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Journal Abstract Search

190 related items for PubMed ID: 7507567

  • 1. Correlation between senescence and DNA repair in cells from young and old individuals and in premature aging syndromes.
    Weirich-Schwaiger H, Weirich HG, Gruber B, Schweiger M, Hirsch-Kauffmann M.
    Mutat Res; 1994 Feb; 316(1):37-48. PubMed ID: 7507567
    [Abstract] [Full Text] [Related]

  • 2. The premature ageing syndromes: insights into the ageing process.
    Dyer CA, Sinclair AJ.
    Age Ageing; 1998 Jan; 27(1):73-80. PubMed ID: 9504370
    [No Abstract] [Full Text] [Related]

  • 3. Genetic effects on the longevity of cultured human fibroblasts. II. DNA repair deficient syndromes.
    Thompson KV, Holliday R.
    Gerontology; 1983 Jan; 29(2):83-8. PubMed ID: 6840563
    [Abstract] [Full Text] [Related]

  • 4. [Determinants of aging processes-medical and biochemical aspects (author's transl)].
    Platt D.
    Aktuelle Gerontol; 1982 May; 12(3):83-7. PubMed ID: 6124142
    [No Abstract] [Full Text] [Related]

  • 5. Premature aging syndromes.
    Brown WT.
    Curr Probl Dermatol; 1987 May; 17():152-65. PubMed ID: 2954770
    [No Abstract] [Full Text] [Related]

  • 6. Aneuploidy analysis in fibroblasts of human premature aging syndromes by FISH during in vitro cellular aging.
    Mukherjee AB, Costello C.
    Mech Ageing Dev; 1998 Jun 15; 103(2):209-22. PubMed ID: 9701772
    [Abstract] [Full Text] [Related]

  • 7. p38 (MAPK) stress signalling in replicative senescence in fibroblasts from progeroid and genomic instability syndromes.
    Tivey HS, Brook AJ, Rokicki MJ, Kipling D, Davis T.
    Biogerontology; 2013 Feb 15; 14(1):47-62. PubMed ID: 23112078
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 2(4):191-9. PubMed ID: 12934712
    [Abstract] [Full Text] [Related]

  • 9. Neurodegeneration in accelerated aging.
    Scheibye-Knudsen M.
    Dan Med J; 2016 Nov 15; 63(11):. PubMed ID: 27808039
    [Abstract] [Full Text] [Related]

  • 10. Mechanisms of formation of chromosomal aberrations: insights from studies with DNA repair-deficient cells.
    Palitti F.
    Cytogenet Genome Res; 2004 Nov 15; 104(1-4):95-9. PubMed ID: 15162020
    [Abstract] [Full Text] [Related]

  • 11. DNA repair and transcription in human premature aging disorders.
    Bohr VA, Dianov G, Balajee A, May A, Orren DK.
    J Investig Dermatol Symp Proc; 1998 Aug 15; 3(1):11-3. PubMed ID: 9732050
    [Abstract] [Full Text] [Related]

  • 12. Gene expression and DNA repair in progeroid syndromes and human aging.
    Kyng KJ, Bohr VA.
    Ageing Res Rev; 2005 Nov 15; 4(4):579-602. PubMed ID: 16246641
    [Abstract] [Full Text] [Related]

  • 13. Homologous recombination is elevated in some Werner-like syndromes but not during normal in vitro or in vivo senescence of mammalian cells.
    Cheng RZ, Murano S, Kurz B, Shmookler Reis RJ.
    Mutat Res; 1990 Nov 15; 237(5-6):259-69. PubMed ID: 2079965
    [Abstract] [Full Text] [Related]

  • 14. [Premature aging syndromes : From phenotype to gene].
    Dereure O, Marque M, Guillot B.
    Ann Dermatol Venereol; 2008 Nov 15; 135(6-7):466-78. PubMed ID: 18598796
    [Abstract] [Full Text] [Related]

  • 15. Genetic effects on the longevity of cultured human fibroblasts. III. Correlations with altered glucose-6-phosphate dehydrogenase.
    Holliday R, Thompson KV.
    Gerontology; 1983 Nov 15; 29(2):89-96. PubMed ID: 6840564
    [Abstract] [Full Text] [Related]

  • 16. The premature aging syndromes.
    Pesce K, Rothe MJ.
    Clin Dermatol; 1996 Nov 15; 14(2):161-70. PubMed ID: 9117983
    [No Abstract] [Full Text] [Related]

  • 17. Telomere-based proliferative lifespan barriers in Werner-syndrome fibroblasts involve both p53-dependent and p53-independent mechanisms.
    Davis T, Singhrao SK, Wyllie FS, Haughton MF, Smith PJ, Wiltshire M, Wynford-Thomas D, Jones CJ, Faragher RG, Kipling D.
    J Cell Sci; 2003 Apr 01; 116(Pt 7):1349-57. PubMed ID: 12615976
    [Abstract] [Full Text] [Related]

  • 18. Molecular bases of progeroid syndromes.
    Navarro CL, Cau P, Lévy N.
    Hum Mol Genet; 2006 Oct 15; 15 Spec No 2():R151-61. PubMed ID: 16987878
    [Abstract] [Full Text] [Related]

  • 19. Progeroid syndromes and UV-induced oxidative DNA damage.
    Kamenisch Y, Berneburg M.
    J Investig Dermatol Symp Proc; 2009 Aug 15; 14(1):8-14. PubMed ID: 19675546
    [Abstract] [Full Text] [Related]

  • 20. Werner syndrome: studies in an affected family reveal a cellular phenotype of unaffected siblings.
    Weirich HG, Weirich-Schwaiger H, Kofler H, Sidoroff A, Fritsch P, Schachtschabel DO, Schweiger M, Hirsch-Kauffmann M.
    Mech Ageing Dev; 1996 Jul 05; 88(1-2):1-15. PubMed ID: 8803918
    [Abstract] [Full Text] [Related]

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