Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes-Reference-Cited by-同舟云学术

Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes

Published:1999-11-01 Issue:9 Volume:104 Page:R33-R39
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Macfarlane Wendy M.,Frayling Timothy M.,Ellard Sian,Evans Julie C.,Allen Lisa I.S.,Bulman Michael P.,Ayres Susan,Shepherd Maggie,Clark Penny,Millward Ann,Demaine Andrew,Wilkin Terence,Docherty Kevin,Hattersley Andrew T.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference28 articles.

1. Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus

2. Linkage of type 2 diabetes to the glucokinase gene

3. Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3)

4. Mutations in the hepatocyte nuclear factor-4α gene in maturity-onset diabetes of the young (MODY1)

5. Mutation in hepatocyte nuclear factor–1β gene (TCF2) associated with MODY

Cited by 220 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Unlocking β-cell restoration: The crucial role of PDX1 in diabetes therapy;Pathology - Research and Practice;2024-02

2. Dominant PDX1 deficiency causes highly penetrant diabetes at different ages, associated with obesity and exocrine pancreatic deficiency: Lessons for precision medicine;Diabetes & Metabolism;2024-01

3. Monogenic diabetes;BIDE' s Diabetes Desk Book;2024

4. Dynamic regulation of pancreatic β cell function and gene expression by the SND1 coregulator in vitro;Islets;2023-10-15

5. Early‐onset diabetes mellitus as a presenting feature of Werner's syndrome in an Indian family;Molecular Genetics & Genomic Medicine;2023-10-10