Genetic analysis of thiopurine methyltransferase polymorphism in the Jordanian population

[1] Sahasranaman S(2008)Clinical pharmacology and pharmacogenetics of thiopurines Eur J Clin Pharmacol 64 753-767

[2] Howard D(2006)Clinical pharmacogenomics of thiopurine S-methyltransferase Curr Clin Pharmacol 1 119-128

[3] Roy S(2008)Four human thiopurine smethyltransferase alleles severely affect protein structure and dynamics J Mol Biol 379 803-814

[4] Zhou S(2007)Current use of pharmacogenetic testing: a national survey of thiopurine methyltransferase testing prior to azathioprine prescription J Clin Pharm Ther 32 187-195

[5] Rutherford K(1194)Thiopurine methyltransferase activity in American white subjects and black subjects Clin Pharmacol Ther 55 15-20

[6] Daggett V(2009)TPMT*26 (208F–>L), a novel mutation detected in a Chinese Br J Clin Pharmacol 68 120-123

[7] Fargher EA(1997)Molecular diagnosis of thiopurine S-methyl transferase deficiency: genetic basis for azathioprine and mercaptopurine intolerance Ann Intern Med 126 608-616

[8] Tricker K(2004)Comprehensive analysis of thiopurine S-methyltransferase phenotype-genotype correlation in a large population of German-Caucasians and identification of novel TPMT variants Pharmacogenetics 14 407-417

[9] Newman W(1996)Thiopurine S-methyltransferase deficiency: two nucleotide transitions define the most prevalent mutant allele associated with loss of catalytic activity in Caucasians Am J Hum Genet 58 694-702

[10] Elliott R(1999)Polymorphism of the thiopurine S-methyltransferase gene in African-Americans Human Mol Gen 8 371-376

[1] Sahasranaman S(2008)Clinical pharmacology and pharmacogenetics of thiopurines Eur J Clin Pharmacol 64 753-767

[2] Howard D(2006)Clinical pharmacogenomics of thiopurine S-methyltransferase Curr Clin Pharmacol 1 119-128

[3] Roy S(2008)Four human thiopurine smethyltransferase alleles severely affect protein structure and dynamics J Mol Biol 379 803-814

[4] Zhou S(2007)Current use of pharmacogenetic testing: a national survey of thiopurine methyltransferase testing prior to azathioprine prescription J Clin Pharm Ther 32 187-195

[5] Rutherford K(1194)Thiopurine methyltransferase activity in American white subjects and black subjects Clin Pharmacol Ther 55 15-20

[6] Daggett V(2009)TPMT*26 (208F–>L), a novel mutation detected in a Chinese Br J Clin Pharmacol 68 120-123

[7] Fargher EA(1997)Molecular diagnosis of thiopurine S-methyl transferase deficiency: genetic basis for azathioprine and mercaptopurine intolerance Ann Intern Med 126 608-616

[8] Tricker K(2004)Comprehensive analysis of thiopurine S-methyltransferase phenotype-genotype correlation in a large population of German-Caucasians and identification of novel TPMT variants Pharmacogenetics 14 407-417

[9] Newman W(1996)Thiopurine S-methyltransferase deficiency: two nucleotide transitions define the most prevalent mutant allele associated with loss of catalytic activity in Caucasians Am J Hum Genet 58 694-702

[10] Elliott R(1999)Polymorphism of the thiopurine S-methyltransferase gene in African-Americans Human Mol Gen 8 371-376