Mutations in PTF1A cause pancreatic and cerebellar agenesis-Reference-Cited by-同舟云学术

Mutations in PTF1A cause pancreatic and cerebellar agenesis

Published:2004-11-14 Issue:12 Volume:36 Page:1301-1305
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Sellick Gabrielle S,Barker Karen T,Stolte-Dijkstra Irene,Fleischmann Christina,J Coleman Richard,Garrett Christine,Gloyn Anna L,Edghill Emma L,Hattersley Andrew T,Wellauer Peter K,Goodwin Graham,Houlston Richard S

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1475.pdf

Reference16 articles.

1. Gentz, J.C. & Cornblath, M. Transient diabetes of the newborn. Adv. Pediatr. 16, 345–363 (1969).

2. Shield, J.P.H. et al. Neonatal diabetes: A study of its aetiopathology and genetic basis. Arch. Dis. Child Fetal Neonatal Ed. 76, F39–F42 (1997).

3. Sellick, G.S., Garrett, C. & Houlston, R.S. A novel gene for neonatal diabetes mellitus maps to chromosome 10p12.1-p13. Diabetes 52, 2636–2638 (2003).

4. Krapp, A. et al. The bHLH protein PTF1-p48 is essential for the formation of the exocrine and the correct spatial organization of the endocrine pancreas. Genes Dev. 12, 3752–3763 (1998).

5. Kawaguchi, Y. et al. The role of the transcriptional regulator PTF1A in converting intestinal to pancreatic progenitors. Nat. Genet. 32, 128–134 (2002).

Cited by 384 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. The role of noncoding RNAs in beta cell biology and tissue engineering;Life Sciences;2024-07

2. Defects of Midbrain/Hindbrain Development: Defects of Anteroposterior and Dorsoventral Patterning;Journal of Pediatric Neurology;2024-05-29

3. Anomalies of Midbrain/Hindbrain Development: Malformations of Cerebellum: Diagnosis, Classification, and Rehabilitative Hypothesis;Journal of Pediatric Neurology;2024-05-11

4. Pancreatic Crosstalk in the Disease Setting: Understanding the Impact of Exocrine Disease on Endocrine Function;Comprehensive Physiology;2024-03-29

5. Insulin Secretion Defect in Children and Adolescents with Obesity: Clinical and Molecular Genetic Characterization;Journal of Diabetes Research;2024-03-20