Murine dishevelled 3 functions in redundant pathways with dishevelled 1 and 2 in normal cardiac outflow tract, cochlea, and neural tube development

PLoS Genetics

Volumn 4, Issue 11, 2008, Pages

  Etheridge, S Leah ^a   Ray, Saugata ^a,g   Li, Shuangding ^b   Hamblet, Natasha S ^a,h   Lijam, Nardos ^c   Tsang, Michael ^d   Greer, Joy ^a   Kardos, Natalie ^a   Wang, Jianbo ^a,i   Sussman, Daniel J ^e   Chen, Ping ^b   Wynshaw Boris, Anthony ^a,f  

^a UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

^b EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c Department of Community Education and Workforce Development   (United States)

^d UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^e New Horizons Diagnostics Corporation   (United States)

^f UNIVERSITY OF CALIFORNIA   (United States)

^g BURNHAM INSTITUTE   (United States)

^h EASTERN VIRGINIA MEDICAL SCHOOL   (United States)

ⁱ UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DISHEVELLED 1; DISHEVELLED 2; DISHEVELLED 3; DISHEVELLED PROTEIN; UNCLASSIFIED DRUG; WNT PROTEIN; DISHEVELLED PROTEINS; PHOSPHOPROTEIN; SIGNAL TRANSDUCING ADAPTOR PROTEIN;

ALLELE; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; COCHLEA; CONTROLLED STUDY; CORTI ORGAN; DEVELOPMENT; HEART DEVELOPMENT; HEART OUTFLOW TRACT OBSTRUCTION; HEART RIGHT VENTRICLE DOUBLE OUTLET; MOUSE; MUTANT; NEURAL TUBE; NEURAL TUBE DEFECT; NEURULATION; NONHUMAN; PATENT DUCTUS ARTERIOSUS; PHENOTYPE; PROTEIN FUNCTION; SIGNAL TRANSDUCTION; STEREOCILIUM; TRANSGENE; ANIMAL; ANIMAL EMBRYO; CONGENITAL HEART MALFORMATION; FEMALE; GENETICS; HEART; HEART MUSCLE; HUMAN; MALE; METABOLISM; MORPHOGENESIS; MOUSE MUTANT; PRENATAL DEVELOPMENT;

MAMMALIA; MURINAE; MUS;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ANIMALS; COCHLEA; EMBRYO, MAMMALIAN; FEMALE; HEART; HEART DEFECTS, CONGENITAL; HUMANS; MALE; MICE; MICE, KNOCKOUT; MORPHOGENESIS; MYOCARDIUM; NEURAL TUBE; NEURAL TUBE DEFECTS; PHENOTYPE; PHOSPHOPROTEINS; SIGNAL TRANSDUCTION; WNT PROTEINS;

EID: 57149114315     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1000259     Document Type: Article

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