-
1
-
-
0029736709
-
Genetic polymorphism of thiopurine S-methyltransferase: Clinical importance and molecular mechanisms
-
Krynetski EY, Tai HL, Yates CR, Fessing MY, Loennechen T, Schuetz JD et al (1996) Genetic polymorphism of thiopurine S-methyltransferase: clinical importance and molecular mechanisms. Pharmacogenetics 6:279-290
-
(1996)
Pharmacogenetics
, vol.6
, pp. 279-290
-
-
Krynetski, E.Y.1
Tai, H.L.2
Yates, C.R.3
Fessing, M.Y.4
Loennechen, T.5
Schuetz, J.D.6
-
2
-
-
45849107951
-
Clinical pharmacology and pharmacogenetics of thiopurines
-
Sahasranaman S, Howard D, Roy S (2008) Clinical pharmacology and pharmacogenetics of thiopurines. Eur J Clin Pharmacol 64:753-767
-
(2008)
Eur J Clin Pharmacol
, vol.64
, pp. 753-767
-
-
Sahasranaman, S.1
Howard, D.2
Roy, S.3
-
3
-
-
0024451147
-
Pharmacogenetics of acute azathioprine toxicity: Relationship to thiopurine methyltransferase genetic polymorphism
-
Lennard L, Van Loon JA, Weinshilboum RM (1989) Pharmacogenetics of acute azathioprine toxicity: relationship to thiopurine methyltransferase genetic polymorphism. Clin Pharmacol Ther 46:149-154
-
(1989)
Clin Pharmacol Ther
, vol.46
, pp. 149-154
-
-
Lennard, L.1
Van Loon, J.A.2
Weinshilboum, R.M.3
-
4
-
-
0033771907
-
Genomic structure and multiple single nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene
-
Seki T, Tanaka T, Nakamura Y (2000) Genomic structure and multiple single nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene. J Hum Genet 45:299-302
-
(2000)
J Hum Genet
, vol.45
, pp. 299-302
-
-
Seki, T.1
Tanaka, T.2
Nakamura, Y.3
-
5
-
-
73349138231
-
UGT1A1 genotyping: A predictor of irinotecan-associated side effects and drug efficacy?
-
Schulz C, Boeck S, Heinemann V, Stemmler HJ (2009) UGT1A1 genotyping: a predictor of irinotecan-associated side effects and drug efficacy? Anticancer Drugs 20:867-879
-
(2009)
Anticancer Drugs
, vol.20
, pp. 867-879
-
-
Schulz, C.1
Boeck, S.2
Heinemann, V.3
Stemmler, H.J.4
-
6
-
-
0034652640
-
Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and association with breast cancer among African Americans
-
Guillemette C, Millikan RC, Newman B, Housman DE (2000) Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and association with breast cancer among African Americans. Cancer Res 60:950-956
-
(2000)
Cancer Res
, vol.60
, pp. 950-956
-
-
Guillemette, C.1
Millikan, R.C.2
Newman, B.3
Housman, D.E.4
-
7
-
-
0036157862
-
Genetic polymorphisms of UDP-glucuronosyltransferase in Asians: UGT1A1*28 is a common allele in Indians
-
Balram C, Sabapathy K, Fei G, Khoo KS, Lee EJ (2002) Genetic polymorphisms of UDP-glucuronosyltransferase in Asians: UGT1A1*28 is a common allele in Indians. Pharmacogenetics 12:81-83
-
(2002)
Pharmacogenetics
, vol.12
, pp. 81-83
-
-
Balram, C.1
Sabapathy, K.2
Fei, G.3
Khoo, K.S.4
Lee, E.J.5
-
8
-
-
34748857912
-
Intraethnic differences in genetic variants of the UGT- glucuronosyltransferase 1A1 gene in Chinese populations
-
Zhang A, Xing Q, Qin S, Du J, Wang L, Yu L et al (2007) Intraethnic differences in genetic variants of the UGT-glucuronosyltransferase 1A1 gene in Chinese populations. Pharmacogenomics J 7:333-338
-
(2007)
Pharmacogenomics J
, vol.7
, pp. 333-338
-
-
Zhang, A.1
Xing, Q.2
Qin, S.3
Du, J.4
Wang, L.5
Yu, L.6
-
9
-
-
69349095224
-
UGT1A1, UGT1A6 and UGT1A7 genetic analysis: Repercussion for irinotecan pharmacogenetics in the Sao Miguel Island Population (Azores, Portugal)
-
Pacheco PR, Brilhante MJ, Ballart C, Sigalat F, Polena H, Cabral R et al (2009) UGT1A1, UGT1A6 and UGT1A7 genetic analysis: repercussion for irinotecan pharmacogenetics in the Sao Miguel Island Population (Azores, Portugal). Mol Diagn Ther 13: 261-268
-
(2009)
Mol Diagn Ther
, vol.13
, pp. 261-268
-
-
Pacheco, P.R.1
Brilhante, M.J.2
Ballart, C.3
Sigalat, F.4
Polena, H.5
Cabral, R.6
-
10
-
-
17044450136
-
Frequent co-occurrence of the TATA box mutation associated with Gilbert's syndrome (UGT1A1*28) with other polymorphisms of the UDP- glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and Egyptians
-
Kohle C, Mohrle B, Munzel PA, Schwab M, Wernet D, Badary OA et al (2003) Frequent co-occurrence of the TATA box mutation associated with Gilbert's syndrome (UGT1A1*28) with other polymorphisms of the UDP- glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and Egyptians. Biochem Pharmacol 65:1521-1527
-
(2003)
Biochem Pharmacol
, vol.65
, pp. 1521-1527
-
-
Kohle, C.1
Mohrle, B.2
Munzel, P.A.3
Schwab, M.4
Wernet, D.5
Badary, O.A.6
-
11
-
-
78249277155
-
Genetic polymorphism in the conjugating enzyme UGT1A1 and the risk of head and neck cancer
-
Lacko M, Roelofs HM, Te Morsche RH, Voogd AC, Oude Ophuis MB, Peters WH et al (2010) Genetic polymorphism in the conjugating enzyme UGT1A1 and the risk of head and neck cancer. Int J Cancer 127:2815-2821
-
(2010)
Int J Cancer
, vol.127
, pp. 2815-2821
-
-
Lacko, M.1
Roelofs, H.M.2
Te Morsche, R.H.3
Voogd, A.C.4
Oude Ophuis, M.B.5
Peters, W.H.6
-
12
-
-
40949121607
-
ABC multidrug transporters: Structure, function and role in chemo resistance
-
Sharom FJ (2008) ABC multidrug transporters: structure, function and role in chemo resistance. Pharmacogenomics 9:105-127
-
(2008)
Pharmacogenomics
, vol.9
, pp. 105-127
-
-
Sharom, F.J.1
-
13
-
-
64649101364
-
A synonymous polymorphism in a common MDR1 (ABCB1) haplotype shapes protein function
-
Fung KL, Gottesman MM (2009) A synonymous polymorphism in a common MDR1 (ABCB1) haplotype shapes protein function. Biochim Biophys Acta 1794:860-871
-
(2009)
Biochim Biophys Acta
, vol.1794
, pp. 860-871
-
-
Fung, K.L.1
Gottesman, M.M.2
-
14
-
-
75549088665
-
MDR1 (C3435T) polymorphism: Relation to the risk of breast cancer and therapeutic outcome
-
Cizmarikova M, Wagnerova M, Schonova L, Habalova V, Kohut A, Linkova A et al (2010) MDR1 (C3435T) polymorphism: relation to the risk of breast cancer and therapeutic outcome. Pharmacogenomics J 10:62-69
-
(2010)
Pharmacogenomics J
, vol.10
, pp. 62-69
-
-
Cizmarikova, M.1
Wagnerova, M.2
Schonova, L.3
Habalova, V.4
Kohut, A.5
Linkova, A.6
-
15
-
-
62149090278
-
MDR1 variants and risk of Parkinson disease. Association with pesticide exposure?
-
Zschiedrich K, Konig IR, Bruggemann N, Kock N, Kasten M, Leenders KL et al (2009) MDR1 variants and risk of Parkinson disease. Association with pesticide exposure? J Neurol 256: 115-120
-
(2009)
J Neurol
, vol.256
, pp. 115-120
-
-
Zschiedrich, K.1
Konig, I.R.2
Bruggemann, N.3
Kock, N.4
Kasten, M.5
Leenders, K.L.6
-
17
-
-
70349100893
-
Application of SNaPshot for analysis of thiopurine methyltransferase gene polymorphism
-
Kapoor G, Maitra A, Somlata, Brahmachari V (2009) Application of SNaPshot for analysis of thiopurine methyltransferase gene polymorphism. Indian J Med Res 129:500-505
-
(2009)
Indian J Med Res
, vol.129
, pp. 500-505
-
-
Kapoor, G.1
Maitra, A.2
Somlata3
Brahmachari, V.4
-
18
-
-
58149269041
-
Associations between common variants in the MDR1 (ABCB1) gene and ulcerative colitis among North Indians
-
Juyal G, Midha V, Amre D, Sood A, Seidman E, Thelma BK (2009) Associations between common variants in the MDR1 (ABCB1) gene and ulcerative colitis among North Indians. Pharmacogenet Genomics 19:77-85
-
(2009)
Pharmacogenet Genomics
, vol.19
, pp. 77-85
-
-
Juyal, G.1
Midha, V.2
Amre, D.3
Sood, A.4
Seidman, E.5
Thelma, B.K.6
-
19
-
-
0032898380
-
Thiopurine methyltransferase alleles in British and Ghanaian populations
-
Ameyaw MM, Collie-Duguid ES, Powrie RH, Ofori-Adjei D, McLeod HL (1999) Thiopurine methyltransferase alleles in British and Ghanaian populations. Hum Mol Genet 8:367-370
-
(1999)
Hum Mol Genet
, vol.8
, pp. 367-370
-
-
Ameyaw, M.M.1
Collie-Duguid, E.S.2
Powrie, R.H.3
Ofori-Adjei, D.4
McLeod, H.L.5
-
20
-
-
33645127229
-
Molecular analysis of thiopurine S-methyltransferase alleles in Taiwan aborigines and Taiwanese
-
Lu HF, Shih MC, Chang YS, Chang JY, Ko YC, Chang SJ et al (2006) Molecular analysis of thiopurine S-methyltransferase alleles in Taiwan aborigines and Taiwanese. J Clin Pharm Ther 31:93-98
-
(2006)
J Clin Pharm Ther
, vol.31
, pp. 93-98
-
-
Lu, H.F.1
Shih, M.C.2
Chang, Y.S.3
Chang, J.Y.4
Ko, Y.C.5
Chang, S.J.6
-
21
-
-
77957652268
-
Genetic analysis of thiopurine methyltransferase polymorphism in the Jordanian population
-
Hakooz N, Arafat T, Payne D, Ollier W, Pushpakom S, Andrews J et al (2010) Genetic analysis of thiopurine methyltransferase polymorphism in the Jordanian population. Eur J Clin Pharmacol 66:999-1003
-
(2010)
Eur J Clin Pharmacol
, vol.66
, pp. 999-1003
-
-
Hakooz, N.1
Arafat, T.2
Payne, D.3
Ollier, W.4
Pushpakom, S.5
Andrews, J.6
-
22
-
-
49649083255
-
UGT1A1 and UGT1A9 functional variants, meat intake, and colon cancer, among Caucasians and African-Americans
-
Girard H, Butler LM, Villeneuve L, Millikan RC, Sinha R, Sandler RS et al (2008) UGT1A1 and UGT1A9 functional variants, meat intake, and colon cancer, among Caucasians and African-Americans. Mutat Res 644:56-63
-
(2008)
Mutat Res
, vol.644
, pp. 56-63
-
-
Girard, H.1
Butler, L.M.2
Villeneuve, L.3
Millikan, R.C.4
Sinha, R.5
Sandler, R.S.6
-
23
-
-
0037230427
-
Combined polymorphisms in UDP-glucuronosyltransferases 1A1 and 1A6: Implications for patients with Gilbert's syndrome
-
Peters WH, te Morsche RH, Roelofs HM (2003) Combined polymorphisms in UDP-glucuronosyltransferases 1A1 and 1A6: implications for patients with Gilbert's syndrome. J Hepatol 38:3-8
-
(2003)
J Hepatol
, vol.38
, pp. 3-8
-
-
Peters, W.H.1
Te Morsche, R.H.2
Roelofs, H.M.3
-
24
-
-
67049143800
-
Gilbert syndrome as a predisposing factor for cholelithiasis risk in the Greek adult population
-
Tsezou A, Tzetis M, Giannatou E, Spanos I, Roma E, Fretzayas A et al (2009) Gilbert syndrome as a predisposing factor for cholelithiasis risk in the Greek adult population. Genet Test Mol Biomarkers 13:143-146
-
(2009)
Genet Test Mol Biomarkers
, vol.13
, pp. 143-146
-
-
Tsezou, A.1
Tzetis, M.2
Giannatou, E.3
Spanos, I.4
Roma, E.5
Fretzayas, A.6
-
25
-
-
33846573882
-
UGT1A1(TA)n promoter polymorphism - A new case of a (TA)8 allele in Caucasians
-
Ostanek B, Furlan D, Mavec T, Lukac-Bajalo J (2007) UGT1A1(TA)n promoter polymorphism-a new case of a (TA)8 allele in Caucasians. Blood Cells Mol Dis 38:78-82
-
(2007)
Blood Cells Mol Dis
, vol.38
, pp. 78-82
-
-
Ostanek, B.1
Furlan, D.2
Mavec, T.3
Lukac-Bajalo, J.4
-
26
-
-
53549087240
-
Genotype frequencies of UDP-glucuronosyltransferase 1A1 promoter gene polymorphism in the population of healthy Croatian pre-scholars
-
Marinkovic N, Pasalic D, Grskovic B, Ferencak G, Honovic L, Rukavina AS (2008) Genotype frequencies of UDP-glucuronosyltransferase 1A1 promoter gene polymorphism in the population of healthy Croatian pre-scholars. Coll Antropol 32:725-729
-
(2008)
Coll Antropol
, vol.32
, pp. 725-729
-
-
Marinkovic, N.1
Pasalic, D.2
Grskovic, B.3
Ferencak, G.4
Honovic, L.5
Rukavina, A.S.6
-
27
-
-
56349113665
-
Serum bilirubin levels, UGT1A1 polymorphisms and risk for coronary artery disease
-
Lingenhel A, Kollerits B, Schwaiger JP, Hunt SC, Gress R, Hopkins PN et al (2008) Serum bilirubin levels, UGT1A1 polymorphisms and risk for coronary artery disease. Exp Gerontol 43:1102-1107
-
(2008)
Exp Gerontol
, vol.43
, pp. 1102-1107
-
-
Lingenhel, A.1
Kollerits, B.2
Schwaiger, J.P.3
Hunt, S.C.4
Gress, R.5
Hopkins, P.N.6
-
28
-
-
0037699938
-
UGT1A1*28 allele and coronary heart disease: The Rotterdam study
-
Bosma PJ, van der Meer IM, Bakker CT, Hofman A, Paul-Abrahamse M, Witteman JC (2003) UGT1A1*28 allele and coronary heart disease: the Rotterdam study. Clin Chem 49:1180-1181
-
(2003)
Clin Chem
, vol.49
, pp. 1180-1181
-
-
Bosma, P.J.1
Van Der Meer, I.M.2
Bakker, C.T.3
Hofman, A.4
Paul-Abrahamse, M.5
Witteman, J.C.6
-
29
-
-
0034894346
-
Association of genetic polymorphisms in UGT1A1 with breast cancer and plasma hormone levels
-
Guillemette C, De Vivo I, Hankinson SE, Haiman CA, Spiegelman D, Housman DE et al (2001) Association of genetic polymorphisms in UGT1A1 with breast cancer and plasma hormone levels. Cancer Epidemiol Biomarkers Prev 10:711-714
-
(2001)
Cancer Epidemiol Biomarkers Prev
, vol.10
, pp. 711-714
-
-
Guillemette, C.1
De Vivo, I.2
Hankinson, S.E.3
Haiman, C.A.4
Spiegelman, D.5
Housman, D.E.6
-
30
-
-
62749139545
-
Citrus fruit intake is associated with lower serum bilirubin concentration among women with the UGT1A1*28 polymorphism
-
Saracino MR, Bigler J, Schwarz Y, Chang JL, Li S, Li L et al (2009) Citrus fruit intake is associated with lower serum bilirubin concentration among women with the UGT1A1*28 polymorphism. J Nutr 139:555-560
-
(2009)
J Nutr
, vol.139
, pp. 555-560
-
-
Saracino, M.R.1
Bigler, J.2
Schwarz, Y.3
Chang, J.L.4
Li, S.5
Li, L.6
-
31
-
-
33845532124
-
Further evidence that the UGT1A1*28 allele is not associated with coronary heart disease: The ECTIM Study
-
Gajdos V, Petit FM, Perret C, Mollet-Boudjemline A, Colin P, Capel L et al (2006) Further evidence that the UGT1A1*28 allele is not associated with coronary heart disease: the ECTIM Study. Clin Chem 52:2313-2314
-
(2006)
Clin Chem
, vol.52
, pp. 2313-2314
-
-
Gajdos, V.1
Petit, F.M.2
Perret, C.3
Mollet-Boudjemline, A.4
Colin, P.5
Capel, L.6
-
32
-
-
33845651872
-
The influence of genetic polymorphisms in Ahr, CYP1A1, CYP1A2, CYP1B1, GST M1, GST T1 and UGT1A1 on urine 1-hydroxypyrene glucuronide concentrations in healthy subjects from Rio Grande do Sul, Brazil
-
Abnet CC, Fagundes RB, Strickland PT, Kamangar F, Roth MJ, Taylor PR et al (2007) The influence of genetic polymorphisms in Ahr, CYP1A1, CYP1A2, CYP1B1, GST M1, GST T1 and UGT1A1 on urine 1-hydroxypyrene glucuronide concentrations in healthy subjects from Rio Grande do Sul, Brazil. Carcinogenesis 28:112-117
-
(2007)
Carcinogenesis
, vol.28
, pp. 112-117
-
-
Abnet, C.C.1
Fagundes, R.B.2
Strickland, P.T.3
Kamangar, F.4
Roth, M.J.5
Taylor, P.R.6
-
33
-
-
3042527833
-
Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 (UGT1A1) and risk of breast cancer
-
Adegoke OJ, Shu XO, Gao YT, Cai Q, Breyer J, Smith J et al (2004) Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 (UGT1A1) and risk of breast cancer. Breast Cancer Res Treat 85:239-245
-
(2004)
Breast Cancer Res Treat
, vol.85
, pp. 239-245
-
-
Adegoke, O.J.1
Shu, X.O.2
Gao, Y.T.3
Cai, Q.4
Breyer, J.5
Smith, J.6
-
34
-
-
34548563846
-
Combined UGT1A1 and UGT1A7 variant alleles are associated with increased risk of Gilbert's syndrome in Taiwanese adults
-
Teng HC, Huang MJ, Tang KS, Yang SS, Tseng CS, Huang CS (2007) Combined UGT1A1 and UGT1A7 variant alleles are associated with increased risk of Gilbert's syndrome in Taiwanese adults. Clin Genet 72:321-328
-
(2007)
Clin Genet
, vol.72
, pp. 321-328
-
-
Teng, H.C.1
Huang, M.J.2
Tang, K.S.3
Yang, S.S.4
Tseng, C.S.5
Huang, C.S.6
-
35
-
-
18744407592
-
Single nucleotide polymorphisms of ABCB1 (MDR1) gene and distinct haplotype profile in a West Black African population
-
Allabi AC, Horsmans Y, Issaoui B, Gala JL (2005) Single nucleotide polymorphisms of ABCB1 (MDR1) gene and distinct haplotype profile in a West Black African population. Eur J Clin Pharmacol 61:97-102
-
(2005)
Eur J Clin Pharmacol
, vol.61
, pp. 97-102
-
-
Allabi, A.C.1
Horsmans, Y.2
Issaoui, B.3
Gala, J.L.4
-
36
-
-
52049100135
-
Impact of MDR1 haplotypes derived from C1236T, G2677T/A and C3435T on the pharmacokinetics of single-dose oral digoxin in healthy Chinese volunteers
-
Xu P, Jiang ZP, Zhang BK, Tu JY, Li HD (2008) Impact of MDR1 haplotypes derived from C1236T, G2677T/A and C3435T on the pharmacokinetics of single-dose oral digoxin in healthy Chinese volunteers. Pharmacology 82:221-227
-
(2008)
Pharmacology
, vol.82
, pp. 221-227
-
-
Xu, P.1
Jiang, Z.P.2
Zhang, B.K.3
Tu, J.Y.4
Li, H.D.5
-
37
-
-
0035051412
-
MDR1 pharmacogenetics: Frequency of the C3435T mutation in exon 26 is significantly influenced by ethnicity
-
Ameyaw MM, Regateiro F, Li T, Liu X, Tariq M, Mobarek A et al (2001) MDR1 pharmacogenetics: frequency of the C3435T mutation in exon 26 is significantly influenced by ethnicity. Pharmacogenetics 11:217-221
-
(2001)
Pharmacogenetics
, vol.11
, pp. 217-221
-
-
Ameyaw, M.M.1
Regateiro, F.2
Li, T.3
Liu, X.4
Tariq, M.5
Mobarek, A.6
-
38
-
-
70349472875
-
Reconstructing Indian population history
-
Reich D, Thangaraj K, Patterson N, Price AL, Singh L (2009) Reconstructing Indian population history. Nature 461:489-494
-
(2009)
Nature
, vol.461
, pp. 489-494
-
-
Reich, D.1
Thangaraj, K.2
Patterson, N.3
Price, A.L.4
Singh, L.5
-
39
-
-
44149107150
-
Genetic landscape of the people of India: A canvas for disease gene exploration
-
Indian Genome Variation Consortium
-
Indian Genome Variation Consortium (2008) Genetic landscape of the people of India: a canvas for disease gene exploration. J Genet 87:3-20
-
(2008)
J Genet
, vol.87
, pp. 3-20
-
-
-
40
-
-
0034850189
-
Frequencies of thiopurine S-methyltransferase mutant alleles (TPMT*2, *3A, *3B and *3C) in 151 healthy Japanese subjects and the inheritance of TPMT*3C in the family of a propositus
-
Kubota T, Chiba K (2001) Frequencies of thiopurine S-methyltransferase mutant alleles (TPMT*2, *3A, *3B and *3C) in 151 healthy Japanese subjects and the inheritance of TPMT*3C in the family of a propositus. Br J Clin Pharmacol 51:475-477
-
(2001)
Br J Clin Pharmacol
, vol.51
, pp. 475-477
-
-
Kubota, T.1
Chiba, K.2
-
41
-
-
33745033064
-
Frequency of the thiopurine S-methyltransferase alleles in the ancient genetic population isolate of Sardinia
-
Rossino R, Vincis C, Alves S, Prata MJ, Macis MD, Nucaro AL et al (2006) Frequency of the thiopurine S-methyltransferase alleles in the ancient genetic population isolate of Sardinia. J Clin Pharm Ther 31:283-287
-
(2006)
J Clin Pharm Ther
, vol.31
, pp. 283-287
-
-
Rossino, R.1
Vincis, C.2
Alves, S.3
Prata, M.J.4
MacIs, M.D.5
Nucaro, A.L.6
-
42
-
-
32044460606
-
Determination of intra-ethnic differences in the polymorphisms of thiopurine S-methyltransferase in Chinese
-
Zhang JP, Zhou SF, Chen X, Huang M (2006) Determination of intra-ethnic differences in the polymorphisms of thiopurine S-methyltransferase in Chinese. Clin Chim Acta 365:337-341
-
(2006)
Clin Chim Acta
, vol.365
, pp. 337-341
-
-
Zhang, J.P.1
Zhou, S.F.2
Chen, X.3
Huang, M.4
-
43
-
-
27744602074
-
Molecular analysis of the thiopurine S-methyltransferase alleles in Bolivians and Tibetans
-
Lu HF, Shih MC, Hsueh SC, Chen CM, Chang JY, Chang JG (2005) Molecular analysis of the thiopurine S-methyltransferase alleles in Bolivians and Tibetans. J Clin Pharm Ther 30: 491-496
-
(2005)
J Clin Pharm Ther
, vol.30
, pp. 491-496
-
-
Lu, H.F.1
Shih, M.C.2
Hsueh, S.C.3
Chen, C.M.4
Chang, J.Y.5
Chang, J.G.6
-
44
-
-
46749130445
-
Polymorphisms of the TPMT gene in the Czech healthy population and patients with inflammatory bowel disease
-
Slanar O, Bortlik M, Buzkova H, Donoval R, Pechandova K, Sebesta I et al (2008) Polymorphisms of the TPMT gene in the Czech healthy population and patients with inflammatory bowel disease. Nucleosides Nucleotides Nucleic Acids 27:835-838
-
(2008)
Nucleosides Nucleotides Nucleic Acids
, vol.27
, pp. 835-838
-
-
Slanar, O.1
Bortlik, M.2
Buzkova, H.3
Donoval, R.4
Pechandova, K.5
Sebesta, I.6
-
45
-
-
0033830262
-
Allelic variants of the thiopurine S-methyltransferase deficiency in patients with ulcerative colitis and in healthy controls
-
Corominas H, Domenech M, Gonzalez D, Diaz C, Roca M, Garcia-Gonzalez MA et al (2000) Allelic variants of the thiopurine S-methyltransferase deficiency in patients with ulcerative colitis and in healthy controls. Am J Gastroenterol 95:2313-2317
-
(2000)
Am J Gastroenterol
, vol.95
, pp. 2313-2317
-
-
Corominas, H.1
Domenech, M.2
Gonzalez, D.3
Diaz, C.4
Roca, M.5
Garcia-Gonzalez, M.A.6
-
46
-
-
47349092912
-
Thiopurine S-methyltransferase (TPMT) pharmacogenetics: Three new mutations and haplotype analysis in the Estonian population
-
Tamm R, Oselin K, Kallassalu K, Magi R, Anier K, Remm M et al (2008) Thiopurine S-methyltransferase (TPMT) pharmacogenetics: three new mutations and haplotype analysis in the Estonian population. Clin Chem Lab Med 46:974-979
-
(2008)
Clin Chem Lab Med
, vol.46
, pp. 974-979
-
-
Tamm, R.1
Oselin, K.2
Kallassalu, K.3
Magi, R.4
Anier, K.5
Remm, M.6
-
47
-
-
4444268912
-
Tracing the origin of the most common thiopurine methyltransferase (TPMT) variants: Preliminary data from the patterns of haplotypic association with two CA repeats
-
Alves S, Rocha J, Amorim A, Prata MJ (2004) Tracing the origin of the most common thiopurine methyltransferase (TPMT) variants: preliminary data from the patterns of haplotypic association with two CA repeats. Ann Hum Genet 68:313-323
-
(2004)
Ann Hum Genet
, vol.68
, pp. 313-323
-
-
Alves, S.1
Rocha, J.2
Amorim, A.3
Prata, M.J.4
-
48
-
-
67650097604
-
Thiopurine S-methyltransferase gene polymorphism in Chilean blood donors
-
Luis Alvarez L, Mauricio Venegas S, Milton Larrondo L, Natalia Becerra B, Ariel Castro L, Rodrigo Quera P (2009) Thiopurine S-methyltransferase gene polymorphism in Chilean blood donors. Rev Med Chile 137:185-192
-
(2009)
Rev Med Chile
, vol.137
, pp. 185-192
-
-
Luis Alvarez, L.1
Mauricio Venegas, S.2
Milton Larrondo, L.3
Natalia Becerra, B.4
Ariel Castro, L.5
Rodrigo Quera, P.6
-
49
-
-
77951443953
-
Frequency of thiopurine S-methyltransferase (TPMT) alleles in southeast Iranian population
-
Bahari A, Hashemi M, Bari Z, Moazeni-Roodi A, Kaykhaei MA, Narouie B (2010) Frequency of thiopurine S-methyltransferase (TPMT) alleles in southeast Iranian population. Nucleosides Nucleotides Nucleic Acids 29:237-244
-
(2010)
Nucleosides Nucleotides Nucleic Acids
, vol.29
, pp. 237-244
-
-
Bahari, A.1
Hashemi, M.2
Bari, Z.3
Moazeni-Roodi, A.4
Kaykhaei, M.A.5
Narouie, B.6
-
50
-
-
59449099864
-
TPMT genetic variations in populations of the Russian Federation
-
Samochatova EV, Chupova NV, Rudneva A, Makarova O, Nasedkina TV, Fedorova OE et al (2009) TPMT genetic variations in populations of the Russian Federation. Pediatr Blood Cancer 52:203-208
-
(2009)
Pediatr Blood Cancer
, vol.52
, pp. 203-208
-
-
Samochatova, E.V.1
Chupova, N.V.2
Rudneva, A.3
Makarova, O.4
Nasedkina, T.V.5
Fedorova, O.E.6
-
51
-
-
32544457881
-
Common Cytochrome p4503A (CYP3A4 and CYP3A5) and Thiopurine S-Methyl Transferase (TPMT) Polymorphisms in Turkish Population
-
Sayutoulu MA, Yildiz U, Hatirnaz O, Ozbek U (2006) Common Cytochrome p4503A (CYP3A4 and CYP3A5) and Thiopurine S-Methyl Transferase (TPMT) Polymorphisms In Turkish Population. Turk J Med Sci 36:11-15
-
(2006)
Turk J Med Sci
, vol.36
, pp. 11-15
-
-
Sayutoulu, M.A.1
Yildiz, U.2
Hatirnaz, O.3
Ozbek, U.4
-
52
-
-
44849108267
-
Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and breast cancer risk in Africans
-
Huo D, Kim HJ, Adebamowo CA, Ogundiran TO, Akang EE, Campbell O et al (2008) Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and breast cancer risk in Africans. Breast Cancer Res Treat 110:367-376
-
(2008)
Breast Cancer Res Treat
, vol.110
, pp. 367-376
-
-
Huo, D.1
Kim, H.J.2
Adebamowo, C.A.3
Ogundiran, T.O.4
Akang, E.E.5
Campbell, O.6
-
53
-
-
47249085145
-
MDR1 genotypes do not influence the absorption of a single oral dose of 600 mg valacyclovir in healthy Chinese Han ethnic males
-
Zhang Y, Jiang XH, Hu YQ, Li ZR, Su L, Wang ZG et al (2008) MDR1 genotypes do not influence the absorption of a single oral dose of 600 mg valacyclovir in healthy Chinese Han ethnic males. Br J Clin Pharmacol 66:247-254
-
(2008)
Br J Clin Pharmacol
, vol.66
, pp. 247-254
-
-
Zhang, Y.1
Jiang, X.H.2
Hu, Y.Q.3
Li, Z.R.4
Su, L.5
Wang, Z.G.6
-
54
-
-
32044446731
-
MDR1 C3435T polymorphism is predictive of later onset of ulcerative colitis in Japanese
-
Osuga T, Sakaeda T, Nakamura T, Yamada T, Koyama T, Tamura T et al (2006) MDR1 C3435T polymorphism is predictive of later onset of ulcerative colitis in Japanese. Biol Pharm Bull 29:324-329
-
(2006)
Biol Pharm Bull
, vol.29
, pp. 324-329
-
-
Osuga, T.1
Sakaeda, T.2
Nakamura, T.3
Yamada, T.4
Koyama, T.5
Tamura, T.6
-
55
-
-
77949261605
-
ABCB1 single nucleotide polymorphisms in the Brazilian population
-
Scheiner MA, Damasceno AM, Maia RC (2010) ABCB1 single nucleotide polymorphisms in the Brazilian population. Mol Biol Rep 37:111-118
-
(2010)
Mol Biol Rep
, vol.37
, pp. 111-118
-
-
Scheiner, M.A.1
Damasceno, A.M.2
Maia, R.C.3
-
56
-
-
70350663033
-
Association between genetic polymorphism of multidrug resistance 1 gene and sasang constitutions
-
Kim HJ, Hwang SY, Kim JH, Park HJ, Lee SG, Lee SW et al (2009) Association between Genetic Polymorphism of Multidrug Resistance 1 Gene and Sasang Constitutions. Evid Based Complement Alternat Med 6(Suppl 1):73-80
-
(2009)
Evid Based Complement Alternat Med
, vol.6
, Issue.SUPPL. 1
, pp. 73-80
-
-
Kim, H.J.1
Hwang, S.Y.2
Kim, J.H.3
Park, H.J.4
Lee, S.G.5
Lee, S.W.6
-
57
-
-
33646757531
-
Associations of allelic variants of the multidrug resistance gene (ABCB1 or MDR1) and inflammatory bowel disease and their effects on disease behavior: A case-control and meta-analysis study
-
Onnie CM, Fisher SA, Pattni R, Sanderson J, Forbes A, Lewis CM et al (2006) Associations of allelic variants of the multidrug resistance gene (ABCB1 or MDR1) and inflammatory bowel disease and their effects on disease behavior: a case-control and meta-analysis study. Inflamm Bowel Dis 12:263-271
-
(2006)
Inflamm Bowel Dis
, vol.12
, pp. 263-271
-
-
Onnie, C.M.1
Fisher, S.A.2
Pattni, R.3
Sanderson, J.4
Forbes, A.5
Lewis, C.M.6
-
58
-
-
38649091379
-
No association between MDR1 (ABCB1) 2677G>T and 3435C>T polymorphism and sporadic colorectal cancer among Bulgarian patients
-
Petrova DT, Nedeva P, Maslyankov S, Toshev S, Yaramov N, Atanasova S et al (2008) No association between MDR1 (ABCB1) 2677G>T and 3435C>T polymorphism and sporadic colorectal cancer among Bulgarian patients. J Cancer Res Clin Oncol 134:317-322
-
(2008)
J Cancer Res Clin Oncol
, vol.134
, pp. 317-322
-
-
Petrova, D.T.1
Nedeva, P.2
Maslyankov, S.3
Toshev, S.4
Yaramov, N.5
Atanasova, S.6
-
59
-
-
34447515970
-
Determination of ABCB1 polymorphisms and haplotypes frequencies in a French population
-
Jeannesson E, Albertini L, Siest G, Gomes AM, Ribeiro V, Aslanidis C et al (2007) Determination of ABCB1 polymorphisms and haplotypes frequencies in a French population. Fundam Clin Pharmacol 21:411-418
-
(2007)
Fundam Clin Pharmacol
, vol.21
, pp. 411-418
-
-
Jeannesson, E.1
Albertini, L.2
Siest, G.3
Gomes, A.M.4
Ribeiro, V.5
Aslanidis, C.6
-
60
-
-
34548575127
-
Possible role of MDR1 two-locus genotypes for young-age onset ulcerative colitis but not Crohn's disease
-
Fiedler T, Buning C, Reuter W, Pitre G, Gentz E, Schmidt HH et al (2007) Possible role of MDR1 two-locus genotypes for young-age onset ulcerative colitis but not Crohn's disease. Eur J Clin Pharmacol 63:917-925
-
(2007)
Eur J Clin Pharmacol
, vol.63
, pp. 917-925
-
-
Fiedler, T.1
Buning, C.2
Reuter, W.3
Pitre, G.4
Gentz, E.5
Schmidt, H.H.6
-
61
-
-
34248583543
-
ATP-binding cassette transporter ABCG2 (BCRP) and ABCB1 (MDR1) variants are not associated with disease susceptibility, disease phenotype response to medical therapy or need for surgeryin Hungarian patients with inflammatory bowel diseases
-
Fischer S, Lakatos PL, Lakatos L, Kovacs A, Molnar T, Altorjay I et al (2007) ATP-binding cassette transporter ABCG2 (BCRP) and ABCB1 (MDR1) variants are not associated with disease susceptibility, disease phenotype response to medical therapy or need for surgeryin Hungarian patients with inflammatory bowel diseases. Scand J Gastroenterol 42:726-733
-
(2007)
Scand J Gastroenterol
, vol.42
, pp. 726-733
-
-
Fischer, S.1
Lakatos, P.L.2
Lakatos, L.3
Kovacs, A.4
Molnar, T.5
Altorjay, I.6
-
62
-
-
84655165078
-
MDR-1 polymorphisms (G2677T and C3435T) in B-chronic lymphocytic leukemia: An impact on susceptibility and prognosis
-
doi:10.1007/s1203201095619
-
Penna G, Allegra A, Alonci A, Aguennouz M, Garufi A, Cannavo A et al (2010) MDR-1 polymorphisms (G2677T and C3435T) in B-chronic lymphocytic leukemia: an impact on susceptibility and prognosis. Med Oncol. doi:10.1007/s1203201095619
-
(2010)
Med Oncol.
-
-
Penna, G.1
Allegra, A.2
Alonci, A.3
Aguennouz, M.4
Garufi, A.5
Cannavo, A.6
-
63
-
-
65649099373
-
Frequency of the three most common polymorphisms in the MDR1 gene in Slovak population
-
Krivulcik T, Sedlak J, Bartosova Z (2009) Frequency of the three most common polymorphisms in the MDR1 gene in Slovak population. Neoplasma 56:101-107
-
(2009)
Neoplasma
, vol.56
, pp. 101-107
-
-
Krivulcik, T.1
Sedlak, J.2
Bartosova, Z.3
-
64
-
-
43049156102
-
Common germline MDR1/ABCB1 functional polymorphisms and haplotypes modify susceptibility to colorectal cancers with high microsatellite instability
-
Potocnik U, Glavac D, Dean M (2008) Common germline MDR1/ABCB1 functional polymorphisms and haplotypes modify susceptibility to colorectal cancers with high microsatellite instability. Cancer Genet Cytogenet 183:28-34
-
(2008)
Cancer Genet Cytogenet
, vol.183
, pp. 28-34
-
-
Potocnik, U.1
Glavac, D.2
Dean, M.3
-
65
-
-
32944468151
-
Mdr-1 single nucleotide polymorphisms in ovarian cancer tissue: G2677T/A correlates with response to paclitaxel chemotherapy
-
Green H, Soderkvist P, Rosenberg P, Horvath G, Peterson C (2006) mdr-1 single nucleotide polymorphisms in ovarian cancer tissue: G2677T/A correlates with response to paclitaxel chemotherapy. Clin Cancer Res 12:854-859
-
(2006)
Clin Cancer Res
, vol.12
, pp. 854-859
-
-
Green, H.1
Soderkvist, P.2
Rosenberg, P.3
Horvath, G.4
Peterson, C.5
-
66
-
-
33846558896
-
Ethnicity-related polymorphisms and haplotypes in the human ABCB1 gene
-
Kimchi-Sarfaty C, Marple AH, Shinar S, Kimchi AM, Scavo D, Roma MI et al (2007) Ethnicity-related polymorphisms and haplotypes in the human ABCB1 gene. Pharmacogenomics 8:29-39
-
(2007)
Pharmacogenomics
, vol.8
, pp. 29-39
-
-
Kimchi-Sarfaty, C.1
Marple, A.H.2
Shinar, S.3
Kimchi, A.M.4
Scavo, D.5
Roma, M.I.6
-
67
-
-
48249103546
-
Polymorphism C3435T of the MDR1 gene in Central Americans and Spaniards
-
Vicente J, Sinues B, Fanlo A, Vasquez P, Medina JC, Martinez- Jarreta B (2008) Polymorphism C3435T of the MDR1 gene in Central Americans and Spaniards. Mol Biol Rep 35:473-478
-
(2008)
Mol Biol Rep
, vol.35
, pp. 473-478
-
-
Vicente, J.1
Sinues, B.2
Fanlo, A.3
Vasquez, P.4
Medina, J.C.5
Martinez-Jarreta, B.6
-
68
-
-
33748753681
-
Is C3435T polymorphism of MDR1 related to inflammatory bowel disease or colorectal cancer in Korean?
-
Lee BI, Choi KY, Lee KM, Chung WC, Kim BW, Choi H et al (2006) Is C3435T polymorphism of MDR1 related to inflammatory bowel disease or colorectal cancer in Korean? Korean J Gastroenterol 47:22-29
-
(2006)
Korean J Gastroenterol
, vol.47
, pp. 22-29
-
-
Lee, B.I.1
Choi, K.Y.2
Lee, K.M.3
Chung, W.C.4
Kim, B.W.5
Choi, H.6
-
69
-
-
62549099045
-
Pharmacogenomics of CYP2A6, CYP2B6, CYP2C19, CYP2D6, CYP3A4, CYP3A5 and MDR1 in Vietnam
-
Veiga MI, Asimus S, Ferreira PE, Martins JP, Cavaco I, Ribeiro V et al (2009) Pharmacogenomics of CYP2A6, CYP2B6, CYP2C19, CYP2D6, CYP3A4, CYP3A5 and MDR1 in Vietnam. Eur J Clin Pharmacol 65:355-363
-
(2009)
Eur J Clin Pharmacol
, vol.65
, pp. 355-363
-
-
Veiga, M.I.1
Asimus, S.2
Ferreira, P.E.3
Martins, J.P.4
Cavaco, I.5
Ribeiro, V.6
-
70
-
-
67650246375
-
Associations between ABCB1/MDR1 gene polymorphisms and Crohn's disease: A gene-wide study in a pediatric population
-
Krupoves A, Seidman EG, Mack D, Israel D, Morgan K, Lambrette P et al (2009) Associations between ABCB1/MDR1 gene polymorphisms and Crohn's disease: a gene-wide study in a pediatric population. Inflamm Bowel Dis 15:900-908
-
(2009)
Inflamm Bowel Dis
, vol.15
, pp. 900-908
-
-
Krupoves, A.1
Seidman, E.G.2
MacK, D.3
Israel, D.4
Morgan, K.5
Lambrette, P.6
-
71
-
-
34447560176
-
Genetic polymorphism of cytochrome P450s and P-glycoprotein in the Finnish population
-
Hilli J, Rane A, Lundgren S, Bertilsson L, Laine K (2007) Genetic polymorphism of cytochrome P450s and P-glycoprotein in the Finnish population. Fundam Clin Pharmacol 21:379-386
-
(2007)
Fundam Clin Pharmacol
, vol.21
, pp. 379-386
-
-
Hilli, J.1
Rane, A.2
Lundgren, S.3
Bertilsson, L.4
Laine, K.5
-
72
-
-
34249095800
-
Multidrug resistance 1 gene polymorphism and susceptibility to inflammatory bowel disease
-
Ardizzone S, Maconi G, Bianchi V, Russo A, Colombo E, Cassinotti A et al (2007) Multidrug resistance 1 gene polymorphism and susceptibility to inflammatory bowel disease. Inflamm Bowel Dis 13:516-523
-
(2007)
Inflamm Bowel Dis
, vol.13
, pp. 516-523
-
-
Ardizzone, S.1
MacOni, G.2
Bianchi, V.3
Russo, A.4
Colombo, E.5
Cassinotti, A.6
-
73
-
-
70549093105
-
Association of the MDR1 (ABCB1) gene 3435C>T polymorphism with male infertility
-
Drozdzik M, Stefankiewicz J, Kurzawa R, Gornik W, Baczkowski T, Kurzawski M (2009) Association of the MDR1 (ABCB1) gene 3435C>T polymorphism with male infertility. Pharmacol Rep 61:690-696
-
(2009)
Pharmacol Rep
, vol.61
, pp. 690-696
-
-
Drozdzik, M.1
Stefankiewicz, J.2
Kurzawa, R.3
Gornik, W.4
Baczkowski, T.5
Kurzawski, M.6
-
74
-
-
70449356836
-
Gene polymorphisms in TYMS, MTHFR, p53 and MDR1 as risk factors for breast cancer: A case-control study
-
Henriquez-Hernandez LA, Murias-Rosales A, Hernandez Gonzalez A, Cabrera De Leon A, Diaz-Chico BN, Mori De Santiago M et al (2009) Gene polymorphisms in TYMS, MTHFR, p53 and MDR1 as risk factors for breast cancer: a case-control study. Oncol Rep 22:1425-1433
-
(2009)
Oncol Rep
, vol.22
, pp. 1425-1433
-
-
Henriquez-Hernandez, L.A.1
Murias-Rosales, A.2
Hernandez Gonzalez, A.3
Cabrera De Leon, A.4
Diaz-Chico, B.N.5
Mori De Santiago, M.6
|