{"id":120911,"date":"2014-04-01T13:50:07","date_gmt":"2014-04-01T17:50:07","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/common-molecular-defect-offers-treatment-hope-for-group-of-rare-disorders.php"},"modified":"2014-04-01T13:50:07","modified_gmt":"2014-04-01T17:50:07","slug":"common-molecular-defect-offers-treatment-hope-for-group-of-rare-disorders","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/molecular-medicine\/common-molecular-defect-offers-treatment-hope-for-group-of-rare-disorders.php","title":{"rendered":"Common molecular defect offers treatment hope for group of rare disorders"},"content":{"rendered":"<p><p>    PUBLIC RELEASE DATE:  <\/p>\n<p>    1-Apr-2014  <\/p>\n<p>    Contact: Sarah Avery    <a href=\"mailto:sarah.avery@duke.edu\">sarah.avery@duke.edu<\/a>    919-660-1306    Duke University Medical    Center<\/p>\n<p>    DURHAM, N.C.  Duke Medicine researchers studying tiny,    antennae-like structures called cilia have found a potential    way to ease some of the physical damage of numerous genetic    disorders that result when these essential cellular components    are defective.  <\/p>\n<p>    Different genetic defects cause dysfunction of the cilia, which    often act as sensory organs that receive signals from other    cells. Individually, disorders involving cilia are rare, but    collectively the more than 100 diseases in the category known    as ciliopathies affect as many as one in 1,000 people.    Ciliopathies are characterized by cognitive impairment,    blindness, deafness, kidney and heart disease, infertility,    obesity and diabetes.  <\/p>\n<p>    Recent research has added key insights into the overall role    and function of cilia in cells and what occurs when the    organelle is defective.  <\/p>\n<p>    \"Cilia are required for regulation of a whole host of signaling    pathways for cellular development,\" said Nicholas Katsanis,    PhD, professor of cell biology and director of the Center for    Human Disease Modeling at Duke. \"They are not the only    signaling regulators, but they are critical. It's been    important for us to understand how they do this.\"  <\/p>\n<p>    In the current study, published April 1, 2014, in the    Journal of Clinical Investigation, Katsanis and    colleagues describe a common mechanism that appears to account    for how dysfunctional cilia cause so many different problems in    cellular signaling pathways.  <\/p>\n<p>    Using both cells and animal models, they focused on the    ubiquitin-proteasome system, the cell's machinery tasked with    regulating the cellular environment by breaking down proteins    that are either damaged or in need of removal.  <\/p>\n<p>    \"Imagine regular housekeeping\" Katsanis said. \"Taking out waste    is part and parcel to the process, but not if you end up    throwing away your valuables.\"  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Go here to see the original: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.eurekalert.org\/pub_releases\/2014-04\/dumc-cmd033114.php\/RS=^ADAKgwBbh4wlvrkgkR8ilSjHgDyYsI-\" title=\"Common molecular defect offers treatment hope for group of rare disorders\">Common molecular defect offers treatment hope for group of rare disorders<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> PUBLIC RELEASE DATE: 1-Apr-2014 Contact: Sarah Avery <a href=\"mailto:sarah.avery@duke.edu\">sarah.avery@duke.edu<\/a> 919-660-1306 Duke University Medical Center DURHAM, N.C. Duke Medicine researchers studying tiny, antennae-like structures called cilia have found a potential way to ease some of the physical damage of numerous genetic disorders that result when these essential cellular components are defective <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/molecular-medicine\/common-molecular-defect-offers-treatment-hope-for-group-of-rare-disorders.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"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":[26],"tags":[],"class_list":["post-120911","post","type-post","status-publish","format-standard","hentry","category-molecular-medicine"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/120911"}],"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\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=120911"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/120911\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=120911"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=120911"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=120911"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}