156 related articles for article (PubMed ID: 24168161)
1. Radiation-induced telomere length variations in normal and in Nijmegen Breakage Syndrome cells.
Berardinelli F; Sgura A; Di Masi A; Leone S; Cirrone GA; Romano F; Tanzarella C; Antoccia A
Int J Radiat Biol; 2014 Jan; 90(1):45-52. PubMed ID: 24168161
[TBL] [Abstract][Full Text] [Related]
2. Cleavage of the BRCT tandem domains of nibrin by the 657del5 mutation affects the DNA damage response less than the Arg215Trp mutation.
Mendez G; Cilli D; Berardinelli F; Viganotti M; Ascenzi P; Tanzarella C; Antoccia A; di Masi A
IUBMB Life; 2012 Oct; 64(10):853-61. PubMed ID: 22941933
[TBL] [Abstract][Full Text] [Related]
3. Hsp90α regulates ATM and NBN functions in sensing and repair of DNA double-strand breaks.
Pennisi R; Antoccia A; Leone S; Ascenzi P; di Masi A
FEBS J; 2017 Aug; 284(15):2378-2395. PubMed ID: 28631426
[TBL] [Abstract][Full Text] [Related]
4. Human RAD50 deficiency: Confirmation of a distinctive phenotype.
Ragamin A; Yigit G; Bousset K; Beleggia F; Verheijen FW; de Wit MY; Strom TM; Dörk T; Wollnik B; Mancini GMS
Am J Med Genet A; 2020 Jun; 182(6):1378-1386. PubMed ID: 32212377
[TBL] [Abstract][Full Text] [Related]
5. Importance of Germline and Somatic Alterations in Human
Otahalova B; Volkova Z; Soukupova J; Kleiblova P; Janatova M; Vocka M; Macurek L; Kleibl Z
Int J Mol Sci; 2023 Mar; 24(6):. PubMed ID: 36982687
[TBL] [Abstract][Full Text] [Related]
6. Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder.
Waltes R; Kalb R; Gatei M; Kijas AW; Stumm M; Sobeck A; Wieland B; Varon R; Lerenthal Y; Lavin MF; Schindler D; Dörk T
Am J Hum Genet; 2009 May; 84(5):605-16. PubMed ID: 19409520
[TBL] [Abstract][Full Text] [Related]
7. Mystery of DNA repair: the role of the MRN complex and ATM kinase in DNA damage repair.
Czornak K; Chughtai S; Chrzanowska KH
J Appl Genet; 2008; 49(4):383-96. PubMed ID: 19029686
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. The role of recombination in telomere length maintenance.
Royle NJ; Méndez-Bermúdez A; Gravani A; Novo C; Foxon J; Williams J; Cotton V; Hidalgo A
Biochem Soc Trans; 2009 Jun; 37(Pt 3):589-95. PubMed ID: 19442255
[TBL] [Abstract][Full Text] [Related]
10. Defective signal joint recombination in fanconi anemia fibroblasts reveals a role for Rad50 in V(D)J recombination.
Donahue SL; Tabah AA; Schmitz K; Aaron A; Campbell C
J Mol Biol; 2007 Jul; 370(3):449-58. PubMed ID: 17524422
[TBL] [Abstract][Full Text] [Related]
11. Assembly of functional ALT-associated promyelocytic leukemia bodies requires Nijmegen Breakage Syndrome 1.
Wu G; Jiang X; Lee WH; Chen PL
Cancer Res; 2003 May; 63(10):2589-95. PubMed ID: 12750284
[TBL] [Abstract][Full Text] [Related]
12. Breast cancer risk is associated with the genes encoding the DNA double-strand break repair Mre11/Rad50/Nbs1 complex.
Hsu HM; Wang HC; Chen ST; Hsu GC; Shen CY; Yu JC
Cancer Epidemiol Biomarkers Prev; 2007 Oct; 16(10):2024-32. PubMed ID: 17932350
[TBL] [Abstract][Full Text] [Related]
13. Molecular basis of ataxia telangiectasia and related diseases.
Ball LG; Xiao W
Acta Pharmacol Sin; 2005 Aug; 26(8):897-907. PubMed ID: 16038621
[TBL] [Abstract][Full Text] [Related]
14. Germline variants in MRE11/RAD50/NBN complex genes in childhood leukemia.
Mosor M; Ziółkowska-Suchanek I; Nowicka K; Dzikiewicz-Krawczyk A; Januszkiewicz-Lewandowska D; Nowak J
BMC Cancer; 2013 Oct; 13():457. PubMed ID: 24093751
[TBL] [Abstract][Full Text] [Related]
15. DNA double-strand break induction and repair in irradiated lymphoblastoid, fibroblast cell lines and white blood cells from ATM, NBS and radiosensitive patients.
Strasser H; Grabenbauer GG; Sprung CN; Sauer R; Distel LV
Strahlenther Onkol; 2007 Aug; 183(8):447-53. PubMed ID: 17680225
[TBL] [Abstract][Full Text] [Related]
16. Impact of heterozygous c.657-661del, p.I171V and p.R215W mutations in NBN on nibrin functions.
Dzikiewicz-Krawczyk A; Mosor M; Januszkiewicz D; Nowak J
Mutagenesis; 2012 May; 27(3):337-43. PubMed ID: 22131123
[TBL] [Abstract][Full Text] [Related]
17. The MRN complex in double-strand break repair and telomere maintenance.
Lamarche BJ; Orazio NI; Weitzman MD
FEBS Lett; 2010 Sep; 584(17):3682-95. PubMed ID: 20655309
[TBL] [Abstract][Full Text] [Related]
18. Ataxia-telangiectasia-like disorder (ATLD)-its clinical presentation and molecular basis.
Taylor AM; Groom A; Byrd PJ
DNA Repair (Amst); 2004; 3(8-9):1219-25. PubMed ID: 15279810
[TBL] [Abstract][Full Text] [Related]
19. Active role for nibrin in the kinetics of atm activation.
Cerosaletti K; Wright J; Concannon P
Mol Cell Biol; 2006 Mar; 26(5):1691-9. PubMed ID: 16478990
[TBL] [Abstract][Full Text] [Related]
20. MRE11-RAD50-NBS1 and ATM function as co-mediators of TRF1 in telomere length control.
Wu Y; Xiao S; Zhu XD
Nat Struct Mol Biol; 2007 Sep; 14(9):832-40. PubMed ID: 17694070
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
