CD2 signaling in T cells involves tyrosine phosphorylation and activation and activation of the Tec family kinase, EMT/ITK/TSK
スポンサーリンク
概要
著者
-
REINHERZ Ellis
Laboratory of Immunobiology and Department of Medical Oncology, Dana-Farber Cancer Institute, Depart
-
Reinherz Ellis
Laboratory Of Immunobiology Dana-farber Cancer Institute
-
KING Philip
Immunology Program, Sloan-Kettering Institute for Cancer Research
-
SADRA Ali
Immunology Program, Sloan-Kettering Institute for Cancer Research
-
HAN Arnold
Immunology Program, Sloan-Kettering Institute for Cancer Research
-
LIU Xiao-rong
Immunology Program, Sloan-Kettering Institute for Cancer Research
-
SUNDERP-LASSMANN Raute
Laboratory of Immunobiology, Dana-Farber Cancer Institute
-
DUPONT Bo
Immunology Program, Sloan-Kettering Institute for Cancer Research
-
Liu Xiao-rong
Immunology Program Sloan-kettering Institute For Cancer Research
-
Dupont Bo
Immunology Program Sloan-kettering Institute For Cancer Research
-
King Philip
Immunology Program Sloan-kettering Institute For Cancer Research
-
Han Arnold
Immunology Program Sloan-kettering Institute For Cancer Research
-
Sadra Ali
Immunology Program Sloan-kettering Institute For Cancer Research
-
Sunderp-lassmann Raute
Laboratory Of Immunobiology Dana-farber Cancer Institute
関連論文
- In vivo selection of a TCR Vβ repertoire directed against an immunodominant influenza virus CTL epitope
- CD2 signaling in T cells involves tyrosine phosphorylation and activation and activation of the Tec family kinase, EMT/ITK/TSK
- Mitogenic properties of a bispecific single-chain Fv-lg fusion generated from CD2-specific mAb to distinct epitopes
- Gene expression analysis of thymocyte selection in vivo
- CD2BP3, CIN85 and the structurally related adaptor protein CMS bind to the same CD2 cytoplasmic segment, but elicit divergent functional activities
- CD2-mediated activation of the Tec-family tyrosine kinase ITK is controlled by prolinerich stretch-4 of the CD2 cytoplasmic tail