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 pr...
The calpain-10 gene (CAPN10) has been associated with type 2 diabetes, but information on molecular ...
Genome-wide scans for linkage have provided one of the dominant approaches adopted by researchers in...
Haplotype combination 112/121 and its intrinsic vari-ants (UCSNP43,-19, and-63) identified within th...
Variations in the calpain-10 gene (CAPN10) have been identified among Mexican-Americans, and an at-r...
Variation in CAPN10, the gene encoding the ubiquitously expressed cysteine protease calpain-10, has ...
Genetic variations in the Calpain-10 gene, CAPN10, have been reported to be associated with the risk...
Type 2 diabetes is the most common form of diabetes, affecting approximately 5-10% of the adult popu...
Type 2 diabetes is a complex polygenic metabolic disorder of epidemic proportions. This review provi...
CAPN10, which encodes the cysteine protease calpain 10, was the first type 2 diabetes mellitus (T2DM...
A positional cloning study of type 2 diabetes in Mexican Americans identified a region, termed “NIDD...
Although genomewide scans have identified several potential chromosomal susceptibility regions in se...
A positional cloning study of type 2 diabetes in Mexican Americans identified a region, termed “NIDD...
Recently, a positional cloning study proposed that haplotypes at the calpain-10 locus (CAPN10) are a...
Background: Genome – wide analysis of genetic predisposition to type 2 diabetes mellitus in di...
Variation within the calpain-10 gene (CAPN10) has been proposed to account for linkage to type 2 dia...
The calpain-10 gene (CAPN10) has been associated with type 2 diabetes, but information on molecular ...
Genome-wide scans for linkage have provided one of the dominant approaches adopted by researchers in...
Haplotype combination 112/121 and its intrinsic vari-ants (UCSNP43,-19, and-63) identified within th...
Variations in the calpain-10 gene (CAPN10) have been identified among Mexican-Americans, and an at-r...
Variation in CAPN10, the gene encoding the ubiquitously expressed cysteine protease calpain-10, has ...
Genetic variations in the Calpain-10 gene, CAPN10, have been reported to be associated with the risk...
Type 2 diabetes is the most common form of diabetes, affecting approximately 5-10% of the adult popu...
Type 2 diabetes is a complex polygenic metabolic disorder of epidemic proportions. This review provi...
CAPN10, which encodes the cysteine protease calpain 10, was the first type 2 diabetes mellitus (T2DM...
A positional cloning study of type 2 diabetes in Mexican Americans identified a region, termed “NIDD...
Although genomewide scans have identified several potential chromosomal susceptibility regions in se...
A positional cloning study of type 2 diabetes in Mexican Americans identified a region, termed “NIDD...
Recently, a positional cloning study proposed that haplotypes at the calpain-10 locus (CAPN10) are a...
Background: Genome – wide analysis of genetic predisposition to type 2 diabetes mellitus in di...
Variation within the calpain-10 gene (CAPN10) has been proposed to account for linkage to type 2 dia...
The calpain-10 gene (CAPN10) has been associated with type 2 diabetes, but information on molecular ...
Genome-wide scans for linkage have provided one of the dominant approaches adopted by researchers in...
Haplotype combination 112/121 and its intrinsic vari-ants (UCSNP43,-19, and-63) identified within th...