The RANTES -28 g polymorphism is associated with primary sclerosing cholangitis [10]

Gut

Volumn 56, Issue 6, 2007, Pages 891-892

  Henckaerts, Liesbet ^a   Fevery, Johan ^a   Van Steenbergen, Werner ^a   Verslype, Chris ^a   Nevens, Frederik ^a   Yap, Paul ^a   Roskams, Tania ^a   Rutgeerts, Paul ^a   Vermeire, Severine ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMOKINE RECEPTOR CCR5; RANTES;

BILE DUCT INJURY; CLINICAL FEATURE; CONTROLLED STUDY; CROHN DISEASE; ENTERITIS; GENE DELETION; GENE EXPRESSION; GENE FREQUENCY; GENE MUTATION; GENETIC TRANSCRIPTION; HUMAN; LETTER; MAJOR CLINICAL STUDY; PRIMARY SCLEROSING CHOLANGITIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; SINGLE NUCLEOTIDE POLYMORPHISM; ULCERATIVE COLITIS;

CHOLANGITIS, SCLEROSING; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; POLYMORPHISM, GENETIC; RANTES;

EID: 34249780523     PISSN: 00175749     EISSN: None     Source Type: Journal    
DOI: 10.1136/gut.2006.115329     Document Type: Letter

References (6)

1. Henckaerts L, Fevery J, Van Steenbergen W, et al. CC-type chemokine receptor 5-Delta 32 mutation protects against primary sclerosing cholangitis. Inflamm Bowel Dis 2006;12:272-7.
2. Ansari N, Abdulla J, Zayyani N, et al. Comparison of RANTES expression in Crohn's disease and ulcerative colitis: an aid in the differential diagnosis? J Clin Pathol 2006;59:1066-72.
3. Kucuk C, Sozuer E, Gursoy S, et al. Treatment with Met-RANTES decreases bacterial translocation in experimental colitis. Am J Surg 2006;191:77-83.
4. An P, Nelson GW, Wang LH, et al. Modulating influence on HIV/AIDS by interacting RANTES gene variants. Proc Natl Acad Sci U SA 2002;99:10002-7.
5. Barrett JC, Fry B, Maller J, et al. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 2005;21:263-5.
6. Scheet P, Stephens M. A last and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase. Am J Hum Genet 2006;78:629-44.