Using the emerging Collaborative Cross to probe the immune system

Genes and Immunity

Volumn 15, Issue 1, 2014, Pages 38-46

  Phillippi, J ^a   Xie, Y ^b   Miller, D R ^b,c   Bell, T A ^b,c   Zhang, Z ^d   Lenarcic, A B ^b   Aylor, D L ^b,c   Krovi, S H ^a   Threadgill, D W ^e   Pardo Manuel De Villena, F ^b,c   Wang, W ^f   Valdar, W ^b,c   Frelinger, J A ^a  

^a UNIVERSITY OF ARIZONA COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF NORTH CAROLINA   (United States)

^d Brooks Computer Science Building   (United States)

^e NORTH CAROLINA STATE UNIVERSITY   (United States)

^f University of California   (United States)

Author keywords

Collaborative Cross; Fc R; QTL

Indexed keywords

CD23 ANTIGEN; GLYCOPROTEIN P 15095;

ANIMAL CELL; ANTIGEN EXPRESSION; ANTIGEN PRESENTING CELL; ARTICLE; CD8+ T LYMPHOCYTE; CHROMOSOME 6; CHROMOSOME 8; COLLABORATIVE CROSS; CONTROLLED STUDY; FLOW CYTOMETRY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC VARIABILITY; HAPLOTYPE; IMMUNE SYSTEM; IMMUNOPHENOTYPING; LYMPHOCYTE; LYMPHOCYTE COUNT; LYMPHOCYTE SUBPOPULATION; MALE; MOUSE; NONHUMAN; PHENOTYPE; PHENOTYPIC VARIATION; PLEIOTROPY; PRIORITY JOURNAL; PROTEIN EXPRESSION; QUANTITATIVE TRAIT LOCUS; RECOMBINANT INBRED STRAIN; SPLEEN CELL; STRUCTURAL GENE; T LYMPHOCYTE SUBPOPULATION;

ANIMALS; ANTIGENS, CD11C; B-LYMPHOCYTES; CD8-POSITIVE T-LYMPHOCYTES; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; HAPLOTYPES; IMMUNOGENETICS; LYMPHOCYTE SUBSETS; MICE; MICE, INBRED STRAINS; QUANTITATIVE TRAIT LOCI; RECEPTORS, IGE; T-LYMPHOCYTES;

EID: 84895886695     PISSN: 14664879     EISSN: 14765470     Source Type: Journal    
DOI: 10.1038/gene.2013.59     Document Type: Article

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