ATR maintains select progenitors during nervous system development

EMBO Journal

Volumn 31, Issue 5, 2012, Pages 1177-1189

  Lee, Youngsoo ^a   Shull, Erin R P ^a,b   Frappart, Pierre Olivier ^a,c   Katyal, Sachin ^a   Enriquez Rios, Vanessa ^a,b   Zhao, Jingfeng ^a   Russell, Helen R ^a   Brown, Eric J ^d   McKinnon, Peter J ^a,b  

^a ST JUDE CHILDREN S RESEARCH HOSPITAL   (United States)

^b UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

^c GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

^d UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

ATM; ATR; DNA damage; neural development; Seckel syndrome

Indexed keywords

ATR PROTEIN; PHOSPHOTRANSFERASE; PROTEIN P16; PROTEIN P53;

ANIMAL CELL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; ATM GENE; ATR GENE; BRAIN REGION; CELL PROLIFERATION; CONTROLLED STUDY; DNA DAMAGE; DNA REPLICATION; EMBRYO; GENE; GENE DELETION; GENE INACTIVATION; GENOME; MOUSE; NERVOUS SYSTEM DEVELOPMENT; NEURAL STEM CELL; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; TELENCEPHALON;

ANIMALS; APOPTOSIS; BRAIN; CELL CYCLE PROTEINS; CELL PROLIFERATION; HISTOCYTOCHEMISTRY; IMMUNOHISTOCHEMISTRY; MICE; MICE, KNOCKOUT; MICROSCOPY; PROTEIN-SERINE-THREONINE KINASES; STEM CELLS;

ATAXIA TELANGIECTASIA; MURINAE;

EID: 84862777854     PISSN: 02614189     EISSN: 14602075     Source Type: Journal    
DOI: 10.1038/emboj.2011.493     Document Type: Article

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