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Volumn 10, Issue 6, 2009, Pages 547-566

Polymorphisms in methotrexate pathways: What is clinically relevant, what is not, and what is promising

Author keywords

Acute lymphoblastic leuk mia; Efficiency; Folate; Methotrexate; Polymorphism; Rheumatoid arthritis; Toxicity

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); ADENOSINE; ADENOSINE MONOPHOSPHATE DEAMINASE; ADENOSINE RECEPTOR; ALANINE; CORTICOSTEROID; CYCLOSPORIN A; CYSTEINE; DIHYDROFOLATE REDUCTASE; DISEASE MODIFYING ANTIRHEUMATIC DRUG; FLUOROURACIL; FOLIC ACID; FOLYLPOLYGLUTAMATE SYNTHASE; GAMMA GLUTAMYL HYDROLASE; GLYCINE; GLYCINE HYDROXYMETHYLTRANSFERASE; HOMOCYSTEINE; INOSINE TRIPHOSPHATE; INOSINE TRIPHOSPHATE PYROPHOSPHATASE; MEPREDNISONE; METHIONINE SYNTHASE; METHIONINE SYNTHASE REDUCTASE; METHOTREXATE; METHYLENETETRAHYDROFOLATE DEHYDROGENASE; PHOSPHORIBOSYLAMINOIMIDAZOLECARBOXAMIDE FORMYLTRANSFERASE; REDUCED FOLATE CARRIER; SALAZOSULFAPYRIDINE; THREONINE; THYMIDYLATE SYNTHASE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 70450241056     PISSN: 13892002     EISSN: None     Source Type: Journal    
DOI: 10.2174/138920009789375414     Document Type: Review
Times cited : (36)

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