-
2
-
-
0026544724
-
Cytogenetic findings in three primary hepatcellular carcinomas
-
Bardi G., Johanson B., Pandis N., Heim S., Mandahl N., Andrén-Sandberg A., Hagerstrand I., Mitelman F. Cytogenetic findings in three primary hepatcellular carcinomas. Cancer Genet Cytogenet. 58:1992;191-195.
-
(1992)
Cancer Genet Cytogenet
, vol.58
, pp. 191-195
-
-
Bardi, G.1
Johanson, B.2
Pandis, N.3
Heim, S.4
Mandahl, N.5
Andrén-Sandberg, A.6
Hagerstrand, I.7
Mitelman, F.8
-
3
-
-
0029995126
-
Chromosome 1p aberrations are frequent in human primary hepatocellular carcinoma
-
Chen H.L., Chen Y.C., Chen D.S. Chromosome 1p aberrations are frequent in human primary hepatocellular carcinoma. Cancer Genet Cytogenet. 86:1996;102-106.
-
(1996)
Cancer Genet Cytogenet
, vol.86
, pp. 102-106
-
-
Chen, H.L.1
Chen, Y.C.2
Chen, D.S.3
-
4
-
-
0029947043
-
Report of a complex karyotype in recurrent metastatic fibrolamellar hepatocellular carcinoma and a review of hepatocellular carcinoma cytogenetics
-
Lowichik A., Schneider N.R., Tonk V., Ansari M.Q., Timmons C.F. Report of a complex karyotype in recurrent metastatic fibrolamellar hepatocellular carcinoma and a review of hepatocellular carcinoma cytogenetics. Cancer Genet Cytogenet. 88:1996;170-174.
-
(1996)
Cancer Genet Cytogenet
, vol.88
, pp. 170-174
-
-
Lowichik, A.1
Schneider, N.R.2
Tonk, V.3
Ansari, M.Q.4
Timmons, C.F.5
-
5
-
-
0028111570
-
Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas
-
Yeh S.H., Chen P.J., Chen H.L., Lai M.Y., Wang C.C., Chen D.S. Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas. Cancer Res. 54:1994;4188-4192.
-
(1994)
Cancer Res
, vol.54
, pp. 4188-4192
-
-
Yeh, S.H.1
Chen, P.J.2
Chen, H.L.3
Lai, M.Y.4
Wang, C.C.5
Chen, D.S.6
-
6
-
-
0028982642
-
Accumulation of genetic changes during development and progression of hepatocellur carcinoma: Loss of heterozygosity on chromosome arm 1p occurs at an early stage of hepatocarcinogenesis
-
Kuroki T., Fujiwara Y., Tsuchiya E., Nakamori S., Imaoka S., Kanematsu T., Nakamura Y. Accumulation of genetic changes during development and progression of hepatocellur carcinoma. loss of heterozygosity on chromosome arm 1p occurs at an early stage of hepatocarcinogenesis Genes Chromosom Cancer. 13:1995;163-167.
-
(1995)
Genes Chromosom Cancer
, vol.13
, pp. 163-167
-
-
Kuroki, T.1
Fujiwara, Y.2
Tsuchiya, E.3
Nakamori, S.4
Imaoka, S.5
Kanematsu, T.6
Nakamura, Y.7
-
7
-
-
0025801654
-
Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatomas
-
Simon D., Knowles B.B., Weith A. Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatomas. Oncogene. 6:1991;765-770.
-
(1991)
Oncogene
, vol.6
, pp. 765-770
-
-
Simon, D.1
Knowles, B.B.2
Weith, A.3
-
8
-
-
0030031136
-
Allelic loss on chromosome 4q and 16q in hepatocellular carcinoma: Association with alpha-fetoprotein production
-
Yeh S.H., Chen P.J., Lai M.Y., Chen D.S. Allelic loss on chromosome 4q and 16q in hepatocellular carcinoma. association with alpha-fetoprotein production Gastroenterology. 110:1996;184-192.
-
(1996)
Gastroenterology
, vol.110
, pp. 184-192
-
-
Yeh, S.H.1
Chen, P.J.2
Lai, M.Y.3
Chen, D.S.4
-
9
-
-
0025269663
-
Frequent loss of heterozygosity on chromosomes 16 and 4 in human hepatocellular carcinoma
-
Zhang W., Hirohashi S., Tsuda H., Shimosato Y., Yokota J., Terada M., Sugimura T. Frequent loss of heterozygosity on chromosomes 16 and 4 in human hepatocellular carcinoma. Jpn J Cancer Res. 81:1990;108-111.
-
(1990)
Jpn J Cancer Res
, vol.81
, pp. 108-111
-
-
Zhang, W.1
Hirohashi, S.2
Tsuda, H.3
Shimosato, Y.4
Yokota, J.5
Terada, M.6
Sugimura, T.7
-
10
-
-
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., Nakamura Y. Allelotype study of primary hepatocellular carcinoma. Cancer Res. 51:1991;89-93.
-
(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
-
11
-
-
0029031943
-
Frequent loss of heterozygosity on 6q at the mannose 6-phosphate/insulin-like growth factor II receptor locus in human hepatocellular tumors
-
De Souza A.T., Hankins G.R., Washington M.K., Fine R.L., Orton T.C., Jirtle R.L. Frequent loss of heterozygosity on 6q at the mannose 6-phosphate/insulin-like growth factor II receptor locus in human hepatocellular tumors. Oncogene. 10:1995;1725-1729.
-
(1995)
Oncogene
, vol.10
, pp. 1725-1729
-
-
De Souza, A.T.1
Hankins, G.R.2
Washington, M.K.3
Fine, R.L.4
Orton, T.C.5
Jirtle, R.L.6
-
12
-
-
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., Jirtle R.L. M6P/IGF2R gene is mutated in human hepatocellular carcinomas with loss of heterozygosity. Nat Genet. 11:1995;447-449.
-
(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
-
13
-
-
0026656360
-
Frequent loss of heterozygosity for loci on chromosome 8p in hepatocellular carcinoma, colorectal cancer, and lung cancer
-
Emi M., Fujiwara Y., Nakajima T., Tsuchia E., Tsuda H., Hirohashi S., Maeda Y., Tsuruta K., Miyaki M., Nakamura Y. Frequent loss of heterozygosity for loci on chromosome 8p in hepatocellular carcinoma, colorectal cancer, and lung cancer. Cancer Res. 52:1992;5368-5372.
-
(1992)
Cancer Res
, vol.52
, pp. 5368-5372
-
-
Emi, M.1
Fujiwara, Y.2
Nakajima, T.3
Tsuchia, E.4
Tsuda, H.5
Hirohashi, S.6
Maeda, Y.7
Tsuruta, K.8
Miyaki, M.9
Nakamura, Y.10
-
14
-
-
0027267036
-
Allelic loss at chromosome band 8p21.3-p22 is associated with progression of hepatocellular carcinoma
-
Emi M., Fujiwara Y., Ohata H., Tsuda H., Hirohashi S., Koike M., Miyaki M., Monden M., Nakamura Y. Allelic loss at chromosome band 8p21.3-p22 is associated with progression of hepatocellular carcinoma. Genes Chromosom Cancer. 7:1993;152-157.
-
(1993)
Genes Chromosom Cancer
, vol.7
, pp. 152-157
-
-
Emi, M.1
Fujiwara, Y.2
Ohata, H.3
Tsuda, H.4
Hirohashi, S.5
Koike, M.6
Miyaki, M.7
Monden, M.8
Nakamura, Y.9
-
15
-
-
0024263645
-
Deletions in human chromosome arms 11p and 13q in primary hepatocellular carcinomas
-
Wang H.P., Rogler C.E. Deletions in human chromosome arms 11p and 13q in primary hepatocellular carcinomas. Cytogenet Cell Genet. 48:1988;72-78.
-
(1988)
Cytogenet Cell Genet
, vol.48
, pp. 72-78
-
-
Wang, H.P.1
Rogler, C.E.2
-
16
-
-
0026684402
-
Accumulation of allelic loss on arms of chromosomes 13q, 16q, and 1p in the advanced stages of human hepatocellular carcinoma
-
Nishida N., Fukuda Y., Kokuryu H., Sadamoto T., Isowa G., Honda K., Yamaoka Y., Ikenaga M., Imura H., Ishizaki K. Accumulation of allelic loss on arms of chromosomes 13q, 16q, and 1p in the advanced stages of human hepatocellular carcinoma. Int J Cancer. 51:1992;862-868.
-
(1992)
Int J Cancer
, vol.51
, pp. 862-868
-
-
Nishida, N.1
Fukuda, Y.2
Kokuryu, H.3
Sadamoto, T.4
Isowa, G.5
Honda, K.6
Yamaoka, Y.7
Ikenaga, M.8
Imura, H.9
Ishizaki, K.10
-
17
-
-
0028023861
-
Deletions of chromosome 13q, mutations in retinoblastoma 1, and retinoblastoma protein state in human hepatocellular carcinoma
-
Zhang X., Xu H.J., Murakami Y., Sachse R., Yashima K., Hirohashi S., Hu S.X., Benedict W.F., Sekiya T. Deletions of chromosome 13q, mutations in retinoblastoma 1, and retinoblastoma protein state in human hepatocellular carcinoma. Cancer Res. 54:1994;4177-4182.
-
(1994)
Cancer Res
, vol.54
, pp. 4177-4182
-
-
Zhang, X.1
Xu, H.J.2
Murakami, Y.3
Sachse, R.4
Yashima, K.5
Hirohashi, S.6
Hu, S.X.7
Benedict, W.F.8
Sekiya, T.9
-
18
-
-
0027243142
-
P53 gene mutations and 17p allelic deletions in hepatocellular carcinoma from Japan
-
Nose H., Imazeki F., Ohto M., Omata M. p53 gene mutations and 17p allelic deletions in hepatocellular carcinoma from Japan. Cancer. 72:1993;355-360.
-
(1993)
Cancer
, vol.72
, pp. 355-360
-
-
Nose, H.1
Imazeki, F.2
Ohto, M.3
Omata, M.4
-
19
-
-
0027276536
-
Frequent loss of heterozygosity on chromosome 22 in hepatocellular carcinoma
-
Takahashi K., Kudo J., Ishibashi H., Hirata Y., Hino Y. Frequent loss of heterozygosity on chromosome 22 in hepatocellular carcinoma. Hepatology. 17:1993;794-799.
-
(1993)
Hepatology
, vol.17
, pp. 794-799
-
-
Takahashi, K.1
Kudo, J.2
Ishibashi, H.3
Hirata, Y.4
Hino, Y.5
-
20
-
-
0031022784
-
Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization
-
Marchio A., Meddeb M., Pineau P., Danglot G., Tiollais P., Berheim A., Deiean A. Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization. Genes Chromosom Cancer. 18:1997;59-65.
-
(1997)
Genes Chromosom Cancer
, vol.18
, pp. 59-65
-
-
Marchio, A.1
Meddeb, M.2
Pineau, P.3
Danglot, G.4
Tiollais, P.5
Berheim, A.6
Deiean, A.7
-
21
-
-
15144361323
-
Concerted nonsyntenic allelic losses in hyperploid hepatocellular carcinoma as determined by a high-resolution allelotype
-
Boige V., Laurent-Puig P., Fouchet P., Fléjou J.F., Monges G., Bedossa P., Bioulac-Sage P., Capron F., Schmitz A., Olschwang S., Thomas G. Concerted nonsyntenic allelic losses in hyperploid hepatocellular carcinoma as determined by a high-resolution allelotype. Cancer Res. 57:1997;1986-1990.
-
(1997)
Cancer Res
, vol.57
, pp. 1986-1990
-
-
Boige, V.1
Laurent-Puig, P.2
Fouchet, P.3
Fléjou, J.F.4
Monges, G.5
Bedossa, P.6
Bioulac-Sage, P.7
Capron, F.8
Schmitz, A.9
Olschwang, S.10
Thomas, G.11
-
22
-
-
0030849123
-
Comprehensive allelotyping of human hepatcellular carcinoma
-
Nagai H., Pineau P., Tiollais P., Buendia M.A., Dejean A. Comprehensive allelotyping of human hepatcellular carcinoma. Oncogene. 14:1997;2927-2933.
-
(1997)
Oncogene
, vol.14
, pp. 2927-2933
-
-
Nagai, H.1
Pineau, P.2
Tiollais, P.3
Buendia, M.A.4
Dejean, A.5
-
23
-
-
0029911967
-
Fluorescence in situ hybridization evaluation of chromosome deletion patterns in prostate cancer
-
Huang S.F., Xiao S., Renshaw A.A., Loughlin K.R., Hudson T.J., Fletcher J.A. Fluorescence in situ hybridization evaluation of chromosome deletion patterns in prostate cancer. Am J Pathol. 149:1996;1565-1573.
-
(1996)
Am J Pathol
, vol.149
, pp. 1565-1573
-
-
Huang, S.F.1
Xiao, S.2
Renshaw, A.A.3
Loughlin, K.R.4
Hudson, T.J.5
Fletcher, J.A.6
-
24
-
-
0028270326
-
Homozygous deletion on chromosome 9p and loss of heterozygosity on 9q, 6p and 6q in primary human small cell lung cancer
-
Merlo A., Gabielson E., Mabry M., Vollmer R., Baylin S.B., Sidransky D. Homozygous deletion on chromosome 9p and loss of heterozygosity on 9q, 6p and 6q in primary human small cell lung cancer. Cancer Res. 54:1994;2322-2326.
-
(1994)
Cancer Res
, vol.54
, pp. 2322-2326
-
-
Merlo, A.1
Gabielson, E.2
Mabry, M.3
Vollmer, R.4
Baylin, S.B.5
Sidransky, D.6
-
25
-
-
0027991276
-
Common region of deletion on the long arm of chromosome 6 in non-Hodgkin's lymphoma and acute lymphoblastic leukemia
-
Menasce L.P., Orphanos V., Santibanez-Koref M., Boyle J.M., Harrison C.J. Common region of deletion on the long arm of chromosome 6 in non-Hodgkin's lymphoma and acute lymphoblastic leukemia. Genes Chromosom Cancer. 10:1994;286-288.
-
(1994)
Genes Chromosom Cancer
, vol.10
, pp. 286-288
-
-
Menasce, L.P.1
Orphanos, V.2
Santibanez-Koref, M.3
Boyle, J.M.4
Harrison, C.J.5
-
26
-
-
0028855714
-
Proximal 6q, a region showing allele loss in primary breast cancer
-
Orphanos V., McGown G., Hey Y., Boyle J.M., Santibanez-Koref M. Proximal 6q, a region showing allele loss in primary breast cancer. Br J Cancer. 71:1995;290-293.
-
(1995)
Br J Cancer
, vol.71
, pp. 290-293
-
-
Orphanos, V.1
McGown, G.2
Hey, Y.3
Boyle, J.M.4
Santibanez-Koref, M.5
-
27
-
-
0029597872
-
Trisomy 1 and 8 occur frequently in hepatocellular carcinoma but not in liver cell adenoma and focal nodular hyperplasia: A fluorescence in situ hybridization study
-
Nasarek A., Werner M., Nolte M., Klempnauer J., Georgii A. Trisomy 1 and 8 occur frequently in hepatocellular carcinoma but not in liver cell adenoma and focal nodular hyperplasia. a fluorescence in situ hybridization study Virchows Arch. 427:1995;373-378.
-
(1995)
Virchows Arch
, vol.427
, pp. 373-378
-
-
Nasarek, A.1
Werner, M.2
Nolte, M.3
Klempnauer, J.4
Georgii, A.5
-
28
-
-
13344261389
-
Cytogenetic analyses of hepatocellular carcinoma by in situ hybridization with a chromosome-specific DNA probe
-
Kimura H., Kagawa K., Deguchi T., Nakajima T., Kakushi M., Okawara T., Katagishi T., Okanoue T., Kashima K., Ashihara T. Cytogenetic analyses of hepatocellular carcinoma by in situ hybridization with a chromosome-specific DNA probe. Cancer. 77:1996;271-277.
-
(1996)
Cancer
, vol.77
, pp. 271-277
-
-
Kimura, H.1
Kagawa, K.2
Deguchi, T.3
Nakajima, T.4
Kakushi, M.5
Okawara, T.6
Katagishi, T.7
Okanoue, T.8
Kashima, K.9
Ashihara, T.10
-
29
-
-
0029960338
-
Interphase cytogenetic studies of human hepatocellular carcinomas by fluorescence in situ hybridization
-
Hamon-Benais C., Ingster O., Terris B., Couturier-Turpin M.H., Berheim A., Feldmann G. Interphase cytogenetic studies of human hepatocellular carcinomas by fluorescence in situ hybridization. Hepatology. 23:1996;429-435.
-
(1996)
Hepatology
, vol.23
, pp. 429-435
-
-
Hamon-Benais, C.1
Ingster, O.2
Terris, B.3
Couturier-Turpin, M.H.4
Berheim, A.5
Feldmann, G.6
-
30
-
-
0031917334
-
Numerical aberrations of chromosomes 16, 17, and 18 in hepatocellular carcinoma: A FISH and FCM analysis of 20 cases
-
Kato A., Kubo K., Kurokawa F., Okita K., Oga A., Murakami T. Numerical aberrations of chromosomes 16, 17, and 18 in hepatocellular carcinoma. a FISH and FCM analysis of 20 cases Digest Dis Sci. 43:1998;1-7.
-
(1998)
Digest Dis Sci
, vol.43
, pp. 1-7
-
-
Kato, A.1
Kubo, K.2
Kurokawa, F.3
Okita, K.4
Oga, A.5
Murakami, T.6
-
31
-
-
0030758205
-
Interphase cytogenetic analysis reveals numerical chromosome aberrations in large liver cell dysplasia
-
Terris B., Ingster O., Rubbia L., Dubois S., Belghiti J., Feldmann G., Degott C., Henin D. Interphase cytogenetic analysis reveals numerical chromosome aberrations in large liver cell dysplasia. J Hepatol. 27:1997;313-319.
-
(1997)
J Hepatol
, vol.27
, pp. 313-319
-
-
Terris, B.1
Ingster, O.2
Rubbia, L.3
Dubois, S.4
Belghiti, J.5
Feldmann, G.6
Degott, C.7
Henin, D.8
-
32
-
-
0030297139
-
Numerical chromosome aberrations in hepatocellular carcinoma detected by fluorescence in situ hybridization
-
Ohasawa N., Sakamoto M., Saito T., Kobayashi M., Hirohashi S. Numerical chromosome aberrations in hepatocellular carcinoma detected by fluorescence in situ hybridization. J Hepatol. 25:1996;655-662.
-
(1996)
J Hepatol
, vol.25
, pp. 655-662
-
-
Ohasawa, N.1
Sakamoto, M.2
Saito, T.3
Kobayashi, M.4
Hirohashi, S.5
-
33
-
-
0028935143
-
Detection of CDKN2 deletion in tumor cell lines and primary glioma by interphase fluorescence in situ hybridization
-
Dreyling M.H., Bohlander S.K., Adeyanju M.O., Olopade O.I. Detection of CDKN2 deletion in tumor cell lines and primary glioma by interphase fluorescence in situ hybridization. Cancer Res. 55:1995;984-988.
-
(1995)
Cancer Res
, vol.55
, pp. 984-988
-
-
Dreyling, M.H.1
Bohlander, S.K.2
Adeyanju, M.O.3
Olopade, O.I.4
-
34
-
-
0028799264
-
Novel fluorescence in situ hybridization approaches in solid tumors: Characterization of frozen specimens, touch preparations, and cytologic preparations
-
Xiao S., Renshaw A.A., Cibas E.S., Hudson T.J., Fletcher J.A. Novel fluorescence in situ hybridization approaches in solid tumors. characterization of frozen specimens, touch preparations, and cytologic preparations Am J Pathol. 147:1995;896-904.
-
(1995)
Am J Pathol
, vol.147
, pp. 896-904
-
-
Xiao, S.1
Renshaw, A.A.2
Cibas, E.S.3
Hudson, T.J.4
Fletcher, J.A.5
-
35
-
-
0027516041
-
Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast
-
Pandis N., Jin Y., Limon J., Bardi G., Idvall I., Mandahl N., Mitelman F., Heim S. Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast. Genes Chromosom Cancer. 6:1993;151-155.
-
(1993)
Genes Chromosom Cancer
, vol.6
, pp. 151-155
-
-
Pandis, N.1
Jin, Y.2
Limon, J.3
Bardi, G.4
Idvall, I.5
Mandahl, N.6
Mitelman, F.7
Heim, S.8
-
36
-
-
0026550844
-
Three distinct regions involved in 3p deletion in human lung cancer
-
Hibi K., Takahashi T., Yamakawa K., Ueda R., Sekido Y., Ariyoshi Y., Suyama M., Takagi H., Nakamura Y. Three distinct regions involved in 3p deletion in human lung cancer. Oncogene. 7:1992;445-449.
-
(1992)
Oncogene
, vol.7
, pp. 445-449
-
-
Hibi, K.1
Takahashi, T.2
Yamakawa, K.3
Ueda, R.4
Sekido, Y.5
Ariyoshi, Y.6
Suyama, M.7
Takagi, H.8
Nakamura, Y.9
-
37
-
-
0028158010
-
Distinct deletions of chromosome 9p associated with melanoma versus glioma, lung cancer, and leukemia
-
Coleman A., Fountain J.W., Nobori T., Olopade O.I., Roberston G., Housman D.E., Lugo T.G. Distinct deletions of chromosome 9p associated with melanoma versus glioma, lung cancer, and leukemia. Cancer Res. 54:1994;344-348.
-
(1994)
Cancer Res
, vol.54
, pp. 344-348
-
-
Coleman, A.1
Fountain, J.W.2
Nobori, T.3
Olopade, O.I.4
Roberston, G.5
Housman, D.E.6
Lugo, T.G.7
-
38
-
-
0023949872
-
In situ hybridization as a tool to study numerical chromosome aberrations in solid bladder tumors
-
Hopman A.H., Ramaekers F.C., Raap A.K., Beck J.L., Devilee P., van der Ploeg M., Vooijs G.P. In situ hybridization as a tool to study numerical chromosome aberrations in solid bladder tumors. Histochemistry. 89:1988;307-316.
-
(1988)
Histochemistry
, vol.89
, pp. 307-316
-
-
Hopman, A.H.1
Ramaekers, F.C.2
Raap, A.K.3
Beck, J.L.4
Devilee, P.5
Van Der Ploeg, M.6
Vooijs, G.P.7
-
39
-
-
0024332123
-
Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma
-
Buetow K.H., Murray J.C., Israel J.L., Lodon W.T., Smith M., Kew M., Blanquet V., Brechot C., Redeker A., Govindarajah S. Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma. Proc Natl Acad Sci USA. 86:1989;8852-8856.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 8852-8856
-
-
Buetow, K.H.1
Murray, J.C.2
Israel, J.L.3
Lodon, W.T.4
Smith, M.5
Kew, M.6
Blanquet, V.7
Brechot, C.8
Redeker, A.9
Govindarajah, S.10
-
42
-
-
0029005855
-
Loss of heterozygosity from the short arm of chromosome 8 is an early event in breast cancers
-
Yaremko M.L., Recant W.M., Westbrook C.A. Loss of heterozygosity from the short arm of chromosome 8 is an early event in breast cancers. Genes Chromosom Cancer. 13:1995;186-191.
-
(1995)
Genes Chromosom Cancer
, vol.13
, pp. 186-191
-
-
Yaremko, M.L.1
Recant, W.M.2
Westbrook, C.A.3
-
43
-
-
9344222738
-
Analysis of 99 microdissected prostate carcinomas reveals a high frequency of allelic loss on chromosome 8p12-21
-
Vocke C.D., Pozzatti R.O., Bostwick D.G., Florence C.D., Jennings S.B., Strup S.E., Duray P.H., Liotta L.A., Emmert-Buck M.R., Linehan W.M. Analysis of 99 microdissected prostate carcinomas reveals a high frequency of allelic loss on chromosome 8p12-21. Cancer Res. 56:1996;2411-2416.
-
(1996)
Cancer Res
, vol.56
, pp. 2411-2416
-
-
Vocke, C.D.1
Pozzatti, R.O.2
Bostwick, D.G.3
Florence, C.D.4
Jennings, S.B.5
Strup, S.E.6
Duray, P.H.7
Liotta, L.A.8
Emmert-Buck, M.R.9
Linehan, W.M.10
-
44
-
-
0028275733
-
Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers
-
Nobori T., Miura K., Wu D.J., Lois A., Takabayashi K., Carson A. Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers. Nature. 368:1994;753-754.
-
(1994)
Nature
, vol.368
, pp. 753-754
-
-
Nobori, T.1
Miura, K.2
Wu, D.J.3
Lois, A.4
Takabayashi, K.5
Carson, A.6
-
45
-
-
0028338514
-
Frequent somatic mutation of the MTS1/CDK4I (multiple tumor suppressor/cyclin-dependnet kinase 4 inhibitor) gene in esophageal squamous cell carcinoma
-
Mori T., Miura K., Aoki T., Nishihira T., Mori S., Nakamura Y. Frequent somatic mutation of the MTS1/CDK4I (multiple tumor suppressor/cyclin-dependnet kinase 4 inhibitor) gene in esophageal squamous cell carcinoma. Cancer Res. 54:1994;3396-3397.
-
(1994)
Cancer Res
, vol.54
, pp. 3396-3397
-
-
Mori, T.1
Miura, K.2
Aoki, T.3
Nishihira, T.4
Mori, S.5
Nakamura, Y.6
-
46
-
-
0029155471
-
Codeletion of p15 and p16 in primary malignant mesothelioma
-
Xiao S., Li D., Vijg J., Sugarbaker D.J., Corson J.M., Fletcher J.A. Codeletion of p15 and p16 in primary malignant mesothelioma. Oncogene. 11:1995;511-515.
-
(1995)
Oncogene
, vol.11
, pp. 511-515
-
-
Xiao, S.1
Li, D.2
Vijg, J.3
Sugarbaker, D.J.4
Corson, J.M.5
Fletcher, J.A.6
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