-
1
-
-
0018736628
-
Hereditary renal-cell carcinoma associated with a chromosomal translocation
-
Cohen A.J., Li F.P., Berg S., Marchetto D.J., Tsai S., Jacobs S.C., et al. Hereditary renal-cell carcinoma associated with a chromosomal translocation. N Engl J Med 1979, 301:592-595.
-
(1979)
N Engl J Med
, vol.301
, pp. 592-595
-
-
Cohen, A.J.1
Li, F.P.2
Berg, S.3
Marchetto, D.J.4
Tsai, S.5
Jacobs, S.C.6
-
2
-
-
0023835155
-
Loss of der(3) in renal cell carcinoma cells of a patient with constitutional t(3;12)
-
Kovacs G., Hoene E. Loss of der(3) in renal cell carcinoma cells of a patient with constitutional t(3;12). Hum Genet 1988, 78:148-150.
-
(1988)
Hum Genet
, vol.78
, pp. 148-150
-
-
Kovacs, G.1
Hoene, E.2
-
3
-
-
0024517466
-
Tissue specific expression of a constitutional 3;6 translocation: development of multiple bilateral renal cell carcinomas
-
Kovacs G., Brusa P., DeRiese W. Tissue specific expression of a constitutional 3;6 translocation: development of multiple bilateral renal cell carcinomas. Int J Cancer 1989, 43:422-427.
-
(1989)
Int J Cancer
, vol.43
, pp. 422-427
-
-
Kovacs, G.1
Brusa, P.2
DeRiese, W.3
-
4
-
-
0023217943
-
Specific chromosome aberration in human renal cell carcinoma
-
Kovacs G., Szücs S., De Riese W., Baumgärtel H. Specific chromosome aberration in human renal cell carcinoma. Int J Cancer 1987, 40:171-178.
-
(1987)
Int J Cancer
, vol.40
, pp. 171-178
-
-
Kovacs, G.1
Szücs, S.2
De Riese, W.3
Baumgärtel, H.4
-
5
-
-
0011153988
-
Consistent 3p deletion and loss of heterozygosity in renal cell carcinoma
-
Kovacs G., Erlandsson R., Boldog F., Ingvarsson S., Müller-Brechlin R., Klein G., et al. Consistent 3p deletion and loss of heterozygosity in renal cell carcinoma. Proc Natl Acad Sci U S A 1988, 85:591-595.
-
(1988)
Proc Natl Acad Sci U S A
, vol.85
, pp. 591-595
-
-
Kovacs, G.1
Erlandsson, R.2
Boldog, F.3
Ingvarsson, S.4
Müller-Brechlin, R.5
Klein, G.6
-
6
-
-
0026080061
-
Cytogenetics of renal cell carcinomas associated with von Hippel-Lindau disease
-
Kovacs G., Emanuel A., Neumann H.P.H., Kung H. Cytogenetics of renal cell carcinomas associated with von Hippel-Lindau disease. Genes Chromosomes Cancer 1991, 3:256-262.
-
(1991)
Genes Chromosomes Cancer
, vol.3
, pp. 256-262
-
-
Kovacs, G.1
Emanuel, A.2
Neumann, H.P.H.3
Kung, H.4
-
7
-
-
0024599830
-
Clonal chromosome abnormalities in tumor cells from patients with sporadic renal cell carcinomas
-
Kovacs G., Frisch S. Clonal chromosome abnormalities in tumor cells from patients with sporadic renal cell carcinomas. Cancer Res 1989, 49:651-659.
-
(1989)
Cancer Res
, vol.49
, pp. 651-659
-
-
Kovacs, G.1
Frisch, S.2
-
8
-
-
0026057382
-
Nonhomologous chromatid exchange in hereditary and sporadic renal cell carcinomas
-
Kovacs G., Kung H.F. Nonhomologous chromatid exchange in hereditary and sporadic renal cell carcinomas. Proc Natl Acad Sci U S A 1991, 88:194-198.
-
(1991)
Proc Natl Acad Sci U S A
, vol.88
, pp. 194-198
-
-
Kovacs, G.1
Kung, H.F.2
-
9
-
-
0023181644
-
Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma
-
Zbar B., Brauch H., Talmadge C., Linehan M. Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma. Nature 1987, 327:721-724.
-
(1987)
Nature
, vol.327
, pp. 721-724
-
-
Zbar, B.1
Brauch, H.2
Talmadge, C.3
Linehan, M.4
-
10
-
-
0030768425
-
Detailed microsatellite analysis of chromosome 3p region in nonpapillary renal cell carcinomas
-
Chudek J., Wilhelm M., Bugert P., Herbers J., Kovacs G. Detailed microsatellite analysis of chromosome 3p region in nonpapillary renal cell carcinomas. Int J Cancer 1997, 73:225-229.
-
(1997)
Int J Cancer
, vol.73
, pp. 225-229
-
-
Chudek, J.1
Wilhelm, M.2
Bugert, P.3
Herbers, J.4
Kovacs, G.5
-
11
-
-
0029975354
-
A gene from human chromosomal band 3p21.1 encodes a highly conserved arginine-rich protein and is mutated in renal cell carcinomas
-
Shridhar V., Rivard S., Shridhar R., Mullins C., Bostick L., Sakr W., et al. A gene from human chromosomal band 3p21.1 encodes a highly conserved arginine-rich protein and is mutated in renal cell carcinomas. Oncogene 1996, 12:1931-1939.
-
(1996)
Oncogene
, vol.12
, pp. 1931-1939
-
-
Shridhar, V.1
Rivard, S.2
Shridhar, R.3
Mullins, C.4
Bostick, L.5
Sakr, W.6
-
12
-
-
0033561527
-
Molecular cloning of a candidate tumor suppressor gene, DLC1, from chromosome 3p21.3
-
Daigo Y., Nishiwaki T., Kawasoe T., Tamari M., Tsuchiya E., Nakamura Y. Molecular cloning of a candidate tumor suppressor gene, DLC1, from chromosome 3p21.3. Cancer Res 1999, 59:1966-1972.
-
(1999)
Cancer Res
, vol.59
, pp. 1966-1972
-
-
Daigo, Y.1
Nishiwaki, T.2
Kawasoe, T.3
Tamari, M.4
Tsuchiya, E.5
Nakamura, Y.6
-
13
-
-
0035476868
-
Epigenetic inactivation of the RASSF1A 3p21.3 tumor suppressor gene in both clear cell and papillary renal cell carcinoma
-
Morrissey C., Martinez A., Zatyka M., Agathanggelou A., Honorio S., Astuti D., et al. Epigenetic inactivation of the RASSF1A 3p21.3 tumor suppressor gene in both clear cell and papillary renal cell carcinoma. Cancer Res 2001, 61:7277-7281.
-
(2001)
Cancer Res
, vol.61
, pp. 7277-7281
-
-
Morrissey, C.1
Martinez, A.2
Zatyka, M.3
Agathanggelou, A.4
Honorio, S.5
Astuti, D.6
-
14
-
-
0027240519
-
Identification of the von Hippel-Lindau disease tumor suppressor gene
-
Latif F., Tory K., Gnarra J., Yao M., Duh F.M., Orcutt M.L., et al. Identification of the von Hippel-Lindau disease tumor suppressor gene. Science 1993, 260:1317-1320.
-
(1993)
Science
, vol.260
, pp. 1317-1320
-
-
Latif, F.1
Tory, K.2
Gnarra, J.3
Yao, M.4
Duh, F.M.5
Orcutt, M.L.6
-
15
-
-
0027954044
-
Mutations of the VHL tumour suppressor gene in renal carcinoma
-
Gnarra J.R., Tory K., Weng Y., Schmidt L., Wei M.H., Li H., et al. Mutations of the VHL tumour suppressor gene in renal carcinoma. Nat Genet 1994, 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
-
16
-
-
0028072991
-
Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma
-
Herman J.G., Latif F., Weng Y., Lerman M.I., Zbar B., Liu S., et al. Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma. Proc Natl Acad Sci U S A 1994, 91:9700-9704.
-
(1994)
Proc Natl Acad Sci U S A
, 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
-
17
-
-
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., Cotticelli M.G., Kastury K., Baffa R., Palazzo J., et al. 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 1996, 84:587-597.
-
(1996)
Cell
, vol.84
, pp. 587-597
-
-
Ohta, M.1
Inoue, H.2
Cotticelli, M.G.3
Kastury, K.4
Baffa, R.5
Palazzo, J.6
-
18
-
-
0032482964
-
The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8
-
Gemmill R.M., West J.D., Boldog F., Tanaka N., Robinson L.J., Smith D.I., et al. The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8. Proc Natl Acad Sci U S A 1998, 95:9572-9577.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 9572-9577
-
-
Gemmill, R.M.1
West, J.D.2
Boldog, F.3
Tanaka, N.4
Robinson, L.J.5
Smith, D.I.6
-
19
-
-
0030001342
-
Evaluation of the FHIT gene in colorectal cancers
-
Thiagalingam S., Lisitsyn N.A., Hamaguchi M., Wigler M.H., Willson J.K., Markowitz S.D., et al. Evaluation of the FHIT gene in colorectal cancers. Cancer Res 1996, 56:2936-2939.
-
(1996)
Cancer Res
, vol.56
, pp. 2936-2939
-
-
Thiagalingam, S.1
Lisitsyn, N.A.2
Hamaguchi, M.3
Wigler, M.H.4
Willson, J.K.5
Markowitz, S.D.6
-
20
-
-
0030930173
-
FHIT gene and the FRA3B region are not involved in the genetics of renal cell carcinomas
-
Bugert P., Wilhelm M., Kovacs G. FHIT gene and the FRA3B region are not involved in the genetics of renal cell carcinomas. Genes Chromosomes Cancer 1997, 20:9-15.
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 9-15
-
-
Bugert, P.1
Wilhelm, M.2
Kovacs, G.3
-
21
-
-
0035084097
-
Association of a novel constitutional translocation t(1q;3q) with familial renal cell carcinoma
-
Kanayama H., Lui W.O., Takahashi M., Naroda T., Kedra D., Wong F.K., et al. Association of a novel constitutional translocation t(1q;3q) with familial renal cell carcinoma. J Med Genet 2001, 38:165-170.
-
(2001)
J Med Genet
, vol.38
, pp. 165-170
-
-
Kanayama, H.1
Lui, W.O.2
Takahashi, M.3
Naroda, T.4
Kedra, D.5
Wong, F.K.6
-
22
-
-
10744226004
-
The t(1;3) breakpoint-spanning genes LSAMP and NORE1 are involved in clear cell renal cell carcinomas
-
Chen J., Lui W.-O., Vos M.D., Clark G.J., Takahashi M., Schoumans J., et al. The t(1;3) breakpoint-spanning genes LSAMP and NORE1 are involved in clear cell renal cell carcinomas. Cancer Cell 2003, 4:405-413.
-
(2003)
Cancer Cell
, vol.4
, pp. 405-413
-
-
Chen, J.1
Lui, W.-O.2
Vos, M.D.3
Clark, G.J.4
Takahashi, M.5
Schoumans, J.6
-
23
-
-
0034765270
-
The DIRC1 gene at chromosome 2q33 spans a familial RCC-associated t(2;3)(q33;q21) chromosome translocation
-
Druck T., Podolski J., Byrski T., Wyrwicz L., Zajaczek S., Kata G., et al. The DIRC1 gene at chromosome 2q33 spans a familial RCC-associated t(2;3)(q33;q21) chromosome translocation. J Hum Genet 2001, 46:583-589.
-
(2001)
J Hum Genet
, vol.46
, pp. 583-589
-
-
Druck, T.1
Podolski, J.2
Byrski, T.3
Wyrwicz, L.4
Zajaczek, S.5
Kata, G.6
-
24
-
-
15144359971
-
A familial case of renal cell carcinoma and t(2;3) chromosome translocation
-
Koolen M.I., van der Meyden A.P., Bodmer D., Eleveld M., van der Looij E., Brunner H., et al. A familial case of renal cell carcinoma and t(2;3) chromosome translocation. Kidney Int 1998, 53:273-275.
-
(1998)
Kidney Int
, vol.53
, pp. 273-275
-
-
Koolen, M.I.1
van der Meyden, A.P.2
Bodmer, D.3
Eleveld, M.4
van der Looij, E.5
Brunner, H.6
-
25
-
-
0037087560
-
Disruption of a novel MFS transporter gene, DIRC2, by a familial renal cell carcinoma-associated t(2;3)(q35;q21)
-
Bodmer D., Eleveld M., Kater-Baats E., Janssen B., Weterman M., Schoenmakers E., et al. Disruption of a novel MFS transporter gene, DIRC2, by a familial renal cell carcinoma-associated t(2;3)(q35;q21). Hum Mol Genet 2002, 11:641-649.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 641-649
-
-
Bodmer, D.1
Eleveld, M.2
Kater-Baats, E.3
Janssen, B.4
Weterman, M.5
Schoenmakers, E.6
-
26
-
-
0042334606
-
Disruption of a novel gene, DIRC3, and expression of DIRC3-HSPBAP1 fusion transcripts in a case of familial cell cancer and t(2;3)(q35;q21)
-
Bodmer D., Schepens M., Eleveld M.J., Schoenmakers E.F., Geurts van Kessel A. Disruption of a novel gene, DIRC3, and expression of DIRC3-HSPBAP1 fusion transcripts in a case of familial cell cancer and t(2;3)(q35;q21). Genes Chromosomes Cancer 2003, 38:107-116.
-
(2003)
Genes Chromosomes Cancer
, vol.38
, pp. 107-116
-
-
Bodmer, D.1
Schepens, M.2
Eleveld, M.J.3
Schoenmakers, E.F.4
Geurts van Kessel, A.5
-
27
-
-
35548942595
-
Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene
-
Bonne A., Vreede L., Kuiper R.P., Bodmer D., Jansen C., Eleveld M., et al. Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene. Cancer Genet Cytogenet 2007, 179:11-18.
-
(2007)
Cancer Genet Cytogenet
, vol.179
, pp. 11-18
-
-
Bonne, A.1
Vreede, L.2
Kuiper, R.P.3
Bodmer, D.4
Jansen, C.5
Eleveld, M.6
-
28
-
-
0035060261
-
Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15)
-
Eleveld M.J., Bodmer D., Merkx G., Siepman A., Sprenger S.H., Weterman M.A., et al. Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15). Genes Chromosomes Cancer 2001, 31:23-32.
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 23-32
-
-
Eleveld, M.J.1
Bodmer, D.2
Merkx, G.3
Siepman, A.4
Sprenger, S.H.5
Weterman, M.A.6
-
29
-
-
33947158579
-
Characterization of a 3;6 translocation associated with renal cell carcinoma
-
Foster R.E., Abdulrahman M., Morris M.R., Prigmore E., Gribble S., Ng B., et al. Characterization of a 3;6 translocation associated with renal cell carcinoma. Genes Chromosomes Cancer 2007, 46:311-317.
-
(2007)
Genes Chromosomes Cancer
, vol.46
, pp. 311-317
-
-
Foster, R.E.1
Abdulrahman, M.2
Morris, M.R.3
Prigmore, E.4
Gribble, S.5
Ng, B.6
-
30
-
-
2442485921
-
Cloning of a new familial t(3;8) translocation associated with conventional renal cell carcinoma reveals a 5 kb microdeletion and no gene involved in the rearrangement
-
Rodríguez-Perales S., Meléndez B., Gribble S.M., Valle L., Carter N.P., Santamaría I., et al. Cloning of a new familial t(3;8) translocation associated with conventional renal cell carcinoma reveals a 5 kb microdeletion and no gene involved in the rearrangement. Hum Mol Genet 2004, 13:983-990.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 983-990
-
-
Rodríguez-Perales, S.1
Meléndez, B.2
Gribble, S.M.3
Valle, L.4
Carter, N.P.5
Santamaría, I.6
-
31
-
-
21044454401
-
About the origin and development of hereditary conventional renal cell carcinoma in a four-generation t(3;8)(p14.1;q24.23) family
-
Valle L., Cascón A., Melchor L., Otero I., Rodríguez-Perales S., Sánchez L., et al. About the origin and development of hereditary conventional renal cell carcinoma in a four-generation t(3;8)(p14.1;q24.23) family. Eur J Hum Genet 2005, 13:570-578.
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 570-578
-
-
Valle, L.1
Cascón, A.2
Melchor, L.3
Otero, I.4
Rodríguez-Perales, S.5
Sánchez, L.6
-
32
-
-
0037932459
-
Molecular study of a new family with hereditary renal cell carcinoma and a translocation t(3;8)(p13;q24.1)
-
Meléndez B., Rodríguez-Perales S., Martínez-Delgado B., Otero I., Robledo M., Martínez-Ramírez A., et al. Molecular study of a new family with hereditary renal cell carcinoma and a translocation t(3;8)(p13;q24.1). Hum Genet 2003, 112:178-185.
-
(2003)
Hum Genet
, vol.112
, pp. 178-185
-
-
Meléndez, B.1
Rodríguez-Perales, S.2
Martínez-Delgado, B.3
Otero, I.4
Robledo, M.5
Martínez-Ramírez, A.6
-
33
-
-
70949090198
-
The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer
-
Kuiper R.P., Vreede L., Venkatachalam R., Ricketts C., Kamping E., Verwiel E., et al. The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer. Cancer Genet Cytogenet 2009, 195:105-111.
-
(2009)
Cancer Genet Cytogenet
, vol.195
, pp. 105-111
-
-
Kuiper, R.P.1
Vreede, L.2
Venkatachalam, R.3
Ricketts, C.4
Kamping, E.5
Verwiel, E.6
-
34
-
-
17344376286
-
Tomosyn: a syntaxin-1-binding protein that forms a novel complex in the neurotransmitter release process
-
Fujita Y., Shirataki H., Sakisaka T., Asakura T., Ohya T., Kotani H., et al. Tomosyn: a syntaxin-1-binding protein that forms a novel complex in the neurotransmitter release process. Neuron 1998, 20:905-915.
-
(1998)
Neuron
, vol.20
, pp. 905-915
-
-
Fujita, Y.1
Shirataki, H.2
Sakisaka, T.3
Asakura, T.4
Ohya, T.5
Kotani, H.6
-
35
-
-
0028790326
-
Terminal deletion of chromosome 3p sequences in nonpapillary renal cell carcinoma: a breakpoint cluster between loci D3S1285 and D3S1603
-
Wilhelm M., Bugert P., Kenck C., Staehler G., Kovacs G. Terminal deletion of chromosome 3p sequences in nonpapillary renal cell carcinoma: a breakpoint cluster between loci D3S1285 and D3S1603. Cancer Res 1995, 55:5383-5385.
-
(1995)
Cancer Res
, vol.55
, pp. 5383-5385
-
-
Wilhelm, M.1
Bugert, P.2
Kenck, C.3
Staehler, G.4
Kovacs, G.5
-
36
-
-
0030483383
-
Refining a proximal breakpoint cluster at chromosome 3p11.2 in nonpapillary renal cell carcinomas
-
Bugert P., Kenck C., Wilhelm M., Kovacs G. Refining a proximal breakpoint cluster at chromosome 3p11.2 in nonpapillary renal cell carcinomas. Int J Cancer 1996, 68:723-726.
-
(1996)
Int J Cancer
, vol.68
, pp. 723-726
-
-
Bugert, P.1
Kenck, C.2
Wilhelm, M.3
Kovacs, G.4
-
37
-
-
0037439819
-
Deletion of chromosome 3p14.2-p25 involving the VHL and FHIT genes in conventional renal cell carcinoma
-
Sükösd F., Kuroda N., Beothe T., Kaur A., Kovacs G. Deletion of chromosome 3p14.2-p25 involving the VHL and FHIT genes in conventional renal cell carcinoma. Cancer Res 2003, 63:455-457.
-
(2003)
Cancer Res
, vol.63
, pp. 455-457
-
-
Sükösd, F.1
Kuroda, N.2
Beothe, T.3
Kaur, A.4
Kovacs, G.5
-
38
-
-
0001650645
-
Parenchymal abnormalities associated with papillary renal cell tumors: a morphologic study
-
Kovacs A., Kovacs G. Parenchymal abnormalities associated with papillary renal cell tumors: a morphologic study. J Urol Pathol 1993, 1:301-312.
-
(1993)
J Urol Pathol
, vol.1
, pp. 301-312
-
-
Kovacs, A.1
Kovacs, G.2
-
39
-
-
33749000005
-
Rising incidence of small renal masses: a need to reassess treatment effect
-
Hollingsworth J.M., Miller D.C., Daignault S., Hollenbeck B.K. Rising incidence of small renal masses: a need to reassess treatment effect. J Natl Cancer Inst 2006, 98:1331-1334.
-
(2006)
J Natl Cancer Inst
, vol.98
, pp. 1331-1334
-
-
Hollingsworth, J.M.1
Miller, D.C.2
Daignault, S.3
Hollenbeck, B.K.4
-
40
-
-
0036799546
-
Understanding familial and non-familial renal cell cancer
-
Bodmer D., van der Hurk W., van Groningen J.J.M., Eleveld M.J., Martens G.J.M., Weterman M.A.J., et al. Understanding familial and non-familial renal cell cancer. Hum Mol Genet 2002, 11:2489-2498.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2489-2498
-
-
Bodmer, D.1
van der Hurk, W.2
van Groningen, J.J.M.3
Eleveld, M.J.4
Martens, G.J.M.5
Weterman, M.A.J.6
-
41
-
-
17044452288
-
HIF activation identified early lesions in VHL kidneys: evidence for site-specific tumor suppressor function in the nephron
-
Mandriota S.J., Turner K.J., Davies D.R., Murray P.G., Morgan N.V., Sowter H.M., et al. HIF activation identified early lesions in VHL kidneys: evidence for site-specific tumor suppressor function in the nephron. Cancer Cell 2002, 1:459-468.
-
(2002)
Cancer Cell
, vol.1
, pp. 459-468
-
-
Mandriota, S.J.1
Turner, K.J.2
Davies, D.R.3
Murray, P.G.4
Morgan, N.V.5
Sowter, H.M.6
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