-
1
-
-
0020080870
-
The highly polymorphic region near the human insulin gene is composed of simple tandemly repeated sequences
-
Bell GI, Selby M, Rutter WJ. The highly polymorphic region near the human insulin gene is composed of simple tandemly repeated sequences. Nature 1982; 295:31-35.
-
(1982)
Nature
, vol.295
, pp. 31-35
-
-
Bell, G.I.1
Selby, M.2
Rutter, W.J.3
-
2
-
-
0020683694
-
Complete nucleotide sequence of the T24 human bladder carcinoma oncogene and its normal homologue
-
Capon DJ, Chen EY, Levinson AD, Seeburg PH, Goedderand DV. Complete nucleotide sequence of the T24 human bladder carcinoma oncogene and its normal homologue. Nature 1983; 302:33-37.
-
(1983)
Nature
, vol.302
, pp. 33-37
-
-
Capon, D.J.1
Chen, E.Y.2
Levinson, A.D.3
Seeburg, P.H.4
Goedderand, D.V.5
-
3
-
-
0027518279
-
Current methods of mutation detection
-
Cotton RG. Current methods of mutation detection. Mutat Res 1993; 285:125-144.
-
(1993)
Mutat Res
, vol.285
, pp. 125-144
-
-
Cotton, R.G.1
-
4
-
-
0025808919
-
Estimation of allele frequencies for VNTR loci
-
Devlin B, Risch N, Roeder K. Estimation of allele frequencies for VNTR loci. Am J Hum Genet 1991: 48:662-676.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 662-676
-
-
Devlin, B.1
Risch, N.2
Roeder, K.3
-
5
-
-
0025837127
-
Altered mercaptopurine metabolism, toxic effects, and dosage requirement in a thiopurine methyltransferase-delicient child with acute lymphocytic leukemia
-
Evans WE, Horner M, Chi YQ, Kalwinsky D, Roberts WM. Altered mercaptopurine metabolism, toxic effects, and dosage requirement in a thiopurine methyltransferase-delicient child with acute lymphocytic leukemia. J Pediatr 1991; 119:985-989.
-
(1991)
J Pediatr
, vol.119
, pp. 985-989
-
-
Evans, W.E.1
Horner, M.2
Chi, Y.Q.3
Kalwinsky, D.4
Roberts, W.M.5
-
6
-
-
0021979069
-
Hypervariable minisatellite region in human DNA
-
Jeffreys AJ, Wilson V. Thein SL. Hypervariable minisatellite region in human DNA. Nature 1985; 314:67-73.
-
(1985)
Nature
, vol.314
, pp. 67-73
-
-
Jeffreys, A.J.1
Wilson, V.2
Thein, S.L.3
-
7
-
-
0027214689
-
An association between the risk of cancer and mutations in the HRAS1 minisatellite locus
-
Krontiris TG, Devlin B, Karp DD, Robert NJ, Rish N. An association between the risk of cancer and mutations in the HRAS1 minisatellite locus. N Engl J Med 1993; 329:517-523.
-
(1993)
N Engl J Med
, vol.329
, pp. 517-523
-
-
Krontiris, T.G.1
Devlin, B.2
Karp, D.D.3
Robert, N.J.4
Rish, N.5
-
8
-
-
0029157488
-
Minisatellites and human disease
-
Krontiris TG. Minisatellites and human disease. Science 1995; 269:1682-1683.
-
(1995)
Science
, vol.269
, pp. 1682-1683
-
-
Krontiris, T.G.1
-
9
-
-
0028861745
-
A single point mutation leading to loss of catalytic activity in human thiopurine S-methyltransferase
-
Krynetski EY, Schuetz JD. Galpin AJ. Pui CH, Relling MV, Evans 1WE. A single point mutation leading to loss of catalytic activity in human thiopurine S-methyltransferase. Proc Natl Acad Sci USA 1995; 92:949-953.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 949-953
-
-
Krynetski, E.Y.1
Schuetz, J.D.2
Galpin, A.J.3
Pui, C.H.4
Relling, M.V.5
Evans, W.E.6
-
10
-
-
0029736709
-
Genetic polymorphism of thiopurine S-methyltransferase: Clinical importance and molecular mechanisms
-
Krynetski EY, Tai HL, Yates CR, Fessing MY, Loennechen T, Schuetz JD, Relling MV, Evans WE. Genetic polymorphism of thiopurine S-methyltransferase: clinical importance and molecular mechanisms. Pharmacogenetics 1996; 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
Relling, M.V.7
Evans, W.E.8
-
11
-
-
0031423467
-
Promoter and intronic sequences of the human thiopurine S-methyltransferase (TPMT) gene isolated from the human PACI genomic library
-
Krynetski EY, Fessing MY, Yates CR, Sun D, Schuetz JD, Evans WE. Promoter and intronic sequences of the human thiopurine S-methyltransferase (TPMT) gene isolated from the human PACI genomic library. Pharm Res 1997; 14:1672-1678.
-
(1997)
Pharm Res
, vol.14
, pp. 1672-1678
-
-
Krynetski, E.Y.1
Fessing, M.Y.2
Yates, C.R.3
Sun, D.4
Schuetz, J.D.5
Evans, W.E.6
-
12
-
-
0028913757
-
Thiopurine methyltransferase pharmacogenetics. Cloning of human liver cDNA and a processed pseudogene on human chromosome 18q21.1
-
Lee D, Szumlanski C, Houtman J, Honchel R, Rojas K, Overhauser J, et al. Thiopurine methyltransferase pharmacogenetics. Cloning of human liver cDNA and a processed pseudogene on human chromosome 18q21.1. Drug Metab Dispos 1995; 23:398-405.
-
(1995)
Drug Metab Dispos
, vol.23
, pp. 398-405
-
-
Lee, D.1
Szumlanski, C.2
Houtman, J.3
Honchel, R.4
Rojas, K.5
Overhauser, J.6
-
13
-
-
0023119219
-
Thiopurine pharmacogenetics in leukemia: Correlation of erythrocyte thiopurine methyltransferase activity and 6-thioguanine nucleotide concentrations
-
Lennard L, Van Loon JA, Lilleyman JS, Weinshilboum RM, Thiopurine pharmacogenetics in leukemia: correlation of erythrocyte thiopurine methyltransferase activity and 6-thioguanine nucleotide concentrations. Clin Pharmacol Ther 1987; 41:18-25.
-
(1987)
Clin Pharmacol Ther
, vol.41
, pp. 18-25
-
-
Lennard, L.1
Van Loon, J.A.2
Lilleyman, J.S.3
Weinshilboum, R.M.4
-
14
-
-
0024451147
-
Pharmacogenetics of acute azathioprine toxicity: Relationship to thiopurine methyltransferase genetic polymorphism
-
Lennard L, Van Loon JA. Weinshilboum RM. Pharmacogenetics acute azathioprine toxicity: relationship to thiopurine methyltransferase genetic polymorphism. Clin Pharmacol Ther 1989; 46:149-154.
-
(1989)
Clin Pharmacol Ther
, vol.46
, pp. 149-154
-
-
Lennard, L.1
Van Loon, J.A.2
Weinshilboum, R.M.3
-
15
-
-
0025331198
-
Genetic variation in response to 6-mercaptopurine for childhood acute lymphoblastic leukaemia
-
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.
-
(1990)
Lancet
, vol.336
, pp. 225-229
-
-
Lennard, L.1
Lilleyman, J.S.2
Van Loon, J.3
Weinshilboum, R.M.4
-
16
-
-
0027524983
-
Congenital thiopurine methyltransferase deficiency and 6-mercaptopurine toxicity during treatment for acute lymphoblastic leukaemia
-
Lennard L, Gibson BE, Nicole T, Lilleyman JS. Congenital thiopurine methyltransferase deficiency and 6-mercaptopurine toxicity during treatment for acute lymphoblastic leukaemia. Arch Dis Child 1993; 69:577-579.
-
(1993)
Arch Dis Child
, vol.69
, pp. 577-579
-
-
Lennard, L.1
Gibson, B.E.2
Nicole, T.3
Lilleyman, J.S.4
-
17
-
-
0002496513
-
Commonly used techniques in molecular cloning
-
Ford N., Nolan C., Ferguson M., Oekler M., editors. New York: Cold Spring Harbor
-
Maniatis T, Sambrook J, Fritsh EF. Commonly used techniques in molecular cloning. In: Ford N, Nolan C, Ferguson M, Oekler M, editors. Molecular cloning, a laboratory manual. New York: Cold Spring Harbor; 1989. pp. E1-E8.
-
(1989)
Molecular Cloning, A Laboratory Manual
-
-
Maniatis, T.1
Sambrook, J.2
Fritsh, E.F.3
-
18
-
-
0027285234
-
Azathioprine-induced myclosuppression in thiopurine methyltransferase deficient heart transplant recipient
-
McLeod HL, Miller DR, Evans WE. Azathioprine-induced myclosuppression in thiopurine methyltransferase deficient heart transplant recipient. Lancet 1993; 341:1151.
-
(1993)
Lancet
, vol.341
, pp. 1151
-
-
McLeod, H.L.1
Miller, D.R.2
Evans, W.E.3
-
19
-
-
0024595101
-
Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms
-
Orita M, Iwabana H, Kanazawa H, Hayashi K. Sekiya T. Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. Proc Natl Acad Sci USA 1989; 86:2766-2770.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 2766-2770
-
-
Orita, M.1
Iwabana, H.2
Kanazawa, H.3
Hayashi, K.4
Sekiya, T.5
-
20
-
-
0009649472
-
Human thiopurine methyltransferase pharmacogenetics: Identification of a novel variant allele
-
Otterness D, Szumlanski C, Weinshilboum RM. Human thiopurine methyltransferase pharmacogenetics: identification of a novel variant allele (abstract). J Invest Med 1996; 44:248.
-
(1996)
J Invest Med
, vol.44
, pp. 248
-
-
Otterness, D.1
Szumlanski, C.2
Weinshilboum, R.M.3
-
21
-
-
12644291917
-
Human thiopurine methyltransferase pharmacogenetics: Gene sequence polymorphisms
-
Otterness D, Szumlanski C, Lennard L, Klemetsdal B, Aabakke J. Park-Hah JO, et al. Human thiopurine methyltransferase pharmacogenetics: Gene sequence polymorphisms. Clin Pharmacol Ther 1997; 62:60-73.
-
(1997)
Clin Pharmacol Ther
, vol.62
, pp. 60-73
-
-
Otterness, D.1
Szumlanski, C.2
Lennard, L.3
Klemetsdal, B.4
Aabakke, J.5
Park-Hah, J.O.6
-
22
-
-
0025995937
-
Different activation domains of SpI govern formation of multimers and mediate transcriptional synergism
-
Pascal E, Tjian R. Different activation domains of SpI govern formation of multimers and mediate transcriptional synergism. Genes Dev 1991; 5:1646-1656.
-
(1991)
Genes Dev
, vol.5
, pp. 1646-1656
-
-
Pascal, E.1
Tjian, R.2
-
23
-
-
0030823111
-
Mini- and microsatellites
-
Ramel C. Mini- and microsatellites. Environ Health Perspect 1997; 105:781-789.
-
(1997)
Environ Health Perspect
, vol.105
, pp. 781-789
-
-
Ramel, C.1
-
24
-
-
0027401302
-
Azathioprine-induced myelosuppression in thiopurine methyltransferase deficient heart transplant recipient
-
Schütz E, Gummert J. Mohr F, Oellerich M. Azathioprine-induced myelosuppression in thiopurine methyltransferase deficient heart transplant recipient. Lancet 1993; 341:436.
-
(1993)
Lancet
, vol.341
, pp. 436
-
-
Schütz, E.1
Gummert, J.2
Mohr, F.3
Oellerich, M.4
-
25
-
-
0031880735
-
An efficient PCR-SSCP strategy for detection of known and new mutations of the thiopurine S-methyltransferase gene
-
Spire-Vayron de la Moureyre C, Debuysere H, Sabbagh N, Marez D, Vinner E, Alcaïde E, et al. An efficient PCR-SSCP strategy for detection of known and new mutations of the thiopurine S-methyltransferase gene. Hum Mutat 1998; 12:177-185.
-
(1998)
Hum Mutat
, vol.12
, pp. 177-185
-
-
Spire-Vayron de la Moureyre, C.1
Debuysere, H.2
Sabbagh, N.3
Marez, D.4
Vinner, E.5
Alcaïde, E.6
-
26
-
-
0026907122
-
Human liver thiopurine methyltransferase pharmacogenetics: Biochemical properties, liver-erythrocyte correlation and presence of isozymes
-
Szumlanski C, Honchel R, Scott M, Weinshilboum RM. Human liver thiopurine methyltransferase pharmacogenetics: biochemical properties, liver-erythrocyte correlation and presence of isozymes. Pharmacogenetics 1992: 2:148-159.
-
(1992)
Pharmacogenetics
, vol.2
, pp. 148-159
-
-
Szumlanski, C.1
Honchel, R.2
Scott, M.3
Weinshilboum, R.M.4
-
27
-
-
0030048791
-
Thiopurine methyltransferase pharmacogenetics: Human gene cloning and characterization of a common polymorphism
-
Szumlanski C, Otterness D, Her C, Lee D, Brandriff B, Kelsell D, et al. Thiopurine methyltransferase pharmacogenetics: human gene cloning and characterization of a common polymorphism, DNA Cell Biol 1996; 15:17-30.
-
(1996)
DNA Cell Biol
, vol.15
, pp. 17-30
-
-
Szumlanski, C.1
Otterness, D.2
Her, C.3
Lee, D.4
Brandriff, B.5
Kelsell, D.6
-
28
-
-
0029919807
-
Thiopurine S-methyltransferase deficiency: Two nucleotide transitions define the most prevalent mutant allele associated with loss of catalytic activity in Caucasians
-
Tai HL, Krynetski EY, Yates CR, Loennechen T, Fessing MY, Krynetskaia NF, Evans WE. 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 1996; 58:694-702.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 694-702
-
-
Tai, H.L.1
Krynetski, E.Y.2
Yates, C.R.3
Loennechen, T.4
Fessing, M.Y.5
Krynetskaia, N.F.6
Evans, W.E.7
-
29
-
-
0028814076
-
Segregation analysis of human and red blood cell (RBC) thiopurine methyltransferase (TPMT) activity
-
Vuchetich JP, Weinshilboum RM, Price PA. Segregation analysis of human and red blood cell (RBC) thiopurine methyltransferase (TPMT) activity. Genet Epidemiol 1995: 12:1-11.
-
(1995)
Genet Epidemiol
, vol.12
, pp. 1-11
-
-
Vuchetich, J.P.1
Weinshilboum, R.M.2
Price, P.A.3
-
30
-
-
0017880983
-
Human crythrocyte thiopurine methyltransferase: Radiochemical microassay and biochemical properties
-
Weinshilboum R, Raymond F, Pazmino P. Human crythrocyte thiopurine methyltransferase: radiochemical microassay and biochemical properties. Clin Chim Acta 1978; 85:323-333.
-
(1978)
Clin Chim Acta
, vol.85
, pp. 323-333
-
-
Weinshilboum, R.1
Raymond, F.2
Pazmino, P.3
-
31
-
-
0018822866
-
Mercaptopurine pharmacogenetics: Monogenic inheritance of erythrocyte thiopurine methyltransferase activity
-
Weinshilboum RM, Sladek SL. Mercaptopurine pharmacogenetics: monogenic inheritance of erythrocyte thiopurine methyltransferase activity. Am J Hum Genet 1980; 32:651-662.
-
(1980)
Am J Hum Genet
, vol.32
, pp. 651-662
-
-
Weinshilboum, R.M.1
Sladek, S.L.2
-
32
-
-
0019956940
-
Pharmacogenetics of human thiopurine methyltransferase: Kidney-erythrocyte correlation and immunolitration studies
-
Woodson LC, Dunnette J, Weinshilboum RM. Pharmacogenetics of human thiopurine methyltransferase: kidney-erythrocyte correlation and immunolitration studies. J Pharmacol Exp Ther 1982; 222:174-181.
-
(1982)
J Pharmacol Exp Ther
, vol.222
, pp. 174-181
-
-
Woodson, L.C.1
Dunnette, J.2
Weinshilboum, R.M.3
-
33
-
-
0030934850
-
Molecular diagnosis of thiopurine S-methyltransferase deficiency: Genetic basis for azathioprine and mercaptopurine intolerance
-
Yates CR, Krynetski EY, Loennechen T, Fessing MY, Tai HL, Pui CH, et al. Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basis for azathioprine and mercaptopurine intolerance. Ann Intern Med 1997; 126:608-614.
-
(1997)
Ann Intern Med
, vol.126
, pp. 608-614
-
-
Yates, C.R.1
Krynetski, E.Y.2
Loennechen, T.3
Fessing, M.Y.4
Tai, H.L.5
Pui, C.H.6
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