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Biochemistry – | University of Utah

Posted: November 26, 2016 at 8:45 am

ResearchNov 08, 2016 Unmasking a Silent Killer: A Culprit Behind Polycystic Kidney Disease kidney disease

Published in October in Cell as part of a study led by scientists at the University of Utah School of Medicine, the structure reveals how specific mistakes in PKD2 triggers polycystic kidney disease, the most common inherited kidney disorder.... Read More

A team of physicians and laboratory scientists has taken a key step toward a cure for sickle cell disease, using CRISPR-Cas9 gene editing to fix the mutated gene responsible for the disease in stem cells from the blood of affected patients. For the first time, they have corrected the mutation in a proportion of stem cells that is high enough to produce a substantial benefit in sickle cell patients.... Read More

University of Utah researchers have found that the structure of an insulin molecule produced by predatory cone snails may be an improvement over current fast-acting therapeutic insulin. The finding suggests that the cone snail insulin, produced by the snails to stun their prey, could begin working in as few as five minutes, compared with 15 minutes for the fastest-acting insulin currently available. ... Read More

University of Utah biochemist Danny Chou, Ph.D., is one of four researchers worldwide to receive a grant from the Juvenile Diabetes Research Foundation (JDRF) and the pharmaceutical company Sanofi US Services Inc. to develop glucose-responsive insulin to help millions of people with Type 1 diabetes (T1D) maintain proper blood glucose levels. ... Read More

One of the most fundamental challenges that a cell faces is how to bring membranes that are far apart, close together. New research in Science shows how cellular machinery, called ESCRT (Endosomal Sorting Complexes Required for Transport), accomplishes this essential task. ... Read More

Jared Rutter, Ph.D., is one of only 26 to receive prestigious Honor ... Read More

Distinguished professor of biochemistry receives one of science's highest honors ... Read More

Program honors 15 researchers nationwide with funds to support their work... Read More

By looking at the ends of double-stranded RNA, Dicer enzyme tells difference ... Read More

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Turmeric and black pepper fight cancer stem cells

Posted: November 26, 2016 at 8:43 am

A new study shows that a combination of turmeric and piperine can limit the growth of stem cells for breast cancer -- the cells that conventional treatment have the hardest time eliminating.

My friend Madhuri Kakarala is a physician at the University of Michigan; she's a cancer specialist and a PhD researcher. But she's also a nutritionist, and, like me, during her final years of medical studies she was diagnosed with cancer -- a stage IV cancer of the thyroid. Madhuri decided to invest all her talent as a researcher and clinician in the task of getting well, and she rapidly arrived at the conclusion that nutritional change could significantly improve her response to her cancer treatment.

Because Madhuri is from an Indian background, she was most interested in the medical and culinary traditions of her country, and particularly fascinated by the promising effects of turmeric in the prevention and treatment of cancers.

This month Madhuri published an important article on the effect of turmeric on breast cancer stem cells. [1] Stem cells are at the center of a theory that seeks to explain why cancer can sometimes return, despite apparently effective treatment. This is because even when all the cancer cells have been eliminated these cancer stem cells that have lied dormant and escaped treatments may be able to form entire new colonies of cancer cells. So to prevent relapse, it's essential that we learn how to eliminate the stem cells. But unfortunately, because they don't actively renew themselves through cell division like other cancer cells do, most existing treatments that target cancerous cells (like radiotherapy and chemotherapy) aren't effective against stem cells. For this reason, the pharmaceutical industry has a whole sector of research devoted to developing new therapies to target and destroy stem cells.

For several years now, Madhuri's lab at the University of Michigan has been studying the effect on breast cancer of curcumin -- one of the most active substances in turmeric -- and piperine, which is a substance active in black pepper. In her latest study she demonstrates that concentrations of curcumin and piperine which can be obtained through diet or from dietary supplements are capable of eliminating breast cancer stem cells, without causing any damage to the normal breast cells. In other words, this isn't a general toxic effect on cells, like conventional anti-cancer treatments have, but an ultra-selective impact on cancer stem cells alone.

"This shows that these compounds are not toxic to normal breast tissue," Madhuri says. "Women at high risk of breast cancer right now can choose to take the drugs tamoxifen or raloxifene for prevention, but most women won't take these drugs because there is too much toxicity. The concept that dietary compounds can help is attractive, and curcumin and piperine appear to have very low toxicity."

The possible anti-cancer properties of curcumin and piperine have been the object of many other studies. But this study is the first to show that they may have a targeted effect on stem cells. Medications like tamoxifen or raloxifene only act against cancers that are sensitive to estrogen. If curcumin and piperine can target stem cells, they have the potential to be useful in many types of breast cancer, particularly those that aren't estrogen-sensitive -- and these are often the most aggressive.

Madhuri's study was performed on cell colonies in Petri dishes, in lab conditions. So we haven't yet reached the stage of a clinical study that would establish guidelines for recommendations to take turmeric supplements at specific dosages for certain types of cancer. However, given that turmeric and pepper, taken as part of a normal diet, are practically never toxic in any way, it seems to me to be perfectly reasonable to recommend that all of us regularly consume a soupspoon of turmeric every day, with a pinch of pepper. You can use it in all your cooking, just like I've been doing for years.

CAUTION: Note that it is often safest to avoid turmeric during chemotherapy as well as a three days before and after the treatment. This is because it can rarely, but it can interfere with some chemotherapy treatments and reduce their benefits.

REFERENCE 1. Kakarala, M., et al., Targeting breast stem cells with the cancer preventive compounds curcumin and piperine. Breast Cancer Research & Treatment, 2009.

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Portal:Biotechnology – Wikipedia

Posted: November 26, 2016 at 8:42 am

From Wikipedia, the free encyclopedia

The Biotechnology Portal

Welcome to the Biotechnology portal. Biotechnology is a technology based on biology, especially when used in agriculture, food science, and medicine.

Of the many different definitions available, the one declared by the UN Convention on Biological Diversity is one of the broadest:

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Cloning is the process of creating an identical copy of an original. A clone in the biological sense, therefore, is a single cell (like bacteria, lymphocytes etc.) or multi-cellular organism that is genetically identical to another living organism. Sometimes this can refer to "natural" clones made either when an organism reproduces asexually or when two genetically identical individuals are produced by accident (as with identical twins), but in common parlance the clone is an identical copy by some conscious design. Also see clone (genetics). The term clone is derived from , the Greek word for "twig". In horticulture, the spelling clon was used until the twentieth century; the final e came into use to indicate the vowel is a "long o" instead of a "short o". Since the term entered the popular lexicon in a more general context, the spelling clone has been used exclusively.

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The Maryland Stem Cell Research Fund (MSCRF) | Tedco

Posted: November 25, 2016 at 8:45 am

The Maryland Stem Cell Research Fund (MSCRF)

The Maryland Stem Cell Research Fund was established by the Governor and the Maryland General Assembly under the Maryland Stem Cell Research Act of 2006. The purpose of the Fund is to promote State-funded human stem cell research and medical treatments through Grants to public and private entities in the State. More information at http://www.mscrf.org.

The purpose of this Investigator-Initiated Research Grants Program is to attract and support Investigators, who wish to conduct basic, translational and/or clinical research involving human stem cells. The results from this application should broaden and advance the knowledge of human stem cell biology and develop clinical applications for the prevention, diagnosis, treatment and cure of human diseases, injuries and conditions.

Principal Investigators and all other MSCRF-funded personnel must be employed or retained by an eligible Maryland-based research organization while conducting State-funded stem cell research. Such affiliations may be permanent or temporary, full-time or part-time. Applicants from Maryland-based public and private, for-profit and not-for-profit research organizations of all types are eligible for this Award (e.g., universities, colleges, research institutes, companies and medical centers).

Applicants for all Maryland Stem Cell Research Grant Programs may request from $110,000 up to $750,000 over a maximum period of three (3) years.

Once a year cycle with new RFA coming out in early October. Letter of Intent due by mid-November. Full application due by mid-January.

- MSCRF Investigator-Initiated - MSCRF Pre-Clinical or Clinical - MSCRF Exploratory - MSCRF Fellowship

Dan Gincel Vice President, University Partnerships & Executive Director, MD Stem Cell Research Fund dgincel@tedco.md 410.715.4172

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The Benefits of Stem Cell Science to Your Health

Posted: November 25, 2016 at 8:45 am

What is a Stem Cell?

The National Institute of Health defines a Stem Cell in this way: Stem cells have the remarkable potential to develop into many different cell types in the body. Serving as a sort of repair system for the body, they can theoretically divide without limit or replenish other cells as long as the person is still alive. When a stem cell divides, each new cell has the potential to remain either a stem cell or become another type of cell with a more specialized function, such as a muscle cell, a red blood cell or a brain cell.

Adult Stem Cells are predominantly formed in the bone marrow. And, just as in the beginnings of life, adult stem cells can literally change into any type of cell in the body throughout life. The adult stem cells are released from the bone marrow then move into circulation in the blood stream to seek out problem areas, then renew and restore those tissues in need of repair.

Example -Repairing The Heart muscle: When circulating stem cells find the heart in reduced health, they exit the bloodstream, attach to the heart and actually become brand new heart muscle cells, analogous to the original cells that originally created the once infant heart. They then begin dividing into still more new heart muscle cells.

The same process occurs in the liver, the kidneys, the brain, the skin, eyes, any organ, tissue, muscle, bone, connective tissue literally any part of the body that is in need of restoration.

The National Institute of Health identifies 74 treatable diseases using adult stem cells in therapy. These costly and complex therapies typically deliver a large quantity of adult stem cells to the area undergoing treatment. Most require that stem cells be harvested from the patient or adult donor, programmed in a lab to become a specific type and cell and then injected into the body. For treatment of disease these therapies are many times the best method of recovery, producing truly remarkable results. Thankfully, most of us dont have issues that require these extensive procedures.

What do the experts say?One of the USAs leading experts in adult stem cell science is Dr. David A Prentice, Ph.D., a professor at Indiana University School of Medicine. The National Institute of Health funds much of his research. In 2003, he presented a detailed paper to the Presidents Council on Bioethics, referring to many studies. In closing, he added:

Adult stem cells have significant capabilities for growth, repair and regeneration of damaged cells and tissues in the body, akin to a built-in repair kit or maintenance crew that needs only activation and stimulation to accomplish repair of damage. Direct stimulation of endogenous (already present in the body) adult stem cells within a tissue may be the easiest, safest and most efficient way to stimulate tissue regeneration. Such stimulation need not rely on any added stem cells

He could not have known then that in 2006, stem cell technology would provide a product as simple as a daily supplement in capsule form that would directly suport the natural release of stem cells in the manner he was describing.

According to medical science, adult stem cells assist in: Cancer, leukaemia, auto immune disease including diabetes, lupus, Crohns disease and arthritis; cardiovascular disease, including acute heart damage and chronic coronary artery disease; corneal regeneration; Parkinson's, stroke; anaemia and other blood conditions; liver and blood disease and many many more conditions.

For those of us just wanting to maintain optimal health or fight the effects of ageing, injury and day to day wear and tear, a smaller but steady release of our existing stem cells into the blood stream can produce considerable health benefits.

When stem cell nutrition is used as a daily supplement over time, the stimulation of billions of additional stem cells in the blood stream could be one of the safest and most efficient methods for maintaining optimal health and wellbeing that science has ever discovered.

The most recent evolution of Stem Cell Nutrition is calledCeruleStemEnhance Ultraand You can enhance the Ability of Stem Cells to find tissues in need of repair and also to calm inflammation withCeruleCyactive. You can improve the ability of Stem Cells to move around your bloodstream to get to the repair sites withCerulePlasmaFlo

Young, old, weak, strong, elite athlete, casual athlete, non-athlete, someone recovering from injury, everyone enjoys having strength, flexibility and stamina. For professional athletes and the weekend warriors fast healing and complete recovery is in demand. The opportunities for Stem Cells to enhance this procedure and shorten time-frames for recovery are becoming evident. The numbers of your own stem cells available in your body can be enhanced by an average of 25% within 1 hour Adult Stem Cells the best anti-ageing system ever known. Knowing what adult stem cells do in the human body, doesnt it make sense that having more of them in the blood stream will undoubtedly have profound effects on your health, wellbeing, and provide an until now, untapped resource for fighting the effects of ageing?

PubMed.gov From the National Library of Medicine and The National Institutes of HealthThe documentation of adult stem cell function by mainstream science and medical research are virtually endless. To find more, just visit the science and medical communitys online source for retrieving such papers and articles https://www.ncbi.nlm.nih.gov/pubmed Type "stem cells" in the search box and have access to more than 265,000 studies. A search there for "Adult stem cells" will yield 53,000+ papers.

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Cord Blood Banking Cost – Cryo-Cell International

Posted: November 25, 2016 at 8:42 am

We also offer special discounts for multiple births, military families, medical professionals and more.Please call 800.786.7235 for details. Annual Storage

Service

Annual

Service

20 Years Prepaid

(Includes initial processing fee, 1st year of storage and additional 20 years of storage)

Service

Standard (HES)

Down payment is due at enrollment. *Actual monthly payment will be slightly lower than what is being shown. Cannot be combined with other offers or discounts. Add $50 to down payment for medical courier service from Alaska, Hawaii and Puerto Rico. After the first year annual storage fees will apply, $150 for cord blood and $150 for cord tissue. A monthly service fee is included in the monthly payment.

Down payment is due at enrollment. *Actual monthly payment will be slightly lower than what is being shown. Cannot be combined with other offers or discounts. Add $50 to down payment for medical courier service from Alaska, Hawaii and Puerto Rico. After the second year annual storage fees will apply, $150 for cord blood and $150 for cord tissue. A monthly service fee is included in the monthly payment.

*Fee schedule subject to change without notice. If a client has received a kit and discontinues services prior to collection, there is no cancellation fee if the kit is returned within two weeks from cancellation notice. Additional courier service fee applies for Alaska, Hawaii and Puerto Rico. Applies to 1-year plan and promotional plan only. After the first year, an annual storage fee will apply. Cryo-Cell guarantees to match any written offer for product determined to be similar at Cryo-Cells sole discretion. ** Promotional Plan cannot be combined with any other promotional offers, coupons or financing.

In order to preserve more types and quantity of umbilical cord stem cells and to maximize possible future health options, Cryo-Cells umbilical cord tissue service provides expectant families with the opportunity to cryogenically store their newborns umbilical cord tissue cells contained within substantially intact cord tissue. Should umbilical cord tissue cells be considered for potential utilization in a future therapeutic application, further laboratory processing may be necessary. Regarding umbilical cord tissue, all private blood banks activities for New York State residents are limited to collection, processing, and long-term storage of umbilical cord tissue stem cells. The possession of a New York State license for such collection, processing and long-term storage does not indicate approval or endorsement of possible future uses or future suitability of these cells.

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Faculty Directory UConn Health

Posted: November 25, 2016 at 8:42 am

Extra IoN Seminar, Dendritic Spikes and Dendritic UP states in Cortical Pyramidal Neurons Voltage-sensitive dye Imaging Talk Newcastle Univ. Institute of Neuroscience 2015 Newcastle, UK Branch specific and spike-order specific action potential invasion in basal, oblique, and apical dendrites of cortical pyramidal neurons. Talk Ministry of Science, Serbia 2015 Eight Photonics Workshop 2015 (Kopaonik) Dendritic Mechanisms for Detecting Strong Glutamatergic Inputs Talk Department of Neuroscience, UConn Health 2015 Farmington, CT Sodium-calcium imaging of glutamate-mediated dendritic spikes Talk MBL, Woods Hole, MA 2015 MBL, Woods Hole, MA NeuroImaging Seminar Series: Glutamate-mediated Plateau Potentials in thin Dendritic Branches: Dendritic UP States Lecture MBL, Woods Hole, MA 2015 MBL, Woods Hole, MA Dendritic spikes and dendritic UP states. Talk Computational Neuroscience 2015 Brandeis University Neuroscience Journal Club - Responsible Research Conduct Talk Neuroscience Department 2015 Sparse, Strong and Large Area Targeting of Genetically Encoded Indicators Poster NIH Investigator Meeting 2015 Bethesda, MD Extrasynaptic receptors and dentritic spikes. See more at: https://royalsociety.org/events/2015/01/chemical-transmitters/ Talk The Royal Society, London 2015 London, UK Optical recordings of dendritic membrane potential and calcium transients. Talk Ministry of Science, Serbia 2014 Seventh Photonics Workshop 2014 (Kopaonik) Synapse discussion Other CT science festival neuroscience 2014 The Richard D. Berlin Center for Cell Analysis and Modeling (CCAM) NMDA Spikes and Plateau Potentials in Thin Dendrites of Cortical Pyramidal Neurons - Voltage-sensitive Dye Imaging - See more at: http://www.gc.cuny.edu/Public-Programming/Calendar/Detail?id=22817#sthash.6B8BHEaz.dpuf Talk CUNY 2014 The Graduate Center 365 Fifth Avenue, New York The use of lasers for functional dendritic imaging-voltage-sensitive and calcium-sensitive dye recordings from dendritic branches.See more at: http://www.scribd.com/doc/237736432/IBRO-NERKA-School-on-Neurophotonics-2014-Program#scribd Lecture International Brain Research Organisation (IBRO) 2014 IBRO NERKA School on Neurophotonics 2014 Branch-specific and Spike order-specific Action Potential Backpropagation in Basal, Oblique and Apical Tuft Dendrites of Cortical Pyramidal Neurons. Talk Neuroplex Workshop 2014 Hamilton Crowne Plaza Hotel, 1001 14th St NW, Washington, D.C. Inconsistent Efficacy of the Action Potential Back-propagation Observed in Rat Prefrontal Cortex Layer 5 Pyramidal Neurons. Talk Marine Biological Laboratory 2013 Woods Hole, MA The use of lasers and voltage sensitive-dyes in neurobiology Talk Photonics Workshop 2013 2013 Institute of Physics, Serbia The Physiology and Genetics of Human Neurodifferentiation Inspire Some Ideas about Mental Diseases Talk Department of Neuroscience 2013 Farmington, CT Studying Human Embryonic Stem Cells with the RedShirtImaging Camera Talk SFN Satellite Event 2012 New Orleans, LO Glutamate Evoked Potentials in Dendrites of Pyramidal Neurons Talk Southern Illinois University 2012 Carbondale, IL Integration of Glutamatergic Inputs in Thin and Spiny Dendrites - Voltage-Sensitive Dye Imaging Talk Rutgers University 2012 Newark, NJ Dendritic Spine Group, Dendrites Swim in Glutamate Talk CCAM and Dept of Neuroscience 2012 CCAM, 400 Farmington Ave. Stem Cell Physiology and Chemistry Core Talk 2012 Connecticut Stem Cell Research Retreat 2012 Yale University School of Medicine Voltage spikes in thin dendrites of pyramidal neurons Talk Janelia Voltage Imaging Workshop 2012 Janelia Farm Dopamine Potentiates Differentiation of Human Embryonic Stem Cells into Neurons, Glenn S. Belinsky, Shaina M. Short, Anna R. Moore, Matthew T. Rich and Srdjan D. Antic Poster Connecticut Innovations, Department of Public Health 2011 Farmington, CT AP Propagation in Oblique and Apical Tuft Dendrites of CA1 Pyramidal Cells, Wen-Liang Zhou and Srdjan D. Antic Poster Gordon Research Conference 2011 Ventura, CA Physiology of the Human Fetal Cortex in Health and Disease; Srdjan D. Antic, Seminar, Neuroscience Retreat 2011 Talk Department of Neuroscience 2011 Farmington, CT Dopaminergic and GABAergic Modulation of Dendritic Calcium Transients in the Rat Prefrontal Cortex, Wen-Liang Zhou and Srdjan D. Antic Poster Neuroscience at Storrs 2011 Storrs, CT Dopaminergic and GABAergic Modulation of Dendritic Calcium Transients in the Rat Prefrontal Cortex, Wen-Liang Zhou and Srdjan D. Antic Poster Society for Neuroscience 2011 Washington, DC CCAM Seminar: "Dendritic Spines for Students" Talk Richard D. Berlin Center for Cell Analysis & Modeling 2010 CCAM, 400 Farmington Ave. NeuroPlex Workshop, Satellite Society of Neuroscience Meeting, San Diego, CA. Talk RedShirtImaging 2010 Hilton San Diego Gaslight Quarter. Seminar Speaker: Srdjan D. Antic, Cell and Genome Sciences Inaugural Symposium. Talk Cell and Genome Sciences 2010 400 Farmington Ave, Farmington CT. International Symposium - 100 Years of Belgrade School of Physiology Talk University of Belgrade 2010 Belgrade, Serbia AP Propagation in Oblique Dendrites of CA1 Pyramidal Cells, Wenliang Zhou and Srdjan Antic Poster Society for Neuroscience 2010 San Diego, CA, USA Neuroscience Journal Club Faculty Presentation; Publication presented: /Science/ 325(5941):756-60. Talk Department of Neuroscience 2009 UCHC Room E-4036 Microelectrode Techniques for Cell Physiology Workshop Talk Marine Biological Association of the UK 2009 Plymouth, England NeuroPlex Workshop, Satellite Society of Neuroscience Meeting, Chicago, IL. Talk RedShirtImaging 2009 Chicago, IL Transient stimulation of somatic dopamine receptors on layer 5 pyramidal neurons of the rat prefrontal cortex Anna R. Moore, Wen-Liang Zhou and Srdjan D. Antic Poster Society for Neuroscience, Chicago, IL. 2009 Chicago, IL Heterogeneity among individual dendritic branches belonging to the same pyramidal cell, Wenliang Zhou and Srdjan Antic Poster Gordon Research Conference, Italy 2009 Toscany, Italy Glutamate-evoked Plateau Potentials in Thin Dendrites Talk University of Bonn 2009 Bonn, Germany Invited Seminar, Department of Physiology and Biophysics Talk Dalhousie University 2008 Halifax, Canada Voltage-Sensitive Dye Workshop Talk FASEB (European Society for Neuroscience) 2008 Geneva, Switzerland

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Stem cell laws – Wikipedia

Posted: November 25, 2016 at 8:41 am

Stem cell laws are the law rules, and policy governance concerning the sources, research, and uses in treatment of stem cells in humans. These laws have been the source of much controversy and vary significantly by country.[1] In the European Union, stem cell research using the human embryo is permitted in Sweden, Finland, Belgium, Greece, Britain, Denmark and the Netherlands; however, it is illegal in Germany, Austria, Ireland, Italy, and Portugal. The issue has similarly divided the United States, with several states enforcing a complete ban and others giving financial support.[2] Elsewhere, Japan, India, Iran, Israel, South Korea, China, and Australia are supportive. However, New Zealand, most of Africa (except South Africa), and most of South America (except Brazil) are restrictive.

The information presented here covers the legal implications of embryonic stem cells (ES), rather than induced pluripotent stem cells (iPSCs). The laws surrounding the two differ because while both have similar capacities in differentiation, their modes of derivation are not. While embryonic stem cells are taken from embryoblasts, induced pluripotent stem cells are undifferentiated from somatic adult cells.[3]

Stem cells are cells found in most, if not all, multi-cellular organisms. A common example of a stem cell is the Hematopoietic stem cell (HSC) which are multipotent stem cells that give rise to cells of the blood lineage. In contrast to multipotent stem cells, embryonic stem cells are pluripotent and are thought to be able to give rise to all cells of the body. Embryonic stem cells were isolated in mice in 1981, and in humans in 1998.[4]

Stem cell treatments are a type of cell therapy that introduce new cells into adult bodies for possible treatment of cancer, Somatic cell nuclear transfer, diabetes, and other medical conditions. Cloning also might be done with stem cells. Stem cells have been used to repair tissue damaged by disease.[5]

Because Embryonic Stem (ES) cells are cultured from the embryoblast 45 days after fertilization, harvesting them is most often done from donated embryos from in vitro fertilization (IVF) clinics. In January 2007, researchers at Wake Forest University reported that "stem cells drawn from amniotic fluid donated by pregnant women hold much of the same promise as embryonic stem cells."[4]

In 2000, the NIH, under the administration of President Bill Clinton, issued guidelines that allow federal funding of embryonic stem-cell research.[4]

The European Union has yet to issue consistent regulations with respect to stem cell research in member states. Whereas Germany, Austria, Italy, Finland, Ireland, Portugal and the Netherlands prohibit or severely restrict the use of embryonic stem cells, Greece, Sweden and the United Kingdom have created the legal basis to support this research.[6]Belgium bans reproductive cloning but allows therapeutic cloning of embryos.[1]France prohibits reproductive cloning and embryo creation for research purposes, but enacted laws (with a sunset provision expiring in 2009) to allow scientists to conduct stem cell research on imported a large amount of embryos from in vitro fertilization treatments.[1]Germany has restrictive policies for stem cell research, but a 2008 law authorizes "the use of imported stem cell lines produced before May 1, 2007."[1]Italy has a 2004 law that forbids all sperm or egg donations and the freezing of embryos, but allows, in effect, using existing stem cell lines that have been imported.[1]Sweden forbids reproductive cloning, but allows therapeutic cloning and authorized a stem cell bank.[1][6]

In 2001, the British Parliament amended the Human Fertilisation and Embryology Act 1990 (since amended by the Human Fertilisation and Embryology Act 2008) to permit the destruction of embryos for hESC harvests but only if the research satisfies one of the following requirements:

The United Kingdom is one of the leaders in stem cell research, in the opinion of Lord Sainsbury, Science and Innovation Minister for the UK.[7] A new 10 million stem cell research centre has been announced at the University of Cambridge.[8]

The primary legislation in South Africa that deals with embryo research is the Human Tissue Act, which is set to be replaced by Chapter 8 of the National Health Act. The NHA Chapter 8 has been enacted by parliament, but not yet signed into force by the president. The process of finalising these regulations is still underway. The NHA Chapter 8 allows the Minister of Health to give permission for research on embryos not older than 14 days. The legislation on embryo research is complemented by the South African Medical Research Council's Ethics Guidelines. These Guidelines advise against the creation of embryos for the sole purpose of research. In the case of Christian Lawyers Association of South Africa & others v Minister of Health & others[9] the court ruled that the Bill of Rights is not applicable to the unborn. It has therefore been argued based on constitutional grounds (the right to human dignity, and the right to freedom of scientific research) that the above limitations on embryo research are overly inhibitive of the autonomy of scientists, and hence unconstitutional.[10]

China prohibits human reproductive cloning but allows the creation of human embryos for research and therapeutic purposes.[1]India banned in 2004 reproductive cloning, permitted therapeutic cloning.[1] In 2004, Japans Council for Science and Technology Policy voted to allow scientists to conduct stem cell research for therapeutic purposes, though formal guidelines have yet to be released.[1] The South Korean government promotes therapeutic cloning, but forbids cloning.[1] The Philippines prohibits human embryonic and aborted human fetal stem cells and their derivatives for human treatment and research. In 1999, Israel passed legislation banning reproductive, but not therapeutic, cloning.[1][6]Saudi Arabia religious officials issued a decree that sanctions the use of embryos for therapeutic and research purposes.[1] According to the Royan Institute for Reproductive Biomedicine, Iran has some of the most liberal laws on stem cell research and cloning.[11][12]

Brazil has passed legislation to permit stem cell research using excess in vitro fertilized embryos that have been frozen for at least three years.[1]

Federal law places restrictions on funding and use of hES cells through amendments to the budget bill.[13] In 2001, George W. Bush implemented a policy limiting the number of stem cell lines that could be used for research.[4] There were some state laws concerning stem cells that were passed in the mid-2000s. New Jersey's 2004 S1909/A2840 specifically permitted human cloning for the purpose of developing and harvesting human stem cells, and Missouri's 2006 Amendment Two legalized certain forms of embryonic stem cell research in the state. On the other hand, Arkansas, Indiana, Louisiana, Michigan, North Dakota and South Dakota passed laws to prohibit the creation or destruction of human embryos for medical research.[13]

During Bush's second term, in July 2006, he used his first Presidential veto on the Stem Cell Research Enhancement Act. The Stem Cell Research Enhancement Act was the name of two similar bills, and both were vetoed by President George W. Bush and were not enacted into law. New Jersey congressman Chris Smith wrote a Stem Cell Therapeutic and Research Act of 2005, which made some narrow exceptions, and was signed into law by President George W. Bush.

In November 2004, California voters approved Proposition 71, creating a US$3 billion state taxpayer-funded institute for stem cell research, the California Institute for Regenerative Medicine. It hopes to provide $300 million a year.

President Barack Obama removed the restriction of federal funding passed by Bush in 2001, which only allowed funding on the 21 cell lines already created. However, the Dickey Amendment to the budget, The Omnibus Appropriations Act of 2009, still bans federal funding of creating new cell lines. In other words, the federal government will now fund research which uses the hundreds of more lines created by public and private funds.[14]

In March 2002, the Canadian Institutes of Health Research announced the first ever guidelines for human pluripotent stem cell research in Canada. The federal granting agencies, CIHR, Natural Sciences and Engineering Research Council, and Social Sciences and Humanities Research Council of Canada teamed up and agreed that no research with human IPSCs would be funded without review and approval from the Stem Cell Oversight Committee (SCOC).[15]

In March 2004, Canadian parliament enacted the Assisted Human Reproduction Act (AHRA), modeled on the United Kingdoms Human Fertilization and Embryology Act of 1990. Highlights of the act include prohibitions against the creation of embryos for research purposes and the criminalization of commercial transactions in human reproductive tissues.[16]

In 2005, Canada enacted a law permitting research on discarded embryos from in vitro fertilization procedures. However, it prohibits the creation of human embryos for research.[1]

On June 30, 2010, The Updated Guidelines for Human Pluripotent Stem Cell Research outline that:

Canada's National Embryonic Stem Cell Registry:

Australia is partially supportive (exempting reproductive cloning yet allowing research on embryonic stem cells that are derived from the process of IVF). New Zealand, however, restricts stem cell research.[17]

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Hormone replacement therapy (HRT) – webmd.com

Posted: November 23, 2016 at 7:46 pm

If youre looking for relief from menopause symptoms, knowing the pros and cons of hormone replacement therapy (HRT) can help you decide whether its right for you.

HRT (also known as hormone therapy, menopausal hormone therapy, and estrogen replacement therapy) uses female hormones -- estrogen and progesterone -- to treat common symptoms of menopause and aging. Doctors can prescribe it during or after menopause.

After your period stops, your hormone levels fall, causing uncomfortable symptoms like hot flashes and vaginal dryness, and sometimes conditions like osteoporosis. HRT replaces hormones your body no longer makes. Its the most effective treatment for menopause symptoms.

You might think of pregnancy when you think of estrogen. In women of child-bearing age, it gets the uterus ready to receive a fertilized egg. It has other roles, too -- it controls how your body uses calcium, which strengthens bones, and raises good cholesterol in the blood.

If you still have your uterus, taking estrogen without progesterone raises your risk for cancer of the endometrium, the lining of the uterus. Since the cells from the endometrium arent leaving your body during your period any more, they may build up in your uterus and lead to cancer. Progesterone lowers that risk by thinning the lining.

Once you know the hormones that make up HRT, think about which type of HRT you should get:

Estrogen Therapy: Doctors generally suggest a low dose of estrogen for women who have had a hysterectomy, the surgery to remove the uterus. Estrogen comes in different forms. The daily pill and patch are the most popular, but the hormone also is available in a vaginal ring, gel, or spray.

Estrogen/Progesterone/Progestin Hormone Therapy: This is often called combination therapy, since it combines doses of estrogen and progestin, the synthetic form of progesterone. Its meant for women who still have their uterus.

The biggest debate about HRT is whether its risks outweigh its benefits.

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U.Va. Smashes Barrier to Growing Organs from Stem Cells …

Posted: November 23, 2016 at 7:46 pm

Scientists at the University of Virginia School of Medicine have overcome one of the greatest challenges in biology and taken a major step toward being able to grow whole organs and tissues from stem cells. By manipulating the appropriate signaling, the U.Va. researchers have turned embryonic stem cells into a fish embryo, essentially controlling embryonic development.

The research will have dramatic impact on the future use of stem cells to better the human condition, providing a framework for future studies in the field of regenerative medicine aimed at constructing tissues and organs from populations of cultured pluripotent cells.

In accomplishing this, U.Va. scientists Bernard and Chris Thisse have overcome the most massive of biological barriers. We have generated an animal by just instructing embryonic cells the right way, said Chris Thisse of the School of Medicines Department of Cell Biology.

The importance of that is profound. If we know how to instruct embryonic cells, she said, we can pretty much do what we want. For example, scientists will be able one day to instruct stem cells to grow into organs needed for transplant.

Directing Embryonic Development

The researchers were able to identify the signals sufficient for starting the cascade of molecular and cellular processes that lead to a fully developed fish embryo. With this study came an answer to the longstanding question of how few signals can initiate the processes of development: amazingly, only two.

The study has shed light on the important roles these two signals play for the formation of organs and full development of a zebrafish embryo. Moreover, the Thisses are now able to direct embryonic development and formation of tissues and organs by controlling signal locations and concentrations.

The embryo they generated was smaller than a normal embryo, because they instructed a small pool of embryonic stem cells, but otherwise he has everything in terms of appropriate development, said Bernard Thisse of the Department of Cell Biology.

Their next steps will be to attempt to reproduce their findings using mice. They expect molecular and cellular mechanisms will be extremely similar in mice and other mammals including humans.

The findings have been published online by Science and will appear in a forthcoming print edition of the prestigious journal. The article was written by U.Va.s Peng-Fei Xu, Nathalie Houssin, Karine F. Ferri-Lagneau, Bernard Thisse and Christine Thisse.

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