No evidence for deletions of the NBS1 gene in lymphomas

Cancer Genetics and Cytogenetics

Volumn 126, Issue 1, 2001, Pages 60-62

  Stumm, Markus ^a   Von Ruskowsky, Andreas ^a   Siebert, Reiner ^b   Harder, Svetlana ^b   Varon, Raymonda ^c   Wieacker, Peter ^a   Schlegelberger, Brigitte ^b  

^a OTTO VON GUERICKE UNIVERSITY   (Germany)

^b UNIVERSITY OF KIEL   (Germany)

^c CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BRCA1 PROTEIN; BRCA2 PROTEIN; GENE PRODUCT; NIBRIN; UNCLASSIFIED DRUG;

ARTICLE; B CELL LYMPHOMA; CARCINOGENESIS; CHROMOSOME 8Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CONTROLLED STUDY; DNA RECOMBINATION; DNA REPAIR; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; HUMAN; HUMAN CELL; LYMPHOMA; NIJMEGEN BREAKAGE SYNDROME; NONHODGKIN LYMPHOMA; PRIORITY JOURNAL; T CELL LYMPHOMA; TUMOR SUPPRESSOR GENE;

GENE DELETION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LYMPHOMA, B-CELL; LYMPHOMA, T-CELL; NUCLEAR PROTEINS;

EID: 0035306631     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(00)00390-3     Document Type: Article

References (14)

1. Non-Hodgkin's lymphoma in pediatric patients with chromosomal breakage syndromes (AT and NBS); experience from the BFM trials
2. The hMre11/hRad50 protein complex and Nijmegen breakage syndrome; linkage of double-strand break repair to the cellular DNA damage response
3. Nibrin, a novel double-strand break repair protein, is mutated in Nijmegen breakage syndrome
4. Association of BRCA1 with Rad51 in mitotic and meiotic cells
5. Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2
6. Mutations in the RAD54 recombination gene in primary cancers
7. Clustering of missense mutations in the ataxia-telangiectasia gene in a sporadic T-cell leukaemia
8. Biallelic mutations in the ATM gene in T-prolymphocytic leukemia
9. Somatic ATM mutations indicate a pathogenic role of ATM in B-cell chronic lymphocytic leukemia
10. Allelic imbalances at NBS1 is frequent in both proximal and distal colorectal carcinoma
11. Radiation, DNA damage and cancer
12. Chromosomeninstabilität, Strahlenempfindlichkeit und Krebs; ataxia-telangiektasia und das Mijmegen Breakage Syndrom
13. 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