DOI: 10.1016/s0165-4608(00)00390-3. No evidence for deletions of the NBS1 gene in lymphomas

No evidence for deletions of the NBS1 gene in lymphomas

10.1016/s0165-4608(00)00390-3

Crossref journal-article

Elsevier BV

Cancer Genetics and Cytogenetics (78)

Bibliography

Stumm, M., von Ruskowsky, A., Siebert, R., Harder, S., Varon, R., Wieacker, P., & Schlegelberger, B. (2001). No evidence for deletions of the NBS1 gene in lymphomas. Cancer Genetics and Cytogenetics, 126(1), 60â62.

Authors 7

Markus Stumm (first)
Andreas von Ruskowsky (additional)
Reiner Siebert (additional)
Svetlana Harder (additional)
Raymonda Varon (additional)
Peter Wieacker (additional)
Brigitte Schlegelberger (additional)

References 14 Referenced 19

Wegner RD, Chzernowska K, Sperling K, Stumm M. Ataxia telangiectasia variants (Nijmegen breakage syndrome). In: Ochs, Smith, Puck, editors. Immunodeficiency disorders: a molecular and genetic approach. New York: Oxford University Press, 1999. pp. 324–34.
10.1023/A:1008391923792 / Ann Oncol / Non-Hodgkin's lymphoma in pediatric patients with chromosomal breakage syndromes (AT and NBS) by Seidemann (2000)
10.1016/S0092-8674(00)81175-7 / Cell / The hMre11/hRad50 protein complex and Nijmegen breakage syndrome by Carney (1998)
10.1016/S0092-8674(00)81174-5 / Cell / Nibrin, a novel double-strand break repair protein, is mutated in Nijmegen breakage syndrome by Varon (1998)
10.1016/S0092-8674(00)81847-4 / Cell / Association of BRCA1 with Rad51 in mitotic and meiotic cells by Scully (1997)
10.1038/386804a0 / Nature / Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2 by Sharan (1997)
10.1038/sj.onc.1202692 / Oncogene / Mutations in the RAD54 recombination gene in primary cancers by Matsuda (1999)
10.1038/ng0997-96 / Watine Genet / Clustering of missense mutations in the ataxia-telangiectasia gene in a sporadic T-cell leukaemia by Vorechovsky (1997)
10.1038/nm1097-1155 / Nat Med / Biallelic mutations in the ATM gene in T-prolymphocytic leukemia by Stilgenbauer (1997)
10.1182/blood.V94.2.748 / Blood / Somatic ATM mutations indicate a pathogenic role of ATM in B-cell chronic lymphocytic leukemia by Schaffner (1999)
{'key': '10.1016/S0165-4608(00)00390-3_BIB11', 'first-page': '427', 'article-title': 'Allelic imbalances at NBS1 is frequent in both proximal and distal colorectal carcinoma', 'volume': '7', 'author': 'Uhrhammer', 'year': '2000', 'journal-title': 'Oncol Rep'} / Oncol Rep / Allelic imbalances at NBS1 is frequent in both proximal and distal colorectal carcinoma by Uhrhammer (2000)
10.1016/S1357-4310(99)01435-5 / Mol Med Today / Radiation, DNA damage and cancer by Hall (1999)
{'key': '10.1016/S0165-4608(00)00390-3_BIB13', 'first-page': '274', 'article-title': 'Chromosomeninstabilität, Strahlenempfindlichkeit und Krebs', 'volume': '10', 'author': 'Sperling', 'year': '1998', 'journal-title': 'Med Genet'} / Med Genet / Chromosomeninstabilität, Strahlenempfindlichkeit und Krebs by Sperling (1998)
10.1046/j.1365-2141.2000.01973.x / Br J Haematol / 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 by Stanulla (2000)

Dates

Type	When
Created	23 years, 1 month ago (July 25, 2002, 1:53 p.m.)
Deposited	5 years, 7 months ago (Jan. 28, 2020, 8:18 a.m.)
Indexed	1 year, 9 months ago (Nov. 19, 2023, 8:38 a.m.)
Issued	24 years, 4 months ago (April 1, 2001)
Published	24 years, 4 months ago (April 1, 2001)
Published Print	24 years, 4 months ago (April 1, 2001)

Funders 0

None

BibTeX

@article{Stumm_2001, title={No evidence for deletions of the NBS1 gene in lymphomas}, volume={126}, ISSN={0165-4608}, url={http://dx.doi.org/10.1016/s0165-4608(00)00390-3}, DOI={10.1016/s0165-4608(00)00390-3}, number={1}, journal={Cancer Genetics and Cytogenetics}, publisher={Elsevier BV}, author={Stumm, Markus and von Ruskowsky, Andreas and Siebert, Reiner and Harder, Svetlana and Varon, Raymonda and Wieacker, Peter and Schlegelberger, Brigitte}, year={2001}, month=apr, pages={60–62} }

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