Opposite phenotypes of hypomorphic and Y766 phosphorylation site mutations reveal a function for Fgfr1 in anteroposterior patterning of mouse embryos

Genes and Development

Volumn 12, Issue 15, 1998, Pages 2332-2344

  Partanen, Juha ^a   Schwartz, Lois ^a   Rossant, Janet ^a,b  

^a MOUNT SINAI HOSPITAL   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

Fibroblast growth factor; Homeotic transformation; Hox gene; Limb patterning; Phospholipase C; Somite

Indexed keywords

ARTICLE; AUTOPHOSPHORYLATION; DEVELOPMENTAL GENETICS; EMBRYO; EMBRYO DEVELOPMENT; GENE ACTIVITY; GENE CONTROL; GENE LOCUS; GENE MUTATION; GENE TARGETING; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION;

MAMMALIA;

EID: 0032146074     PISSN: 08909369     EISSN: None     Source Type: Journal    
DOI: 10.1101/gad.12.15.2332     Document Type: Article

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