(Q45001863)

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Characterization of a conserved aphidicolin-sensitive common fragile site at human 4q22 and mouse 6C1: possible association with an inherited disease and cancer

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scholarly article

1 reference

Europe PubMed Central

8 December 2017

Characterization of a conserved aphidicolin-sensitive common fragile site at human 4q22 and mouse 6C1: possible association with an inherited disease and cancer (English)

1 reference

Europe PubMed Central

8 December 2017

author name string

Lorène Rozier

1

1 reference

Europe PubMed Central

8 December 2017

Eliane El-Achkar

2

1 reference

Europe PubMed Central

8 December 2017

Françoise Apiou

3

1 reference

Europe PubMed Central

8 December 2017

Michelle Debatisse

4

1 reference

Europe PubMed Central

8 December 2017

language of work or name

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publication date

1 September 2004

1 reference

Europe PubMed Central

8 December 2017

1 reference

Europe PubMed Central

8 December 2017

23

1 reference

Europe PubMed Central

8 December 2017

6872-6880

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Europe PubMed Central

8 December 2017

41

1 reference

Europe PubMed Central

8 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.onc.1207809

0 references

Common fragile sites.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

Evidence that instability within the FRA3B region extends four megabases

1 reference

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21 January 2018

Specific association between alcohol intake, high grade of differentiation and 4q34-q35 deletions in hepatocellular carcinomas identified by high resolution allelotyping

1 reference

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21 January 2018

A mortality gene(s) for the human adenocarcinoma line HeLa maps to a 130-kb region of human chromosome 4q22-q23

1 reference

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21 January 2018

Genetics of hepatocellular carcinoma

1 reference

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21 January 2018

New targets of beta-catenin signaling in the liver are involved in the glutamine metabolism

1 reference

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21 January 2018

Characteristic chromosomal fragility of human embryonic cells exposed in vitro to aphidicolin.

1 reference

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21 January 2018

Initiation of the breakage-fusion-bridge mechanism through common fragile site activation in human breast cancer cells: the model of PIP gene duplication from a break at FRA7I

1 reference

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21 January 2018

Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons

1 reference

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21 January 2018

Induction of multiple double-strand breaks within an hsr by meganucleaseI-SceI expression or fragile site activation leads to formation of double minutes and other chromosomal rearrangements

1 reference

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21 January 2018

A new role for hypoxia in tumor progression: induction of fragile site triggering genomic rearrangements and formation of complex DMs and HSRs

1 reference

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21 January 2018

Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer.

1 reference

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21 January 2018

Alterations in the common fragile site gene Parkin in ovarian and other cancers

1 reference

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21 January 2018

Rodent common fragile sites: are they conserved? Evidence from mouse and rat.

1 reference

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21 January 2018

Muir-Torre-like syndrome in Fhit-deficient mice

1 reference

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21 January 2018

Functional evidence for a squamous cell carcinoma mortality gene(s) on human chromosome 4.

1 reference

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21 January 2018

Increased expression of aphidicolin-induced common fragile sites in Tourette syndrome: the key to understand the genetics of comorbid phenotypes?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

Loss of FHIT protein expression is a marker of adverse evolution in good prognosis localized breast cancer.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

The human glutamate receptor delta 2 gene (GRID2) maps to chromosome 4q22

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

FRA3B and other common fragile sites: the weakest links

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

The common fragile site FRA16D and its associated gene WWOX are highly conserved in the mouse at Fra8E1

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

Hotfoot mouse mutations affect the delta 2 glutamate receptor gene and are allelic to lurcher.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

Neurobiological effects of a null mutation depend on genetic context: comparison between two hotfoot alleles of the delta-2 ionotropic glutamate receptor

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

Genetic alterations associated with hepatocellular carcinomas define distinct pathways of hepatocarcinogenesis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

Beta-catenin mutations in hepatocellular carcinoma correlate with a low rate of loss of heterozygosity.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

Cell type-dependent difference in the distribution and frequency of aphidicolin-induced fragile sites: T and B lymphocytes and bone marrow cells

1 reference

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21 January 2018

Deletion 4q21/4q22 syndrome: two patients with de novo 4q21.3q23 and 4q13.2q23 deletions

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

Interspersed repeats and other mementos of transposable elements in mammalian genomes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

The clinical significance of fragile sites on human chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

An 8-cM interstitial deletion on 4q21-q22 in DNA from an infant with hepatoblastoma overlaps with a commonly deleted region in adult liver cancers.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

A hot spot for hotfoot mutations in the gene encoding the delta2 glutamate receptor

1 reference

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21 January 2018

Constitutive fragile sites and cancer.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

The delta2 glutamate receptor: 10 years later

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

Allelic loss on chromosomes 4q and 16q in hepatocellular carcinoma: Association with elevated alpha-fetoprotein production

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

Comprehensive allelotyping of human hepatocellular carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

The Characterization of the Common Fragile Site FRA16D and Its Involvement in Multiple Myeloma Translocations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

21 January 2018

Characterization of the common fragile site FRA9E and its potential role in ovarian cancer

1 reference

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7 January 2021

based on heuristic

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Transcriptional profiling reveals that several common fragile-site genes are downregulated in ovarian cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

7 January 2021

based on heuristic

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Common fragile sites in chromosomes of bone marrow cells and peripheral blood lymphocytes from healthy persons and leukemia patients

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

7 January 2021

based on heuristic

inferred from DOI database lookup

A role for common fragile site induction in amplification of human oncogenes

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

A simple method for simultaneous R- or G-banding and fluorescence in situ hybridization of small single-copy genes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207809

7 January 2021

based on heuristic

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Mapping FRA11A, a folate-sensitive fragile site in human chromosome band 11q13.3.

1 reference

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7 January 2021

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Identification of homozygous deletions at chromosome 16q23 in aflatoxin B1 exposed hepatocellular carcinoma

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.ONC.1207809

1 reference

Europe PubMed Central

8 December 2017

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1 reference

Europe PubMed Central

8 December 2017

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