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Article

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

Genes, chromosomes & cancer - 1 Nov 2002

Cerosaletti Karen M, Morrison V Anne, Sabath Daniel E, Willerford Dennis M, Concannon Patrick

Abstract excerpt

Non-Hodgkin lymphomas (NHLs) are characterized by chromosomal translocations that juxtapose loci encoding lymphoid antigen receptors with cellular proto-oncogenes. These translocations are thought to arise from inaccurate processing of DNA breaks created during physiologic recombination of the antigen receptor genes in lymphocytes. The inherited disorders ataxia-telangiectasia and Nijmegen breakage syndrome are...

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Identifiers

PMID: 12353271
DOI: 10.1002/gcc.10114

Genes

ATM

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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Mutations and molecular variants of the NBS1 gene in non-Hodgkin lymphoma.PMID 12353271Read ↗

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A systematic evaluation of the ataxia telangiectasia mutated gene does not show an association with non-Hodgkin lymphoma.Semantic proximity Read ↗

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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.Semantic proximity Read ↗

New mutations and protein variants of NBS1 are identified in cancer cell lines.Semantic proximity Read ↗

657del5 mutation in the gene for Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controls.Semantic proximity Read ↗

Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish pediatric patients with sporadic lymphoid malignancies.Semantic proximity Read ↗

Molecular variants of the ATM gene in Hodgkin's disease in children.Semantic proximity Read ↗

Mutational inactivation of the nijmegen breakage syndrome gene (NBS1) in glioblastomas is associated with multiple TP53 mutations.Semantic proximity Read ↗

Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemiaSemantic proximity Read ↗

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