176 related articles for article (PubMed ID: 30606610)
1. Double-strand break repair plays a role in repeat instability in a fragile X mouse model.
Gazy I; Hayward B; Potapova S; Zhao X; Usdin K
DNA Repair (Amst); 2019 Feb; 74():63-69. PubMed ID: 30606610
[TBL] [Abstract][Full Text] [Related]
2. MutLγ promotes repeat expansion in a Fragile X mouse model while EXO1 is protective.
Zhao X; Zhang Y; Wilkins K; Edelmann W; Usdin K
PLoS Genet; 2018 Oct; 14(10):e1007719. PubMed ID: 30312299
[TBL] [Abstract][Full Text] [Related]
3. Repeat Instability in the Fragile X-Related Disorders: Lessons from a Mouse Model.
Zhao X; Gazy I; Hayward B; Pintado E; Hwang YH; Tassone F; Usdin K
Brain Sci; 2019 Mar; 9(3):. PubMed ID: 30832215
[TBL] [Abstract][Full Text] [Related]
4. Heterozygosity for a hypomorphic Polβ mutation reduces the expansion frequency in a mouse model of the Fragile X-related disorders.
Lokanga RA; Senejani AG; Sweasy JB; Usdin K
PLoS Genet; 2015 Apr; 11(4):e1005181. PubMed ID: 25886163
[TBL] [Abstract][Full Text] [Related]
5. Modifiers of Somatic Repeat Instability in Mouse Models of Friedreich Ataxia and the Fragile X-Related Disorders: Implications for the Mechanism of Somatic Expansion in Huntington's Disease.
Zhao X; Kumari D; Miller CJ; Kim GY; Hayward B; Vitalo AG; Pinto RM; Usdin K
J Huntingtons Dis; 2021; 10(1):149-163. PubMed ID: 33579860
[TBL] [Abstract][Full Text] [Related]
6. Human DNA polymerase η promotes RNA-templated error-free repair of DNA double-strand breaks.
Chakraborty A; Tapryal N; Islam A; Sarker AH; Manohar K; Mitra J; Hegde ML; Hazra T
J Biol Chem; 2023 Mar; 299(3):102991. PubMed ID: 36758800
[TBL] [Abstract][Full Text] [Related]
7. FAN1 protects against repeat expansions in a Fragile X mouse model.
Zhao XN; Usdin K
DNA Repair (Amst); 2018 Sep; 69():1-5. PubMed ID: 29990673
[TBL] [Abstract][Full Text] [Related]
8. The transcription-coupled repair protein ERCC6/CSB also protects against repeat expansion in a mouse model of the fragile X premutation.
Zhao XN; Usdin K
Hum Mutat; 2015 Apr; 36(4):482-7. PubMed ID: 25726753
[TBL] [Abstract][Full Text] [Related]
9. C-Terminal region of DNA ligase IV drives XRCC4/DNA ligase IV complex to chromatin.
Liu S; Liu X; Kamdar RP; Wanotayan R; Sharma MK; Adachi N; Matsumoto Y
Biochem Biophys Res Commun; 2013 Sep; 439(2):173-8. PubMed ID: 23994631
[TBL] [Abstract][Full Text] [Related]
10. Impairment of the non-homologous end joining and homologous recombination pathways of DNA double strand break repair: Impact on spontaneous and radiation-induced mammary and intestinal tumour risk in Apc min/+ mice.
Haines JW; Coster M; Bouffler SD
DNA Repair (Amst); 2015 Nov; 35():19-26. PubMed ID: 26435054
[TBL] [Abstract][Full Text] [Related]
11. The role of the Mre11-Rad50-Nbs1 complex in double-strand break repair-facts and myths.
Takeda S; Hoa NN; Sasanuma H
J Radiat Res; 2016 Aug; 57 Suppl 1(Suppl 1):i25-i32. PubMed ID: 27311583
[TBL] [Abstract][Full Text] [Related]
12. Deficiency of XLF and PAXX prevents DNA double-strand break repair by non-homologous end joining in lymphocytes.
Hung PJ; Chen BR; George R; Liberman C; Morales AJ; Colon-Ortiz P; Tyler JK; Sleckman BP; Bredemeyer AL
Cell Cycle; 2017 Feb; 16(3):286-295. PubMed ID: 27830975
[TBL] [Abstract][Full Text] [Related]
13. Structural role for DNA Ligase IV in promoting the fidelity of non-homologous end joining.
Stinson BM; Carney SM; Walter JC; Loparo JJ
Nat Commun; 2024 Feb; 15(1):1250. PubMed ID: 38341432
[TBL] [Abstract][Full Text] [Related]
14. A point mutation in the nuclease domain of MLH3 eliminates repeat expansions in a mouse stem cell model of the Fragile X-related disorders.
Hayward BE; Steinbach PJ; Usdin K
Nucleic Acids Res; 2020 Aug; 48(14):7856-7863. PubMed ID: 32619224
[TBL] [Abstract][Full Text] [Related]
15. [Double strand break repair, one mechanism can hide another: alternative non-homologous end joining].
Rass E; Grabarz A; Bertrand P; Lopez BS
Cancer Radiother; 2012 Feb; 16(1):1-10. PubMed ID: 21737335
[TBL] [Abstract][Full Text] [Related]
16. Impaired DNA double-strand break repair contributes to the age-associated rise of genomic instability in humans.
Li Z; Zhang W; Chen Y; Guo W; Zhang J; Tang H; Xu Z; Zhang H; Tao Y; Wang F; Jiang Y; Sun FL; Mao Z
Cell Death Differ; 2016 Nov; 23(11):1765-1777. PubMed ID: 27391797
[TBL] [Abstract][Full Text] [Related]
17. Role of the yeast DNA repair protein Nej1 in end processing during the repair of DNA double strand breaks by non-homologous end joining.
Yang H; Matsumoto Y; Trujillo KM; Lees-Miller SP; Osley MA; Tomkinson AE
DNA Repair (Amst); 2015 Jul; 31():1-10. PubMed ID: 25942368
[TBL] [Abstract][Full Text] [Related]
18. Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency.
Buijsen RA; Visser JA; Kramer P; Severijnen EA; Gearing M; Charlet-Berguerand N; Sherman SL; Berman RF; Willemsen R; Hukema RK
Hum Reprod; 2016 Jan; 31(1):158-68. PubMed ID: 26537920
[TBL] [Abstract][Full Text] [Related]
19. A human iPSC model of Ligase IV deficiency reveals an important role for NHEJ-mediated-DSB repair in the survival and genomic stability of induced pluripotent stem cells and emerging haematopoietic progenitors.
Tilgner K; Neganova I; Moreno-Gimeno I; Al-Aama JY; Burks D; Yung S; Singhapol C; Saretzki G; Evans J; Gorbunova V; Gennery A; Przyborski S; Stojkovic M; Armstrong L; Jeggo P; Lako M
Cell Death Differ; 2013 Aug; 20(8):1089-100. PubMed ID: 23722522
[TBL] [Abstract][Full Text] [Related]
20. PARP-1 and Ku compete for repair of DNA double strand breaks by distinct NHEJ pathways.
Wang M; Wu W; Wu W; Rosidi B; Zhang L; Wang H; Iliakis G
Nucleic Acids Res; 2006; 34(21):6170-82. PubMed ID: 17088286
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
