The association of MYO9B gene in Italian patients with inflammatory bowel diseases

Alimentary Pharmacology and Therapeutics

Volumn 27, Issue 3, 2008, Pages 241-248

  Latiano, A ^a   Palmieri, O ^a   Valvano, M R ^a   D'Inca R ^b   Caprilli, R ^c   Cucchiara, S ^c   Sturniolo, G C ^b   Bossa, F ^a   Andriulli, A ^a   Annese, V ^a  

^a CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

^b UNIVERSITY OF PADOVA   (Italy)

^c SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; MYOSIN; MYOSIN IXB; STEROID; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; CARD15 GENE; CHILD; COLON RESECTION; CONTROLLED STUDY; CROHN DISEASE; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; ENTERITIS; ETHNIC GROUP; FAMILY HISTORY; FEMALE; GENE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC POLYMORPHISM; HUMAN; INTESTINE MUCOSA PERMEABILITY; ITALY; MAJOR CLINICAL STUDY; MALE; MY09B GENE; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STEROID THERAPY; ULCERATIVE COLITIS;

ADOLESCENT; ADULT; AGED; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; COLITIS, ULCERATIVE; CROHN DISEASE; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; INFANT; INFLAMMATORY BOWEL DISEASES; INTESTINAL MUCOSA; ITALY; LINKAGE DISEQUILIBRIUM; MALE; MIDDLE AGED; MYOSINS; NOD2 SIGNALING ADAPTOR PROTEIN; ODDS RATIO; PERMEABILITY; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 37549053624     PISSN: 02692813     EISSN: 13652036     Source Type: Journal    
DOI: 10.1111/j.1365-2036.2007.03551.x     Document Type: Article

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