Combined deletion of Id2 and Id3 genes reveals multiple roles for e proteins in invariant NKT cell development and expansion

Journal of Immunology

Volumn 191, Issue 10, 2013, Pages 5052-5064

  Li, Jia ^a   Wu, Di ^b,c   Jiang, Ning ^b,c   Zhuang, Yuan ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b The University of Texas at Austin   (United States)

^c UNIVERSITY OF TEXAS AT AUSTIN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CD4 ANTIGEN; E PROTEIN; T LYMPHOCYTE RECEPTOR; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; CD8 ANTIGEN; IDB2 PROTEIN, MOUSE; IDB3 PROTEIN, MOUSE; INHIBITOR OF DIFFERENTIATION 2; INHIBITOR OF DIFFERENTIATION PROTEIN; LYMPHOCYTE ANTIGEN RECEPTOR;

ANIMAL CELL; ARTICLE; CELL EXPANSION; CELL FATE; CELL MATURATION; CONTROLLED STUDY; DELETION MUTANT; GENE; GENE DELETION; GENETIC CODE; ID2 GENE; ID3 GENE; LYMPHOCYTE COUNT; LYMPHOCYTE PROLIFERATION; MOUSE; NATURAL KILLER T CELL; NONHUMAN; PRE T LYMPHOCYTE; PRIORITY JOURNAL; PROTEIN FUNCTION; ANIMAL; C57BL MOUSE; CELL DIFFERENTIATION; CELL LINEAGE; CELL PROLIFERATION; GENETICS; METABOLISM; TRANSGENIC MOUSE;

ANIMALS; ANTIGENS, CD4; ANTIGENS, CD8; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; CELL DIFFERENTIATION; CELL LINEAGE; CELL PROLIFERATION; INHIBITOR OF DIFFERENTIATION PROTEIN 2; INHIBITOR OF DIFFERENTIATION PROTEINS; LYMPHOCYTE COUNT; MICE; MICE, INBRED C57BL; MICE, TRANSGENIC; NATURAL KILLER T-CELLS; RECEPTORS, ANTIGEN, T-CELL, ALPHA-BETA;

EID: 84887642858     PISSN: 00221767     EISSN: 15506606     Source Type: Journal    
DOI: 10.4049/jimmunol.1301252     Document Type: Article

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