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For: Shamanna RA, Croteau DL, Lee JH, Bohr VA. Recent Advances in Understanding Werner Syndrome. F1000Res 2017;6:1779. [PMID: 29043077 DOI: 10.12688/f1000research.12110.1] [Cited by in Crossref: 44] [Cited by in F6Publishing: 43] [Article Influence: 8.8] [Reference Citation Analysis]
Number Citing Articles
1 Gilmour BC, Gudmundsrud R, Frank J, Hov A, Lautrup S, Aman Y, Røsjø H, Brenner C, Ziegler M, Tysnes OB, Tzoulis C, Omland T, Søraas A, Holmøy T, Bergersen LH, Storm-Mathisen J, Nilsen H, Fang EF. Targeting NAD+ in translational research to relieve diseases and conditions of metabolic stress and ageing. Mech Ageing Dev 2020;186:111208. [PMID: 31953124 DOI: 10.1016/j.mad.2020.111208] [Cited by in Crossref: 13] [Cited by in F6Publishing: 15] [Article Influence: 6.5] [Reference Citation Analysis]
2 Geng L, Liu Z, Zhang W, Li W, Wu Z, Wang W, Ren R, Su Y, Wang P, Sun L, Ju Z, Chan P, Song M, Qu J, Liu GH. Chemical screen identifies a geroprotective role of quercetin in premature aging. Protein Cell. 2018;. [PMID: 30069858 DOI: 10.1007/s13238-018-0567-y] [Cited by in Crossref: 38] [Cited by in F6Publishing: 35] [Article Influence: 9.5] [Reference Citation Analysis]
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4 Singh A, Ganguly S, Chhabra N, Yadav H, Oshima J. A Case Report of Werner's Syndrome With a Novel Mutation From India. Cureus 2020;12:e8025. [PMID: 32528764 DOI: 10.7759/cureus.8025] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
5 James CD, Das D, Morgan EL, Otoa R, Macdonald A, Morgan IM. Werner Syndrome Protein (WRN) Regulates Cell Proliferation and the Human Papillomavirus 16 Life Cycle during Epithelial Differentiation. mSphere 2020;5:e00858-20. [PMID: 32938703 DOI: 10.1128/mSphere.00858-20] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Hussain M, Krishnamurthy S, Patel J, Kim E, Baptiste BA, Croteau DL, Bohr VA. Skin Abnormalities in Disorders with DNA Repair Defects, Premature Aging, and Mitochondrial Dysfunction. J Invest Dermatol 2021;141:968-75. [PMID: 33353663 DOI: 10.1016/j.jid.2020.10.019] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
7 Lee JH, Shamanna RA, Kulikowicz T, Borhan Fakouri N, Kim EW, Christiansen LS, Croteau DL, Bohr VA. CDK2 phosphorylation of Werner protein (WRN) contributes to WRN's DNA double-strand break repair pathway choice. Aging Cell 2021;20:e13484. [PMID: 34612580 DOI: 10.1111/acel.13484] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
8 Sommers JA, Kulikowicz T, Croteau DL, Dexheimer T, Dorjsuren D, Jadhav A, Maloney DJ, Simeonov A, Bohr VA, Brosh RM Jr. A high-throughput screen to identify novel small molecule inhibitors of the Werner Syndrome Helicase-Nuclease (WRN). PLoS One 2019;14:e0210525. [PMID: 30625228 DOI: 10.1371/journal.pone.0210525] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 3.3] [Reference Citation Analysis]
9 Gerlach SU, Herranz H. Genomic instability and cancer: lessons from Drosophila. Open Biol 2020;10:200060. [PMID: 32485126 DOI: 10.1098/rsob.200060] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
10 Lu H, Davis AJ. Human RecQ Helicases in DNA Double-Strand Break Repair. Front Cell Dev Biol 2021;9:640755. [PMID: 33718381 DOI: 10.3389/fcell.2021.640755] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
11 Phan T, Khalid F, Iben S. Nucleolar and Ribosomal Dysfunction-A Common Pathomechanism in Childhood Progerias? Cells 2019;8:E534. [PMID: 31167386 DOI: 10.3390/cells8060534] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
12 Wu Z, Shi Y, Lu M, Song M, Yu Z, Wang J, Wang S, Ren J, Yang YG, Liu GH, Zhang W, Ci W, Qu J. METTL3 counteracts premature aging via m6A-dependent stabilization of MIS12 mRNA. Nucleic Acids Res 2020;48:11083-96. [PMID: 33035345 DOI: 10.1093/nar/gkaa816] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 4.5] [Reference Citation Analysis]
13 Lebel M, Monnat RJ Jr. Werner syndrome (WRN) gene variants and their association with altered function and age-associated diseases. Ageing Res Rev 2018;41:82-97. [PMID: 29146545 DOI: 10.1016/j.arr.2017.11.003] [Cited by in Crossref: 26] [Cited by in F6Publishing: 20] [Article Influence: 6.5] [Reference Citation Analysis]
14 Fang EF, Hou Y, Lautrup S, Jensen MB, Yang B, SenGupta T, Caponio D, Khezri R, Demarest TG, Aman Y, Figueroa D, Morevati M, Lee HJ, Kato H, Kassahun H, Lee JH, Filippelli D, Okur MN, Mangerich A, Croteau DL, Maezawa Y, Lyssiotis CA, Tao J, Yokote K, Rusten TE, Mattson MP, Jasper H, Nilsen H, Bohr VA. NAD+ augmentation restores mitophagy and limits accelerated aging in Werner syndrome. Nat Commun 2019;10:5284. [PMID: 31754102 DOI: 10.1038/s41467-019-13172-8] [Cited by in Crossref: 62] [Cited by in F6Publishing: 60] [Article Influence: 20.7] [Reference Citation Analysis]
15 Norouzi M, Shafiei M, Abdollahi Z, Miar P, Galehdari H, Emami MH, Zeinalian M, Tabatabaiefar MA. WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family. Front Oncol 2021;11:648649. [PMID: 34164337 DOI: 10.3389/fonc.2021.648649] [Reference Citation Analysis]
16 Mukherjee S, Sinha D, Bhattacharya S, Srinivasan K, Abdisalaam S, Asaithamby A. Werner Syndrome Protein and DNA Replication. Int J Mol Sci 2018;19:E3442. [PMID: 30400178 DOI: 10.3390/ijms19113442] [Cited by in Crossref: 20] [Cited by in F6Publishing: 17] [Article Influence: 5.0] [Reference Citation Analysis]
17 Mojumdar A. Mutations in conserved functional domains of human RecQ helicases are associated with diseases and cancer: A review. Biophysical Chemistry 2020;265:106433. [DOI: 10.1016/j.bpc.2020.106433] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
18 Park S, Kim BK, Park SK. Supplementation with phosphatidylethanolamine confers anti-oxidant and anti-aging effects via hormesis and reduced insulin/IGF-1-like signaling in C. elegans. Mech Ageing Dev 2021;197:111498. [PMID: 33974957 DOI: 10.1016/j.mad.2021.111498] [Reference Citation Analysis]
19 Guio H, Poterico JA, Levano KS, Cornejo-Olivas M, Mazzetti P, Manassero-Morales G, Ugarte-Gil MF, Acevedo-Vásquez E, Dueñas-Roque M, Piscoya A, Fujita R, Sanchez C, Casavilca-Zambrano S, Jaramillo-Valverde L, Sullcahuaman-Allende Y, Iglesias-Pedraz JM, Abarca-Barriga H. Genetics and genomics in Peru: Clinical and research perspective. Mol Genet Genomic Med 2018;6:873-86. [PMID: 30584990 DOI: 10.1002/mgg3.533] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
20 Gudmundsrud R, Skjånes TH, Gilmour BC, Caponio D, Lautrup S, Fang EF. Crosstalk among DNA Damage, Mitochondrial Dysfunction, Impaired Mitophagy, Stem Cell Attrition, and Senescence in the Accelerated Ageing Disorder Werner Syndrome. Cytogenet Genome Res 2021;161:297-304. [PMID: 34433164 DOI: 10.1159/000516386] [Reference Citation Analysis]
21 Das D, Bristol ML, Smith NW, James CD, Wang X, Pichierri P, Morgan IM. Werner Helicase Control of Human Papillomavirus 16 E1-E2 DNA Replication Is Regulated by SIRT1 Deacetylation. mBio 2019;10:e00263-19. [PMID: 30890607 DOI: 10.1128/mBio.00263-19] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
22 Lautrup S, Caponio D, Cheung HH, Piccoli C, Stevnsner T, Chan WY, Fang EF. Studying Werner syndrome to elucidate mechanisms and therapeutics of human aging and age-related diseases. Biogerontology 2019;20:255-69. [PMID: 30666569 DOI: 10.1007/s10522-019-09798-2] [Cited by in Crossref: 15] [Cited by in F6Publishing: 12] [Article Influence: 5.0] [Reference Citation Analysis]
23 Abbasi S, Parmar G, Kelly RD, Balasuriya N, Schild-Poulter C. The Ku complex: recent advances and emerging roles outside of non-homologous end-joining. Cell Mol Life Sci 2021;78:4589-613. [PMID: 33855626 DOI: 10.1007/s00018-021-03801-1] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
24 Li M, Liu B, Yi J, Yang Y, Wang J, Zhu WG, Luo J. MIB1-mediated degradation of WRN promotes cellular senescence in response to camptothecin treatment. FASEB J 2020;34:11488-97. [PMID: 32652764 DOI: 10.1096/fj.202000268RRR] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
25 Qiu GH, Zheng X, Fu M, Huang C, Yang X. The protective function of non-coding DNA in DNA damage accumulation with age and its roles in age-related diseases. Biogerontology 2019;20:741-61. [PMID: 31473864 DOI: 10.1007/s10522-019-09832-3] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
26 Epiney DG, Salameh C, Cassidy D, Zhou LT, Kruithof J, Milutinović R, Andreani TS, Schirmer AE, Bolterstein E. Characterization of Stress Responses in a Drosophila Model of Werner Syndrome. Biomolecules 2021;11:1868. [PMID: 34944512 DOI: 10.3390/biom11121868] [Reference Citation Analysis]
27 Iglesias-Pedraz JM, Fossatti-Jara DM, Valle-Riestra-Felice V, Cruz-Visalaya SR, Ayala Felix JA, Comai L. WRN modulates translation by influencing nuclear mRNA export in HeLa cancer cells. BMC Mol Cell Biol 2020;21:71. [PMID: 33054770 DOI: 10.1186/s12860-020-00315-9] [Reference Citation Analysis]
28 Wong SK, Ima-Nirwana S, Chin KY. Can telomere length predict bone health? A review of current evidence. Bosn J Basic Med Sci 2020;20:423-9. [PMID: 32156247 DOI: 10.17305/bjbms.2020.4664] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
29 Fernandez RJ 3rd, Johnson FB. A regulatory loop connecting WNT signaling and telomere capping: possible therapeutic implications for dyskeratosis congenita. Ann N Y Acad Sci 2018;1418:56-68. [PMID: 29722029 DOI: 10.1111/nyas.13692] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 2.7] [Reference Citation Analysis]
30 Yoon YS, Jin M, Sin DD. Accelerated lung aging and chronic obstructive pulmonary disease. Expert Rev Respir Med 2019;13:369-80. [PMID: 30735057 DOI: 10.1080/17476348.2019.1580576] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
31 Aumailley L, Lebel M. The Impact of Vitamin C on Different System Models of Werner Syndrome. Antioxid Redox Signal 2021;34:856-74. [PMID: 33202145 DOI: 10.1089/ars.2020.8147] [Reference Citation Analysis]
32 James CD, Das D, Bristol ML, Morgan IM. Activating the DNA Damage Response and Suppressing Innate Immunity: Human Papillomaviruses Walk the Line. Pathogens 2020;9:E467. [PMID: 32545729 DOI: 10.3390/pathogens9060467] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
33 Tu J, Wan C, Zhang F, Cao L, Law PWN, Tian Y, Lu G, Rennert OM, Chan WY, Cheung HH. Genetic correction of Werner syndrome gene reveals impaired pro-angiogenic function and HGF insufficiency in mesenchymal stem cells. Aging Cell 2020;19:e13116. [PMID: 32320127 DOI: 10.1111/acel.13116] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
34 Lee JH, Kim EW, Croteau DL, Bohr VA. Heterochromatin: an epigenetic point of view in aging. Exp Mol Med 2020;52:1466-74. [PMID: 32887933 DOI: 10.1038/s12276-020-00497-4] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 4.5] [Reference Citation Analysis]
35 Paull TT. DNA damage and regulation of protein homeostasis. DNA Repair (Amst) 2021;105:103155. [PMID: 34116476 DOI: 10.1016/j.dnarep.2021.103155] [Reference Citation Analysis]
36 Oshima J, Kato H, Maezawa Y, Yokote K. RECQ helicase disease and related progeroid syndromes: RECQ2018 meeting. Mech Ageing Dev 2018;173:80-3. [PMID: 29752965 DOI: 10.1016/j.mad.2018.05.002] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 2.3] [Reference Citation Analysis]
37 Charlier CF, Martins RAP. Protective Mechanisms Against DNA Replication Stress in the Nervous System. Genes (Basel) 2020;11:E730. [PMID: 32630049 DOI: 10.3390/genes11070730] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
38 Hsu T, Zhang B, L'etoile ND, Juang B. C. elegans orthologs MUT-7/CeWRN-1 of Werner syndrome protein regulate neuronal plasticity. eLife 2021;10:e62449. [DOI: 10.7554/elife.62449] [Reference Citation Analysis]
39 Kim SH, Kim BK, Park S, Park SK. Phosphatidylcholine Extends Lifespan via DAF-16 and Reduces Amyloid-Beta-Induced Toxicity in Caenorhabditis elegans. Oxid Med Cell Longev 2019;2019:2860642. [PMID: 31379987 DOI: 10.1155/2019/2860642] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 2.3] [Reference Citation Analysis]
40 Wu Z, Zhang W, Song M, Wang W, Wei G, Li W, Lei J, Huang Y, Sang Y, Chan P, Chen C, Qu J, Suzuki K, Belmonte JCI, Liu GH. Differential stem cell aging kinetics in Hutchinson-Gilford progeria syndrome and Werner syndrome. Protein Cell 2018;9:333-50. [PMID: 29476423 DOI: 10.1007/s13238-018-0517-8] [Cited by in Crossref: 32] [Cited by in F6Publishing: 29] [Article Influence: 8.0] [Reference Citation Analysis]
41 Wong SK, Chin KY, Ima-Nirwana S. Vitamin C: A Review on its Role in the Management of Metabolic Syndrome. Int J Med Sci 2020;17:1625-38. [PMID: 32669965 DOI: 10.7150/ijms.47103] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
42 Chen TI, Hsu YK, Chou CY, Chen YH, Hsu ST, Liou YS, Dai YC, Chang MF, Chang SC. Hepatitis C Virus NS3 Protein Plays a Dual Role in WRN-Mediated Repair of Nonhomologous End Joining. J Virol 2019;93:e01273-19. [PMID: 31462559 DOI: 10.1128/JVI.01273-19] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
43 Cassidy D, Epiney DG, Salameh C, Zhou LT, Salomon RN, Schirmer AE, McVey M, Bolterstein E. Evidence for premature aging in a Drosophila model of Werner syndrome. Exp Gerontol 2019;127:110733. [PMID: 31518666 DOI: 10.1016/j.exger.2019.110733] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
44 Maezawa Y, Kato H, Takemoto M, Watanabe A, Koshizaka M, Ishikawa T, Sargolzaeiaval F, Kuzuya M, Wakabayashi H, Kusaka T, Yokote K, Oshima J. Biallelic WRN Mutations in Newly Identified Japanese Werner Syndrome Patients. Mol Syndromol 2018;9:214-8. [PMID: 30140198 DOI: 10.1159/000489055] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
45 Das D, Bristol ML, Pichierri P, Morgan IM. Using a Human Papillomavirus Model to Study DNA Replication and Repair of Wild Type and Damaged DNA Templates in Mammalian Cells. Int J Mol Sci 2020;21:E7564. [PMID: 33066318 DOI: 10.3390/ijms21207564] [Reference Citation Analysis]