Associated Papers
ABCC4, ITPA, NUDT15, TPMT and their interaction as genetic predictors of 6-mercaptopurine intolerance in chinese patients with acute lymphoblastic leukemia.
Fan POL et al.
Pediatric Hematology and Oncology, 2022
Inosine triphosphate pyrophosphohydrolase (ITPA) polymorphic sequence variants in Chinese ALL children and possible association with mercaptopurine related toxicity.
Ma X et al.
International Journal of Clinical and Experimental Pathology, 2014
Inosine triphosphate pyrophosphohydrolase (ITPA) polymorphic sequence variants in adult hematological malignancy patients and possible association with mitochondrial DNA defects.
Zamzami MA et al.
Journal of Hematology & Oncology, 2013
Clinical pharmacology and pharmacogenetics of thiopurines.
Sahasranaman S et al.
European Journal of Clinical Pharmacology, 2008
Pharmacogenomics in inflammatory bowel disease.
Egan LJ et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association, 2006
Inosine triphosphate pyrophosphatase and thiopurine s-methyltransferase genotypes relationship to azathioprine-induced myelosuppression.
Zelinkova Z et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association, 2006
Allele frequency of inosine triphosphate pyrophosphatase gene polymorphisms in a Japanese population.
Marinaki AM et al.
Nucleosides, Nucleotides & Nucleic Acids, 2004
Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency.
Sumi S et al.
Human Genetics, 2002
ITPA polymorphisms do not predict additional risk beyond TPMT and NUDT15 for thiopurine-induced cytopenia in inflammatory bowel disease.
Jena A et al.
Revista De Gastroenterologia De Mexico (english), 0
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