-
1
-
-
0011153988
-
Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma
-
Kovacs G., Erlandsson R., Boldog F., et al. Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma. Proc Natl Acad Sci U S A 1989, 85:1571-1575.
-
(1989)
Proc Natl Acad Sci U S A
, vol.85
, pp. 1571-1575
-
-
Kovacs, G.1
Erlandsson, R.2
Boldog, F.3
-
2
-
-
0033559942
-
Loss of heterozygosity at 3p14.2 in clear cell renal cell carcinoma is an early event and is highly localized to the FHIT gene locus
-
Velickovic M., Delahunt B., Grebe S.K. Loss of heterozygosity at 3p14.2 in clear cell renal cell carcinoma is an early event and is highly localized to the FHIT gene locus. Cancer Res 1999, 59:1323-1326.
-
(1999)
Cancer Res
, vol.59
, pp. 1323-1326
-
-
Velickovic, M.1
Delahunt, B.2
Grebe, S.K.3
-
3
-
-
0033011629
-
Comparative allelotyping of the short arm human chromosome 3 in epithelial tumors of 4 different types
-
Braga E., Pugacheva E., Bazov I., et al. Comparative allelotyping of the short arm human chromosome 3 in epithelial tumors of 4 different types. FEBS Lett 1999, 454:215-219.
-
(1999)
FEBS Lett
, vol.454
, pp. 215-219
-
-
Braga, E.1
Pugacheva, E.2
Bazov, I.3
-
4
-
-
0027953797
-
Common regions of deletion in chromosome regions 3p12 and 3p14.2 in primary clear cell renal carcinomas
-
Lubinski J., Hadaczek P., Podolski J., et al. Common regions of deletion in chromosome regions 3p12 and 3p14.2 in primary clear cell renal carcinomas. Cancer Res 1994, 54:3710-3713.
-
(1994)
Cancer Res
, vol.54
, pp. 3710-3713
-
-
Lubinski, J.1
Hadaczek, P.2
Podolski, J.3
-
5
-
-
0037439819
-
Deletion of chromosome 3p14.2-p25 involving the VHL and FHIT genes in conventional renal cell carcinoma
-
Sukosd F., Kuroda N., Beothe T., et al. 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
-
-
Sukosd, F.1
Kuroda, N.2
Beothe, T.3
-
6
-
-
16644373473
-
Role of VHL gene mutation in human cancer
-
Kim W., Kaelin W.G. Role of VHL gene mutation in human cancer. J Clin Oncol 2004, 22:4993-5004.
-
(2004)
J Clin Oncol
, vol.22
, pp. 4993-5004
-
-
Kim, W.1
Kaelin, W.G.2
-
7
-
-
14644440800
-
The genetic basis of kidney cancer: Implications for gene-specific clinical management
-
Linehan W.M., Grubb R.L., Coleman J.A., et al. The genetic basis of kidney cancer: Implications for gene-specific clinical management. BJU Int 2005, 95(Suppl):2-7.
-
(2005)
BJU Int
, vol.95
, Issue.SUPPL.
, pp. 2-7
-
-
Linehan, W.M.1
Grubb, R.L.2
Coleman, J.A.3
-
9
-
-
0027954044
-
Mutation of the VHL tumor suppressor gene in renal cell carcinoma
-
Gnarra J.R., Tory K., Weng Y., et al. Mutation of the VHL tumor suppressor gene in renal cell 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
-
10
-
-
0034116801
-
Role of chromosome 3p12-p21 tumor suppressor genes in clear cell renal cell carcinoma: Analysis of VHL dependent and VHL independent pathways of tumorigenesis
-
Martinez A., Fullwood P., Kondo K., et al. Role of chromosome 3p12-p21 tumor suppressor genes in clear cell renal cell carcinoma: Analysis of VHL dependent and VHL independent pathways of tumorigenesis. Mol Pathol 2000, 53:137-144.
-
(2000)
Mol Pathol
, vol.53
, pp. 137-144
-
-
Martinez, A.1
Fullwood, P.2
Kondo, K.3
-
11
-
-
0034026499
-
Familial clear cell renal cell carcinoma (FCRC): Clinical features and mutation analysis of the VHL, MET, and CUL2 candidate genes
-
Woodward E.R., Clifford S.C., Astuti D., et al. Familial clear cell renal cell carcinoma (FCRC): Clinical features and mutation analysis of the VHL, MET, and CUL2 candidate genes. J Med Genet 2000, 37:348-353.
-
(2000)
J Med Genet
, vol.37
, pp. 348-353
-
-
Woodward, E.R.1
Clifford, S.C.2
Astuti, D.3
-
12
-
-
0031776704
-
Inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL independent pathway in clear cell renal tumorigenesis
-
Clifford S.C., Prowse A.H., Affara N.A., et al. Inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL independent pathway in clear cell renal tumorigenesis. Genes Chromosomes Cancer 1998, 22:200-209.
-
(1998)
Genes Chromosomes Cancer
, vol.22
, pp. 200-209
-
-
Clifford, S.C.1
Prowse, A.H.2
Affara, N.A.3
-
13
-
-
0028313966
-
A tumor suppressor locus within 3p14-p12 mediates rapid cell death of renal cell carcinoma in vivo
-
Sanchez Y., el-Naggar A., Pathak S., et al. A tumor suppressor locus within 3p14-p12 mediates rapid cell death of renal cell carcinoma in vivo. Proc Natl Acad Sci U S A 1994, 91:3383-3387.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 3383-3387
-
-
Sanchez, Y.1
el-Naggar, A.2
Pathak, S.3
-
14
-
-
0026443728
-
Definition of a tumor suppressor locus within human chromosome 3p21-p22
-
Killary A.M., Wolf E.M., Giambernardi T.A., et al. Definition of a tumor suppressor locus within human chromosome 3p21-p22. Proc Natl Acad Sci U S A 1992, 89:10877-10881.
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, pp. 10877-10881
-
-
Killary, A.M.1
Wolf, E.M.2
Giambernardi, T.A.3
-
15
-
-
0035030905
-
Proliferating cell nuclear antigen(PCNA) and epidermal growth factor receptor (EGFr) in renal cell carcinoma (RCC) patients with polysomy of chromosome 7
-
Amare Kadam P.S., Varghese C., Bharde S., et al. Proliferating cell nuclear antigen(PCNA) and epidermal growth factor receptor (EGFr) in renal cell carcinoma (RCC) patients with polysomy of chromosome 7. Cancer Genet Cytogenet 2000, 125:59-66.
-
(2000)
Cancer Genet Cytogenet
, vol.125
, pp. 59-66
-
-
Amare Kadam, P.S.1
Varghese, C.2
Bharde, S.3
-
16
-
-
0029653615
-
A second-generation YAC contig map of human chromosome 3
-
Gemmill R.M., Chumakov I., Scott P., et al. A second-generation YAC contig map of human chromosome 3. Nature 1995, 377(Suppl):299-319.
-
(1995)
Nature
, vol.377
, Issue.SUPPL.
, pp. 299-319
-
-
Gemmill, R.M.1
Chumakov, I.2
Scott, P.3
-
17
-
-
1642352674
-
Constitutional genomic instability, chromosome aberrations in tumor cells, and retinoblastoma
-
Amare P.S., Ghule P., Jose J., et al. Constitutional genomic instability, chromosome aberrations in tumor cells, and retinoblastoma. Cancer Genet Cytogenetics 2004, 150:33-43.
-
(2004)
Cancer Genet Cytogenetics
, vol.150
, pp. 33-43
-
-
Amare, P.S.1
Ghule, P.2
Jose, J.3
-
18
-
-
14744268243
-
Identification of various MLL gene aberrations that lead to MLL gene mutation in patients with acute lymphoblastic leukemia (ALL) and infants with acute leukemia
-
Pais A., Amare P.S., Raje G., et al. Identification of various MLL gene aberrations that lead to MLL gene mutation in patients with acute lymphoblastic leukemia (ALL) and infants with acute leukemia. Leukemia Res 2005, 29:517-526.
-
(2005)
Leukemia Res
, vol.29
, pp. 517-526
-
-
Pais, A.1
Amare, P.S.2
Raje, G.3
-
19
-
-
84884672162
-
Investigation of recurrent deletion loci specific to conventional renal cell carcinoma (cRCC) by comparative allelotyping in major epithelial carcinomas
-
in press
-
Bhat Singh R.R., Amare Kadam P.S. Investigation of recurrent deletion loci specific to conventional renal cell carcinoma (cRCC) by comparative allelotyping in major epithelial carcinomas. Ind J Urol 2011, in press.
-
(2011)
Ind J Urol
-
-
Bhat Singh, R.R.1
Amare Kadam, P.S.2
-
20
-
-
0037055570
-
Critical TSG regions on chromosome 3p in major human epithelial malignancies: Allelotyping and quantitative real-time PCR
-
Braga E., Senchenko V., Bazov I., et al. Critical TSG regions on chromosome 3p in major human epithelial malignancies: Allelotyping and quantitative real-time PCR. Int J Cancer 2002, 100:534-541.
-
(2002)
Int J Cancer
, vol.100
, pp. 534-541
-
-
Braga, E.1
Senchenko, V.2
Bazov, I.3
-
21
-
-
0033119769
-
Comparative genomic hybridization of breast tumors stratified by histological grade reveals new insights into the biological progression of breast cancer
-
Roylance R., Gorman P., Harris W., et al. Comparative genomic hybridization of breast tumors stratified by histological grade reveals new insights into the biological progression of breast cancer. Cancer Res 1999, 59:1433-1436.
-
(1999)
Cancer Res
, vol.59
, pp. 1433-1436
-
-
Roylance, R.1
Gorman, P.2
Harris, W.3
-
22
-
-
0034813489
-
Chromosome 3p allele loss in early invasive breast cancer: Detailed mapping and association with clinicopathologic features
-
Martinez A., Walker R.A., Shaw J.A., et al. Chromosome 3p allele loss in early invasive breast cancer: Detailed mapping and association with clinicopathologic features. Mol Pathol 2001, 54:300-306.
-
(2001)
Mol Pathol
, vol.54
, pp. 300-306
-
-
Martinez, A.1
Walker, R.A.2
Shaw, J.A.3
-
23
-
-
0035406393
-
High-resolution chromosome 3p allelotyping of breast carcinomas and precursor lesions demonstrates frequent loss of heterozygosity and a discontinuous pattern of allele loss
-
Maitra A., Wistuba I.I., Washington C., et al. High-resolution chromosome 3p allelotyping of breast carcinomas and precursor lesions demonstrates frequent loss of heterozygosity and a discontinuous pattern of allele loss. Am J Pathol 2001, 159:119-130.
-
(2001)
Am J Pathol
, vol.159
, pp. 119-130
-
-
Maitra, A.1
Wistuba, I.I.2
Washington, C.3
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