Stat6 and IRS-2 cooperate in interleukin 4 (IL-4)-induced proliferation and differentiation but are dispensable for IL-4-dependent rescue from apoptosis

Molecular and Cellular Biology

Volumn 22, Issue 1, 2002, Pages 117-126

  Wurster, A L ^a   Withers, D J ^a   Uchida, T ^a   Grusby, M F ^a   White, M J ^a  

^a HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIN DEPENDENT KINASE INHIBITOR; INSULIN RECEPTOR SUBSTRATE 2; INTERLEUKIN 4; INTERLEUKIN 4 RECEPTOR; PROTEIN P27; PROTEIN TYROSINE PHOSPHATASE; PROTEIN TYROSINE PHOSPHATASE INHIBITOR; STAT6 PROTEIN;

ANIMAL CELL; APOPTOSIS; ARTICLE; CELL DIFFERENTIATION; CELL PROLIFERATION; CONTROLLED STUDY; ENZYME ACTIVITY; GENE EXPRESSION; MOUSE; NONHUMAN; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; T LYMPHOCYTE;

1-PHOSPHATIDYLINOSITOL 3-KINASE; ANIMALS; APOPTOSIS; CELL CYCLE PROTEINS; CELL DIFFERENTIATION; CELL DIVISION; CELL SEPARATION; CELLS, CULTURED; CYCLIN-DEPENDENT KINASE INHIBITOR P27; ENZYME INHIBITORS; FLOW CYTOMETRY; INTERLEUKIN-4; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MICE; MICE, KNOCKOUT; PHOSPHOPROTEINS; SIGNAL TRANSDUCTION; STAT6 TRANSCRIPTION FACTOR; T-LYMPHOCYTES; TH2 CELLS; TRANS-ACTIVATORS; TUMOR SUPPRESSOR PROTEINS;

ANIMALIA;

EID: 0036133110     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.22.1.117-126.2002     Document Type: Article

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