(Q44666439)

English

Mutations of the Huntington's disease protein impact on the ATM-dependent signaling and repair pathways of the radiation-induced DNA double-strand breaks: corrective effect of statins and bisphosphonates.

scientific article published on 26 November 2013

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24277524%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

Mutations of the Huntington's disease protein impact on the ATM-dependent signaling and repair pathways of the radiation-induced DNA double-strand breaks: corrective effect of statins and bisphosphonates (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24277524%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

Huntington's disease

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Guillaume Vogin

7

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24277524%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

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Mélanie L Ferlazzo

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24277524%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

Laurène Sonzogni

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24277524%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

Adeline Granzotto

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24277524%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

Larry Bodgi

4

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Europe PubMed Central

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1 March 2020

Océane Lartin

5

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24277524%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

Clément Devic

6

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24277524%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

Sandrine Pereira

8

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24277524%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

Nicolas Foray

9

1 reference

Europe PubMed Central

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1 March 2020

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26 November 2013

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Europe PubMed Central

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1 March 2020

Molecular Neurobiology

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24277524%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

49

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Europe PubMed Central

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1 March 2020

3

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1 March 2020

1200-1211

1 reference

Europe PubMed Central

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1 March 2020

https://scigraph.springernature.com/pub.10.1007/s12035-013-8591-7

0 references

Huntington disease and the huntingtin protein

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

The incidence and prevalence of Huntington's disease: a systematic review and meta-analysis

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Beyond the brain: widespread pathology in Huntington's disease

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat number

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Site of (CCG) polymorphism in the HD gene

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

An in vitro perspective on the molecular mechanisms underlying mutant huntingtin protein toxicity

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

DNA repair mechanisms in Huntington's disease

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Mutant huntingtin impairs Ku70-mediated DNA repair

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Presymptomatic diagnosis of Huntington's disease?

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Radiosensitivity in Huntington's disease: implications for pathogenesis and presymptomatic diagnosis

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

A review of human cell radiosensitivity in vitro

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

DNA double-strand breaks: their cellular and clinical impact?

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

DNA double-strand break repair defects in syndromes associated with acute radiation response: at least two different assays to predict intrinsic radiosensitivity?

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Evidence for a lack of DNA double-strand break repair in human cells exposed to very low x-ray doses

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

A single formula to describe radiation-induced protein relocalization: towards a mathematical definition of individual radiosensitivity.

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Hypersensitivity of ataxia telangiectasia fibroblasts to ionizing radiation is associated with a repair deficiency of DNA double-strand breaks

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

A subset of ATM- and ATR-dependent phosphorylation events requires the BRCA1 protein

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Combined treatment with statins and aminobisphosphonates extends longevity in a mouse model of human premature aging.

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Consequences of the bleed-through phenomenon in immunofluorescence of proteins forming radiation-induced nuclear foci

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Normal huntingtin function: an alternative approach to Huntington's disease

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

HP1 and the dynamics of heterochromatin maintenance

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

The emerging role of HP1 in the DNA damage response

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Heterochromatin formation in mammalian cells: interaction between histones and HP1 proteins

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Oxidative genome damage and its repair: implications in aging and neurodegenerative diseases.

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Observations of radiation-induced chromosome fragment loss in live mammalian cells in culture, and its effect on colony-forming ability

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Inherent cellular radiosensitivity as a basic concept for human tumor radiotherapy.

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

DNA breakage and induction of DNA damage response proteins precede the appearance of visible mutant huntingtin aggregates

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Deregulation of BRCA1 leads to impaired spatiotemporal dynamics of γ-H2AX and DNA damage responses in Huntington's disease

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

ATM is a cytoplasmic protein in mouse brain required to prevent lysosomal accumulation.

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Dysfunction of the cholesterol biosynthetic pathway in Huntington's disease.

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Altered cholesterol homeostasis contributes to enhanced excitotoxicity in Huntington's disease.

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Study on the variation in X-ray sensitivity of human diploid skin fibroblasts. Normal radiosensitivity of cells derived from patients with Huntington's disease

1 reference

https://api.crossref.org/works/10.1007%2FS12035-013-8591-7

21 January 2018

Xeroderma pigmentosum: its overlap with trichothiodystrophy, Cockayne syndrome and other progeroid syndromes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/24277524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A quantitative comparison of potentially lethal damage repair and the rejoining of interphase chromosome breaks in low passage normal human fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/24277524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

53BP1, an activator of ATM in response to DNA damage

1 reference

https://pubmed.ncbi.nlm.nih.gov/24277524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sensitivity to ionising radiation of lymphocytes from Huntington's chorea patients compared to controls

1 reference

https://pubmed.ncbi.nlm.nih.gov/24277524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficient recovery from potentially lethal damage in some gamma-irradiated human fibroblast cell strains

1 reference

https://pubmed.ncbi.nlm.nih.gov/24277524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Radiation sensitivity of fibroblast strains from patients with Usher's syndrome, Duchenne muscular dystrophy, and Huntington's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/24277524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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