Regulation of Autophagy by Cytosolic Acetyl-Coenzyme A

The Hallmarks of Aging

López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2013) · Cell · doi:10.1016/j.cell.2013.05.039 · Cited by 14,982

Autophagy in the Pathogenesis of Disease

Levine, B., & Kroemer, G. (2008) · Cell · doi:10.1016/j.cell.2007.12.018 · Cited by 7,069

Autophagy: Renovation of Cells and Tissues

Mizushima, N., & Komatsu, M. (2011) · Cell · doi:10.1016/j.cell.2011.10.026 · Cited by 6,615

Autophagy and the Integrated Stress Response

Kroemer, G., Mariño, G., & Levine, B. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.023 · Cited by 3,506

TFEB Links Autophagy to Lysosomal Biogenesis

Settembre, C., Di Malta, C., Polito, V. A., Arencibia, M. G., Vetrini, F., Erdin, S., Erdin, S. U., Huynh, T., Medina, D., Colella, P., et al. (2011) · Science · doi:10.1126/science.1204592 · Cited by 3,365

AMPK regulates energy expenditure by modulating NAD+ metabolism and SIRT1 activity

Cantó, C., Gerhart-Hines, Z., Feige, J. N., Lagouge, M., Noriega, L., Milne, J. C., Elliott, P. J., Puigserver, P., & Auwerx, J. (2009) · Nature · doi:10.1038/nature07813 · Cited by 3,300

ATP-citrate lyase links cellular metabolism to histone acetylation

Wellen, K. E., Hatzivassiliou, G., Sachdeva, U. M., Bui, T. V., Cross, J. R., & Thompson, C. B. (2009) · Science · doi:10.1126/science.1164097 · Cited by 2,298

In Vivo Analysis of Autophagy in Response to Nutrient Starvation Using Transgenic Mice Expressing a Fluorescent Autophagosome Marker

Mizushima, N., Yamamoto, A., Matsui, M., Yoshimori, T., & Ohsumi, Y. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-09-0704 · Cited by 2,105

Induction of autophagy by spermidine promotes longevity

Eisenberg, T., Knauer, H., Schauer, A., Büttner, S., Ruckenstuhl, C., Carmona-Gutierrez, D., Ring, J., Schroeder, S., Magnes, C., Antonacci, L., et al. (2009) · Nature Cell Biology · doi:10.1038/ncb1975 · Cited by 1,680

Network organization of the human autophagy system

Behrends, C., Sowa, M. E., Gygi, S. P., & Harper, J. W. (2010) · Nature · doi:10.1038/nature09204 · Cited by 1,554

Moving towards a novel therapeutic strategy for hyperammonemia that targets glutamine metabolism

Fukui, K., Takahashi, T., Matsunari, H., Uchikura, A., Watanabe, M., Nagashima, H., Ishihara, N., Kakuma, T., Watanabe, Y., Yamashita, Y., et al. (2022) · Journal of Inherited Metabolic Disease · doi:10.1002/jimd.12540 · Cited by 4

Mitochondrial Signaling

Raimundo, N., Fernández-Mosquera, L., & Yambire, K. F. (2016) · Springer eBooks · doi:10.1007/978-1-4939-3612-0_9 · Cited by 4

Epi-Regulation of Cell Death in Cancer

Beato, A., Torre, L. D., Capone, V., Carannante, D., Favale, G., Verrilli, G., Altucci, L., & Carafa, V. (2023) · Biochemistry · doi:10.5772/intechopen.108919 · Cited by 4

The mechanism and role of intracellular α-ketoglutarate reduction in hepatic stellate cell activation

Zhao, J., Jiang, Y., Sun, X., Liu, X.-S., Liu, F., Song, M., & Zhang, L. (2020) · Bioscience Reports · doi:10.1042/bsr20193385 · Cited by 4

Cysteamine-bicalutamide combination treatment restores alpha-ketoglutarate and corrects proximal tubule phenotype in cystinosisPreprint

Jamalpoor, A., van Gelder, C. A. G. H., Yengej, F. A. Y., Zaal, E. A., Berlingerio, S. P., Veys, K. R. P., Casellas, C. P., Voskuil, K., Essa, K., Ammerlaan, C. M. E., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.10.941799 · Cited by 4

Autophagic signaling promotes systems-wide remodeling in skeletal muscle upon oncometabolic stressPreprint

Karlstaedt, A., Vitrac, H., Salazar, R., Gould, B. D., Soedkamp, D., Spivia, W. R., Raedschelders, K., Dinh, A. Q., Guzman, A. G., Tan, L., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.13.338202 · Cited by 4

Loss of hepatic ME1 ameliorates MASLD by Suppressing peroxisomal β-Oxidation and Activating Lipophagy/Lipolysis

Zhang, J., Wu, D., Lei, R., Zhang, F., Wu, W., Wu, Y. Z., Zhang, Z., Han, D., Chen, L., Yu, Y., et al. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2025.09.008 · Cited by 3

Crosstalk between acetylation modification and autophagy in cancer: roles, mechanisms, and therapeutic potential

Liu, Y., Yan, Z., Fu, Z., Wu, X., Wang, F., & Yuan, Y. (2025) · Cell Death Discovery · doi:10.1038/s41420-025-02809-x · Cited by 3

The Roles of Caloric Restriction Mimetics in Central Nervous System Demyelination and Remyelination

Kaffe, D., Kaplanis, S. I., & Karagogeos, D. (2023) · Current Issues in Molecular Biology · doi:10.3390/cimb45120596 · Cited by 4

Hydroxycitrate-loaded exosomes demonstrate enhanced therapeutic efficacy against lung adenocarcinoma by inhibiting the metabolic enzyme ATP citrate lyase

Phutela, K., Bal, A., Singh, N., & Sharma, S. (2025) · Nanoscale Advances · doi:10.1039/d5na00094g · Cited by 3

Mitochondrial modulators

Naumova, N., Koliada, A. K., Kuzub, N., & Vaiserman, A. M. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-823679-6.00012-6 · Cited by 3

Calorie Restriction Mimetics From Functional Foods

Sun, W. Y., & Wang, Y. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805376-8.00022-8 · Cited by 3

Autophagie et système cardiovasculaire

Kheloufi, M., Rautou, P., & Boulanger, C. M. (2017) · médecine/sciences · doi:10.1051/medsci/20173303015 · Cited by 4

Starvation and Climate Change—How to Constrain Cancer Cell Epigenetic Diversity and Adaptability to Enhance Treatment Efficacy

Gregg, C. J. (2021) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2021.693781 · Cited by 4

A mechanistic perspective on the health promoting effects of alcohol – A focus on epigenetics modification

Guan, S. P., Kumar, S. N., Fann, D. Y., & Kennedy, B. K. (2022) · Alcohol · doi:10.1016/j.alcohol.2022.07.009 · Cited by 3

Methionine coordinates a hierarchically organized anabolic program enabling proliferationPreprint

Walvekar, A. S., Srinivasan, R., Gupta, R., & Laxman, S. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/249367 · Cited by 3

High-fat diet intake modulates maternal intestinal adaptations to pregnancy, and results in placental hypoxia and impaired fetal gut developmentPreprint

Gohir, W., Kennedy, K. M., Wallace, J. G., Saoi, M., Bellissimo, C. J., Britz‐McKibbin, P., Petrik, J., Surette, M. G., & Sloboda, D. M. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/436816 · Cited by 3

Polyamines and autophagy as a dynamic regulatory network in skeletal muscle regeneration and aging

Attili, L., Rossi, M. N., Santo, R. D., Duranti, G., Ceci, R., & Cervelli, M. (2026) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2026.112188 · Cited by 3

Delineating the role of autophagy in driving the resistance to cancer chemotherapy

Shantanu, P. A., Syamprasad, N. P., Rajdev, B., Gawali, B., Kumar, A., Rahman, T., & Naidu, V. G. M. (2021) · Annals of Oncology Research and Therapy · doi:10.4103/aort.aort_26_21 · Cited by 2

A big picture of the mitochondria-mediated signals: From mitochondria to organism

Acar, N. V., & Özgül, R. K. (2023) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2023.08.032 · Cited by 2

Involvement of transcriptional co-activator p300 in upregulated expression of HSP70 by aquareovirus non-structural protein NS31

Yu, F., Hu, G., Xu, J., Song, S., Zhao, Z., & Lu, L. (2023) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2023.105077 · Cited by 2

Acetylation of microtubule-binding PinX1 orchestrates ribosome biogenesis to nutrient starvation via the RNA polymerase I preinitiation complex

Lü, G., Yang, L., Zhang, Q., Zhang, S., Xiong, Y., Li, T., Zhang, Y. L., Liu, M., Zhang, Y., Wu, J., et al. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.110465 · Cited by 2

Vascular endothelial growth factor blockade elicits a stable metabolic shift in tumor cells: therapeutic implications

Indraccolo, S. (2015) · Molecular & Cellular Oncology · doi:10.1080/23723556.2015.1008307 · Cited by 2

Regulation of Macroautophagy by Nutrients and Metabolites

Lorin, S., Pattingre, S., Meijer, A. J., & Codogno, P. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802167-5.00014-1 · Cited by 2

Role of Autophagy in Cancer Metabolism

Cheong, H. (2016) · InTech eBooks · doi:10.5772/64025 · Cited by 2

Heterogeneous cellular effects of α-ketoglutarate esters

Galluzzi, L. (2019) · Aging · doi:10.18632/aging.102028 · Cited by 2

Pathogenic hyperactivation of mTORC1 by cytoplasmic EP300 in Hutchinson-Gilford progeria syndrome

Ferret, L., Kroemer, G., & Djavaheri‐Mergny, M. (2024) · Cell Stress · doi:10.15698/cst2024.04.295 · Cited by 2

Transcription factor EP300 targets SIRT5 to promote autophagy of nucleus pulposus cells and attenuate intervertebral disc degeneration

Liu, X., Huang, S., Xu, P., Xu, H.-W., Wang, D., & Wang, S.-J. (2025) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2025.119933 · Cited by 2

The Role of Autophagy during Nontuberculous Mycobacterial Infection

Kim, Y. J., Sapkota, A., Lee, B., Park, E., & Jo, E. (2025) · Journal of Bacteriology and Virology · doi:10.4167/jbv.2025.55.3.205 · Cited by 1

MCD enzyme deficiency drives early mortality and multiorgan metabolic disruption in Dahl salt-sensitive rats

Kravtsova, O., Tan, Y., Levchenko, V., Kovalenko, E., Tiwari, R., Zietara, A. P., Bohovyk, R., Dissanayake, L. V., Van, T., Sharp, T. E., et al. (2025) · iScience · doi:10.1016/j.isci.2025.114505 · Cited by 1

Fueling Disease: ACSS2 in Obesity‐Associated Metabolic Disorders and Cancer Progression

Chen, L., Wang, Y., & Yang, J. (2026) · Obesity Reviews · doi:10.1111/obr.70096 · Cited by 1

Adaptive crosstalk between polyamine metabolism, translation, and autophagy sustains energy homeostasis in mammals during starvation: a scoping review

Karimi, K., Roberts, S. C., Carter, N. S., Hofer, S. J., & Karimi, R. (2026) · Amino Acids · doi:10.1007/s00726-026-03512-6 · Cited by 1

The Temporal Architecture of Human Cells: Organelle Clocks and Distributed Circadian Time

Bautista, J., & López‐Cortés, A. (2026) · BioEssays · doi:10.1002/bies.70157 · Cited by 2

Metabolic danger signals: TCA cycle metabolites regulate immunity and disease

Ryan, T. A. J., & Zanoni, I. (2026) · Cell chemical biology · doi:10.1016/j.chembiol.2026.07.004 · Cited by 1

Cardiac Autophagy and Its Regulation by Reversible Protein Acetylation

Xie, M., & Hill, J. A. (2016) · Cardiac and vascular biology · doi:10.1007/978-3-319-41457-7_10 · Cited by 1

Spermidine and its role in inducing autophagy in cardiac muscle to prevent cardiac dysfunction

Hassan, I., & Mirbahai, L. (2020) · Reinvention an International Journal of Undergraduate Research · doi:10.31273/reinvention.v13i1.519 · Cited by 1

Linking Cellular Metabolism to Epigenetics in Melanoma

Guo, W., & Li, C. (2021) · International Journal of Dermatology and Venereology · doi:10.1097/jd9.0000000000000191 · Cited by 1

Molecular dynamics of autophagy in cancer metabolism

Pandey, R., Kanwar, J. R., Kumar, D., Gupta, V. K., & Kumar, A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-99879-6.00005-5 · Cited by 1

“Diet and Exercise Will Help You Live Longer”: The Meme that Turns on Housekeeping Genes

Escobar, K. A., Visconti, L. M., Wallace, A., & VanDusseldorp, T. A. (2019) · Advances in Geriatric Medicine and Research · doi:10.20900/agmr20200002 · Cited by 2

De novo lipogenesis fuels adipocyte autophagosome membrane dynamicsPreprint

Rowland, L. A., Guilherme, A., Henriques, F. D. S., DiMarzio, C., Wetoska, N., Kelly, M., Reddig, K. R., Hendricks, G. M., Pan, M., Han, X., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.25.493413 · Cited by 1

Mechanisms and Dynamics of Protein Acetylation in

Baeza, M., Smallegan, M. J., & Denu, J. M. (2016)

Rerouting 'coenzyme A' biosynthesis

Srinivasan, B. (2015) · University of Groningen research database (University of Groningen / Centre for Information Technology)

A metabolic master regulator of autophagy and longevity

Schroeder, S., Pendl, T., Zimmermann, A., Eisenberg, T., Carmona‐Gutiérrez, D., Ruckenstuhl, C., Mariño, G., Pietrocola, F., Harger, A., Magnes, C., et al. (2014)

Metabolomics in Assessment of Nutritional Status

Hanhineva, K. (2017) · Wiley eBooks · doi:10.1002/9781119105916.ch5

Role of human arylamine n-acetyltransferase 1 in tumorigenesis and cancer biology.

Stepp, M. W. (2017) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/2862

Verdauung und Darmerkrankungen

Fegerl, S. P., Sartor, H., & Witasek, A. (2019) · Springer eBooks · doi:10.1007/978-3-662-58111-7_6

A systems chemoproteomic analysis of acyl-CoA/protein interaction networksPreprint

Levy, M. J., Montgomery, D. C., Sardiu, M. E., Bergholtz, S. E., Nance, K. D., Montano, J., Thorpe, A. L., Fox, S. D., Lin, Q., Andresson, T., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/665281

Diagnostik und Therapie nach F. X. Mayr

Fegerl, S. P., & Witasek, A. (2019) · Springer eBooks · doi:10.1007/978-3-662-48879-9_22

Avaliação da via autofágica no parasito Schistosoma mansoni: uma abordagem por bioinformática e microscopia

Bastos, J. A. (2018) · doi:10.14393/ufu.di.2019.362

Dependence of the Viability of Ras-Expressing Cells on Damage to Mitochondria Caused by Antitumor Agents

Kochetkova, E. Y., Blinova, G. I., Boytsov, A., Поспелов, В. А., & Pospelova, T. V. (2020) · Cell and Tissue Biology · doi:10.1134/s1990519x20060061

Diet’s impact dictated by synonymous mitochondrial SNP interacting with nucleotypePreprint

Dobson, A. J., Voigt, S., Kumpitsch, L., Langer, L., Voigt, E., Ibrahim, R., Dowling, D. K., & Reinhardt, K. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.07.434274

Metabolic aspects of canonical versus noncanonical autophagy

Castoldi, F., & Pietrocola, F. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820538-9.00001-6

Autophagy and aging

Escobar, K. A., & VanDusseldorp, T. A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-817990-1.00050-0

Creating a bottleneck: Robust LC3B lipidation analysis by adjusting autophagic flux with low concentrations of Bafilomycin A1Preprint

Liebl, M. P., Meister, S. C., Frey, L., Hendrich, K., Klemmer, A., Pohl, C., & Lakics, V. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.12.452036

Dysregulated myogenesis and autophagy in genetically induced pulmonary emphysemaPreprint

Balnis, J., Drake, L. A., Singer, D. V., Vincent, C. E., Korponay, T. C., D'Armiento, J. M., Lee, C. G., Elias, J. A., Singer, H. A., & Jaitovich, A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.08.450201

Untersuchungen zur Bedeutung des mitochondrialen CLPXP-Komplexes für den Energie-Metabolismus von Podospora anserina

Heinz, D. (2021) · Publication Server of Goethe University Frankfurt am Main (Goethe University Frankfurt) · doi:10.21248/gups.65210

Advances in the Regulation of Autophagy

夏, 丹. (2019) · Advances in Clinical Medicine · doi:10.12677/acm.2019.93027

Faculty Opinions recommendation of Leucine Signals to mTORC1 via Its Metabolite Acetyl-Coenzyme A.

Bogan, J. S. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733953691.793554906

Faculty Opinions recommendation of Mechanisms and dynamics of protein acetylation in mitochondria.

Ji, L. L. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.726108102.793564356

Identification and characterisation of potent anti-MRSA phloroglucinol derivatives of Dryopteris crassirhizoma NakaiPreprint

Bhowmick, S., Beckmann, M., Shen, J., & Mur, L. A. J. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.23.493049

Spermidine activates authophagy but does not rescue human neuroblastoma SH-SY5Y cells from effects of arginine starvation

Nishtuk, Y. V., Stasyk, O. V., & Stasyk, O. G. (2022) · Studia Biologica · doi:10.30970/sbi.1603.691

Mechanism for Suppressing Visceral Fat Accumulation of Resveratrol

Yanai, T. (2018) · JOURNAL OF THE BREWING SOCIETY OF JAPAN · doi:10.6013/jbrewsocjapan.113.2

Rhapontigenin Improves Non-alcoholic Fatty Liver Disease by Inducing Lipophagy Through the ACOX1 and mTOR/ULK1 Pathways

Wang, Y.-X., Ke, X.-G., Wang, C., Peng, K., Wu, H., & Yang, Y. (2023) · Pharmacognosy Magazine · doi:10.1177/09731296231197299

The anti-cancer transition-state inhibitor MTDIA inhibits human MTAP, inducing autophagy in humanized yeast

Coorey, N., Tollestrup, I., Bircham, P. W., Sheridan, J. P., Evans, G. B., Schramm, V. L., Atkinson, P. H., & Munkacsi, A. B. (2025) · Disease Models & Mechanisms · doi:10.1242/dmm.052173

Shengyang Sanhuo Decoction and Disassembled Prescriptions Improve Chronic Fatigue Syndrome in Mice: Insights from Lipid MetabolismPreprint

Li, L.-L., Zhang, Y., Fu, Y., Jiang, H., Zhang, X., Yin, T., Li, X., Ren, Q., & Lu, Y. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5371522

Ketone Body Supplementation Upon a Standard High-Carbohydrate Diet Induces Autophagy-Mediated Developmental Delay in Drosophila Melanogaster Larvae

Becher, M. L., Zhai, F., Gilbert, M. L., Mota, D. I., Griffiths, L. A., Pierre, M., Athreya, A. R., Boyd, F. S., Cameron, A. M., Cameron, M. R., et al. (2024) · Developmental Biology · doi:10.1016/j.ydbio.2025.07.020

Eat, Heal, Repeat: How zebrafish master regeneration

Pérez-Montes, C., Lavado-Fernández, E., Martínez-Rojo, I., Santos-Ledo, A., & García-Macia, M. (2025) · International review of cytology · doi:10.1016/bs.ircmb.2025.10.008

Additional file 1 of Unstructured regions of large enzymatic complexes control the availability of metabolites with signaling functions

Skalidis, I., Tüting, C., & Kastritis, P. L. (2020) · Figshare · doi:10.6084/m9.figshare.12864899

Additional file 3 of Post-translational regulation of autophagy is involved in intra-microbiome suppression of fungal pathogens

Wang, J., Xu, C., Sun, Q., Xu, J., Chai, Y., Berg, G., Cernava, T., Ma, Z., & Chen, Y. (2021) · Figshare · doi:10.6084/m9.figshare.14741192

Additional file 2 of Post-translational regulation of autophagy is involved in intra-microbiome suppression of fungal pathogens

Wang, J., Xu, C., Sun, Q., Xu, J., Chai, Y., Berg, G., Cernava, T., Ma, Z., & Chen, Y. (2021) · Figshare · doi:10.6084/m9.figshare.14741189

ATG4D loss leads to late-onset cardiomyopathy and stress-induced heart failure in mice, and its repression marks maladaptive cardiac remodeling in humansPreprint

Mariño, G., Tamargo‐Gómez, I., García, R., Martínez-García, G. G., Suárez, M. F., Cimadevilla, O. C. F., Caravia, X. M., Pérez, R. F., Rey, V., Calvo, M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.29.678527

Epigenetic modifications and aging: intermittent fasting as a catalyst for positive epigenetic changes

Sharma, B., Negi, R., Jain, S., Chaudhury, S., & Singh, P. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-30060-8.00011-x · Cited by 1

Disruption of zinc homeostasis reduces histone acetylation levels in normal and tumor cells

Xu, S., Hu, Y., Tang, C., & Xu, W. (2026) · Scientific Reports · doi:10.1038/s41598-026-35270-6

Metabolic axis of autophagy: A key player in tumor maintenance and opportunities for therapeutic exploitation

Garg, M. (2026) · World Journal of Clinical Oncology · doi:10.5306/wjco.v17.i3.115094

Regulation of Autophagy by Acetyl Coenzime A : From the Mechanisms to a Revised Definition of Caloric Restriction Mimetics

Pietrocola, F. (2015) · theses.fr (ABES) · doi:10.70675/42d6808dzc206z4e0fzb806z29f806b2f781 · Cited by 1

Obésité et méta-inflammation : rôle du système lysosomal-autophagique et des protéines associées

Soussi, H. (2016) · theses.fr (ABES) · doi:10.70675/77e61e80zde3cz4030z95f1z194698d236d8

Vanin-1 et la réponse mésenchymateuse à un stress inflammatoire ou tumoral

Giessner, C. (2015) · theses.fr (ABES) · doi:10.70675/ad91f126zab69z4befzb47bz6ebe23e41f19

Role of Chloride in Modulating Autophagy : Cystic Fibrosis as a Disease Model

Zhang, S. (2018) · theses.fr (ABES) · doi:10.70675/aade8b2ez4194z4addza263z0496a36afc12

A proteomic approach for understanding the metabolic adaptations in non-small cell lung cancer

Martín-Bernabé, A. (2018) · theses.fr (ABES) · doi:10.70675/426e7b40z057az4326z8cfez7da3a5c12c7e

Aspirin recapitulates features of caloric restriction

Castoldi, F. (2018) · theses.fr (ABES) · doi:10.70675/02f5de46z9573z4f0dz9b29z3fa5274e9088

Modulation de l'autophagie neuronale par la sérine protéase tPA en conditions ischémiques

Thiebaut, A. M. (2019) · theses.fr (ABES) · doi:10.70675/6586c0abz9e4cz455fz95ffzc52ec76397f8

Bénéfice des modulateurs métaboliques en combinaison aux chimio-immunothérapies anticancéreuses

Lévesque, S. (2019) · doi:10.70675/db466876zeec8z4537za0e0zc0f1fa485cea

Functional characterisation of Drosophila M1BP

Barthez, M. (2019) · theses.fr (ABES) · doi:10.70675/38635cdczfedaz4361zb0a3z7b6850e707ed

Biochemical characterization of mTORC1 regulation by glutamine metabolism

Bodineau, C. (2020) · theses.fr (ABES) · doi:10.70675/9d5aaabdz81bdz4118zb3edze237bdd8dee0

Autophagy mediates the hormonal regulation of neuronal homeostasis and brain aging

Rivagorda, M. (2021) · theses.fr (ABES) · doi:10.70675/e4cd7313zfed5z4ebezb547z9b4557da55e6

Metabolic Roles of Acyl Coenzyme A-Binding Protein (ACBP)/Diazepam Binding Inhibitor (DBI)

Joseph, A. (2021) · theses.fr (ABES) · doi:10.70675/b045685ezd444z4b46zb0f9z0e726ceac466

Biochemical, biophysical and structural study of proteins associated to human diseases : tcDAC2 and ADAT complex

Ramos‐Morales, E. (2021) · theses.fr (ABES) · doi:10.70675/c6b28473zf6b6z4024z99bfz05629f0484d7

Le métabolisme de l'inflammation dans les maladies microcristallines

Pham, C. N. (2024) · theses.fr (ABES) · doi:10.70675/f0753276z83c0z49a8zaacfz19b5d72e5627

Inflammaging: Immune–Metabolic Crosstalk Between the Prostate–Testis and Musculoskeletal System

Bossio, S., Russa, D. L., Rago, V., Dio, M. D., Aversa, A., & Perri, A. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27083612 · Cited by 1

Inhibition of the mitochondrial pyruvate carrier attenuates the integrated stress response activation in a cellular model of Huntington’s disease

Oliveira, Â. Z., Almeida, L. M., Oliveira, J. M. A., & Pinho, B. R. (2026) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-026-05573-3

Research progress on spermidine for the amelioration of metabolic diseases

Shuang-Bin, W. A. N. G., Rui-Ze, A. I., Zhang, Y.-J., HUANG, Q.-C., Xiao-Xia, F. A. N., & Le-Le, J. I. (2026) · Shengming kexue · doi:10.3724/cbls.2026049

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Transcriptomic and epigenetic characterization of paraventricular thalamic nucleus neurons in Polg1 mutant mice

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PolyCore, a bimodal peritoneal dialysis solution based on xylitol, L-carnitine, and icodextrin: In vitro evidence of the peritoneal membrane protection, rationale, and design of the phase II pilot study EXCITE

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The polycentric aging framework: epigenetic regulation as a dominant lifespan-limiting center in human aging

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Revisiting Inherited Metabolic Diseases ( IMDs ) Through the Lens of Selective Autophagy

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Nutrients and Their Role in Autophagy Regulation

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Regulation of Autophagy by Acetyl Coenzime A : From the Mechanisms to a Revised Definition of Caloric Restriction Mimetics

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Acetyl-coenzyme A

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Nucleocytosolic depletion of the energy metabolite acetyl-coenzyme a stimulates autophagy and prolongs lifespan

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