-
1
-
-
0035029986
-
CTLA-4 and not CD28 is a susceptibility gene for thyroid autoantibody production
-
Tomer Y, Greenberg DA, Barbesino G, Concepcion E, Davies TF. CTLA-4 and not CD28 is a susceptibility gene for thyroid autoantibody production. J Clin Endocrinol Metab 2001: 86: 1687-93.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 1687-1693
-
-
Tomer, Y.1
Greenberg, D.A.2
Barbesino, G.3
Concepcion, E.4
Davies, T.F.5
-
2
-
-
0030598879
-
An Mse I RFLP in the human CTLA4 promotor
-
Deichmann K, Heinzmann A, Bruggenolte E, Forster J, Kuehr J. An Mse I RFLP in the human CTLA4 promotor. Biochem Biophys Res Commun 1996: 225: 817-8.
-
(1996)
Biochem Biophys Res Commun
, vol.225
, pp. 817-818
-
-
Deichmann, K.1
Heinzmann, A.2
Bruggenolte, E.3
Forster, J.4
Kuehr, J.5
-
3
-
-
0034935542
-
Association of CTLA-4 but not CD28 gene polymorphisms with systemic lupus erythematosus in the Japanese population
-
Ahmed S, Ihara K, Kanemitsu S et al. Association of CTLA-4 but not CD28 gene polymorphisms with systemic lupus erythematosus in the Japanese population. Rheumatology 2001: 40: 662-7.
-
(2001)
Rheumatology
, vol.40
, pp. 662-667
-
-
Ahmed, S.1
Ihara, K.2
Kanemitsu, S.3
-
4
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koeleman BP, Koster T. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994: 369: 64-7.
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.2
Koster, T.3
-
5
-
-
0035881368
-
Heterozygosity for the factor V Leiden (G1691A) mutation predisposes renal transplant recipients to thrombotic complications and graft loss
-
Wuthrich RP, Cicvara-Muzar S, Booy C, Maly FE. Heterozygosity for the factor V Leiden (G1691A) mutation predisposes renal transplant recipients to thrombotic complications and graft loss. Transplantation 2001: 72: 549-50.
-
(2001)
Transplantation
, vol.72
, pp. 549-550
-
-
Wuthrich, R.P.1
Cicvara-Muzar, S.2
Booy, C.3
Maly, F.E.4
-
6
-
-
0029850530
-
A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
-
Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996: 88: 3698-703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
8
-
-
27944442250
-
-
http://cts.med.uni-heidelberg.de/public/reagents.html.
-
-
-
-
9
-
-
27944500923
-
Computer simulation of stochastic processes through model-sampling (Monte Carlo) techniques
-
Sheppard CW. Computer simulation of stochastic processes through model-sampling (Monte Carlo) techniques. FEBS Lett 1969: 2 (Suppl. 1): 14-21.
-
(1969)
FEBS Lett
, vol.2
, Issue.SUPPL. 1
, pp. 14-21
-
-
Sheppard, C.W.1
-
10
-
-
0033006003
-
Allelic discrimination using fluorogenic probes and the 5′nuclease assay
-
Livak KJ. Allelic discrimination using fluorogenic probes and the 5′nuclease assay. Genet Anal 1999: 14: 143-9.
-
(1999)
Genet Anal
, vol.14
, pp. 143-149
-
-
Livak, K.J.1
-
11
-
-
4143075080
-
A novel MALDITOF based methodology for genotyping single nucleotide polymorphisms
-
Blondal T, Waage BG, Smarason SV et al. A novel MALDITOF based methodology for genotyping single nucleotide polymorphisms. Nucleic Acids Res 2003: 31: 155.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 155
-
-
Blondal, T.1
Waage, B.G.2
Smarason, S.V.3
-
12
-
-
1642525984
-
High-throughput single nucleotide polymorphism typing by fluorescent single-strand conformation polymorphism analysis with capillary electrophoresis
-
Doi K, Doi H, Noiri E, Nakao A, Fujita T, Tokunaga K. High-throughput single nucleotide polymorphism typing by fluorescent single-strand conformation polymorphism analysis with capillary electrophoresis. Electrophoresis 2004: 25: 833-8.
-
(2004)
Electrophoresis
, vol.25
, pp. 833-838
-
-
Doi, K.1
Doi, H.2
Noiri, E.3
Nakao, A.4
Fujita, T.5
Tokunaga, K.6
-
13
-
-
0032933161
-
Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylenetetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR
-
Hessner MJ, Luhm RA, Pearson SL, Endean DJ, Friedmann KD, Montgomery RR. Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylenetetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR. Thromb Haemost 1999: 81: 733-8.
-
(1999)
Thromb Haemost
, vol.81
, pp. 733-738
-
-
Hessner, M.J.1
Luhm, R.A.2
Pearson, S.L.3
Endean, D.J.4
Friedmann, K.D.5
Montgomery, R.R.6
-
14
-
-
0033869814
-
Genotyping of factor V G1691A (Leiden) without the use of PCR by invasive cleavage of oligonucleotide probes
-
Hessner MJ, Budish MA, Friedmann KD. Genotyping of factor V G1691A (Leiden) without the use of PCR by invasive cleavage of oligonucleotide probes. Clin Chem 2000: 46: 1051-6.
-
(2000)
Clin Chem
, vol.46
, pp. 1051-1056
-
-
Hessner, M.J.1
Budish, M.A.2
Friedmann, K.D.3
-
15
-
-
0031955592
-
Factor V Leiden (G1691A), the prothrombin 3′-untranslated region variant (G20210A) and thermolabile methylenetetrahydrofolate reductase (C677T): A single genetic test genotypes all three loci - Determination of frequencies in the S. Wales population of the UK
-
Bowen DJ, Bowley S, John M, Collins PW. Factor V Leiden (G1691A), the prothrombin 3′-untranslated region variant (G20210A) and thermolabile methylenetetrahydrofolate reductase (C677T): a single genetic test genotypes all three loci - determination of frequencies in the S. Wales population of the UK. Thromb Haemost 1998: 79: 949-54.
-
(1998)
Thromb Haemost
, vol.79
, pp. 949-954
-
-
Bowen, D.J.1
Bowley, S.2
John, M.3
Collins, P.W.4
-
16
-
-
0034827541
-
Age-dependent prevalence of vascular disease-associated polymorphisms among 2689 volunteer blood donors
-
Hessner MJ, Dinauer DM, Kwiatkowski R, Neri B, Raife TJ. Age-dependent prevalence of vascular disease-associated polymorphisms among 2689 volunteer blood donors. Clin Chem 2001: 47: 1879-84.
-
(2001)
Clin Chem
, vol.47
, pp. 1879-1884
-
-
Hessner, M.J.1
Dinauer, D.M.2
Kwiatkowski, R.3
Neri, B.4
Raife, T.J.5
-
17
-
-
0028810738
-
World distribution of factor V Leiden
-
Rees DC, Cox M, Clegg JB. World distribution of factor V Leiden. Lancet 1995: 346: 1133-4.
-
(1995)
Lancet
, vol.346
, pp. 1133-1134
-
-
Rees, D.C.1
Cox, M.2
Clegg, J.B.3
-
18
-
-
0033824437
-
Prothrombin activation is increased among asymptomatic carriers of the prothrombin G20210A and factor V Arg506Gln mutations
-
Bauer KA, Humphries S, Smillie B. Prothrombin activation is increased among asymptomatic carriers of the prothrombin G20210A and factor V Arg506Gln mutations. Thromb Haemost 2000: 84: 396-400.
-
(2000)
Thromb Haemost
, vol.84
, pp. 396-400
-
-
Bauer, K.A.1
Humphries, S.2
Smillie, B.3
-
19
-
-
0005601318
-
Effect of MTHFR 677C/T on plasma total homocysteine levels in renal graft recipients
-
Fodinger M, Wolfl G, Fischer G. Effect of MTHFR 677C/T on plasma total homocysteine levels in renal graft recipients. Kidney Int 1999: 55: 1072-80.
-
(1999)
Kidney Int
, vol.55
, pp. 1072-1080
-
-
Fodinger, M.1
Wolfl, G.2
Fischer, G.3
-
20
-
-
0037990070
-
The impact of costimulatory molecule gene polymorphisms on clinical outcomes in liver transplantation
-
Marder BA, Schröppel B, Lin M et al. The impact of costimulatory molecule gene polymorphisms on clinical outcomes in liver transplantation. Am J Transplant 2003: 3: 424-31.
-
(2003)
Am J Transplant
, vol.3
, pp. 424-431
-
-
Marder, B.A.1
Schröppel, B.2
Lin, M.3
-
21
-
-
3042811442
-
Prevalence of resistance against activated protein C resulting from factor V Leiden is significantly increased in myocardial infarction: Investigation of 507 patients with myocardial infarction
-
Middendorf K, Gohring P, Huehns TY, Seidel D, Steinbeck G, Nikol S. Prevalence of resistance against activated protein C resulting from factor V Leiden is significantly increased in myocardial infarction: investigation of 507 patients with myocardial infarction. Am Heart J 2004: 147: 897-904.
-
(2004)
Am Heart J
, vol.147
, pp. 897-904
-
-
Middendorf, K.1
Gohring, P.2
Huehns, T.Y.3
Seidel, D.4
Steinbeck, G.5
Nikol, S.6
-
22
-
-
0141538396
-
Analyzes of three common thrombophilic gene mutations in German women with recurrent abortions
-
Pauer HU, Voigt-Tschirschwitz T, Hinney B et al. Analyzes of three common thrombophilic gene mutations in German women with recurrent abortions. Acta Obstet Gynecol Scand 2003: 82: 942-7.
-
(2003)
Acta Obstet Gynecol Scand
, vol.82
, pp. 942-947
-
-
Pauer, H.U.1
Voigt-Tschirschwitz, T.2
Hinney, B.3
-
23
-
-
0034977211
-
Factors explaining the difference of total homocysteine between men and women in the European Investigation into Cancer and Nutrition Potsdam study
-
Dierkes J, Jeckel A, Ambrosch A, Westphal S, Luley C, Boeing H. Factors explaining the difference of total homocysteine between men and women in the European Investigation Into Cancer and Nutrition Potsdam study. Metabolism 2001: 50: 640-5.
-
(2001)
Metabolism
, vol.50
, pp. 640-645
-
-
Dierkes, J.1
Jeckel, A.2
Ambrosch, A.3
Westphal, S.4
Luley, C.5
Boeing, H.6
-
24
-
-
0035098317
-
The codon 17 polymorphism of the CTLA4 gene in type 2 diabetes mellitus
-
Rau H, Braun J, Donner H et al. The codon 17 polymorphism of the CTLA4 gene in type 2 diabetes mellitus. J Clin Endocrinol Metab 2001: 86: 653-5.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 653-655
-
-
Rau, H.1
Braun, J.2
Donner, H.3
-
25
-
-
0035013326
-
Factor V Leiden mutation: Potential thrombogenic role in renal vein, dialysis graft and transplant vascular thrombosis
-
Wuthrich RP. Factor V Leiden mutation: potential thrombogenic role in renal vein, dialysis graft and transplant vascular thrombosis. Curr Opin Nephrol Hypertens 2001: 10: 409-14.
-
(2001)
Curr Opin Nephrol Hypertens
, vol.10
, pp. 409-414
-
-
Wuthrich, R.P.1
-
26
-
-
0032858734
-
Heterozygous prothrombin gene mutation: A new risk factor for early renal allograft thrombosis
-
Oh J, Schaefer F, Veldmann A et al. Heterozygous prothrombin gene mutation: a new risk factor for early renal allograft thrombosis. Transplantation 1999: 68: 575-8.
-
(1999)
Transplantation
, vol.68
, pp. 575-578
-
-
Oh, J.1
Schaefer, F.2
Veldmann, A.3
-
27
-
-
0345486986
-
Early loss of renal transplants in patients with thrombophilia
-
Fischereder M, Gohring P, Schneeberger H et al. Early loss of renal transplants in patients with thrombophilia. Transplantation 1998: 65: 936-9.
-
(1998)
Transplantation
, vol.65
, pp. 936-939
-
-
Fischereder, M.1
Gohring, P.2
Schneeberger, H.3
-
28
-
-
0030734382
-
Codon 17 polymorphism of the cytotoxic T lymphocyte antigen 4 gene in Hashimoto's thyroiditis and Addison's disease
-
Donner H, Braun J, Seidl C et al. Codon 17 polymorphism of the cytotoxic T lymphocyte antigen 4 gene in Hashimoto's thyroiditis and Addison's disease. J Clin Endocrinol Metab 1997: 82: 4130-2.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 4130-4132
-
-
Donner, H.1
Braun, J.2
Seidl, C.3
-
29
-
-
0031014716
-
CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus
-
Donner H, Rau H, Walfish PG et al. CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus. J Clin Endocrinol Metab 1997: 82: 143-6.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 143-146
-
-
Donner, H.1
Rau, H.2
Walfish, P.G.3
-
30
-
-
0032964170
-
The CTLA-4 gene is associated with multiple sclerosis
-
Ligers A, Xu C, Saarinen S, Hillert J, Olerup O. The CTLA-4 gene is associated with multiple sclerosis. J Neuroimmunol 1999: 97: 182-90.
-
(1999)
J Neuroimmunol
, vol.97
, pp. 182-190
-
-
Ligers, A.1
Xu, C.2
Saarinen, S.3
Hillert, J.4
Olerup, O.5
-
31
-
-
0031963283
-
CTLA4 codon 17 dimorphism in patients with rheumatoid arthritis
-
Seidl C, Donner H, Fischer B et al. CTLA4 codon 17 dimorphism in patients with rheumatoid arthritis. Tissue Antigens 1998: 51: 62-6.
-
(1998)
Tissue Antigens
, vol.51
, pp. 62-66
-
-
Seidl, C.1
Donner, H.2
Fischer, B.3
-
32
-
-
0010690218
-
Polymorphism in the promoter and exon 1 of the cytotoxic T lymphocyte antigen-4 gene associated with autoimmune thyroid disease in Koreans
-
Park YJ, Chung HK, Park DJ et al. Polymorphism in the promoter and exon 1 of the cytotoxic T lymphocyte antigen-4 gene associated with autoimmune thyroid disease in Koreans. Thyroid 2000: 10: 453-9.
-
(2000)
Thyroid
, vol.10
, pp. 453-459
-
-
Park, Y.J.1
Chung, H.K.2
Park, D.J.3
-
33
-
-
0346121389
-
Recipient ctla-4 +49 G/G genotype is associated with reduced incidence of acute rejection after liver transplantation
-
De Reuver P, Pravica V, Hop W. Recipient ctla-4 +49 G/G genotype is associated with reduced incidence of acute rejection after liver transplantation. Am J Transplant 2003: 3: 1587-94.
-
(2003)
Am J Transplant
, vol.3
, pp. 1587-1594
-
-
De Reuver, P.1
Pravica, V.2
Hop, W.3
-
34
-
-
0035451084
-
Linkage disequilibrium and disease-associated CTLA4 gene polymorphisms
-
Holopainen PM, Partanen JA. Linkage disequilibrium and disease-associated CTLA4 gene polymorphisms. J Immunol 2001: 167: 2457-8.
-
(2001)
J Immunol
, vol.167
, pp. 2457-2458
-
-
Holopainen, P.M.1
Partanen, J.A.2
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