Fibroblast growth factor 10 plays a causative role in the tracheal cartilage defects in a mouse model of apert syndrome

Pediatric Research

Volumn 66, Issue 4, 2009, Pages 386-390

  Tiozzo, Caterina ^a   Langhe, Stijn De ^b   Carraro, Gianni ^c   Alam, Denise Al ^c   Nagy, Andre ^c   Wigfall, Clarence ^c   Hajihosseini, Mohammad K ^d   Warburton, David ^c   Minoo, Parviz ^a   Bellusci, Saverio ^c  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^b DEPARTMENT OF MEDICINE   (United States)

^c CHILDREN S HOSPITAL LOS ANGELES   (United States)

^d UNIVERSITY OF EAST ANGLIA   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR 10; FIBROBLAST GROWTH FACTOR RECEPTOR 2; TRANSCRIPTION FACTOR TBX5;

ACROCEPHALOSYNDACTYLY; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL PROLIFERATION; CHONDROPATHY; CONTROLLED STUDY; EMBRYO; EXPERIMENTAL MOUSE; FEMALE; MESENCHYME CELL; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; TRACHEA STENOSIS;

ACROCEPHALOSYNDACTYLIA; ANIMALS; BODY PATTERNING; CARTILAGE; EMBRYO, MAMMALIAN; FIBROBLAST GROWTH FACTOR 10; HUMANS; MICE; MICE, TRANSGENIC; PHENOTYPE; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; SIGNAL TRANSDUCTION; T-BOX DOMAIN PROTEINS; TRACHEA;

EID: 70350441830     PISSN: 00313998     EISSN: 15300447     Source Type: Journal    
DOI: 10.1203/PDR.0b013e3181b45580     Document Type: Article

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