Conditional gene inactivation reveals roles for Fgf10 and Fgfr2 in establishing a normal pattern of epithelial branching in the mouse lung

Developmental Dynamics

Volumn 238, Issue 8, 2008, Pages 1999-2013

  Abler, Lisa L ^a   Mansour, Suzanne L ^b   Sun, Xin ^a  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

^b UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

Branching morphogenesis; Cell survival; Development; Fgf10; Fgfr2; Lung; Proximal distal patterning

Indexed keywords

BETA GALACTOSIDASE; FIBROBLAST GROWTH FACTOR 10; FIBROBLAST GROWTH FACTOR RECEPTOR 2; MUTANT PROTEIN; SURFACTANT PROTEIN C; TRANSCRIPTION FACTOR SOX2; TRANSCRIPTION FACTOR SOX9;

ALLELE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BRANCHING MORPHOGENESIS; BRONCHUS; CELL DEATH; CONTROLLED STUDY; DOWN REGULATION; EMBRYO; GENE INACTIVATION; GENE LOCATION; LUNG ALVEOLUS EPITHELIUM; LUNG DEVELOPMENT; LUNG LOBE; MESENCHYME; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; UPREGULATION;

ANIMALS; BASE SEQUENCE; BODY PATTERNING; CELL DEATH; CELL SURVIVAL; DNA PRIMERS; EPITHELIUM; FEMALE; FIBROBLAST GROWTH FACTOR 10; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENE TARGETING; LUNG; MESODERM; MICE; MICE, KNOCKOUT; MICE, MUTANT STRAINS; MICE, TRANSGENIC; PREGNANCY; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; SIGNAL TRANSDUCTION; SOX9 TRANSCRIPTION FACTOR; SOXB1 TRANSCRIPTION FACTORS;

EID: 67650792487     PISSN: 10588388     EISSN: 10970177     Source Type: Journal    
DOI: 10.1002/dvdy.22032     Document Type: Article

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