Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease-Reference-Cited by-同舟云学术

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Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease

Published:1995-05-01 Issue:5 Volume:4 Page:821-830
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Angrist M.,Bolk S.,Thiel B.,Puffenberger E. G.,Hofstra R. M.,Buys C. H. C. M.,Cass D. T.,Chakravarti A.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/4/5/821/2088916/4-5-821.pdf

Cited by 224 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 interplay of common genetic variants NRG1 rs2439302 and RET rs2435357 increases the risk of developing Hirschsprung’s disease;Frontiers in Cell and Developmental Biology;2023-07-07

2. Comprehensive characterization of the genetic landscape of familial Hirschsprung’s disease;World Journal of Pediatrics;2023-03-01

3. RET Proto-Oncogene—Not Such an Obvious Starting Point in Cancer Therapy;Cancers;2022-10-27

4. Association of rs2435357 and rs2506030 polymorphisms in RET with susceptibility to hirschsprung disease: A systematic review and meta-analysis;Frontiers in Pediatrics;2022-10-17

5. The <i>RET</i> gene encodes RET protein, which triggers intracellular signaling pathways for enteric neurogenesis, and <i>RET</i> mutation results in Hirschsprung's disease;AIMS Neuroscience;2022

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