Calorie restriction extends yeast life span by lowering the level of NADH

Methods in yeast genetics

Sherman, F., Fink, G. R., & Hicks, J. B. (1979) · Cold Spring Harbor Laboratory eBooks · Cited by 7,430

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

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

Requirement of NAD and SIR2 for Life-Span Extension by Calorie Restriction in Saccharomyces cerevisiae

Lin, S.-J., Defossez, P.-A., & Guarente, L. (2000) · Science · doi:10.1126/science.289.5487.2126 · Cited by 1,775

A new efficient gene disruption cassette for repeated use in budding yeast

Güldener, U. (1996) · Nucleic Acids Research · doi:10.1093/nar/24.13.2519 · Cited by 1,657

Increased dosage of a sir-2 gene extends lifespan in Caenorhabditis elegans

Tissenbaum, H. A., & Guarente, L. (2001) · Nature · doi:10.1038/35065638 · Cited by 1,603

Calorie restriction extends Saccharomyces cerevisiae lifespan by increasing respiration

Lin, S.-J., Kaeberlein, M., Andalis, A. A., Sturtz, L. A., Defossez, P.-A., Culotta, V. C., Fink, G. R., & Guarente, L. (2002) · Nature · doi:10.1038/nature00829 · Cited by 1,057

Inhibition of Silencing and Accelerated Aging by Nicotinamide, a Putative Negative Regulator of Yeast Sir2 and Human SIRT1

Bitterman, K. J., Anderson, R. M., Cohen, H. Y., Latorre-Esteves, M., & Sinclair, D. A. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m205670200 · Cited by 1,002

The silencing protein SIR2 and its homologs are NAD-dependent protein deacetylases

Landry, J., Sutton, A., Tafrov, S. T., Heller, R. C., Stebbins, J., Pillus, L., & Sternglanz, R. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.110148297 · Cited by 970

Nicotinamide and PNC1 govern lifespan extension by calorie restriction in Saccharomyces cerevisiae

Anderson, R. M., Bitterman, K. J., Wood, J. G., Medvedik, O., & Sinclair, D. A. (2003) · Nature · doi:10.1038/nature01578 · Cited by 736

A Mitochondria-Targeted Fluorescent Probe for Monitoring NADPH Overproduction during Influenza Virus Infection

Chang, H., Hu, X., Tang, X., Tian, S., Li, Y., Lv, X., & Shang, L. (2023) · ACS Sensors · doi:10.1021/acssensors.2c02458 · Cited by 21

Caloric restriction, Sirtuins, and cardiovascular diseases

Wei, Z., Yang, B., Wang, H., Lv, S., Chen, H., & Liu, D. (2024) · Chinese Medical Journal · doi:10.1097/cm9.0000000000003056 · Cited by 22

Multiple Pathways Regulating the Calorie Restriction Response in Yeast

Rahat, O., Maoz, N., & Cohen, H. Y. (2010) · The Journals of Gerontology Series A · doi:10.1093/gerona/glq165 · Cited by 21

NAMPT inhibition synergizes with NQO1-targeting agents in inducing apoptotic cell death in non-small cell lung cancer cells

Liu, H., Qing-Ran, L. I., Cheng, X., Wang, G., & Hao, H. (2016) · Chinese Journal of Natural Medicines · doi:10.1016/s1875-5364(16)30068-1 · Cited by 21

Non-Coding RNA Molecules Connect Calorie Restriction and Lifespan

Abraham, K. J., Ostrowski, L., & Mekhail, K. (2016) · Journal of Molecular Biology · doi:10.1016/j.jmb.2016.08.020 · Cited by 21

Methylene blue decreases mitochondrial lysine acetylation in the diabetic heart

Berthiaume, J. M., Hsiung, C., Austin, A. B., McBrayer, S. P., Depuydt, M. M., Chandler, M. P., Miyagi, M., & Rosca, M. G. (2017) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-017-2993-1 · Cited by 22

The epigenetic and morphogenetic effects of molecular oxygen and its derived reactive species in development

Hitchler, M. J., & Domann, F. E. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.01.008 · Cited by 20

Skeletal Muscle Gene Expression Profile in Response to Caloric Restriction and Aging: A Role for SirT1

Myers, M. J., Shaik, F., Shaik, F., Alway, S. E., & Mohamed, J. S. (2021) · Genes · doi:10.3390/genes12050691 · Cited by 19

NAD+ Metabolism in Age-Related Hearing Loss

Kim, H. (2014) · Aging and Disease · doi:10.14336/ad.2014.0500150 · Cited by 20

Genome-Wide Analysis of Yeast Aging

Sutphin, G. L., Olsen, B., Kennedy, B. K., & Kaeberlein, M. R. (2011) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-94-007-2561-4_12 · Cited by 21

Less is more: Nutrient limitation induces cross-talk of nutrient sensing pathways with NAD+ homeostasis and contributes to longevity

Tsang, F. A., & Lin, S.-J. (2015) · Frontiers in Biology · doi:10.1007/s11515-015-1367-x · Cited by 21

Low ergosterol content in yeast adh1 mutant enhances chitin maldistribution and sensitivity to paraquat‐induced oxidative stress

Marisco, G., Saito, S. T., Ganda, I. S., Brendel, M., & Pungartnik, C. (2011) · Yeast · doi:10.1002/yea.1844 · Cited by 20

Deteriorated Stress Response in Stationary-Phase Yeast: Sir2 and Yap1 Are Essential for Hsf1 Activation by Heat Shock and Oxidative Stress, Respectively

Nussbaum, I., Weindling, E., Jubran, R., Cohen, A., & Bar‐Nun, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111505 · Cited by 23

Tolerance to NADH/NAD+ imbalance anticipates aging and anti-aging interventions

Alonso-Lavin, A. J., Bajić, D., & Poyatos, J. F. (2021) · iScience · doi:10.1016/j.isci.2021.102697 · Cited by 17

Pharmacological modulation of adaptive thermogenesis: new clues for obesity management?

Genchi, V. A., Palma, G., Sorice, G. P., D’Oria, R., Caccioppoli, C., Marrano, N., Biondi, G., Caruso, I., Cignarelli, A., Natalicchio, A., et al. (2023) · Journal of Endocrinological Investigation · doi:10.1007/s40618-023-02125-0 · Cited by 19

Biochemical and Mutational Analysis of a Novel Nicotinamidase from Oceanobacillus iheyensis HTE831

Sánchez-Carrón, G., García-García, M. I., Perez, R. Z., Takami, H., García‐Carmona, F., & Sánchez‐Ferrer, Á. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056727 · Cited by 19

Epigenetic Manifestation of Metabolic Syndrome and Dietary Management

Chaudhary, N., Nakka, K. K., Maulik, N., & Chattopadhyay, S. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.4387 · Cited by 19

Perspectives on the mitochondrial etiology of replicative aging in yeast

Ugidos, A., Nyström, T., & Caballero, A. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.02.002 · Cited by 18

Mitochondrial-targeting fluorescent probe awakened by nitroreductase for hypoxic imaging and surgical navigation of solid tumors

Xie, H., Li, Q., Yang, H., Gao, W., Zhang, Q., Zhang, P., & Ding, C. (2023) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2023.134556 · Cited by 18

Fatty Acid Biosynthesis Inhibition Increases Reduction Potential in Neuronal Cells under Hypoxia

Brose, S. A., Golovko, S. A., & Golovko, M. Y. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00546 · Cited by 18

Less is more or more is less: Implications of glucose metabolism in the regulation of the reproductive potential and total lifespan of the Saccharomyces cerevisiae yeast

Maślanka, R., & Zadrąg‐Tęcza, R. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28386 · Cited by 20

Evidence of a sirtuin gene family in grapevine (Vitis vinifera L.)

Busconi, M., Reggi, S., Fogher, C., & Bavaresco, L. (2009) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2009.03.003 · Cited by 18

Sirtuins and β‐cell function

Bordone, L., & Guarente, L. (2007) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2007.00769.x · Cited by 18

Wine, sirtuins and nephroprotection: Not only resveratrol

Mannari, C., Bertelli, A. A. E., Stiaccini, G., & Giovannini, L. (2010) · Medical Hypotheses · doi:10.1016/j.mehy.2010.08.004 · Cited by 18

Sirt1 Regulates Insulin Secretion by Repressing UCP2 in Pancreatic b Cells

Bordone, L., Motta, M. C., Picard, F., Jhala, U. S., Apfeld, J., McDonagh, T., Lemieux, M. E., McBurney, M. W., Easlon, E. J., & Guarente, L. (2006) · Cited by 17

An NAD + -Dependent Sirtuin Depropionylase and Deacetylase (Sir2La) from the Probiotic Bacterium Lactobacillus acidophilus NCFM

Olesen, S. V., Rajabi, N., Svensson, B., Olsen, C. A., & Madsen, A. S. (2018) · Biochemistry · doi:10.1021/acs.biochem.8b00306 · Cited by 16

Saffron, Its Active Components, and Their Association with DNA and Histone Modification: A Narrative Review of Current Knowledge

Rashid, M., Brim, H., & Ashktorab, H. (2022) · Nutrients · doi:10.3390/nu14163317 · Cited by 20

Up-regulation of nicotinamide phosphoribosyltransferase and increase of NAD+ levels by glucose restriction extend replicative lifespan of human fibroblast Hs68 cells

Yang, N.-C., Song, T., Chang, Y., Chen, M.-Y., & Hu, M. (2014) · Biogerontology · doi:10.1007/s10522-014-9528-x · Cited by 17

Inactivation of mitochondrial aspartate aminotransferase contributes to the respiratory deficit of yeast frataxin-deficient cells

Sliwa, D., Dairou, J., Camadro, J., & Santos, R. (2011) · Biochemical Journal · doi:10.1042/bj20111574 · Cited by 17

Redox responses in yeast to acetate as the carbon source

Minard, K. I., & McAlister-Henn, L. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.12.014 · Cited by 17

Molecular Docking and Dynamics Simulation, Receptor‐based Hypothesis: Application to Identify Novel Sirtuin 2 Inhibitors

Sakkiah, S., Thangapandian, S., Park, C., Son, M., & Lee, K. W. (2012) · Chemical Biology & Drug Design · doi:10.1111/j.1747-0285.2012.01406.x · Cited by 17

Real-Time Assessment of the Metabolic Profile of Living Cells with Genetically Encoded NADH Sensors

Zhao, Y., Yang, Y. A., & Loscalzo, J. (2014) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/b978-0-12-416618-9.00018-2 · Cited by 19

Improved mass spectrometry-based activity assay reveals oxidative and metabolic stress as sirtuin-1 regulators

Shao, D., Yao, C., Kim, M. H., Fry, J., Cohen, R. A., Costello, C. E., Matsui, R., Seta, F., McComb, M. E., & Bachschmid, M. M. (2019) · Redox Biology · doi:10.1016/j.redox.2019.101150 · Cited by 16

Nicotinamide riboside restores nicotinamide adenine dinucleotide levels and alleviates brain injury by inhibiting oxidative stress and neuroinflammation in a mouse model of intracerebral hemorrhage

She, J., Zhang, H., Xu, H. Z., Li, Y., Wu, J., Han, R., Lin, F., Wang, Y., Sheng, R., Gu, J., et al. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04335-w · Cited by 16

The Lifespan-Promoting Effect of Otophylloside B in Caenorhabditis elegans

Yang, J., Wan, Q.-L., Mu, Q., Wu, C., Ding, A.-J., Yang, Z., Qiu, M., & Luo, H. (2015) · Natural Products and Bioprospecting · doi:10.1007/s13659-015-0064-4 · Cited by 16

Cultivation and quantitative single‐cell analysis of Saccharomyces cerevisiae on a multifunctional microfluidic device

Stratz, S., Verboket, P. E., Hasler, K., & Dittrich, P. S. (2017) · Electrophoresis · doi:10.1002/elps.201700253 · Cited by 16

Transcriptional response to dietary restriction in Drosophila melanogaster

Ding, F., Gil, M. P., Franklin, M., Ferreira, J., Tatar, M., Helfand, S. L., & Neretti, N. (2014) · Journal of Insect Physiology · doi:10.1016/j.jinsphys.2014.05.002 · Cited by 17

Altered Expression of Mitochondrial NAD+ Carriers Influences Yeast Chronological Lifespan by Modulating Cytosolic and Mitochondrial Metabolism

Orlandi, I., Stamerra, G., & Vai, M. (2018) · Frontiers in Genetics · doi:10.3389/fgene.2018.00676 · Cited by 16

Enhanced cellular longevity arising from environmental fluctuations

Liu, Y., Zhou, Z., Su, H., Wu, S., Ni, G., Zhang, A., Tsimring, L. S., Hasty, J., & Hao, N. (2024) · Cell Systems · doi:10.1016/j.cels.2024.07.007 · Cited by 16

The Elusive Magic Pill: Finding Effective Therapies for Mitochondrial Disorders

Goldstein, A. C., & Wolfe, L. A. (2013) · Neurotherapeutics · doi:10.1007/s13311-012-0175-0 · Cited by 16

Dietary restriction increases site-specific histone H3 acetylation in rat liver: Possible modulation by sirtuins

Kawakami, K., Nakamura, A., & Goto, S. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.01.120 · Cited by 15

The Contentious History of Sirtuin Debates

Naiman, S., & Cohen, H. Y. (2012) · Rambam Maimonides Medical Journal · doi:10.5041/rmmj.10093 · Cited by 15

Dietary Restriction, Hormesis, and Small Molecule Mimetics

Sinclair, D. A., & Howitz, K. T. (2005) · Elsevier eBooks · doi:10.1016/b978-012088387-5/50006-6 · Cited by 15

Nicotinamide riboside activates SIRT5 deacetylation

Curry, A. M., Rymarchyk, S., Herrington, N. B., Donu, D., Kellogg, G. E., & Cen, Y. (2023) · FEBS Journal · doi:10.1111/febs.16887 · Cited by 14

Keep the fire burning: Current avenues in the quest of treating mitochondrial disorders

Tischner, C., & Wenz, T. (2015) · Mitochondrion · doi:10.1016/j.mito.2015.06.002 · Cited by 14

Hypothermic machine perfusion ameliorates inflammation during ischemia-reperfusion injury via sirtuin-1-mediated deacetylation of nuclear factor-κB p65 in rat livers donated after circulatory death

Zeng, C., Hu, X., He, W., Wang, Y., Li, L., Xiong, Y., & Ye, Q. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.7738 · Cited by 14

ChIP-exo analysis highlights Fkh1 and Fkh2 transcription factors as hubs that integrate multi-scale networks in budding yeast

Mondeel, T. D. G. A., Holland, P., Nielsen, J., & Barberis, M. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz603 · Cited by 14

Krüppel-like factor 6 (KLF6) requires its amino terminal domain to promote villous trophoblast cell fusion

Miranda, A. L., Racca, A. C., Kourdova, L. T., Rojas, M. L., Puerto, M. M. C. D., Rodríguez-Lombardi, G., Salas, A. V., Travella, C., da Silva, E. C. O., de Souza, S. T., et al. (2021) · Placenta · doi:10.1016/j.placenta.2021.12.006 · Cited by 14

Activation of Protein Kinase C-Mitogen-activated Protein Kinase Signaling in Response to Inositol Starvation Triggers Sir2p-dependent Telomeric Silencing in Yeast

Lee, S., Gaspar, M. L., Aregullin, M. A., Jesch, S. A., & Henry, S. A. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.493072 · Cited by 14

Muscle type-specific responses to NAD+ salvage biosynthesis promote muscle function in Caenorhabditis elegans

Vrablik, T. L., Wang, W., Upadhyay, A., & Hanna‐Rose, W. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.11.014 · Cited by 14

Surprising sirtuin crosstalk in the heart

Schug, T. T., & Li, X. (2010) · Aging · doi:10.18632/aging.100128 · Cited by 14

Kynurenic Acid and Its Analogs Are Beneficial Physiologic Attenuators in Bdelloid Rotifers

Datki, Z., Galik-Olah, Z., Bohár, Z., Zádori, D., Fülöp, F., Szatmári, I., Gálik, B., Kálmán, J., & Vécsei, L. (2019) · Molecules · doi:10.3390/molecules24112171 · Cited by 14

Reactive Oxygen Species in the Induction of Toxicity

Lenaz, G., & Strocchi, P. (2009) · Wiley eBooks · doi:10.1002/9780470744307.gat024 · Cited by 15

High-affinity Na+-dependent dicarboxylate cotransporter promotes cellular senescence by inhibiting SIRT1

Liu, W., Hong, Q., Bai, X., Fu, B., Xie, Y., Zhang, X., Li, J., Shi, S., Lv, Y., & Sun, X. (2010) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2010.08.006 · Cited by 14

Influence of chronological aging on the survival and nucleotide content of cells grown in different conditions: occurrence of a high concentration of UDP--acetylglucosamine in stationary cells grown in 2% glucose

Osório, H., Silles, E., MAIA, R., Peleteiro, B., Moradas‐Ferreira, P., Sillero, M. A. G., & Sillero, A. (2004) · FEMS Yeast Research · doi:10.1016/j.femsyr.2004.10.001 · Cited by 12

Sirtuins in Aging and Age-Related Diseases

Haigis, M. C., & Sinclair, D. A. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-378638-8.00011-7 · Cited by 13

Growth phase-dependent roles of Sir2 in oxidative stress resistance and chronological lifespan in yeast

Kang, W. K., Kim, Y. H., Kim, B.-S., & Kim, J. (2014) · The Journal of Microbiology · doi:10.1007/s12275-014-4173-2 · Cited by 14

Looking for putative functions of the Leishmania cytosolic SIR2 deacetylase

Séréno, D., Vergnes, B., Mathieu-Daudé, F., Cordeiro‐da‐Silva, A., & Ouaissi, A. (2006) · Parasitology Research · doi:10.1007/s00436-006-0280-2 · Cited by 13

Sirtuins, Tissue Maintenance, and Tumorigenesis

Mohrin, M., & Chen, D. (2013) · Genes & Cancer · doi:10.1177/1947601912474930 · Cited by 11

Molecular evolutionary patterns of NAD+/Sirtuin aging signaling pathway across taxa

Gaur, U., Tu, J., Li, D., Gao, Y., Lian, T., Sun, B., Yang, D., Fan, X., & Yang, M. (2017) · PLoS ONE · doi:10.1371/journal.pone.0182306 · Cited by 12

Evaluation of lifespan promoting effects of biofortified wheat in Drosophila melanogaster

Pandey, M., Bansal, S., & Chawla, G. (2022) · Experimental Gerontology · doi:10.1016/j.exger.2022.111697 · Cited by 11

The Involvement of Sirtuin 1 Dysfunction in High-Fat Diet-Induced Vascular Dysfunction in Mice

Xia, N., Reifenberg, G., Schirra, C., & Li, H. (2022) · Antioxidants · doi:10.3390/antiox11030541 · Cited by 13

The effects of temperature and diet on age grading and population age structure determination in Drosophila

Aw, W. C., & Ballard, J. W. O. (2013) · Journal of Insect Physiology · doi:10.1016/j.jinsphys.2013.07.005 · Cited by 12

Genetic perturbation of key central metabolic genes extends lifespan in Drosophila and affects response to dietary restriction

Talbert, M. E., Barnett, B., Hoff, R., Amella, M., Kuczynski, K., Lavington, E., Koury, S. A., Brud, E., & Eanes, W. F. (2015) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2015.1646 · Cited by 12

Mitogen-activated protein kinases, Fus3 and Kss1, regulate chronological lifespan in yeast

Aluru, M. R., McKinney, T., Venero, A.-K. L., Choudhury, S., & Torres, M. P. (2017) · Aging · doi:10.18632/aging.101350 · Cited by 13

NaDC3 Induces Premature Cellular Senescence by Promoting Transport of Krebs Cycle Intermediates, Increasing NADH, and Exacerbating Oxidative Damage

Ma, Y., Bai, X., Du, X., Fu, B., & Chen, X. (2014) · The Journals of Gerontology Series A · doi:10.1093/gerona/glu198 · Cited by 12

The Pivotal Role of One-Carbon Metabolism in Neoplastic Progression During the Aging Process

Majumder, A., Bano, S., & Nayak, K. B. (2024) · Biomolecules · doi:10.3390/biom14111387 · Cited by 11

Promising drug discovery strategies for sirtuin modulators: what lessons have we learnt?

Garg, G., Singh, A. K., Singh, S., & Rizvi, S. I. (2021) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2021.1915980 · Cited by 11

Changing ROS, NAD and AMP: A path to longevity via mitochondrial therapeutics

Lushchak, O. V., Gospodaryov, D. V., Strilbytska, O. M., & Bayliak, M. M. (2023) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2023.03.005 · Cited by 11

Metabolite modulation of HeLa cell response to ENOX2 inhibitors EGCG and phenoxodiol

Wu, L., Luca, T. D., Watanabe, T., Morré, D. M., & Morré, D. J. (2011) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2011.04.011 · Cited by 11

Articulatory-Acoustic Analyses of Mandarin Words in Emotional Context Speech for Smart Campus

Ren, G., Zhang, X., & Duan, S. (2018) · IEEE Access · doi:10.1109/access.2018.2865831 · Cited by 11

Combined In-Cell NMR and Simulation Approach to Probe Redox-Dependent Pathway Control

Jensen, P. R., Matos, M. R. A., Sonnenschein, N., & Meier, S. (2019) · Analytical Chemistry · doi:10.1021/acs.analchem.9b00660 · Cited by 11

Overexpression ofgrappaencoding a histone methyltransferase enhances stress resistance inDrosophila

List, O., Togawa, T., Tsuda, M., Matsuo, T., Elard, L., & Aigaki, T. (2009) · Hereditas · doi:10.1111/j.1601-5223.2008.02080.x · Cited by 12

Longevity and Aging in Budding Yeast

Kaeberlein, M. R. (2006) · Elsevier eBooks · doi:10.1016/b978-012369391-4/50019-9 · Cited by 12

A quantitative yeast aging proteomics analysis reveals novel aging regulators

Sun, Y., Yu, R., Guo, H., Qin, H. H., & Dang, W. (2021) · GeroScience · doi:10.1007/s11357-021-00412-3 · Cited by 11

The emerging importance of NAD+ metabolome for nutrition and food sciences: A bibliometric analysis

Alegre, G. F. S., & Pastore, G. M. (2023) · Food Bioscience · doi:10.1016/j.fbio.2023.103126 · Cited by 10

3D imaging of the mitochondrial redox state of rat hearts under normal and fasting conditions

Xu, H. N., Zhou, R., Moon, L., Feng, M., & Li, L. Z. (2013) · Journal of Innovative Optical Health Sciences · doi:10.1142/s1793545813500454 · Cited by 10

Mechanistic perspectives of calorie restriction on vascular homeostasis

Liu, Y., Chen, H., & Liu, D. (2014) · Science China Life Sciences · doi:10.1007/s11427-014-4709-z · Cited by 10

Quantification of Protein Copy Number in Yeast: The NAD+ Metabolome

Mei, S.-C., & Brenner, C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0106496 · Cited by 10

Genetic engineering of AtAOX1a in Saccharomyces cerevisiae prevents oxidative damage and maintains redox homeostasis

Vishwakarma, A., Dalal, A., Tetali, S. D., Kirti, P. B., & Padmasree, K. (2016) · FEBS Open Bio · doi:10.1002/2211-5463.12028 · Cited by 11

[Manipulation of NADH metabolism in industrial strains].

Qin, Y., Dong, Z., Liu, L., & Chen, J. (2009) · PubMed · Cited by 10

A budding yeast's perspective on aging: The shape I'm in

Smith, J. T., Wright, J., & Schneider, B. L. (2015) · Experimental Biology and Medicine · doi:10.1177/1535370215577584 · Cited by 10

NAD+ and metabolic regulation of age-related proteoxicity: A possible role for methylglyoxal?

Hipkiss, A. R. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.03.006 · Cited by 10

Mitochondrial Dysfunction And Lipid Accumulation In The Human Diaphragm During Mechanical Ventilation

Picard, M. A., Liang, F., Hussain, S. N., Goldberg, P., Danialou, G., Chaturvedi, R. K., Matecki, S., Jaber, S., Rosiers, C. D., Karpati, G., et al. (2011) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a4257 · Cited by 9

Mitochondrial Targetable Turn-On Fluorescent Probe for Fast Detection of NAD(P)H in Living Cells and In Vivo

Magesh, K., Lu, Y., Wu, S., & Velmathi, S. (2024) · ACS Applied Bio Materials · doi:10.1021/acsabm.4c00755 · Cited by 9

Improvement of natural isolates of Saccharomyces cerevisiae strains for synthesis of a chiral building block using classic genetics

Nir, N., Bahalul, M., Feingersch, R., Katz-Ezov, T., Kashi, Y., & Fishman, A. (2008) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-008-1344-2 · Cited by 9

The Gender Association of the SIRT1 rs7895833 Polymorphism with Pediatric Obesity: A 3-Year Panel Study

Lee, M., Choi, S. R., Lee, Y., & Oh, H. (2016) · Lifestyle Genomics · doi:10.1159/000454713 · Cited by 10

Virtually identical does not mean exactly identical: Discrepancy in energy metabolism between glucose and fructose fermentation influences the reproductive potential of yeast cells

Maślanka, R., Bednarska, S., & Zadrąg‐Tęcza, R. (2024) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2024.110021 · Cited by 9

Redox Modulating Factors Affect Longevity Regulation in Rotifers

Mácsai, L., Galik-Olah, Z., Bush, A. I., Gálik, B., Ónody, R., Kálmán, J., & Datki, Z. (2018) · The Journals of Gerontology Series A · doi:10.1093/gerona/gly193 · Cited by 8

The Many Roles Mitochondria Play in Mammalian Aging

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Molecular probe to visualize the effect of a glycolytic inhibitor on reducing NADH levels in a cellular system

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Heruth, D. P., Zhang, L. Q., & Ye, S. Q. (2011) · Journal of Bioanalysis & Biomedicine · doi:10.4172/1948-593x.1000047 · Cited by 6

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Anekonda, T. S. (2009) · Open Longevity Science · doi:10.2174/1876326x00903010028 · Cited by 7

Vitamin-Dependent Modifications of Chromatin

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(2004) · Science s STKE · doi:10.1126/stke.2142004tw13

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Increased life span due to calorie restriction in respiratory deficient yeast

Kaeberlein, M. R., Hu, D., Kerr, E. O., Tsuchiya, M., Westman, E. A., Dang, N., Fields, S., & Kennedy, B. K. (2005) · PLoS Genetics · doi:10.1371/journal.pgen.0010069.eor · Cited by 8

Doi: 10.1111/j.1474-9726.2006.00240.x Sirtuin-independent effects of nicotinamide on lifespan Blackwell Publishing Ltd extension from calorie restriction in yeast

Tsuchiya, M., Dang, N., Kerr, E. O., Hu, D., Steffen, K. K., Oakes, J. A., Kennedy, B. K., & Kaeberlein, M. R. (2013)