These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

81 related articles for article (PubMed ID: 491660)

  • 21. Insulin receptor synthesis and turnover in differentiating 3T3-L1 preadipocytes.
    Lane MD; Reed BC; Clements PR
    Prog Clin Biol Res; 1981; 66 Pt A():523-42. PubMed ID: 6171829
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Comparison of the phosphorylation events in membranes from proliferating vs. quiescent endothelial cells.
    Kazlauskas A; DiCorleto PE
    J Cell Physiol; 1987 Feb; 130(2):228-44. PubMed ID: 3818801
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Differential effects of transforming growth factor-beta and epidermal growth factor on the cell cycle of cultured rabbit articular chondrocytes.
    Vivien D; Galéra P; Lebrun E; Loyau G; Pujol JP
    J Cell Physiol; 1990 Jun; 143(3):534-45. PubMed ID: 2358472
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Inhibition of DNA synthesis and cell division by a cell surface sialoglycopeptide.
    Fattaey H; Johnson TC; Chou HH
    J Cell Physiol; 1989 May; 139(2):269-74. PubMed ID: 2715187
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Potassium transport in normal and transformed mouse 3T3 cells.
    Spaggiare S; Wallach MJ; Tupper JT
    J Cell Physiol; 1976 Nov; 89(3):403-16. PubMed ID: 977660
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A high level of cell surface phosphatidylinositol-specific phospholipase C activity is characteristic of growth-arrested 3T3 fibroblasts but not of transformed variants.
    Volwerk JJ; Birrell GB; Hedberg KK; Griffith OH
    J Cell Physiol; 1992 Jun; 151(3):613-22. PubMed ID: 1338336
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Resumption of cell cycle in BALB/c-3T3 fibroblasts arrested by polyamine depletion: relation with "competence" gene expression.
    Charollais RH; Mester J
    J Cell Physiol; 1988 Dec; 137(3):559-64. PubMed ID: 3142887
    [TBL] [Abstract][Full Text] [Related]  

  • 28. CDGF (chicken embryo fibroblast-derived growth factor) is mitogenically related to TGF-beta and modulates PDGF, bFGF, and IGF-I action on sparse NIH/3T3 cells.
    Geistlich A; Gehring H
    Exp Cell Res; 1993 Feb; 204(2):329-35. PubMed ID: 8440329
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mode of estrogen action on cell proliferation in CAMA-1 cells: II. Sensitivity of G1 phase population.
    Leung BS; Potter AH
    J Cell Biochem; 1987 Jul; 34(3):213-25. PubMed ID: 3611201
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Density-dependent inhibition of mouse embryo fibroblast growth: involvement of IGFBP-3.
    Blat C; Villaudy J; Harel L
    Exp Cell Res; 1994 Nov; 215(1):114-8. PubMed ID: 7525322
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Arrest of 3T3 cells in G1 phase in suspension culture.
    Otsuka H; Moskowitz M
    J Cell Physiol; 1975 Dec; 87(2):213-9. PubMed ID: 1214003
    [TBL] [Abstract][Full Text] [Related]  

  • 32. EGF induces cell cycle arrest of A431 human epidermoid carcinoma cells.
    MacLeod CL; Luk A; Castagnola J; Cronin M; Mendelsohn J
    J Cell Physiol; 1986 Apr; 127(1):175-82. PubMed ID: 3007537
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Inhibition of serum and transforming growth factor beta (TGF-beta1)-induced DNA synthesis in confluent airway smooth muscle by heparin.
    Okona-Mensah KB; Shittu E; Page C; Costello J; Kilfeather SA
    Br J Pharmacol; 1998 Oct; 125(4):599-606. PubMed ID: 9831891
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Permeable FGF-1 nuclear localization signal peptide stimulates DNA synthesis in various cell types but is cell-density sensitive and unable to support cell proliferation.
    Komi A; Suzuki M; Imamura T
    Exp Cell Res; 1998 Sep; 243(2):408-14. PubMed ID: 9743600
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Growth hormone attenuation of epidermal growth factor-induced mitogenesis.
    Wiepz GJ; Houtman JC; Cha D; Bertics PJ
    J Cell Physiol; 1997 Oct; 173(1):44-53. PubMed ID: 9326448
    [TBL] [Abstract][Full Text] [Related]  

  • 36. ADP-ribosylation of the rhoA gene product by botulinum C3 exoenzyme causes Swiss 3T3 cells to accumulate in the G1 phase of the cell cycle.
    Yamamoto M; Marui N; Sakai T; Morii N; Kozaki S; Ikai K; Imamura S; Narumiya S
    Oncogene; 1993 Jun; 8(6):1449-55. PubMed ID: 8502473
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Growth inhibition of BALB/c mouse keratinocytes by TGF-beta 1 and CeReS-18 appears to act through distinct mechanisms.
    Betz NA; Fattaey HK; Johnson TC
    Exp Cell Res; 1996 Aug; 227(1):47-54. PubMed ID: 8806450
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Subcellular distribution of the p53 protein during the cell cycle of Balb/c 3T3 cells.
    Shaulsky G; Ben-Ze'ev A; Rotter V
    Oncogene; 1990 Nov; 5(11):1707-11. PubMed ID: 2267137
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Inhibition of cell growth: effects of the tyrosine kinase inhibitor CGP 53716.
    Major TC; Keiser JA
    J Pharmacol Exp Ther; 1997 Oct; 283(1):402-10. PubMed ID: 9336349
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Subcellular structures involved in internalization and degradation of epidermal growth factor.
    Fine RE; Goldenberg R; Sorrentino J; Herschman HR
    J Supramol Struct Cell Biochem; 1981; 15(3):235-51. PubMed ID: 6267315
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.