Mutation of the mouse hepatocyte nuclear factor/forkhead homologue 4 gene results in an absence of cilia and random left-right asymmetry

Journal of Clinical Investigation

Volumn 102, Issue 6, 1998, Pages 1077-1082

  Chen, Jianchun ^a   Knowles, Heather J ^a   Hebert, Jennifer L ^a   Hackett, Brian P ^a,b  

^a WASHINGTON UNIVERSITY   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Cilia; Dynein; Left right asymmetry; Situs; Winged helix

Indexed keywords

DYNEIN ADENOSINE TRIPHOSPHATASE; NUCLEAR FACTOR I; TRANSCRIPTION FACTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CILIARY MOTILITY; CONTROLLED STUDY; EMBRYO; EMBRYO AXIS; FEMALE; GENE EXPRESSION REGULATION; GENE MUTATION; GENE TARGETING; GROWTH DISORDER; HYDROCEPHALUS; IN SITU HYBRIDIZATION; KARTAGENER SYNDROME; MALE; MOUSE; MOUSE MUTANT; MULTIGENE FAMILY; NONHUMAN; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SITUS INVERSUS;

EID: 0032530312     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI4786     Document Type: Article

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