Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2000-11-8
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF089087, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF089088, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF089089, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF089090, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF089091, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF089092, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF089093, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF089094, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF089095, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF089096, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF158748, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF200349, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF300795
pubmed:abstractText
Type 2 or non-insulin-dependent diabetes mellitus (NIDDM) is the most common form of diabetes worldwide, affecting approximately 4% of the world's adult population. It is multifactorial in origin with both genetic and environmental factors contributing to its development. A genome-wide screen for type 2 diabetes genes carried out in Mexican Americans localized a susceptibility gene, designated NIDDM1, to chromosome 2. Here we describe the positional cloning of a gene located in the NIDDM1 region that shows association with type 2 diabetes in Mexican Americans and a Northern European population from the Botnia region of Finland. This putative diabetes-susceptibility gene encodes a ubiquitously expressed member of the calpain-like cysteine protease family, calpain-10 (CAPN10). This finding suggests a novel pathway that may contribute to the development of type 2 diabetes.
pubmed:grant
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1061-4036
pubmed:author
pubmed:issnType
Print
pubmed:volume
26
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
163-75
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:11017071-Adult, pubmed-meshheading:11017071-Amino Acid Sequence, pubmed-meshheading:11017071-Calpain, pubmed-meshheading:11017071-Chromosome Mapping, pubmed-meshheading:11017071-Chromosomes, Human, Pair 2, pubmed-meshheading:11017071-Diabetes Mellitus, Type 2, pubmed-meshheading:11017071-European Continental Ancestry Group, pubmed-meshheading:11017071-Finland, pubmed-meshheading:11017071-Gene Frequency, pubmed-meshheading:11017071-Genetic Markers, pubmed-meshheading:11017071-Genetic Predisposition to Disease, pubmed-meshheading:11017071-Genetic Variation, pubmed-meshheading:11017071-Genome, Human, pubmed-meshheading:11017071-Haplotypes, pubmed-meshheading:11017071-Humans, pubmed-meshheading:11017071-Mexican Americans, pubmed-meshheading:11017071-Molecular Sequence Data, pubmed-meshheading:11017071-Polymorphism, Genetic, pubmed-meshheading:11017071-Risk Assessment, pubmed-meshheading:11017071-United States
pubmed:year
2000
pubmed:articleTitle
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.
pubmed:affiliation
Howard Hughes Medical Institute, The University of Chicago, Chicago, Illinois, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't