Clonally diverse T cell homeostasis is maintained by a common program of cell-cycle control

Journal of Immunology

Volumn 190, Issue 8, 2013, Pages 3985-3993

  Hogan, Thea ^a,d   Shuvaev, Andrey ^b,e   Commenges, Daniel ^b   Yates, Andrew ^c   Callard, Robin ^a   Thiebaut, Rodolphe ^b   Seddon, Benedict ^d  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b INSERM   (France)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^d NATIONAL INSTITUTE FOR MEDICAL RESEARCH   (United Kingdom)

^e SIBERIAN FEDERAL UNIVERSITY   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

LYMPHOCYTE ANTIGEN;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CELL CLONE; CELL CYCLE REGULATION; CELL DIVISION; CELL TYPE; CELLULAR PARAMETERS; CONTROLLED STUDY; HOMEOSTASIS; IN VIVO STUDY; LYMPHOCYTE COUNT; LYMPHOCYTE DIFFERENTIATION; LYMPHOCYTE PROLIFERATION; LYMPHOCYTOPENIA; MATHEMATICAL MODEL; MOUSE; NONHUMAN; PREDICTION; PRIORITY JOURNAL; STOCHASTIC MODEL; T LYMPHOCYTE;

ADOPTIVE TRANSFER; ANIMALS; CELL CYCLE; CELL DIFFERENTIATION; CELL DIVISION; CELL LINE; CLONE CELLS; HOMEOSTASIS; IMMUNOPHENOTYPING; LYMPHOCYTE ACTIVATION; LYMPHOPENIA; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MICE, TRANSGENIC; MODELS, IMMUNOLOGICAL; RECEPTORS, ANTIGEN, T-CELL; T-LYMPHOCYTE SUBSETS;

EID: 84875979256     PISSN: 00221767     EISSN: 15506606     Source Type: Journal    
DOI: 10.4049/jimmunol.1203213     Document Type: Article

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