Association study of ITGAM, ITGAX, and CD58 autoimmune risk loci in systemic sclerosis: Results from 2 large european caucasian cohorts

Journal of Rheumatology

Volumn 38, Issue 6, 2011, Pages 1033-1038

  Coustet, Baptiste ^a,b   Agarwal, Sandeep K ^c   Gourh, Pravitt ^c   Guedj, Mickael ^d   Mayes, Maureen D ^c   Dieude, Philippe ^a   Wipff, Julien ^a   Avouac, Jerome ^a   Hachulla, Eric ^e   Diot, Elisabeth ^f   Cracowski, Jean Luc ^g   Tiev, Kiet ^h   Sibilia, Jean ⁱ   Mouthon, Luc ^a   Frances, Camille ^j   Amoura, Zahir ^j   Carpentier, Patrick ^g   Meyer, Olivier ^a   Kahan, Andre ^a   Boileau, Catherine ^k   Arnett, Frank C ^c   Allanore, Yannick ^a,b   more..

^a UNIVERSITÉ PARIS DESCARTES   (France)

^b INSTITUT COCHIN   (France)

^c UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^d UNIVERSITÉ D EVRY VAL D ESSONNE   (France)

^e UNIV LILLE   (France)

^f CHU BRETONNEAU   (France)

^g GRENOBLE UNIVERSITY HOSPITAL   (France)

^h HÔPITAL SAINT ANTOINE   (France)

ⁱ UNIVERSITÉ DE STRASBOURG   (France)

^j SORBONNE UNIVERSITÉ   (France)

^k LABORATOIRE DES SCIENCES DU CLIMAT ET DE L ENVIRONNEMENT   (France)

more..

Author keywords

Autoimmunity; CD58; ITGAM; ITGAX; Single nucleotide polymorphism; Systemic lupus erythematosus; Systemic sclerosis

Indexed keywords

ALPHA INTEGRIN; AUTOANTIBODY; LYMPHOCYTE FUNCTION ASSOCIATED ANTIGEN 3;

ANTIBODY SPECIFICITY; ARTICLE; AUTOIMMUNITY; CAUCASIAN; CD58 GENE; COHORT ANALYSIS; CONTROLLED STUDY; EUROPE; FEMALE; FIBROSING ALVEOLITIS; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; ITGAM GENE; ITGAX GENE; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; POPULATION GENETICS; PRIORITY JOURNAL; RISK ASSESSMENT; SINGLE NUCLEOTIDE POLYMORPHISM; SYSTEMIC SCLEROSIS;

ANTIGENS, CD11B; ANTIGENS, CD11C; ANTIGENS, CD58; AUTOIMMUNE DISEASES; CASE-CONTROL STUDIES; COHORT STUDIES; DATA INTERPRETATION, STATISTICAL; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; FRANCE; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MALE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS; SCLERODERMA, SYSTEMIC; UNITED STATES;

EID: 79957843890     PISSN: 0315162X     EISSN: 14992752     Source Type: Journal    
DOI: 10.3899/jrheum.101053     Document Type: Article

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