213 related articles for article (PubMed ID: 16840438)
1. Cancer incidence in Nijmegen breakage syndrome is modulated by the amount of a variant NBS protein.
Krüger L; Demuth I; Neitzel H; Varon R; Sperling K; Chrzanowska KH; Seemanova E; Digweed M
Carcinogenesis; 2007 Jan; 28(1):107-11. PubMed ID: 16840438
[TBL] [Abstract][Full Text] [Related]
2. An inducible null mutant murine model of Nijmegen breakage syndrome proves the essential function of NBS1 in chromosomal stability and cell viability.
Demuth I; Frappart PO; Hildebrand G; Melchers A; Lobitz S; Stöckl L; Varon R; Herceg Z; Sperling K; Wang ZQ; Digweed M
Hum Mol Genet; 2004 Oct; 13(20):2385-97. PubMed ID: 15333589
[TBL] [Abstract][Full Text] [Related]
3. Extreme variation in apoptosis capacity amongst lymphoid cells of Nijmegen breakage syndrome patients.
Thierfelder N; Demuth I; Burghardt N; Schmelz K; Sperling K; Chrzanowska KH; Seemanova E; Digweed M
Eur J Cell Biol; 2008 Feb; 87(2):111-21. PubMed ID: 17977616
[TBL] [Abstract][Full Text] [Related]
4. Clinical variability and expression of the NBN c.657del5 allele in Nijmegen Breakage Syndrome.
Lins S; Kim R; Krüger L; Chrzanowska KH; Seemanova E; Digweed M
Gene; 2009 Nov; 447(1):12-7. PubMed ID: 19635536
[TBL] [Abstract][Full Text] [Related]
5. Nijmegen breakage syndrome: the clearance pathway for mutant nibrin protein is allele specific.
Salewsky B; Wessendorf P; Hirsch D; Krenzlin H; Digweed M
Gene; 2013 May; 519(2):217-21. PubMed ID: 23458873
[TBL] [Abstract][Full Text] [Related]
6. Unique morphological spectrum of lymphomas in Nijmegen breakage syndrome (NBS) patients with high frequency of consecutive lymphoma formation.
Gładkowska-Dura M; Dzierzanowska-Fangrat K; Dura WT; van Krieken JH; Chrzanowska KH; van Dongen JJ; Langerak AW
J Pathol; 2008 Nov; 216(3):337-44. PubMed ID: 18788073
[TBL] [Abstract][Full Text] [Related]
7. Mild Nijmegen breakage syndrome phenotype due to alternative splicing.
Varon R; Dutrannoy V; Weikert G; Tanzarella C; Antoccia A; Stöckl L; Spadoni E; Krüger LA; di Masi A; Sperling K; Digweed M; Maraschio P
Hum Mol Genet; 2006 Mar; 15(5):679-89. PubMed ID: 16415040
[TBL] [Abstract][Full Text] [Related]
8. Nijmegen breakage syndrome: clinical manifestation of defective response to DNA double-strand breaks.
Digweed M; Sperling K
DNA Repair (Amst); 2004; 3(8-9):1207-17. PubMed ID: 15279809
[TBL] [Abstract][Full Text] [Related]
9. New mutations and protein variants of NBS1 are identified in cancer cell lines.
Tessitore A; Biordi L; Flati V; Toniato E; Marchetti P; Ricevuto E; Ficorella C; Scotto L; Giannini G; Frati L; Masciocchi C; Tombolini V; Gulino A; Martinotti S
Genes Chromosomes Cancer; 2003 Feb; 36(2):198-204. PubMed ID: 12508248
[TBL] [Abstract][Full Text] [Related]
10. Identification of the interactors of human nibrin (NBN) and of its 26 kDa and 70 kDa fragments arising from the NBN 657del5 founder mutation.
Cilli D; Mirasole C; Pennisi R; Pallotta V; D'Alessandro A; Antoccia A; Zolla L; Ascenzi P; di Masi A
PLoS One; 2014; 9(12):e114651. PubMed ID: 25485873
[TBL] [Abstract][Full Text] [Related]
11. Nibrin functions in Ig class-switch recombination.
Kracker S; Bergmann Y; Demuth I; Frappart PO; Hildebrand G; Christine R; Wang ZQ; Sperling K; Digweed M; Radbruch A
Proc Natl Acad Sci U S A; 2005 Feb; 102(5):1584-9. PubMed ID: 15668383
[TBL] [Abstract][Full Text] [Related]
12. The role of nibrin in doxorubicin-induced apoptosis and cell senescence in Nijmegen Breakage Syndrome patients lymphocytes.
Alster O; Bielak-Zmijewska A; Mosieniak G; Moreno-Villanueva M; Dudka-Ruszkowska W; Wojtala A; Kusio-Kobiałka M; Korwek Z; Burkle A; Piwocka K; Siwicki JK; Sikora E
PLoS One; 2014; 9(8):e104964. PubMed ID: 25119968
[TBL] [Abstract][Full Text] [Related]
13. The defect in humoral immunity in patients with Nijmegen breakage syndrome is explained by defects in peripheral B lymphocyte maturation.
Piątosa B; van der Burg M; Siewiera K; Pac M; van Dongen JJ; Langerak AW; Chrzanowska KH; Bernatowska E
Cytometry A; 2012 Oct; 81(10):835-42. PubMed ID: 22851427
[TBL] [Abstract][Full Text] [Related]
14. The clinical manifestation of a defective response to DNA double-strand breaks as exemplified by Nijmegen breakage syndrome.
Demuth I; Digweed M
Oncogene; 2007 Dec; 26(56):7792-8. PubMed ID: 18066092
[TBL] [Abstract][Full Text] [Related]
15. Cancer risk of heterozygotes with the NBN founder mutation.
Seemanová E; Jarolim P; Seeman P; Varon R; Digweed M; Swift M; Sperling K
J Natl Cancer Inst; 2007 Dec; 99(24):1875-80. PubMed ID: 18073374
[TBL] [Abstract][Full Text] [Related]
16. Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability.
Seemanová E; Sperling K; Neitzel H; Varon R; Hadac J; Butova O; Schröck E; Seeman P; Digweed M
J Med Genet; 2006 Mar; 43(3):218-24. PubMed ID: 16033915
[TBL] [Abstract][Full Text] [Related]
17. DNA damage in Nijmegen Breakage Syndrome cells leads to PARP hyperactivation and increased oxidative stress.
Krenzlin H; Demuth I; Salewsky B; Wessendorf P; Weidele K; Bürkle A; Digweed M
PLoS Genet; 2012; 8(3):e1002557. PubMed ID: 22396666
[TBL] [Abstract][Full Text] [Related]
18. Expression of full-length NBS1 protein restores normal radiation responses in cells from Nijmegen breakage syndrome patients.
Ito A; Tauchi H; Kobayashi J; Morishima K; Nakamura A; Hirokawa Y; Matsuura S; Ito K; Komatsu K
Biochem Biophys Res Commun; 1999 Nov; 265(3):716-21. PubMed ID: 10600486
[TBL] [Abstract][Full Text] [Related]
19. Mutations in the Nijmegen breakage syndrome gene in medulloblastomas.
Huang J; Grotzer MA; Watanabe T; Hewer E; Pietsch T; Rutkowski S; Ohgaki H
Clin Cancer Res; 2008 Jul; 14(13):4053-8. PubMed ID: 18593981
[TBL] [Abstract][Full Text] [Related]
20. Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL).
Varon R; Reis A; Henze G; von Einsiedel HG; Sperling K; Seeger K
Cancer Res; 2001 May; 61(9):3570-2. PubMed ID: 11325820
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
