Ablation of Csk in neural crest lineages causes corneal anomaly by deregulating collagen fibril organization and cell motility

Developmental Biology

Volumn 315, Issue 2, 2008, Pages 474-488

  Takatsuka, Atsuko ^a   Yagi, Reiko ^a   Koike, Masato ^b   Oneyama, Chitose ^a   Nada, Shigeyuki ^a   Schmedt, Christian ^c   Uchiyama, Yasuo ^b   Okada, Masato ^a  

^a OSAKA UNIVERSITY   (Japan)

^b OSAKA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^c Genomics Institute   (United States)

Author keywords

Cas; Cdc42; Cell motility; Cell polarity; Cornea; Cre loxP; Csk; Protein zero; Rac1; Src family kinases

Indexed keywords

CELL PROTEIN; COLLAGEN FIBRIL; COLLAGEN TYPE 1; COLLAGEN TYPE 1A1; CRE RECOMBINASE; CRK ASSOCIATED SUBSTRATE PROTEIN; METALLOPROTEINASE; PROTEIN CDC42; PROTEIN TYROSINE KINASE; PROTEIN ZERO; RAC1 PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL MOTILITY; COLLAGEN SYNTHESIS; CONTROLLED STUDY; CORNEA DISEASE; CORNEA ENDOTHELIUM; CORNEA OPACITY; CYTOSKELETON; DEVELOPMENT; DYSPLASIA; EMBRYO; ENZYME ACTIVITY; FACE DEFORMITY; FLUORESCENCE RESONANCE ENERGY TRANSFER; LOXP SITE; MESENCHYME CELL; MOUSE; NEURAL CREST; NONHUMAN; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN EXPRESSION; PROTEIN PHOSPHORYLATION;

MUS;

EID: 39949083006     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ydbio.2008.01.004     Document Type: Article

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