BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 25309043)

  • 1. [Werner syndrome. A prototypical form of segmental progeria.].
    Lessel D; Oshima J; Kubisch C
    Med Genet; 2012 Dec; 24(4):262-267. PubMed ID: 25309043
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Werner syndrome and mutations of the WRN and LMNA genes in France.
    Uhrhammer NA; Lafarge L; Dos Santos L; Domaszewska A; Lange M; Yang Y; Aractingi S; Bessis D; Bignon YJ
    Hum Mutat; 2006 Jul; 27(7):718-9. PubMed ID: 16786514
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Severe metabolic disorders coexisting with Werner syndrome: a case report.
    Li H; Yang M; Shen H; Wang S; Cai H
    Endocr J; 2021 Mar; 68(3):261-267. PubMed ID: 33087645
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome.
    Donadille B; D'Anella P; Auclair M; Uhrhammer N; Sorel M; Grigorescu R; Ouzounian S; Cambonie G; Boulot P; Laforêt P; Carbonne B; Christin-Maitre S; Bignon YJ; Vigouroux C
    Orphanet J Rare Dis; 2013 Jul; 8():106. PubMed ID: 23849162
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Werner syndrome presenting as early-onset diabetes: A case report.
    Wang X; Liu S; Qin F; Liu Q; Wang Q
    J Diabetes Investig; 2022 Mar; 13(3):592-598. PubMed ID: 34564935
    [TBL] [Abstract][Full Text] [Related]  

  • 6. POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome.
    Lessel D; Hisama FM; Szakszon K; Saha B; Sanjuanelo AB; Salbert BA; Steele PD; Baldwin J; Brown WT; Piussan C; Plauchu H; Szilvássy J; Horkay E; Högel J; Martin GM; Herr AJ; Oshima J; Kubisch C
    Hum Mutat; 2015 Nov; 36(11):1070-9. PubMed ID: 26172944
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prematurely aged children: molecular alterations leading to Hutchinson-Gilford progeria and Werner syndromes.
    Domínguez-Gerpe L; Araújo-Vilar D
    Curr Aging Sci; 2008 Dec; 1(3):202-12. PubMed ID: 20021393
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pathways and functions of the Werner syndrome protein.
    Lee JW; Harrigan J; Opresko PL; Bohr VA
    Mech Ageing Dev; 2005 Jan; 126(1):79-86. PubMed ID: 15610765
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Current advances in unraveling the function of the Werner syndrome protein.
    Ozgenc A; Loeb LA
    Mutat Res; 2005 Sep; 577(1-2):237-51. PubMed ID: 15946710
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases.
    Shen JC; Loeb LA
    Trends Genet; 2000 May; 16(5):213-20. PubMed ID: 10782115
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Werner's Syndrome RecQ helicase/exonuclease at the nexus of cancer and aging.
    Chun SG; Shaeffer DS; Bryant-Greenwood PK
    Hawaii Med J; 2011 Mar; 70(3):52-5. PubMed ID: 21365542
    [TBL] [Abstract][Full Text] [Related]  

  • 12. WRN protein and Werner syndrome.
    Luo J
    N Am J Med Sci (Boston); 2010; 3(4):205-207. PubMed ID: 22180828
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of Werner syndrome without metabolic abnormality: implications for the early pathophysiology.
    Takada-Watanabe A; Yokote K; Takemoto M; Fujimoto M; Irisuna H; Honjo S; Futami K; Furuichi Y; Saito Y
    Geriatr Gerontol Int; 2012 Jan; 12(1):140-6. PubMed ID: 22188495
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [WRN gene].
    Katsuya T; Morishita R
    Nihon Rinsho; 2009 Jul; 67(7):1277-82. PubMed ID: 19591272
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. WRN helicase defective in the premature aging disorder Werner syndrome genetically interacts with topoisomerase 3 and restores the top3 slow growth phenotype of sgs1 top3.
    Aggarwal M; Brosh RM
    Aging (Albany NY); 2009 Feb; 1(2):219-33. PubMed ID: 20157511
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Do you know this syndrome? Werner syndrome.
    Bilgiç Ö
    An Bras Dermatol; 2017; 92(2):271-272. PubMed ID: 28538897
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry.
    Saha B; Lessel D; Nampoothiri S; Rao AS; Hisama FM; Peter D; Bennett C; Nürnberg G; Nürnberg P; Martin GM; Kubisch C; Oshima J
    Mol Genet Genomic Med; 2013 May; 1(1):7-14. PubMed ID: 23936869
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.