319 related articles for article (PubMed ID: 12427531)
1. Recombinational DNA repair and human disease.
Thompson LH; Schild D
Mutat Res; 2002 Nov; 509(1-2):49-78. PubMed ID: 12427531
[TBL] [Abstract][Full Text] [Related]
2. Human syndromes with genomic instability and multiprotein machines that repair DNA double-strand breaks.
De la Torre C; Pincheira J; López-Sáez JF
Histol Histopathol; 2003 Jan; 18(1):225-43. PubMed ID: 12507302
[TBL] [Abstract][Full Text] [Related]
3. Chromosome instability syndromes.
Taylor AM
Best Pract Res Clin Haematol; 2001 Sep; 14(3):631-44. PubMed ID: 11640873
[TBL] [Abstract][Full Text] [Related]
4. Chromosome breakage syndromes and cancer.
Duker NJ
Am J Med Genet; 2002 Oct; 115(3):125-9. PubMed ID: 12407692
[TBL] [Abstract][Full Text] [Related]
5. Werner syndrome helicase has a critical role in DNA damage responses in the absence of a functional fanconi anemia pathway.
Aggarwal M; Banerjee T; Sommers JA; Iannascoli C; Pichierri P; Shoemaker RH; Brosh RM
Cancer Res; 2013 Sep; 73(17):5497-507. PubMed ID: 23867477
[TBL] [Abstract][Full Text] [Related]
6. Disorders of DNA replication and repair.
Auerbach AD; Verlander PC
Curr Opin Pediatr; 1997 Dec; 9(6):600-16. PubMed ID: 9425594
[TBL] [Abstract][Full Text] [Related]
7. Ataxia-telangiectasia and the Nijmegen breakage syndrome: related disorders but genes apart.
Shiloh Y
Annu Rev Genet; 1997; 31():635-62. PubMed ID: 9442910
[TBL] [Abstract][Full Text] [Related]
8. Oxidative stress, mitochondrial abnormalities and antioxidant defense in Ataxia-telangiectasia, Bloom syndrome and Nijmegen breakage syndrome.
Maciejczyk M; Mikoluc B; Pietrucha B; Heropolitanska-Pliszka E; Pac M; Motkowski R; Car H
Redox Biol; 2017 Apr; 11():375-383. PubMed ID: 28063379
[TBL] [Abstract][Full Text] [Related]
9. Chromosomal breakage syndromes and the BRCA1 genome surveillance complex.
Futaki M; Liu JM
Trends Mol Med; 2001 Dec; 7(12):560-5. PubMed ID: 11733219
[TBL] [Abstract][Full Text] [Related]
10. Chromosome instability syndromes.
Taylor AMR; Rothblum-Oviatt C; Ellis NA; Hickson ID; Meyer S; Crawford TO; Smogorzewska A; Pietrucha B; Weemaes C; Stewart GS
Nat Rev Dis Primers; 2019 Sep; 5(1):64. PubMed ID: 31537806
[TBL] [Abstract][Full Text] [Related]
11. DNA strand break repair and human genetic disease.
McKinnon PJ; Caldecott KW
Annu Rev Genomics Hum Genet; 2007; 8():37-55. PubMed ID: 17887919
[TBL] [Abstract][Full Text] [Related]
12. ATM-dependent phosphorylation of nibrin in response to radiation exposure.
Gatei M; Young D; Cerosaletti KM; Desai-Mehta A; Spring K; Kozlov S; Lavin MF; Gatti RA; Concannon P; Khanna K
Nat Genet; 2000 May; 25(1):115-9. PubMed ID: 10802669
[TBL] [Abstract][Full Text] [Related]
13. Fanconi anemia and Bloom's syndrome crosstalk through FANCJ-BLM helicase interaction.
Suhasini AN; Brosh RM
Trends Genet; 2012 Jan; 28(1):7-13. PubMed ID: 22024395
[TBL] [Abstract][Full Text] [Related]
14. Genetic diseases associated with DNA and chromosomal instability.
Lambert WC
Dermatol Clin; 1987 Jan; 5(1):85-108. PubMed ID: 3549081
[TBL] [Abstract][Full Text] [Related]
15. DNA helicases, genomic instability, and human genetic disease.
van Brabant AJ; Stan R; Ellis NA
Annu Rev Genomics Hum Genet; 2000; 1():409-59. PubMed ID: 11701636
[TBL] [Abstract][Full Text] [Related]
16. ATM's Role in the Repair of DNA Double-Strand Breaks.
Shibata A; Jeggo PA
Genes (Basel); 2021 Aug; 12(9):. PubMed ID: 34573351
[TBL] [Abstract][Full Text] [Related]
17. Regulation of ATM in DNA double strand break repair accounts for the radiosensitivity in human cells exposed to high linear energy transfer ionizing radiation.
Xue L; Yu D; Furusawa Y; Okayasu R; Tong J; Cao J; Fan S
Mutat Res; 2009 Nov; 670(1-2):15-23. PubMed ID: 19583974
[TBL] [Abstract][Full Text] [Related]
18. Homologous recombination and cell cycle checkpoints: Rad51 in tumour progression and therapy resistance.
Henning W; Stürzbecher HW
Toxicology; 2003 Nov; 193(1-2):91-109. PubMed ID: 14599770
[TBL] [Abstract][Full Text] [Related]
19. Phenotypic Analysis of ATM Protein Kinase in DNA Double-Strand Break Formation and Repair.
Mian E; Wiesmüller L
Methods Mol Biol; 2017; 1599():317-334. PubMed ID: 28477129
[TBL] [Abstract][Full Text] [Related]
20. SGS1, the Saccharomyces cerevisiae homologue of BLM and WRN, suppresses genome instability and homeologous recombination.
Myung K; Datta A; Chen C; Kolodner RD
Nat Genet; 2001 Jan; 27(1):113-6. PubMed ID: 11138010
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
