Log on / register
Feedback | Support | My details
Compound developmental eye disorders following inactivation of TGFbeta signaling in neural-crest stem cells.
Ittner LM, Wurdak H, Schwerdtfeger K, Kunz T, Ille F, Leveen P, Hjalt TA, Suter U, Karlsson S, Hafezi F, Born W, Sommer L
J Biol 2005, 4:11
[Full text] [PubMed] [Related articles] [Cited on BioMed Central]


printer friendly 
to  [Help]

PubMed Central articles that cite the above article:

1.
Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities.
Dixon J, Jones NC, Sandell LL, Jayasinghe SM, Crane J, Rey JP, Dixon MJ, Trainor PA
Proc Natl Acad Sci U S A 2006 Sep 5, 103:13403-8
[PubMed Central] [PubMed] [Related articles]

2.
Genetic and epigenetic mechanisms of gene regulation during lens development.
Cvekl A, Duncan MK
Prog Retin Eye Res 2007 Nov, 26:555-97
[PubMed Central] [PubMed] [Related articles]

3.
Identification of pax6-dependent gene regulatory networks in the mouse lens.
Wolf LV, Yang Y, Wang J, Xie Q, Braunger B, Tamm ER, Zavadil J, Cvekl A
PLoS One 2009, 4:e4159
[PubMed Central] [PubMed] [Related articles]

4.
Heparan sulfate deficiency leads to Peters anomaly in mice by disturbing neural crest TGF-beta2 signaling.
Iwao K, Inatani M, Matsumoto Y, Ogata-Iwao M, Takihara Y, Irie F, Yamaguchi Y, Okinami S, Tanihara H
J Clin Invest 2009 Jul, 119:1997-2008
[PubMed Central] [PubMed] [Related articles]


This article is also cited by 3 articles in BioMed Central

printer friendly 
to  [Help]

© 1999-2009 BioMed Central Ltd unless otherwise stated. Part of Springer Science+Business Media.