Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus

Nature Genetics

Volumn 40, Issue 2, 2008, Pages 211-216

  Kozyrev, Sergey V ^a   Abelson, Anna Karin ^a   Wojcik, Jerome ^b   Zaghlool, Ammar ^a   Linga Reddy, M V Prasad ^a   Sanchez, Elena ^c   Gunnarsson, Iva ^d   Svenungsson, Elisabet ^d   Sturfelt, Gunnar ^e   Jönsen, Andreas ^e   Truedsson, Lennart ^e   Pons Estel, Bernardo A ^f   Witte, Torsten ^g   D'Alfonso, Sandra ^h   Barrizzone, Nadia ^h   Danieli, Maria Giovanna ⁱ   Gutierrez, Carmen ^j   Suarez, Ana ^j   Junker, Peter ^k   Laustrup, Helle ^k   González Escribano, Maria Francisca ^l   Martin, Javier ^c   Abderrahim, Hadi ^b   Alarcón Riquelme, Marta E ^a   more..

^a UPPSALA UNIVERSITY   (Sweden)

^b MERCK SERONO S A   (Switzerland)

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

^d KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^e LUND UNIVERSITY   (Sweden)

^f Sanatorio Parque   (Argentina)

^g HANNOVER MEDICAL SCHOOL   (Germany)

^h UNIVERSITY OF EASTERN PIEDMONT   (Italy)

ⁱ UNIVERSITÀ POLITECNICA DELLE MARCHE   (Italy)

^j HOSPITAL UNIVERSITARIO CENTRAL DE ASTURIAS   (Spain)

^k ODENSE UNIVERSITY HOSPITAL   (Denmark)

^l HOSPITAL UNIVERSITARIO VIRGEN DEL ROCÍO   (Spain)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ANKYRIN; B LYMPHOCYTE RECEPTOR; COMPLEMENTARY DNA; PROTEIN BANK1; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; B LYMPHOCYTE; CONTROLLED STUDY; EXON; GENE EXPRESSION; GENE FUNCTION; GENE REPLICATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC CODE; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DOMAIN; RNA SPLICING; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; SYSTEMIC LUPUS ERYTHEMATOSUS;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ALLELES; ALTERNATIVE SPLICING; AMINO ACID MOTIFS; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ANKYRIN REPEAT; B-LYMPHOCYTES; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN; COHORT STUDIES; DNA, COMPLEMENTARY; EXONS; GENE DELETION; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; HAPLOTYPES; HISTIDINE; HUMANS; INTRONS; LINKAGE DISEQUILIBRIUM; LOGISTIC MODELS; LUPUS ERYTHEMATOSUS, SYSTEMIC; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; PHYSICAL CHROMOSOME MAPPING; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN ISOFORMS; PROTEIN STRUCTURE, TERTIARY; SEQUENCE ANALYSIS, DNA; SWEDEN; VARIATION (GENETICS);

EID: 38649138296     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.79     Document Type: Article

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