SCOPUS 정보 검색 플랫폼

Volumn 210, Issue 11, 2013, Pages 2403-2414

Pathogenic CD4+ T cells recognizing an unstable peptide of insulin are directly recruited into islets bypassing local lymph nodes

(4) Mohan, James F a Calderon, Boris a Anderson, Mark S b Unanue, Emil R a

a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE (United States)

b UNIVERSITY OF CALIFORNIA (United States)

Author keywords

[No Author keywords available]

Indexed keywords

IMMUNOGLOBULIN G; INSULIN; INSULIN ANTIBODY; T LYMPHOCYTE RECEPTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIBODY PRODUCTION; ANTIGEN PRESENTATION; ANTIGEN PRESENTING CELL; ANTIGEN RECOGNITION; ARTICLE; CD4+ T LYMPHOCYTE; CD8+ T LYMPHOCYTE; CELL CONTACT; CONTROLLED STUDY; FEMALE; IMMUNOPATHOGENESIS; LYMPH NODE; LYMPHOCYTE FUNCTION; MOUSE; NONHUMAN; NONOBESE DIABETIC MOUSE; PANCREAS ISLET; PANCREAS ISLET BETA CELL; PATHOGENICITY; PRIORITY JOURNAL; PURIFYING SELECTION; SPLEEN; THYMUS; TRANSGENIC MOUSE;

AMINO ACID SEQUENCE; ANIMALS; CD4-POSITIVE T-LYMPHOCYTES; FEMALE; INSULIN; ISLETS OF LANGERHANS; LYMPH NODES; MICE; MICE, INBRED NOD; MICE, TRANSGENIC; MOLECULAR SEQUENCE DATA; PEPTIDES; PROTEIN STABILITY; RECEPTORS, ANTIGEN, T-CELL;

EID: 84886837181 PISSN: 00221007 EISSN: 15409538 Source Type: Journal
DOI: 10.1084/jem.20130582 Document Type: Article

Times cited : (46)

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