Association of haplotypes of the TLR8 locus with susceptibility to Crohn's and Behçet's diseases

Clinical and Experimental Rheumatology

Volumn 33, Issue , 2015, Pages 117-122

  Ortiz Fernández, Lourdes ^a   García Lozano, José Raúl ^a   Montes Cano, Marco Antonio ^a   Conde Jaldón, Marta ^a   Leo, Eduardo ^a   Ortego Centeno, Norberto ^b   Gómez García, María ^c   García Hernández, Francisco José ^a   Márquez, José Luis ^a   Espinosa, Gerard ^d   Graña Gil, Genaro ^e   Sánchez Bursón, Juan ^f   Juliá, María Rosa ^g   Blanco, Ricardo ^h   Barnosi Marín, Ana Celia ⁱ   Solans, Roser ^j   Fanlo, Patricia ^k   Rodríguez Carballeira, Mónica ^l   Camps, Teresa ^m   Castañeda, Santos ⁿ   Martín, Javier ^o   González Escribano, María Francisca ^a   more..

^a HOSPITAL UNIVERSITARIO VIRGEN DEL ROCÍO   (Spain)

^b HOSPITAL UNIVERSITARIO SAN CECILIO   (Spain)

^c HOSPITAL UNIVERSITARIO VIRGEN DE LAS NIEVES   (Spain)

^d HOSPITAL CLÍNIC   (Spain)

^e HOSPITAL JUAN CANALEJO   (Spain)

^f HOSPITAL UNIVERSITARIO DE VALME   (Spain)

^g HOSPITAL UNIVERSITARIO SON ESPASES   (Spain)

^h HOSPITAL UNIVERSITARIO MARQUÉS DE VALDECILLA   (Spain)

ⁱ Hospital de Torrecardenas   (Spain)

^j HOSPITAL UNIVERSITARI VALL D HEBRON   (Spain)

^k Instituto de Investigación Sanitaria de Navarra   (Spain)

^l HOSPITAL MÚTUA DE TERRASSA   (Spain)

^m HOSPITAL REGIONAL UNIVERSITARIO DE MÁLAGA   (Spain)

ⁿ HOSPITAL UNIVERSITARIO DE LA PRINCESA   (Spain)

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

more..

Author keywords

Beh et's disease; Crohn's disease; TLR8

Indexed keywords

TOLL LIKE RECEPTOR 8; TLR8 PROTEIN, HUMAN;

ARTICLE; BEHCET DISEASE; CONTROLLED STUDY; CROHN DISEASE; DISEASE ACTIVITY; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; FEMALE; GENE; GENE EXPRESSION; GENE FREQUENCY; GENE FUNCTION; GENE IDENTIFICATION; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENOTYPING TECHNIQUE; HUMAN; IMMUNE RESPONSE; MALE; MOLECULAR PATHOLOGY; PRIORITY JOURNAL; SEX DIFFERENCE; SINGLE NUCLEOTIDE POLYMORPHISM; TOLL LIKE RECEPTOR 8 GENE; TREND STUDY; X CHROMOSOME; ADULT; BEHCET SYNDROME; CASE CONTROL STUDY; CHI SQUARE DISTRIBUTION; CLINICAL TRIAL; COMPUTER SIMULATION; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETICS; HAPLOTYPE; IMMUNOLOGY; MIDDLE AGED; MULTICENTER STUDY; ODDS RATIO; PHENOTYPE; PROTECTION; RISK ASSESSMENT; RISK FACTOR; SPAIN; YOUNG ADULT;

ADULT; BEHCET SYNDROME; CASE-CONTROL STUDIES; CHI-SQUARE DISTRIBUTION; COMPUTER SIMULATION; CROHN DISEASE; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MIDDLE AGED; ODDS RATIO; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTECTIVE FACTORS; RISK ASSESSMENT; RISK FACTORS; SEX FACTORS; SPAIN; TOLL-LIKE RECEPTOR 8; YOUNG ADULT;

EID: 84954597839     PISSN: 0392856X     EISSN: 1593098X     Source Type: Journal    
DOI: None     Document Type: Article

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