(Q52903919)

9 May 2018

title

High prevalence of the NBN gene mutation c.657-661del5 in Southeast Germany. (English)

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9 May 2018

author name string

M H Maurer

1

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9 May 2018

K Hoffmann

2

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9 May 2018

K Sperling

3

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9 May 2018

R Varon

4

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9 May 2018

publication date

1 January 2010

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9 May 2018

Journal of Applied Genetics

published in

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9 May 2018

volume

51

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9 May 2018

issue

2

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9 May 2018

page(s)

211-214

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9 May 2018

https://scigraph.springernature.com/pub.10.1007/bf03195730

exact match

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cites work

Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours.

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12 December 2020

Germline 657del5 mutation in the NBS1 gene in breast cancer patients

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12 December 2020

Non-Hodgkin lymphoma (NHL) in children with Nijmegen Breakage syndrome (NBS)

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

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Determination of the frequency of the common 657Del5 Nijmegen breakage syndrome mutation in the German population: no association with risk of breast cancer

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12 December 2020

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

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Correspondence re: R. Varon et al., Mutations in the Nijmegen breakage syndrome gene (NBS1) in childhood acute lymphoblastic leukemia. Cancer Res., 61: 3570-3572, 2001

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12 December 2020

Positional cloning of the gene for Nijmegen breakage syndrome

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12 December 2020

Germline 657del5 mutation in the NBS1 gene in patients with malignant melanoma of the skin.

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12 December 2020

Nijmegen Breakage Syndrome mutations and risk of breast cancer

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12 December 2020

Differing responses of Nijmegen breakage syndrome and ataxia telangiectasia cells to ionizing radiation

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12 December 2020

Radiosensitivity of ataxia telangiectasia and Nijmegen breakage syndrome homozygotes and heterozygotes as determined by three-color FISH chromosome painting

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12 December 2020

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

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12 December 2020

Role of Nbs1 in the activation of the Atm kinase revealed in humanized mouse models

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12 December 2020

Frequency of 657del(5) mutation of the NBS1 gene in the Czech population by polymerase chain reaction with sequence specific primers

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12 December 2020

Non-Hodgkin's lymphoma in pediatric patients with chromosomal breakage syndromes (AT and NBS): experience from the BFM trials

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12 December 2020

Cancer risk of heterozygotes with the NBN founder mutation.

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12 December 2020

Nijmegen breakage syndrome. The International Nijmegen Breakage Syndrome Study Group

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Individual differences in chromosomal aberrations after in vitro irradiation of cells from healthy individuals, cancer and cancer susceptibility syndrome patients.

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12 December 2020

Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland

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12 December 2020

Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL).

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12 December 2020

NBS1 657del5 mutation may contribute only to a limited fraction of breast cancer cases in Russia.

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12 December 2020

Mystery of DNA repair: the role of the MRN complex and ATM kinase in DNA damage repair

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NBS1 is a prostate cancer susceptibility gene.

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

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12 December 2020

Identifiers

DOI

10.1007/BF03195730

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9 May 2018

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9 May 2018