BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 38277397)

  • 21. Sex differences in symptom presentation and their impact on diagnostic accuracy in Werner syndrome.
    Kaneko H; Maezawa Y; Tsukagoshi-Yamaguchi A; Koshizaka M; Takada-Watanabe A; Nakamura R; Funayama S; Aono K; Teramoto N; Sawada D; Maeda Y; Minamizuka T; Hayashi A; Ide K; Ide S; Shoji M; Kitamoto T; Takemoto M; Kato H; Yokote K
    Geriatr Gerontol Int; 2024 Jan; 24(1):161-167. PubMed ID: 38062994
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Diabetes mellitus coexisted with progeria: a case report of atypical Werner syndrome with novel LMNA mutations and literature review.
    He G; Yan Z; Sun L; Lv Y; Guo W; Gang X; Wang G
    Endocr J; 2019 Nov; 66(11):961-969. PubMed ID: 31270292
    [TBL] [Abstract][Full Text] [Related]  

  • 23. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.
    Friedrich K; Lee L; Leistritz DF; Nürnberg G; Saha B; Hisama FM; Eyman DK; Lessel D; Nürnberg P; Li C; Garcia-F-Villalta MJ; Kets CM; Schmidtke J; Cruz VT; Van den Akker PC; Boak J; Peter D; Compoginis G; Cefle K; Ozturk S; López N; Wessel T; Poot M; Ippel PF; Groff-Kellermann B; Hoehn H; Martin GM; Kubisch C; Oshima J
    Hum Genet; 2010 Jul; 128(1):103-11. PubMed ID: 20443122
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Case Report: A novel
    Peng H; Wang J; Liu Y; Yang H; Li L; Ma Y; Zhuo H; Jiang H
    Front Endocrinol (Lausanne); 2022; 13():918979. PubMed ID: 35909544
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Homozygous and compound heterozygous mutations at the Werner syndrome locus.
    Oshima J; Yu CE; Piussan C; Klein G; Jabkowski J; Balci S; Miki T; Nakura J; Ogihara T; Ells J; Smith M; Melaragno MI; Fraccaro M; Scappaticci S; Matthews J; Ouais S; Jarzebowicz A; Schellenberg GD; Martin GM
    Hum Mol Genet; 1996 Dec; 5(12):1909-13. PubMed ID: 8968742
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A novel mutation of the WRN gene in a Chinese patient with Werner syndrome.
    Zhao N; Hao F; Qu T; Zuo YG; Wang BX
    Clin Exp Dermatol; 2008 May; 33(3):278-81. PubMed ID: 18205852
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Werner syndrome (WRN) gene variants and their association with altered function and age-associated diseases.
    Lebel M; Monnat RJ
    Ageing Res Rev; 2018 Jan; 41():82-97. PubMed ID: 29146545
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Ectopic hTERT expression facilitates reprograming of fibroblasts derived from patients with Werner syndrome as a WS cellular model.
    Wang S; Liu Z; Ye Y; Li B; Liu T; Zhang W; Liu GH; Zhang YA; Qu J; Xu D; Chen Z
    Cell Death Dis; 2018 Sep; 9(9):923. PubMed ID: 30206203
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes.
    Maierhofer A; Flunkert J; Oshima J; Martin GM; Poot M; Nanda I; Dittrich M; Müller T; Haaf T
    Aging Cell; 2019 Oct; 18(5):e12995. PubMed ID: 31259468
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The Impact of Vitamin C on Different System Models of Werner Syndrome.
    Aumailley L; Lebel M
    Antioxid Redox Signal; 2021 Apr; 34(11):856-874. PubMed ID: 33202145
    [No Abstract]   [Full Text] [Related]  

  • 31. Meningioma in a patient with Werner syndrome.
    Pattankar S; Churi O; Misra BK
    Neurol India; 2020; 68(2):483-486. PubMed ID: 32415031
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genetic correction of Werner syndrome gene reveals impaired pro-angiogenic function and HGF insufficiency in mesenchymal stem cells.
    Tu J; Wan C; Zhang F; Cao L; Law PWN; Tian Y; Lu G; Rennert OM; Chan WY; Cheung HH
    Aging Cell; 2020 May; 19(5):e13116. PubMed ID: 32320127
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Werner syndrome: clinical evaluation of two cases and a novel mutation.
    Mansur AT; Elçioglu NH; Demirci GT
    Genet Couns; 2014; 25(2):119-27. PubMed ID: 25059010
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.
    Yu CE; Oshima J; Wijsman EM; Nakura J; Miki T; Piussan C; Matthews S; Fu YH; Mulligan J; Martin GM; Schellenberg GD
    Am J Hum Genet; 1997 Feb; 60(2):330-41. PubMed ID: 9012406
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Comparative aspects of the Werner syndrome gene.
    Oshima J
    In Vivo; 2000; 14(1):165-72. PubMed ID: 10757074
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Search and insights into novel genetic alterations leading to classical and atypical Werner syndrome.
    Oshima J; Hisama FM
    Gerontology; 2014; 60(3):239-46. PubMed ID: 24401204
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Characterization of Stress Responses in a
    Epiney DG; Salameh C; Cassidy D; Zhou LT; Kruithof J; Milutinović R; Andreani TS; Schirmer AE; Bolterstein E
    Biomolecules; 2021 Dec; 11(12):. PubMed ID: 34944512
    [TBL] [Abstract][Full Text] [Related]  

  • 39. WRN mutations in Werner syndrome.
    Moser MJ; Oshima J; Monnat RJ
    Hum Mutat; 1999; 13(4):271-9. PubMed ID: 10220139
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetic analyses of two cases of Werner's syndrome.
    Sogabe Y; Yasuda M; Yokoyama Y; Tamura A; Negishi I; Ohnishi K; Shinozaki T; Ishikawa O
    Eur J Dermatol; 2004; 14(6):379-82. PubMed ID: 15564200
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.