Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans
about
Computer assisted cloning of human neutral alpha-glucosidase C (GANC): a new paralog in the glycosyl hydrolase gene family 31.Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locusThe Siblings With Ischemic Stroke Study (SWISS) protocolGap junctionsSeven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families.Genetics of type 1 diabetes mellitusGenomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia studyIntegrative analysis for finding genes and networks involved in diabetes and other complex diseasesGenetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitusAllegro, a new computer program for multipoint linkage analysisIdentifying gene interaction enrichment for gene expression dataLinkage analysis of GAW14 simulated data: comparison of multimarker, multipoint, and conditional approaches.Comparison of affected sibling-pair linkage methods to identify gene x gene interaction in GAW15 simulated dataTwo-locus heterogeneity cannot be distinguished from two-locus epistasis on the basis of affected-sib-pair data.Common and unique susceptibility loci in Graves and Hashimoto diseases: results of whole-genome screening in a data set of 102 multiplex families.Search for haplotype interactions that influence susceptibility to type 1 diabetes, through use of unphased genotype data.Novel analytical methods applied to type 1 diabetes genome-scan data.Methods for detecting gene x gene interaction in multiplex extended pedigreesSearching for epistatic interactions in nuclear families using conditional linkage analysis.Detection of gene x gene interactions in genome-wide association studies of human population data.Lack of association of genetic variation in chromosome region 15q14-22.1 with type 2 diabetes in a Japanese population.Exploiting gene x gene interaction in linkage analysis.The CAPN10 gene is associated with insulin resistance phenotypes in the Spanish population.Identifying hypothetical genetic influences on complex disease phenotypes.Something old and something new: wedding recombinant inbred lines with traditional line cross analysis increases power to describe gene interactionsFAM-MDR: a flexible family-based multifactor dimensionality reduction technique to detect epistasis using related individuals.INSIG1 influences obesity-related hypertriglyceridemia in humans.Reconstructability analysis as a tool for identifying gene-gene interactions in studies of human diseases.Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.Age-related macular degeneration--a genome scan in extended families.Are variants in the CAPN10 gene related to risk of type 2 diabetes? A quantitative assessment of population and family-based association studies.Abnormal glucose homeostasis and pancreatic islet function in mice with inactivation of the Fem1b gene.Insights into insulin resistance and type 2 diabetes from knockout mouse models.A genome screen of families with multiple cases of prostate cancer: evidence of genetic heterogeneity.Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthmaA genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1qA genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.Incorporation of molecular data and redefinition of phenotype: new approaches to genetic epidemiology of bipolar manic depressive illness and schizophrenia.Subsets of Finns with high HDL to total cholesterol ratio show evidence for linkage to type 2 diabetes on chromosome 6q.Genetics of schizophrenia and the new millennium: progress and pitfalls.
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Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans
description
im Februar 1999 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в лютому 1999
@uk
name
Loci on chromosomes 2 (NIDDM1) ...... diabetes in Mexican Americans
@en
Loci on chromosomes 2
@nl
type
label
Loci on chromosomes 2 (NIDDM1) ...... diabetes in Mexican Americans
@en
Loci on chromosomes 2
@nl
prefLabel
Loci on chromosomes 2 (NIDDM1) ...... diabetes in Mexican Americans
@en
Loci on chromosomes 2
@nl
P2093
P356
P1433
P1476
Loci on chromosomes 2 (NIDDM1) ...... diabetes in Mexican Americans
@en
P2093
Augustine Kong
Craig L. Hanis
Dan L. Nicolae
Graeme I. Bell
Mike Frigge
P2888
P304
P356
10.1038/6002
P407
P577
1999-02-01T00:00:00Z