Science 1995 Jul
Threadgill DW, Dlugosz AA, Hansen LA, Tennenbaum T, Lichti U, Yee D, LaMantia C, Mourton T, Herrup K, Harris RC
Abstract
Gene targeting was used to create a null allele at the epidermal growth factor receptor locus (Egfr). The phenotype was dependent on genetic background. EGFR deficiency on a CF-1 background resulted in peri-implantation death due to degeneration of the inner cell mass. On a 129/Sv background, homozygous mutants died at mid-gestation due to placental defects; on a CD-1 background, the mutants lived for up to 3 weeks and showed abnormalities in skin, kidney, brain, liver, and gastrointestinal trac
...[more]t. The multiple abnormalities associated with EGFR deficiency indicate that the receptor is involved in a wide range of cellular activities.
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Mesh Headings:
Abnormalities, Multiple, Animals, Base Sequence, Brain, Cell Division, Digestive System, Digestive System Abnormalities, Embryonic and Fetal Development, Female, Gene Targeting, Hair, Homozygote, Kidney, Lung, Male, Mice, Molecular Sequence Data, Mutation, Phenotype, Receptor, Epidermal Growth Factor, Skin, Skin Abnormalities