Mutations in the coding region of the neurogenin 3 gene (NEUROG3) are not a common cause of maturity-onset diabetes of the young in Japanese subjects

Diabetes

Volumn 50, Issue 3, 2001, Pages 694-696

  Del Bosque Plata, Laura ^a   Lin, Joseph ^c   Horikawa, Yukio ^a   Schwarz, Peter E H ^a   Cox, Nancy J ^a   Iwasaki, Naoko ^b   Ogata, Makiko ^b   Iwamoto, Yasuhiko ^b   German, Michael S ^c   Bell, Graeme I ^a  

^a UNIVERSITY OF CHICAGO   (United States)

^b TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

INSULIN; NEUROGENIN 3; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

5' UNTRANSLATED REGION; AMINO ACID SUBSTITUTION; ARTICLE; CENTRAL NERVOUS SYSTEM; CODON; GENE DELETION; GENE EXPRESSION; GENE MUTATION; GENETIC POLYMORPHISM; GENETIC SCREENING; HUMAN; JAPAN; MAJOR CLINICAL STUDY; MATURITY ONSET DIABETES MELLITUS; NUCLEOTIDE SEQUENCE; PANCREAS ISLET BETA CELL; PRIORITY JOURNAL; PROMOTER REGION;

EID: 0035119823     PISSN: 00121797     EISSN: None     Source Type: Journal    
DOI: 10.2337/diabetes.50.3.694     Document Type: Article

References (15)

1. Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3)
2. Mutation in hepatocyte nuclear factor-1β gene (TCF2) associated with MODY
3. Mutations in the hepatocyte nuclear factor-4α gene in maturity-onset diabetes of the young (MODY1)
4. Early-onset type-II diabetes mellitus (MODY4) linked to IPF1
5. Mutations in NEUROD1 are associated with the development of type 2 diabetes
6. Expression of neurogenin3 reveals an islet cell precursor population in the pancreas
7. Notch signalling controls pancreatic cell differentiation
8. Independent development of pancreatic α-and β-cells from neurogenin3-expressing precursors: A role for the notch pathway in repression of premature differentiation
9. Neurogenin3 is required for the development of the four endocrine cell lineages of the pancreas
10. Reduced pancreatic polypeptide response to hypoglycemia and amylin response to arginine in subjects with a mutation in the HNF-4α/MODY 1 gene
11. β-cell transcription factors and diabetes: Mutations in the coding region of the BETA2/NeuroD1 (NEUROD1) and Nkx2.2 (NKX2B) genes are not associated with maturity-onset diabetes of the young in Japanese
12. β-cell transcription factors and diabetes: No evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3β gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young
13. Organization and partial sequence of the hepatocyte nuclear factor-4α/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY
14. Recommendations for a nomenclature system for human gene mutations: Nomenclature Working Group