-
1
-
-
0034966656
-
Thirteen UDPglucuronosyltransferase genes are encoded at the human UGT1 gene complex locus
-
Gong QH, Cho JW, Huang T et al. Thirteen UDPglucuronosyltransferase genes are encoded at the human UGT1 gene complex locus. Pharmacogenetics 11, 357-368 (2001).
-
(2001)
Pharmacogenetics
, vol.11
, pp. 357-368
-
-
Gong, Q.H.1
Cho, J.W.2
Huang, T.3
-
2
-
-
0041930641
-
Vertebrate UDP-glucuronosyltransferases: Functional and evolutionary aspects
-
Bock KW. Vertebrate UDP-glucuronosyltransferases: functional and evolutionary aspects. Biochem. Pharmacol. 66, 691-396 (2003).
-
(2003)
Biochem. Pharmacol.
, vol.66
, pp. 691-396
-
-
Bock, K.W.1
-
3
-
-
0028867826
-
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome
-
Bosma PJ, Chowdhury JR, Bakker C et al. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome. N. Engl. J. Med. 333, 1171-1175 (1995).
-
(1995)
N. Engl. J. Med.
, vol.333
, pp. 1171-1175
-
-
Bosma, P.J.1
Chowdhury, J.R.2
Bakker, C.3
-
4
-
-
0028081366
-
Discrimination between Crigler-Najjar Type I and II by expression of mutant bilirubin uridine diphosphate-glucuronosyltransferase
-
Seppen J, Bosma PJ, Goldhoorn BG et al. Discrimination between Crigler-Najjar Type I and II by expression of mutant bilirubin uridine diphosphate-glucuronosyltransferase. J. Clin. Invest. 94, 2385-2391 (1994).
-
(1994)
J. Clin. Invest.
, vol.94
, pp. 2385-2391
-
-
Seppen, J.1
Bosma, P.J.2
Goldhoorn, B.G.3
-
5
-
-
0031595660
-
The UGT1A1*28 allele is relatively rare in a Japanese population
-
Ando Y, Chida M, Nakayama K et al. The UGT1A1*28 allele is relatively rare in a Japanese population. Pharmacogenetics 8, 357-360 (1998).
-
(1998)
Pharmacogenetics
, vol.8
, pp. 357-360
-
-
Ando, Y.1
Chida, M.2
Nakayama, K.3
-
6
-
-
0034671387
-
Polymorphisms of UDP-glucuronosyltransferase gene and irinotecan toxicity: A pharmacogenetic analysis
-
Ando Y, Saka H, Ando M et al. Polymorphisms of UDP- glucuronosyltransferase gene and irinotecan toxicity: a pharmacogenetic analysis. Cancer Res. 60, 6921-6926 (2000). • First retrospective case-control study that demonstrated an important role of UGT1A1*28 allele associated with the development of toxicity after irinotecan chemotherapy.
-
(2000)
Cancer Res.
, vol.60
, pp. 6921-6926
-
-
Ando, Y.1
Saka, H.2
Ando, M.3
-
7
-
-
0036148810
-
Polymorphisms of UDP-glucuronosyltransferase and pharmacokinetics of irinotecan
-
Ando Y, Ueoka H, Sugiyama T et al. Polymorphisms of UDP- glucuronosyltransferase and pharmacokinetics of irinotecan. Ther. Drug Monit. 24, 111-116 (2002).
-
(2002)
Ther. Drug Monit.
, vol.24
, pp. 111-116
-
-
Ando, Y.1
Ueoka, H.2
Sugiyama, T.3
-
8
-
-
12244271026
-
Haplotype structure of the UDP-glucuronosyltransferase 1A1 promoter in different ethnic groups
-
Innocenti F, Grimsley C, Das S et al. Haplotype structure of the UDP-glucuronosyltransferase 1A1 promoter in different ethnic groups. Pharmacogenetics 12, 725-733 (2002).
-
(2002)
Pharmacogenetics
, vol.12
, pp. 725-733
-
-
Innocenti, F.1
Grimsley, C.2
Das, S.3
-
9
-
-
0036025450
-
UGT1A1*28 polymorphism as a determinant of irinotecan disposition and toxicity
-
Iyer L, Das S, Janisch L et al. UGT1A1*28 polymorphism as a determinant of irinotecan disposition and toxicity. Pharmacogenomics J. 2, 43-47 (2002). • First prospective pharmacogenetic investigation of the influence of the UGT1A1*28 polymorphism on the disposition and toxicity of irinotecan.
-
(2002)
Pharmacogenomics J.
, vol.2
, pp. 43-47
-
-
Iyer, L.1
Das, S.2
Janisch, L.3
-
10
-
-
2342459714
-
Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecan
-
Innocenti F, Undevia SD, Iyer L et al. Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecan. J. Clin. Oncol. 22, 1382-1388 (2004). • Prospective study that evaluated the association between the prevalence of severe toxicity and UGT1A1 polymorphism.
-
(2004)
J. Clin. Oncol.
, vol.22
, pp. 1382-1388
-
-
Innocenti, F.1
Undevia, S.D.2
Iyer, L.3
-
11
-
-
4344632633
-
UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer
-
Marcuello E, Altes A, Menoyo A et al. UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer. Br. J. Cancer 91, 678-682 (2004).
-
(2004)
Br. J. Cancer
, vol.91
, pp. 678-682
-
-
Marcuello, E.1
Altes, A.2
Menoyo, A.3
-
12
-
-
3242769758
-
Influence of genetic variants in UGT1A1 and UGT1A9 on the in vivo glucuronidation of SN-38
-
Paoluzzi L, Singh AS, Price DK et al. Influence of genetic variants in UGT1A1 and UGT1A9 on the in vivo glucuronidation of SN-38. J. Clin. Pharmacol. 44, 854-860 (2004).
-
(2004)
J. Clin. Pharmacol.
, vol.44
, pp. 854-860
-
-
Paoluzzi, L.1
Singh, A.S.2
Price, D.K.3
-
13
-
-
21944434407
-
Genetic polymorphism in the phenobarbital-responsive enhancer module of the UDP-glucuronosyltransferase 1A1 gene and irinotecan toxicity
-
Kitagawa C, Ando M, Ando Y et al. Genetic polymorphism in the phenobarbital-responsive enhancer module of the UDP-glucuronosyltransferase 1A1 gene and irinotecan toxicity. Pharmacogenet. Genomics 15, 35-41 (2005).
-
(2005)
Pharmacogenet. Genomics
, vol.15
, pp. 35-41
-
-
Kitagawa, C.1
Ando, M.2
Ando, Y.3
-
14
-
-
26444594410
-
Clinical pharmacogenetics of irinotecan (CPT-11)
-
Ando Y, Hasegawa Y. Clinical pharmacogenetics of irinotecan (CPT-11). Drug Metab. Rev. 37, 565-574 (2005).
-
(2005)
Drug Metab. Rev.
, vol.37
, pp. 565-574
-
-
Ando, Y.1
Hasegawa, Y.2
-
15
-
-
0037050354
-
Irinotecan plus cisplatin compared with etoposide plus cisplatin for extensive small-cell lung cancer
-
Noda K, Nishiwaki Y, Kawahara M et al. Irinotecan plus cisplatin compared with etoposide plus cisplatin for extensive small-cell lung cancer. N. Engl. J. Med. 346, 85-91 (2002).
-
(2002)
N. Engl. J. Med.
, vol.346
, pp. 85-91
-
-
Noda, K.1
Nishiwaki, Y.2
Kawahara, M.3
-
16
-
-
0034727063
-
Irinotecan plus fluorouracil and leucovorin for metastatic colorectal cancer
-
Irinotecan Study Group
-
Saltz LB, Cox JV, Blanke C et al. Irinotecan plus fluorouracil and leucovorin for metastatic colorectal cancer. Irinotecan Study Group. N. Engl. J. Med. 343, 905-914 (2000).
-
(2000)
N. Engl. J. Med.
, vol.343
, pp. 905-914
-
-
Saltz, L.B.1
Cox, J.V.2
Blanke, C.3
-
17
-
-
26444610679
-
Post-marketing surveillance (PMS) of all patients treated with irinotecan in Japan: Clinical experience and ADR profile of 13,935 patients
-
Abstract 1033
-
Tadokoro J, Hasegawa H, Hayakawa K et al. Post-marketing surveillance (PMS) of all patients treated with irinotecan in Japan: clinical experience and ADR profile of 13,935 patients. Proc. Am. Soc. Clin. Oncol. 21(Suppl.), 259a (2002) (Abstract 1033).
-
(2002)
Proc. Am. Soc. Clin. Oncol.
, vol.21
, Issue.SUPPL.
-
-
Tadokoro, J.1
Hasegawa, H.2
Hayakawa, K.3
-
18
-
-
0032519431
-
Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes
-
Iyer L, King CD, Whitington PF et al. Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes. J. Clin. Invest. 101, 847-854 (1998).
-
(1998)
J. Clin. Invest.
, vol.101
, pp. 847-854
-
-
Iyer, L.1
King, C.D.2
Whitington, P.F.3
-
19
-
-
0032934383
-
Phenotype-genotype correlation of in vitro SN-38 (active metabolite of irinotecan) and bilirubin glucuronidation in human liver tissue with UGT1A1 promoter polymorphism
-
Iyer L, Hall D, Das S et al. Phenotype-genotype correlation of in vitro SN-38 (active metabolite of irinotecan) and bilirubin glucuronidation in human liver tissue with UGT1A1 promoter polymorphism. Clin. Pharmacol. Ther. 65, 576-582 (1999).
-
(1999)
Clin. Pharmacol. Ther.
, vol.65
, pp. 576-582
-
-
Iyer, L.1
Hall, D.2
Das, S.3
-
20
-
-
0027991904
-
Investigation of the substrate specificity of a cloned expressed human bilirubin UDP-glucuronosyltransferase: UDP-sugar specificity and involvement in steroid and xenobiotic glucuronidation
-
Senafi SB, Clarke DJ, Burchell B. Investigation of the substrate specificity of a cloned expressed human bilirubin UDP-glucuronosyltransferase: UDP-sugar specificity and involvement in steroid and xenobiotic glucuronidation. Biochem. J. 303(Pt 1), 233-240 (1994).
-
(1994)
Biochem. J.
, vol.303
, Issue.1 PART
, pp. 233-240
-
-
Senafi, S.B.1
Clarke, D.J.2
Burchell, B.3
-
21
-
-
0026701911
-
A novel complex locus UGT1 encodes human bilirubin, phenol, and other UDP-glucuronosyltransferase isozymes with identical carboxyl termini
-
Ritter JK, Chen F, Sheen YY et al. A novel complex locus UGT1 encodes human bilirubin, phenol, and other UDP-glucuronosyltransferase isozymes with identical carboxyl termini. J. Biol. Chem. 267, 3257-3261 (1992).
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 3257-3261
-
-
Ritter, J.K.1
Chen, F.2
Sheen, Y.Y.3
-
22
-
-
8544224973
-
The UDP glycosyltransferase gene superfamily: Recommended nomenclature update based on evolutionary divergence
-
Mackenzie PI, Owens IS, Burchell B et al. The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergence. Pharmacogenetics 7, 255-269 (1997).
-
(1997)
Pharmacogenetics
, vol.7
, pp. 255-269
-
-
Mackenzie, P.I.1
Owens, I.S.2
Burchell, B.3
-
23
-
-
0030030762
-
Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome
-
Monaghan G, Ryan M, Seddon R et al. Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome. Lancet 347, 578-581 (1996).
-
(1996)
Lancet
, vol.347
, pp. 578-581
-
-
Monaghan, G.1
Ryan, M.2
Seddon, R.3
-
24
-
-
0031616354
-
Analysis of bilirubin uridine 5′-diphosphate (UDP)- glucuronosyltransferase gene mutations in seven patients with Crigler-Najjar syndrome Type II
-
Yamamoto K, Soeda Y, Kamisako T et al. Analysis of bilirubin uridine 5′-diphosphate (UDP)-glucuronosyltransferase gene mutations in seven patients with Crigler-Najjar syndrome Type II. J. Hum. Genet. 43, 111-114 (1998).
-
(1998)
J. Hum. Genet.
, vol.43
, pp. 111-114
-
-
Yamamoto, K.1
Soeda, Y.2
Kamisako, T.3
-
25
-
-
2342558617
-
Irinotecan pharmacogenetics: Is it time to intervene?
-
McLeod HL, Watters JW. Irinotecan pharmacogenetics: is it time to intervene? J. Clin. Oncol. 22, 1356-1359 (2004).
-
(2004)
J. Clin. Oncol.
, vol.22
, pp. 1356-1359
-
-
McLeod, H.L.1
Watters, J.W.2
-
26
-
-
0031719562
-
Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene: A common missense mutation among Japanese, Koreans and Chinese
-
Akaba K, Kimura T, Sasaki A et al. Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese. Biochem. Mol. Biol. Int. 46, 21-26 (1998).
-
(1998)
Biochem. Mol. Biol. Int.
, vol.46
, pp. 21-26
-
-
Akaba, K.1
Kimura, T.2
Sasaki, A.3
-
27
-
-
0032493441
-
Racial variability in the UDPglucuronosyltransferase 1 (UGT1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism?
-
Beutler E, Gelbart T, Demina A. Racial variability in the UDPglucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism? Proc. Natl Acad. Sci. USA 95, 8170-8174 (1998).
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 8170-8174
-
-
Beutler, E.1
Gelbart, T.2
Demina, A.3
-
28
-
-
2942527225
-
UGT1A1 haplotypes associated with reduced glucuronidation and increased serum bilirubin in irinotecan-administered Japanese patients with cancer
-
Sai K, Saeki M, Saito Y et al. UGT1A1 haplotypes associated with reduced glucuronidation and increased serum bilirubin in irinotecan-administered Japanese patients with cancer. Clin. Pharmacol. Ther. 75, 501-515 (2004).
-
(2004)
Clin. Pharmacol. Ther.
, vol.75
, pp. 501-515
-
-
Sai, K.1
Saeki, M.2
Saito, Y.3
-
29
-
-
6544244602
-
Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese
-
Akaba K, Kimura T, Sasaki A et al. Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese. J. Hum. Genet. 44, 22-25 (1999).
-
(1999)
J. Hum. Genet.
, vol.44
, pp. 22-25
-
-
Akaba, K.1
Kimura, T.2
Sasaki, A.3
-
30
-
-
0033001454
-
Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism
-
Maruo Y, Nishizawa K, Sato H et al. Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism. Pediatrics 103, 1224-1227 (1999).
-
(1999)
Pediatrics
, vol.103
, pp. 1224-1227
-
-
Maruo, Y.1
Nishizawa, K.2
Sato, H.3
-
31
-
-
0031864410
-
Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome Type II
-
Yamamoto K, Sato H, Fujiyama Y et al. Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome Type II. Biochim. Biophys. Acta 1406, 267-273 (1998).
-
(1998)
Biochim. Biophys. Acta
, vol.1406
, pp. 267-273
-
-
Yamamoto, K.1
Sato, H.2
Fujiyama, Y.3
-
32
-
-
0030053274
-
The genetic basis of Gilbert's syndrome
-
Sato H, Adachi Y, Koiwai O. The genetic basis of Gilbert's syndrome. Lancet 347, 557-558 (1996).
-
(1996)
Lancet
, vol.347
, pp. 557-558
-
-
Sato, H.1
Adachi, Y.2
Koiwai, O.3
-
33
-
-
33744804311
-
Comprehensive analysis of UGT1A polymorphisms predictive for pharmacokinetics and treatment outcome in patients with non-small-cell lung cancer treated with irinotecan and cisplatin
-
Han JY, Lim HS, Shin ES et al. Comprehensive analysis of UGT1A polymorphisms predictive for pharmacokinetics and treatment outcome in patients with non-small-cell lung cancer treated with irinotecan and cisplatin. J. Clin. Oncol. 24, 2237-2244 (2006).
-
(2006)
J. Clin. Oncol.
, vol.24
, pp. 2237-2244
-
-
Han, J.Y.1
Lim, H.S.2
Shin, E.S.3
-
34
-
-
3242743744
-
Rapid detection of UGT1A1 gene polymorphisms by newly developed Invader assay
-
Hasegawa Y, Sarashina T, Ando M et al. Rapid detection of UGT1A1 gene polymorphisms by newly developed Invader assay. Clin. Chem. 50, 1479-1480 (2004). • First report on the development of the Invader® UGT1A1 Molecular Assay, and the evaluation with clinical samples.
-
(2004)
Clin. Chem.
, vol.50
, pp. 1479-1480
-
-
Hasegawa, Y.1
Sarashina, T.2
Ando, M.3
-
35
-
-
0032998425
-
Polymorphism identification and quantitative detection of genomic DNA by invasive cleavage of oligonucleotide probes
-
Lyamichev V, Mast AL, Hall JG et al. Polymorphism identification and quantitative detection of genomic DNA by invasive cleavage of oligonucleotide probes. Nat. Biotechnol. 17, 292-296 (1999).
-
(1999)
Nat. Biotechnol.
, vol.17
, pp. 292-296
-
-
Lyamichev, V.1
Mast, A.L.2
Hall, J.G.3
-
36
-
-
0028043309
-
Real time kinetics of restriction endonuclease cleavage monitored by fluorescence resonance energy transfer
-
Ghosh SS, Eis PS, Blumeyer K et al. Real time kinetics of restriction endonuclease cleavage monitored by fluorescence resonance energy transfer. Nucleic Acids Res. 22, 3155-3159 (1994).
-
(1994)
Nucleic Acids Res.
, vol.22
, pp. 3155-3159
-
-
Ghosh, S.S.1
Eis, P.S.2
Blumeyer, K.3
-
37
-
-
2342514163
-
Detection of genomic polymorphisms associated with venous thrombosis using the invader biplex assay
-
Patnaik M, Dlott JS, Fontaine RN et al. Detection of genomic polymorphisms associated with venous thrombosis using the invader biplex assay. J. Mol. Diagn. 6, 137-144 (2004).
-
(2004)
J. Mol. Diagn.
, vol.6
, pp. 137-144
-
-
Patnaik, M.1
Dlott, J.S.2
Fontaine, R.N.3
-
38
-
-
0036597896
-
Characterization of cytochrome P450 2D6 alleles using the Invader System
-
Neville M, Selzer R, Aisenstein B et al. Characterization of cytochrome P450 2D6 alleles using the Invader System. Biotechniques 32, S34-S43 (2002).
-
(2002)
Biotechniques
, vol.32
-
-
Neville, M.1
Selzer, R.2
Aisenstein, B.3
-
39
-
-
26444611844
-
Genetic polymorphisms of the multidrug resistance-associated protein 2 gene (ABCC2) and irinotecan toxicity
-
Abstract 2009
-
Kitagawa C, Ando M, Ando Y et al. Genetic polymorphisms of the multidrug resistance-associated protein 2 gene (ABCC2) and irinotecan toxicity. Proc. Am. Soc. Clin. Oncol. 22(Suppl.), 129 (2004) (Abstract 2009).
-
(2004)
Proc. Am. Soc. Clin. Oncol.
, vol.22
, Issue.SUPPL.
, pp. 129
-
-
Kitagawa, C.1
Ando, M.2
Ando, Y.3
-
40
-
-
6344282495
-
Pharmacogenetic analysis of interindividual irinotecan (CPT-11) pharmacokinetic (PK) variability: Evidence for a functional variant of ABCC2
-
Abstract 2010
-
Innocenti F, Undevia SD, Chen PX et al. Pharmacogenetic analysis of interindividual irinotecan (CPT-11) pharmacokinetic (PK) variability: evidence for a functional variant of ABCC2. Proc. Am. Soc. Clin. Oncol. 22(Suppl.), 129 (2004) (Abstract 2010).
-
(2004)
Proc. Am. Soc. Clin. Oncol.
, vol.22
, Issue.SUPPL.
, pp. 129
-
-
Innocenti, F.1
Undevia, S.D.2
Chen, P.X.3
-
41
-
-
33746814672
-
-
Human UGT Allele Tables http://som.flinders.edu.au/FUSA/ClinPharm/UGT/ allele_table.html
-
Human UGT Allele Tables
-
-
|