-
1
-
-
0022922229
-
Polysomy of chromosome 7 is correlated with overexpression of the erbB oncogene in human glioblastoma cell lines
-
Henn W., Blin N., Zang K.D. Polysomy of chromosome 7 is correlated with overexpression of the erbB oncogene in human glioblastoma cell lines. Hum Genet. 74:1986;104-106
-
(1986)
Hum Genet
, vol.74
, pp. 104-106
-
-
Henn, W.1
Blin, N.2
Zang, K.D.3
-
2
-
-
0028911133
-
Chromosomal abnormalities in glioblastoma multiforme tumors and glioma cell lines detected by comparative genomic hybridization
-
Kim D.H., Mohapatra G., Bollen A., Waldman F.M., Feuerstein B.G. Chromosomal abnormalities in glioblastoma multiforme tumors and glioma cell lines detected by comparative genomic hybridization. Int J Cancer. 60:1995;812-819
-
(1995)
Int J Cancer
, vol.60
, pp. 812-819
-
-
Kim, D.H.1
Mohapatra, G.2
Bollen, A.3
Waldman, F.M.4
Feuerstein, B.G.5
-
3
-
-
0029010921
-
Detection of multiple gains and losses of genetic material in ten glioma cell lines by comparative genomic hybridization
-
Mohapatra G., Kim D.H., Feuerstein B.G. Detection of multiple gains and losses of genetic material in ten glioma cell lines by comparative genomic hybridization. Genes Chromosomes Cancer. 13:1995;86-93
-
(1995)
Genes Chromosomes Cancer
, vol.13
, pp. 86-93
-
-
Mohapatra, G.1
Kim, D.H.2
Feuerstein, B.G.3
-
4
-
-
0031929455
-
Genetic analysis of glioblastoma multiforme provides evidence for subgroups within the grade
-
Mohapatra G., Bollen A.W., Kim D.H., Lamborn K., Moore D., Prados M.D., Feuerstein B.G. Genetic analysis of glioblastoma multiforme provides evidence for subgroups within the grade. Genes Chromosomes Cancer. 21:1998;195-206
-
(1998)
Genes Chromosomes Cancer
, vol.21
, pp. 195-206
-
-
Mohapatra, G.1
Bollen, A.W.2
Kim, D.H.3
Lamborn, K.4
Moore, D.5
Prados, M.D.6
Feuerstein, B.G.7
-
5
-
-
0033048809
-
Chromosomal abnormalities in glioblastoma multiforme by comparative genomic hybridization: Correlation with radiation treatment outcome
-
Huhn S.L., Mohapatra G., Bollen A., Lamborn K., Prados M.D., Feuerstein B.G. Chromosomal abnormalities in glioblastoma multiforme by comparative genomic hybridization: correlation with radiation treatment outcome. Clin Cancer Res. 5:1999;1435-1443
-
(1999)
Clin Cancer Res
, vol.5
, pp. 1435-1443
-
-
Huhn, S.L.1
Mohapatra, G.2
Bollen, A.3
Lamborn, K.4
Prados, M.D.5
Feuerstein, B.G.6
-
6
-
-
0035887448
-
Genetic subgroups of anaplastic astrocytomas correlate with patient age and survival
-
Kunwar S., Mohapatra G., Bollen A., Lamborn K.R., Prados M., Feuerstein B.G. Genetic subgroups of anaplastic astrocytomas correlate with patient age and survival. Cancer Res. 61:2001;7683-7688
-
(2001)
Cancer Res
, vol.61
, pp. 7683-7688
-
-
Kunwar, S.1
Mohapatra, G.2
Bollen, A.3
Lamborn, K.R.4
Prados, M.5
Feuerstein, B.G.6
-
7
-
-
0035111058
-
Analysis of complex relationships between age, p53, epidermal growth factor receptor, and survival in glioblastoma patients
-
Simmons M.L., Lamborn K.R., Takahashi M., Chen P., Israel M.A., Berger M.S., Godfrey T., Nigro J., Prados M., Chang S., Barker F.G. 2nd, Aldape K. Analysis of complex relationships between age, p53, epidermal growth factor receptor, and survival in glioblastoma patients. Cancer Res. 61:2001;1122-1128
-
(2001)
Cancer Res
, vol.61
, pp. 1122-1128
-
-
Simmons, M.L.1
Lamborn, K.R.2
Takahashi, M.3
Chen, P.4
Israel, M.A.5
Berger, M.S.6
Godfrey, T.7
Nigro, J.8
Prados, M.9
Chang, S.10
Barker II, F.G.11
Aldape, K.12
-
8
-
-
0026298348
-
DNA sequence localization in metaphase and interphase cells by fluorescence in situ hybridization
-
Trask B.J. DNA sequence localization in metaphase and interphase cells by fluorescence in situ hybridization. Methods Cell Biol. 35:1991;3-35
-
(1991)
Methods Cell Biol
, vol.35
, pp. 3-35
-
-
Trask, B.J.1
-
9
-
-
0038214755
-
Multicolor spectral karyotyping of human chromosomes
-
Schrock E., du Manoir S., Veldman T., Schoell B., Wienberg J., Ferguson-Smith M.A., Ning Y., Ledbetter D.H., Bar-Am I., Soenksen D., Garini Y., Ried T. Multicolor spectral karyotyping of human chromosomes. Science. 273:1996;494-497
-
(1996)
Science
, vol.273
, pp. 494-497
-
-
Schrock, E.1
Du Manoir, S.2
Veldman, T.3
Schoell, B.4
Wienberg, J.5
Ferguson-Smith, M.A.6
Ning, Y.7
Ledbetter, D.H.8
Bar-Am, I.9
Soenksen, D.10
Garini, Y.11
Ried, T.12
-
11
-
-
0026495364
-
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
-
Kallioniemi A., Kallioniemi O.P., Sudar D., Rutovitz D., Gray J.W., Waldman F., Pinkel D. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science. 258:1992;818-821
-
(1992)
Science
, vol.258
, pp. 818-821
-
-
Kallioniemi, A.1
Kallioniemi, O.P.2
Sudar, D.3
Rutovitz, D.4
Gray, J.W.5
Waldman, F.6
Pinkel, D.7
-
12
-
-
17344371740
-
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
-
Pinkel D., Segraves R., Sudar D., Clark S., Poole I., Kowbel D., Collins C., Kuo W.L., Chen C., Zhai Y., Dairkee S.H., Ljung B.M., Gray J.W., Albertson D.G. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat Genet. 20:1998;207-211
-
(1998)
Nat Genet
, vol.20
, pp. 207-211
-
-
Pinkel, D.1
Segraves, R.2
Sudar, D.3
Clark, S.4
Poole, I.5
Kowbel, D.6
Collins, C.7
Kuo, W.L.8
Chen, C.9
Zhai, Y.10
Dairkee, S.H.11
Ljung, B.M.12
Gray, J.W.13
Albertson, D.G.14
-
13
-
-
0035179871
-
Assembly of microarrays for genome-wide measurement of DNA copy number
-
Snijders A.M., Nowak N., Segraves R., Blackwood S., Brown N., Conroy J., Hamilton G., Hindle A.K., Huey B., Kimura K., Law S., Myambo K., Palmer J., Ylstra B., Yue J.P., Gray J.W., Jain A.N., Pinkel D., Albertson D.G. Assembly of microarrays for genome-wide measurement of DNA copy number. Nat Genet. 29:2001;263-264
-
(2001)
Nat Genet
, vol.29
, pp. 263-264
-
-
Snijders, A.M.1
Nowak, N.2
Segraves, R.3
Blackwood, S.4
Brown, N.5
Conroy, J.6
Hamilton, G.7
Hindle, A.K.8
Huey, B.9
Kimura, K.10
Law, S.11
Myambo, K.12
Palmer, J.13
Ylstra, B.14
Yue, J.P.15
Gray, J.W.16
Jain, A.N.17
Pinkel, D.18
Albertson, D.G.19
-
14
-
-
0036180003
-
Fully automatic quantification of microarray image data
-
Jain A.N., Tokuyasu T.A., Snijders A.M., Segraves R., Albertson D.G., Pinkel D. Fully automatic quantification of microarray image data. Genome Res. 12:2002;325-332
-
(2002)
Genome Res
, vol.12
, pp. 325-332
-
-
Jain, A.N.1
Tokuyasu, T.A.2
Snijders, A.M.3
Segraves, R.4
Albertson, D.G.5
Pinkel, D.6
-
15
-
-
0030690049
-
Analyses of brain tumor cell lines confirm a simple model of relationships among fluorescence in situ hybridization, DNA index, and comparative genomic hybridization
-
Mohapatra G., Moore D.H., Kim D.H., Grewal L., Hyun W.C., Waldman F.M., Pinkel D., Feuerstein B.G. Analyses of brain tumor cell lines confirm a simple model of relationships among fluorescence in situ hybridization, DNA index, and comparative genomic hybridization. Genes Chromosomes Cancer. 20:1997;311-319
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 311-319
-
-
Mohapatra, G.1
Moore, D.H.2
Kim, D.H.3
Grewal, L.4
Hyun, W.C.5
Waldman, F.M.6
Pinkel, D.7
Feuerstein, B.G.8
-
16
-
-
0019462206
-
Isolation, karyotype, and clonal growth of heterogeneous subpopulations of human malignant gliomas
-
Shapiro J.R., Yung W.K., Shapiro W.R. Isolation, karyotype, and clonal growth of heterogeneous subpopulations of human malignant gliomas. Cancer Res. 41:1981;2349-2359
-
(1981)
Cancer Res
, vol.41
, pp. 2349-2359
-
-
Shapiro, J.R.1
Yung, W.K.2
Shapiro, W.R.3
-
18
-
-
0026345679
-
Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes
-
Collins C., Kuo W.L., Segraves R., Fuscoe J., Pinkel D., Gray J.W. Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes. Genomics. 11:1991;997-1006
-
(1991)
Genomics
, vol.11
, pp. 997-1006
-
-
Collins, C.1
Kuo, W.L.2
Segraves, R.3
Fuscoe, J.4
Pinkel, D.5
Gray, J.W.6
-
19
-
-
0031963355
-
Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21)
-
Roberts T., Chernova O., Cowell J.K. Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21). Cancer Genet Cytogenet. 100:1998;10-20
-
(1998)
Cancer Genet Cytogenet
, vol.100
, pp. 10-20
-
-
Roberts, T.1
Chernova, O.2
Cowell, J.K.3
-
20
-
-
0037313331
-
T(11;19) (q21;p13) translocation in mucoepidermoid carcinoma creates a novel fusion product that disrupts a Notch signaling pathway
-
[Erratum: Nat Genet 200333:430.]
-
Tonon G., Modi S., Wu L., Kubo A., Coxon A.B., Komiya T., O'Neil K., Stover K., El-Naggar A., Griffin J.D., Kirsch I.R., Kaye F.J. t(11;19) (q21;p13) translocation in mucoepidermoid carcinoma creates a novel fusion product that disrupts a Notch signaling pathway. [Erratum: Nat Genet 200333:430.] Nat Genet. 33:2003;208-213
-
(2003)
Nat Genet
, vol.33
, pp. 208-213
-
-
Tonon, G.1
Modi, S.2
Wu, L.3
Kubo, A.4
Coxon, A.B.5
Komiya, T.6
O'Neil, K.7
Stover, K.8
El-Naggar, A.9
Griffin, J.D.10
Kirsch, I.R.11
Kaye, F.J.12
-
21
-
-
0020965275
-
Occurrence and evolution of homogeneously staining regions may be due to breakage-fusion-bridge cycles following telomere loss
-
Cowell J.K., Miller O.J. Occurrence and evolution of homogeneously staining regions may be due to breakage-fusion-bridge cycles following telomere loss. Chromosoma. 88:1983;216-221
-
(1983)
Chromosoma
, vol.88
, pp. 216-221
-
-
Cowell, J.K.1
Miller, O.J.2
-
22
-
-
12944329959
-
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
-
Gisselsson D., Pettersson L., Hoglund M., Heidenblad M., Gorunova L., Wiegant J., Mertens F., Dal Cin P., Mitelman F., Mandahl N. Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity. Proc Natl Acad Sci U S A. 97:2000;5357-5362
-
(2000)
Proc Natl Acad Sci U S a
, vol.97
, pp. 5357-5362
-
-
Gisselsson, D.1
Pettersson, L.2
Hoglund, M.3
Heidenblad, M.4
Gorunova, L.5
Wiegant, J.6
Mertens, F.7
Dal Cin, P.8
Mitelman, F.9
Mandahl, N.10
-
23
-
-
0036849512
-
Initiation of the breakage-fusion-bridge mechanism through common fragile site activation in human breast cancer cells: The model of PIP gene duplication from a break at FRA7I
-
Ciullo M., Debily M.A., Rozier L., Autiero M., Billault A., Mayau V., El Marhomy S., Guardiola J., Bernheim A., Coullin P., Piatier-Tonneau D., Debatisse M. Initiation of the breakage-fusion-bridge mechanism through common fragile site activation in human breast cancer cells: the model of PIP gene duplication from a break at FRA7I. Hum Mol Genet. 11:2002;2887-2894
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2887-2894
-
-
Ciullo, M.1
Debily, M.A.2
Rozier, L.3
Autiero, M.4
Billault, A.5
Mayau, V.6
El Marhomy, S.7
Guardiola, J.8
Bernheim, A.9
Coullin, P.10
Piatier-Tonneau, D.11
Debatisse, M.12
-
24
-
-
0033860991
-
Molecular cytogenetic analysis of medulloblastomas and supratentorial primitive neuroectodermal tumors by using conventional banding, comparative genomic hybridization, and spectral karyotyping
-
Bayani J., Zielenska M., Marrano P., Kwan Ng Y., Taylor M.D., Jay V., Rutka J.T., Squire J.A. Molecular cytogenetic analysis of medulloblastomas and supratentorial primitive neuroectodermal tumors by using conventional banding, comparative genomic hybridization, and spectral karyotyping. J Neurosurg. 93:2000;437-448
-
(2000)
J Neurosurg
, vol.93
, pp. 437-448
-
-
Bayani, J.1
Zielenska, M.2
Marrano, P.3
Kwan Ng, Y.4
Taylor, M.D.5
Jay, V.6
Rutka, J.T.7
Squire, J.A.8
-
25
-
-
0345552243
-
Genomic imbalances of 7p and 17q in malignant peripheral nerve sheath tumors are clinically relevant
-
Schmidt H., Wurl P., Taubert H., Meye A., Bache M., Holzhausen H.J., Hinze R. Genomic imbalances of 7p and 17q in malignant peripheral nerve sheath tumors are clinically relevant. Genes Chromosomes Cancer. 25:1999;205-211
-
(1999)
Genes Chromosomes Cancer
, vol.25
, pp. 205-211
-
-
Schmidt, H.1
Wurl, P.2
Taubert, H.3
Meye, A.4
Bache, M.5
Holzhausen, H.J.6
Hinze, R.7
-
26
-
-
0034738802
-
Gains in chromosomes 7, 8q, 15q and 17q are characteristic changes in malignant but not in benign peripheral nerve sheath tumors from patients with Recklinghausen's disease
-
Schmidt H., Taubert H., Meye A., Wurl P., Bache M., Bartel F., Holzhausen H.J., Hinze R. Gains in chromosomes 7, 8q, 15q and 17q are characteristic changes in malignant but not in benign peripheral nerve sheath tumors from patients with Recklinghausen's disease. Cancer Lett. 155:2000;181-190
-
(2000)
Cancer Lett
, vol.155
, pp. 181-190
-
-
Schmidt, H.1
Taubert, H.2
Meye, A.3
Wurl, P.4
Bache, M.5
Bartel, F.6
Holzhausen, H.J.7
Hinze, R.8
-
27
-
-
0035099106
-
Chromosomal abnormalities subdivide ependymal tumors into clinically relevant groups
-
Hirose Y., Aldape K., Bollen A., James C.D., Brat D., Lamborn K., Berger M., Feuerstein B.G. Chromosomal abnormalities subdivide ependymal tumors into clinically relevant groups. Am J Pathol. 158:2001;1137-1143
-
(2001)
Am J Pathol
, vol.158
, pp. 1137-1143
-
-
Hirose, Y.1
Aldape, K.2
Bollen, A.3
James, C.D.4
Brat, D.5
Lamborn, K.6
Berger, M.7
Feuerstein, B.G.8
-
28
-
-
0037081817
-
Karyotypic heterogeneity and clonal evolution in squamous cell carcinomas of the head and neck
-
Jin C., Jin Y., Wennerberg J., Akervall J., Dictor M., Mertens F. Karyotypic heterogeneity and clonal evolution in squamous cell carcinomas of the head and neck. Cancer Genet Cytogenet. 132:2002;85-96
-
(2002)
Cancer Genet Cytogenet
, vol.132
, pp. 85-96
-
-
Jin, C.1
Jin, Y.2
Wennerberg, J.3
Akervall, J.4
Dictor, M.5
Mertens, F.6
-
29
-
-
0035220183
-
Comparative genomic hybridization analysis suggests a gain of chromosome 7p associated with lymph node metastasis in non-small cell lung cancer
-
Ubagai T., Matsuura S., Tauchi H., Itou K., Komatsu K. Comparative genomic hybridization analysis suggests a gain of chromosome 7p associated with lymph node metastasis in non-small cell lung cancer. Oncol Rep. 8:2001;83-88
-
(2001)
Oncol Rep
, vol.8
, pp. 83-88
-
-
Ubagai, T.1
Matsuura, S.2
Tauchi, H.3
Itou, K.4
Komatsu, K.5
-
30
-
-
17744391051
-
A comparison of DNA copy number changes detected by comparative genomic hybridization in malignancies of the liver, biliary tract and pancreas
-
Shiraishi K., Okita K., Kusano N., Harada T., Kondoh S., Okita S., Ryozawa S., Ohmura R., Noguchi T., Iida Y., Akiyama T., Oga A., Fukumoto Y., Furuya T., Kawauchi S., Sasaki K. A comparison of DNA copy number changes detected by comparative genomic hybridization in malignancies of the liver, biliary tract and pancreas. Oncology. 60:2001;151-161
-
(2001)
Oncology
, vol.60
, pp. 151-161
-
-
Shiraishi, K.1
Okita, K.2
Kusano, N.3
Harada, T.4
Kondoh, S.5
Okita, S.6
Ryozawa, S.7
Ohmura, R.8
Noguchi, T.9
Iida, Y.10
Akiyama, T.11
Oga, A.12
Fukumoto, Y.13
Furuya, T.14
Kawauchi, S.15
Sasaki, K.16
-
31
-
-
0035206246
-
Correlation of histologic subtypes and replication error phenotype with comparative genomic hybridization in gastric cancer
-
Wu M.S., Chang M.C., Huang S.P., Tseng C.C., Sheu J.C., Lin Y.W., Shun C.T., Lin M.T., Lin J.T. Correlation of histologic subtypes and replication error phenotype with comparative genomic hybridization in gastric cancer. Genes Chromosomes Cancer. 30:2001;80-86
-
(2001)
Genes Chromosomes Cancer
, vol.30
, pp. 80-86
-
-
Wu, M.S.1
Chang, M.C.2
Huang, S.P.3
Tseng, C.C.4
Sheu, J.C.5
Lin, Y.W.6
Shun, C.T.7
Lin, M.T.8
Lin, J.T.9
-
32
-
-
0035135616
-
Molecular cytogenetic analysis of prostatic adenocarcinomas from screening studies: Early cancers may contain aggressive genetic features
-
Alers J.C., Krijtenburg P.J., Vis A.N., Hoedemaeker R.F., Wildhagen M.F., Hop W.C., van Der Kwast T.T., Schroder F.H., Tanke H.J., van Dekken H. Molecular cytogenetic analysis of prostatic adenocarcinomas from screening studies: early cancers may contain aggressive genetic features. Am J Pathol. 158:2001;399-406
-
(2001)
Am J Pathol
, vol.158
, pp. 399-406
-
-
Alers, J.C.1
Krijtenburg, P.J.2
Vis, A.N.3
Hoedemaeker, R.F.4
Wildhagen, M.F.5
Hop, W.C.6
Van Der Kwast, T.T.7
Schroder, F.H.8
Tanke, H.J.9
Van Dekken, H.10
-
33
-
-
0028282920
-
Clonal chromosome abnormalities in 54 cases of ovarian carcinoma
-
Thompson F.H., Emerson J., Alberts D., Liu Y., Guan X.Y., Burgess A., Fox S., Taetle R., Weinstein R., Makar R., Powell D., Trent J. Clonal chromosome abnormalities in 54 cases of ovarian carcinoma. Cancer Genet Cytogenet. 73:1994;33-45
-
(1994)
Cancer Genet Cytogenet
, vol.73
, pp. 33-45
-
-
Thompson, F.H.1
Emerson, J.2
Alberts, D.3
Liu, Y.4
Guan, X.Y.5
Burgess, A.6
Fox, S.7
Taetle, R.8
Weinstein, R.9
Makar, R.10
Powell, D.11
Trent, J.12
-
34
-
-
1842369666
-
Genetic alteration mapping on chromosome 7 in primary breast cancer
-
Bieche I., Khodja A., Driouch K., Lidereau R. Genetic alteration mapping on chromosome 7 in primary breast cancer. Clin Cancer Res. 3:1997;1009-1016
-
(1997)
Clin Cancer Res
, vol.3
, pp. 1009-1016
-
-
Bieche, I.1
Khodja, A.2
Driouch, K.3
Lidereau, R.4
-
35
-
-
0033504868
-
Cytogenetic analyses of secondary liver tumors reveal significant differences in genomic imbalances between primary and metastatic colon carcinomas
-
Parada L.A., Maranon A., Hallen M., Tranberg K.G., Stenram U., Bardi G., Johansson B. Cytogenetic analyses of secondary liver tumors reveal significant differences in genomic imbalances between primary and metastatic colon carcinomas. Clin Exp Metastasis. 17:1997;471-479
-
(1997)
Clin Exp Metastasis
, vol.17
, pp. 471-479
-
-
Parada, L.A.1
Maranon, A.2
Hallen, M.3
Tranberg, K.G.4
Stenram, U.5
Bardi, G.6
Johansson, B.7
-
36
-
-
0027974256
-
Neurofibromatosis and childhood leukaemia/lymphoma: A population-based UKCCSG study
-
Stiller C.A., Chessells J.M., Fitchett M. Neurofibromatosis and childhood leukaemia/lymphoma: a population-based UKCCSG study. Br J Cancer. 70:1994;969-972
-
(1994)
Br J Cancer
, vol.70
, pp. 969-972
-
-
Stiller, C.A.1
Chessells, J.M.2
Fitchett, M.3
-
37
-
-
2542501864
-
-
University of California Santa Cruz Human Genome Project. Human genome database [Internet]. Available at: http://genome.ucsc.edu/. Accessed July 2003 freeze.
-
Human Genome Database [Internet]
-
-
|