A molecular basis for differential developmental anomalies in Axenfeld-Rieger syndrome-Reference-Cited by-同舟云学术

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A molecular basis for differential developmental anomalies in Axenfeld-Rieger syndrome

Published:2002-04-01 Issue:7 Volume:11 Page:743-753
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
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Author:

Espinoza H. M.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/11/7/743/2398312/ddf084.pdf

Cited by 56 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. HMGN2 represses gene transcription via interaction with transcription factors Lef-1 and Pitx2 during amelogenesis;Journal of Biological Chemistry;2022-09

2. Axenfeld-Rieger syndrome: more than meets the eye;Journal of Medical Genetics;2022-07-26

3. Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 Variants;Cornea;2022-03-30

4. Mechanistic Insights into Axenfeld–Rieger Syndrome from Zebrafish foxc1 and pitx2 Mutants;International Journal of Molecular Sciences;2021-09-16

5. The Ocular Neural Crest: Specification, Migration, and Then What?;Frontiers in Cell and Developmental Biology;2020-12-23

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