By Philip M. Parker

In March 2001, the nationwide Institutes of healthiness issued the next caution: "The variety of sites supplying health-related assets grows each day. Many websites supply priceless info, whereas others can have details that's unreliable or misleading." in addition, due to the quick bring up in Internet-based info, many hours may be wasted looking out, identifying, and printing. for the reason that merely the smallest fraction of data facing myotonic dystrophy is listed in se's, corresponding to www.google.com or others, a non-systematic method of net study should be not just time eating, but in addition incomplete. This booklet was once created for doctors, scholars, and individuals of most of the people who are looking to behavior clinical learn utilizing the main complex instruments to be had and spending the smallest amount of time doing so.

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Neurology; University of Minnesota Twin Cities 450 Mcnamara Alumni Center Minneapolis, Mn 554552070 Timing: Fiscal Year 2007; Project Start 01-APR-2007; Project End 31-MAR-2012 Summary: (provided by applicant): Myotonic Dystrophy (DM), one of the most common forms of muscular dystrophy, is a multisystemic disorder caused by mutations on either chromosome 19 (DM1) or chromosome 3 (DM2). The pathophysiological effects of the DM1 mutation have been controversial because it is an untranslated CTG expansion in the 3' region of a gene, and thus causes this severe dominantly inherited disease without affecting the coding portion of a gene.

Projects 1, 2, & 3 interact with the Repository Core and this Core will interact with the other MDCRCs. ; Professor of Neurology and Member; Fred Hutchinson Cancer Research Center Box 19024, 1100 Fairview Ave N Seattle, Wa 981091024 Timing: Fiscal Year 2005; Project Start 01-SEP-1998; Project End 30-JUN-2008 Summary: (provided by applicant): The most prevalent form of myotonic dystrophy is caused by the expansion of a CTG triplet repeat in agene-rich region of chromosome 19 at the DM1 locus. The CTG repeat is in the non-coding region of the DMPK gene and adjacent to the regulatory region of the neighboring SIX5 gene.

RNA also plays roles in human disease, including Prader-Willi and myotonic dystrophy. g. with RNAi, antisense technology, or with therapeutic ribozymes, requires an understanding of the structures of these RNA sequences. RNAstructure is a software package for RNA secondary structure prediction and analysis. edu and has been downloaded by a total of over 11,000 users. The specific aims of this proposal include both development and maintenance for the RNAstructure package: 1) Develop enthalpy nearest neighbor parameters for RNA secondary structure formation to allow structure prediction and analysis at other temperatures.

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