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Results:
1-16
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Results: 16
Authors:
Padilla-Nash, HM
Heselmeyer-Haddad, K
Wangsa, N
Zhang, HG
Ghadimi, BM
Macville, M
Augustus, M
Schrock, E
Hilgenfeld, E
Ried, T
Citation: Hm. Padilla-nash et al., Jumping translocations are common in solid tumor cell lines and result in recurrent fusions of whole chromosome arms, GENE CHROM, 30(4), 2001, pp. 349-363
Authors:
Hilgenfeld, E
Padilla-Nash, H
McNeil, N
Knutsen, T
Montagna, C
Tchinda, J
Horst, J
Ludwig, WD
Serve, H
Buchner, T
Berdel, WE
Schrock, E
Ried, T
Citation: E. Hilgenfeld et al., Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2, BR J HAEM, 113(2), 2001, pp. 305-317
Authors:
Hilgenfeld, E
Padilla-Nash, H
Haas, OA
Serve, H
Schrock, E
Ried, T
Citation: E. Hilgenfeld et al., Spectral karyotyping (SKY) of hematologic malignancies, METH MOL M, 55, 2001, pp. 65-79
Authors:
Ghadimi, BM
Sackett, DL
Difilippantonio, MJ
Schrock, E
Neumann, T
Jauho, A
Auer, G
Ried, T
Citation: Bm. Ghadimi et al., Centrosome amplification and instability occurs exclusively in aneuploid, but not in diploid colorectal cancer cell lines, and correlates with numerical chromosomal aberrations, GENE CHROM, 27(2), 2000, pp. 183-190
Authors:
Schrock, E
Padilla-Nash, H
Citation: E. Schrock et H. Padilla-nash, Spectral karyotyping and multicolor fluorescence in situ hybridization reveal new tumor-specific chromosomal aberrations, SEM HEMATOL, 37(4), 2000, pp. 334-347
Authors:
Wolf, NG
Abdul-Karim, FW
Farver, C
Schrock, E
du Manoir, S
Schwartz, S
Citation: Ng. Wolf et al., Analysis of ovarian borderline tumors using comparative genomic hybridization and fluorescence in situ hybridization, GENE CHROM, 25(4), 1999, pp. 307-315
Authors:
Ried, T
Heselmeyer-Haddad, K
Blegen, H
Schrock, E
Auer, G
Citation: T. Ried et al., Genomic changes defining the genesis, progression, and malignancy potential in solid human tumors: A phenotype genotype correlation, GENE CHROM, 25(3), 1999, pp. 195-204
Authors:
Weaver, ZA
McCormack, SJ
Liyanage, M
du Manoir, S
Coleman, A
Schrock, E
Dickson, RB
Ried, T
Citation: Za. Weaver et al., A recurring pattern of chromosomal aberrations in mammary gland tumors of MMTV-cmyc transgenic mice, GENE CHROM, 25(3), 1999, pp. 251-260
Authors:
Padilla-Nash, HM
Nash, WG
Padilla, GM
Roberson, KM
Robertson, CN
Macville, M
Schrock, E
Ried, T
Citation: Hm. Padilla-nash et al., Molecular cytogenetic analysis of the bladder carcinoma cell line BK-10 byspectral karyotyping, GENE CHROM, 25(1), 1999, pp. 53-59
Authors:
Ning, Y
Laundon, CH
Schrock, E
Buchanan, P
Ried, T
Citation: Y. Ning et al., Prenatal diagnosis of a mosaic extra structurally abnormal chromosome by spectral karyotyping, PRENAT DIAG, 19(5), 1999, pp. 480-482
Authors:
Peschka, B
Leygraaf, J
Hansmann, D
Hansmann, M
Schrock, E
Ried, T
Engels, H
Schwanitz, G
Schubert, R
Citation: B. Peschka et al., Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping, PRENAT DIAG, 19(12), 1999, pp. 1143-1149
Authors:
Liang, JC
Ning, Y
Wang, RY
Padilla-Nash, HM
Schrock, E
Soenksen, D
Nagarajan, L
Ried, T
Citation: Jc. Liang et al., Spectral karyotypic study of the HL-60 cell line: Detection of complex rearrangements involving chromosomes 5, 7, and 16 and delineation of critical region of deletion on 5q31.1, CANC GENET, 113(2), 1999, pp. 105-109
Authors:
Hilgenfeld, E
Padilla-Nash, H
Schrock, E
Ried, T
Citation: E. Hilgenfeld et al., Analysis of B-cell neoplasias by spectral karyotyping (SKY), CURR T MICR, 246, 1999, pp. 169-174
Authors:
Macville, M
Schrock, E
Padilla-Nash, H
Keck, C
Ghadimi, BM
Zimonjic, D
Popescu, N
Ried, T
Citation: M. Macville et al., Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping, CANCER RES, 59(1), 1999, pp. 141-150
Authors:
Ghadimi, BM
Schrock, E
Walker, RL
Wangsa, D
Jauho, A
Meltzer, PS
Ried, T
Citation: Bm. Ghadimi et al., Specific chromosomal aberrations and amplification of the AIB1 nuclear receptor coactivator gene in pancreatic carcinomas, AM J PATH, 154(2), 1999, pp. 525-536
Authors:
Haddad, BR
Schrock, E
Meck, J
Cowan, J
Young, H
Ferguson-Smith, MA
du Manoir, S
Ried, T
Citation: Br. Haddad et al., Identification of de novo chromosomal markers and derivatives by spectral karyotyping, HUM GENET, 103(5), 1998, pp. 619-625
Risultati:
1-16
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