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Results: 26-50/2230
Authors:
Tsao, SW
Wong, N
Wang, XH
Liu, Y
Wan, TSK
Fung, LF
Lancaster, WD
Gregoire, L
Wong, YC
Citation: Sw. Tsao et al., Nonrandom chromosomal imbalances in human ovarian surface epithelial cellsimmortalized by HPV16-E6E7 viral oncogenes, CANC GENET, 130(2), 2001, pp. 141-149
Authors:
Hamaguchi, H
Yamaguchi, M
Nagata, K
Koike, E
Imagunbai, M
Tsurukubo, Y
Yamamoto, K
Citation: H. Hamaguchi et al., Aggressive NK cell lymphoma/leukemia with clonal der(3)t(1;3) (q12;p25), del(6)(q13) and del(13)(q12q14), CANC GENET, 130(2), 2001, pp. 150-154
Authors:
Ray, GN
Shahid, M
Husain, SA
Citation: Gn. Ray et al., Status of chromosome breaks and gaps in breast cancer: a follow-up study, CANC GENET, 130(2), 2001, pp. 155-159
Authors:
Paulsson, K
Sall, T
Fioretos, T
Mitelman, F
Johansson, B
Citation: K. Paulsson et al., The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology, CANC GENET, 130(2), 2001, pp. 160-165
Authors:
Achuthan, R
Bell, SM
Roberts, P
Leek, JP
Horgan, K
Markham, AF
MacLennan, KA
Speirs, V
Citation: R. Achuthan et al., Genetic events during the transformation of a tamoxifen-sensitive human breast cancer cell line into a drug-resistant clone, CANC GENET, 130(2), 2001, pp. 166-172
Authors:
Sandberg, AA
Bridge, JA
Citation: Aa. Sandberg et Ja. Bridge, Updates on the cytogenetics and molecular genetics of bone and soft tissuetumors: clear cell sarcoma (malignant melanoma of soft parts), CANC GENET, 130(1), 2001, pp. 1-7
Authors:
Odero, MD
Soto, JL
Matutes, E
Martin-Subero, JI
Zudaire, I
Rao, PH
Cigudosa, JC
Ardanaz, MT
Chaganti, RSK
Perucho, M
Calasanz, MJ
Citation: Md. Odero et al., Comparative genomic hybridization and amplotyping by arbitrarily primed PCR in stage A B-CLL, CANC GENET, 130(1), 2001, pp. 8-13
Authors:
Zielenska, M
Bayani, J
Pandita, A
Toledo, S
Marrano, P
Andrade, J
Petrilli, A
Thorner, P
Sorensen, P
Squire, JA
Citation: M. Zielenska et al., Comparative genomic hybridization analysis identifies gains of 1p35 similar to p36 and chromosome 19 in osteosarcoma, CANC GENET, 130(1), 2001, pp. 14-21
Authors:
Koo, SH
Ihm, CH
Kwon, KC
Park, JW
Kim, JM
Kong, G
Citation: Sh. Koo et al., Genetic alterations in hepatocellular carcinoma and intrahepatic cholangiocarcinoma, CANC GENET, 130(1), 2001, pp. 22-28
Authors:
Smith, A
St Heaps, L
Sharma, P
Jarvis, A
Forsyth, C
Citation: A. Smith et al., Abnormal dicentric chromosome with co-amplification of sequences from chromosomes 11 and 19: a novel rearrangement in a patient with myelodysplastic syndrome transforming to acute myeloid leukemia, CANC GENET, 130(1), 2001, pp. 29-32
Authors:
Liu, SH
Li, Q
Pang, WX
Bo, LJ
Qin, S
Liu, XP
Teng, QL
Qian, LS
Wang, JX
Citation: Sh. Liu et al., A new complex variant t(4;15;17) in acute promyelocytic leukemia: fluorescence in situ hybridization confirmation and literature review, CANC GENET, 130(1), 2001, pp. 33-37
Authors:
Yamamoto, K
Nakamura, Y
Arai, H
Aoyagi, M
Saito, K
Furusawa, S
Mitani, K
Citation: K. Yamamoto et al., Translocation (14;19)(q32;q13) detected by spectral karyotyping and lack of BCL3 rearrangement in CD5-positive B-cell lymphoma associated with hemophagocytic syndrome, CANC GENET, 130(1), 2001, pp. 38-41
Authors:
Ueda, C
Yamada, H
Akasaka, T
Ohmori, K
Sasada, M
Uchiyama, T
Ohno, H
Citation: C. Ueda et al., Establishment and characterization of a new human myeloma cell line, KY delta-1, producing the delta/kappa type immunoglobulin, CANC GENET, 130(1), 2001, pp. 42-50
Authors:
Rogalla, P
Blank, C
Helbig, R
Wosniok, W
Bullerdiek, J
Citation: P. Rogalla et al., Significant correlation between the breakpoints of rare clonal aberrationsin benign solid tumors and the assignment of HMGIY retropseudogenes, CANC GENET, 130(1), 2001, pp. 51-56
Authors:
Brisset, S
Schleiermacher, G
Peter, M
Mairal, A
Oberlin, O
Delattre, O
Aurias, A
Citation: S. Brisset et al., CGH analysis of secondary genetic changes in Ewing tumors: correlation with metastatic disease in a series of 43 cases, CANC GENET, 130(1), 2001, pp. 57-61
Authors:
Fabris, V
Ernst, G
Lopes, EC
Garcia, M
Hajos, S
Alvarez, E
Merani, S
Citation: V. Fabris et al., Chromosome studies of murine T-cell lymphoid leukemia and derived cell lines, CANC GENET, 130(1), 2001, pp. 62-67
Authors:
Gonzalez, FA
Anguita, E
Mora, A
Asenjo, S
Lopez, I
Polo, M
Villegas, A
Citation: Fa. Gonzalez et al., Deletion of BCR region 3 ' in chronic myelogenous leukemia, CANC GENET, 130(1), 2001, pp. 68-74
Authors:
Finelli, P
Francchiolla, NS
Giardino, D
Gottardi, G
Deliliers, DL
Cortelezzi, A
Larizza, L
Deliliers, GL
Citation: P. Finelli et al., FISH characterization of t(8;12)(q12;p13) observed as the sole karyotypic anomaly in a myelodysplastic syndrome patient, CANC GENET, 130(1), 2001, pp. 75-78
Authors:
Granzow, M
Popp, S
Weber, S
Schoell, B
Holtgreve-Grez, H
Senf, L
Hager, D
Boschert, J
Scheurlen, W
Jauch, A
Citation: M. Granzow et al., Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics, CANC GENET, 130(1), 2001, pp. 79-83
Authors:
Berger, R
Busson, M
Daniel, MT
Citation: R. Berger et al., B-cell acute lymphoblastic leukemia with tandem t(14;14)(q11;q32), CANC GENET, 130(1), 2001, pp. 84-86
Authors:
Silva, MLM
de Brito, GD
Simoes, F
Otero, L
Land, MGP
Guerra, MC
Salles, TJM
Pombo-de-Oliveira, MS
Citation: Mlm. Silva et al., A new case of t(5;15)(p15;q11 similar to q13) in infant acute lymphoblastic leukemia, CANC GENET, 130(1), 2001, pp. 87-88
Authors:
Fowler, DJ
DeAngelo, DJ
Ariyanaygam, S
Atkins, L
Citation: Dj. Fowler et al., A new case of isolated del(12)(q15q22) in myelodysplastic syndrome, CANC GENET, 130(1), 2001, pp. 89-91
Authors:
Gursky, S
Olopade, OI
Rowley, JD
Citation: S. Gursky et al., Identification of a 1.2 Kb cDNA fragment from a region on 9p21 commonly deleted in multiple tumor types, CANC GENET, 129(2), 2001, pp. 93-101
Authors:
Nishio, J
Iwasaki, H
Ohjimi, Y
Ishiguro, M
Isayama, T
Naito, M
Kaneko, Y
Kikuchi, M
Citation: J. Nishio et al., Supernumerary ring chromosomes in dermatofibrosarcoma protuberans may contain sequences from 8q11.2 similar to qter and 17q21 similar to qter: a combined cytogenetic and comparative genomic hybridization study, CANC GENET, 129(2), 2001, pp. 102-106
Authors:
Reddy, KS
Parsons, L
Mak, L
Chan, JA
Citation: Ks. Reddy et al., An hsr on chromosome 7 was shown to be an insertion of four copies of the 11q23 MLL gene region in an HIV-related lymphoma, CANC GENET, 129(2), 2001, pp. 107-111