183 related articles for article (PubMed ID: 19635536)
21. The Slavic NBN Founder Mutation: A Role for Reproductive Fitness?
Seemanova E; Varon R; Vejvalka J; Jarolim P; Seeman P; Chrzanowska KH; Digweed M; Resnick I; Kremensky I; Saar K; Hoffmann K; Dutrannoy V; Karbasiyan M; Ghani M; Barić I; Tekin M; Kovacs P; Krawczak M; Reis A; Sperling K; Nothnagel M
PLoS One; 2016; 11(12):e0167984. PubMed ID: 27936167
[TBL] [Abstract][Full Text] [Related]
22. Nijmegen breakage syndrome associated with porokeratosis.
Wolf EK; Shwayder TA
Pediatr Dermatol; 2009; 26(1):106-8. PubMed ID: 19250427
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Directed Alternative Splicing in Nijmegen Breakage Syndrome: Proof of Principle Concerning Its Therapeutical Application.
Salewsky B; Hildebrand G; Rothe S; Parplys AC; Radszewski J; Kieslich M; Wessendorf P; Krenzlin H; Borgmann K; Nussenzweig A; Sperling K; Digweed M
Mol Ther; 2016 Feb; 24(1):117-24. PubMed ID: 26265251
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. 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]
27. Telomere attrition and dysfunction: a potential trigger of the progeroid phenotype in nijmegen breakage syndrome.
Habib R; Kim R; Neitzel H; Demuth I; Chrzanowska K; Seemanova E; Faber R; Digweed M; Voss R; Jäger K; Sperling K; Walter M
Aging (Albany NY); 2020 Jun; 12(12):12342-12375. PubMed ID: 32564008
[TBL] [Abstract][Full Text] [Related]
28. Nijmegen breakage syndrome: consequences of defective DNA double strand break repair.
Digweed M; Reis A; Sperling K
Bioessays; 1999 Aug; 21(8):649-56. PubMed ID: 10440861
[TBL] [Abstract][Full Text] [Related]
29. Screening of Nijmegen breakage syndrome 1 mutations in four unrelated families by polymerase chain reaction using sequence-specific primers.
Di Masi A; Antoccia A; Spadoni E; Varon-Mateeva R; Maraschio P; Tanzarella C
Genet Test; 2006; 10(1):24-30. PubMed ID: 16544999
[TBL] [Abstract][Full Text] [Related]
30. Nijmegen breakage syndrome (NBS).
Chrzanowska KH; Gregorek H; Dembowska-Bagińska B; Kalina MA; Digweed M
Orphanet J Rare Dis; 2012 Feb; 7():13. PubMed ID: 22373003
[TBL] [Abstract][Full Text] [Related]
31. Nijmegen breakage syndrome.
Kondratenko I; Paschenko O; Polyakov A; Bologov A
Adv Exp Med Biol; 2007; 601():61-7. PubMed ID: 17712992
[TBL] [Abstract][Full Text] [Related]
32. Nijmegen breakage syndrome in 13% of age-matched Czech children with primary microcephaly.
Seeman P; Gebertová K; Paderová K; Sperling K; Seemanová E
Pediatr Neurol; 2004 Mar; 30(3):195-200. PubMed ID: 15033202
[TBL] [Abstract][Full Text] [Related]
33. Secondary acute monocytic leukemia positive for 11q23 rearrangement in Nijmegen breakage syndrome.
Pastorczak A; Szczepanski T; Trelinska J; Finalet Ferreiro J; Wlodarska I; Mycko K; Polucha A; Sedek L; Meyer C; Marschalek R; Młynarski W
Pediatr Blood Cancer; 2014 Aug; 61(8):1469-71. PubMed ID: 24619942
[TBL] [Abstract][Full Text] [Related]
34. Nijmegen breakage syndrome: case report and review of literature.
Hasbaoui BE; Elyajouri A; Abilkassem R; Agadr A
Pan Afr Med J; 2020; 35():85. PubMed ID: 32537088
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. [Nijmegen Breakage syndrome].
Erdos M; Tóth B; Juhász P; Mahdi M; Maródi L
Orv Hetil; 2010 Apr; 151(16):665-73. PubMed ID: 20353920
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours.
Nowak J; Mosor M; Ziółkowska I; Wierzbicka M; Pernak-Schwarz M; Przyborska M; Roznowski K; Pławski A; Słomski R; Januszkiewicz D
Eur J Cancer; 2008 Mar; 44(4):627-30. PubMed ID: 18280732
[TBL] [Abstract][Full Text] [Related]
39. DNA repair functional analyses of NBN hypomorphic variants associated with NBN-related infertility.
Fiévet A; Bellanger D; Zahed L; Burglen L; Derrien AC; Dubois d'Enghien C; Lespinasse J; Parfait B; Pedespan JM; Rieunier G; Stoppa-Lyonnet D; Stern MH
Hum Mutat; 2020 Mar; 41(3):608-618. PubMed ID: 31729086
[TBL] [Abstract][Full Text] [Related]
40. 657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish population.
Tekin M; Akcayoz D; Ucar C; Gulen H; Akar N
Hum Biol; 2005 Jun; 77(3):393-7. PubMed ID: 16392640
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]