http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-200404100-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a01717442a2a920617ac88dbdf9caacc
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 2003-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a3a49d3748ae0b9c7d8825abf888bbd3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b0b591b9842483362bc1da8fa52636c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_30080fea368ef7e6453636d5d5772a6c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a4f058f8b9d139cdc4c85ebc4b2f4f5f
publicationDate 2004-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-200404100-A
titleOfInvention Methods for analyzing sorbs1 polymorphisms and use in diagnosis of predisposition to insulin disorders and treatment of insulin disorders
abstract The present invention identifies mutations in the human sorbin and SH3-domain-containing-1 (SORBS1) gene, particularly at one or more of positions 220, 249, -7 with respect to exon 5, -25 with respect to exon 6, 682, +64 with respect to exon 9, +61 with respect to exon 10, +69 with respect to exon 11, +33 with respect to exon 16, 1482, 1518, -6 with respect to exon 22, +79 with respect to exon 24, and 2337. A polymorphism at position 682 within exon 7, the T228A allele, correlates with the phenotypes of low blood pressure and low body mass index, and is a protective marker for both obesity and diabetes. The invention also relates to methods and materials for detecting single nucleotide polymorphisms in the SORBS1 gene and to the use of SORBS1 polymorphisms in the diagnosis, screening, and treatment of type 2 diabetes, obesity, hypertension, atherosclerosis, and metabolic syndrome. The invention is predicated on the identification of the human SORBS1 gene.
priorityDate 2002-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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