148 related articles for article (PubMed ID: 22037268)
21. Association of a missense single nucleotide polymorphism, Cys1367Arg of the WRN gene, with the risk of bone and soft tissue sarcomas in Japan.
Nakayama R; Sato Y; Masutani M; Ogino H; Nakatani F; Chuman H; Beppu Y; Morioka H; Yabe H; Hirose H; Sugimura H; Sakamoto H; Ohta T; Toyama Y; Yoshida T; Kawai A
Cancer Sci; 2008 Feb; 99(2):333-9. PubMed ID: 18271933
[TBL] [Abstract][Full Text] [Related]
22. WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brazil.
Pinto GR; Yoshioka FK; Clara CA; Santos MJ; Almeida JR; Burbano RR; Rey JA; Casartelli C
J Neurooncol; 2008 Dec; 90(3):253-8. PubMed ID: 18670736
[TBL] [Abstract][Full Text] [Related]
23. The Werner Protein Acts as a Coactivator of Nuclear Factor κB (NF-κB) on HIV-1 and Interleukin-8 (IL-8) Promoters.
Mizutani T; Ishizaka A; Furuichi Y
J Biol Chem; 2015 Jul; 290(30):18391-9. PubMed ID: 26037922
[TBL] [Abstract][Full Text] [Related]
24. Functional role of the Werner syndrome RecQ helicase in human fibroblasts.
Dhillon KK; Sidorova J; Saintigny Y; Poot M; Gollahon K; Rabinovitch PS; Monnat RJ
Aging Cell; 2007 Feb; 6(1):53-61. PubMed ID: 17266675
[TBL] [Abstract][Full Text] [Related]
25. Werner protein cooperates with the XRCC4-DNA ligase IV complex in end-processing.
Kusumoto R; Dawut L; Marchetti C; Wan Lee J; Vindigni A; Ramsden D; Bohr VA
Biochemistry; 2008 Jul; 47(28):7548-56. PubMed ID: 18558713
[TBL] [Abstract][Full Text] [Related]
26. Predictive impact of genetic polymorphisms in DNA repair genes on susceptibility and therapeutic outcomes to colorectal cancer patients.
Sun K; Gong A; Liang P
Tumour Biol; 2015 Mar; 36(3):1549-59. PubMed ID: 25355595
[TBL] [Abstract][Full Text] [Related]
27. The Werner syndrome helicase/exonuclease processes mobile D-loops through branch migration and degradation.
Opresko PL; Sowd G; Wang H
PLoS One; 2009; 4(3):e4825. PubMed ID: 19283071
[TBL] [Abstract][Full Text] [Related]
28. The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis.
Muftuoglu M; Oshima J; von Kobbe C; Cheng WH; Leistritz DF; Bohr VA
Hum Genet; 2008 Nov; 124(4):369-77. PubMed ID: 18810497
[TBL] [Abstract][Full Text] [Related]
29. Adult progeria: a new mutation in the WRN gene.
Rocha ML; Chicharo AT; Sequeira G; Teixeira V
BMJ Case Rep; 2022 Nov; 15(11):. PubMed ID: 36396328
[TBL] [Abstract][Full Text] [Related]
30. A Novel WRN Frameshift Mutation Identified by Multiplex Genetic Testing in a Family with Multiple Cases of Cancer.
Yang L; Wang G; Zhao X; Ye S; Shen P; Wang W; Zheng S
PLoS One; 2015; 10(8):e0133020. PubMed ID: 26241669
[TBL] [Abstract][Full Text] [Related]
31. CASP8, XRCC1, WRN, NF2, and BRIP1 Polymorphisms Analysis Shows Their Genetic Susceptibility for Meningioma Risk and the Association with Tumor-Related Phenotype in a Chinese Population.
Huang G; Feng J; Hao S; Li D; Wang K; Wang L; Wu Z; Wan H; Zhang L; Zhang J
World Neurosurg; 2018 Jun; 114():e883-e891. PubMed ID: 29581016
[TBL] [Abstract][Full Text] [Related]
32. Telomere ResQue and preservation--roles for the Werner syndrome protein and other RecQ helicases.
Opresko PL
Mech Ageing Dev; 2008; 129(1-2):79-90. PubMed ID: 18054793
[TBL] [Abstract][Full Text] [Related]
33. [Case report: A case of Werner syndrome with compound heterozygous mutations of WRN gene].
Tamori Y; Takahashi T; Nakajima S; Nishimoto Y; Ohno K; Takemoto M; Yokote K; Kita T; Tsutsumi M
Nihon Naika Gakkai Zasshi; 2011 Jun; 100(6):1642-4. PubMed ID: 21770289
[No Abstract] [Full Text] [Related]
34. Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancer.
Wirtenberger M; Frank B; Hemminki K; Klaes R; Schmutzler RK; Wappenschmidt B; Meindl A; Kiechle M; Arnold N; Weber BH; Niederacher D; Bartram CR; Burwinkel B
Carcinogenesis; 2006 Aug; 27(8):1655-60. PubMed ID: 16501249
[TBL] [Abstract][Full Text] [Related]
35. WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair.
Chen L; Huang S; Lee L; Davalos A; Schiestl RH; Campisi J; Oshima J
Aging Cell; 2003 Aug; 2(4):191-9. PubMed ID: 12934712
[TBL] [Abstract][Full Text] [Related]
36. The Werner's syndrome 4330T>C (Cys1367Arg) gene variant does not affect the in vitro cytotoxicity of topoisomerase inhibitors and platinum compounds.
Innocenti F; Mirkov S; Nagasubramanian R; Ramírez J; Liu W; Bleibel WK; Shukla SJ; Hennessy K; Rosner GL; Cook E; Eileen Dolan M; Ratain MJ
Cancer Chemother Pharmacol; 2009 Apr; 63(5):881-7. PubMed ID: 18677484
[TBL] [Abstract][Full Text] [Related]
37. Possible associations between successful aging and polymorphic markers in the Werner gene region.
Sild M; Koca C; Bendixen MH; Frederiksen H; McGue M; Kølvraa S; Christensen K; Nexø B
Ann N Y Acad Sci; 2006 May; 1067():309-10. PubMed ID: 16804003
[TBL] [Abstract][Full Text] [Related]
38. Polymorphisms in DNA repair genes, hair dye use, and the risk of non-Hodgkin lymphoma.
Guo H; Bassig BA; Lan Q; Zhu Y; Zhang Y; Holford TR; Leaderer B; Boyle P; Qin Q; Zhu C; Li N; Rothman N; Zheng T
Cancer Causes Control; 2014 Oct; 25(10):1261-70. PubMed ID: 25178586
[TBL] [Abstract][Full Text] [Related]
39. DNA binding residues in the RQC domain of Werner protein are critical for its catalytic activities.
Tadokoro T; Kulikowicz T; Dawut L; Croteau DL; Bohr VA
Aging (Albany NY); 2012 Jun; 4(6):417-29. PubMed ID: 22713343
[TBL] [Abstract][Full Text] [Related]
40. Functional deficit associated with a missense Werner syndrome mutation.
Tadokoro T; Rybanska-Spaeder I; Kulikowicz T; Dawut L; Oshima J; Croteau DL; Bohr VA
DNA Repair (Amst); 2013 Jun; 12(6):414-21. PubMed ID: 23583337
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]