SIRT1 Functionally Interacts with the Metabolic Regulator and Transcriptional Coactivator PGC-1α

Oxidants, oxidative stress and the biology of ageing

Finkel, T., & Holbrook, N. J. (2000) · Nature · doi:10.1038/35041687 · Cited by 9,413

Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1

Wu, Z., Puigserver, P., Andersson, U., Zhang, C., Adelmant, G., Mootha, V., Troy, A., Cinti, S., Lowell, B., Scarpulla, R. C., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)80611-x · Cited by 4,139

Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase

Imai, S.-I., Armstrong, C. M., Kaeberlein, M., & Guarente, L. (2000) · Nature · doi:10.1038/35001622 · Cited by 3,510

Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase

Brunet, A., Sweeney, L. B., Sturgill, J. F., Chua, K. F., Greer, P. L., Lin, Y., Tran, H., Ross, S. E., Mostoslavsky, R., Cohen, H. Y., et al. (2004) · Science · doi:10.1126/science.1094637 · Cited by 3,239

Modulation of NF‐κB‐dependent transcription and cell survival by the SIRT1 deacetylase

Yeung, F., Hoberg, J. E., Ramsey, C. S., Keller, M. D., Jones, D. R., Frye, R. A., & Mayo, M. W. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600244 · Cited by 2,750

hSIR2SIRT1 Functions as an NAD-Dependent p53 Deacetylase

Vaziri, H., Dessain, S. K., Eaton, E. N., Imai, S., Frye, R. A., Pandita, T. K., Guarente, L., & Weinberg, R. A. (2001) · Cell · doi:10.1016/s0092-8674(01)00527-x · Cited by 2,690

The SIR2/3/4 complex and SIR2 alone promote longevity in Saccharomyces cerevisiae by two different mechanisms

Kaeberlein, M., McVey, M., & Guarente, L. (1999) · Genes & Development · doi:10.1101/gad.13.19.2570 · Cited by 2,253

Negative Control of p53 by Sir2α Promotes Cell Survival under Stress

Luo, J., Nikolaev, A. Y., Imai, S.-I., Chen, D., Su, F., Shiloh, A., Guarente, L., & Gu, W. (2001) · Cell · doi:10.1016/s0092-8674(01)00524-4 · Cited by 2,081

Peroxisome Proliferator-Activated Receptor-γ Coactivator 1α (PGC-1α): Transcriptional Coactivator and Metabolic Regulator

Puigserver, P., & Spiegelman, B. M. (2003) · Endocrine Reviews · doi:10.1210/er.2002-0012 · Cited by 2,076

Calorie restriction promotes mammalian cell survival by inducing the SIRT1 deacetylase

Cohen, H. Y., Miller, C., Bitterman, K. J., Wall, N. R., Hekking, B., Kessler, B., Howitz, K. T., Gorospe, M., de Cabo, R., & Sinclair, D. A. (2004) · Science · doi:10.1126/science.1099196 · Cited by 1,924

SIRT1 AS A KEY CELL REGULATOR OF METABOLISM AND OXIDATIVE STRESS

Voznesenskaya, T. Y., Stupchuk, M. S., Kaleinikova, O. N., & Блашків, Т. В. (2018) · Bulletin of Problems Biology and Medicine · doi:10.29254/2077-4214-2018-1-1-142-20-25 · Cited by 3

Reversal of metabolic shift in post-infarct-remodelled hearts: possible novel therapeutic approach

Tanno, M., & Kuno, A. (2012) · Cardiovascular Research · doi:10.1093/cvr/cvs364 · Cited by 3

Decoding NAD+ Metabolism in COVID-19: Implications for Immune Modulation and Therapy

Song, S., Gan, J., Long, Q., Gao, Z., & Zheng, Y. (2024) · Vaccines · doi:10.3390/vaccines13010001 · Cited by 2

Deacetylation of SOD3 by sirtuins restores furin cleavage

Mitchem, E. C., Harris, P. S., Michel, C. R., McGinnis, C. D., Ray, S., Mallela, K. M. G., Roede, J. R., Petersen, S. V., Nozik‐Grayck, E., & Fritz, K. S. (2025) · Redox Biochemistry and Chemistry · doi:10.1016/j.rbc.2025.100062 · Cited by 2

Lactobacillus johnsonii JNU3402 Ameliorates Age‐Related Liver Dysfunction Through Stimulating PGC ‐1α‐Mediated SIRT1 Expression

Hong, E., Yang, G., Oh, S., & Kim, E. (2025) · BioFactors · doi:10.1002/biof.70069 · Cited by 2

Stimulatory Effects of (+)-Epicatechin on Mitochondrial Biogenesis and Function in Skeletal Muscle of Aged Rats: Underlying Mechanisms

Ramírez‐Sánchez, I., Ordóñez‐Razo, R. M., Najera, V., Ceballos, G. M., & Villarreal, F. J. (2026) · Journal of Medicinal Food · doi:10.1177/1096620x261421080 · Cited by 2

Dapagliflozin Protects Cardiomyocytes against Doxorubicin-Induced Toxicity by Modulating Sirtuin 1/Sirtuin 3 and Ferroptosis Pathway

Khine, H. E. E., Mangmool, S., & Parichatikanond, W. (2026) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.5c00760 · Cited by 2

Modulation of Tumorigenesis by Dietary Intervention Is Not Mediated by SIRT1 Catalytic Activity

Clark-Knowles, K. V., Dewar‐Darch, D., Jardine, K. E., & McBurney, M. W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0112406 · Cited by 2

Exploring the signal-dependent transcriptional regulation involved in the liver pathology of type 2 diabetes

Sakai, M. (2022) · Diabetology International · doi:10.1007/s13340-022-00610-0 · Cited by 2

Maladaptive response following glucose overload in GLUT4 ‐overexpressing H9C2 cardiomyoblasts

Stratmann, B., Eggers, B., Mattern, Y., de Carvalho, T. S., Marcus, K., & Tschoepe, D. (2024) · Diabetes Obesity and Metabolism · doi:10.1111/dom.15553 · Cited by 2

Mechanisms of SIRT1/SIRT3-mediated reduction of mitochondrial regeneration and inflammatory response in diabetic cerebral ischemia-reperfusion injury

Xin, C., Liu, O., Sun, M., Han, P., Li, X., Niu, Q., Ma, N., Yang, X. C., Hei, C., & Liu, P. (2025) · Metabolic Brain Disease · doi:10.1007/s11011-025-01662-2 · Cited by 2

SRT1720 ameliorates LPS-induced depressive-like behaviors in mice and activates Parkin-mediated mitophagy

Sun, L., Li, C., Shi, J., Zeng, W., Wu, L., Wan, S., & Wang, Y. (2025) · BMC Neuroscience · doi:10.1186/s12868-025-00968-2 · Cited by 2

Sirtuin-Dependent Metabolic Control and Its Role in the Aging Process

Calvo, S. S.-C., Navas, P., & López‐Lluch, G. (2012) · InTech eBooks · doi:10.5772/35702 · Cited by 2

Photobiomodulation on Bax and Bcl-2 Proteins and SIRT1/PGC-1αAxis mRNA Expression Levels of Aging Rat Skeletal Muscle

Li, F., Liu, Y.-Y., Qin, F., Luo, Q., Yang, H., Zhang, Q.-G., & Liu, T. C. (2014) · International Journal of Photoenergy · doi:10.1155/2014/384816 · Cited by 2

Anti-obesity Effects of Ethanolic Extract of Polygonatum sibiricum Rhizome in High-fat Diet-fed Mice

Ko, J.-H., Jeon, W.-J., Kwon, H.-S., Yeon, S.-W., & Kang, J. (2015) · Korean Journal of Food Science and Technology · doi:10.9721/kjfst.2015.47.4.499 · Cited by 2

Activity of Panax ginseng C.A. Meyer on Energy Production in Mammals

Pannacci, M., Lucini, V., Dugnani, S., Ciracì, R., Zangara, A., & Scaglione, F. (2016) · Biochemistry & Pharmacology Open Access · doi:10.4172/2167-0501.1000221 · Cited by 2

Sirtuins and Aging

Dong, Y., & Zou, S. (2009) · Springer eBooks · doi:10.1007/978-1-4419-0639-7_5 · Cited by 2

Sirtuins as Metabolic Modulators of Muscle Plasticity

Menzies, K. J., Zaldivar‐Jolissaint, J. F., & Auwerx, J. H. (2016) · Springer eBooks · doi:10.1007/978-94-024-0962-8_9 · Cited by 2

The bifunctional roles of sirtuins and their therapeutic potential in cancer

Lee, Y. T., Tan, Y. J., Mok, P. Y., Subramaniam, A. V., & Oon, C. E. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822467-0.00009-7 · Cited by 2

Sirtuins in the biology of aging

Wątroba, M., & Szukiewicz, D. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-814118-2.00002-1 · Cited by 3

Beneficial Effects of Resveratrol on Neurological Disorders

Farooqui, A. A. (2012) · Springer eBooks · doi:10.1007/978-1-4614-3804-5_7 · Cited by 2

Correction: Effects of Resveratrol and SIRT1 on PGC-1α Activity and Mitochondrial Biogenesis: A Reevaluation

Higashida, K., Kim, S. H., Jung, S. R., Asaka, M., Holloszy, J. O., & Han, D. (2014) · PLoS Biology · doi:10.1371/annotation/900c9397-eeb9-4d4e-9a05-ff18d657be79 · Cited by 2

Prospect of Mitochondria-Targeted Antioxidants as a Hepatoprotective and Anti-Alcoholic Liver Disease AgentPreprint

Abugri, J., & Adu‐Frimpong, M. (2021) · Preprints.org · doi:10.20944/preprints202103.0143.v1 · Cited by 2

Mitochondrial Function and Dysfunction in White Adipocytes and Therapeutic Implications

Wang, F., Huynh, P. M., & An, Y. (2024) · Comprehensive physiology · doi:10.1002/cphy.c230009 · Cited by 10

Developmental Programming of Nonalcoholic Fatty Liver Disease (NAFLD)

Bruce, K. D., & Cagampang, F. R. A. (2016) · Springer eBooks · doi:10.1007/978-1-4939-6386-7_12 · Cited by 1

Optical Redox Imaging of Breast Cancer NADH Redox Status Associated with PGC1α Gene Expression

Lin, Z., Wen, Y., Xu, H. N., Zhang, L., Zeng, C., Lin, T. R., Floros, J., Mach, R. H., & Li, L. Z. (2025) · Academic Radiology · doi:10.1016/j.acra.2025.11.014 · Cited by 1

Circulating eNAMPT in Glaucoma: A Semi-Quantitative Plasma Analysis Before and After Nicotinamide Supplementation

Vallbona-Garcia, A., Gustavsson, S. T., Gorgels, T. G. M. F., Tribble, J. R., Webers, C. A. B., Smeets, H. J. M., Jóhannesson, G., Williams, P. A., & Benedikter, B. J. (2026) · Translational Vision Science & Technology · doi:10.1167/tvst.15.1.37 · Cited by 2

Targeting the SARM1-NAD⁺ axis: A review of new strategy for reversing the imbalance of energy and mitochondrial homeostasis in metabolic diseases

Xiong, A., Lv, W., Shao, X., Lv, Y., & Zhang, Y. (2026) · Pharmacological Research · doi:10.1016/j.phrs.2026.108128 · Cited by 1

Fangchinoline alleviates hypertensive heart failure via PGC‐1α/STAT6/PPARγ activation of mitophagy against ferroptosis

Liu, C., Wang, Z., Zhang, L., Yang, D., Zhang, Z., Cui, X., Eid, A. H., & Wang, M. (2026) · British Journal of Pharmacology · doi:10.1111/bph.70552 · Cited by 1

Targeting Sirtuin Signaling in Parkinson’s Disease and Neurodegeneration: Molecular Insights and Translational Potential

Kumari, S., Singh, H., Kamiya, A., & Taliyan, R. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-06062-w · Cited by 2

CPT2 as a Convergent Node Linking Age-Associated Neuronal H3K27me3 Remodeling to Nicotinamide Mononucleotide (NMN)-Induced Expression Rescue in Metabolic Tissues

Cheung, N. (2026) · Cureus · doi:10.7759/cureus.112906 · Cited by 1

Sirt1 inhibits the recruitment of RNA polymerase II to metabolic gene promoter during pressure overload through competition with the preinitiation complex on Sub1

Oka, S., Mourad, Y., Veera, S., Zhai, P., Alcendor, R. R., Guo, Y., Ades, J., Kashyap, S., Xu, X., Hu, C., et al. (2026) · Cardiovascular Research · doi:10.1093/cvr/cvag178 · Cited by 1

Cellular and Molecular Mechanisms of Resveratrol and Its Derivatives

Stuart, J. A., & Robb, E. L. (2013) · Springer eBooks · doi:10.1007/978-1-4614-6968-1_3 · Cited by 1

Molecular Mechanisms of Cardiovascular Aging

Meiliana, A., & Wijaya, A. (2013) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v5i3.64 · Cited by 1

Signaling pathway cross talk in Alzheimer's

Godoy, J. A., Ríos, J. A., Zolezzi, J. M., Braidy, N., & Inestrosa, N. C. (2014) · Cited by 1

REVIEW ARTICLE Mechanisms of neurodegeneration in Huntington's disease

Gil‐Mohapel, J., & Rego, A. C. (2008) · Cited by 1

THE ROLE OF PXR AND IKKβ SIGNALING IN CARDIOMETABOLIC DISEASE

Helsley, R. N. (2016) · UKnowledge (University of Kentucky) · doi:10.13023/etd.2016.040 · Cited by 1

The influence of rs2273773 and rs7895833 SIRT1 gene polymorphisms on life expectancy in context of metabolic factors in Silesian population

Grzeszczak, W., Woźny, Ł., Stefanowicz, M., & Danikiewicz, M. (2017) · Annales Academiae Medicae Silesiensis · doi:10.18794/aams/64164 · Cited by 1

Metabolic Flexibility and Mitochondrial Bioenergetics in the Failing Heart. Therapeutic Approaches

Rosca, M. G. (2021) · Romanian Journal of Cardiology · doi:10.47803/rjc.2021.31.2.269 · Cited by 1

Phosphodiesterase-1 inhibitor modulates Ca2+ regulation in sirtuin 1-deficient mouse cardiomyocytes

Yang, H., Lin, C.-Y., Lin, F., Yu, P., Huang, S., Chen, Y., Tsai, C., & Yang, H.-Y. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.174498 · Cited by 1

miR181a/b-1 controls osteocyte metabolism and mechanical properties independently of bone morphology

Yoon, J., Kaya, S., Matsumae, G., Dole, N. S., & Alliston, T. N. (2023) · Bone · doi:10.1016/j.bone.2023.116836 · Cited by 2

Signaling Cascades in Heart Failure: From Cardiomyocytes Growth and Survival to Mitochondrial Signaling Pathways

Marı́n-Garcı́a, J. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-147-9_7 · Cited by 1

Computational model of circadian oscillator in mammals: Interaction with NAD+/SIRT1 system and age-related changes in the expression of circadian oscillator genes

Podkolodnyy, N. L., Tverdokhleb, N. N., & Podkolodnaya, O. A. (2017) · Russian Journal of Genetics Applied Research · doi:10.1134/s2079059717050161 · Cited by 1

Sir2D, a Sirtuin family protein, regulates adenylate cyclase A expression through interaction with the MybB transcription factor early in Dictyostelium development upon starvation

Taniura, H., Soeda, S., Ohta, T., Oki, M., & Tsuboi, R. (2019) · Heliyon · doi:10.1016/j.heliyon.2019.e01301 · Cited by 1

Epigenetic Dysregulation in Aging and Cancer

Komninou, D., & Richie, J. P. (2009) · Epigenetics and human health · doi:10.1002/9783527628384.ch17 · Cited by 1

Models of acetylation and the regulation of longevity: From yeast to humans

Finkel, M., & Cohen, H. Y. (2005) · Drug Discovery Today Disease Models · doi:10.1016/j.ddmod.2005.11.003 · Cited by 1

NRF2 AS A NUTRIENT SENSITIVE TRANSCRIPTION FACTOR

Kulkarni, S. R. (2012) · Digital Commons - URI (University of Rhode Island) · doi:10.23860/diss-kulkarni-supriya-2012 · Cited by 1

Sirtuin Function in Longevity

Smith, D. L., & Smith, J. S. (2009) · Springer eBooks · doi:10.1007/978-90-481-3465-6_6 · Cited by 1

The role of resveratrol treatment and regular physical activity on sirtuins in brain of rats artificially selected for intrinsic aerobic running capacity

Szűcs, L. (2015) · REAL-PhD (Hungarian Academy of Sciences) · doi:10.17624/tf.2015.03 · Cited by 1

Functional analysis of hepatic FOXO3 signalling in glucose and lipid metabolism

Gul, S. (2014) · OPen Access Repositorium der Universität Ulm (OPARU) (Ulm University) · doi:10.18725/oparu-3289 · Cited by 1

Pharmacological and fasting-induced activation of SIRT1/LXRα signaling alleviates diabetes-induced retinopathyPreprint

Hammer, S. S., Vieira, C. P., McFarland, D., Sandler, M., Levitsky, Y., Dorweiler, T. F., Lydic, T. A., Asare‐Bediako, B., Adu-Agyeiwaah, Y., Sielski, M. S., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/871822 · Cited by 1

Midbrain on Fire: mtDNA Ignites Neuroinflammation in PRKN‐P

Narendra, D. P., & Thayer, J. A. (2022) · Movement Disorders · doi:10.1002/mds.29073 · Cited by 1

Modulation of exercise-induced gene expression in human skeletal muscle by exercise intensity, training status and short- term endurance training

Egan, B. (2008) · Dublin City University Open Access Institutional Repository (Dublin City University)

Metabolic and Antioxidant Adaptation to Exercise: Role of Redox Signaling

Ji, L. L. (2015) · Healthy ageing and longevity · doi:10.1007/978-3-319-14830-4_6

The Cross-Talk Between Mitochondria and the Nucleus in the Response to Oxidative Stress Associated with Mitochondrial Dysfunction in Mitochondrial Encephalomyopathies

Wu, Y., Lee, W., Wu, S., & Wei, Y. (2011) · InTech eBooks · doi:10.5772/19713

Functional characterization of roles of histone deacetylases in the regulation of DNA damage response

Yuan, Z. (2007) · Digital Commons - University of South Florida (University of South Florida)

A Potential Tumor Suppressive Role of SIRT1 in Cancer

Kabra, N. (2010) · Digital Commons - University of South Florida (University of South Florida)

Factors affecting growth, differentiation and apoptosis of osteoblastic and osteosarcoma cells

Li, Y. (2008) · Figshare

Queen Honeybee and Me: Forever Young? Conserved Pathways for Longevity

Knäblein, J., & Huber, R. (2013) · Wiley eBooks · doi:10.1002/9783527669417.ch26

Chapter 12 Regulation of PGC-1 in humans with insulin resistance and type 2 diabetes: Functional implications

Pihlajamäki, J., & Patti, M. (2006) · Advances in molecular and cellular endocrinology · doi:10.1016/s1569-2566(06)05012-5

Neurovascular Mechanisms of Ischemia Tolerance Against Brain Injury

Dave, K. R., Thompson, J. W., Neumann, J. T., Pérez‐Pinzón, M. A., & Lin, H. W. (2013) · Springer eBooks · doi:10.1007/978-1-4614-8690-9_10

Effects of core temperature on exercise-induced mitochondrial biogenesis: Potential role of PGC-1α, AMPK eNOS, SIRT1, and SIRT3

Hodge, T. (2014) · W&M Publish (College of William & Mary)

Dietary Energy Balance, Calorie Restriction, and Cancer Prevention

Hursting, S. D., Smith, S. M., Nogueira, L., de Angel, R. E., Lashinger, L. M., & Perkins, S. N. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-627-6_7

The skinny on SIRT1 regulation

Schug, T. T. (2010) · Disease Models & Mechanisms · doi:10.1242/dmm.005629

The Role of Sirtuins in Arthritis

Kyburz, D., & Niederer, F. (2012) · Springer eBooks · doi:10.1007/978-1-4614-6166-1_18

Contemporary Reviews in Cardiovascular Medicine Cellular Senescence, Vascular Disease, and Aging Part 1 of a 2-Part Review

Kovacic, J. C., & Nabel, E. G. (2016)

Towards endophenotyping multiple sclerosis

Strijbis, E. M. M. (2014) · Pure Amsterdam UMC

Calorie Restriction, Exercise, and Colon Cancer Prevention: A Mechanistic Perspective

Rogers, C. J., Colbert, L. H., Perkins, S. N., & Hursting, S. D. (2010) · Springer eBooks · doi:10.1007/978-1-4419-7551-5_5

Mitochondrial energetic metabolism in hereditary neuropathies associated with OPA1 and MFN2 genes mutations.

Guillet, V., & REYNIER, P. (2009) · OpenGrey (Institut de l'Information Scientifique et Technique)

Role of cardiac FoxO1 in conditions of insulin resistance, nutrient excess, and diabetes

Puthanveetil, P. (2012) · cIRcle (University of British Columbia) · doi:10.14288/1.0072615

Characterization of Sirt2 using conditional RNAi in mice

Reiss, M. (2011) · Kölner Universitäts PublikationsServer (Universität zu Köln)

OXIDATIVE STRESS-INDUCED VASCULAR DYSFUNCTION: MECHANISTIC PERSPECTIVES AND PREVENTIVE STRATEGIES

Vasamsetti, S. B., & Kotamraju, S. (2011)

Role of phosphodiesterase-4 in alcohol-induced organ injury.

Avila, D. V. (2016) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/2405

Role of Sirtuins in Aging and Tumorigenesis

Bai, W., Nicosia, S. V., Hsieh, T., & Zhang, X. M. (2008) · CRC Press eBooks · doi:10.1201/9781420045802.ch9

Def-eating senescence?

Maulucci, G., & Pani, G. (2012)

Role of Occludin in the Regulation of Epithelial Tight Junctions

Manda, B. (2016) · doi:10.21007/etd.cghs.2016.0415

Role of Autophagy Inhibition in Regulating Hepatic Lipid Metabolism

Li, X., & Li, L. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805420-8.00004-4

Regulation of SIRT1, SIRT3, PGC-1α, and LRP130 in Response to Energetic Stress in Human Skeletal Muscle

Edgett, B. A. (2017) · QSpace (Queen's University Library)

THE ACUTE IMPACT OF A SINGLE DOSE OF RESVERATROL ON INSULIN SENSITIVITY, WHOLE BODY FAT OXIDATION, AND INTRACELLULAR SIGNALING IN SKELETAL MUSCLE AND ADIPOSE TISSUE IN OVERWEIGHT AND OBESE MEN

Williams, C. (2013) · QSpace (Queen's University Library)

Shear Stress-Induced Mitochondrial Biogenesis Decreases the

Kim, J., Kim, B., Lee, H., Thakkar, S. R., Babbitt, D. M., Eguchi, S., Michael, D., & Park, J. (2015)

CALL FOR PAPERS Biomarkers in Lung Diseases: from Pathogenesis to Prediction to New Therapies Decreased endothelial nitric oxide synthase expression and function contribute to impaired mitochondrial biogenesis and oxidative stress in fetal lambs with persistent pulmonary hypertension

Afolayan, A. J., Eis, A., Alexander, M., Michalkiewicz, T., Teng, R., Lakshminrusimha, S., Konduri, G. G., Afolayan, A. J., Eis, A., & Rj, T. (2016)

HAT-HDAC System in Asthma

Sun, X., Chen, Z. H., & Wang, X. (2018) · Translational bioinformatics · doi:10.1007/978-981-10-8764-6_12

Role of Lysine Acetylation in the Control of Cardiac Energy Metabolism

Alrub, A. (2014) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3g15tk4x

Genetics of Life Span: Lessons from Model Organisms

Marı́n-Garcı́a, J., Goldenthal, M. J., & Moe, G. W. P. L. (2007) · Springer eBooks · doi:10.1007/978-0-387-74072-0_12

Comparing and contrasting the effects of aerobic exercise and the exercise mimetic, resveratrol, on neurocognitive function

Hussey, R. C. (2013) · Trinity's Access to Research Output (TARA) (Trinity College Dublin)

Effects of Natural Antioxidants on Motor and Cognitive Deficits in an Animal Model of Aging and Obesity and Dopaminergic-Like SH-SY5Y Cell Line

Potdar, S. (2018)

Neuroprotective Effect of Resveratrol via Sirtuin 1 Pathway in a Rat Model of Chronic Ocular Hypertension

Heo, H., Sung, M. S., & Park, S. W. (2018) · Journal of the Korean Glaucoma Society · doi:10.36299/jkgs.2018.7.1.1

Advancing transcriptome analysis in models of disease and ageing

de Jong, T. V. (2019) · doi:10.33612/diss.99203371

Pathological Interaction between DNA Repair and Mitochondrial Dysfunction in ALS

Bermúdez-Guzmán, L., & Leal, A. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.90217

Modulation of neuronal mitochondrial dynamics, autophagy and huntingtin proteostasis by HDAC inhibitors: Insights for Huntington's disease

Dias, P. G. G. (2015) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · doi:10.34626/3xwd-bf33

MicroRNAs linking oxidative stress and diabetes

Friedrich, J., & Krenning, G. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-815776-3.00010-3

mtDNA maintenance: disease and therapy

Quadalti, C., & Garone, C. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819656-4.00016-4

Nutritional Regulation of Mitochondrial Health and Its Implication in Treating Obesity and Diabetes: Lessons Learned From the Resveratrol–Sirt1 Axis

Tao, Z., Shi, L., & Cheng, Z. (2020) · Royal Society of Chemistry eBooks · doi:10.1039/9781839160608-00164 · Cited by 1

Endometrial Factors Causing Subfertility in CowsPreprint

Matsuyama, S., Nakamura, S., Minabe, S., Sakatani, M., Takenouchi, N., Sasaki, T., Iwata, H., & Kimura, K. (2021) · Research Square · doi:10.21203/rs.3.rs-200187/v1

Sex Differences in the Effects of Osteocalcin and Exercise on Cognition and Behaviour in a High-fat Diet Model of Type 2 Diabetes

Winberg, J. (2020) · TSpace (University of Toronto)

Nutrient-Dependent Acetylation Controls Basic Regulatory Metabolic Switches and Cellular Reprogramming

Uigserver, P. P. (2012)

Protective Effect of Ginsenoside Rd on Military Aviation Noise-Induced Cochlear Hair Cell DamagePreprint

Chen, X., Yu-hui, L. I. U., Ji, S., Xue, X., Liu, P., Cong-cong, L. I., ZHANG, M., CHANG, Y.-M., & Xiao-cheng, W. A. N. G. (2021) · Research Square · doi:10.21203/rs.3.rs-673642/v1

Control of Mitochondrial Homeostasis In Disused and Aging Skeletal Muscle: Role of Pgc-1Alpha and Sirtuins

Yeo, D. (2020) · University of Minnesota Digital Conservancy (University of Minnesota)

Sirt1 and the Mitochondria

Luen Tang, B. (2016) · Molecules and Cells · doi:10.14348/molcells.2016.2318 · Cited by 740

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