Association of an NKG2D gene variant with systemic lupus erythematosus in two populations

Human Immunology

Volumn 71, Issue 1, 2010, Pages 74-78

  Kabalak, Gamze ^a   Thomas, Rachel M ^a   Martin, Javier ^b   Ortego Centeno, Noberto ^c   Jimenez Alonso, Juan ^d   de Ramón, Enrique ^e   Buyny, Sabine ^a   Hamsen, Sandra ^a   Gross, Wolfgang L ^f   Schnarr, Sebastian ^g   Zeidler, Henning ^h   Gromnica Ihle, Erika ⁱ   Schmidt, Reinhold E ^a   Witte, Torsten ^a  

^a HANNOVER MEDICAL SCHOOL   (Germany)

^b INSTITUTO DE PARASITOLOGÍA Y BIOMEDICINA LÓPEZ NEYRA   (Spain)

^c HOSPITAL UNIVERSITARIO SAN CECILIO   (Spain)

^d HOSPITAL UNIVERSITARIO VIRGEN DE LAS NIEVES   (Spain)

^e HOSPITAL REGIONAL UNIVERSITARIO DE MÁLAGA   (Spain)

^f UNIVERSITY OF LÜBECK   (Germany)

^g Rheumaklinik Oberbayern ^*  (Germany)

^h Rheumatologicum Hannover   (Germany)

ⁱ MARTIN LUTHER KRANKENHAUS   (Germany)

Author keywords

Genetics; NKG2D; SLE

Indexed keywords

NATURAL KILLER CELL RECEPTOR NKG2D;

ARTICLE; CONTROLLED STUDY; FEMALE; GENE EXPRESSION; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; GERMANY; HUMAN; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; POPULATION GENETICS; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM; SPAIN; SYSTEMIC LUPUS ERYTHEMATOSUS;

ALLELES; CELL PROLIFERATION; CELLS, CULTURED; GENE EXPRESSION REGULATION; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LUPUS ERYTHEMATOSUS, SYSTEMIC; NK CELL LECTIN-LIKE RECEPTOR SUBFAMILY K; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 71449104169     PISSN: 01988859     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.humimm.2009.09.352     Document Type: Article

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