Bibliography
- LONG RM: Planning for a national effort to enable and accelerate discoveries in pharmacogenetics: the NIH Pharmacogenetics Research Network. Clin. Pharmacol. Ther. (2007) 81:450-454.
- EVANS WE, MCLEOD HL: Pharmacogenomics – drug disposition, drug targets, and side effects. N. Engl. J. Med. (2003) 348:538-549.
- KIRCHHEINER J, FUHR U, BROCKMOLLER J: Pharmacogenetics-based therapeutic recommendations – ready for clinical practice? Nat. Rev. (2005) 4:639-647.
- WEINSHILBOUM R, WAND L: Pharmacogenomics: bench to bedside. Nat. Rev. Drug Discov. (2004) 3:739-748.
- DELEON J, ARMSTRONG SC, COZZA KL: Clinical guidelines for psychiatrists for the use of pharmacogenetic testing for CYP450 2D6 and CYP450 2C19. Psychosomatics (2006) 47:75-85.
- BAILEY DS, BONDAR A, FURNESS LM: Pharmacogenomics – it's not just pharmacogenetics. Curr. Opin. Biotechnol. (1998) 9:595-601.
- TSONGALIS GJ, COLEMAN WB: Clinical genotyping: the need for interrogation of single nucleotide polymorphisms and mutations in the clinical laboratory. Clin. Chim. Acta (2006) 363:127-137.
- NEBERT DW, INGELMAN-SUNDBERG M, DALY AK: Genetic epidemiology of environmental toxicity and cancer susceptibility: human allelic polymorphisms in drug metabolizing genes, their functional importance and nomenclature issues. Drug Metab. Rev. (1999) 31:467-487.
- LAZAROU J, POMERANZ BH, COREY PN: Incidence of adverse drug reactions in hospitalized patients: a meta-analysis of prospective studies. JAMA (1998) 279:1200-1205.
- SHASTRY BS: Pharmacogenetics and the concept of individualized medicine. Pharmacogenom. J. (2006) 6:16-21.
- VOGEL F: Moderne probleme der Humangenetik. Ergeb Inn. Med. Kinderheilkd (1959) 12:52-125.
- NEBERT D: Pharmacogenetics and pharmacogenomics: why is this relevant to the clinical geneticist? Clin. Genet. (1999) 56:247-258.
- WEBER WW: Populations and genetic polymorphisms. Mol. Diagn. (1999) 4:299-307.
- MAGER J, GLAASER G, RAZIN A, IZAK G, BIEN S, NOAM M: Metabolic effects of pyrimidines derived from fava bean glycosides on human erythrocytes deficient in glucose-6-phosphate dehydrogenase. Biochem. Biophys. Res. Commun. (1965) 20:235-240.
- PODDA M, FIORELLI G, IDEO G, SPANO G, DIOGUARDI N: In-vitro-effect of a fava bean extract and of its fractions on reduced glutathione in glucose-6-phosphate dehydrogenase deficient red cells. Folia Haematol. Int. Mag. Klin. Morphol. Blutforsch. (1969) 91:51-55.
- SNYDER LH: Studies in human inheritance. The inheritance of taste deficiency in man. Ohio J. Sci. (1932) 32:436-468.
- EVANS DAP: N-acetyltransferase. Pharmaco. Ther. (1989) 42:157-234.
- CARSON PE, FLANAGAN CL, ICKES CE, ALVING AS: Enzymatic deficiency in primaquine-sensitive erythrocytes. Science (1956) 124:484-485.
- HAMMER W, SJOQVIST F. Plasma levels of monomethylated tricyclic antidepressants during treatment with imipramine-like compounds. Life Sci. (1967) 6:1895-903.
- KALOW W: Familial incidence of low pseudocholinesterase level. Lancet (1956) 211:576-577.
- WEINSHILBOUM R: Inheritance and drug response. N. Engl. J. Med. (2003) 348:529-537.
- HUGHES HB, BIEHL JP, JONES AP, SCHMIDT LH: Metabolism of isoniazid in man as related to the occurrence of peripheral neuritis. Am. Rev. Tuberc. (1954) 70:266-273.
- EVANS WE, RELLING MV: Pharmacogenomics: translating functional genomics into rational therapeutics. Science (1999) 286:487-491.
- GARDINER SJ, BEGG EJ: Pharmacogenetics, drug metabolizing enzymes and clinical practice. Pharmacol. Rev. (2006) 58:521-581.
- INGELMAN-SUNDBERG M: Genetic polymorphisms of cytochrome P450 2D6 (CYP2D6): clinical consequences, evolutionary aspects and functional diversity. Pharmacogenom. J. (2005) 5:6-13.
- INGELMAN-SUNDBERG M: Pharmacogenetics of cytochrome P450 and its applications in drug therapy: the past, present and future. Trends Pharmacol. Sci. (2004) 25:193-200.
- HEIM MH, MEYER UA: Evolution of a highly polymorphic human cytochrome P450 gene cluster: CYP2D6. Genomics (1992) 14:49-58.
- LEDESMA MC, AGUNDEZ JA: Identification of subtypes of CYP2D gene rearrangements among carriers of CYP2D6 gene deletion and duplication. Clin. Chem. (2005) 51:939-943.
- ANDERSSON T, FLOCKHART DA, GOLDSTEIN DB et al.: Drug-metabolizing enzymes: evidence for clinical utility of pharmacogenomic tests. Clin. Pharmacol. Ther. (2005) 78:559-581.
- LEE HK, LEWIS LD, TSONGALIS GJ et al.: Negative urine opioid screening caused by rifampin-mediated induction of oxycodone hepatic metabolism. Clin. Chim. Acta (2006) 367:196-200.
- LOCKHART AC, TIRONA RG, KIM RB: Pharmacogenetics of ATP-binding cassette transporters in cancer and chemotherapy. Mol. Cancer Ther. (2003) 2:685-698.
- MARZOLINI C, TIRONA RG, KIM RB: Pharmacogenomics of the OATP and OAT families. Pharmacogenomics (2004) 5:273-282.
- URQUHART BL, TIRONA RG, KIM RB: Nuclear receptors and the regulation of drug-metabolizing enzymes and drug transporters: implications for interindividual variability in response to drugs. J. Clin. Pharmacol. (2007) 47:566-578.
- BORST P, SCHINKEL AH, SMIT JJ et al.: Classical and novel forms of multidrug resistance and the physiological functions of P-glycoproteins in mammals. Pharmacol. Ther. (1993) 60:289-299.
- KUSUHARA H, SUZUKI H, SUGIYAMA Y: The role of P-glycoprotein and canalicular multispecific organic anion transporter in the hepatobiliary excretion of drugs. J. Pharm. Sci. (1998) 87:1025-1040.
- TANIGAWARA Y: Role of P-glycoprotein in drug disposition. Ther. Drug Monit. (2000) 22:137-140.
- AMBUDKAR SV, DEY S, HRYCYNA CA: Biochemical, cellular, and pharmacological aspects of the multidrug transporter. Ann. Rev. Pharmacol. Toxicol. (1999) 39:361-398.
- HIGGINS CF, CALLAGHAN R, LINTON KJ et al.: Structure of the multidrug resistance P-glycoprotein. Semin. Cancer Biol. (1997) 8:135-142.
- ROSENBERG MF, CALLAGHAN R, FORD RC, HIGGINS CF: Structure of the multidrug resistance P-glycoprotein to 2.5 nm resolution determined by electron microscopy and image analysis. J. Biol. Chem. (1997) 272:10685-10694.
- SAKAEDA T, NAKAMURA T, OKUMURA K: MDR1 genotype-related pharmacokinetics and pharmacodynamics. Biol. Pharm. Bull. (2002) 25:1391-1400.
- HOFFMEYER S, BURK O, VON RICHTER O et al.: Functional polymorphisms of the human multidrug-resistance gene: multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. Proc. Natl. Acad. Sci. USA (2000) 97:3473-3478.
- JAMROZIAK K, ROBAK T: Pharmacogenomics of MDR1/ABCB1 gene: the influence on risk and clinical outcome of haematological malignancies. Hematology (2004) 9:91-105.
- VAN DER KOLK DM, DE VRIES EG, NOORDHOEK L et al.: Activity and expression of the multidrug resistance proteins P-glycoprotein, MRP1, MRP2, MRP3 and MRP5 in de novo and relapsed acute myeloid leukemia. Leukemia (2001) 15:1544-1553.
- SCHAICH M, SOUCEK S, THIEDE C et al.: MDR1 and MRP1 gene expression are independent predictors for treatment outcome in adult acute myeloid leukaemia. Br. J. Haematol. (2005) 128:324-332.
- JAMROZIAK K, BALCERCZAK E, CEBULA B et al.: No influence of 3435C > T ABCB1 (MDR1) gene polymorphism on risk of adult acute myeloid leukemia and P-glycoprotein expression in blast cells. Ther. Drug Monit. (2006) 28:707-711.
- VAN DER HOLT B, VAN DEN HEUVEL-EIBRINK MM et al.: ABCB1 gene polymorphisms are not associated with treatment outcome in elderly acute myeloid leukemia patients. Clin. Pharmacol. Ther. (2006) 80:427-439.
- KIMCHI-SARFATY C, OH JM, KIM IW et al.: A ‘silent’ polymorphism in the MDR1 gene changes substrate specificity. Science (2007) 315:525-528.
- SAMANI NJ, O'TOOLE L, CHANNER K, WOODS KL: A meta analysis of the association of the deletion allele of the angiotensin converting enzyme gene with myocardial infarction. Circulation (1996) 94:708-712.
- GREEN SA, COLE G, JACINTO M, INNIS M, LIGGETT SB: A polymorphism of the human β2-adrenergic receptor within the fourth membrane alters ligand binding and functional properties of the receptor. J. Biol. Chem. (1993) 268:23116-23121.
- SCHAAK S, MIALET-PEREZ J, FLORDELLIS C, PARIS H: Genetic variation of human adrenergic receptors: from molecular and functional properties to clinical and pharmacogenetic implications. Curr. Top. Med. Chem. (2007) 7:217-231.
- Bhatnagar P, GULERIA R, KUKRETI R: Pharmacogenomics of β2-agonist: key focus on signaling pathways. Pharmacogenomics (2006) 7:919-933.
- SHANKAR DB, LI J, TAPANG P, MCCALL JO et al.: ABT-869, a multitargeted receptor kinase inhibitor: inhibition of FLT3 phosphorylation and signaling in acute myeloid leukemia. Blood (2007) 109:3400-3408.
- GOETZ MP, RAE JM, SUMAN VJ et al.: Pharmacogenetics of tamoxifen biotransformation is associated with clinical outcomes of efficacy and hot flashes. J. Clin. Oncol. (2005) 23:9312-9318.
- GROUP EBCTC: Tamoxifen for early breast cancer: an overview of the randomized trials. Early Breast Cancer Trialists' Collaborative Group. Lancet (1998) 351:1451-1467.
- POON GK, CHUI YC, MCCAGUE R et al.: Analysis of Phase I and Phase II metabolites of tamoxifen in breast cancer patients. Drug Metab. Dispos. (1993) 21:1119-1124.
- KLEIN TE, CHANG JT, CHO MK et al.: Integrating genotype and phenotype information: an overview of the PharmGKB project. Pharmacogenom. J. (2001) 1:167-170.
- JIN Y, DESTA Z, STEARNS V et al.: CYP2D6 genotype, antidepressant use, and tamoxifen metabolism during adjuvant breast cancer treatment. J. NCI (2005) 97:30-39.
- SACHSE C, BROCKMÖLLER J, BAUER S, ROOTS I: Cytochrome P450 2D6 variants in a Caucasian population: allele frequencies and phenotypic consequences. Am. J. Hum. Genet. (1997) 60(2):284-295.
- LENNARD L, REES CA, LILLEYMAN JS, MADDOCKS JL: Childhood leukaemia: a relationship between intracellular 6-mercaptopurine metabolites and neutropenia. Br. J. Clin. Pharmacol. (2004) 58:S867-S871.
- SALAVAGGIONE OE, WANG L, WIEPERT M, YEE VC, WEINSHILBOUM RM: Thiopurine S-methyltransferase pharmacogenetics: variant allele functional and comparative genomics. Pharmacogenet. Genom. (2005) 15:801-815.
- WEINSHILBOUM RM, SLADEK SL: Mercaptopurine pharmacogenetics: monogenic inheritance of erythrocyte thiopurine methyltransferase activity. Am. J. Hum. Genet. (1980) 32:651-662.
- YATES CR, KRYNETSKI EY, LOENNECHEN T et al.: Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basis for azathioprine and mercaptopurine intolerance. Ann. Intern. Med. (1997) 126:608-614.
- LENNARD L, LILLEYMAN JS, VAN LOON J, WEINSHILBOUM RM: Genetic variation in response to 6-mercaptopurine for childhood acute lymphoblastic leukaemia. Lancet (1990) 336:225-229.
- WASSERMAN E, MYARA A, LOKIEC F et al.: Severe CPT-11 toxicity in patients with Gilbert's syndrome: two case reports. Ann. Oncol. (1997) 8:1049-1051.
- HUMERICKHOUSE R, LOHRBACH K, LI L, BOSRON WF, DOLAN ME: Characterization of CPT-11 hydrolysis by human liver carboxylesterase isoforms hCE-1 and hCE-2. Cancer Res. (2000) 60:1189-1192.
- HARTMANN JT, LIPP HP: Camptothecin and podophyllotoxin derivatives: inhibitors of topoisomerase I and II – mechanisms of action, pharmacokinetics and toxicity profile. Drug Saf. (2006) 29:209-230.
- MAITLAND ML, VASISHT K, RATAIN MJ: TPMT, UGT1A1 and DPYD: genotyping to ensure safer cancer therapy? Trends Pharmacol. Sci. (2006) 27:432-437.
- LINDER MW, PROUGH RA, VALDES R Jr: Pharmacogenetics: a laboratory tool for optimizing therapeutic efficiency. Clin. Chem. (1997) 43:254-266.
- SCHUR BC, BJERKE J, NUWAYHID N, WONG SH: Genotyping of cytochrome P450 2D6*3 and *4 mutations using conventional PCR. Clin. Chim. Acta (2001) 308:25-31.
- LUCAS T, LOSERT D, ALLEN M et al.: Combination of allele-specific real time PCR for differentiation of β2-adrenergic receptor coding single nucelotide polymorphisms. Clin. Chem. (2004) 50:769-772.
- LEE HK, LEWIS LD, TSONGALIS GJ et al.: Validation of a CYP2D6 genotyping panel on the nanochip molecular biology workstation. Clin. Chem. (2007) 53:823-828.
- FERRARI M, CREMONESI L, BONINI P et al.: Single-nucleotide polymorphism and mutation identification by the nanogen microelectronic chip technology. Methods Mol. Med. (2005) 114:93-106.
- ERALI M, SCHMIDT B, LYON E, WITTWER C: Evaluation of electronic microarrays for genotyping factor V, factor II, and MTHFR. Clin. Chem. (2003) 49:732-739.
- JAIN KK: Applications of AmpliChip CYP450. Mol. Diagn. (2005) 9:119-127.
- VAIRAVAN R: AutoGenomics, Inc. Pharmacogenomics (2004) 5:585-588.
- BORTOLIN S, BLACK M, MODI H et al.: Analytical validation of the tag-it high-throughput microsphere-based universal array genotyping platform: application to the multiplex detection of a panel of thrombophilia-associated single-nucleotide polymorphisms. Clin. Chem (2004) 50:2028-2036.
Website
- http://gai.nci.nih.gov/cgi-bin/histo.cgi National Cancer Institute's Cancer Genome Anatomy Project.