(Q79264601)

English

A FISH comparison of variant derivatives of the recurrent dic(17;20) of myelodysplastic syndromes and acute myeloid leukemia: Obligatory retention of genes on 17p and 20q may explain the formation of dicentric chromosomes

scientific article published on 01 January 2007

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scholarly article

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Europe PubMed Central

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20 December 2019

A FISH comparison of variant derivatives of the recurrent dic(17;20) of myelodysplastic syndromes and acute myeloid leukemia: Obligatory retention of genes on 17p and 20q may explain the formation of dicentric chromosomes (English)

1 reference

Europe PubMed Central

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20 December 2019

acute myeloid leukemia

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author name string

Ruth N MacKinnon

1

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20 December 2019

Cris Patsouris

2

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20 December 2019

Ilse Chudoba

3

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20 December 2019

Lynda J Campbell

4

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20 December 2019

publication date

1 January 2007

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20 December 2019

Genes, Chromosomes and Cancer

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20 December 2019

46

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20 December 2019

1

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20 December 2019

27-36

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Europe PubMed Central

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20 December 2019

Centromeric breakage and highly rearranged chromosome derivatives associated with mutations of TP53 are common in therapy-related MDS and AML after therapy with alkylating agents: an M-FISH study

1 reference

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7 January 2021

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Increased frequency of dicentric chromosomes in therapy-related MDS and AML compared to de novo disease is significantly related to previous treatment with alkylating agents and suggests a specific susceptibility to chromosome breakage at the centro

1 reference

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7 January 2021

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An essential role for DNA methyltransferase DNMT3B in cancer cell survival

1 reference

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7 January 2021

based on heuristic

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Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes

1 reference

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7 January 2021

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Proposals for the Classification of the Acute Leukaemias French-American-British (FAB) Co-operative Group

1 reference

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7 January 2021

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Proposal for the recognition of minimally differentiated acute myeloid leukaemia (AML-MO)

1 reference

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7 January 2021

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A case of isodicentric 7p as sole abnormality in a patient with acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

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Interphase FISH screening for the LCR-mediated common rearrangement of isochromosome 17q in primary myelofibrosis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

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Changes in apoptosis-related pathways in acute myelocytic leukemia

1 reference

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7 January 2021

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Monosomy 20 as a pointer to dicentric (9;20) in acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH study

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

The management of patients with leukaemia: the role of cytogenetics in this molecular era.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

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Dicentric (9;20)(p11;q11) identified by fluorescence in situ hybridization in four pediatric acute lymphoblastic leukemia patients

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

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Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

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Detailed characterization of a homozygously deleted region corresponding to a candidate tumor suppressor locus at distal 17p13.3 in human lung cancer.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical and molecular cytogenetic studies in seven patients with myeloid diseases characterized by i(20q-)

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

FISH studies identify the i(20q-) anomaly as a der(20)del(20)(q11q13)idic(20)(p11)

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytogenetic profile of myelodysplastic syndromes with complex karyotypes: an analysis using spectral karyotyping

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Isochromosome breakpoints on 17p in medulloblastoma are flanked by different classes of DNA sequence repeats

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Double 20q- anomaly in myelodysplastic syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromosome stability is maintained by short intercentromeric distance in functionally dicentric human Robertsonian translocations

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

The isochromosome (17q) in chronic myelocytic leukaemia: mechanism of origin, centromeric function and clonal evolution

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

A new nonrandom unbalanced t(17;20) in myeloid malignancies

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a commonly deleted region at 17p13.3 in leukemia and lymphoma associated with 17p abnormality

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q)

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

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Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Demonstration of i(17q) in metaphase and interphase of malignant hematopoietic cells by fluorescence in situ hybridization

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

DNA methyltransferase 3b contributes to oncogenic transformation induced by SV40T antigen and activated Ras.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of centromeric antigens in dicentric Robertsonian translocations: CENP-C and CENP-E are necessary components of functional centromeres

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Stable dicentric X chromosomes with two functional centromeres.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using M-FISH.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

dic(5;17): a recurring abnormality in malignant myeloid disorders associated with mutations of TP53

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

17p- syndrome arising from a novel dicentric translocation in a patient with acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Increased gene copy numbers at chromosome 20q are frequent in both squamous cell carcinomas and adenocarcinomas of the cervix

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20385

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.20385

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17048234%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17048234%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

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