-
1
-
-
0027295745
-
A suggested nomenclature for designated mutations
-
Beaudet AL, Tsui L-C (1993) A suggested nomenclature for designated mutations. Hum Mutat 2:245-248
-
(1993)
Hum Mutat
, vol.2
, pp. 245-248
-
-
Beaudet, A.L.1
Tsui, L.-C.2
-
2
-
-
0018736628
-
Hereditary renal cell carcinoma associated with chromosomal translocation
-
Cohen A, Li F, Berg S, Marchetto D, Tsai S, Jacobs S, Brown R (1979) Hereditary renal cell carcinoma associated with chromosomal translocation. N Engl J Med 301:592-595
-
(1979)
N Engl J Med
, vol.301
, pp. 592-595
-
-
Cohen, A.1
Li, F.2
Berg, S.3
Marchetto, D.4
Tsai, S.5
Jacobs, S.6
Brown, R.7
-
3
-
-
0031047993
-
The von Hippel-Lindau tumor suppressor gene, a rare and intriguing disease opening new insight into basic mechanisms of carcinogenesis
-
Decker HJH, Weidt EJ, Brieger J (1997) The von Hippel-Lindau tumor suppressor gene, a rare and intriguing disease opening new insight into basic mechanisms of carcinogenesis. Cancer Genet Cytogenet 93:74-83
-
(1997)
Cancer Genet Cytogenet
, vol.93
, pp. 74-83
-
-
Decker, H.J.H.1
Weidt, E.J.2
Brieger, J.3
-
4
-
-
0028587585
-
Somatic mutations of the von Hippel-Lindau disease tumor suppressor gene in non-familial clear cell renal carcinoma
-
Foster K, Prowse A, van den Berg A, Fleming S, Hulsbeek MMF, Crossey PA, Richards FM, et al (1994) Somatic mutations of the von Hippel-Lindau disease tumor suppressor gene in non-familial clear cell renal carcinoma. Hum Mol Genet 3:2169-2173
-
(1994)
Hum Mol Genet
, vol.3
, pp. 2169-2173
-
-
Foster, K.1
Prowse, A.2
Van Den Berg, A.3
Fleming, S.4
Hulsbeek, M.M.F.5
Crossey, P.A.6
Richards, F.M.7
-
5
-
-
0020957754
-
Expression of human myeloid-associated surface antigens in human-mouse myeloid cell hybrids
-
Geurts van Kessel A, Tetteroo PAT, Von dem Borne AEGK, Hagemeijer A, Bootsma D (1983) Expression of human myeloid-associated surface antigens in human-mouse myeloid cell hybrids. Proc Natl Acad Sci USA 80:3748-3752
-
(1983)
Proc Natl Acad Sci USA
, vol.80
, pp. 3748-3752
-
-
Geurts Van Kessel, A.1
Tetteroo, P.A.T.2
Von Dem Borne, A.E.G.K.3
Hagemeijer, A.4
Bootsma, D.5
-
6
-
-
0028897420
-
Genetics of renal-cell carcinoma and evidence for a critical role for von Hippel-Lindau in renal tumorigenesis
-
Gnarra JR, Lerman MI, Zbar B, Linehan WM (1995) Genetics of renal-cell carcinoma and evidence for a critical role for von Hippel-Lindau in renal tumorigenesis. Semin Oncol 22: 3-8
-
(1995)
Semin Oncol
, vol.22
, pp. 3-8
-
-
Gnarra, J.R.1
Lerman, M.I.2
Zbar, B.3
Linehan, W.M.4
-
7
-
-
0027954044
-
Mutations of the VHL tumor suppressor gene in renal carcinoma
-
Gnarra JR, Tory K, Weng Y, Schmidt L, Wei MH, Li H, Latif F, et al (1994) Mutations of the VHL tumor suppressor gene in renal carcinoma. Nat Genet 7:85-90
-
(1994)
Nat Genet
, vol.7
, pp. 85-90
-
-
Gnarra, J.R.1
Tory, K.2
Weng, Y.3
Schmidt, L.4
Wei, M.H.5
Li, H.6
Latif, F.7
-
8
-
-
0028072991
-
Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma
-
Herman JG, Latif F, Weng Y, Lerman MI, Zbar B, Liu S, Samid D, et al (1994) Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma. Proc Natl Acad Sci USA 91:9700-9704
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 9700-9704
-
-
Herman, J.G.1
Latif, F.2
Weng, Y.3
Lerman, M.I.4
Zbar, B.5
Liu, S.6
Samid, D.7
-
9
-
-
0027504088
-
Antioncogenes and human cancer
-
Knudson AG (1993) Antioncogenes and human cancer. Proc Natl Acad Sci USA 90:10914-10921
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 10914-10921
-
-
Knudson, A.G.1
-
10
-
-
0000177603
-
VHL gene mutation and clear-cell renal carcinomas
-
_ (1995) VHL gene mutation and clear-cell renal carcinomas. Cancer J Sci Am 1:180-181
-
(1995)
Cancer J Sci Am
, vol.1
, pp. 180-181
-
-
-
11
-
-
0029919109
-
Hereditary cancer: Two hits revisited
-
_ (1996) Hereditary cancer: two hits revisited. Cancer Res Clin Oncol 122:135-140
-
(1996)
Cancer Res Clin Oncol
, vol.122
, pp. 135-140
-
-
-
12
-
-
0031004936
-
Deletions of the short arm of chromosome 3 in solid tumors and the search for suppressor genes
-
Kok K, Naylor SL, Buys CHCM (1997) Deletions of the short arm of chromosome 3 in solid tumors and the search for suppressor genes. Adv Cancer Res 71:27-92
-
(1997)
Adv Cancer Res
, vol.71
, pp. 27-92
-
-
Kok, K.1
Naylor, S.L.2
Buys, C.H.C.M.3
-
13
-
-
15144359971
-
A familial case of renal cell carcinoma and a t(2;3) chromosome translocation
-
Koolen MI, Van der Meyden APM, Bodmer D, Eleveld M, Van der Looij E, Brunner H, Smits A, et al (1998) A familial case of renal cell carcinoma and a t(2;3) chromosome translocation. Kidney Int 53:273-275
-
(1998)
Kidney Int
, vol.53
, pp. 273-275
-
-
Koolen, M.I.1
Van Der Meyden, A.P.M.2
Bodmer, D.3
Eleveld, M.4
Van Der Looij, E.5
Brunner, H.6
Smits, A.7
-
14
-
-
0027442691
-
Molecular cytogenetics of renal cell tumors
-
Kovacs G (1993) Molecular cytogenetics of renal cell tumors. Adv Cancer Res 62:89-124
-
(1993)
Adv Cancer Res
, vol.62
, pp. 89-124
-
-
Kovacs, G.1
-
15
-
-
0024517466
-
Tissue-specific expression of a constitutional 3;6 translocation development of multiple bilateral renal-cell carcinomas
-
Kovacs G, Brusa P, De Riese W (1989) Tissue-specific expression of a constitutional 3;6 translocation development of multiple bilateral renal-cell carcinomas. Int J Cancer 43: 422-427
-
(1989)
Int J Cancer
, vol.43
, pp. 422-427
-
-
Kovacs, G.1
Brusa, P.2
De Riese, W.3
-
16
-
-
0024599830
-
Clonal chromosome abnormalities in tumor cells from patients with sporadic renal cell carcinomas
-
Kovacs G, Frisch S (1989) Clonal chromosome abnormalities in tumor cells from patients with sporadic renal cell carcinomas. Cancer Res 49:651-659
-
(1989)
Cancer Res
, vol.49
, pp. 651-659
-
-
Kovacs, G.1
Frisch, S.2
-
17
-
-
0023835155
-
Loss of der(3) in renal carcinoma cell of a patient with constitutional t(3;12)
-
Kovacs G, Hoene E (1988) Loss of der(3) in renal carcinoma cell of a patient with constitutional t(3;12). Hum Genet 78: 148-150
-
(1988)
Hum Genet
, vol.78
, pp. 148-150
-
-
Kovacs, G.1
Hoene, E.2
-
18
-
-
0026057382
-
Nonhomologous chromatid exchange in hereditary and sporadic renal cell carcinomas
-
Kovacs G, Kung HF (1991) Nonhomologous chromatid exchange in hereditary and sporadic renal cell carcinomas. Proc Natl Acad Sci USA 88:194-198
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 194-198
-
-
Kovacs, G.1
Kung, H.F.2
-
19
-
-
0027074832
-
Clinical and genetic studies of renal cell carcinomas in a family with a constitutional chromosome 3;8 translocation: Genetics of familial renal carcinoma
-
Li FP, Decker HH, Zbar B, Stanton VP, Kovacs G, Seizinger BR, Aburatani H, et al (1993) Clinical and genetic studies of renal cell carcinomas in a family with a constitutional chromosome 3;8 translocation: genetics of familial renal carcinoma. Ann Intern Med 18:106-111
-
(1993)
Ann Intern Med
, vol.18
, pp. 106-111
-
-
Li, F.P.1
Decker, H.H.2
Zbar, B.3
Stanton, V.P.4
Kovacs, G.5
Seizinger, B.R.6
Aburatani, H.7
-
20
-
-
0026759647
-
Reviews on chromosome studies in urological tumors
-
Meloni AM, Bridge J, Sandberg AA (1992) Reviews on chromosome studies in urological tumors. J Urol 148:253-265
-
(1992)
J Urol
, vol.148
, pp. 253-265
-
-
Meloni, A.M.1
Bridge, J.2
Sandberg, A.A.3
-
22
-
-
13344279424
-
The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers
-
Ohta M, Inoue H, Cottecelli MG, Kastury K, Baffa R, Palazzo J, Siprashvili Z, et al (1996) The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers. Cell 84:587-597
-
(1996)
Cell
, vol.84
, pp. 587-597
-
-
Ohta, M.1
Inoue, H.2
Cottecelli, M.G.3
Kastury, K.4
Baffa, R.5
Palazzo, J.6
Siprashvili, Z.7
-
23
-
-
17344381429
-
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas
-
Schmidt L, Duh FM, Chen F, Kishida T, Glenn G, Choyke P, Scherer SW, et al (1997) Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas. Nat Genet 16:68-73
-
(1997)
Nat Genet
, vol.16
, pp. 68-73
-
-
Schmidt, L.1
Duh, F.M.2
Chen, F.3
Kishida, T.4
Glenn, G.5
Choyke, P.6
Scherer, S.W.7
-
24
-
-
0000191647
-
Mechanism of tumorigenesis of renal carcinomas associated with the constitutional chromosome 3;8 translocation
-
Schmidt L, Li F, Brown RS, Berg S, Chen F, Wei MH, Tory K, et al (1995) Mechanism of tumorigenesis of renal carcinomas associated with the constitutional chromosome 3;8 translocation. Cancer J Sci Am 1:191-195
-
(1995)
Cancer J Sci Am
, vol.1
, pp. 191-195
-
-
Schmidt, L.1
Li, F.2
Brown, R.S.3
Berg, S.4
Chen, F.5
Wei, M.H.6
Tory, K.7
-
25
-
-
0028235907
-
Frequent somatic mutations and loss of heterozygosity of the von Hippel-Lindau tumor suppressor gene in primary human renal cell carcinomas
-
Shuin T, Kondo K, Torigoe S, Kishida T, Kubota Y, Hosaka M, Nagashima Y, et al (1994) Frequent somatic mutations and loss of heterozygosity of the von Hippel-Lindau tumor suppressor gene in primary human renal cell carcinomas. Cancer Res 54:2852-2855
-
(1994)
Cancer Res
, vol.54
, pp. 2852-2855
-
-
Shuin, T.1
Kondo, K.2
Torigoe, S.3
Kishida, T.4
Kubota, Y.5
Hosaka, M.6
Nagashima, Y.7
-
26
-
-
10144257193
-
The t(X;1)(p11.2;q21.2) translocation in papillary renal cell carcinoma fuses a novel gene PRCC to the TFE3 transcription factor gene
-
Sidhar SK, Clark J, Gill S, Hamoundi R, Crew AJ, Gwilliam R, Ross M, et al (1996) The t(X;1)(p11.2;q21.2) translocation in papillary renal cell carcinoma fuses a novel gene PRCC to the TFE3 transcription factor gene. Hum Mol Genet 5:1333-1338
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1333-1338
-
-
Sidhar, S.K.1
Clark, J.2
Gill, S.3
Hamoundi, R.4
Crew, A.J.5
Gwilliam, R.6
Ross, M.7
-
27
-
-
0028936830
-
Report of the Fifth International Workshop on Human Chromosome 3 Mapping 1994
-
Smith DI, Glover TW, Gemill RM, Drabkin HA, O'Connell P, Naylor SL (1995) Report of the Fifth International Workshop on Human Chromosome 3 Mapping 1994. Cytogenet Cell Genet 68:125-146
-
(1995)
Cytogenet Cell Genet
, vol.68
, pp. 125-146
-
-
Smith, D.I.1
Glover, T.W.2
Gemill, R.M.3
Drabkin, H.A.4
O'Connell, P.5
Naylor, S.L.6
-
28
-
-
0029940485
-
Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996
-
Spurr NK, Bashir R, Bushby K, Cox A, Cox S, Hildebrandt F, Hill N, et al (1996) Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996. Cytogenet Cell Genet 73:255-273
-
(1996)
Cytogenet Cell Genet
, vol.73
, pp. 255-273
-
-
Spurr, N.K.1
Bashir, R.2
Bushby, K.3
Cox, A.4
Cox, S.5
Hildebrandt, F.6
Hill, N.7
-
29
-
-
0029003196
-
Familial and sporadic human renal cell carcinoma: Evidence against a double loss mechanism of carcinogenesis
-
Stein WD, Stein AD (1995) Familial and sporadic human renal cell carcinoma: evidence against a double loss mechanism of carcinogenesis. J Clin Epidemiol 48:767-777
-
(1995)
J Clin Epidemiol
, vol.48
, pp. 767-777
-
-
Stein, W.D.1
Stein, A.D.2
-
30
-
-
0030983281
-
Involvement of multiple loci on chromosome 3 in renal cell cancer development
-
van den Berg A, Buys CHCM (1997) Involvement of multiple loci on chromosome 3 in renal cell cancer development. Genes Chromosom Cancer 19:59-76
-
(1997)
Genes Chromosom Cancer
, vol.19
, pp. 59-76
-
-
Van Den Berg, A.1
Buys, C.H.C.M.2
-
31
-
-
0030811819
-
Normal FHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B region
-
van den Berg A, Draaijers TG, Kok K, Timmer T, Van der Veen AY, Veldhuis PMJF, De Leij L, et al (1997a) Normal FHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B region. Genes Chromosom Cancer 19:220-227
-
(1997)
Genes Chromosom Cancer
, vol.19
, pp. 220-227
-
-
Van Den Berg, A.1
Draaijers, T.G.2
Kok, K.3
Timmer, T.4
Van Der Veen, A.Y.5
Veldhuis, P.M.J.F.6
De Leij, L.7
-
32
-
-
0030034627
-
Major role for a 3p21 region and lack of involvement of the t(3;8) breakpoint region in the development of renal cell carcinoma suggested by loss of heterozygosity analysis
-
van den Berg A, Hulsbeek MMF, De Jong D, Kok K, Veldhuis PMJF, Roche J, Buys CHCM (1996) Major role for a 3p21 region and lack of involvement of the t(3;8) breakpoint region in the development of renal cell carcinoma suggested by loss of heterozygosity analysis. Genes Chromosom Cancer 15:64-72
-
(1996)
Genes Chromosom Cancer
, vol.15
, pp. 64-72
-
-
Van Den Berg, A.1
Hulsbeek, M.M.F.2
De Jong, D.3
Kok, K.4
Veldhuis, P.M.J.F.5
Roche, J.6
Buys, C.H.C.M.7
-
33
-
-
0030929318
-
Cytogenetic classification of renal cell cancer
-
van den Berg E, Dijkhuizen T, Oosterhuis JW, Geurts van Kessel A, De Jong B, Störkel S (1997b) Cytogenetic classification of renal cell cancer. Cancer Genet Cytogenet 95:103-107
-
(1997)
Cancer Genet Cytogenet
, vol.95
, pp. 103-107
-
-
Van Den Berg, E.1
Dijkhuizen, T.2
Oosterhuis, J.W.3
Geurts Van Kessel, A.4
De Jong, B.5
Störkel, S.6
-
34
-
-
0030463172
-
Fusion of the transcription factor TFE3 gene to a novel gene, PRCC, in t(X;1)(p11;q21)-positive papillary renal cell carcinomas
-
Weterman M, Wilbrink M, Geurts van Kessel A (1996a) Fusion of the transcription factor TFE3 gene to a novel gene, PRCC, in t(X;1)(p11;q21)-positive papillary renal cell carcinomas. Proc Natl Acad Sci USA 93:15294-15298
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 15294-15298
-
-
Weterman, M.1
Wilbrink, M.2
Geurts Van Kessel, A.3
-
35
-
-
0030480923
-
Molecular cloning of the papillary renal cell carcinoma-associated t(X;1)(p11;q21) breakpoint
-
Weterman M, Wilbrink M, Janssen I, Janssen H, van den Berg E, Fisher S, Craig I, et al (1996b) Molecular cloning of the papillary renal cell carcinoma-associated t(X;1)(p11;q21) breakpoint. Cytogenet Cell Genet 75:2-6
-
(1996)
Cytogenet Cell Genet
, vol.75
, pp. 2-6
-
-
Weterman, M.1
Wilbrink, M.2
Janssen, I.3
Janssen, H.4
Van Den Berg, E.5
Fisher, S.6
Craig, I.7
-
36
-
-
16144365122
-
Germline mutations in the von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan
-
Zbar B, Kishida T, Chen F, Schmidt L, Maher ER, Richards FM, Crossey PA, et al (1996) Germline mutations in the von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan. Hum Mutat 8:348-357
-
(1996)
Hum Mutat
, vol.8
, pp. 348-357
-
-
Zbar, B.1
Kishida, T.2
Chen, F.3
Schmidt, L.4
Maher, E.R.5
Richards, F.M.6
Crossey, P.A.7
-
37
-
-
0029759214
-
Detection of von Hippel-Lindau disease gene mutations in paraffin-embedded sporadic renal cell carcinoma specimens
-
Zhuang Z, Gnarra JR, Dudley CF, Zbar B, Linehan WM, Lubensky IA (1996) Detection of von Hippel-Lindau disease gene mutations in paraffin-embedded sporadic renal cell carcinoma specimens. Mod Pathol 9:838-842
-
(1996)
Mod Pathol
, vol.9
, pp. 838-842
-
-
Zhuang, Z.1
Gnarra, J.R.2
Dudley, C.F.3
Zbar, B.4
Linehan, W.M.5
Lubensky, I.A.6
|