CD2ϵ and CD3ξ cytoplasmic domains can independently generate signals for T cell development and function

Immunity

Volumn 2, Issue 4, 1995, Pages 401-411

  Shlnkal, Yoichl ^a   Ma, Averll ^a   Cheng, Hwei Lang ^a   Alt, Frederick W ^a  

^a HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CD3 ANTIGEN; INTERLEUKIN 2 RECEPTOR; T LYMPHOCYTE RECEPTOR; CELL RECEPTOR; RECEPTORS, INTERLEUKIN 2;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CELL DEATH; LYMPHOCYTE DIFFERENTIATION; LYMPHOCYTE PROLIFERATION; MOUSE; NONHUMAN; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; TRANSGENE; TRANSGENIC MOUSE; ANIMAL; CELL DIFFERENTIATION; GENETICS; METABOLISM; MOLECULAR CLONING; PHYSIOLOGY; SECOND MESSENGER; T LYMPHOCYTE;

ANIMAL; ANTIGENS, CD3; CELL DEATH; CELL DIFFERENTIATION; CLONING, MOLECULAR; MICE; MICE, TRANSGENIC; RECEPTORS, CYTOPLASMIC AND NUCLEAR; RECEPTORS, INTERLEUKIN-2; SECOND MESSENGER SYSTEMS; SIGNAL TRANSDUCTION; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; T-LYMPHOCYTES;

EID: 0028986925     PISSN: 10747613     EISSN: None     Source Type: Journal    
DOI: 10.1016/1074-7613(95)90148-5     Document Type: Article

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