BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

243 related articles for article (PubMed ID: 19011155)

  • 21. Differential regulation of PAI-1 gene expression in human fibroblasts predisposed to a fibrotic phenotype.
    Higgins PJ; Slack JK; Diegelmann RF; Staiano-Coico L
    Exp Cell Res; 1999 May; 248(2):634-42. PubMed ID: 10222156
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A comparative analysis of the proteins between the fibroblasts from Werner's syndrome patients and age-matched normal individuals using two-dimensional gel electrophoresis.
    Toda T; Satoh M; Sugimoto M; Goto M; Furuichi Y; Kimura N
    Mech Ageing Dev; 1998 Jan; 100(2):133-43. PubMed ID: 9541134
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The Werner's syndrome 4330T>C (Cys1367Arg) gene variant does not affect the in vitro cytotoxicity of topoisomerase inhibitors and platinum compounds.
    Innocenti F; Mirkov S; Nagasubramanian R; Ramírez J; Liu W; Bleibel WK; Shukla SJ; Hennessy K; Rosner GL; Cook E; Eileen Dolan M; Ratain MJ
    Cancer Chemother Pharmacol; 2009 Apr; 63(5):881-7. PubMed ID: 18677484
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Downregulated expression of the signaling molecules Nck, c-Crk, Grb2/Ash, PI 3-kinase p110 alpha and WRN during fibroblast aging in vitro.
    Matuoka K; Takenawa T
    Biochim Biophys Acta; 1998 Feb; 1401(2):211-5. PubMed ID: 9531977
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Bone and calcium metabolism in Werner's syndrome.
    Shiraki M; Aoki C; Goto M
    Endocr J; 1998 Aug; 45(4):505-12. PubMed ID: 9881900
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The expression of proliferation-dependent antigens during the lifespan of normal and progeroid human fibroblasts in culture.
    Kill IR; Faragher RG; Lawrence K; Shall S
    J Cell Sci; 1994 Feb; 107 ( Pt 2)():571-9. PubMed ID: 7911472
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cycling Werner's syndrome fibroblasts display calcium-dependent potassium currents.
    Faragher RG; Hardy SP; Davis T; Dropcova S; Allen MC
    Exp Cell Res; 1997 Feb; 231(1):119-22. PubMed ID: 9056418
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Identification and biochemical characterization of a Werner's syndrome protein complex with Ku70/80 and poly(ADP-ribose) polymerase-1.
    Li B; Navarro S; Kasahara N; Comai L
    J Biol Chem; 2004 Apr; 279(14):13659-67. PubMed ID: 14734561
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism.
    Salk D; Au K; Hoehn H; Martin GM
    Cytogenet Cell Genet; 1981; 30(2):92-107. PubMed ID: 7273860
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mitogen-mediated protein phosphorylation in Werner's syndrome fibroblasts.
    Hirai M; Amagai M; Tajima S; Nishikawa T; Shimizu N
    Cell Struct Funct; 1988 Dec; 13(6):471-80. PubMed ID: 2468420
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Accelerated aging and nucleolar fragmentation in yeast sgs1 mutants.
    Sinclair DA; Mills K; Guarente L
    Science; 1997 Aug; 277(5330):1313-6. PubMed ID: 9271578
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Premature aging and predisposition to cancers caused by mutations in RecQ family helicases.
    Furuichi Y
    Ann N Y Acad Sci; 2001 Apr; 928():121-31. PubMed ID: 11795503
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Analysis of Werner's expression within the brain and primary neuronal culture.
    Gee J; Ding Q; Keller JN
    Brain Res; 2002 Jun; 940(1-2):44-8. PubMed ID: 12020873
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Regional differences in insulin receptor function in Werner's syndrome.
    Yamasaki H; Akazawa S; Okuno S; Ikari N; Yamaguchi Y; Chikuba N; Yamamoto H; Maeda Y; Tahara D; Nagataki S
    Diabetes Res Clin Pract; 1992 Feb; 15(2):105-11. PubMed ID: 1563326
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular analysis of insulin receptor gene in Werner's syndrome.
    Uotani S; Yamaguchi Y; Yokota A; Yamasaki H; Takino H; Chikuba N; Goto Y; Fujishima N; Yano M; Matsumoto K
    Diabetes Res Clin Pract; 1994 Dec; 26(3):171-6. PubMed ID: 7736897
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Werner's syndrome: a review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrations.
    Salk D
    Hum Genet; 1982; 62(1):1-5. PubMed ID: 6759366
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Down-regulation of the defective transcripts of the Werner's syndrome gene in the cells of patients.
    Yamabe Y; Sugimoto M; Satoh M; Suzuki N; Sugawara M; Goto M; Furuichi Y
    Biochem Biophys Res Commun; 1997 Jul; 236(1):151-4. PubMed ID: 9223443
    [TBL] [Abstract][Full Text] [Related]  

  • 39. From old organisms to new molecules: integrative biology and therapeutic targets in accelerated human ageing.
    Cox LS; Faragher RG
    Cell Mol Life Sci; 2007 Oct; 64(19-20):2620-41. PubMed ID: 17660942
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Ageing: Heterochromatin disorganization associated with premature ageing.
    Jones B
    Nat Rev Genet; 2015 Jun; 16(6):318. PubMed ID: 25982170
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.