Inactivation of Cdc42 in neural crest cells causes craniofacial and cardiovascular morphogenesis defects

Developmental Biology

Volumn 383, Issue 2, 2013, Pages 239-252

  Liu, Yang ^a   Jin, Yixin ^a   Li, Jieli ^a   Seto, Edward ^a   Kuo, Enoch ^a   Yu, Wei ^b   Schwartz, Robert J ^b   Blazo, Maria ^c   Zhang, Shenyuan L ^a   Peng, Xu ^a  

^a TEXAS A M COLLEGE OF MEDICINE   (United States)

^b University of Houston   (United States)

^c TEXAS A AND M HEALTH SCIENCE CENTER   (United States)

Author keywords

Cdc42; Craniofacial malformation; GTPase; Migration; Neural crest cell; Persistent truncus arteriosus

Indexed keywords

BONE MORPHOGENETIC PROTEIN 2; PROTEIN CDC42;

ANIMAL CELL; ANIMAL CELL CULTURE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; AORTA ARCH; ARTERIAL TRUNK; ARTICLE; BLOOD VESSEL; CARDIOVASCULAR MALFORMATION; CELL ISOLATION; CLEFT LIP; CONTROLLED STUDY; CRANIOFACIAL MALFORMATION; CYTOSKELETON; EMBRYO; EMBRYO DEVELOPMENT; FEMALE; HISTOLOGY; IMMUNOFLUORESCENCE; KNOCKOUT MOUSE; LETHALITY; MOUSE; MUTANT; NEURAL CREST CELL; NONHUMAN; OSSIFICATION; PRIORITY JOURNAL; PULMONARY ARTERY; SKULL;

MUS; VERTEBRATA;

EID: 84885850901     PISSN: 00121606     EISSN: 1095564X     Source Type: Journal    
DOI: 10.1016/j.ydbio.2013.09.013     Document Type: Article

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