Fibronectin synthesis and degradation in human fibroblasts with aging

[1]  Z. Medvedev.  Age changes of chromatin. A review , 1984, Mechanisms of Ageing and Development.

[2]  M A Levitt,et al.  The effect of the extracellular matrix on the detachment of human endothelial cells , 1984, Journal of cellular physiology.

[3]  A. J. Millis,et al.  Fibronectin distribution on the surfaces of young and old human fibroblasts , 1984, Mechanisms of Ageing and Development.

[4]  U. Langenbeck,et al.  Intracellular levels and metabolism of leucine and alpha-ketoisocaproate in normal and maple syrup urine disease fibroblasts. , 1984, Biochemical medicine.

[5]  S. Goto,et al.  Codon recognition fidelity of ribosomes at the first and second positions does not decrease during aging , 1983, Mechanisms of Ageing and Development.

[6]  A. Bittles,et al.  The effects of in vitro ageing on the composition of the intracellular free amino acid pool of human diploid fibroblasts , 1982, Mechanisms of Ageing and Development.

[7]  R. O. Kelley,et al.  Loss of organized fibronectin matrix from the surface of aging diploid fibroblasts (IMR-90) , 1981, Mechanisms of Ageing and Development.

[8]  S. Aizawa,et al.  Cell surface changes accompanying aging in human diploid fibroblasts. V. Role of large major cell surface protein and surface negative charge in aging- and transformation-associated changes in concanavalin A-mediated red blood cell adsorption. , 1980, Experimental cell research.

[9]  S. Goldstein,et al.  Fidelity of protein synthesis does not decline during aging of cultured human fibroblasts , 1980, Journal of cellular physiology.

[10]  A. J. Millis,et al.  Fibronectin from aged fibroblasts is defective in promoting cellular adhesion , 1980, Journal of cellular physiology.

[11]  H. Crissman,et al.  Development of the aging cell surface. Reduction of gap junction-mediated metabolic cooperation with progressive subcultivation of human embryo fibroblasts (IMR-90). , 1979, Experimental cell research.

[12]  B. Hoskins,et al.  Spreading behavior and surface characteristics of young and senescent WI38 fibroblasts revealed by scanning electron microscopy. , 1979, Experimental cell research.

[13]  Kenneth M. Yamada,et al.  Mechanism of the decrease in the major cell surface protein of chick embryo fibroblasts after transformation , 1977, Cell.

[14]  I. Pastan,et al.  Microfilament bundles and cell shape are related to adhesiveness to substratum and are dissociable from growth control in cultured fibroblasts , 1977, Cell.

[15]  E. Schneider,et al.  Relationship between cell replication and volume in senescent human diploid fibroblasts , 1976, Mechanisms of Ageing and Development.

[16]  E. Schneider,et al.  The relationship between in vitro cellular aging and in vivo human age. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[17]  I. Pastan,et al.  Cell surface protein partially restores morphology, adhesiveness, and contact inhibition of movement to transformed fibroblasts. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[18]  Y. Courtois,et al.  Surface labelling of senescent chick fibroblasts by lactoperoxidase-catalysed iodination. , 1976, Gerontology.

[19]  P. Good.  Aging in mammalian cell populations: A review , 1975, Mechanisms of Ageing and Development.

[20]  P. Bowman,et al.  Aging of human fibroblasts in vitro: Surface features and behavior of aging WI 38 cells , 1975, Mechanisms of Ageing and Development.

[21]  J. Bye,et al.  Density and cell cycle dependence of cell surface proteins in hamster fibroblasts. , 1974, Cell.

[22]  W. D. Barnes,et al.  Genealogies of clones of diploid fibroblasts. Cinemicrophotographic observations of cell division patterns in relation to population age. , 1974, Experimental cell research.

[23]  L. Hayflick,et al.  The serial cultivation of human diploid cell strains. , 1961, Experimental cell research.

[24]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.