-
1
-
-
0031963294
-
Cancer statistics, 1998
-
Landis, S. H., Murray, T., Bolden, S., and Wingo, P. A. Cancer statistics, 1998. CA Cancer J. Clin., 48: 6-29, 1998.
-
(1998)
CA Cancer J. Clin.
, vol.48
, pp. 6-29
-
-
Landis, S.H.1
Murray, T.2
Bolden, S.3
Wingo, P.A.4
-
2
-
-
0025312728
-
A genetic model for colorectal tumorigenesis
-
Fearon, E. R., and Vogelstein, B. A genetic model for colorectal tumorigenesis. Cell. 61: 759-767, 1990.
-
(1990)
Cell
, vol.61
, pp. 759-767
-
-
Fearon, E.R.1
Vogelstein, B.2
-
3
-
-
0028857682
-
Genetic alterations in breast cancer
-
Bièche, I., and Lidereau, R. Genetic alterations in breast cancer. Genes Chromosomes Cancer, 14: 227-251, 1995.
-
(1995)
Genes Chromosomes Cancer
, vol.14
, pp. 227-251
-
-
Bièche, I.1
Lidereau, R.2
-
4
-
-
0025250745
-
Allelotype of breast cancer: Cumulative allele losses promote tumor progression in primary breast cancer
-
Sato, T., Tanigami, A., Yamakawa, K., Akiyama, F., Kasumi, F., Sakamoto, G., and Nakamura, Y. Allelotype of breast cancer: cumulative allele losses promote tumor progression in primary breast cancer. Cancer Res., 50: 7184-7189, 1990.
-
(1990)
Cancer Res.
, vol.50
, pp. 7184-7189
-
-
Sato, T.1
Tanigami, A.2
Yamakawa, K.3
Akiyama, F.4
Kasumi, F.5
Sakamoto, G.6
Nakamura, Y.7
-
5
-
-
0026589399
-
Heterogeneity for allelic loss in human breast cancer
-
Chen, L. C., Kurisu, W., Ljung, B. M., Goldman, E. S., Moore, D., II, and Smith, H. S. Heterogeneity for allelic loss in human breast cancer. J. Natl. Cancer Inst., 84: 506-510, 1992.
-
(1992)
J. Natl. Cancer Inst.
, vol.84
, pp. 506-510
-
-
Chen, L.C.1
Kurisu, W.2
Ljung, B.M.3
Goldman, E.S.4
Moore D. II5
Smith, H.S.6
-
6
-
-
0027953579
-
Loss of heterozygosity and p53 gene mutations in breast cancer
-
Deng, G., Chen, L. C., Schott, D. R., Thor, A., Bhargava, V., Ljung, B. M., Chew, K., and Smith, H. S. Loss of heterozygosity and p53 gene mutations in breast cancer. Cancer Res., 54: 499-505, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 499-505
-
-
Deng, G.1
Chen, L.C.2
Schott, D.R.3
Thor, A.4
Bhargava, V.5
Ljung, B.M.6
Chew, K.7
Smith, H.S.8
-
7
-
-
0031938046
-
Mapping of a new target region of allelic loss to a 2-cm interval at 22q13.1 in primary breast cancer
-
Iida, A., Kurose, K., Isobe, R., Akiyama, F., Sakamoto, G., Yoshimoto, M., Kasumi, F., Nakamura, Y., and Emi, M. Mapping of a new target region of allelic loss to a 2-cM interval at 22q13.1 in primary breast cancer. Genes Chromosomes Cancer, 21: 108-112, 1998.
-
(1998)
Genes Chromosomes Cancer
, vol.21
, pp. 108-112
-
-
Iida, A.1
Kurose, K.2
Isobe, R.3
Akiyama, F.4
Sakamoto, G.5
Yoshimoto, M.6
Kasumi, F.7
Nakamura, Y.8
Emi, M.9
-
8
-
-
0032545728
-
Loss of heterozygosity at loci from chromosome arm 22q in human sporadic breast carcinomas
-
Allione, F., Eisenger, F., Parc, P., Noguchi, T., Sobol, H., and Birnbaum, D. Loss of heterozygosity at loci from chromosome arm 22q in human sporadic breast carcinomas. Int. J. Cancer, 75: 181-186, 1998.
-
(1998)
Int. J. Cancer
, vol.75
, pp. 181-186
-
-
Allione, F.1
Eisenger, F.2
Parc, P.3
Noguchi, T.4
Sobol, H.5
Birnbaum, D.6
-
9
-
-
0027405720
-
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor
-
Trofatter, J. A., MacCollin, M. M., Rutter, J. L., Murrell, J. R., Duyao, M. P., Parry, D. M., Eldridge, R., Kley, N., Menon, A. G., Pulaski, K., Haase, V. H., Ambrose, C. M., Munroe, D., Bove, C., Haines, J. L., Martuza, R. L., MacDonald, M. E., Seizinger, B. R., Short, M. P., Buckler, A. J., and Gusella, J. F. A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor. Cell, 72: 791-800, 1993.
-
(1993)
Cell
, vol.72
, pp. 791-800
-
-
Trofatter, J.A.1
MacCollin, M.M.2
Rutter, J.L.3
Murrell, J.R.4
Duyao, M.P.5
Parry, D.M.6
Eldridge, R.7
Kley, N.8
Menon, A.G.9
Pulaski, K.10
Haase, V.H.11
Ambrose, C.M.12
Munroe, D.13
Bove, C.14
Haines, J.L.15
Martuza, R.L.16
MacDonald, M.E.17
Seizinger, B.R.18
Short, M.P.19
Buckler, A.J.20
Gusella, J.F.21
more..
-
10
-
-
0030050417
-
Neurofibromatosis 2: Loss of Merlin's protective spell
-
Gusella, J. F., Ramesh, V., MacCollin, M., and Jacoby, L. B. Neurofibromatosis 2: loss of Merlin's protective spell. Curr. Opin. Genet. Dev., 6: 87-92, 1996.
-
(1996)
Curr. Opin. Genet. Dev.
, vol.6
, pp. 87-92
-
-
Gusella, J.F.1
Ramesh, V.2
MacCollin, M.3
Jacoby, L.B.4
-
11
-
-
0032835528
-
Mapping of a target region of allelic loss to a 0.5-cM interval on chromosome 22q13 in human colorectal cancer
-
Castells, A., Ino, Y., Louis, D. N., Ramesh, V., Gusella, J. F., and Rustgi, A. K. Mapping of a target region of allelic loss to a 0.5-cM interval on chromosome 22q13 in human colorectal cancer. Gastroenterology, 117: 831-837, 1999.
-
(1999)
Gastroenterology
, vol.117
, pp. 831-837
-
-
Castells, A.1
Ino, Y.2
Louis, D.N.3
Ramesh, V.4
Gusella, J.F.5
Rustgi, A.K.6
-
12
-
-
0030041917
-
Localization of an ovarian cancer tumor supressor gene to a 0.5-cM region between D22S284 and CYP2D. on chromosome 22q
-
Bryan, E. J., Watson, R. H., Davis, M., Hitchcock, A., Foulkes, W. D., and Campbell, I. G. Localization of an ovarian cancer tumor supressor gene to a 0.5-cM region between D22S284 and CYP2D. on chromosome 22q. Cancer Res., 56: 719-721. 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 719-721
-
-
Bryan, E.J.1
Watson, R.H.2
Davis, M.3
Hitchcock, A.4
Foulkes, W.D.5
Campbell, I.G.6
-
13
-
-
0032809735
-
Common regions of deletion on chromosome 22q12.3-q13.1 and 22q13.2 in human astrocytomas appear related to malignancy grade
-
Ino, Y., Silver, J. S., Blazejewski, L., Nishikawa, R., Matsutani, M., von Deimling, A., and Louis, D. N. Common regions of deletion on chromosome 22q12.3-q13.1 and 22q13.2 in human astrocytomas appear related to malignancy grade. J. Neuropathol. Exp. Neurol., 58: 881-885, 1999.
-
(1999)
J. Neuropathol. Exp. Neurol.
, vol.58
, pp. 881-885
-
-
Ino, Y.1
Silver, J.S.2
Blazejewski, L.3
Nishikawa, R.4
Matsutani, M.5
Von Deimling, A.6
Louis, D.N.7
-
14
-
-
0031687584
-
Allelic loss on chromosome 22 in oral cancer: Possibility of the existence of a tumor suppressor gene on 22q13
-
Miyakawa, A., Wang, X. L., Nakanishi, H., Imai, F. L., Shiiba, M., Miya, T., Imai, Y., and Tanzawa, H. Allelic loss on chromosome 22 in oral cancer: possibility of the existence of a tumor suppressor gene on 22q13. Int. J. Oncol., 13: 705-709, 1998.
-
(1998)
Int. J. Oncol.
, vol.13
, pp. 705-709
-
-
Miyakawa, A.1
Wang, X.L.2
Nakanishi, H.3
Imai, F.L.4
Shiiba, M.5
Miya, T.6
Imai, Y.7
Tanzawa, H.8
-
15
-
-
0032529238
-
Localization of putative tumor suppressor loci by genome-wide allelotyping in human pancreatic endocrine tumors
-
Chung, D. C., Brown, S. B., Graeme-Cook, F., Tillotson, L. G., Warshaw, A. L., Jensen, R. T., and Arnold, A. Localization of putative tumor suppressor loci by genome-wide allelotyping in human pancreatic endocrine tumors. Cancer Res., 58: 3706-3711, 1998.
-
(1998)
Cancer Res.
, vol.58
, pp. 3706-3711
-
-
Chung, D.C.1
Brown, S.B.2
Graeme-Cook, F.3
Tillotson, L.G.4
Warshaw, A.L.5
Jensen, R.T.6
Arnold, A.7
-
16
-
-
79960655760
-
The DNA sequence of chromosome 22
-
Dunham, I., Shimizu, N., Roe, B. A., Chissoe, S., et al. The DNA sequence of chromosome 22. Nature (Lond.), 402: 489-495, 1999.
-
(1999)
Nature (Lond.)
, vol.402
, pp. 489-495
-
-
Dunham, I.1
Shimizu, N.2
Roe, B.A.3
Chissoe, S.4
-
17
-
-
0022495380
-
Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma
-
Seizinger, B. R., Martuza, R. L., and Gusella, J. F. Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma. Nature (Lond.), 322: 644-647, 1986.
-
(1986)
Nature (Lond.)
, vol.322
, pp. 644-647
-
-
Seizinger, B.R.1
Martuza, R.L.2
Gusella, J.F.3
-
18
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib, C., Faure, S., Fizames, C., Samson, D., Drouot, N., Vignal, A., Millasscau, P., Marc, S., Hazan, J., Seboun, E., Lathrop, M., Gyapay, G., Morissette, J., and Weissenhach, J. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature (Lond.), 380: 152-154, 1996.
-
(1996)
Nature (Lond.)
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasscau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
Lathrop, M.11
Gyapay, G.12
Morissette, J.13
Weissenhach, J.14
-
19
-
-
0345003786
-
Deletion mapping of chromosomal region 1p32-pter in primary breast cancer
-
Bièche, I., Khodja, A., and Lidereau, R. Deletion mapping of chromosomal region 1p32-pter in primary breast cancer. Genes Chromosomes Cancer, 14: 255-263, 1999.
-
(1999)
Genes Chromosomes Cancer
, vol.14
, pp. 255-263
-
-
Bièche, I.1
Khodja, A.2
Lidereau, R.3
-
20
-
-
1842369666
-
Genetic alteration mapping on chromosome 7 in primary breast cancer
-
Bièche, I., Khodja, A., Driouch, K., and Lidereau, R. Genetic alteration mapping on chromosome 7 in primary breast cancer. Clin. Cancer Res., 3: 1009-1016, 1997.
-
(1997)
Clin. Cancer Res.
, vol.3
, pp. 1009-1016
-
-
Bièche, I.1
Khodja, A.2
Driouch, K.3
Lidereau, R.4
-
21
-
-
0033566763
-
Two regions of deletion in 9p23-23 in sporadic breast cancer
-
An, H. X., Claas, A., Savelyeva, L., Seitz, S., Schlag, P., Scheerneck, S., and Schwab, M. Two regions of deletion in 9p23-23 in sporadic breast cancer. Cancer Res., 59: 3941-3943, 1999.
-
(1999)
Cancer Res.
, vol.59
, pp. 3941-3943
-
-
An, H.X.1
Claas, A.2
Savelyeva, L.3
Seitz, S.4
Schlag, P.5
Scheerneck, S.6
Schwab, M.7
-
22
-
-
0030593038
-
DPC4, a candidate tumor suppressor gene at human chromosome 18q21.1
-
Hahn, S. A., Schutte, M., Shamsul Hoque, A. T. M., Moskaluk, C. A., daCosta, L. T., Rozenblum, E., Weinstein, C. L., Fischer, A., Yeo, C. J., Hraban, R. H., and Kern, S. E. DPC4, a candidate tumor suppressor gene at human chromosome 18q21.1. Science (Washington DC), 271: 350-353, 1996.
-
(1996)
Science (Washington DC)
, vol.271
, pp. 350-353
-
-
Hahn, S.A.1
Schutte, M.2
Shamsul Hoque, A.T.M.3
Moskaluk, C.A.4
DaCosta, L.T.5
Rozenblum, E.6
Weinstein, C.L.7
Fischer, A.8
Yeo, C.J.9
Hraban, R.H.10
Kern, S.E.11
-
23
-
-
0030892416
-
Comparative genomic hybridization of ductal carcinoma in situ of the breast; identification of regions of DNA amplification and deletion in common with invasive breast carcinoma
-
James, L. A., Mitchell, E. L. D., Menasce, L., and Varley, J. M. Comparative genomic hybridization of ductal carcinoma in situ of the breast; identification of regions of DNA amplification and deletion in common with invasive breast carcinoma. Oncogene, 14: 1059-1065, 1997.
-
(1997)
Oncogene
, vol.14
, pp. 1059-1065
-
-
James, L.A.1
Mitchell, E.L.D.2
Menasce, L.3
Varley, J.M.4
-
24
-
-
0025066085
-
Genomic alteration in human breast carcinomas
-
Larsson, C., Bystrom, C., Skoog, L., Rotstein, S., and Nordenskjold, M. Genomic alteration in human breast carcinomas. Genes Chromosomes Cancer, 2: 191-197. 1990.
-
(1990)
Genes Chromosomes Cancer
, vol.2
, pp. 191-197
-
-
Larsson, C.1
Bystrom, C.2
Skoog, L.3
Rotstein, S.4
Nordenskjold, M.5
-
25
-
-
0032532082
-
Comparative genomic hybridization analysis of lobular carcinoma in situ and atypical lobular hyperplasia and potential roles for gains and losses of genetic material in breast neoplasia
-
Lu, Y. J., Osin, P., Lakhani, S. R., Di Palma, S., Gusterson, B. A., and Shipley, J. M. Comparative genomic hybridization analysis of lobular carcinoma in situ and atypical lobular hyperplasia and potential roles for gains and losses of genetic material in breast neoplasia. Cancer Res., 58: 4721-4727, 1998.
-
(1998)
Cancer Res.
, vol.58
, pp. 4721-4727
-
-
Lu, Y.J.1
Osin, P.2
Lakhani, S.R.3
Di Palma, S.4
Gusterson, B.A.5
Shipley, J.M.6
|