(Q54594491)

1 June 2018

title

Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia. (English)

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1 June 2018

Danuta Januszkiewicz-Lewandowska

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4

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author name string

Mosor M

1

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1 June 2018

Ziółkowska I

2

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1 June 2018

Pernak-Schwarz M

3

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Nowak J

5

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1 June 2018

publication date

29 June 2006

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1 June 2018

published in

Leukemia

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1 June 2018

volume

20

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1 June 2018

issue

8

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page(s)

1454-1456

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https://scigraph.springernature.com/pub.10.1038/sj.leu.2404285

exact match

0 references

cites work

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.LEU.2404285

Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404285

Mutations and molecular variants of the NBS1 gene in non-Hodgkin lymphoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404285

NBS1 localizes to gamma-H2AX foci through interaction with the FHA/BRCT domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404285

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404285

7 January 2021

Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish pediatric patients with sporadic lymphoid malignancies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404285

7 January 2021

The common deletion 657del5 in the Nibrin gene is not a major risk factor for B or T cell non-Hodgkin lymphoma in a pediatric population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404285

7 January 2021

First case of aplastic anemia in a Japanese child with a homozygous missense mutation in the NBS1 gene (I171V) associated with genomic instability

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404285

7 January 2021

Identifiers

DOI

10.1038/SJ.LEU.2404285

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1 June 2018

Dimensions Publication ID

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1 June 2018