(Q73048185)

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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

scientific article published on 01 October 2000

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31 October 2019

Karyotypic dissection of Hodgkin's disease cell lines reveals ectopic subtelomeres and ribosomal DNA at sites of multiple jumping translocations and genomic amplification (English)

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31 October 2019

Hans Guenter Drexler

7

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H G Drexler

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31 October 2019

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R A MacLeod

1

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31 October 2019

D Spitzer

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31 October 2019

I Bar-Am

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31 October 2019

J E Sylvester

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31 October 2019

M Kaufmann

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31 October 2019

A Wernich

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31 October 2019

publication date

1 October 2000

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31 October 2019

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31 October 2019

14

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31 October 2019

10

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31 October 2019

1803-1814

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31 October 2019

https://scigraph.springernature.com/pub.10.1038/sj.leu.2401894

0 references

Chromosomes of Sternberg-Reed cells

1 reference

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Cytogenetics of Hodgkin's disease

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Unique display of a pathologic karyotype in Hodgkin's disease by Reed-Sternberg cells

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The Reed-Sternberg cells of Hodgkin disease are clonal

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Hodgkin and Reed-Sternberg cells in Hodgkin's disease represent the outgrowth of a dominant tumor clone derived from (crippled) germinal center B cells.

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Phenotype, genotype and clonality of Reed-Sternberg cells in nodular sclerosis Hodgkin's disease: results of a single-cell study

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Hodgkin's disease with monoclonal and polyclonal populations of Reed-Sternberg cells

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THE ORIGIN OF HODGKIN AND REED/STERNBERG CELLS IN HODGKIN'S DISEASE

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Rare occurrence of classical Hodgkin's disease as a T cell lymphoma

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Multicolor FISHing: what's the catch?

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Multicolor Spectral Karyotyping of Human Chromosomes

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Hodgkin's disease derived cell lines HDLM-2 and L-428: comparison of morphology, immunological and isoenzyme profiles

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B7-1 (CD80) as target for immunotoxin therapy for Hodgkin's disease

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Soluble vascular cell adhesion molecule-1 (sVCAM-1) is an independent prognostic marker in Hodgkin's disease

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The mummified Hodgkin cell: cell death in Hodgkin's disease

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Clonal deleterious mutations in the IkappaBalpha gene in the malignant cells in Hodgkin's lymphoma

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Defective IkappaBalpha in Hodgkin cell lines with constitutively active NF-kappaB.

1 reference

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The human ribosomal RNA genes: structure and organization of the complete repeating unit

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Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' end.

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Oligonucleotide-primed in situ DNA synthesis (PRINS): a method for chromosome mapping, banding, and investigation of sequence organization

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Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

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Detection of amplified DNA sequences by reverse chromosome painting using genomic tumor DNA as probe

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Ribosomal DNA clusters in pulsed-field gel electrophoretic analysis of human acrocentric chromosomes

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Cytogenetic and molecular genetic analysis of abnormal cells in Hodgkin's disease

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Chromosomal abnormalities in malignant lymphoma and Hodgkin's disease

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Karyotypic abnormalities and immunoglobulin gene rearrangements in Hodgkin's disease

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Clonal cytogenetic abnormalities in Hodgkin's disease

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Recurring chromosome abnormalities in Hodgkin's disease

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Phenotypic and genotypic characterization of Hodgkin's disease

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A breakpoint map of recurrent chromosomal rearrangements in human neoplasia

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Complete sequence of the 43-kb human ribosomal DNA repeat: analysis of the intergenic spacer

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Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization

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Aneuploidy and cancer

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Occurrence of TEL-AML1 fusion resulting from (12;21) translocation in human early B-lineage leukemia cell lines

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Fluorescence in situ hybridization assessment of the telomeric regions of jumping translocations in a case of aggressive B-cell non-Hodgkin lymphoma

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Interstitial telomeric sequences at the junction site of a jumping translocation

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Molecular characterization of jumping translocations reveals spatial and temporal breakpoint heterogeneity

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Instability of dinucleotide repeats in Hodgkin's disease.

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Chromosomal in situ hybridization of a Hodgkin's disease-derived cell line (L540) using DNA probes for TCRA, TCRB, MET, and rRNA.

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Nucleoli and AgNORs in Hodgkin's disease

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1 reference

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