Type 2 diabetes locus on 12q15 further mapping and mutation screening of two candidate genes

Diabetes

Volumn 50, Issue 1, 2001, Pages 204-208

  Bektas, Arsun ^a,b   Hughes, Jennifer N ^a   Warram, James H ^a   Krolewski, Andrzej S ^a,b   Doria, Alessandro ^a,b  

^a JOSLIN DIABETES CENTER   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 12Q; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; HUMAN; NON INSULIN DEPENDENT DIABETES MELLITUS; PRIORITY JOURNAL;

EID: 0035157481     PISSN: 00121797     EISSN: None     Source Type: Journal    
DOI: 10.2337/diabetes.50.1.204     Document Type: Article

References (20)

1. A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2
2. Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families
3. Molecular genetics of maturity-onset diabetes of the young
4. Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus
5. A gene for maturity onset diabetes of the young maps to chromosome 12q
6. Mutations in the hepatocyte nuclear factor-1α gene are a common cause of maturity-onset diabetes of the young in the U.K
7. Clinical characteristics of early-onset autosomal dominant type 2 diabetes unlinked to known MODY genes
8. Evidence of a novel type 2 diabetes locus 50 cM centromeric to NIDDM2 on chromosome 12q
9. An STS-based map of the human genome
10. Deafness linked to DFNA2: One locus but how many genes?
11. Insulin action and the insulin signaling network
12. Molecular cloning of phogrin, a protein-tyrosine phosphatase homologue localized to insulin secretory granule membranes
13. A physical map of 30,000 human genes
14. Molecular cloning and sequencing of the cDNA for human membrane-bound carboxypeptidase M: Comparison with carboxypeptidases A, B, H, and N
15. Carboxypeptidase E is a regulated secretory pathway sorting receptor: Genetic obliteration leads to endocrine disorders in Cpe (fat) mice
16. Hyperproinsulinaemia in obese fat/fat mice associated with a carboxypeptidase E mutation which reduces enzyme activity
17. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
18. Parametric and nonparametric linkage analysis: A unified multipoint approach
19. Dideoxy fingerprinting (ddF): A rapid and efficient screen for the presence of mutations
20. Trinucleotide repeats at the rad locus: Allele distributions in NIDDM and mapping to a 3-cM region on chromosome 16q