-
1
-
-
0034624697
-
Combined LOH/CGH analysis proves the existence of interstitial 3p deletions in renal cell carcinoma
-
Alimov A, Kost-Alimova M, Liu J, Li C, Bergerheim U, Imreh S, Klein G, Zabarovsky ER. 2000. Combined LOH/CGH analysis proves the existence of interstitial 3p deletions in renal cell carcinoma. Oncogene 19:1392-1399.
-
(2000)
Oncogene
, vol.19
, pp. 1392-1399
-
-
Alimov, A.1
Kost-Alimova, M.2
Liu, J.3
Li, C.4
Bergerheim, U.5
Imreh, S.6
Klein, G.7
Zabarovsky, E.R.8
-
2
-
-
0035030905
-
Proliferating cell nuclear antigen and epidermal growth factor receptor (EGFr) status in renal cell carcinoma patients with polysomy of chromosome 7
-
Amare Kadam PS, Varghese C, Bharde SH, Narasimhamoorthy NK, Desai S, Advani SH, Havaldar R, Kulkarni JN. 2001. Proliferating cell nuclear antigen and epidermal growth factor receptor (EGFr) status in renal cell carcinoma patients with polysomy of chromosome 7. Cancer Genet Cytogenet 125:139-146.
-
(2001)
Cancer Genet Cytogenet
, vol.125
, pp. 139-146
-
-
Amare Kadam, P.S.1
Varghese, C.2
Bharde, S.H.3
Narasimhamoorthy, N.K.4
Desai, S.5
Advani, S.H.6
Havaldar, R.7
Kulkarni, J.N.8
-
3
-
-
0026556942
-
Molecular and cellular characterization of human renal cell carcinoma cell lines
-
Anglard P, Trahan E, Liu S, Latif F, Merino MJ, Lerman MI, Zbar B, Linehan WM. 1992. Molecular and cellular characterization of human renal cell carcinoma cell lines. Cancer Res 52:348-356.
-
(1992)
Cancer Res
, vol.52
, pp. 348-356
-
-
Anglard, P.1
Trahan, E.2
Liu, S.3
Latif, F.4
Merino, M.J.5
Lerman, M.I.6
Zbar, B.7
Linehan, W.M.8
-
5
-
-
8044261435
-
Correlations of allelic imbalance of chromosome 14 with adverse prognostic parameters in 148 renal cell carcinomas
-
Beroud C, Fournet JC, Jeanpierre C, Droz D, Bouvier R, Froger D, Chretien Y, Marechal JM, Weissenbach J, Junien C. 1996. Correlations of allelic imbalance of chromosome 14 with adverse prognostic parameters in 148 renal cell carcinomas. Genes Chromosomes Cancer 17:215-224.
-
(1996)
Genes Chromosomes Cancer
, vol.17
, pp. 215-224
-
-
Beroud, C.1
Fournet, J.C.2
Jeanpierre, C.3
Droz, D.4
Bouvier, R.5
Froger, D.6
Chretien, Y.7
Marechal, J.M.8
Weissenbach, J.9
Junien, C.10
-
6
-
-
0034660401
-
The tcf17 gene at chromosome 5q is not involved in the development of conventional renal cell carcinoma
-
Bugert P, Pesti T, Kovacs G. 2000. The tcf17 gene at chromosome 5q is not involved in the development of conventional renal cell carcinoma. Int J Cancer 86:806-810.
-
(2000)
Int J Cancer
, vol.86
, pp. 806-810
-
-
Bugert, P.1
Pesti, T.2
Kovacs, G.3
-
7
-
-
0027198847
-
Detection of allele loss in colorectal tumours using microsatellites and fluorescent DNA technology
-
Cawkwell L, Bell SM, Lewis FA, Dixon MF, Taylor GR, Quirke P. 1993. Detection of allele loss in colorectal tumours using microsatellites and fluorescent DNA technology. Br J Cancer 67:1262-1267.
-
(1993)
Br J Cancer
, vol.67
, pp. 1262-1267
-
-
Cawkwell, L.1
Bell, S.M.2
Lewis, F.A.3
Dixon, M.F.4
Taylor, G.R.5
Quirke, P.6
-
8
-
-
0031776704
-
Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: Evidence for a VHL-independent pathway in clear cell renal tumourigenesis
-
Clifford SC, Prowse AH, Affara NA, Buys CH, Maher ER. 1998. Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL-independent pathway in clear cell renal tumourigenesis. Genes Chromosomes Cancer 22:200-209.
-
(1998)
Genes Chromosomes Cancer
, vol.22
, pp. 200-209
-
-
Clifford, S.C.1
Prowse, A.H.2
Affara, N.A.3
Buys, C.H.4
Maher, E.R.5
-
9
-
-
0027954044
-
Mutations of the VHL tumour suppressor gene in renal carcinoma
-
Gnarra JR, Tory K, Weng Y, Schmidt L, Wei MH, Li H, Latif F, Liu S, Chen F, Duh F-M, Lubensky IA, Duan R, Florence C, Pozzatti R, Walther MM, Bander NH, Grossman HB, Brauch H, Pomer S, Brooks JD, Issacs WB, Lerman MI, Zbar B, Linehan WM. 1994. Mutations of the VHL tumour 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
Liu, S.8
Chen, F.9
Duh, F.-M.10
Lubensky, I.A.11
Duan, R.12
Florence, C.13
Pozzatti, R.14
Walther, M.M.15
Bander, N.H.16
Grossman, H.B.17
Brauch, H.18
Pomer, S.19
Brooks, J.D.20
Issacs, W.B.21
Lerman, M.I.22
Zbar, B.23
Linehan, W.M.24
more..
-
10
-
-
0035503345
-
Prognostic impacts of cytogenetic findings in clear cell renal cell carcinoma: Gain of 5q31-qter predicts a distinct clinical phenotype with favorable prognosis
-
Gunawan B, Huber W, Holtrup M, von Heydebreck A, Efferth T, Poustka A, Ringert RH, Jakse G, Fuzesi L. 2001. Prognostic impacts of cytogenetic findings in clear cell renal cell carcinoma: gain of 5q31-qter predicts a distinct clinical phenotype with favorable prognosis. Cancer Res 61:7731-7738.
-
(2001)
Cancer Res
, vol.61
, pp. 7731-7738
-
-
Gunawan, B.1
Huber, W.2
Holtrup, M.3
Von Heydebreck, A.4
Efferth, T.5
Poustka, A.6
Ringert, R.H.7
Jakse, G.8
Fuzesi, L.9
-
11
-
-
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, Duan DS, Gnarra JR, Linehan WM, Baylin S. 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
Duan, D.S.8
Gnarra, J.R.9
Linehan, W.M.10
Baylin, S.11
-
12
-
-
0026495364
-
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
-
Kallioniemi A, Kallioniemi OP, Sudar D, Rutovitz D, Gray JW, Waldman F, Pinkel D. 1992. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 258:818-821.
-
(1992)
Science
, vol.258
, pp. 818-821
-
-
Kallioniemi, A.1
Kallioniemi, O.P.2
Sudar, D.3
Rutovitz, D.4
Gray, J.W.5
Waldman, F.6
Pinkel, D.7
-
13
-
-
0002166920
-
SKY: A comprehensive diagnostic and research tool. A review of the first 300 published cases
-
Knutsen T, Ried T. 2000. SKY: a comprehensive diagnostic and research tool. A review of the first 300 published cases. J Assoc Genet Tech 26:3-15.
-
(2000)
J Assoc Genet Tech
, vol.26
, pp. 3-15
-
-
Knutsen, T.1
Ried, T.2
-
14
-
-
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
-
15
-
-
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
-
16
-
-
0027240519
-
Identification of the von Hippel-Lindau disease tumor suppressor gene
-
Latif F, Tory K, Gnarra J, Yao M, Duh FM, Orcutt ML, Stackhouse T, Kuzmin I, Modi W, Geil L, Schmidt L, Zhou F, Li H, Wei MH, Chen F, Glenn G, Choyke P, Walther MM, Weng Y, Duan DSR, Dean M, Glavac D, Richards FM, Crossey PA, Fergusin-Smith MA, Le Paslier D, Chumakov I, Cohen D, Chinault AC, Maher ER, Linehan WM, Zbar B, Lerman MI. 1993. Identification of the von Hippel-Lindau disease tumor suppressor gene. Science 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
Stackhouse, T.7
Kuzmin, I.8
Modi, W.9
Geil, L.10
Schmidt, L.11
Zhou, F.12
Li, H.13
Wei, M.H.14
Chen, F.15
Glenn, G.16
Choyke, P.17
Walther, M.M.18
Weng, Y.19
Duan, D.S.R.20
Dean, M.21
Glavac, D.22
Richards, F.M.23
Crossey, P.A.24
Fergusin-Smith, M.A.25
Le Paslier, D.26
Chumakov, I.27
Cohen, D.28
Chinault, A.C.29
Maher, E.R.30
Linehan, W.M.31
Zbar, B.32
Lerman, M.I.33
more..
-
17
-
-
0344076342
-
Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping
-
Macville M, Schröck E, Padilla-Nash H, Keck C, Ghadimi BM, Zimonjic D, Popescu N, Ried T. 1999. Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping. Cancer Res 59:141-150.
-
(1999)
Cancer Res
, vol.59
, pp. 141-150
-
-
Macville, M.1
Schröck, E.2
Padilla-Nash, H.3
Keck, C.4
Ghadimi, B.M.5
Zimonjic, D.6
Popescu, N.7
Ried, T.8
-
18
-
-
0030040471
-
Genetic aberrations detected by comparative genomic hybridization are associated with clinical outcome in renal cell carcinoma
-
Moch H, Presti JC Jr, Sauter G, Buchholz N, Jordan P, Mihatsch MJ, Waldman FM. 1996. Genetic aberrations detected by comparative genomic hybridization are associated with clinical outcome in renal cell carcinoma. Cancer Res 56:27-30.
-
(1996)
Cancer Res
, vol.56
, pp. 27-30
-
-
Moch, H.1
Presti J.C., Jr.2
Sauter, G.3
Buchholz, N.4
Jordan, P.5
Mihatsch, M.J.6
Waldman, F.M.7
-
19
-
-
0033938241
-
Signaturebased analysis of MET proto-oncogene mutations using DHPLC
-
Nickerson ML, Weirich G, Zbar B, Schmidt LS. 2000. Signaturebased analysis of MET proto-oncogene mutations using DHPLC. Hum Mutat 16:68-76.
-
(2000)
Hum Mutat
, vol.16
, pp. 68-76
-
-
Nickerson, M.L.1
Weirich, G.2
Zbar, B.3
Schmidt, L.S.4
-
20
-
-
0035064685
-
Molecular cytogenetic characterization of early and late renal cell carcinomas in von Hippel-Lindau (VHL) disease with spectral karyotyping (SKY)
-
Phillips JL, Ghadimi BM, Wangsa D, Padilla-Nash H, Worrell R, Hewitt S, Walther MM, Linehan WM, Klausner RD, Ried T. 2001. Molecular cytogenetic characterization of early and late renal cell carcinomas in von Hippel-Lindau (VHL) disease with spectral karyotyping (SKY). Genes Chromosomes Cancer 31:1-9.
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 1-9
-
-
Phillips, J.L.1
Ghadimi, B.M.2
Wangsa, D.3
Padilla-Nash, H.4
Worrell, R.5
Hewitt, S.6
Walther, M.M.7
Linehan, W.M.8
Klausner, R.D.9
Ried, T.10
-
21
-
-
0032322577
-
Initiating genetic events in small renal neoplasms detected by comparative genomic hybridization
-
Presti JC Jr, Moch H, Gelb AB, Huynh D, Waldman FM. 1998. Initiating genetic events in small renal neoplasms detected by comparative genomic hybridization. J Urol 160:1557-1561.
-
(1998)
J Urol
, vol.160
, pp. 1557-1561
-
-
Presti J.C., Jr.1
Moch, H.2
Gelb, A.B.3
Huynh, D.4
Waldman, F.M.5
-
22
-
-
0036160550
-
Allelic loss on chromosomes 8 and 9 correlates with clinical outcome in locally advanced clear cell carcinoma of the kidney
-
Presti JC Jr, Wilhelm M, Reuter V, Russo P, Motzer R, Waldman F. 2002. Allelic loss on chromosomes 8 and 9 correlates with clinical outcome in locally advanced clear cell carcinoma of the kidney. J Urol 167:1464-1468.
-
(2002)
J Urol
, vol.167
, pp. 1464-1468
-
-
Presti J.C., Jr.1
Wilhelm, M.2
Reuter, V.3
Russo, P.4
Motzer, R.5
Waldman, F.6
-
23
-
-
0027282013
-
Chromosome 17p deletions and p53 mutations in renal cell carcinoma
-
Reiter RE, Anglard P, Liu S, Gnarra JR, Linehan WM. 1993. Chromosome 17p deletions and p53 mutations in renal cell carcinoma. Cancer Res 53:3092-3097.
-
(1993)
Cancer Res
, vol.53
, pp. 3092-3097
-
-
Reiter, R.E.1
Anglard, P.2
Liu, S.3
Gnarra, J.R.4
Linehan, W.M.5
-
24
-
-
0034860286
-
Genomic imbalances in 61 renal cancers from the proximal tubulus detected by comparative genomic hybridization
-
Reutzel D, Mende M, Naumann S, Störkel S, Brenner W, Zabel B, Decker J. 2001. Genomic imbalances in 61 renal cancers from the proximal tubulus detected by comparative genomic hybridization. Cytogenet Cell Genet 93:221-227.
-
(2001)
Cytogenet Cell Genet
, vol.93
, pp. 221-227
-
-
Reutzel, D.1
Mende, M.2
Naumann, S.3
Störkel, S.4
Brenner, W.5
Zabel, B.6
Decker, J.7
-
25
-
-
0030853274
-
Tumor cytogenetics revisited: Comparative genomic hybridization and spectral karyotyping
-
Ried T, Liyanage M, du Manoir S, Heselmeyer K, Auer G, Macville M, Schröck E. 1997. Tumor cytogenetics revisited: comparative genomic hybridization and spectral karyotyping. J Mol Med 75:801-814.
-
(1997)
J Mol Med
, vol.75
, pp. 801-814
-
-
Ried, T.1
Liyanage, M.2
Du Manoir, S.3
Heselmeyer, K.4
Auer, G.5
Macville, M.6
Schröck, E.7
-
26
-
-
0033035955
-
Genomic changes defining the genesis, progression, and malignancy potential in solid human tumors: A phenotype/genotype correlation
-
Ried T, Heselmeyer-Haddad K, Blegen H, Schröck E, Auer G. 1999. Genomic changes defining the genesis, progression, and malignancy potential in solid human tumors: a phenotype/genotype correlation. Genes Chromosomes Cancer 25:195-204.
-
(1999)
Genes Chromosomes Cancer
, vol.25
, pp. 195-204
-
-
Ried, T.1
Heselmeyer-Haddad, K.2
Blegen, H.3
Schröck, E.4
Auer, G.5
-
27
-
-
17344381429
-
Germline and somatic mutations in the tyrosine kinase domain of the MET protooncogene in papillary renal carcinomas
-
Schmidt L, Duh F-M, Chen F, Kishida T, Glenn G, Choyke P, Scherer SW, Zhuang Z, Lubensky IA, Dean M, Allikmets R, Chidambaram A, Bergerheim UR, Feltis TJ, Casadevall C, Zamarron A, Bernues M, Richard S, Lips CJM, Walther MM, Tsui L, Geil L, Orcutt ML, Stackhouse T, Lipan J, Slife L, Brauch H, Decker J, Niehans G, Hughson MD, Moch H, Störkel S, Lerman MI, Linehan WM, Zbar B. 1997. Germline and somatic mutations in the tyrosine kinase domain of the MET protooncogene 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
Zhuang, Z.8
Lubensky, I.A.9
Dean, M.10
Allikmets, R.11
Chidambaram, A.12
Bergerheim, U.R.13
Feltis, T.J.14
Casadevall, C.15
Zamarron, A.16
Bernues, M.17
Richard, S.18
Lips, C.J.M.19
Walther, M.M.20
Tsui, L.21
Geil, L.22
Orcutt, M.L.23
Stackhouse, T.24
Lipan, J.25
Slife, L.26
Brauch, H.27
Decker, J.28
Niehans, G.29
Hughson, M.D.30
Moch, H.31
Störkel, S.32
Lerman, M.I.33
Linehan, W.M.34
Zbar, B.35
more..
-
28
-
-
0038214755
-
Multicolor spectral karyotyping of human chromosomes
-
Schröck E, du Manoir S, Veldman T, Schoell B, Wienberg J, Ferguson-Smith MA, Ning Y, Ledbetter, DH, Bar-Am I, Soenksen D, Garini Y, Ried T. 1996. Multicolor spectral karyotyping of human chromosomes. Science 273:494-497.
-
(1996)
Science
, vol.273
, pp. 494-497
-
-
Schröck, E.1
Du Manoir, S.2
Veldman, T.3
Schoell, B.4
Wienberg, J.5
Ferguson-Smith, M.A.6
Ning, Y.7
Ledbetter, D.H.8
Bar-Am, I.9
Soenksen, D.10
Garini, Y.11
Ried, T.12
-
29
-
-
7844234770
-
Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene
-
Stolle C, Glenn G, Zbar B, Humphrey JS, Choyke P, Walther M, Pack S, Hurley K, Andrey C, Klausner R, Linehan WM. 1998. Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene. Hum Mutat 12:417-423.
-
(1998)
Hum Mutat
, vol.12
, pp. 417-423
-
-
Stolle, C.1
Glenn, G.2
Zbar, B.3
Humphrey, J.S.4
Choyke, P.5
Walther, M.6
Pack, S.7
Hurley, K.8
Andrey, C.9
Klausner, R.10
Linehan, W.M.11
-
30
-
-
0034009646
-
Molecular cytogenetic analysis of 17 renal cancer cell lines: Increased copy number at 5q31-33 in cell lines from nonpapillary carcinomas
-
Yang ZQ, Yoshida MA, Fukuda Y, Kurihara N, Nakamura Y, Inazawa J. 2000. Molecular cytogenetic analysis of 17 renal cancer cell lines: increased copy number at 5q31-33 in cell lines from nonpapillary carcinomas. Jpn J Cancer Res 91:156-163.
-
(2000)
Jpn J Cancer Res
, vol.91
, pp. 156-163
-
-
Yang, Z.Q.1
Yoshida, M.A.2
Fukuda, Y.3
Kurihara, N.4
Nakamura, Y.5
Inazawa, J.6
-
31
-
-
0029165763
-
Renal cell carcinoma. Cytogenetic analysis of tumors and cell lines
-
Zhao WP, Gnarra JR, Liu S, Knutsen T, Linehan WM, Whang-Peng J. 1995. Renal cell carcinoma. Cytogenetic analysis of tumors and cell lines. Cancer Genet Cytogenet 82:128-139.
-
(1995)
Cancer Genet Cytogenet
, vol.82
, pp. 128-139
-
-
Zhao, W.P.1
Gnarra, J.R.2
Liu, S.3
Knutsen, T.4
Linehan, W.M.5
Whang-Peng, J.6
-
32
-
-
17344373892
-
Trisomy 7-harbouring non-random duplication of the mutant MET allele in hereditary papillary renal carcinomas
-
Zhuang Z. Park WS, Pack S, Schmidt L, Vortmeyer AO, Pak E, Pham T, Weil RJ, Candidus S, Lubensky IA, Linehan WM, Zbar B, Weirich G. 1998. Trisomy 7-harbouring non-random duplication of the mutant MET allele in hereditary papillary renal carcinomas. Nat Genet 20:66-69.
-
(1998)
Nat Genet
, vol.20
, pp. 66-69
-
-
Zhuang, Z.1
Park, W.S.2
Pack, S.3
Schmidt, L.4
Vortmeyer, A.O.5
Pak, E.6
Pham, T.7
Weil, R.J.8
Candidus, S.9
Lubensky, I.A.10
Linehan, W.M.11
Zbar, B.12
Weirich, G.13
|