(Q40671217)

English

Combined 24-color karyotyping and comparative genomic hybridization analysis indicates predominant rearrangements of early replicating chromosome regions in neuroblastoma

scientific article published on February 2003

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scholarly article

1 reference

Europe PubMed Central

22 September 2017

Combined 24-color karyotyping and comparative genomic hybridization analysis indicates predominant rearrangements of early replicating chromosome regions in neuroblastoma (English)

1 reference

Europe PubMed Central

22 September 2017

0 references

Isabelle Janoueix-Lerosey

object named as

Isabelle Janoueix-Lerosey

2

0 references

Olivier Delattre

object named as

Olivier Delattre

7

0 references

Gudrun Schleiermacher

1

object named as

Gudrun Schleiermacher

1 reference

Europe PubMed Central

22 September 2017

6

object named as

Alain Aurias

1 reference

Europe PubMed Central

22 September 2017

Valérie Combaret

3

object named as

Valérie Combaret

1 reference

Europe PubMed Central

22 September 2017

author name string

Josette Derré

4

1 reference

Europe PubMed Central

22 September 2017

Jérome Couturier

5

1 reference

Europe PubMed Central

22 September 2017

publication date

1 February 2003

1 reference

Europe PubMed Central

22 September 2017

Cancer Genetics and Cytogenetics

1 reference

Europe PubMed Central

22 September 2017

141

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Europe PubMed Central

22 September 2017

1

1 reference

Europe PubMed Central

22 September 2017

32-42

1 reference

Europe PubMed Central

22 September 2017

Molecular biology of neuroblastoma

1 reference

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7 January 2021

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Comparative genomic hybridization (CGH) analysis of neuroblastomas--an important methodological approach in paediatric tumour pathology

1 reference

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7 January 2021

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Comparative genomic hybridization and telomerase activity analysis identify two biologically different groups of 4s neuroblastomas

1 reference

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7 January 2021

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Genetic heterogeneity of neuroblastoma studied by comparative genomic hybridization.

1 reference

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7 January 2021

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Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

based on heuristic

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1;17 translocations and other chromosome 17 rearrangements in human primary neuroblastoma tumors and cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

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Additional copies of a 25 Mb chromosomal region originating from 17q23.1-17qter are present in 90% of high-grade neuroblastomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

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Promiscuous translocations of chromosome arm 17q in human neuroblastomas

1 reference

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7 January 2021

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Molecular cytogenetic delineation of 17q translocation breakpoints in neuroblastoma cell lines.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

based on heuristic

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Molecular analysis of chromosome arm 17q gain in neuroblastoma

1 reference

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7 January 2021

based on heuristic

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Comprehensive genetic and histopathologic study reveals three types of neuroblastoma tumors.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

based on heuristic

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Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

based on heuristic

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Coordinate deletion of chromosome 3p and 11q in neuroblastoma detected by comparative genomic hybridization

1 reference

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7 January 2021

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Comparative genomic hybridization (CGH) analysis of stage 4 neuroblastoma reveals high frequency of 11q deletion in tumors lackingMYCN amplification

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

based on heuristic

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Gain of chromosome arm 17q is associated with unfavourable prognosis in neuroblastoma, but does not involve mutations in the somatostatin receptor 2(SSTR2) gene at 17q24.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

based on heuristic

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Multicolor Spectral Karyotyping of Human Chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

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Karyotyping human chromosomes by combinatorial multi-fluor FISH.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Coexistence of several unbalanced translocations in a case of neuroblastoma: the contribution of multicolor spectral karyotyping

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY).

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

based on heuristic

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Combined M-FISH and CGH analysis allows comprehensive description of genetic alterations in neuroblastoma cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

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Sensitive detection of numerical and structural aberrations of chromosome 1 in neuroblastoma by interphase fluorescence in situ hybridization. Comparison with restriction fragment length polymorphism and conventional cytogenetic analyses

1 reference

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7 January 2021

based on heuristic

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Cytogenetic and molecular study of two human neuroblastoma cell lines.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

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N-myc expression switched off and class I human leukocyte antigen expression switched on after somatic cell fusion of neuroblastoma cells

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

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Inactivation of the NF1 gene in human melanoma and neuroblastoma cell lines without impaired regulation of GTP.Ras

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7 January 2021

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Metaphase chromosome anomaly: association with drug resistance and cell-specific products

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

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Chromosome analysis of human neuroblastoma cell line TR14 showing double minutes and an aberration involving chromosome 1.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900644-1

7 January 2021

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Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

1 reference

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7 January 2021

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Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analyses

1 reference

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7 January 2021

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Sequence of DNA replication in 277 R- and Q-bands of human chromosomes using a BrdU treatment

1 reference

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Analysis of DNA replication during S-phase by means of dynamic chromosome banding at high resolution

1 reference

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7 January 2021

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Comparative genomic hybridization analysis of human neuroblastomas: detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell lines.

1 reference

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7 January 2021

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N-myc enhances the expression of a large set of genes functioning in ribosome biogenesis and protein synthesis

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The MEIS1 oncogene is highly expressed in neuroblastoma and amplified in cell line IMR32

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Break-induced replication: a review and an example in budding yeast

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Delayed replication timing leads to delayed mitotic chromosome condensation and chromosomal instability of chromosome translocations

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Chromosome-wide assessment of replication timing for human chromosomes 11q and 21q: disease-related genes in timing-switch regions

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Molecular cytogenetic analysis of breast cancer cell lines

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Chromosomal alterations in 15 breast cancer cell lines by comparative genomic hybridization and spectral karyotyping.

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Characterization of chromosome aberrations associated with soft-tissue leiomyosarcomas by twenty-four-color karyotyping and comparative genomic hybridization analysis

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Identifiers

10.1016/S0165-4608(02)00644-1

1 reference

Europe PubMed Central

22 September 2017

1 reference

Europe PubMed Central

22 September 2017

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