Expression of a single ICAM-1 isoform on T cells is sufficient for development of experimental autoimmune encephalomyelitis

European Journal of Immunology

Volumn 44, Issue 4, 2014, Pages 1194-1199

  Bullard, Daniel C ^a   Hu, Xianzhen ^b   Crawford, David ^c   Mcdonald, Kristin ^c   Ramos, Theresa N ^b   Barnum, Scott R ^b  

^a UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^b University of Alabama at Birmingham   (United States)

^c UNIVERSITY OF OKLAHOMA   (United States)

Author keywords

Adhesion molecules; Alternative splicing; Central nervous system; Demyelinating disease; Transgenic animals

Indexed keywords

CD2 ANTIGEN; INTERCELLULAR ADHESION MOLECULE 1; ISOPROTEIN;

ADOPTIVE TRANSFER; ALTERNATIVE RNA SPLICING; ANIMAL CELL; ARTICLE; CELLULAR IMMUNITY; CONTROLLED STUDY; DISEASE COURSE; DISEASE SEVERITY; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; IMMUNOLOGICAL SYNAPSE; IN VITRO STUDY; INTRACELLULAR SIGNALING; MOUSE; MULTIPLE SCLEROSIS; NONHUMAN; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; T LYMPHOCYTE; TRANSGENIC MOUSE;

ADHESION MOLECULES; ALTERNATIVE SPLICING; CENTRAL NERVOUS SYSTEM; DEMYELINATING DISEASE; TRANSGENIC ANIMALS;

ADOPTIVE TRANSFER; ALTERNATIVE SPLICING; ANIMALS; BINDING SITES; BLOTTING, WESTERN; ENCEPHALOMYELITIS, AUTOIMMUNE, EXPERIMENTAL; FLOW CYTOMETRY; HEK293 CELLS; HUMANS; INTERCELLULAR ADHESION MOLECULE-1; MICE; MICE, KNOCKOUT; MICE, TRANSGENIC; PROTEIN ISOFORMS; T-LYMPHOCYTES;

EID: 84897971361     PISSN: 00142980     EISSN: 15214141     Source Type: Journal    
DOI: 10.1002/eji.201344023     Document Type: Article

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