-
1
-
-
0003043601
-
Neoplasms of the central nervous system
-
V. T. DeVita, Jr., S. Hellman, and S. A. Rosenberg (eds.), Philadelphia: Lippincott-Raven Publishers
-
Neoplasms of the central nervous system. In: Louis, D. N., and Cavenee, W. K. In: V. T. DeVita, Jr., S. Hellman, and S. A. Rosenberg (eds.), Cancer: Principles and Practice of Oncology, Ed. 5, pp. 2013-2017. Philadelphia: Lippincott-Raven Publishers, 1997.
-
(1997)
Cancer: Principles and Practice of Oncology, Ed. 5
, pp. 2013-2017
-
-
Louis, D.N.1
Cavenee, W.K.2
-
2
-
-
0029397626
-
Molecular pathways in the formation of gliomas
-
von Deimling, A., Louis, D. N., and Wiestler, O. D. Molecular pathways in the formation of gliomas. Glia, 15: 328-338, 1995.
-
(1995)
Glia
, vol.15
, pp. 328-338
-
-
Von Deimling, A.1
Louis, D.N.2
Wiestler, O.D.3
-
3
-
-
0028618304
-
Deletion of p16 and p15 genes in brain tumors
-
Jen, J., Harper, J. W., Bigner, S. H., Bigner, D. D., Papadopoulos, N., Markowitz, S., Willson, J. K. V., Kinzler, K. W., and Vogelstein, B. Deletion of p16 and p15 genes in brain tumors. Cancer Res., 54: 6353-6358, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 6353-6358
-
-
Jen, J.1
Harper, J.W.2
Bigner, S.H.3
Bigner, D.D.4
Papadopoulos, N.5
Markowitz, S.6
Willson, J.K.V.7
Kinzler, K.W.8
Vogelstein, B.9
-
4
-
-
0028652269
-
CDKN2 (p16/ MTS1) gene deletion or CDK4 amplification occurs in the majority of glioblastomas
-
Schmidt, E. E., Ichimura, K., Reifenberger, G., and Collins. V. P. CDKN2 (p16/ MTS1) gene deletion or CDK4 amplification occurs in the majority of glioblastomas. Cancer Res., 54: 6321-6324, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 6321-6324
-
-
Schmidt, E.E.1
Ichimura, K.2
Reifenberger, G.3
Collins, V.P.4
-
5
-
-
0029736653
-
Human glioblastomas with no alterations of the CDKN2A (p16, INK4A, MTS1) and CDK4 genes have frequent mutations of the retinoblastoma gene
-
Ichimura, K., Schmidt, E. E., Goike, H. M., and Collins, V. P. Human glioblastomas with no alterations of the CDKN2A (p16, INK4A, MTS1) and CDK4 genes have frequent mutations of the retinoblastoma gene. Oncogene. 13: 1065-1072, 1996.
-
(1996)
Oncogene
, vol.13
, pp. 1065-1072
-
-
Ichimura, K.1
Schmidt, E.E.2
Goike, H.M.3
Collins, V.P.4
-
6
-
-
0029397307
-
The p53 gene and its role in human brain tumors
-
Bögler, O., Huang, H. J. S., Kleihues, P., and Cavenee, W. K. The p53 gene and its role in human brain tumors. Glia, 15: 308-327, 1995.
-
(1995)
Glia
, vol.15
, pp. 308-327
-
-
Bögler, O.1
Huang, H.J.S.2
Kleihues, P.3
Cavenee, W.K.4
-
7
-
-
0029398189
-
Gene amplification in human gliomas
-
Collins, V. P. Gene amplification in human gliomas. Glia, 15: 289-296, 1995.
-
(1995)
Glia
, vol.15
, pp. 289-296
-
-
Collins, V.P.1
-
8
-
-
0028198314
-
Alterations of the TP53 gene in human gliomas
-
Rasheed, B. K. A., McLendon, R. E., Herndon, J. E., Friedman, H. S., Friedman, A. H., Bigner, D. D., and Bigner, S. H. Alterations of the TP53 gene in human gliomas. Cancer Res., 54: 1324-1330, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 1324-1330
-
-
Rasheed, B.K.A.1
McLendon, R.E.2
Herndon, J.E.3
Friedman, H.S.4
Friedman, A.H.5
Bigner, D.D.6
Bigner, S.H.7
-
9
-
-
0029992049
-
Deletion mapping of gliomas suggests the presence of two small regions for candidate tumor-suppressor genes in a 17-cM interval on chromosome 10q
-
Albarosa, R., Colombo, B. M., Roz, L., Magnani, I., Pollo, B., Cirenei, N., Giani, C., Conti, A. M. F., DiDonato, S., and Finocchiaro, G. Deletion mapping of gliomas suggests the presence of two small regions for candidate tumor-suppressor genes in a 17-cM interval on chromosome 10q. Am. J. Hum. Genet., 58: 1260-1267, 1996.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1260-1267
-
-
Albarosa, R.1
Colombo, B.M.2
Roz, L.3
Magnani, I.4
Pollo, B.5
Cirenei, N.6
Giani, C.7
Conti, A.M.F.8
DiDonato, S.9
Finocchiaro, G.10
-
10
-
-
0026709506
-
Loss of heterozygosity for 10q loci in human gliomas
-
Rasheed, B. K. A., Fuller, G. N., Friedman, A. H., Darrel, D., Bigner, D. D. and Bigner, S. H. Loss of heterozygosity for 10q loci in human gliomas. Genes Chromosomes & Cancer, 5: 75-82, 1992.
-
(1992)
Genes Chromosomes & Cancer
, vol.5
, pp. 75-82
-
-
Rasheed, B.K.A.1
Fuller, G.N.2
Friedman, A.H.3
Darrel, D.4
Bigner, D.D.5
Bigner, S.H.6
-
11
-
-
0027208575
-
Loss of heterozygosity in malignant gliomas involves at least three distinct regions on chromosome 10
-
Karlbom, A. E., James, C. D., Boethius, J., Cavenee, W. K., Collins, V. P., Norden-Skjöld M., and Larsson, C. Loss of heterozygosity in malignant gliomas involves at least three distinct regions on chromosome 10. Hum. Genet., 92: 169-174, 1993.
-
(1993)
Hum. Genet.
, vol.92
, pp. 169-174
-
-
Karlbom, A.E.1
James, C.D.2
Boethius, J.3
Cavenee, W.K.4
Collins, V.P.5
Norden-Skjöld, M.6
Larsson, C.7
-
12
-
-
0026710064
-
Association of epidermal growth factor receptor gene amplification with loss of chromosome 10 in human glioblastoma multiforme
-
von Deimling, A., Louis, D. N., von Ammon, K., Petersen, I., Hoell, T., Chung, R. Y., Martuza, R. L., Schoenfeld, D. A., Yasargil, G., Wiestler, O. D., and Seizinger, B. R. Association of epidermal growth factor receptor gene amplification with loss of chromosome 10 in human glioblastoma multiforme. J. Neurosurg., 77: 295-301, 1992.
-
(1992)
J. Neurosurg.
, vol.77
, pp. 295-301
-
-
Von Deimling, A.1
Louis, D.N.2
Von Ammon, K.3
Petersen, I.4
Hoell, T.5
Chung, R.Y.6
Martuza, R.L.7
Schoenfeld, D.A.8
Yasargil, G.9
Wiestler, O.D.10
Seizinger, B.R.11
-
13
-
-
0030936323
-
PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer
-
Washington DC
-
Li, J., Yen, C., Liaw, D., Podsypanina, K., Bose, S., Wang, S. I., Puc, J., Miliaresis, C., Rodgers, L., McCombie, R., Bigner, S. H., Giovanella, B. C., Ittmann, M., Tycko, B., Hibshoosh, H., Wigler, M. H., and Parsons, R. PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science (Washington DC), 275: 1943-1947, 1997.
-
(1997)
Science
, vol.275
, pp. 1943-1947
-
-
Li, J.1
Yen, C.2
Liaw, D.3
Podsypanina, K.4
Bose, S.5
Wang, S.I.6
Puc, J.7
Miliaresis, C.8
Rodgers, L.9
McCombie, R.10
Bigner, S.H.11
Giovanella, B.C.12
Ittmann, M.13
Tycko, B.14
Hibshoosh, H.15
Wigler, M.H.16
Parsons, R.17
-
14
-
-
17144436629
-
Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers
-
Steck, P. A., Pershouse, M. A., Jasser, S. A., Yung, W. K. A., Lin, H., Ligon, A. H., Langford, L. A., Baumgard, M. L., Hattier, T., Davis, T., Frye, C., Hu, R., Swedlund, B., Teng, D. H. F., and Tavtigian, S. V. Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers. Nat. Genet., 15: 356-362, 1997.
-
(1997)
Nat. Genet.
, vol.15
, pp. 356-362
-
-
Steck, P.A.1
Pershouse, M.A.2
Jasser, S.A.3
Yung, W.K.A.4
Lin, H.5
Ligon, A.H.6
Langford, L.A.7
Baumgard, M.L.8
Hattier, T.9
Davis, T.10
Frye, C.11
Hu, R.12
Swedlund, B.13
Teng, D.H.F.14
Tavtigian, S.V.15
-
15
-
-
0031001041
-
TEP1, encoded by a candidate tumor suppressor locus, is a novel protein tyrosine phosphatase regulated by transforming growth factor β
-
Li, D., and Sun, H. TEP1, encoded by a candidate tumor suppressor locus, is a novel protein tyrosine phosphatase regulated by transforming growth factor β. Cancer Res., 57: 2124-2129, 1997.
-
(1997)
Cancer Res.
, vol.57
, pp. 2124-2129
-
-
Li, D.1
Sun, H.2
-
16
-
-
0031004088
-
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome
-
Liaw, D., Marsh, D. J., Li, J., Dahia, D. L. M., Wang, S. I., Zheng, Z., Bose, S., Call, K. M., Tsou, H. C., Peacocke, M., Eng, C., and Parsons, R. Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nat. Genet., 16: 64-67, 1997.
-
(1997)
Nat. Genet.
, vol.16
, pp. 64-67
-
-
Liaw, D.1
Marsh, D.J.2
Li, J.3
Dahia, D.L.M.4
Wang, S.I.5
Zheng, Z.6
Bose, S.7
Call, K.M.8
Tsou, H.C.9
Peacocke, M.10
Eng, C.11
Parsons, R.12
-
17
-
-
0028930619
-
MTS1/p16/CDKN2 lesions in primary glioblastoma multiforme
-
Moulton, T., Samara, G., Chung, W. Y., Yuan, L., Desai, R., Sisti, M., Bruce, J., and Tycko, B. MTS1/p16/CDKN2 lesions in primary glioblastoma multiforme. Am. J. Pathol., 146: 613-619, 1995.
-
(1995)
Am. J. Pathol.
, vol.146
, pp. 613-619
-
-
Moulton, T.1
Samara, G.2
Chung, W.Y.3
Yuan, L.4
Desai, R.5
Sisti, M.6
Bruce, J.7
Tycko, B.8
-
18
-
-
0029416826
-
An STS-based map of the human genome
-
Washington DC
-
Hudson, T. J., Stein, L. D., Gerety, S. S., Ma. J., Castle, A. B., Silva, J., Slonim, D. K., Baptista, R., Druglyak, L., Xu, S. H., Hu, X., Colbert, A. M. E., Rosenberg, C., Reeve-Daly, M. P., Rozen, S., Hui, L., Wu, X., Vestergaard, C., Wilson, K. M., Bae, J. S., Maitra, S., Ganiatsas, S., Evans, C. A., DeAngelis, M. M., Ingalls, K. A., Nahf, R. W., Horton, L. T., Jr., Anderson, M. O., Collymore, A. J., Ye, W., Kouyoumjian, V., Zemsteva, I. S., Tam, J., Devine, R., Courtney, D. F., Renaud, M. T., Nguyen, H., O'Connor, T. J., Fizames, C., Faure, S., Gyapay, G., Dib, C., Morissette, J., Orlin, J. B., Birren, B. W., Goodman, N., Weissenbach, J., Hawkins, T. L., Foote, S., Page, D. C., and Landers, E. S. An STS-based map of the human genome. Science (Washington DC), 270: 1945-1954, 1995.
-
(1995)
Science
, vol.270
, pp. 1945-1954
-
-
Hudson, T.J.1
Stein, L.D.2
Gerety, S.S.3
Ma, J.4
Castle, A.B.5
Silva, J.6
Slonim, D.K.7
Baptista, R.8
Druglyak, L.9
Xu, S.H.10
Hu, X.11
Colbert, A.M.E.12
Rosenberg, C.13
Reeve-Daly, M.P.14
Rozen, S.15
Hui, L.16
Wu, X.17
Vestergaard, C.18
Wilson, K.M.19
Bae, J.S.20
Maitra, S.21
Ganiatsas, S.22
Evans, C.A.23
DeAngelis, M.M.24
Ingalls, K.A.25
Nahf, R.W.26
Horton Jr., L.T.27
Anderson, M.O.28
Collymore, A.J.29
Ye, W.30
Kouyoumjian, V.31
Zemsteva, I.S.32
Tam, J.33
Devine, R.34
Courtney, D.F.35
Renaud, M.T.36
Nguyen, H.37
O'Connor, T.J.38
Fizames, C.39
Faure, S.40
Gyapay, G.41
Dib, C.42
Morissette, J.43
Orlin, J.B.44
Birren, B.W.45
Goodman, N.46
Weissenbach, J.47
Hawkins, T.L.48
Foote, S.49
Page, D.C.50
Landers, E.S.51
more..
-
19
-
-
0029091503
-
Frequency of homozygous deletion at p16/CDKN2 in primary human tumours
-
Cairns, P., Polascik, T. J., Eby, Y., Tokino, K., Califano, J., Merlo, A., Mao, L., Herath, J., Jenkins, R., Westra, W., Rutter, J. L., Buckler, A., Gabrielson, E., Tockman, M., Cho, K. R., Hedrick, L., Bova, G. S., Isaacs, W., Koch, W., Schwab, D., and Sidransky, D. 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
Tokino, K.4
Califano, J.5
Merlo, A.6
Mao, L.7
Herath, J.8
Jenkins, R.9
Westra, W.10
Rutter, J.L.11
Buckler, A.12
Gabrielson, E.13
Tockman, M.14
Cho, K.R.15
Hedrick, L.16
Bova, G.S.17
Isaacs, W.18
Koch, W.19
Schwab, D.20
Sidransky, D.21
more..
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