222 related articles for article (PubMed ID: 17304144)
1. Analysis of ITPA phenotype-genotype correlation in the Bulgarian population revealed a novel gene variant in exon 6.
Atanasova S; Shipkova M; Svinarov D; Mladenova A; Genova M; Wieland E; Oellerich M; von Ahsen N
Ther Drug Monit; 2007 Feb; 29(1):6-10. PubMed ID: 17304144
[TBL] [Abstract][Full Text] [Related]
2. Measurement of erythrocyte inosine triphosphate pyrophosphohydrolase (ITPA) activity by HPLC and correlation of ITPA genotype-phenotype in a Caucasian population.
Shipkova M; Lorenz K; Oellerich M; Wieland E; von Ahsen N
Clin Chem; 2006 Feb; 52(2):240-7. PubMed ID: 16384889
[TBL] [Abstract][Full Text] [Related]
3. Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency.
Sumi S; Marinaki AM; Arenas M; Fairbanks L; Shobowale-Bakre M; Rees DC; Thein SL; Ansari A; Sanderson J; De Abreu RA; Simmonds HA; Duley JA
Hum Genet; 2002 Oct; 111(4-5):360-7. PubMed ID: 12384777
[TBL] [Abstract][Full Text] [Related]
4. Frequency of ITPA gene polymorphisms in Iranian patients with acute lymphoblastic leukemia and prediction of its myelosuppressive effects.
Azimi F; Mortazavi Y; Alavi S; Khalili M; Ramazani A
Leuk Res; 2015 Oct; 39(10):1048-54. PubMed ID: 26242828
[TBL] [Abstract][Full Text] [Related]
5. The ITPA c.94C>A and g.IVS2+21A>C sequence variants contribute to missplicing of the ITPA gene.
Arenas M; Duley J; Sumi S; Sanderson J; Marinaki A
Biochim Biophys Acta; 2007 Jan; 1772(1):96-102. PubMed ID: 17113761
[TBL] [Abstract][Full Text] [Related]
6. Association between adverse effects under azathioprine therapy and inosine triphosphate pyrophosphatase activity in patients with chronic inflammatory bowel disease.
Shipkova M; Franz J; Abe M; Klett C; Wieland E; Andus T
Ther Drug Monit; 2011 Jun; 33(3):321-8. PubMed ID: 21544018
[TBL] [Abstract][Full Text] [Related]
7. Inosine triphosphate pyrophosphatase and thiopurine s-methyltransferase genotypes relationship to azathioprine-induced myelosuppression.
Zelinkova Z; Derijks LJ; Stokkers PC; Vogels EW; van Kampen AH; Curvers WL; Cohn D; van Deventer SJ; Hommes DW
Clin Gastroenterol Hepatol; 2006 Jan; 4(1):44-9. PubMed ID: 16431304
[TBL] [Abstract][Full Text] [Related]
8. Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency in the Japanese population.
Maeda T; Sumi S; Ueta A; Ohkubo Y; Ito T; Marinaki AM; Kurono Y; Hasegawa S; Togari H
Mol Genet Metab; 2005 Aug; 85(4):271-9. PubMed ID: 15946879
[TBL] [Abstract][Full Text] [Related]
9. Association between inosine triphosphate pyrophosphohydrolase deficiency and azathioprine-related adverse drug reactions in the Chinese kidney transplant recipients.
Xiong H; Xin HW; Wu XC; Li Q; Xiong L; Yu AR
Fundam Clin Pharmacol; 2010 Jun; 24(3):393-400. PubMed ID: 19682085
[TBL] [Abstract][Full Text] [Related]
10. The effect of ITPA polymorphisms on the enzyme kinetic properties of human erythrocyte inosine triphosphatase toward its substrates ITP and 6-Thio-ITP.
Bakker JA; Lindhout M; Habets DD; van den Wijngaard A; Paulussen AD; Bierau J
Nucleosides Nucleotides Nucleic Acids; 2011 Nov; 30(11):839-49. PubMed ID: 22060550
[TBL] [Abstract][Full Text] [Related]
11. Allele frequency of inosine triphosphate pyrophosphatase (ITPA) and thiopurine-S-methyl transferase (TPMT) genes in the Tunisian population.
Melaouhia S; Fékih M; Garat A; Allorge D; Ferchichi H; Klouz A; Boubaker J; Broly F; Lakhal M
Clin Res Hepatol Gastroenterol; 2012 Apr; 36(2):178-84. PubMed ID: 22225964
[TBL] [Abstract][Full Text] [Related]
12. Adverse drug reactions to azathioprine therapy are associated with polymorphism in the gene encoding inosine triphosphate pyrophosphatase (ITPase).
Marinaki AM; Ansari A; Duley JA; Arenas M; Sumi S; Lewis CM; Shobowale-Bakre el-M; Escuredo E; Fairbanks LD; Sanderson JD
Pharmacogenetics; 2004 Mar; 14(3):181-7. PubMed ID: 15167706
[TBL] [Abstract][Full Text] [Related]
13. TPMT but not ITPA gene polymorphism influences the risk of azathioprine intolerance in renal transplant recipients.
Kurzawski M; Dziewanowski K; Lener A; Drozdzik M
Eur J Clin Pharmacol; 2009 May; 65(5):533-40. PubMed ID: 19229528
[TBL] [Abstract][Full Text] [Related]
14. Pharmacogenetics of thiopurine therapy in paediatric IBD patients.
De Ridder L; Van Dieren JM; Van Deventer HJ; Stokkers PC; Van der Woude JC; Van Vuuren AJ; Benninga MA; Escher JC; Hommes DW
Aliment Pharmacol Ther; 2006 Apr; 23(8):1137-41. PubMed ID: 16611274
[TBL] [Abstract][Full Text] [Related]
15. Mutation in the ITPA gene predicts intolerance to azathioprine.
Marinaki AM; Duley JA; Arenas M; Ansari A; Sumi S; Lewis CM; Shobowale-Bakre M; Fairbanks LD; Sanderson J
Nucleosides Nucleotides Nucleic Acids; 2004 Oct; 23(8-9):1393-7. PubMed ID: 15571265
[TBL] [Abstract][Full Text] [Related]
16. Polymorphism of ITPA 94C>A and risk of adverse effects among patients with acute lymphoblastic leukaemia treated with 6-mercaptopurine.
Wan Rosalina WR; Teh LK; Mohamad N; Nasir A; Yusoff R; Baba AA; Salleh MZ
J Clin Pharm Ther; 2012 Apr; 37(2):237-41. PubMed ID: 21545474
[TBL] [Abstract][Full Text] [Related]
17. Allele frequency of thiopurine methyltransferase and inosine triphosphate pyrophosphatase gene polymorphisms in Korean patients with inflammatory bowel diseases.
Cheon JH; Kim JH; Kim BY; Kim SW; Hong SY; Eun CS; Hong SS; Byeon JS; Kim TI; Han DS; Yang SK; Lee KR; Kim WH
Hepatogastroenterology; 2009; 56(90):421-3. PubMed ID: 19579612
[TBL] [Abstract][Full Text] [Related]
18. Association of inosine triphosphatase 94C>A and thiopurine S-methyltransferase deficiency with adverse events and study drop-outs under azathioprine therapy in a prospective Crohn disease study.
von Ahsen N; Armstrong VW; Behrens C; von Tirpitz C; Stallmach A; Herfarth H; Stein J; Bias P; Adler G; Shipkova M; Oellerich M; Kruis W; Reinshagen M; Schütz E
Clin Chem; 2005 Dec; 51(12):2282-8. PubMed ID: 16214825
[TBL] [Abstract][Full Text] [Related]
19. Distribution of Genetic Polymorphisms of Genes Implicated in Thiopurine Drugs Metabolism.
Chadli Z; Kerkeni E; Hannachi I; Chouchene S; Ben Fredj N; Boughattas NA; Aouam K; Chaabane A
Ther Drug Monit; 2018 Oct; 40(5):655-659. PubMed ID: 30086084
[TBL] [Abstract][Full Text] [Related]
20. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
