Chromosome translocation based on illegitimate recombination in human tumors (original) (raw)
Comparison of constitutional and tumor-associated 11;22 translocations: nonidentical breakpoints on chromosomes 11 and 22
Jacques Ghysdael
Proceedings of the National Academy of Sciences of the United States of America, 1986
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Localization of genetic elements of intact and derivative chromosome 11 and 22 territories in nuclei of Ewing sarcoma cells
Michal Kozubek
Journal of Structural Biology, 2006
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Chromosomes in Ewing's sarcoma. I. An evaluation of 85 cases and remarkable consistency of t (11; 22)(q24; q12)
Christian Volk
Cancer genetics and …, 1988
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Chromosome translocations in cancer: computational evidence for the random generation of double-strand breaks
J. Vizmanos
Trends in Genetics, 2006
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Translocation t(11;14) in multiple myeloma: Analysis of translocation breakpoints on der(11) and der(14) chromosomes suggests complex molecular mechanisms of recombination
Guy Pratt
Genes, Chromosomes and Cancer, 2004
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Detection and molecular cytogenetic characterization of a novel ring chromosome in a histological variant of Ewing sarcoma
Karoly Szuhai
Cancer Genetics and Cytogenetics, 2007
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Recurrent gains of 1q, 8 and 12 in the Ewing family of tumours by comparative genomic hybridization
M. Caballín, O. Myklebost
1997
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Metastatic extraosseous Ewing tumor: Association of the additional translocation der(16)t(1;16) with the variant EWS/ERG rearrangement in a case of cytogenetically inconspicuous chromosome 22
Ian J Cohen
Cancer Genetics and Cytogenetics, 1996
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Bands involved in primary chromosome rearrangements in sarcomas are not constitutionally liable to breakage in sarcoma patients
Anders Rydholm
Human Genetics, 1988
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Translocation of chromosomes 11 and 22 in choroidal metastatic ewing sarcoma detected by fluorescent in situ hybridization
Svetlana Pack
American Journal of Ophthalmology, 1999
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Recurrent chromosomal translocations: Is proximity a rule?
Sonal Bakshi
Indian journal of experimental biology, 2017
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SUPPLEMENTARY DATA MATERIAL: Characterization of Chromosomal Translocation Breakpoint Sequences in Solid Tumours: “An In Silico Analysis”
Afzal Ansari
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Roles of nonhomologous DNA end joining, V(D)J recombination, and class switch recombination in chromosomal translocations
Michael Lieber
DNA Repair, 2006
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The role of chromosomal alterations in human cancer development
marco alessandro pierotti
Journal of Cellular Biochemistry, 2007
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Chromosomal Translocations and Non-B DNA Structures in the Human Genome
Michael Lieber
Cell Cycle, 2004
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Jumping translocations in hematological malignancies: a cytogenetic study of five cases
Vasileios N. Georgakakos, PhD, K. Manola
Cancer genetics and …, 2008
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Characterization of the A673 cell line (Ewing tumor) by molecular cytogenetic techniques
Miguel Urioste
Cancer Genetics and Cytogenetics, 2003
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Prognostic impact of chromosomal aberrations in Ewing tumours
Peter Ambros
2002
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Karyotypic dissection of Hodgkin’s disease cell lines reveals ectopic subtelomeres and ribosomal DNA at sites of multiple jumping translocations and genomic amplification
Irit Bar-am
Leukemia, 2000
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Possible involvement of unstable sites on chromosomes 7 and 14 in human cancer
Jacques Scheres
Cancer Genetics and Cytogenetics, 1986
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High frequency of genomic instability in Ewing family of tumors
Ian J Cohen
Cancer Genetics and Cytogenetics, 2004
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Genetic imbalances revealed by comparative genomic hybridization in Ewing tumors
Werner Boecker
Genes, Chromosomes and Cancer, 2001
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Chromosome 22 abnormalities in Ewing's sarcoma
Alan Craft
Journal of Clinical Pathology, 1989
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Coincidence of synteny breakpoints with malignancy-related deletions on human chromosome 3
Stefan Imreh
Proceedings of the National Academy of Sciences, 2003
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A Method for Accurate Detection of Translocation Junctions in Ewing Family of Tumors
mark bolander
Molecular Biotechnology, 2001
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Molecular analysis of DNA junctions produced by illegitimate recombination in human cells
Alain Sarasin
Nucleic Acids Research, 1992
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Restoring mismatch repair does not stop the formation of reciprocal translocations in the colon cancer cell line HCA7 but further destabilizes chromosome number
H. Lohi
Oncogene, 2005
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Evidence for Replicative Repair of DNA Double-Strand Breaks Leading to Oncogenic Translocation and Gene Amplification
maria jasin
2002
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Illegitimate recombination leading to allelic loss and unbalanced translocation in p53-mutated human lymphoblastoid cells
Makoto Hayashi
Molecular and cellular biology, 1997
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Segmental duplications and evolutionary plasticity at tumor chromosome break-prone regions
Stefan Imreh
Genome Research, 2008
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Dysfunctional homologous recombination mediates genomic instability and progression in myeloma
Hemanta Koley
Blood, 2009
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A DNA damage repair mechanism is involved in the origin of chromosomal translocations t(4;11) in primary leukemic cells
Arndt Borkhardt, Rolf Marschalek
Oncogene, 1999
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