(Q54774700)

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Multiplex single-tube screening for mutations in the Nijmegen Breakage Syndrome (NBS1) gene in Hodgkin's and non-Hodgkin's lymphoma patients of Slavic origin.

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scholarly article

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12734548

Multiplex single-tube screening for mutations in the Nijmegen Breakage Syndrome (NBS1) gene in Hodgkin's and non-Hodgkin's lymphoma patients of Slavic origin. (English)

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12734548

Nijmegen breakage syndrome

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12734548

3

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Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12734548

Anne-Lise Børresen-Dale

7

object named as

Anne-Lise Børresen-Dale

1 reference

Europe PubMed Central

3 June 2018

Vessela Kristensen

8

object named as

Vessela N Kristensen

1 reference

Europe PubMed Central

3 June 2018

Grethe Grenaker Alnæs

5

object named as

Grethe Grenaker Alnaes

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12734548

author name string

Ivan Gut

2

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12734548

Eva Skovlund

4

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12734548

Tom Kristensen

6

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Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12734548

publication date

1 May 2003

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Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12734548

European Journal of Human Genetics

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Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12734548

11

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3 June 2018

http://europepmc.org/abstract/MED/12734548

416-419

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3 June 2018

http://europepmc.org/abstract/MED/12734548

5

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12734548

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200972

0 references

ATM-dependent phosphorylation of nibrin in response to radiation exposure

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

21 January 2018

Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

21 January 2018

Cancer in patients with ataxia-telangiectasia and in their relatives in the nordic countries

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

21 January 2018

Positional cloning of the gene for Nijmegen breakage syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

21 January 2018

Association of BRCA1 with the hRad50-hMre11-p95 complex and the DNA damage response

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

21 January 2018

Nbs1 potentiates ATP-driven DNA unwinding and endonuclease cleavage by the Mre11/Rad50 complex

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

21 January 2018

Chk2 activation dependence on Nbs1 after DNA damage

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

21 January 2018

The Nijmegen breakage syndrome protein is essential for Mre11 phosphorylation upon DNA damage

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

21 January 2018

Targeted disruption of the Nijmegen breakage syndrome gene NBS1 leads to early embryonic lethality in mice.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

21 January 2018

An alternative mode of translation permits production of a variant NBS1 protein from the common Nijmegen breakage syndrome allele

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

21 January 2018

Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slav populations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

21 January 2018

Genetic polymorphisms of biotransformation enzymes in patients with Hodgkin's and non-Hodgkin's lymphomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

21 January 2018

An increased risk for malignant neoplasms in heterozygotes for a syndrome of microcephaly, normal intelligence, growth retardation, remarkable facies, immunodeficiency and chromosomal instability.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

7 January 2021

based on heuristic

inferred from DOI database lookup

No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non-Hodgkin's lymphoma of childhood and adolescence

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200972

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.EJHG.5200972

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12734548

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12734548

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