Interstitial and large chromosome 1p deletion occurs in localized and disseminated neuroblastomas and predicts an unfavourable outcome (Q59672669)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9751260%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

title

Interstitial and large chromosome 1p deletion occurs in localized and disseminated neuroblastomas and predicts an unfavourable outcome (English)

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4 December 2019

5

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4 December 2019

Paola Ghisellini

7

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4 December 2019

Maria F. Faienza

8

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4 December 2019

Massimo Conte

11

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4 December 2019

author name string

A Iolascon

1

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4 December 2019

C Lo Cunsolo

2

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4 December 2019

L Giordani

3

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4 December 2019

R Cusano

4

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4 December 2019

M Boumgartner

6

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4 December 2019

L Boni

9

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4 December 2019

B De Bernardi

10

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4 December 2019

G Romeo

12

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4 December 2019

G P Tonini

13

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4 December 2019

language of work or name

English

0 references

publication date

1 August 1998

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4 December 2019

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4 December 2019

volume

130

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4 December 2019

issue

1-2

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4 December 2019

page(s)

83-92

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Amplified DNA with limited homology to myc cellular oncogene is shared by human neuroblastoma cell lines and a neuroblastoma tumour

4 December 2019

cites work

1 reference

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7 January 2021

Abnormalities of chromosome 1p in human neuroblastoma tumors and cell lines

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Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas

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Analysis of N-myc amplification in relation to disease stage and histologic types in human neuroblastomas

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Age-dependent prognostic significance of N-myc amplification in neuroblastoma. The Italian experience

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MYCN oncogene amplification in neuroblastoma is associated with worse prognosis, except in stage 4s: the Italian experience with 295 children

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7 January 2021

Two distinct deleted regions on the short arm of chromosome I in neuroblastoma

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7 January 2021

Gene amplification in human neuroblastomas: basic mechanisms and clinical implications

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7 January 2021

Cytogenetic findings and prognosis in neuroblastoma with emphasis on marker chromosome 1.

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Fluorescence in situ hybridization combined with immunohistochemistry for highly sensitive detection of chromosome 1 aberrations in neuroblastoma

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7 January 2021

Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification

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7 January 2021

PCR assay for chromosome 1p deletion in small neuroblastoma samples

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7 January 2021

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

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7 January 2021

There may be two tumor suppressor genes on chromosome arm 1p closely associated with biologically distinct subtypes of neuroblastoma

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7 January 2021

International criteria for diagnosis, staging, and response to treatment in patients with neuroblastoma

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7 January 2021

Peculiar allelotype associated with susceptibility to neuroblastoma

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7 January 2021

A comprehensive genetic map of the human genome based on 5,264 microsatellites

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7 January 2021

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

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7 January 2021

Detection of specific sequences among DNA fragments separated by gel electrophoresis

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7 January 2021

Cloning, chromosomal localization, physical mapping, and genomic characterization of HKR3

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7 January 2021

Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers

1 reference

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7 January 2021

Genomic instability in 1p and human malignancies

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7 January 2021

N-myc gene amplification/expression in localized stroma-rich neuroblastoma (ganglioneuroblastoma)

1 reference

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7 January 2021

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Identifiers

DOI

1 reference

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4 December 2019

1 reference