-
1
-
-
0022547592
-
Hepatitis B virus DNA integration in a sequence homologous to v-erb-A and steroid receptor genes in a hepatocellular carcinoma
-
Dejean, A., Bougueleret, L., Grzeschik, K. H. and Tiollais, P. Hepatitis B virus DNA integration in a sequence homologous to v-erb-A and steroid receptor genes in a hepatocellular carcinoma. Nature, 322, 70-72 (1986).
-
(1986)
Nature
, vol.322
, pp. 70-72
-
-
Dejean, A.1
Bougueleret, L.2
Grzeschik, K.H.3
Tiollais, P.4
-
2
-
-
0025022001
-
Hepatitis B virus integration in a cyclin A gene in a hepatocellular carcinoma
-
Wang, J., Chenivesse, X., Henglein, B. and Bréchot, C. Hepatitis B virus integration in a cyclin A gene in a hepatocellular carcinoma. Nature, 343, 555-557 (1990).
-
(1990)
Nature
, vol.343
, pp. 555-557
-
-
Wang, J.1
Chenivesse, X.2
Henglein, B.3
Bréchot, C.4
-
3
-
-
0015043748
-
Mutation and cancer: Statistical study of retinoblastoma
-
Knudson, A. G. Mutation and cancer: statistical study of retinoblastoma. Proc. Natl. Acad. Sci. USA, 68, 820-823 (1971).
-
(1971)
Proc. Natl. Acad. Sci. USA
, vol.68
, pp. 820-823
-
-
Knudson, A.G.1
-
4
-
-
0027504088
-
Antioncogenes and human cancer
-
Knudson, A. G. Antioncogenes and human cancer. Proc. Natl. Acad. Sci. USA, 90, 10914-10921 (1993).
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 10914-10921
-
-
Knudson, A.G.1
-
5
-
-
0024263645
-
Deletions in human chromosome arms 11p and 13q in primary hepatocellular carcinomas
-
Wang, H. P. and Rogler, C. E. Deletions in human chromosome arms 11p and 13q in primary hepatocellular carcinomas. Cytogenet. Cell Genet., 48, 72-78 (1988).
-
(1988)
Cytogenet. Cell Genet.
, vol.48
, pp. 72-78
-
-
Wang, H.P.1
Rogler, C.E.2
-
6
-
-
0024332123
-
Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma
-
Buetow, K. H., Murray, J., Israel, J., London, W., Smith, M., Kew, M., Blanquet, V., Bréchot, C., Redeker, A. and Govindarajah, S. Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma. Proc. Natl. Acad. Sci. USA, 86, 8852-8856 (1989).
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 8852-8856
-
-
Buetow, K.H.1
Murray, J.2
Israel, J.3
London, W.4
Smith, M.5
Kew, M.6
Blanquet, V.7
Bréchot, C.8
Redeker, A.9
Govindarajah, S.10
-
7
-
-
0025134850
-
Allele loss on chromosome 16 associated with progression of human hepatocellular carcinoma
-
Tsuda, H., Zhang, W., Shimosato, Y., Yokota, J., Terada, M., Sugimura. T., Miyamura, T. and Hirohashi, S. Allele loss on chromosome 16 associated with progression of human hepatocellular carcinoma. Proc. Natl. Acad. Sci. USA, 87, 6791-6794 (1990).
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 6791-6794
-
-
Tsuda, H.1
Zhang, W.2
Shimosato, Y.3
Yokota, J.4
Terada, M.5
Sugimura, T.6
Miyamura, T.7
Hirohashi, S.8
-
8
-
-
0026656360
-
Frequent loss of heterozygosity for loci on chromosome 8p in hepatocellular carcinoma, colorectal cancer, and lung cancer
-
Emi, M., Fujiwara, Y., Nakajima, T., Tsuchiya, E., Tsuda, H., Hirohashi, S., Maeda, Y., Tsuruta, K., Miyaki, M. and Nakamura, Y. Frequent loss of heterozygosity for loci on chromosome 8p in hepatocellular carcinoma, colorectal cancer, and lung cancer. Cancer Res., 52, 5368-5372 (1992).
-
(1992)
Cancer Res.
, vol.52
, pp. 5368-5372
-
-
Emi, M.1
Fujiwara, Y.2
Nakajima, T.3
Tsuchiya, E.4
Tsuda, H.5
Hirohashi, S.6
Maeda, Y.7
Tsuruta, K.8
Miyaki, M.9
Nakamura, Y.10
-
9
-
-
0028111570
-
Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas
-
Yeh, S. H., Chen, P. J., Chen, H. L., Wang, C. C. and Chen, D. S. Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas. Cancer Res., 54, 4188-4192 (1994).
-
(1994)
Cancer Res.
, vol.54
, pp. 4188-4192
-
-
Yeh, S.H.1
Chen, P.J.2
Chen, H.L.3
Wang, C.C.4
Chen, D.S.5
-
10
-
-
0028804071
-
M6P/IGF2R gene is mutated in human hepatocellular carcinomas with loss of heterozygosity
-
De Souza, A. T., Hankins, G. R., Washington, M. K., Orton, T. C. and Jirtle, R. L. M6P/IGF2R gene is mutated in human hepatocellular carcinomas with loss of heterozygosity. Nat. Genet., 11, 447-449 (1995).
-
(1995)
Nat. Genet.
, vol.11
, pp. 447-449
-
-
De Souza, A.T.1
Hankins, G.R.2
Washington, M.K.3
Orton, T.C.4
Jirtle, R.L.5
-
11
-
-
0026022684
-
Allelotype study of primary hepatocellular carcinoma
-
Fujimori, M., Tokino, T., Hino, O., Kitagawa, T., Imamura, T., Okamoto, E., Mitsunobu, M., Ishikawa, T., Nakagama, H., Harada, H., Yagura, M., Matsubara, K. and Nakamura, Y. Allelotype study of primary hepatocellular carcinoma. Cancer Res., 51, 89-93 (1991).
-
(1991)
Cancer Res.
, vol.51
, pp. 89-93
-
-
Fujimori, M.1
Tokino, T.2
Hino, O.3
Kitagawa, T.4
Imamura, T.5
Okamoto, E.6
Mitsunobu, M.7
Ishikawa, T.8
Nakagama, H.9
Harada, H.10
Yagura, M.11
Matsubara, K.12
Nakamura, Y.13
-
12
-
-
0030849123
-
Comprehensive allelotyping of human hepatocellular carcinoma
-
Nagai, H., Pineau, P., Tiollais, P., Buendia, M. A. and Dejean, A. Comprehensive allelotyping of human hepatocellular carcinoma. Oncogene, 14, 2927-2933 (1997).
-
(1997)
Oncogene
, vol.14
, pp. 2927-2933
-
-
Nagai, H.1
Pineau, P.2
Tiollais, P.3
Buendia, M.A.4
Dejean, A.5
-
13
-
-
0027276536
-
Frequent loss of heterozygosity on chromosome 22 in hepatocellular carcinoma
-
Takahashi, K., Kudo, J., Ishibashi, H., Hirata, Y. and Niho, Y. Frequent loss of heterozygosity on chromosome 22 in hepatocellular carcinoma. Hepatology, 17, 794-799 (1993).
-
(1993)
Hepatology
, vol.17
, pp. 794-799
-
-
Takahashi, K.1
Kudo, J.2
Ishibashi, H.3
Hirata, Y.4
Niho, Y.5
-
14
-
-
0028912246
-
Loss of heterozygosity and analysis of mutation of p53 in hepatocellular carcinoma
-
Yumoto, Y., Hanafusa, T., Hada, H., Morita, T., Ooguchi, S., Shinji, N., Mitani, T., Hamaya, K., Koide, N. and Tsuji, T. Loss of heterozygosity and analysis of mutation of p53 in hepatocellular carcinoma. J. Gastroenterol. Hepatol., 10, 179-185 (1995).
-
(1995)
J. Gastroenterol. Hepatol.
, vol.10
, pp. 179-185
-
-
Yumoto, Y.1
Hanafusa, T.2
Hada, H.3
Morita, T.4
Ooguchi, S.5
Shinji, N.6
Mitani, T.7
Hamaya, K.8
Koide, N.9
Tsuji, T.10
-
15
-
-
0032484502
-
Allelotype analysis of hepatocellular carcinoma
-
Piao, Z., Park, C., Park, J. H. and Kim, H. Allelotype analysis of hepatocellular carcinoma. Int. J. Cancer, 75, 29-33 (1998).
-
(1998)
Int. J. Cancer
, vol.75
, pp. 29-33
-
-
Piao, Z.1
Park, C.2
Park, J.H.3
Kim, H.4
-
16
-
-
0030936323
-
PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer
-
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, 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
-
17
-
-
17144436629
-
Identification of a candidate tumor 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., Lin, H., Ligon, A. H., Langford, L. A., Baumgard, M. L., Hattier, T., Davis, T., Frye, C., Hu, R., Swedlund, B., Teng, D. H. and Tavtigian, S. V. Identification of a candidate tumor 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.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.14
Tavtigian, S.V.15
-
18
-
-
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, P. L., 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, P.L.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
-
19
-
-
0031203265
-
Germline mutations in PTEN are present in Bannayan-Zonana syndrome
-
Marsh, D. J., Dahia, P. L., Zheng, Z., Liaw, D., Parsons, R., Gorlin, R. J. and Eng, C. Germline mutations in PTEN are present in Bannayan-Zonana syndrome. Nat. Genet., 16, 333-334 (1997).
-
(1997)
Nat. Genet.
, vol.16
, pp. 333-334
-
-
Marsh, D.J.1
Dahia, P.L.2
Zheng, Z.3
Liaw, D.4
Parsons, R.5
Gorlin, R.J.6
Eng, C.7
-
20
-
-
0030837555
-
P-TEN, the tumor suppressor from human chromosome 10q23, is a dual-specificity phosphatase
-
Myers, M. P., Stolarov, J. P., Eng, C., Li, J., Wang, S. I., Wigler, M. H., Parsons, R. and Tonks, N. K. P-TEN, the tumor suppressor from human chromosome 10q23, is a dual-specificity phosphatase. Proc. Natl. Acad. Sci. USA, 94, 9052-9057 (1997).
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 9052-9057
-
-
Myers, M.P.1
Stolarov, J.P.2
Eng, C.3
Li, J.4
Wang, S.I.5
Wigler, M.H.6
Parsons, R.7
Tonks, N.K.8
-
21
-
-
0030781053
-
PTEN/MMAC1 mutations in endometrial cancers
-
Risinger, J. I., Hayes, A. K., Berchuck, A. and Barrett, J. C. PTEN/MMAC1 mutations in endometrial cancers. Cancer Res., 57, 4736-4738 (1997).
-
(1997)
Cancer Res.
, vol.57
, pp. 4736-4738
-
-
Risinger, J.I.1
Hayes, A.K.2
Berchuck, A.3
Barrett, J.C.4
-
22
-
-
0030801275
-
Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in primary breast carcinomas
-
Rhei, E., Kang, L., Bogomolniy, F., Federici, M. G., Borgen, P. I. and Boyd, J. Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in primary breast carcinomas. Cancer Res., 57, 3657-3659 (1997).
-
(1997)
Cancer Res.
, vol.57
, pp. 3657-3659
-
-
Rhei, E.1
Kang, L.2
Bogomolniy, F.3
Federici, M.G.4
Borgen, P.I.5
Boyd, J.6
-
23
-
-
0031681438
-
Somatic mutations of the PTEN/MMAC1 gene in fifteen japanese endometrial cancers: Evidence for inactivation of both alleles
-
Kurose, K., Bando, K., Fukino, K., Sugisaki, Y., Araki, T. and Emi, M. Somatic mutations of the PTEN/MMAC1 gene in fifteen Japanese endometrial cancers: evidence for inactivation of both alleles. Jpn. J. Cancer Res., 89, 842-848 (1998).
-
(1998)
Jpn. J. Cancer Res.
, vol.89
, pp. 842-848
-
-
Kurose, K.1
Bando, K.2
Fukino, K.3
Sugisaki, Y.4
Araki, T.5
Emi, M.6
-
24
-
-
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
-
25
-
-
0028231090
-
The 1993-1994 Genethon human genetic linkage map
-
Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M. and Weissenbach, J. The 1993-1994 Genethon human genetic linkage map. Nat. Genet., 7, 246-339 (1994).
-
(1994)
Nat. Genet.
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Millasseau, P.6
Marc, S.7
Bernardi, G.8
Lathrop, M.9
Weissenbach, J.10
-
26
-
-
0031014544
-
Localization of a breast cancer tumor suppressor gene to a 3-cM interval within chromosomal region 16q22
-
Iida, A., Isobe, R., Yoshimoto, M., Kasumi, F., Nakamura, Y. and Emi, M. Localization of a breast cancer tumor suppressor gene to a 3-cM interval within chromosomal region 16q22. Br. J. Cancer, 75, 264-267 (1997).
-
(1997)
Br. J. Cancer
, vol.75
, pp. 264-267
-
-
Iida, A.1
Isobe, R.2
Yoshimoto, M.3
Kasumi, F.4
Nakamura, Y.5
Emi, M.6
-
27
-
-
0031647971
-
Five familial hypercholesterolemic kindreds in Japan with novel mutations of the LDL receptor gene
-
Hirayama, T., Yamaki, E., Hata, A., Tsuji, M., Hashimoto, K., Yamamoto, M. and Emi, M. Five familial hypercholesterolemic kindreds in Japan with novel mutations of the LDL receptor gene. J. Hum. Genet., 43, 250-254 (1998).
-
(1998)
J. Hum. Genet.
, vol.43
, pp. 250-254
-
-
Hirayama, T.1
Yamaki, E.2
Hata, A.3
Tsuji, M.4
Hashimoto, K.5
Yamamoto, M.6
Emi, M.7
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