Molecular Basis of the Accumulation of Abnormal Proteins in Progeria and Aging Fibroblasts
- 1 January 1985
- book chapter
- Published by Springer Nature
- Vol. 35, 427-442
- https://doi.org/10.1007/978-1-4899-2218-2_27
Abstract
No abstract availableKeywords
This publication has 48 references indexed in Scilit:
- Molecular clocks, molecular profiles, and optimum diets: Three approaches to the problem of agingPublished by Elsevier ,2003
- Changes in NAD levels in human lymphocytes and fibroblasts during aging and in premature aging syndromesMechanisms of Ageing and Development, 1983
- Increased lability of triosephosphate isomerase in progeria and Werner's syndrome fibroblastsMechanisms of Ageing and Development, 1982
- Molecular basis for the accumulation of acidic isozymes of triosephosphate isomerase on agingMechanisms of Ageing and Development, 1981
- Effects of age on energy status and redox state of lympocytes during blastogenesisBiochemical and Biophysical Research Communications, 1981
- Lysosomal and mitochondrial heat labile enzymes in Werner's syndrome fibroblastsExperimental Gerontology, 1980
- Fidelity of protein synthesis does not decline during aging of cultured human fibroblastsJournal of Cellular Physiology, 1980
- PROTEOLYTIC SUSCEPTIBILITY AND METHIONINE MODIFICATION OF MONODEAMIDATED RIBONUCLEASE AInternational Journal of Peptide and Protein Research, 1978
- Evidence contrary to the protein error hypothesis for in vitro senescenceJournal of Cellular Physiology, 1976
- Primary structure of two COOH-terminal hexapeptides from rabbit muscle aldolase: A difference in the structure of the α and β subunitsBiochemical and Biophysical Research Communications, 1970