By Philip M. Parker
In March 2001, the nationwide Institutes of overall healthiness issued the subsequent caution: "The variety of websites delivering health-related assets grows each day. Many websites offer invaluable info, whereas others could have info that's unreliable or misleading." in addition, as a result swift elevate in Internet-based info, many hours could be wasted looking out, opting for, and printing. due to the fact that purely the smallest fraction of knowledge facing Angelman syndrome is listed in se's, equivalent to www.google.com or others, a non-systematic method of web examine may be not just time eating, but additionally incomplete. This publication was once created for doctors, scholars, and participants of most of the people who are looking to behavior scientific study utilizing the main complex instruments on hand and spending the smallest amount of time doing so.
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Extra info for Angelman Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
The molecular basis for these diseases is deregulation of imprinted gene clusters on 11 p15 and 15q11 caused predominantly by either deletions within imprinting control centers (ICC) or by epigenetic DMA methylation changes in the ICC. Elevated risk for AS and BWS has been associated with assisted reproductive technologies, which are thought to induce epigenetic loss of imprinting during in vitro embryo culture. This proposal tests the overall hypothesis that epigenetic alterations alone can cause developmental pathologies that model these syndromes as a result of global loss of imprinting (LOI), and further tests a therapeutic approach for correcting LOI events.
User registration, a subscription fee, or some other type of fee may be required to access the full text of articles in some journals. gov/pubmed. Type Angelman syndrome (or synonyms) into the search box, and click Go. The following is the type of output you can expect from PubMed for Angelman syndrome (hyperlinks lead to article summaries): • A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp. Author(s): Buiting K, Lich C, Cottrell S, Barnicoat A, Horsthemke B.
Db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=10647904&query_hl=12&itool=pubmed_docsum • A candidate model for Angelman syndrome in the mouse. Author(s): Cattanach BM, Barr JA, Beechey CV, Martin J, Noebels J, Jones J. Source: Mammalian Genome : Official Journal of the International Mammalian Genome Society. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=9195990&query_hl=12&itool=pubmed_docsum • A case of Angelman syndrome arising as a result of a de novo Robertsonian translocation. Author(s): Ramsden S, Gaunt L, Seres-Santamaria A, Clayton-Smith J.
Angelman Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker