Foxn3 is essential for craniofacial development in mice and a putative candidate involved in human congenital craniofacial defects

Biochemical and Biophysical Research Communications

Volumn 400, Issue 1, 2010, Pages 60-65

  Samaan, George ^a   Yugo, Danielle ^a   Rajagopalan, Sangeetha ^a   Wall, Jonathan ^a   Donnell, Robert ^a   Goldowitz, Dan ^b   Gopalakrishnan, Rajaram ^c   Venkatachalam, Sundaresan ^a  

^a UNIVERSITY OF TENNESSEE   (United States)

^b UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^c UNIVERSITY OF MINNESOTA   (United States)

Author keywords

Craniofacial; Fork head; Foxn3; Mammalian development; Mouse model; Transcription factor

Indexed keywords

PROTEIN; PROTEIN FOXN3; UNCLASSIFIED DRUG; CELL CYCLE PROTEIN; FORKHEAD TRANSCRIPTION FACTOR; FOXN3 PROTEIN, HUMAN; FOXN3 PROTEIN, MOUSE; REPRESSOR PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; CRANIOFACIAL DEVELOPMENT; CRANIOFACIAL MALFORMATION; EMBRYO; EYE MALFORMATION; FEMALE; FOXN3 GENE; GENE; GROWTH RETARDATION; HUMAN; MALE; MOUSE; MOUSE MUTANT; NEWBORN; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN FUNCTION; TOOTH MALFORMATION; ANIMAL; EMBRYO DEATH; GENETICS; GROWTH DISORDER; LETHAL GENE; METABOLISM; MUTANT MOUSE STRAIN; MUTATION;

ANIMALS; CELL CYCLE PROTEINS; CRANIOFACIAL ABNORMALITIES; EMBRYO LOSS; EYE ABNORMALITIES; FORKHEAD TRANSCRIPTION FACTORS; GENES, LETHAL; GROWTH DISORDERS; HUMANS; MICE; MICE, MUTANT STRAINS; MUTATION; REPRESSOR PROTEINS; TOOTH ABNORMALITIES;

MAMMALIA; MUS;

EID: 78650852967     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2010.07.142     Document Type: Article

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