-
1
-
-
0343196653
-
Increased copy number at 17q22-q24 by CGH in breast cancer is due to high-level amplification of two separate regions
-
Bärlund M, Tirkkonen M, Forozan F, Tanner MM, Kallioniemi O, Kallioniemi A. 1997. Increased copy number at 17q22-q24 by CGH in breast cancer is due to high-level amplification of two separate regions. Genes Chromosomes Cancer 20:372-376.
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 372-376
-
-
Bärlund, M.1
Tirkkonen, M.2
Forozan, F.3
Tanner, M.M.4
Kallioniemi, O.5
Kallioniemi, A.6
-
2
-
-
0031725944
-
Homogeneously staining regions in 223 breast carcinomas: Cytogenetic and clinicopathological correlations
-
Bernardino J, Gerbault-Seureau M, Zafrani B, Dericke Y, Boudou E, Magdelenat H, Dutrillaux B. 1998. Homogeneously staining regions in 223 breast carcinomas: cytogenetic and clinicopathological correlations. Br J Cancer 78:1214-1218.
-
(1998)
Br J Cancer
, vol.78
, pp. 1214-1218
-
-
Bernardino, J.1
Gerbault-Seureau, M.2
Zafrani, B.3
Dericke, Y.4
Boudou, E.5
Magdelenat, H.6
Dutrillaux, B.7
-
4
-
-
0028580430
-
Somatic genetic changes in human breast cancer
-
Devilee P, Cornelisse CJ. 1994. Somatic genetic changes in human breast cancer. Biochim Biophys Acta 1198:113-130.
-
(1994)
Biochim Biophys Acta
, vol.1198
, pp. 113-130
-
-
Devilee, P.1
Cornelisse, C.J.2
-
5
-
-
0344097450
-
Specific chromosomal aberrations and amplification of the AlB1 nuclear receptor coactivator gene in pancreatic carcinomas
-
Ghadimi BM, Schröck E, Walker RL, Wangsa D, Jauho A, Meltzer PS, Ried T. 1999. Specific chromosomal aberrations and amplification of the AlB1 nuclear receptor coactivator gene in pancreatic carcinomas. Am J Pathol 154:525-536.
-
(1999)
Am J Pathol
, vol.154
, pp. 525-536
-
-
Ghadimi, B.M.1
Schröck, E.2
Walker, R.L.3
Wangsa, D.4
Jauho, A.5
Meltzer, P.S.6
Ried, T.7
-
6
-
-
0028001095
-
Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection
-
Guan X-Y, Meltzer PS, Dalton WS, Trent JM. 1994. Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection. Nat Genet 8:155-161.
-
(1994)
Nat Genet
, vol.8
, pp. 155-161
-
-
Guan, X.-Y.1
Meltzer, P.S.2
Dalton, W.S.3
Trent, J.M.4
-
7
-
-
0031769001
-
Identification of de novo chromosomal markers and derivatives by spectral karyotyping
-
Haddad BR, Schröck E, Meck J, Cowan J, Young H, Ferguson-Smith MA, du Manoir S, Ried T. 1998. Identification of de novo chromosomal markers and derivatives by spectral karyotyping. Hum Genet 103:619-625.
-
(1998)
Hum Genet
, vol.103
, pp. 619-625
-
-
Haddad, B.R.1
Schröck, E.2
Meck, J.3
Cowan, J.4
Young, H.5
Ferguson-Smith, M.A.6
Du Manoir, S.7
Ried, T.8
-
8
-
-
0028874583
-
Genetic aberrations detected by comparative genomic hybridization predict outcome in node-negative breast cancer
-
Isola JJ, Kallioniemi O-P, Chu LW, Fuqua SAW, Hilsenbeck SG, Osborne CK, Waldman FM. 1995. Genetic aberrations detected by comparative genomic hybridization predict outcome in node-negative breast cancer. Am J Pathol 147:905-911.
-
(1995)
Am J Pathol
, vol.147
, pp. 905-911
-
-
Isola, J.J.1
Kallioniemi, O.-P.2
Chu, L.W.3
Fuqua, S.A.W.4
Hilsenbeck, S.G.5
Osborne, C.K.6
Waldman, F.M.7
-
9
-
-
0026495364
-
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
-
Kallioniemi A, Kallioniemi O-P, Sudar D, Rutovitz D, Gray WW, Waldman F, Pinkel D. 1992. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 258: 818-821.
-
(1992)
Science
, vol.258
, pp. 818-821
-
-
Kallioniemi, A.1
Kallioniemi, O.-P.2
Sudar, D.3
Rutovitz, D.4
Gray, W.W.5
Waldman, F.6
Pinkel, D.7
-
10
-
-
0032955441
-
Four-color CGH: A new method for quality control of comparative genomic hybridization
-
Karhu R, Rummukainen J, Lörch T, Isola J. 1999. Four-color CGH: a new method for quality control of comparative genomic hybridization. Genes Chromosomes Cancer 24:112-118.
-
(1999)
Genes Chromosomes Cancer
, vol.24
, pp. 112-118
-
-
Karhu, R.1
Rummukainen, J.2
Lörch, T.3
Isola, J.4
-
11
-
-
0344076342
-
Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping
-
Macville M, Schröck E, Padilla-Nash H, Keck C, Ghadimi BM, Zimonjic D, Popescu N, Ried T. 1999. Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping. Cancer Res 59:141-150.
-
(1999)
Cancer Res
, vol.59
, pp. 141-150
-
-
Macville, M.1
Schröck, E.2
Padilla-Nash, H.3
Keck, C.4
Ghadimi, B.M.5
Zimonjic, D.6
Popescu, N.7
Ried, T.8
-
12
-
-
0030825508
-
Chromosomal imbalance maps of malignant solid tumors: A cytogenetic survey of 3185 neoplasms
-
Mertens F, Johansson B, Höglund M, Mitelman F. 1997. Chromosomal imbalance maps of malignant solid tumors: a cytogenetic survey of 3185 neoplasms. Cancer Res 57:2765-2780.
-
(1997)
Cancer Res
, vol.57
, pp. 2765-2780
-
-
Mertens, F.1
Johansson, B.2
Höglund, M.3
Mitelman, F.4
-
14
-
-
0025901088
-
Parameters of the human genome
-
Morton NE. 1991. Parameters of the human genome. Proc Natl Acad Sci USA 88:7474-7476.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 7474-7476
-
-
Morton, N.E.1
-
15
-
-
0030838976
-
Genetic alterations in primary breast cancers and their metastases: Direct comparison using modified comparative genomic hybridization
-
Nishizaki T, DeVries S, Chew K, Goodson III, WH, Ljung B-M, Thor A, Waldman FM. 1997. Genetic alterations in primary breast cancers and their metastases: Direct comparison using modified comparative genomic hybridization. Genes Chromosomes Cancer 19:267-272.
-
(1997)
Genes Chromosomes Cancer
, vol.19
, pp. 267-272
-
-
Nishizaki, T.1
DeVries, S.2
Chew, K.3
Goodson W.H. III4
Ljung, B.-M.5
Thor, A.6
Waldman, F.M.7
-
16
-
-
0032934462
-
Molecular cytogenetic analysis of the bladder carcinoma cell line BK-10 by spectral karyotyping
-
Padilla-Nash HM, Nash WG, Padilla GM, Roberson KM, Robertson CN, Macville M, Schröck E, Ried T. 1999. Molecular cytogenetic analysis of the bladder carcinoma cell line BK-10 by spectral karyotyping. Genes Chromosomes Cancer 25:53-59.
-
(1999)
Genes Chromosomes Cancer
, vol.25
, pp. 53-59
-
-
Padilla-Nash, H.M.1
Nash, W.G.2
Padilla, G.M.3
Roberson, K.M.4
Robertson, C.N.5
Macville, M.6
Schröck, E.7
Ried, T.8
-
17
-
-
0026496013
-
Whole-arm t(1;16) and i(1q) as sole anomalies identify gain of 1q as a primary chromosomal abnormality in breast cancer
-
Pandis N, Heim S, Bardi G, Idvall I, Mandahl N, Mitelman F. 1992. Whole-arm t(1;16) and i(1q) as sole anomalies identify gain of 1q as a primary chromosomal abnormality in breast cancer. Genes Chromosomes Cancer 5:235-238.
-
(1992)
Genes Chromosomes Cancer
, vol.5
, pp. 235-238
-
-
Pandis, N.1
Heim, S.2
Bardi, G.3
Idvall, I.4
Mandahl, N.5
Mitelman, F.6
-
18
-
-
0032170964
-
Multicolor spectral karyotyping identifies new recurring breakpoints and translocations in multiple myeloma
-
Rao BH, Cigudosa JC, Ning Y, Calasanz MJ, Iida S, Tagawa S, Michaeli J, Klein B, Dalla-Favera R, Jhanwar SC, Ried T, Chaganti RSK. 1998. Multicolor spectral karyotyping identifies new recurring breakpoints and translocations in multiple myeloma. Blood 92:1743-1748.
-
(1998)
Blood
, vol.92
, pp. 1743-1748
-
-
Rao, B.H.1
Cigudosa, J.C.2
Ning, Y.3
Calasanz, M.J.4
Iida, S.5
Tagawa, S.6
Michaeli, J.7
Klein, B.8
Dalla-Favera, R.9
Jhanwar, S.C.10
Ried, T.11
Chaganti, R.S.K.12
-
19
-
-
0028849283
-
Comparative genomic hybridization of formalin-fixed, paraffin-embedded breast carcinomas reveals different patterns of chromosomal gains and losses in fibroadenomas and diploid and ancuploid carcinomas
-
Ried T, Just KE, Holtgreve-Grez H, du Manoir S, Speicher MR, Schröck E, Latham C, Blegen H, Zetterberg A, Cremer T, Auer G. 1995. Comparative genomic hybridization of formalin-fixed, paraffin-embedded breast carcinomas reveals different patterns of chromosomal gains and losses in fibroadenomas and diploid and ancuploid carcinomas. Cancer Res 55:5415-5423.
-
(1995)
Cancer Res
, vol.55
, pp. 5415-5423
-
-
Ried, T.1
Just, K.E.2
Holtgreve-Grez, H.3
Du Manoir, S.4
Speicher, M.R.5
Schröck, E.6
Latham, C.7
Blegen, H.8
Zetterberg, A.9
Cremer, T.10
Auer, G.11
-
20
-
-
0030853274
-
Tumor cytogenetics revisited: Comparative genomic hybridization and spectral karyotyping
-
Ried T, Liyanage M, du Manoir S, Heselmeyer K, Auer G, Macville M, Schröck E. 1997. Tumor cytogenetics revisited: comparative genomic hybridization and spectral karyotyping. J Mol Med 75: 801-814.
-
(1997)
J Mol Med
, vol.75
, pp. 801-814
-
-
Ried, T.1
Liyanage, M.2
Du Manoir, S.3
Heselmeyer, K.4
Auer, G.5
Macville, M.6
Schröck, E.7
-
21
-
-
0038214755
-
Multicolor spectral karyotyping of human chromosomes
-
Schröck E, du Manoir S, Veldman T, Schoell B, Wienberg J, Ferguson-Smith MA, Ning Y, Ledbetter DH, Bar-Am I, Soenksen D, Garini Y, Ried T. 1996. Multicolor spectral karyotyping of human chromosomes. Science 273:494-497.
-
(1996)
Science
, vol.273
, pp. 494-497
-
-
Schröck, 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
-
22
-
-
2642683176
-
Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities
-
Schröck E, Veldman T, Padilla-Nash H, Ning Y, Spurbeck J, Jalal S, Shaffer LG, Papenhausen P, Kozma C, Phelan MC, Kjeldsen E, Schonberg SA, O'Brien P, Biesecker L, du Manoir S, Ried T. 1997. Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities. Hum Genet 101:255-262.
-
(1997)
Hum Genet
, vol.101
, pp. 255-262
-
-
Schröck, E.1
Veldman, T.2
Padilla-Nash, H.3
Ning, Y.4
Spurbeck, J.5
Jalal, S.6
Shaffer, L.G.7
Papenhausen, P.8
Kozma, C.9
Phelan, M.C.10
Kjeldsen, E.11
Schonberg, S.A.12
O'Brien, P.13
Biesecker, L.14
Du Manoir, S.15
Ried, T.16
-
23
-
-
0029912473
-
Karyotyping human chromosomes by combinatorial multi-fluor FISH
-
Speicher MR, Ballard SG, Ward DC. 1996. Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nat Genet 12: 368-375.
-
(1996)
Nat Genet
, vol.12
, pp. 368-375
-
-
Speicher, M.R.1
Ballard, S.G.2
Ward, D.C.3
-
24
-
-
8944227502
-
Independent amplification and frequent co-amplification of three nonsyntenic regions on the long arm of chromosome 20 in human breast cancer
-
Tanner MM, Tirkkonen M, Kallioniemi A, Isola J, Kuukasjärvi T, Collins C, Kowbel D, Guan X-Y, Trent J, Gray JW, Meltzer P, Kallioniemi O-P. 1996. Independent amplification and frequent co-amplification of three nonsyntenic regions on the long arm of chromosome 20 in human breast cancer. Cancer Res 56:3441-3445.
-
(1996)
Cancer Res
, vol.56
, pp. 3441-3445
-
-
Tanner, M.M.1
Tirkkonen, M.2
Kallioniemi, A.3
Isola, J.4
Kuukasjärvi, T.5
Collins, C.6
Kowbel, D.7
Guan, X.-Y.8
Trent, J.9
Gray, J.W.10
Meltzer, P.11
Kallioniemi, O.-P.12
-
25
-
-
0031929177
-
Molecular cytogenetics of primary breast cancer by CGH
-
Tirkkonen M, Tanner M, Karhu R, Kallioniemi A, Isola J, Kallioniemi O-P. 1998. Molecular cytogenetics of primary breast cancer by CGH. Genes Chromosomes Cancer 21:177-184.
-
(1998)
Genes Chromosomes Cancer
, vol.21
, pp. 177-184
-
-
Tirkkonen, M.1
Tanner, M.2
Karhu, R.3
Kallioniemi, A.4
Isola, J.5
Kallioniemi, O.-P.6
-
26
-
-
0030909689
-
Hidden chromosome abnormalities in hematological malignancies detected by multicolor spectral karyotyping
-
Veldman T, Vignon C, Schröck E, Rowley JD, Ried T. 1997. Hidden chromosome abnormalities in hematological malignancies detected by multicolor spectral karyotyping. Nat Genet 15:406-110.
-
(1997)
Nat Genet
, vol.15
, pp. 406-1110
-
-
Veldman, T.1
Vignon, C.2
Schröck, E.3
Rowley, J.D.4
Ried, T.5
-
27
-
-
0032895536
-
Cytogenetic changes in radiation-induced tumors of the thyroid
-
Zitzelsberger H, Lehmann L, Hieber L, Weier H-U, Janish C, Fung J, Negele T, Spelsberg F, Lengfelder E, Demidchik EP, Salassidis K, Kellerer AM, Werner M, Bauchinger M. 1999. Cytogenetic changes in radiation-induced tumors of the thyroid. Cancer Res 59:135-140.
-
(1999)
Cancer Res
, vol.59
, pp. 135-140
-
-
Zitzelsberger, H.1
Lehmann, L.2
Hieber, L.3
Weier, H.-U.4
Janish, C.5
Fung, J.6
Negele, T.7
Spelsberg, F.8
Lengfelder, E.9
Demidchik, E.P.10
Salassidis, K.11
Kellerer, A.M.12
Werner, M.13
Bauchinger, M.14
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