{"id":54947,"date":"2012-10-30T06:58:37","date_gmt":"2012-10-30T06:58:37","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/the-2nd-meeting-of-the-series-days-of-molecular-medicine.php"},"modified":"2012-10-30T06:58:37","modified_gmt":"2012-10-30T06:58:37","slug":"the-2nd-meeting-of-the-series-days-of-molecular-medicine","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/molecular-medicine\/the-2nd-meeting-of-the-series-days-of-molecular-medicine.php","title":{"rendered":"The 2nd meeting of the series Days of Molecular Medicine"},"content":{"rendered":"<p><p>    PARIS--(BUSINESS WIRE)--  <\/p>\n<p>    Each year the American Association for the Advancement of    Science, which publishes the prestigious journals Science and    Science Translational Medicine, the Karolinska institute in    Stockholm, the DMMGF foundation and the Fondation Ipsen    organise a series of meetings entitled Days of Molecular    Medicine. This year the Institute for Molecular Biotechnology    (Vienna) was also involved in the partnership. The meetings are    highly regarded in the field of translational medicine, which    bridges the gap between fundamental research and medical    application. The latest event took place from 8-10 October in    Vienna, Austria. Several well known scientists, including the    Nobel Prize Eric Kandel attended the meeting.  <\/p>\n<p>    Entitled The translational science of rare diseases: Rare for    Care, the meeting focused on an original topic with    far-reaching consequences: research into rare illnesses and how    it can lead to discovering therapies, including for common    illnesses. Rare illnesses are also known as orphan diseases    because they affect few patients and can therefore be    neglected. Yet, although each rare illness only affects a few    patients, together, they affect a lot of people. Their    treatment also plays an essential role in adapting our approach    to human physiology and pathology. Many rare illnesses have    genetic origins that can be elucidated. Pinpointing the gene or    genes involved enables a protein or a biochemical path to be    targeted and acted on, using gene therapy or drugs. Cystic    fibrosis is a remarkable example of this. Many pathogenic    mutations have been identified and their mechanism brought to    light through research into the disease. As Peter Mueller    (Cambridge, USA) demonstrated in Vienna, this resulted in a    drug formulation that can increase a patients life expectancy    by twenty years!  <\/p>\n<p>    Concerning gene therapy, Alain Fischer (Hpital Necker, Paris,    France) presented his pioneering work, while several others    presented on-going trials to treat Canavan disease or    blindness. Many extremely rare and newly identified illnesses    were also presented, among them those discovered through a    special programme instigated by the American National Institute    of Health.  <\/p>\n<p>    About the Fondation Ipsen  <\/p>\n<p>    Established in 1983 under the aegis of the Fondation de France,    the mission of the Fondation Ipsen is to contribute to the    development and dissemination of scientific knowledge. The    long-standing action of the Fondation Ipsen aims at fostering    the interaction between researchers and clinical practitioners,    which is indispensable due to the extreme specialisation of    these professions. The ambition of the Fondation Ipsen is to    initiate a reflection about the major scientific issues of the    forthcoming years. It has developed an important international    network of scientific experts who meet regularly at meetings    known as Colloques Mdecine et Recherche, dedicated to six main    themes: Alzheimer's disease, neurosciences, longevity,    endocrinology, the vascular system and cancer science. Moreover    the Fondation Ipsen has started since 2007 several meetings in    partnership with the Salk Institute, the Karolinska Institutet,    the Massachusetts General Hospital, the Days of Molecular    Medicine Global Foundation as well as with the science journals    Nature, Cell and Science. The Fondation Ipsen produced several    hundreds publications; more than 250 scientists and biomedical    researchers have been awarded prizes and research grants.  <\/p>\n<\/p>\n<p>Go here to see the original:<\/p>\n<p><a target=\"_blank\" href=\"http:\/\/finance.yahoo.com\/news\/2nd-meeting-series-days-molecular-080000644.html;_ylt=A2KJ3CWHeo9QOwEA0JD_wgt.\" title=\"The 2nd meeting of the series Days of Molecular Medicine\">The 2nd meeting of the series Days of Molecular Medicine<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> PARIS--(BUSINESS WIRE)-- Each year the American Association for the Advancement of Science, which publishes the prestigious journals Science and Science Translational Medicine, the Karolinska institute in Stockholm, the DMMGF foundation and the Fondation Ipsen organise a series of meetings entitled Days of Molecular Medicine. This year the Institute for Molecular Biotechnology (Vienna) was also involved in the partnership. The meetings are highly regarded in the field of translational medicine, which bridges the gap between fundamental research and medical application.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/molecular-medicine\/the-2nd-meeting-of-the-series-days-of-molecular-medicine.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-54947","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\/54947"}],"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=54947"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/54947\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=54947"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=54947"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=54947"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}