385 related articles for article (PubMed ID: 23276657)
1. Disease-causing missense mutations in human DNA helicase disorders.
Suhasini AN; Brosh RM
Mutat Res; 2013; 752(2):138-152. PubMed ID: 23276657
[TBL] [Abstract][Full Text] [Related]
2. DNA helicases associated with genetic instability, cancer, and aging.
Suhasini AN; Brosh RM
Adv Exp Med Biol; 2013; 767():123-44. PubMed ID: 23161009
[TBL] [Abstract][Full Text] [Related]
3. Diseases with DNA damage-processing defects.
Timme TL; Moses RE
Am J Med Sci; 1988 Jan; 295(1):40-8. PubMed ID: 3276189
[TBL] [Abstract][Full Text] [Related]
4. Werner syndrome: entering the helicase era.
Epstein CJ; Motulsky AG
Bioessays; 1996 Dec; 18(12):1025-7. PubMed ID: 8976161
[TBL] [Abstract][Full Text] [Related]
5. [Functional analysis of yeast homologue gene associated with human DNA helicase causative syndromes].
Miyajima A
Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku; 2002; (120):53-74. PubMed ID: 12638184
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Warsaw breakage syndrome, a cohesinopathy associated with mutations in the XPD helicase family member DDX11/ChlR1.
van der Lelij P; Chrzanowska KH; Godthelp BC; Rooimans MA; Oostra AB; Stumm M; Zdzienicka MZ; Joenje H; de Winter JP
Am J Hum Genet; 2010 Feb; 86(2):262-6. PubMed ID: 20137776
[TBL] [Abstract][Full Text] [Related]
9. The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes.
Riou L; Zeng L; Chevallier-Lagente O; Stary A; Nikaido O; Taïeb A; Weeda G; Mezzina M; Sarasin A
Hum Mol Genet; 1999 Jun; 8(6):1125-33. PubMed ID: 10332046
[TBL] [Abstract][Full Text] [Related]
10. XPD helicase structures and activities: insights into the cancer and aging phenotypes from XPD mutations.
Fan L; Fuss JO; Cheng QJ; Arvai AS; Hammel M; Roberts VA; Cooper PK; Tainer JA
Cell; 2008 May; 133(5):789-800. PubMed ID: 18510924
[TBL] [Abstract][Full Text] [Related]
11. Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.
Kashiyama K; Nakazawa Y; Pilz DT; Guo C; Shimada M; Sasaki K; Fawcett H; Wing JF; Lewin SO; Carr L; Li TS; Yoshiura K; Utani A; Hirano A; Yamashita S; Greenblatt D; Nardo T; Stefanini M; McGibbon D; Sarkany R; Fassihi H; Takahashi Y; Nagayama Y; Mitsutake N; Lehmann AR; Ogi T
Am J Hum Genet; 2013 May; 92(5):807-19. PubMed ID: 23623389
[TBL] [Abstract][Full Text] [Related]
12. Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndrome.
Suhasini AN; Rawtani NA; Wu Y; Sommers JA; Sharma S; Mosedale G; North PS; Cantor SB; Hickson ID; Brosh RM
EMBO J; 2011 Feb; 30(4):692-705. PubMed ID: 21240188
[TBL] [Abstract][Full Text] [Related]
13. [DNA helicases and human diseases].
Uhring M; Poterszman A
Med Sci (Paris); 2006 Dec; 22(12):1087-94. PubMed ID: 17156731
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Insight into the roles of helicase motif Ia by characterizing Fanconi anemia group J protein (FANCJ) patient mutations.
Guo M; Vidhyasagar V; Ding H; Wu Y
J Biol Chem; 2014 Apr; 289(15):10551-10565. PubMed ID: 24573678
[TBL] [Abstract][Full Text] [Related]
16. Structure of the DNA repair helicase XPD.
Liu H; Rudolf J; Johnson KA; McMahon SA; Oke M; Carter L; McRobbie AM; Brown SE; Naismith JH; White MF
Cell; 2008 May; 133(5):801-12. PubMed ID: 18510925
[TBL] [Abstract][Full Text] [Related]
17. Structural and functional analyses of disease-causing missense mutations in Bloom syndrome protein.
Guo RB; Rigolet P; Ren H; Zhang B; Zhang XD; Dou SX; Wang PY; Amor-Gueret M; Xi XG
Nucleic Acids Res; 2007; 35(18):6297-310. PubMed ID: 17878217
[TBL] [Abstract][Full Text] [Related]
18. Mutational analysis of FANCJ helicase.
Guo M; Vidhyasagar V; Talwar T; Kariem A; Wu Y
Methods; 2016 Oct; 108():118-29. PubMed ID: 27107905
[TBL] [Abstract][Full Text] [Related]
19. Specialization among iron-sulfur cluster helicases to resolve G-quadruplex DNA structures that threaten genomic stability.
Bharti SK; Sommers JA; George F; Kuper J; Hamon F; Shin-ya K; Teulade-Fichou MP; Kisker C; Brosh RM
J Biol Chem; 2013 Sep; 288(39):28217-29. PubMed ID: 23935105
[TBL] [Abstract][Full Text] [Related]
20. Premature aging and predisposition to cancers caused by mutations in RecQ family helicases.
Furuichi Y
Ann N Y Acad Sci; 2001 Apr; 928():121-31. PubMed ID: 11795503
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]