-
1
-
-
0028790326
-
Terminal deletion of chromosome 3p sequences in nonpapillary renal cell carcinomas: A breakpoint cluster between loci D3S1285 and D3S1603
-
Wilhelm M, Bugert P, Kenck C, et al: Terminal deletion of chromosome 3p sequences in nonpapillary renal cell carcinomas: A breakpoint cluster between loci D3S1285 and D3S1603. Cancer Res 55:5383-5385, 1995
-
(1995)
Cancer Res
, vol.55
, pp. 5383-5385
-
-
Wilhelm, M.1
Bugert, P.2
Kenck, C.3
-
2
-
-
0027954044
-
Mutations of the VHL tumour suppressor gene in renal carcinoma
-
Gnarra JR, Tory K, Weng Y, et al: Mutations of the VHL tumour suppressor gene in renal carcinoma. Nat Gen 7:85-90, 1994
-
(1994)
Nat Gen
, vol.7
, pp. 85-90
-
-
Gnarra, J.R.1
Tory, K.2
Weng, Y.3
-
3
-
-
0029944971
-
Mutation of the VHL gene is associated exclusively with the development of non-papillary renal cell carcinomas
-
Kenck C, Wilhelm M, Bugert P, et al: Mutation of the VHL gene is associated exclusively with the development of non-papillary renal cell carcinomas. J Pathol 179:157-161, 1996
-
(1996)
J Pathol
, vol.179
, pp. 157-161
-
-
Kenck, C.1
Wilhelm, M.2
Bugert, P.3
-
5
-
-
0027258065
-
Tumor suppressor gene allelic loss in human renal cancers
-
Brooks JD, Bova GS, Marshall FF, et al: Tumor suppressor gene allelic loss in human renal cancers. J Urol 150:1278-1283, 1993
-
(1993)
J Urol
, vol.150
, pp. 1278-1283
-
-
Brooks, J.D.1
Bova, G.S.2
Marshall, F.F.3
-
6
-
-
0028091126
-
Molecular genetic investigation of sporadic renal cell carcinoma: Analysis of allele loss on chromosomes 3p, 5q, 11p, 17 and 22
-
Foster K, Crossey PA, Cairns P, et al: Molecular genetic investigation of sporadic renal cell carcinoma: analysis of allele loss on chromosomes 3p, 5q, 11p, 17 and 22. Br J Cancer 69:230-234, 1994
-
(1994)
Br J Cancer
, vol.69
, pp. 230-234
-
-
Foster, K.1
Crossey, P.A.2
Cairns, P.3
-
7
-
-
0025017058
-
Allelic losses of chromosomes 9, 11, and 17 in human bladder cancer
-
Tsai YC, Nichols PW, Hiti AL, et al: Allelic losses of chromosomes 9, 11, and 17 in human bladder cancer. Cancer Res 50:44-47, 1990
-
(1990)
Cancer Res
, vol.50
, pp. 44-47
-
-
Tsai, Y.C.1
Nichols, P.W.2
Hiti, A.L.3
-
8
-
-
0027516042
-
Initiation of bladder cancer may involve deletion of a tumour-suppressor gene on chromosome 9
-
Cairns P, Shaw ME, Knowles MA: Initiation of bladder cancer may involve deletion of a tumour-suppressor gene on chromosome 9. Oncogene 8:1083-1085, 1993
-
(1993)
Oncogene
, vol.8
, pp. 1083-1085
-
-
Cairns, P.1
Shaw, M.E.2
Knowles, M.A.3
-
9
-
-
0028158767
-
Frequent loss of chromosome 9 in human primary non-small cell lung cancer
-
Merlo A, Gabrielson E, Askin F, et al: Frequent loss of chromosome 9 in human primary non-small cell lung cancer. Cancer Res 54:640-642, 1994
-
(1994)
Cancer Res
, vol.54
, pp. 640-642
-
-
Merlo, A.1
Gabrielson, E.2
Askin, F.3
-
10
-
-
0026627965
-
Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9
-
Gailani MR, Bale SJ, Leffell DJ, et al: Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9. Cell 69:111-117, 1992
-
(1992)
Cell
, vol.69
, pp. 111-117
-
-
Gailani, M.R.1
Bale, S.J.2
Leffell, D.J.3
-
11
-
-
0028008679
-
Progression of basal cell carcinoma through loss of chromosome 9q and inactivation of a single p53 allele
-
van der Riet P, Karp D, Farmer E, et al: Progression of basal cell carcinoma through loss of chromosome 9q and inactivation of a single p53 allele. Cancer Res 54:25-27, 1994
-
(1994)
Cancer Res
, vol.54
, pp. 25-27
-
-
Van der Riet, P.1
Karp, D.2
Farmer, E.3
-
12
-
-
0031881427
-
Mutations in the human homologue of the Drosophila patched gene in esophageal squamous cell carcinoma
-
Maesawa C, Tamura G, Iwaya T, et al: Mutations in the human homologue of the Drosophila patched gene in esophageal squamous cell carcinoma. Genes Chromosomes Cancer 21:276-279, 1998
-
(1998)
Genes Chromosomes Cancer
, vol.21
, pp. 276-279
-
-
Maesawa, C.1
Tamura, G.2
Iwaya, T.3
-
13
-
-
0031036694
-
Sporadic medulloblastomas contain PTCH mutations
-
Raffel C, Jenkins RB, Frederick L, et al: Sporadic medulloblastomas contain PTCH mutations. Cancer Res 57:842-845, 1997
-
(1997)
Cancer Res
, vol.57
, pp. 842-845
-
-
Raffel, C.1
Jenkins, R.B.2
Frederick, L.3
-
14
-
-
15644373337
-
Mutations of the PATCHED gene in several types of sporadic extracutaneous tumors
-
Xie J, Johnson RL, Zhang X, et al: Mutations of the PATCHED gene in several types of sporadic extracutaneous tumors. Cancer Res 57:2369-2372, 1997
-
(1997)
Cancer Res
, vol.57
, pp. 2369-2372
-
-
Xie, J.1
Johnson, R.L.2
Zhang, X.3
-
15
-
-
0031717394
-
Dinucleotide repeat polymorphism within the tumor suppressor gene PTCH at 9q22
-
Louhelainen J, Lindstrom E, Hemminki K, et al: Dinucleotide repeat polymorphism within the tumor suppressor gene PTCH at 9q22. Clin Genet 54:239-241, 1998
-
(1998)
Clin Genet
, vol.54
, pp. 239-241
-
-
Louhelainen, J.1
Lindstrom, E.2
Hemminki, K.3
-
16
-
-
0003903343
-
-
Woodbury, NY, Cold Spring Harbor Laboratory Press
-
Sambrook J, Fritschookstein EF, Maniatis T: Molecular Cloning: A Laboratory Manual (2nd ed). Woodbury, NY, Cold Spring Harbor Laboratory Press, 1989
-
(1989)
Molecular Cloning: A Laboratory Manual (2nd ed.)
-
-
Sambrook, J.1
Fritschookstein, E.F.2
Maniatis, T.3
-
19
-
-
0028868209
-
Localization of tumor suppressor loci on chromosome 9 in primary human renal cell carcinomas
-
Cairns P, Tokino K, Eby Y, et al: Localization of tumor suppressor loci on chromosome 9 in primary human renal cell carcinomas. Cancer Res 55:224-227, 1995
-
(1995)
Cancer Res
, vol.55
, pp. 224-227
-
-
Cairns, P.1
Tokino, K.2
Eby, Y.3
-
20
-
-
0030848639
-
Loss of heterozygosity at chromosomes 8p, 9p, and 14q is associated with stage and grade of non-papillary renal cell carcinomas
-
Schullerus D, Herbers J, Chudek J, et al: Loss of heterozygosity at chromosomes 8p, 9p, and 14q is associated with stage and grade of non-papillary renal cell carcinomas. J Pathol 183:151-155, 1997
-
(1997)
J Pathol
, vol.183
, pp. 151-155
-
-
Schullerus, D.1
Herbers, J.2
Chudek, J.3
-
21
-
-
0034746254
-
CDKNA2A mutation analysis, protein expression, and deletion mapping of chromosome 9p in conventional clear-cell renal carcinomas: Evidence for a second tumor suppressor gene proximal to CDKN2A
-
Schraml P, Struckmann K, Bednar R, et al: CDKNA2A mutation analysis, protein expression, and deletion mapping of chromosome 9p in conventional clear-cell renal carcinomas: Evidence for a second tumor suppressor gene proximal to CDKN2A. Am J Pathol 158:593-601, 2001
-
(2001)
Am J Pathol
, vol.158
, pp. 593-601
-
-
Schraml, P.1
Struckmann, K.2
Bednar, R.3
-
22
-
-
0032878968
-
Characteristic loss of heterozygosity in chromosome 3P and low frequency of replication errors in sporadic renal cell carcinoma
-
Chino K, Esumi M, Ishida H, et al: Characteristic loss of heterozygosity in chromosome 3P and low frequency of replication errors in sporadic renal cell carcinoma. J Urol 162:614-618, 1999
-
(1999)
J Urol
, vol.162
, pp. 614-618
-
-
Chino, K.1
Esumi, M.2
Ishida, H.3
-
23
-
-
0034322262
-
Genetic alterations in metastatic renal cell carcinoma detected by comparative genomic hybridization: Correlation with clinical and histological data
-
Junker K, Moravek P, Podhola M, et al: Genetic alterations in metastatic renal cell carcinoma detected by comparative genomic hybridization: Correlation with clinical and histological data. Int J Oncol 17:903-908, 2000
-
(2000)
Int J Oncol
, vol.17
, pp. 903-908
-
-
Junker, K.1
Moravek, P.2
Podhola, M.3
-
24
-
-
0029091503
-
Frequency of homozygous deletion at p16/CDKN2 in primary human tumours
-
Cairns P, Polascik TJ, Eby Y, et al: Frequency of homozygous deletion at p16/CDKN2 in primary human tumours. Nat Genet 11:210-212, 1995
-
(1995)
Nat Genet
, vol.11
, pp. 210-212
-
-
Cairns, P.1
Polascik, T.J.2
Eby, Y.3
-
25
-
-
0026483716
-
Homozygous deletions within human chromosome band 9p21 in melanoma
-
Fountain JW, Karayiorgou M, Ernstoff MS, et al: Homozygous deletions within human chromosome band 9p21 in melanoma. Proc Nat Acad Sci USA 89:10557-10561, 1992
-
(1992)
Proc Nat Acad Sci USA
, vol.89
, pp. 10557-10561
-
-
Fountain, J.W.1
Karayiorgou, M.2
Ernstoff, M.S.3
-
26
-
-
0343674751
-
Allelic loss at the D9S171 locus on chromosome 9p13 is associated with progression of papillary renal cell carcinoma
-
Schraml P, Muller D, Bednar R, et al: Allelic loss at the D9S171 locus on chromosome 9p13 is associated with progression of papillary renal cell carcinoma. J Pathol 190:457-461, 2000
-
(2000)
J Pathol
, vol.190
, pp. 457-461
-
-
Schraml, P.1
Muller, D.2
Bednar, R.3
-
27
-
-
15844386165
-
Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome
-
Hahn H, Wicking C, Zaphiropoulous PG, et al: Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. Cell 85:841-851, 1996
-
(1996)
Cell
, vol.85
, pp. 841-851
-
-
Hahn, H.1
Wicking, C.2
Zaphiropoulous, P.G.3
-
28
-
-
15844381336
-
Human homolog of patched, a candidate gene for the basal cell nervus syndrome
-
Johnson RL, Rothman AL, Xie J, et al: Human homolog of patched, a candidate gene for the basal cell nervus syndrome. Science 272:1668-1671, 1996
-
(1996)
Science
, vol.272
, pp. 1668-1671
-
-
Johnson, R.L.1
Rothman, A.L.2
Xie, J.3
-
29
-
-
0030239754
-
Is human patched the gatekeeper of common skin cancers?
-
letter; comment
-
Sidransky D: Is human patched the gatekeeper of common skin cancers? [letter; comment]. Nat Genet 14:7-8, 1996
-
(1996)
Nat Genet
, vol.14
, pp. 7-8
-
-
Sidransky, D.1
-
30
-
-
0030990735
-
Human patched (PTCH) mRNA is overexpressed consistently in tumor cells of both familial and sporadic basal cell carcinoma
-
Unden AB, Zaphiropoulos PG, Bruce K, et al: Human patched (PTCH) mRNA is overexpressed consistently in tumor cells of both familial and sporadic basal cell carcinoma. Cancer Res 57: 2336-2340, 1997
-
(1997)
Cancer Res
, vol.57
, pp. 2336-2340
-
-
Unden, A.B.1
Zaphiropoulos, P.G.2
Bruce, K.3
-
31
-
-
1842330252
-
Trichoepitheliomas contain somatic mutations in the overexpressed PTCH gene: Support for a gatekeeper mechanism in skin tumorigenesis
-
Vorechovsky I, Unden AB, Sandstedt B, et al: Trichoepitheliomas contain somatic mutations in the overexpressed PTCH gene: Support for a gatekeeper mechanism in skin tumorigenesis. Cancer Res 57:4677-4681, 1997
-
(1997)
Cancer Res
, vol.57
, pp. 4677-4681
-
-
Vorechovsky, I.1
Unden, A.B.2
Sandstedt, B.3
-
32
-
-
0030913169
-
Medulloblastomas of the desmoplastic variant carry mutations of the human homologue of Drosophila patched
-
Pietsch T, Waha A, Koch A, et al: Medulloblastomas of the desmoplastic variant carry mutations of the human homologue of Drosophila patched. Cancer Res 57:2085-2088, 1997
-
(1997)
Cancer Res
, vol.57
, pp. 2085-2088
-
-
Pietsch, T.1
Waha, A.2
Koch, A.3
-
33
-
-
0030738693
-
Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system
-
Wolter M, Reifenberger J, Sommer C, et al: Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system. Cancer Res 57:2581-2585, 1997
-
(1997)
Cancer Res
, vol.57
, pp. 2581-2585
-
-
Wolter, M.1
Reifenberger, J.2
Sommer, C.3
-
34
-
-
0030874617
-
Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours
-
Vorechovsky I, Tingby O, Hartman M, et al: Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours. Oncogene 15:361-366, 1997
-
(1997)
Oncogene
, vol.15
, pp. 361-366
-
-
Vorechovsky, I.1
Tingby, O.2
Hartman, M.3
|