{"id":1065121,"date":"2012-04-26T22:10:51","date_gmt":"2012-04-26T22:10:51","guid":{"rendered":"http:\/\/www.longevitymedicine.tv\/new-embryonic-stem-cell-line-will-aid-research-on-nerve-condition\/"},"modified":"2024-08-18T11:09:35","modified_gmt":"2024-08-18T15:09:35","slug":"new-embryonic-stem-cell-line-will-aid-research-on-nerve-condition-2","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/diseases\/new-embryonic-stem-cell-line-will-aid-research-on-nerve-condition-2.php","title":{"rendered":"New embryonic stem cell line will aid research on nerve condition"},"content":{"rendered":"<p><p>    ScienceDaily (Apr. 25, 2012)  The    University of Michigan's second human embryonic stem cell line    has just been placed on the U.S. National Institutes of    Health's registry, making the cells available for    federally-funded research. It is the second of the stem cell    lines derived at U-M to be placed on the registry.  <\/p>\n<p>    The line, known as UM11-1PGD, was derived from a cluster of    about 30 cells removed from a donated five-day-old embryo    roughly the size of the period at the end of this sentence.    That embryo was created for reproductive purposes, tested and    found to be affected with a genetic disorder, deemed not    suitable for implantation, and would therefore have otherwise    been discarded when it was donated in 2011.  <\/p>\n<p>    It carries the gene defect responsible for Charcot-Marie-Tooth    disease, a hereditary neurological disorder characterized by a    slowly progressive degeneration of the muscles in the foot,    lower leg and hand. CMT, as it is known, is one of the most    common inherited neurological disorders, affecting one in 2,500    people in the United States. People with CMT usually begin to    experience symptoms in adolescence or early adulthood.  <\/p>\n<p>    The embryo used to create the cell line was never frozen, but    rather was transported from another IVF laboratory in the state    of Michigan to the U-M in a special container. This may mean    that these stem cells will have unique characteristics and    utilities in understanding CMT disease progression or screening    therapies in comparison to other human embryonic stem cells.  <\/p>\n<p>    \"We are proud to provide this cell line to the scientific    community, in hopes that it may aid the search for new    treatments and even a cure for CMT,\" says Gary Smith, Ph.D.,    who derived the line and also is co-director of the U-M    Consortium for Stem Cell Therapies, part of the A. Alfred    Taubman Medical Research Institute. \"Once again, the acceptance    of these cells to the registry demonstrates our attention to    details of proper oversight, consenting, and following of NIH    guidelines.\"  <\/p>\n<p>    U-M is one of only four institutions -- including two other    universities and one private company -- to have    disease-specific stem cell lines listed in the national    registry. U-M has several other disease-specific hESC lines    submitted to NIH and awaiting approval, says Smith, who is a    professor in the Department of Obstetrics and Gynecology at the    University of Michigan Medical School. The first line, a    genetically normal one, was accepted to the registry in    February.  <\/p>\n<p>    \"Stem cell lines that carry genetic traits linked to specific    diseases are a model system to investigate what causes these    diseases and come up with treatments,\" says Sue O'Shea, Ph.D.,    professor of Cell and Developmental Biology at the U-M Medical    School, and co-director of the Consortium for Stem Cell    Therapies.  <\/p>\n<p>    Each line is the culmination of years of preparation and    cooperation between U-M and Genesis Genetics, a Michigan-based    genetic diagnostic company. This work was made possible by    Michigan voters' November 2008 approval of a state    constitutional amendment permitting scientists to derive    embryonic stem cell lines using surplus embryos from fertility    clinics or embryos with genetic abnormalities and not suitable    for implantation.  <\/p>\n<p>    The amendment also made possible an unusual collaboration that    has blossomed between the University of Michigan and molecular    research scientists at Genesis Genetics, a company that has    grown in only eight years to become the leading global provider    of pre-implantation genetic diagnosis (PGD) testing. PGD is a    testing method used to identify days-old embryos carrying the    genetic mutations responsible for serious inherited diseases.    During a PGD test, a single cell is removed from an    eight-celled embryo. The other seven cells continue to multiply    and on the fifth day form a cluster of roughly 100 cells known    as a blastocyst.  <\/p>\n<p>    Genesis Genetics performs nearly 7,500 PGD tests annually.    Under the arrangement between the company and U-M, patients    with embryos that test positive for a genetic disease now have    the option of donating those embryos to U-M if they have    decided not to use them for reproductive purposes and the    embryos would otherwise be discarded.  <\/p>\n<\/p>\n<p>Excerpt from:<br \/>\n<a target=\"_blank\" href=\"http:\/\/www.sciencedaily.com\/releases\/2012\/04\/120425140459.htm\" title=\"New embryonic stem cell line will aid research on nerve condition\" rel=\"noopener\">New embryonic stem cell line will aid research on nerve condition<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> ScienceDaily (Apr. 25, 2012) The University of Michigan's second human embryonic stem cell line has just been placed on the U.S. National Institutes of Health's registry, making the cells available for federally-funded research <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/diseases\/new-embryonic-stem-cell-line-will-aid-research-on-nerve-condition-2.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":64,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[1246871],"tags":[],"class_list":["post-1065121","post","type-post","status-publish","format-standard","hentry","category-diseases"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/1065121"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/64"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=1065121"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/1065121\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=1065121"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=1065121"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=1065121"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}