Id3 and Id2 act as a dual safety mechanism in regulating the development and population size of innate-like gd t cells

Journal of Immunology

Volumn 192, Issue 3, 2014, Pages 1055-1063

  Zhang, Baojun ^a   Lin, Yen Yu ^a   Dai, Meifang ^a   Zhuang, Yuan ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HEB PROTEIN; INHIBITOR OF DIFFERENTIATION 2; INHIBITOR OF DIFFERENTIATION 3; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR E2A; UNCLASSIFIED DRUG;

ALLELE; ANIMAL CELL; ARTICLE; C57BL 6 MOUSE; CELL EXPANSION; CELL LINEAGE; CELL MATURATION; CELL POPULATION; CELL SURVIVAL; CONTROLLED STUDY; GAMMA DELTA T LYMPHOCYTE; GENE DELETION; KNOCKOUT MOUSE; LINKAGE ANALYSIS; LYMPHOCYTE SUBPOPULATION; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL;

ALLELES; ANIMALS; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; CELL LINEAGE; CROSSES, GENETIC; GENE REARRANGEMENT, DELTA-CHAIN T-CELL ANTIGEN RECEPTOR; GENE REARRANGEMENT, GAMMA-CHAIN T-CELL ANTIGEN RECEPTOR; INHIBITOR OF DIFFERENTIATION PROTEIN 2; INHIBITOR OF DIFFERENTIATION PROTEINS; LYMPHOCYTE COUNT; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; RECEPTORS, ANTIGEN, T-CELL, GAMMA-DELTA; SPECIFIC PATHOGEN-FREE ORGANISMS; T-LYMPHOCYTE SUBSETS; THYMUS GLAND;

EID: 84893381678     PISSN: 00221767     EISSN: 15506606     Source Type: Journal    
DOI: 10.4049/jimmunol.1302694     Document Type: Article

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