High-throughput transcriptome analysis reveals that the loss of Pten activates a novel NKX6-1/RASGRP1 regulatory module to rescue microphthalmia caused by Fgfr2-deficient lenses-Reference-Cited by-同舟云学术

High-throughput transcriptome analysis reveals that the loss of Pten activates a novel NKX6-1/RASGRP1 regulatory module to rescue microphthalmia caused by Fgfr2-deficient lenses

Published:2019-11-05 Issue:11-12 Volume:138 Page:1391-1407
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Padula Stephanie L.,Anand Deepti,Hoang Thanh V.,Chaffee Blake R.,Liu Lin,Liang Chun,Lachke Salil A.^ORCID,Robinson Michael L.^ORCID

Funder

National Eye Institute

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-019-02084-8.pdf

Reference67 articles.

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4. Butler MG, Dasouki MJ, Zhou X-P, Talebizadeh Z, Brown M, Takahashi TN, Eng C et al (2005) Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations. J Med Genet 42(4):318–321

5. Cavalheiro GR, Matos-Rodrigues GE, Zhao Y, Gomes AL, Anand D, Predes D, Martins RAP et al (2017) N-myc regulates growth and fiber cell differentiation in lens development. Dev Biol 429(1):105–117

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