Oxidative stress and protein aggregation during biological aging
暂无分享,去创建一个
[1] C. Schöneich,et al. Protein modification during biological aging: selective tyrosine nitration of the SERCA2a isoform of the sarcoplasmic reticulum Ca2+-ATPase in skeletal muscle. , 1999 .
[2] K. Kuczera,et al. The sensitivity of carboxyl-terminal methionines in calmodulin isoforms to oxidation by H(2)O(2) modulates the ability to activate the plasma membrane Ca-ATPase. , 2000, Chemical research in toxicology.
[3] C. Schöneich,et al. Peroxynitrite modification of protein thiols: oxidation, nitrosylation, and S-glutathiolation of functionally important cysteine residue(s) in the sarcoplasmic reticulum Ca-ATPase. , 1999, Biochemistry.
[4] A. Varshavsky,et al. Detecting and measuring cotranslational protein degradation in vivo. , 2000, Science.
[5] E. Stadtman,et al. Methionine residues as endogenous antioxidants in proteins. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[6] D. Ferrington,et al. Selective Degradation of Oxidized Calmodulin by the 20 S Proteasome* , 2001, The Journal of Biological Chemistry.
[7] F. Murad,et al. An activity in rat tissues that modifies nitrotyrosine-containing proteins. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[8] A. Gafni. Structural Modifications of Proteins During Aging , 1997, Journal of the American Geriatrics Society.
[9] Protein oxidation and age-dependent alterations in calcium homeostasis. , 2000 .
[10] B. Friguet,et al. Age-related decline of rat liver multicatalytic proteinase activity and protection from oxidative inactivation by heat-shock protein 90. , 1996, Archives of biochemistry and biophysics.
[11] W. Vogt. Oxidation of methionyl residues in proteins: tools, targets, and reversal. , 1995, Free radical biology & medicine.
[12] C. K. Lee,et al. Gene expression profile of aging and its retardation by caloric restriction. , 1999, Science.
[13] B. Matthews,et al. Structure and mechanism of peptide methionine sulfoxide reductase, an "anti-oxidation" enzyme. , 2000, Biochemistry.
[14] K. Hensley,et al. Nitrone Inhibition of Age‐Associated Oxidative Damage , 2000, Annals of the New York Academy of Sciences.
[15] S. Meydani,et al. Biomarkers as early predictors of long-term health status and human immune function. , 2009, Nutrition reviews.
[16] S. Gottesman,et al. Posttranslational quality control: folding, refolding, and degrading proteins. , 1999, Science.
[17] M. Beal,et al. Oxidative damage in Alzheimer's , 1996, Nature.
[18] J. Stamler,et al. The Skeletal Muscle Calcium Release Channel Coupled O2 Sensor and NO Signaling Functions , 2000, Cell.
[19] C. Schöneich,et al. Diastereoselective reduction of protein‐bound methionine sulfoxide by methionine sulfoxide reductase , 1999, FEBS letters.
[20] S. Kirischuk,et al. Calcium homeostasis in aged neurones. , 1996, Life sciences.
[21] B. Rogina,et al. Extended life-span conferred by cotransporter gene mutations in Drosophila. , 2000, Science.
[22] L. Guarente,et al. Genetic pathways that regulate ageing in model organisms , 2000, Nature.
[23] T. Reinheckel,et al. Degradation of Oxidized Proteins in K562 Human Hematopoietic Cells by Proteasome* , 1996, The Journal of Biological Chemistry.
[24] Steven N. Austad,et al. Why do we age? , 2000, Nature.
[25] T. Squier,et al. Progressive decline in the ability of calmodulin isolated from aged brain to activate the plasma membrane Ca-ATPase. , 1998, Biochemistry.
[26] R. Floyd,et al. Reversal of age-related increase in brain protein oxidation, decrease in enzyme activity, and loss in temporal and spatial memory by chronic administration of the spin-trapping compound N-tert-butyl-alpha-phenylnitrone. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[27] R. S. Sohal,et al. Mitochondrial adenine nucleotide translocase is modified oxidatively during aging. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[28] T. Squier,et al. Oxidatively modified calmodulin binds to the plasma membrane Ca-ATPase in a nonproductive and conformationally disordered complex. , 2001, Biophysical journal.
[29] J. Turrens. Superoxide Production by the Mitochondrial Respiratory Chain , 1997, Bioscience reports.
[30] R. Weindruch,et al. Oxidative Stress, Caloric Restriction, and Aging , 1996, Science.
[31] W. Baumeister,et al. The 26S proteasome: a molecular machine designed for controlled proteolysis. , 1999, Annual review of biochemistry.
[32] N. Holbrook,et al. Oxidants, oxidative stress and the biology of ageing , 2000, Nature.
[33] J. Blass,et al. Inherent Abnormalities in Energy Metabolism in Alzheimer Disease: Interaction with Cerebrovascular Compromise , 2000, Annals of the New York Academy of Sciences.
[34] E. Stadtman,et al. Protein Oxidation in Aging, Disease, and Oxidative Stress* , 1997, The Journal of Biological Chemistry.
[35] W. Ying. Deleterious network hypothesis of aging. , 1997, Medical hypotheses.
[36] H. Yokosawa,et al. Intracellular calcium mobilization regulates the activity of 26 S proteasome during the metaphase-anaphase transition in the ascidian meiotic cell cycle. , 1994, Developmental biology.
[37] A. Goldberg,et al. Ca2+-free Calmodulin and Calmodulin Damaged byin Vitro Aging Are Selectively Degraded by 26 S Proteasomes without Ubiquitination* , 2000, The Journal of Biological Chemistry.