BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

323 related articles for article (PubMed ID: 23849162)

  • 21. Oxidative stress and antioxidant response in fibroblasts from Werner and atypical Werner syndromes.
    Seco-Cervera M; Spis M; García-Giménez JL; Ibañez-Cabellos JS; Velázquez-Ledesma A; Esmorís I; Bañuls S; Pérez-Machado G; Pallardó FV
    Aging (Albany NY); 2014 Mar; 6(3):231-45. PubMed ID: 24799429
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The transcriptional response to distinct growth factors is impaired in Werner syndrome cells.
    Lutomska A; Lebedev A; Scharffetter-Kochanek K; Iben S
    Exp Gerontol; 2008 Sep; 43(9):820-6. PubMed ID: 18625297
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The Werner syndrome protein: linking the replication checkpoint response to genome stability.
    Pichierri P; Ammazzalorso F; Bignami M; Franchitto A
    Aging (Albany NY); 2011 Mar; 3(3):311-8. PubMed ID: 21389352
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The Werner syndrome protein affects the expression of genes involved in adipogenesis and inflammation in addition to cell cycle and DNA damage responses.
    Turaga RV; Paquet ER; Sild M; Vignard J; Garand C; Johnson FB; Masson JY; Lebel M
    Cell Cycle; 2009 Jul; 8(13):2080-92. PubMed ID: 19502800
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Accelerated aging syndromes, are they relevant to normal human aging?
    Dreesen O; Stewart CL
    Aging (Albany NY); 2011 Sep; 3(9):889-95. PubMed ID: 21931180
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Werner syndrome protein: functions in the response to DNA damage and replication stress in S-phase.
    Cheng WH; Muftuoglu M; Bohr VA
    Exp Gerontol; 2007 Sep; 42(9):871-8. PubMed ID: 17587522
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. A role for WRN in telomere-based DNA damage responses.
    Eller MS; Liao X; Liu S; Hanna K; Bäckvall H; Opresko PL; Bohr VA; Gilchrest BA
    Proc Natl Acad Sci U S A; 2006 Oct; 103(41):15073-8. PubMed ID: 17015833
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. 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]  

  • 31. 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]  

  • 32. Transient overexpression of Werner protein rescues starvation induced autophagy in Werner syndrome cells.
    Maity J; Bohr VA; Laskar A; Karmakar P
    Biochim Biophys Acta; 2014 Dec; 1842(12 Pt A):2387-94. PubMed ID: 25257404
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Estrogen prevents senescence through induction of WRN, Werner syndrome protein.
    Lee SJ; Lee SH; Ha NC; Park BJ
    Horm Res Paediatr; 2010; 74(1):33-40. PubMed ID: 20395656
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Divergent cellular phenotypes of human and mouse cells lacking the Werner syndrome RecQ helicase.
    Dhillon KK; Sidorova JM; Albertson TM; Anderson JB; Ladiges WC; Rabinovitch PS; Preston BD; Monnat RJ
    DNA Repair (Amst); 2010 Jan; 9(1):11-22. PubMed ID: 19896421
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Nonfunctional mutant Wrn protein leads to neurological deficits, neuronal stress, microglial alteration, and immune imbalance in a mouse model of Werner syndrome.
    Hui CW; St-Pierre MK; Detuncq J; Aumailley L; Dubois MJ; Couture V; Skuk D; Marette A; Tremblay JP; Lebel M; Tremblay MÈ
    Brain Behav Immun; 2018 Oct; 73():450-469. PubMed ID: 29908963
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Primary lipodystrophies].
    Capeau J; Magré J; Lascols O; Caron M; Béréziat V; Vigouroux C
    Ann Endocrinol (Paris); 2007 Feb; 68(1):10-20. PubMed ID: 17320032
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Ascorbate improves metabolic abnormalities in Wrn mutant mice but not the free radical scavenger catechin.
    Lebel M; Massip L; Garand C; Thorin E
    Ann N Y Acad Sci; 2010 Jun; 1197():40-4. PubMed ID: 20536831
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. Type A insulin resistance syndrome revealing a novel lamin A mutation.
    Young J; Morbois-Trabut L; Couzinet B; Lascols O; Dion E; Béréziat V; Fève B; Richard I; Capeau J; Chanson P; Vigouroux C
    Diabetes; 2005 Jun; 54(6):1873-8. PubMed ID: 15919811
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.