Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome-Reference-Cited by-同舟云学术

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Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome

Published:2009-08-10 Issue:8 Volume:4 Page:e6568
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Rosenfeld Jill A.,Ballif Blake C.,Lucas Ann,Spence Edward J.,Powell Cynthia,Aylsworth Arthur S.,Torchia Beth A.,Shaffer Lisa G.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference32 articles.

1. Novel transcription factor Satb2 interacts with matrix attachment region DNA elements in a tissue-specific manner and demonstrates cell-type-dependent expression in the developing mouse CNS.;O Britanova;Eur J Neurosci,2005

2. SUMO modification of a novel MAR-binding protein, SATB2, modulates immunoglobulin mu gene expression.;G Dobreva;Genes Dev,2003

3. Satb2 regulates callosal projection neuron identity in the developing cerebral cortex.;EA Alcamo;Neuron,2008

4. SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation.;G Dobreva;Cell,2006

5. Identification of SATB2 as the cleft palate gene on 2q32-q33.;DR FitzPatrick;Hum Mol Genet,2003

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