{"id":1065146,"date":"2012-04-26T22:10:55","date_gmt":"2012-04-26T22:10:55","guid":{"rendered":"http:\/\/www.longevitymedicine.tv\/second-um-stem-cell-line-now-available-to-help-cure-nerve-condition\/"},"modified":"2024-08-18T11:09:47","modified_gmt":"2024-08-18T15:09:47","slug":"second-um-stem-cell-line-now-available-to-help-cure-nerve-condition-2","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/diseases\/second-um-stem-cell-line-now-available-to-help-cure-nerve-condition-2.php","title":{"rendered":"Second UM Stem Cell Line Now Available To Help Cure Nerve Condition"},"content":{"rendered":"<p><p>    ANN ARBOR  The University of Michigans second human embryonic    stem cell line has just been placed on the U.S. National    Institutes of Healths registry, making the cells available for    federally funded research. It is the second of the stem cell    lines derived at UM 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 UM 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 UM    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>    UM 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. UM has several    other disease-specific hESClines 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 OShea,    professor of cell and developmental biology at the UM 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 UM 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.    PGDis 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 UM, patients with    embryos that test positive for a genetic disease now have the    option of donating those embryos to UM if they have decided not    to use them for reproductive purposes and the embryos would    otherwise be discarded.  <\/p>\n<\/p>\n<p>View post:<br \/>\n<a target=\"_blank\" href=\"http:\/\/detroit.cbslocal.com\/2012\/04\/25\/second-um-stem-cell-line-now-available-to-help-cure-nerve-condition\/\" title=\"Second UM Stem Cell Line Now Available To Help Cure Nerve Condition\" rel=\"noopener\">Second UM Stem Cell Line Now Available To Help Cure Nerve Condition<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> ANN ARBOR The University of Michigans second human embryonic stem cell line has just been placed on the U.S. National Institutes of Healths registry, making the cells available for federally funded research. It is the second of the stem cell lines derived at UM to be placed on the registry <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/diseases\/second-um-stem-cell-line-now-available-to-help-cure-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-1065146","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\/1065146"}],"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=1065146"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/1065146\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=1065146"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=1065146"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=1065146"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}