132 related articles for article (PubMed ID: 11301316)
1. A novel protein interacts with the Werner's syndrome gene product physically and functionally.
Kawabe Yi ; Branzei D; Hayashi T; Suzuki H; Masuko T; Onoda F; Heo SJ; Ikeda H; Shimamoto A; Furuichi Y; Seki M; Enomoto T
J Biol Chem; 2001 Jun; 276(23):20364-9. PubMed ID: 11301316
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. The N-terminal region of Sgs1, which interacts with Top3, is required for complementation of MMS sensitivity and suppression of hyper-recombination in sgs1 disruptants.
Ui A; Satoh Y; Onoda F; Miyajima A; Seki M; Enomoto T
Mol Genet Genomics; 2001 Jul; 265(5):837-50. PubMed ID: 11523801
[TBL] [Abstract][Full Text] [Related]
4. Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases.
Yamagata K; Kato J; Shimamoto A; Goto M; Furuichi Y; Ikeda H
Proc Natl Acad Sci U S A; 1998 Jul; 95(15):8733-8. PubMed ID: 9671747
[TBL] [Abstract][Full Text] [Related]
5. Werner interacting protein 1 promotes binding of Werner protein to template-primer DNA.
Kanamori M; Seki M; Yoshimura A; Tsurimoto T; Tada S; Enomoto T
Biol Pharm Bull; 2011; 34(8):1314-8. PubMed ID: 21804224
[TBL] [Abstract][Full Text] [Related]
6. Elevation of sister chromatid exchange in Saccharomyces cerevisiae sgs1 disruptants and the relevance of the disruptants as a system to evaluate mutations in Bloom's syndrome gene.
Onoda F; Seki M; Miyajima A; Enomoto T
Mutat Res; 2000 Apr; 459(3):203-9. PubMed ID: 10812332
[TBL] [Abstract][Full Text] [Related]
7. Characterisation of the interaction between WRN, the helicase/exonuclease defective in progeroid Werner's syndrome, and an essential replication factor, PCNA.
Rodríguez-López AM; Jackson DA; Nehlin JO; Iborra F; Warren AV; Cox LS
Mech Ageing Dev; 2003 Feb; 124(2):167-74. PubMed ID: 12633936
[TBL] [Abstract][Full Text] [Related]
8. Werner complex deficiency in cells disrupts the Nuclear Pore Complex and the distribution of lamin B1.
Li Z; Zhu Y; Zhai Y; R Castroagudin M; Bao Y; White TE; Glavy JS
Biochim Biophys Acta; 2013 Dec; 1833(12):3338-3345. PubMed ID: 24050918
[TBL] [Abstract][Full Text] [Related]
9. Sgs1 helicase activity is required for mitotic but apparently not for meiotic functions.
Miyajima A; Seki M; Onoda F; Shiratori M; Odagiri N; Ohta K; Kikuchi Y; Ohno Y; Enomoto T
Mol Cell Biol; 2000 Sep; 20(17):6399-409. PubMed ID: 10938117
[TBL] [Abstract][Full Text] [Related]
10. Crystal structure of the HRDC domain of human Werner syndrome protein, WRN.
Kitano K; Yoshihara N; Hakoshima T
J Biol Chem; 2007 Jan; 282(4):2717-28. PubMed ID: 17148451
[TBL] [Abstract][Full Text] [Related]
11. Characterization of the slow-growth phenotype of S. cerevisiae Whip/Mgs1 Sgs1 double deletion mutants.
Branzei D; Seki M; Onoda F; Yagi H; Kawabe Y; Enomoto T
DNA Repair (Amst); 2002 Aug; 1(8):671-82. PubMed ID: 12509289
[TBL] [Abstract][Full Text] [Related]
12. Covalent modification of the Werner's syndrome gene product with the ubiquitin-related protein, SUMO-1.
Kawabe Y; Seki M; Seki T; Wang WS; Imamura O; Furuichi Y; Saitoh H; Enomoto T
J Biol Chem; 2000 Jul; 275(28):20963-6. PubMed ID: 10806190
[TBL] [Abstract][Full Text] [Related]
13. Unwinding the molecular basis of the Werner syndrome.
Shen J; Loeb LA
Mech Ageing Dev; 2001 Jul; 122(9):921-44. PubMed ID: 11348659
[TBL] [Abstract][Full Text] [Related]
14. Accelerated aging and nucleolar fragmentation in yeast sgs1 mutants.
Sinclair DA; Mills K; Guarente L
Science; 1997 Aug; 277(5330):1313-6. PubMed ID: 9271578
[TBL] [Abstract][Full Text] [Related]
15. Werner's syndrome lymphoblastoid cells are hypersensitive to topoisomerase II inhibitors in the G2 phase of the cell cycle.
Pichierri P; Franchitto A; Mosesso P; Proietti de Santis L; Balajee AS; Palitti F
Mutat Res; 2000 Mar; 459(2):123-33. PubMed ID: 10725663
[TBL] [Abstract][Full Text] [Related]
16. Functional interaction between the Werner Syndrome protein and DNA polymerase delta.
Kamath-Loeb AS; Johansson E; Burgers PM; Loeb LA
Proc Natl Acad Sci U S A; 2000 Apr; 97(9):4603-8. PubMed ID: 10781066
[TBL] [Abstract][Full Text] [Related]
17. The N-terminal domain of the large subunit of human replication protein A binds to Werner syndrome protein and stimulates helicase activity.
Shen JC; Lao Y; Kamath-Loeb A; Wold MS; Loeb LA
Mech Ageing Dev; 2003; 124(8-9):921-30. PubMed ID: 14499497
[TBL] [Abstract][Full Text] [Related]
18. Requirements for the nucleolytic processing of DNA ends by the Werner syndrome protein-Ku70/80 complex.
Li B; Comai L
J Biol Chem; 2001 Mar; 276(13):9896-902. PubMed ID: 11152456
[TBL] [Abstract][Full Text] [Related]
19. Identification and biochemical characterization of a Werner's syndrome protein complex with Ku70/80 and poly(ADP-ribose) polymerase-1.
Li B; Navarro S; Kasahara N; Comai L
J Biol Chem; 2004 Apr; 279(14):13659-67. PubMed ID: 14734561
[TBL] [Abstract][Full Text] [Related]
20. Functions of RecQ family helicases: possible involvement of Bloom's and Werner's syndrome gene products in guarding genome integrity during DNA replication.
Enomoto T
J Biochem; 2001 Apr; 129(4):501-7. PubMed ID: 11275547
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]