2018 Naples, Italy; 2nd International Probiotics, Nutrition & Microbiome Conference October 10-12, 2018 Amsterdam, Netherlands

Related Societies:

Related Biotechnology Conferences | Genetic Engineering Conferences | Pharmaceutical Chemistry Conferences | Biological Engineering Conferences | Bio economy Conferences | Biomedicine Conferences | Microbiology Conferences | Molecular Biology Conferences | Nano-Biotechnology Conferences | Biology Conferences | Embryology Conferences | Pharmacogenomics Conferences

4th Synthetic Biology Conferences October 18-19, 2018 Rome, Italy; 4th Tissue Engineering Conferences; October 18-19, 2018 Rome, Italy; 11th Tissue Engineering Conferences October 18-20, 2018 Rome, Italy; 11th Regenerative Medicine Conferences October 18-20, 2018 at Rome, Italy; 10th Stem Cell Conferences October 08-09, 2018 Zurich, Switzerland; 10th Regenerative Medicine Conferences October 08-09, 2018 Zurich, Switzerland; 9th Cell Conferences March 21-23, 2019 Rome, Italy; 9th Gene Therapy Exhibitions March 21-23, 2019 Rome, Italy; 4th Glycobiology World Congress September 17-19, 2018 Rome, Italy; 13th Metabolomics Conferences October 11-12, 2018 Zurich, Switzerland; 13th Systems Biology Conferences October 11-12, 2018 Zurich, Switzerland; BIO World Congress on Industrial Biotechnology July 16 - 19, 2018 Philadelphia, Pennsylvania; World Biotechnology Conference June 25-27, 2018 Stockholm, Sweden; International Biotechnology and Research Conference April 25-27, 2018 Rome, Italy; 2nd World Congress and Expo on Biotechnology and Bioengineering June 25-27, 2018, Dubai, UAE; BIO Asia International Conference March 5 - 6, 2019 Tokyo, Japan; BIO Patient and Health Advocacy Summit October 25 - 26, 2018 Washington, DC

Related Societies:

Related Societies:

Related Societies:

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Biotech – Scientific American

October 8th, 2018 11:45 am

Draft guidelines permit gene-editing tools for research into early human development, but would discourage manipulation of embryos for reproduction

5 minutes ago David Cyranoski and Nature magazine

James P. Allison and Tasuku Honjo share the Nobel Prize for their work on harnessing the cancer patient's own immune system to destroy tumors.

October 1, 2018 Steve Mirsky

Researchers at the Mount Sinai Diabetes Center have already developed an artificial pancreas. Next, a drug that could regenerate pancreatic cells in the body.

September 12, 2018

Immunologist James Allison has spent over thirty years studying T cells and developing strategies for cancer immunotherapy. Now, hes looking at new ways to unleash the immune system to eradicate cancer.

September 12, 2018

Interview: Joan Argetsinger Steitz weighs in on #MeToo and working with James Watson

September 11, 2018 Dina Fine Maron

New device gives an amputee the ability to feel the location of his foot

August 9, 2018 Simon Makin

As Ebola outbreaks occur again and again, the scramble for answers and medications is ongoing

August 6, 2018

Shutting down an overactive enzyme could become a general treatment, rather than one solely intended for the few who inherit a mutated Parkinsons gene

August 6, 2018 Emily Willingham

A flurry of recent findings highlighta contentious question in this area

July 16, 2018 Sharon Begley and STAT

A next-generation cochlear implant might allow the hearing-impaired to listen to music and cope with noise

July 16, 2018 Simon Makin

Activating the reward system boosts anti-tumor immunity in mice

July 13, 2018 Esther Landhuis

The controversy over how many genes are contained in the human genome continues to simmer

June 19, 2018 Cassandra Willyard and Nature magazine

The preliminary findings raise questions about one of the ways this tech edits genomes

June 12, 2018 Sharon Begley and STAT

Three patients in Japan will receive the experimental therapy in the next year

May 30, 2018 David Cyranoski and Nature magazine

The swallowable device looks promising in pigs

May 24, 2018 Andrew Joseph and STAT

A new technique could replace the need for human embryos in some lab experiments

May 24, 2018 Sara Reardon and Nature magazine

Racing pigeons is big businessand doping is common. Now scientists have devised a way to detect doping in the avian athletes. Christopher Intagliata reports.

May 15, 2018 Christopher Intagliata

Researchers are intent on decoding body-brain nerve signals to diagnose ailments

May 10, 2018 Tim Hornyak

Chinas move is expected to complement other countriesrelated initiatives

April 6, 2018 David Cyranoski and Nature magazine

Cancerous cells may pick up the characteristics of nearby organs, evading treatment

March 29, 2018 Meghana Keshavan and STAT

Discover world-changing science. Explore our digital archive back to 1845, including articles by more than 150 Nobel Prize winners.

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Department of Microbiology and Molecular Genetics

October 7th, 2018 12:44 am

I welcome you to the Department of Microbiology and Molecular Genetics. Our department is uniquely positioned in two colleges at the University of Vermont: the Robert Larner, M.D., College of Medicine (LCOM) and the College of Agriculture and Life Sciences (CALS). At CALS, MMG hosts two outstanding undergraduate majors, Microbiology and Molecular Genetics. Our highly-recognized faculty educators work closely with our undergraduate students throughout their years at UVM as they become excellent scientists and innovative, critical thinkers. At LCOM, our faculty are closely engaged with teaching and training medical students, as well as graduate students, in our Cellular, Molecular and Biomedical Sciences (CMB) Ph.D. program and Medical Masters program.

Our faculty are highly focused on research, which spans from basic-science inquiry in the fields of Microbiology; Cell, Molecular and Structural biology; to applied and translational research in human immunology, vaccine, and bioinformatics and genetics. MMG hosts a nationally recognized team exploring the mechanisms of DNA Repair, research that is critically important to human diseases, including cancer. The recent addition of the UVM Vaccine Testing Center team to MMG complements our research portfolio by adding significant new depth in clinical and translational human immunology and vaccinology, as well as U.S.-based and international clinical trials, all with a focus on preventing and controlling infectious diseases of global importance.

Thank you for your interest in MMG. We look forward to hearing from you!

Beth Kirkpatrick, M.D.Professor and Chair, Department of Microbiology and Molecular GeneticsDirector, Vaccine Testing Center

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Integrative Medicine of Central New York, PC | Chittenango …

October 7th, 2018 12:42 am

Meet Your Practitioners

HEIDI S. PUC MD, FACP, ABIHM

Heidi S. Puc MD, FACP, ABIHM, is a board-certified hematologist and medical oncologist with over 20 years of experience in the private practice of adult hematology and oncology, after having completed fellowship training at Memorial Sloan Kettering Cancer Center. She received specialty training in Integrative Medicine through the Scripps Clinic in California, and also completed a two-year fellowship program run by Dr. Andrew Weil at the University of Arizona. She developed an integrative oncology consultative practice within her conventional hematology/oncology position at HOACNY, until she joined The Stram Center for Integrative Medicine in October 2015. At The Stram Center, Dr. Puc provided integrative medicine and integrative oncology consultations and services in conjunction with conventional approaches provided by the primary oncologist. These integrative approaches included incorporating nutritional and herbal supplements, and mind-body therapies. There, she also managed patients with Lyme disease, and has undergone training through the International Lyme and Associated Diseases Society (ILADS) as well as a mentorship with Dr. Richard Horowitz, a specialist in the field. She is a Fellow of the American College of Physicians and a Diplomate of the American Board of Integrative Holistic Medicine. She is a member of the American Society of Clinical Oncology, The American College of Physicians, the Society for Integrative Oncology, and ILADS.Dr. Puc also has Energy Medicine Certifications in Reiki Levels I and II, Basic Pranic Healing, and is a Seichim Master, and personally practices Transcendental Meditation. Dr. Heidi Puc is very excited to announce the opening of her own integrative medicine practice in her Syracuse area home town.

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Integrative Health Services for Adults | NYU Langone Health

October 7th, 2018 12:42 am

NYU Langone offers integrative health, health promotion, and wellness programs to complement your conventional healthcare. Services are offered to patients, caregivers, and anyone in the NYU Langone community through the Lerner Health Promotions Program.

Integrative health practitioners can help you manage the physical and emotional side effects of your treatment, as well as provide services that help you stay well. We help as you prepare for treatment and provide care during your hospital stay and after you return home.

Our services include mindbody bedside care, acupuncture, guided imagery, massage, energy therapies, yoga, and more. Our staff of licensed professionals works with nearly 5,000 people per year, including more than 3,000 through our MindBody Patient Bedside Program and more than 400 through the Prepare for Surgery, Heal Faster program. We also partner with The Monday Campaigns to share healthy behavior reminders with patients and staff on topics such as eating less meat, exercising more, and limiting stress.

To learn more about our integrative health programs, please call 212-263-5767 or email mindbody@nyulangone.org. Patients at Tisch Hospital and Kimmel Pavilion can ask your healthcare provider to make a referral.

We thank Sid and Helaine Lerner, who since 1996 have provided generous support for our integrative health and health promotion services.

Learn more about our integrative health services at NYU Langones Rusk Rehabilitation, Hassenfeld Childrens Hospital at NYU Langone, Perlmutter Cancer Center, and Stephen D. Hassenfeld Childrens Center for Cancer and Blood Disorders.

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Integrative Medicine Clinic in Ashburn, VA

October 6th, 2018 5:45 am

Integrative Medical Approach

Integrative medicine places the patient at the center of a holistic approach to medical care. Patient's individual needs, risks, and goals are the main driving forces of any integrative therapy. Physicians practicing integrative medicine emphasize that treatment of every aspect of a person's health is crucial to the success of the healing process:

To request more information, please contact our Ashburn integrative medicine clinic today! Call (703) 327-2434 or contact Dr. Andrew Heyman online.

Integrative medicine is a multi-disciplinary approach that combines the scientific advances and a variety of effective therapies to treat disease.

Integrative medicine combines conventional and complementary treatment options to achieve optimal health for the patient. It is based on the research which demonstrates that the human body has an innate healing mechanism. Illness occurs when the regenerative processes in the body are disturbed, and the body can no longer keep itself healthy.

Integrative medicine emphasizes the use of the least invasive treatment options necessary to bring the body to a healthy state.

Integrative medicine physicians focus on health optimization and often combine a variety of methods to optimize their patients' health:

To request more information, please contact our Ashburn integrative medicine clinic today! Call (703) 327-2434 or contact Dr. Andrew Heyman online.

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Integrative Medicine Clinic in Ashburn, VA

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Fat-Derived Stem Cells vs Bone Marrow – ThriveMD

October 5th, 2018 3:44 am

Stromal vascular fraction was dramatically better than bone marrow concentrate in its ability to differentiate into cartilage.Two other important features were also well documented. SVF created significantlymore colony forming units than BMC, another significant predictor of healingresponse. And perhaps most importantly, SVF was dramatically better than BMC inits ability to differentiate into cartilage.

Second, arecent study byHan Chao et alhas also demonstrated that fat derived stem cells also have a higher proliferation potential for neural tissue and are a better source for not only cartilage regeneration but also for nervous system regeneration.

Adipose fat tissue provides the largest volume of adult stem cells (1,000 to 2,000 times the number of cells per volume found in bone marrow). Bone marrow provides some stem cells but more importantly provides a large volume of growth factors to aid in the repair process. In addition to adult stem cells, fat tissue also contains numerous other regenerative cells that are important to the healing process. Stem cells derived from adipose fat tissue have been shown to be a much better source for the repair of cartilage degeneration and recent studies have demonstrated its superior ability to differentiate into cartilage.

The studies gavea very comprehensive look at comparing BMC and SVF in the abilityto repair cartilage damage in a same procedure protocol. Every significantmeasurement comparing bone marrow to adipose tissue for stem cell harvesting demonstrated that adipose providedbetter cell content and superior ability to differentiate into cartilage than bone marrow. Our extensive clinical experience withthe procedureforColorado patientsclearly indicates the same.

*Individual patient results may vary. Contact us today to find out if stem cell therapy may be able to help you.

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EasySep Human Nave CD4+ T Cell Isolation Kit

October 3rd, 2018 8:42 pm

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EasySep Human Nave CD4+ T Cell Isolation Kit

EasySep Human Nave CD4+ T Cell Isolation Kit

For even faster cell isolations, we recommend the new EasySep Human Nave CD4+ T Cell Isolation Kit II (17555) which isolates cells in just 11 minutes.

Advantages:

Fast, easy-to-use and column-free Up to 96% purity Isolated cells are untouched

Magnet Compatibility:

EasySep Magnet (Catalog #18000)

The Big Easy EasySep Magnet (Catalog #18001)

Easy 50 EasySep Magnet (Catalog #18002)

EasyEights EasySep Magnet (Catalog #18103)

RoboSep-S (Catalog #21000)

Subtype:

Cell Isolation Kits

Cell Type:

T Cells; T Cells, CD4+

Selection Method:

Negative

Application:

Cell Isolation

Area of Interest:

Immunology

Document Type

Product Name

Catalog #

Lot #

Language

Yes. The EasySep kits use either a negative selection approach by targeting and removing unwanted cells or a positive selection approach targeting desired cells. Depletion kits are also available for the removal of cells with a specific undesired marker (e.g. GlyA).

Magnetic particles are crosslinked to cells using Tetrameric Antibody Complexes (TAC). When placed in the EasySep Magnet, labeled cells migrate to the wall of the tube. The unlabeled cells are then poured off into a separate fraction.

The EasySep procedure is column-free. That's right - no columns!

The Product Information Sheet provided with each EasySep kit contains detailed staining information.

Yes. RoboSep, the fully automated cell separator, automates all EasySep labeling and cell separation steps.

Yes. We recommend a cell concentration of 2x108 cells/mL and a minimum working volume of 100 L. Samples containing 2x107 cells or fewer should be suspended in 100 L of buffer.

Yes, the EasySep particles are flow cytometry-compatible, as they are very uniform in size and about 5000X smaller than other commercially available magnetic beads used with column-free systems.

No, but due to the small size of these particles, they will not interfere with downstream applications.

Yes; however, this may impact the kit's performance. The provided EasySep protocols have already been optimized to balance purity, recovery and time spent on the isolation.

Yes, the purity of targeted cells will increase with additional rounds of separations; however, cell recovery will decrease.

If particle binding is a key concern, we offer two options for negative selection. The EasySep negative selection kits can isolate untouched cells with comparable purities, while RosetteSep can isolate untouched cells directly from whole blood without using particles or magnets.

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This product is designed for use in the following research area(s) as part of the highlighted workflow stage(s). Explore these workflows to learn more about the other products we offer to support each research area.

Research Area Workflow Stages for

Workflow Stages

Figure 1. Typical EasySep Human Nave CD4+ T Cell Isolation Profile

Starting with a single-cell suspension of PBMCs, the nave CD4+ T cell (CD3+CD4+CD45RA+CD45RO-) content of the isolated fraction typically ranges from 91.3% - 96.9%. In the example above, the purities of the start and isolated fraction are 11.1% and 93.2%, respectively.

Bjö et al.

Staphylococcus aureus (S. aureus) is a human pathogen as well as a frequent colonizer of skin and mucosa. This bacterium potently activates conventional T-cells through superantigens and it is suggested to induce T-cell cytokine-production as well as to promote a regulatory phenotype in T-cells in order to avoid clearance. This study aimed to investigate how S. aureus impacts the production of regulatory and pro-inflammatory cytokines and the expression of CD161 and HELIOS by peripheral CD4(+)FOXP3(+) T-cells. Stimulation of PBMC with S. aureus 161:2-cell free supernatant (CFS) induced expression of IL-10, IFN- and IL-17A in FOXP3(+) cells. Further, CD161 and HELIOS separated the FOXP3(+) cells into four distinct populations regarding cytokine-expression. Monocyte-depletion decreased S. aureus 161:2-induced activation of FOXP3(+) cells while pre-stimulation of purified monocytes with S. aureus 161:2-CFS and subsequent co-culture with autologous monocyte-depleted PBMC was sufficient to mediate activation of FOXP3(+) cells. Together, these data show that S. aureus potently induces FOXP3(+) cells and promotes a diverse phenotype with expression of regulatory and pro-inflammatory cytokines connected to increased CD161-expression. This could indicate potent regulation or a contribution of FOXP3(+) cells to inflammation and repression of immune-suppression upon encounter with S. aureus.

STEMCELL TECHNOLOGIES INC.S QUALITY MANAGEMENT SYSTEM IS CERTIFIED TO ISO 13485. PRODUCTS ARE FOR RESEARCH USE ONLY AND NOT INTENDED FOR HUMAN OR ANIMAL DIAGNOSTIC OR THERAPEUTIC USES UNLESS OTHERWISE STATED.

Internal Search Keywords: 19555|19555RF|19555C|19515|19155|19155RF|19155C|19115|Easy sep naive CD-4|Easy sep naive CD4 T

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Center for Sight | Ophthalmology in Pensacola, Gulf Breeze …

October 3rd, 2018 6:42 am

What is a Cataract?

A cataract is a clouding of the natural lens inside the eye that prevents you from seeing a clear image of objects at distance for reading and/or close work. Primarily because of the eyes natural aging process, cataracts begin developing in almost everyone before they reach the age of 60.

Most cataracts are associated with a gradual aging process in the natural lens of the eye over a period of years, and annual eye exams can best judge the progression of these changes. At this time, there is no current medical treatment for cataracts although the National Eye Institute (NEI) is funding studies to see whether taking certain vitamins and minerals can prevent or delay cataracts.

Common cataract symptoms

The detection of a cataract can only be accomplished by a thorough dilated eye examination. An eye physician must determine if your vision is being affected by a cataract or other eye disorders which may present similar vision problems. Patients with a family history of eye disorders, medical problems such as diabetes, or previous injuries to the eye are especially prone to vision problems.

Cataract surgery is an outpatient procedure performed in a sterile operating room. It takes approximately 30 minutes to perform. A very small incision into the eye is made to allow the insertion of a fine probe which then breaks the cataract up into small pieces that are easily removed. Next, an intraocular lens (IOL) is inserted into the same location where the cataract was removed. Like the natural lens of the eye, an IOL focuses images onto the retina, which are then transferred by the optic nerve to the brain. The IOL is made of a flexible silicone or acrylic material designed to be compatible with the natural eye tissue. Your IOL will hold the appropriate prescription providing you with the best vision possible. The cost of cataract surgery is generally covered by standard medical insurance policies, with the exception of co-pays and deductibles.

At least two weeks prior to surgery, a technician will measure your eyes in order to determine your IOL prescription. This measurement is called an ASCAN or LenSTAR. This measurement will allow your doctor to choose the type of IOL that is right for you. IOL types consist of standard, Monofocal, Multifocal, and Toric.

When Monofocals are chosen, the IOLs are set in order to improve distance vision. Therefore, you will likely use reading glasses to view objects up close. Likewise, if the IOLs are set to improve near vision, glasses will likely be used to clearly view objects from a distance. After the age of 40, a condition called Presbyopia takes effect on the eyes natural lens. Presbyopia weakens the flexibility of the lens, making near vision more difficult. Consequently, even without the presence of cataracts, reading glasses or an equivalent form of vision corrective surgery could be required.

Multifocal IOLs are embedded with a series of focal rings. The rings allow both near and far images to be seen clearly, based on where the incoming light is focused through the rings. The need to use glasses always varies from person to person, but is generally decreased with the use of Multifocal IOLs in both eyes. Usually it takes 6 to 12 weeks after surgery is completed on the second eye for the brain to fully adapt and for your vision to fully improve. This is true for all types of IOLs.

*Be aware that Multifocal lenses, while helping to improve both near and far vision, may allow for certain side effects such as halos around lights or decreased sharpness or contrast at night. Not all who use Multifocals are susceptible to these side effects, it just depends on how the brain adapts to your corrected vision. If you frequently drive at night or need to focus on near objects for an extended amount of time, you may be more satisfied with Monofocal IOLs.

The AcrySof IQ Toric IOLs are designed to correct corneal astigmatism, which is the inability of the eye to focus clearly at any distance because of different curvatures on the cornea. With astigmatism the cornea is curved like a football rather than round and smooth like a baseball. Toric lenses are most accommodating to those who have astigmatism to a substantial degree.

*We are proud to offer Multifocal Intraocular Lenses and IQ Toric intraocular Lenses. HOWEVER, please note that while cataract surgery is covered by insurance, these special lenses are not covered by insurance and will cost full price.

We offer surgical services at the following locations:

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Surrogacy laws by country – Wikipedia

October 3rd, 2018 6:42 am

Legal regulation of surrogacy in the world:

Both gainful and altruistic forms are legal

No legal regulation

Only altruistic is legal

Allowed between relatives up to second degree of consanguinity

Banned

Unregulated/uncertain situation

The legal aspects of surrogacy in any particular jurisdiction tend to hinge on a few central questions:

Laws differ widely from one jurisdiction to another.

In Australia, all jurisdictions except the Northern Territory allow altruistic surrogacy; with commercial surrogacy being a criminal offense. The Northern Territory has no legislation governing surrogacy.[1] In New South Wales, Queensland and the Australian Capital Territory it is an offence to enter into international commercial surrogacy arrangements with potential penalties extending to imprisonment for up to one year in Australian Capital Territory, up to two years imprisonment in New South Wales and up to three years imprisonment in Queensland.

In 2004, the Australian Capital Territory made only altruistic surrogacy legal.[2]

In 2006, Australian senator Stephen Conroy and his wife Paula Benson announced that they had arranged for a child to be born through egg donation and gestational surrogacy. Unusually, Conroy was put on the birth certificate as the father of the child. Previously, couples who used to make surrogacy arrangements in Australia had to adopt the child after it was registered as born to the natural mother; rather than being recognized as birth parents, however now that surrogacy is more regular practice for childless parents; most states have switched to such arrangements to give the intended parents proper rights.[3][4]After the announcement, Victoria passed the Assisted Reproductive Treatment Act 2008, effective since 1 January 2010 to make only altruistic surrogacy legal.[5]

In 2009, Western Australia[6] passed a law to allow only altruistic surrogacy for couples of the opposite-sex only, and to prohibit it for single people and same-sex couples. In 2010, Queensland made only altruistic surrogacy legal,[7] as did New South Wales,[8] and Tasmania did the same in 2013 with the Surrogacy Act No 34 and the Surrogacy (Consequential Amendments) Act No 31[9][10][11][12]

In 2017, South Australia passed a bill to allow gay couples equal access to both surrogacy and IVF. The bill received royal assent on 15 March 2017 and went into effect on 21 March 2017.[13][14][15][16][17]

A Medicare rebate is not available for IVF treatment for surrogacy.

Altrustic surrogacy is legal in Belgium.[18]

The Assisted Human Reproduction Act (AHRC) permits only altruistic surrogacy: surrogate mothers may be reimbursed for approved expenses but payment of any other consideration or fee is illegal.[19] Quebec law, however, does not recognize surrogacy arrangements, whether commercial or altruistic.

The Quebec Civil Code renders all surrogacy contracts, whether commercial or altruistic, unenforceable.[20]

There are no clear rules in Colombia as of today regarding surrogacy and a loophole persists. The current laws applied are those from a natural childbirth. This means the child must be registered with the surnames of the surrogate mother and her partner or spouse, if she has any. Only through a challenging paternity lawsuit before a judge may the commissioning parents be recognized as legal parents, and it may include genetic tests.[21]

In July 2016, a right wing political party, Democratic Center, has introduced for the second time a bill in order to determine the concept of surrogacy and to forbid any types of it.[22][23]

Surrogacy is not legally regulated in the Czech Republic and so is generally considered legal.[24] The only mention of the phrase "surrogate motherhood" can be found in 804 of the law n. 89/2012, where the law designates an exception to the ban of adoption by siblings for siblings carried by a surrogate mother.[25]

Altruistic surrogacy is legal in Denmark.

All surrogacy arrangements (both commercial and altruistic) have been illegal since 2007. Commercial surrogacy arrangements were illegal even before 2007.

In France, since 1994, any surrogacy arrangement that is commercial or altruistic, is illegal or unlawful and is not sanctioned by the law (art 16-7 of the Code Civil).[26]The French Court of Cassation already took this point of view in 1991. It held that if any couple makes an agreement or arranges with another person that she is to bear the husband's child and surrender it on birth to the couple, and that she is choosing that she will not keep the child, the couple making such an agreement or arrangement is not allowed to adopt the child. In its judgement the court held that such an agreement is illegal on the basis of articles 6, 353 and 1128 of the Code Civil.[27] In 2018, France government plans to allow surrogacy in France.

All surrogacy arrangements (both commercial and altruistic) are illegal. German party FDP wants to allow altruistic surrogacy.[28]

Surrogacy, along with ovum and sperm donation, has been legal in the country of Georgia since 1992. A donor or surrogate mother has no parental rights over such a child.[citation needed]

Law 3305/2005 (Enforcement of Medically Assisted Reproduction)Surrogacy in Greece is fully legal and is only one of a handful of countries in the world to give legal protection to intended parents. Intended parents must meet certain qualifications, and will go before a family judge before starting their journey. As long as they meet the qualifications, the court appearance is procedural and will be granted their application. At present, intended parents must be in a heterosexual partnership or be a single female. Females must be able to prove there is a medical indication they cannot carry and be no older than 50 at the time of the contract. As in all jurisdictions, surrogates must pass medical and psychological tests so they can prove to the court that they are medically and mentally fit. What is unique about Greece is that it is the only country in Europe, and one of only countries in the world where the surrogate then has no rights over the child. The intended parents become the legal parents from conception and there is no mention of the surrogate mother anywhere on hospital or birth documents. The intended parent(s) are listed as the parents. This even applies if an egg or sperm donor is used by one of the partners.An added advantage for Europeans is that, due to the Schengen Treaty, they can freely travel home as soon as the baby is born and deal with citizenship issues at that time, as opposed to applying at their own embassy in Greece.The old regime (pursuant to art. 8 of Law 3089/2002), one of the prerequisites for granting the judicial permission for surrogacy was also the fact that the surrogate mother and the commissioning parents should be Greek citizens or permanent residents.However, the law has recently (in July 2014) changed and the new provisions of L. 4272/2014 foresee now that the surrogacy is allowed to applicants or surrogate mothers who have their permanent or temporary residence in Greece.With this new law Greece becomes the only EU country with a comprehensive framework to regulate, facilitate and enforce surrogacy, as according to the explanatory statement of the art. 17 of the L. 4272/2014: The possibility is now extending also to applicants or surrogate mothers who have their permanent residence outside Greece.

Commercial surrogacy is criminal under the Human Reproductive Technology Ordinance 2000. The law is phrased in a manner that no one can pay a surrogate, no surrogate can receive money, and no one can arrange a commercial surrogacy (the same applies to the supply of gametes), no matter within or outside Hong Kong. Normally only the gametes of the intended parents can be used.

In October 2010, Peter Lee, the eldest son and one of the presumed heirs of billionnaire Lee Shau Kee obtained three sons through a surrogate mother, reportedly from California. Since the junior Lee is single, the news attracted criticism on both moral and legal grounds. A vicar general of the territory's Roman Catholic diocese was critical. In December the case was reportedly referred to police after questions were asked in Legco.[29]

Commercial surrogacy is illegal in Hungary.

All surrogacy arrangements (both commercial and altruistic) are illegal.

As of November 4, 2015 commercial surrogacy is not legal in India. Those commissioned before 11/4/2015 are reviewed on case by case situation; however, no new surrogacies will be started.[30]

Before 2015, commercial surrogacy was legal in India.[31] India was a desitination for surrogacy-related fertility tourism because of the relatively low cost. Including the costs of flight tickets, medical procedures, and hotels, it was roughly a third of the price compared with going through the procedure in the UK.[32] In the case of Balaz v. Union of India the Honorable Supreme Court of India has given the verdict that the citizenship of the child born through this process will have the citizenship of its surrogate mother. Surrogacy was regulated by the Indian Council of Medical Research guidelines, 2005.

There is no law in Ireland governing surrogacy. In 2005 a Government appointed Commission published a very comprehensive report on Assisted Human Reproduction, which made many recommendations on the broader area of assisted human reproduction. In relation to surrogacy it recommended that the commissioning couple would under Irish law be regarded as the parents of the child. Despite the publication there has been no legislation published and the area essentially remains unregulated. Due to mounting pressure from Irish citizens going abroad to have children through surrogacy, the Minister for Justice, Equality and Defence published guidelines for them on 21 February 2012.[33]

In March 1996, the Israeli government legalized gestational surrogacy under the "Embryo Carrying Agreements Law." This law made Israel the first country in the world to implement a form of state-controlled surrogacy in which each and every contract must be approved directly by the state.[34] A state-appointed committee permits surrogacy arrangements to be filed only by Israeli citizens who share the same religion.[35]The numerous restrictions on surrogacy under Israeli law have prompted some intended parents to turn to surrogates outside of the country. Same-sex couples can enter a surrogacy arrangement outside of Israel and have their legal parenthood recognized within Israel.

All surrogacy arrangements (both commercial and altruistic) are legal and popular. Many couples from middle east do the surrogacy in Iran due to the legal easiness.

All surrogacy arrangements (both commercial and altruistic) are illegal.

In March 2008, the Science Council of Japan proposed a ban on surrogacy and said that doctors, agents and their clients should be punished for commercial surrogacy arrangements.

Altruistic surrogacy is legal in the Netherlands.[36] Only commercial surrogacy is illegal in Belgium and the Netherlands. Although altrustic surrogacy is legal, there is only one hospital taking in couples and there are extremely strict rules to get in. This makes a lot of couples seek their treatment outside the Netherlands or Belgium.[37]

Altruistic surrogacy is legal.

Gestational surrogacy is currently practiced in Nigeria by a few IVF clinics. The guidelines are as approved by the practice guidelines of the Association of Fertility and Reproductive Health (AFRH) of Nigeria. The ART regulation that is currently being considered by the Senate permits surrogacy and allows some inducement to be paid for transport and other expenses.[38]

Surrogacy is illegal in Pakistan.[39]

Surrogacy is mostly unregulated in Poland.[40] A 2015 news report estimated there are likely dozens surrogate mothers in Poland.[41]

In 2016, Gestational surrogacy was legalized in Portugal. Discussions on the adoption of this law lasted more than 3 years. The first version of the law was adopted May 13, 2016, but the president vetoed it. He demanded that the law contained rights and obligations of all participants in the process of surrogacy. As a result, the text of the law has been updated, and now surrogacy is legalized and regulated by law in Portugal.

The basic rules of the law on surrogacy in PortugalUse the surrogacy services can only those couples, where the woman can not carry and give birth to a child for medical reasons. This should be documentally confirmed.Surrogate motherhood should be altruistic, the woman who agrees to carry and give birth to a child, shouldnt pay for services.The written agreement must be necessarily issued between the surrogate mother and the genetic parents. The rights and obligations of the parties as well as their actions in cases of force majeure should be included in it.After the birth, parental rights over the child belong to the genetic parents.According to the law, the surrogate mother is a woman of child-bearing age who agrees to carry and give birth to a child for the genetic parents, and she doesnt lay claim to be his mother.

Traditional surrogacy is illegal in Portugal except for some situations that give the right for a surrogate mother to be genetic (for example, if the future adoptive mother is completely barren).

Adoption of the law caused some debate within several Portuguese Christian Churches, though not among the once dominant Roman Catholic Church. Representatives of Brazilian and US based evangelical and Pentecostal churches condemn surrogacy and suggest that infertile couples can/must (depending on the Church) pursue conventional adoption (national or transnational even though the later is banned by law).

Heterosexual and Lesbian Couples can become parents via surrogacy in Portugal as by 2016 all the risks of the program are provided and regulated by law (for example, the occurrence of developmental defects of the baby, miscarriage or abortion). Male Homosexual couples and single men and women of any sexual orientation have not yet been included, but they are not addressed specifically by the law which leaves an opening for a future revision in a more encompassing way. One such revision is on the current manifestos of several parties: the [Left Bloc (B.E)], [PeopleAnimalsNature (PAN)-and [(Ecologist Party "The Greens" (Os Verdes - The Greens)]. They can count on the repeated opposition of the populist right party CDS People's Party (PP-CDS) and the Social Democratic Party (PPD-PSD), the most socially conservative parties in parliament. The Communist Party (P.C.P) voted against the first proposal, because it was against the recommendations of the National Ethics Counsil, this was also President's argument to decline its approval. Most of the Socialist Party voted favourably, as well. By now, this means that gay couples are banned from altruistic surrogacy within Portugal and since the Constitution of Portugal explicitly bans discrimination on the basis of sexual orientation, this could be unconstitutional, which is being discussed by the Portuguese Constitutional Court.[42][43][44][45]

Gestational surrogacy, even commercial, is legal in Russia,[46] being available to practically all adults willing to be parents.[47] There must be one of several medical indications for surrogacy: absence of uterus, deformity of the uterine cavity or cervix, uterine cavity synechia, somatic diseases contraindicating child bearing, or repeated failure of IVF despite high-quality embryos.[46]

The first surrogacy program in Russia was successfully implemented in 1995 at the IVF centre of the Obstetrics and Gynecology Institute in St. Petersburg.[48] Public opinion in general is surrogacy-friendly; recent cases of a famous singer and a well-known businesswoman who openly used services of gestational surrogates received positive news coverage. Meanwhile, the Russian Orthodox Church has officially condemned surrogacy. As regards the baptism of the children born through surrogacy, the Russian Orthodox Church holds that a "child born with the assistance of surrogate motherhood can be Baptized according to the wishes of the party that will be raising it, if such are either its biological parents or its surrogate mother, only after they have recognized that, from the Christian point of view, such reproductive technology is morally reprehensible and have borne ecclesial repentance regardless of whither they ignored the Churchs position consciously or unconsciously".[49]

A few Russian women, such as Ekaterina Zakharova,[50] Natalija Klimova,[51] and Lamara Kelesheva,[52] became grandmothers through post-mortem gestational surrogacy programs, their surrogate grandsons being conceived posthumously after the deaths of their sons.

Registration of children born through surrogacy is regulated by the Family Code of Russia (art. 51-52) and the Law on Acts on Civil Status (art. 16). A surrogates consent is needed for that. Apart from that consent, no adoption nor court decision is required. The surrogates name is never listed on the birth certificate.There is no requirement for the child to be genetically related to at least one of the commissioning parents.[53]

Children born to heterosexual couples who are not officially married or single intended parents through gestational surrogacy are registered in accordance to analogy of jus (art. 5 of the Family Code). A court decision may be needed in that case. On 5 August 2009 a St. Petersburg court definitely resolved a dispute as to whether single women could apply for surrogacy and obliged the State Registration Authority to register a 35-year=old single intended mother, Nataliya Gorskaya, as the mother of her surrogate son.[54]

On 4 August 2010 a Moscow court ruled that a single man who applied for gestational surrogacy (using donor eggs) could be registered as the only parent of his son, becoming the first man in Russia to defend his right to become a father through court proceedings.[55] The surrogate mothers name was not listed on the birth certificate; the father was listed as the only parent. After that a few more identical decisions concerning single men who became fathers through surrogacy were issued by different courts in Russia, listing men as the only parents of their surrogate children and confirming that prospective single parents, regardless of their sex or sexual orientation, can exercise their right to parenthood through surrogacy in Russia.

Liberal legislation makes Russia attractive for "reproductive tourists" looking for techniques not available in their countries. Intended parents go there for oocyte donation because of advanced age or marital status (single women and single men) and when surrogacy is considered. Foreigners have the same rights for assisted reproduction as Russian citizens. Within 3 days after the birth, the commissioning parents obtain a Russian birth certificate with both their names on it. Genetic relation to the child (in case of donation) does not matter.[56]

Religious authorities in Saudi Arabia do not allow the use of surrogate mothers, instead suggesting medical procedures to restore fertility and ability to deliver.[57]

All surrogacy arrangements (both commercial and altruistic) are illegal. A draft of the new civil law is said to allow surogacy mother, but Serbian Assembly still did not adopt this law yet. On April 21, 2017, the Serbian Assembly started a discussion a legislation on assisted reproductive technology that bans all forms of surrogacy. (The legislation is being discussed.)

The South Africa Children's Act of 2005 (which came fully into force in 2010) enabled the "commissioning parents" and the surrogate to have their surrogacy agreement validated by the High Court even before fertilization. This allows the commissioning parents to be recognized as legal parents from the outset of the process and helps prevent uncertainty - although if the surrogate mother is the genetic mother she has until 60 days after the birth of the child to change her mind. The law permits single people and gay couples to be commissioning parents.[58] However, only those domiciled in South Africa benefit from the protection of the law, no non-validated agreements will be enforced, and agreements must be altruistic rather than commercial. If there is only one commissioning parent, s/he must be genetically related to the child. If there are two, they must both be genetically related to the child unless that is physically impossible due to infertility or sex (as in the case of a same sex couple). The Commissioning parent or parents must be physically unable to birth a child independently. The surrogate mother must have had at least one pregnancy and viable delivery and have at least one living child. The surrogate mother has the right to unilaterally terminate the pregnancy, but she must consult with and inform the commissioning parents, and if she is terminating for a non-medical reason, may be obliged to refund any medical reimbursements she had received.[59]

As of mid-2010s, surrogacy was available and mostly unregulated in South Korea. The practice is often morally stigmatized. Surrogacy has declined since mid-2000s, as some aspects of commercial surrogacy became illegal.[60]

Whereas surrogacy is not legal in Spain (the biological mother's renouncement contract is not legally valid), it is legal to perform the surrogacy in a country where it is legal, having the mother the nationality from that same country.[61]

Surrogacy is not clearly regulated in Swedish law.[62] The legal procedure most equivalent to it is making an adoption of the child from the surrogate mother. However, the surrogate mother has the right to keep the child if she changes her mind before the adoption. The biological father may nevertheless claim the right to the child.

It is illegal for Swedish fertility clinics to make surrogate arrangements. As an alternative, Sweden sanctioned the world's first uterus transplant in an infertile woman. The woman was 36 years old.

Surrogacy is regulated in the "Bundesgesetz ber die medizinisch untersttzte Fortpflanzung (Fortpflanzungsmedizingesetz, FMedG) vom 18. Dezember 1998" and illegal in Switzerland. Art. 4 forbids surrogacy, Art. 31 regulates the punishment of clinicians who apply in vitro fertilisation for surrogacy or persons who arrange surrogacy. The surrogate mother is not punished by law. She will be the legal mother of the child.

On 24 August 2014, the Administrative Court of the Canton of St. Gallen granted parentship to two men of a child born in the USA.[63]

In response to the controversial Baby Gammy incident in 2014, Thailand since July 30, 2015, has banned foreign people travelling to Thailand, to have commercial surrogacy contract arrangement, under the Protection of Children Born from Assisted Reproductive Technologies Act. Only opposite-sex married couples as Thailand residents are allowed to have a commercial surrogacy contract arrangement. In the past Thailand was a popular destination for couples seeking surrogate mothers.[64][65][66]

Since 2002, surrogacy and surrogacy in combination with egg/sperm donation has been absolutely legal in Ukraine. According to the law a donor or a surrogate mother has no parental rights over the child born and the child born is legally the child of the prospective parents.

In Ukraine the start of introduction of methods of supporting reproductive medicine was given in eighties of the preceding century. It was Kharkov where the extracorporeal fertilization method was for the first time successfully applied in Ukraine, and in 1991 a girl named Katy was born. Kharkiv was also the first city in CIS countries to realize surrogacy. Many clinics dealing with surrogacy have been opened in Kiev[67] and Lviv.

Ukrainian surrogacy laws are very favorable and fully support the individual's reproductive rights. Surrogacy is officially regulated by Clause 123 of the Family Code of Ukraine and the order of the Ministry of health of Ukraine "On approval of the application of assisted reproductive technologies in Ukraine" from 09.09.2013 787. You can choose between Gestational Surrogacy, Egg/sperm Donation, special Embryo adoption programs and their combinations. No specific permission from any regulatory body is required for that. A written informed consent of all parties (intended parents and surrogate) participating in the surrogacy program is mandatory.

Ukrainian legislation allows intended parents to carry on a surrogacy program and their names will be on Birth certificate of the child born as a result of the surrogacy program from the very beginning. The child is considered to be legally "belonging" to the prospective parents from the very moment of conception. The surrogates name is never listed on the birth certificate. The surrogate can't keep the child after the birth. Even if a donation program took place and there is no biological relation between the child and the intended mother, their names will be on Birth certificate (Clause 3 of article 123 of the Family Code of Ukraine).

Embryo research is also allowed, gamete and embryo donation permitted on a commercial level. Single women can be treated by known or anonymous donor insemination. Gestational surrogacy is an option for officially married couples and single women. There is no such concept as gay/lesbian marriage in Ukraine, meanwhile such patients can be treated as single women/men.

Commercial surrogacy arrangements are not legal in the United Kingdom. Such arrangements were prohibited by the Surrogacy Arrangements Act 1985.[68] Whilst it is illegal in the UK to pay more than expenses for a surrogacy, the relationship is recognised under section 30 of the Human Fertilisation and Embryology Act 1990. Regardless of contractual or financial consideration for expenses, surrogacy arrangements are not legally enforceable so a surrogate mother maintains the legal right of determination for the child, even if they are genetically unrelated. Unless a parental order or adoption order is made, the surrogate mother remains the legal mother of the child.

Surrogacy and its attendant legal issues fall under state jurisdiction and the legal situation for surrogacy varies greatly from state to state. Some states have written legislation, while others have developed common law regimes for dealing with surrogacy issues. Some states facilitate surrogacy and surrogacy contracts, others simply refuse to enforce them, and some penalize commercial surrogacy. Surrogacy friendly states tend to enforce both commercial and altruistic surrogacy contracts and facilitate straightforward ways for the intended parents to be recognized as the child's legal parents. Some relatively surrogacy friendly states only offer support for married heterosexual couples. Generally, only gestational surrogacy is supported and traditional surrogacy finds little to no legal support.

States generally considered to be surrogacy friendly include California,[69] Illinois,[70] Arkansas,[71] Maryland,[72] Washington D.C., Oregon,[73] and New Hampshire[74] among others. Both New Jersey and Washington State commercial surrogacy laws become effective from 1/1/2019.

For legal purposes, key factors are where the contract is completed, where the surrogate mother resides, and where the birth takes place. Therefore, individuals living in a non-friendly state can still benefit from the policies of surrogacy friendly states by working with a surrogate who lives and will give birth in a friendly state.

Arkansas was one of the first states to enact surrogacy friendly laws. In 1989, under then Governor Bill Clinton, it passed Act 647, which states that in a surrogacy arrangement, the biological father and his wife will be recognized as the child's legal parents from birth, even if his wife is not genetically related to the child (i.e., in a traditional surrogacy arrangement). If he is unmarried, he alone will be recognized as the legal parent. A woman may also be recognized as the legal mother of the surrogate birth mother's genetic child as long as that child was conceived with anonymous donor sperm.[75] On the other hand, it is unclear how or whether same sex couples could benefit these laws, since the 2008 ballot measure that made it illegal for unmarried, cohabiting individuals to adopt or provide foster care to minors.[76] On June 26, 2015, the 2008 ballot issue is moot because of Obergefell v. Hodges.

California is known to be a surrogacy-friendly state. It permits commercial surrogacy, regularly enforces gestational surrogacy contracts, and makes it possible for all intended parents, regardless of marital status or sexual orientation, to establish their legal parentage prior to the birth and without adoption proceedings (pre-birth orders).[77][78]

Michigan forbids absolutely all surrogacy agreements. It is a felony to enter into such an agreement, punishable by a fine of up to $50,000 and up to five years in prison. The law makes surrogacy agreements unenforceable.[79]

Since 2014, New Hampshire is recognized as a surrogacy friendly state, with laws in place to protect all parties to a surrogacy arrangement. All intended parents, irrespective of marital status, sexual orientation, or a genetic connection to the child, are able to establish their legal parental rights through pre-birth orders placing their names directly on the child's initial birth certificate. Reasonable compensation to the surrogate is permitted by statute.[80]

New York law holds that commercial surrogacy contracts contravene public policy and provides for civil penalties for those who participate in or facilitate a commercial surrogacy contract in New York.[81] Altruistic surrogacy contracts are not penalized, but neither are they enforced. New York does recognize pre-birth orders from other states, and has provided a post-birth adoption alternative for altruistic surrogate parents via orders of maternal and paternal filiation.[82]

Baby M: New Jersey 1988. The surrogate mother in a gestational surrogacy arrangement decided to keep the resulting child. The intended parents sued to have themselves recognized as the legal parents. The New Jersey Supreme Court found that the surrogacy contract was invalid as a matter of New Jersey public policy. However, the intended parents were given custody of the child because the courts thought they would provide a better home for the baby than the surrogate mother, who was instead given visitation rights.

Surrogacy for humanitarian purposes have been allowed in Vietnam from 2015 after The amended Family and Marriage Law passed with nearly 60 percent of votes from the National Assembly.

Under the new law, surrogacy will only be allowed among married couples, who do not have any common child, after doctors confirm the wife can not give birth even with technical support. The surrogate must be a relative of either the husband or wife, and have already given birth successfully. A woman is only allowed to be a surrogate once in her life and must produce her husbands approval if shes married. The embryo must be created by the intended parents' sperm and ovum.[83] The process must be voluntary and follow in-vitro fertilization regulations.

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