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3. 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]
4. Contact-inhibited revertant cell lines isolated from SV40-transformed cells. I. Biologic, virologic, and chemical properties. Culp LA; Grimes WJ; Black PH J Cell Biol; 1971 Sep; 50(3):682-90. PubMed ID: 4329153 [TBL] [Abstract][Full Text] [Related]
5. Regulation of adenosine 3',5'-cyclic monophosphate phosphodiesterase activity in fibroblasts by intracellular concentrations of cyclic adenosine monophosphate (3T3-dibutyryl cyclic AMP-SV40-transformed cells-michaelis constants-L cells-prostaglandin E 1 ). D'Armiento M; Johnson GS; Pastan I Proc Natl Acad Sci U S A; 1972 Feb; 69(2):459-62. PubMed ID: 4333987 [TBL] [Abstract][Full Text] [Related]
7. Effect of dithiothreitol on plasma membrane intramembranous particle topography in BALB/c 3T3 and simian virus-transformed 3T3 cells and plasma membrane vesicles. Scott RE; Maercklein PB J Natl Cancer Inst; 1980 Aug; 65(2):415-9. PubMed ID: 6249950 [TBL] [Abstract][Full Text] [Related]
8. Protein turnover and proliferation. Failure of SV-3T3 cells to increase lysosomal proteinases, increase protein degradation and cease net protein accumulation. Lockwood TD; Minassian IA Biochem J; 1982 Aug; 206(2):251-8. PubMed ID: 6293461 [TBL] [Abstract][Full Text] [Related]
9. Hyaluronate-binding protein of simian virus 40-transformed 3T3 cells: membrane distribution and reconstitution into lipid vesicles. Chi-Rosso G; Toole BP J Cell Biochem; 1987 Mar; 33(3):173-83. PubMed ID: 2437135 [TBL] [Abstract][Full Text] [Related]
10. Effect of plasma membranes on solute transport in 3T3 cells. Lieberman MA; Raben DM; Whittenberger B; Glaser L J Biol Chem; 1979 Jul; 254(14):6357-61. PubMed ID: 221497 [TBL] [Abstract][Full Text] [Related]
12. An altered rate of uridine transport in membrane vesicles isolated from growing and quiescent mouse 3T3 fibroblast cells. Quinlan DC; Hochstadt J Proc Natl Acad Sci U S A; 1974 Dec; 71(12):5000-3. PubMed ID: 4531032 [TBL] [Abstract][Full Text] [Related]
13. Differences in membrane fluidity and structure in contact-inhibited and transformed cells. Barnett RE; Furcht LT; Scott RE Proc Natl Acad Sci U S A; 1974 May; 71(5):1992-4. PubMed ID: 4365580 [TBL] [Abstract][Full Text] [Related]
14. A simplified procedure for isolating plasma membranes from cultured mouse fibroblast cells: 3T3 and SV-3T3. Harshman S; Conlin JG Anal Biochem; 1978 Oct; 90(1):98-106. PubMed ID: 215053 [No Abstract] [Full Text] [Related]
15. Cell-cell contact and growth regulation of pinocytosis in 3T3 cells. Davies PF J Supramol Struct; 1980; 13(2):211-7. PubMed ID: 6264231 [TBL] [Abstract][Full Text] [Related]
16. Dependence of intracellular alkali-ion concentrations of 3T3 and SV 40-3T3 cells on growth density. Ernst M; Adam G Cytobiologie; 1979 Feb; 18(3):450-9. PubMed ID: 218856 [TBL] [Abstract][Full Text] [Related]
17. Cell contact-dependent increase in membrane D-galactopyranosyl-like residues on normal, but not virus- or spontaneously-transformed, murine fibroblasts. Nicolson GL; Lacorbiere M Proc Natl Acad Sci U S A; 1973 Jun; 70(6):1672-6. PubMed ID: 4352648 [TBL] [Abstract][Full Text] [Related]
18. Age-dependent decrease of growth responsiveness in density inhibited 3T3 cell populations and their interactions with SV 40-3T3 cells. van der Bosch J J Cell Physiol; 1980 Aug; 104(2):127-36. PubMed ID: 7410486 [TBL] [Abstract][Full Text] [Related]