(Q37986682)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22351161%20AND%20SRC:MED&resulttype=core&format=json

23 January 2020

title

Molecular nature of radiation injury and DNA repair disorders associated with radiosensitivity (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22351161%20AND%20SRC:MED&resulttype=core&format=json

23 January 2020

1 reference

18 February 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22351161%20AND%20SRC:MED&resulttype=core&format=json

International Journal of Hematology

23 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22351161%20AND%20SRC:MED&resulttype=core&format=json

23 January 2020

volume

95

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22351161%20AND%20SRC:MED&resulttype=core&format=json

23 January 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22351161%20AND%20SRC:MED&resulttype=core&format=json

23 January 2020

page(s)

239-245

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22351161%20AND%20SRC:MED&resulttype=core&format=json

Reactions of oxyl radicals with DNA.

23 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Oxidative damage to DNA in mammalian chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Instability and decay of the primary structure of DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Solution conformation of the major adduct between the carcinogen (+)-anti-benzo[a]pyrene diol epoxide and DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Inverse radiation dose-rate effects on somatic and germ-line mutations and DNA damage rates

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Chromosome instability and X-ray hypersensitivity in a microcephalic and growth-retarded child

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

A family showing no evidence of linkage between the ataxia telangiectasia gene and chromosome 11q22-23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

A single ataxia telangiectasia gene with a product similar to PI-3 kinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Positional cloning of the gene for Nijmegen breakage syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Further delineation of the Nijmegen breakage syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Eleven Polish patients with microcephaly, immunodeficiency, and chromosomal instability: the Nijmegen breakage syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Immortalization and characterization of Nijmegen Breakage syndrome fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Conserved modes of recruitment of ATM, ATR and DNA-PKcs to sites of DNA damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Mre11-Rad50-Nbs1 is a keystone complex connecting DNA repair machinery, double-strand break signaling, and the chromatin template.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

MDC1 is a mediator of the mammalian DNA damage checkpoint

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

MDC1 is coupled to activated CHK2 in mammalian DNA damage response pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Mre11 protein complex prevents double-strand break accumulation during chromosomal DNA replication.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

ATM phosphorylates histone H2AX in response to DNA double-strand breaks

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

MDC1 is required for the intra-S-phase DNA damage checkpoint

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Activation of the ATM kinase by ionizing radiation and phosphorylation of p53

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Functional interaction of H2AX, NBS1, and p53 in ATM-dependent DNA damage responses and tumor suppression

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

DNA-dependent protein kinase catalytic subunit: a relative of phosphatidylinositol 3-kinase and the ataxia telangiectasia gene product

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

A structural model for regulation of NHEJ by DNA-PKcs autophosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Functional and biochemical dissection of the structure-specific nuclease ARTEMIS

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

The Artemis:DNA-PKcs endonuclease cleaves DNA loops, flaps, and gaps

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Activity of DNA ligase IV stimulated by complex formation with XRCC4 protein in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Mammalian DNA double-strand break repair protein XRCC4 interacts with DNA ligase IV

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Immunoglobulin metabolism in ataxia telangiectasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Nijmegen Breakage syndrome: a progress report

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Decreased immunoglobulin class switching in Nijmegen Breakage syndrome due to the DNA repair defect.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Heterogeneity of humoral immune abnormalities in children with Nijmegen breakage syndrome: an 8-year follow-up study in a single centre.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

ATM is not required in somatic hypermutation of VH, but is involved in the introduction of mutations in the switch mu region

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

ATM is required for efficient recombination between immunoglobulin switch regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Immunoglobulin class switch recombination is impaired in Atm-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Nibrin functions in Ig class-switch recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Genomic instability, endoreduplication, and diminished Ig class-switch recombination in B cells lacking Nbs1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

A new type of radiosensitive T-B-NK+ severe combined immunodeficiency caused by a LIG4 mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Defective DNA-dependent protein kinase activity is linked to V(D)J recombination and DNA repair defects associated with the murine scid mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

SCID in Jack Russell terriers: a new animal model of DNA-PKcs deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Leaky Scid phenotype associated with defective V(D)J coding end processing in Artemis-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Impaired lymphocyte development and antibody class switching and increased malignancy in a murine model of DNA ligase IV syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Critical role for Atm in suppressing V(D)J recombination-driven thymic lymphoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Therapy for non-Hodgkin lymphoma in children with primary immunodeficiency: analysis of 19 patients from the BFM trials.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Posttransplant T-cell lymphoma. Report of three cases and a review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

A patient with mutations in DNA Ligase IV: clinical features and overlap with Nijmegen breakage syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

A severe form of human combined immunodeficiency due to mutations in DNA ligase IV.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Genetic pathway to recurrent chromosome translocations in murine lymphoma involves V(D)J recombinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Irradiation promotes V(D)J joining and RAG-dependent neoplastic transformation in SCID T-cell precursors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1008-Y

A kinase-negative mutation of DNA-PK(CS) in equine SCID results in defective coding and signal joint formation

21 January 2018

1 reference

12 December 2020

Splitting the ATM: distinct repair and checkpoint defects in ataxia–telangiectasia

1 reference

12 December 2020

Alternative end joining during switch recombination in patients with ataxia-telangiectasia

1 reference

12 December 2020

Inhibition of DNA synthesis by ionizing radiation: a marker for an S-phase checkpoint

1 reference

12 December 2020

A DNA-PKcs mutation in a radiosensitive T-B- SCID patient inhibits Artemis activation and nonhomologous end-joining.

1 reference

12 December 2020

Severe combined immunodeficiency among the Navajo. I. Characterization of phenotypes, epidemiology, and population genetics

1 reference

12 December 2020

Hypersensitivity to ionizing radiation, in vitro, in a new chromosomal breakage disorder, the Nijmegen Breakage Syndrome.

1 reference

12 December 2020

Damage-resistant DNA synthesis in eukaryotes

1 reference

12 December 2020

Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients

1 reference

12 December 2020

Radiation reaction in ataxia telangiectasia

1 reference

12 December 2020

Single-strand break repair and genetic disease

1 reference

12 December 2020

Variant of ataxia-telangiectasia with low-level radiosensitivity

1 reference

12 December 2020

Partial T and B lymphocyte immunodeficiency and predisposition to lymphoma in patients with hypomorphic mutations in Artemis

1 reference

12 December 2020

Leukemia and lymphoma in ataxia telangiectasia

1 reference

12 December 2020

Epstein-Barr virus-associated B-cell lymphoma in a patient with DNA ligase IV (LIG4) syndrome

1 reference

12 December 2020

Ataxia-telangiectasia: A multiparameter analysis of eight families

1 reference

12 December 2020

Ataxia-telangiectasia

1 reference

12 December 2020

IgG2 deficiency in ataxia-telangiectasia

1 reference

12 December 2020

Studies on depurination of DNA by heat

1 reference

12 December 2020

Ataxia telangiectasia. Neoplasia, untoward response to x-irradiation, and tuberous sclerosis

1 reference

12 December 2020

DNA damage produced by ionizing radiation in mammalian cells: identities, mechanisms of formation, and reparability

1 reference

12 December 2020

Nijmegen Breakage Syndrome: a progress report

1 reference

12 December 2020

10.1007/S12185-012-1008-Y

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22351161%20AND%20SRC:MED&resulttype=core&format=json

23 January 2020

1 reference