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pump due to three novel ABCB11 mutations in intrahepatic cholestasis. J Hepatol 43:
536-543.
179. Torok HP, Glas J, Tonenchi L, Lohse P, Muller-Myhsok B, Limbersky O, Neugebauer C,
Schnitzler F, Seiderer J, Tillack C, et al. 2005. Polymorphisms in the DLG5 and OCTN
cation transporter genes in Crohn's disease. Gut 54:1421-1427.
180. Tosa M, Negoro K, Kinouchi Y, Abe H, Nomura E, Takagi S, Aihara H, Oomori S,
Sugimura M, Takahashi K, et al. 2006. Lack of association between IBD5 and Crohn's
disease in Japanese patients demonstrates population-specific differences in inflammatory
bowel disease. Scand J Gastroenterol 41:48-53.
181. Gazouli M, Mantzaris G, Archimandritis AJ, Nasioulas G, Anagnou NP. 2005. single-
nucleotide polymorphisms of OCTN1, OCTN2, and DLG5 genes in Greek patients with
Crohn's disease. World J Gastroenterol 11:7525-7530.
182. Vermeire S, Pierik M, Hlavaty T, Claessens G, van Schuerbeeck N, Joossens S, Ferrante
M, Henckaerts L, Bueno de Mesquita M, Vlietinck R, Rutgeerts P. 2005. Association of
organic cation transporter risk haplotype with perianal penetrating Crohn's disease but
not with susceptibility to IBD. Gastroenterology 129:1845-1853.
183. Noble CL, Nimmo ER, Drummond H, Ho GT, Tenesa A, Smith L, Anderson N, Arnott
ID, Satsangi J. 2005. The contribution of OCTN1/2 variants within the IBD5 locus
to disease susceptibility and severity in Crohn's disease. Gastroenterology 129:1854-
1864.
184. Barton A, Eyre S, Bowes J, Ho P, John S, Worthington J. 2005. Investigation of the
SLC22A4 gene (associated with rheumatoid arthritis in a Japanese population) in a United
Kingdom population of rheumatoid arthritis patients. Arthritis Rheum 52:752-758.
185. Newman B, Wintle RF, van Oene M, Yazdanpanah M, Owen J, Johnson B, Gu X, Amos
CI, Keystone E, Rubin LA, Siminovitch KA. 2005. SLC22A4 polymorphisms implicated
in rheumatoid arthritis and Crohn's disease are not associated with rheumatoid arthritis
in a Canadian Caucasian population. Arthritis Rheum 52:425-429.
186. Wang W, Xue S, Ingles SA, Chen Q, Diep AT, Frankl HD, Stolz A, Haile RW. 2001.
An association between genetic polymorphisms in the ileal sodium-dependent bile acid
transporter gene and the risk of colorectal adenomas. Cancer Epidemiol Biomark Prev
10:931-936.
187. Page T, Hodgkinson AD, Ollerenshaw M, Hammonds JC, Demaine AG. 2005. Glucose
transporter polymorphisms are associated with clear-cell renal carcinoma. Cancer Genet
Cytogenet 163:151-155.
188. Jamroziak K, Balcerczak E, Cebula B, Kowalczyk M, Panczyk M, Janus A, Smolewski
P, Mirowski M, Robak T. 2005. Multi-drug transporter MDR1 gene polymorphism and
prognosis in adult acute lymphoblastic leukemia. Pharmacol Rep 57:882-888.
189. Jamroziak K, Mlynarski W, Balcerczak E, Mistygacz M, Trelinska J, Mirowski M, Bo-
dalski J, Robak T. 2004. Functional C3435T polymorphism of MDR1 gene: an impact on
genetic susceptibility and clinical outcome of childhood acute lymphoblastic leukemia.
Eur J Haematol 72:314-321.
190. Kishi S, Yang W, Boureau B, Morand S, Das S, Chen P, Cook EH, Rosner GL, Schuetz E,
Pui CH, Relling MV. 2004. Effects of prednisone and genetic polymorphisms on etoposide
disposition in children with acute lymphoblastic leukemia. Blood 103:67-72.
191. Efferth T, Sauerbrey A, Steinbach D, Gebhart E, Drexler HG, Miyachi H, Chitambar
CR, Becker CM, Zintl F, Humeny A. 2003. Analysis of single nucleotide polymorphism
 
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