mTORC1 Controls Mitochondrial Activity and Biogenesis through 4E-BP-Dependent Translational Regulation

Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation

Vander Heiden, M. G., Cantley, L. C., & Thompson, C. B. (2009) · Science · doi:10.1126/science.1160809 · Cited by 16,197

Bioconductor: open software development for computational biology and bioinformatics

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mTOR Signaling in Growth Control and Disease

Laplante, M., & Sabatini, D. M. (2012) · Cell · doi:10.1016/j.cell.2012.03.017 · Cited by 8,509

Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex

Sarbassov, D. D., Guertin, D. A., Ali, S. M., & Sabatini, D. M. (2005) · Science · doi:10.1126/science.1106148 · Cited by 6,216

mTOR: from growth signal integration to cancer, diabetes and ageing

Zoncu, R., Efeyan, A., & Sabatini, D. M. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3025 · Cited by 3,941

Metabolic Reprogramming: A Cancer Hallmark Even Warburg Did Not Anticipate

Ward, P. S., & Thompson, C. B. (2012) · Cancer Cell · doi:10.1016/j.ccr.2012.02.014 · Cited by 3,233

mTOR Interacts with Raptor to Form a Nutrient-Sensitive Complex that Signals to the Cell Growth Machinery

Kim, D., Sarbassov, D. D., Ali, S. M., King, J. E., Latek, R. R., Erdjument‐Bromage, H., Tempst, P., & Sabatini, D. M. (2002) · Cell · doi:10.1016/s0092-8674(02)00808-5 · Cited by 3,051

Rictor, a Novel Binding Partner of mTOR, Defines a Rapamycin-Insensitive and Raptor-Independent Pathway that Regulates the Cytoskeleton

Sarbassov, D. D., Ali, S. M., Kim, D.-H., Guertin, D. A., Latek, R. R., Erdjument-Bromage, H., Tempst, P., & Sabatini, D. M. (2004) · Current Biology · doi:10.1016/j.cub.2004.06.054 · Cited by 2,665

Mammalian TOR complex 2 controls the actin cytoskeleton and is rapamycin insensitive

Jacinto, E., Loewith, R., Schmidt, A., Lin, S., Rüegg, M. A., Hall, A., & Hall, M. N. (2004) · Nature Cell Biology · doi:10.1038/ncb1183 · Cited by 2,097

Cellular energy utilization and molecular origin of standard metabolic rate in mammals

Rolfe, D. F., & Brown, G. C. (1997) · Physiological Reviews · doi:10.1152/physrev.1997.77.3.731 · Cited by 2,021

RNA‐Binding Proteins: Function, Biological Mechanisms, and Therapeutic Opportunities

Li, L., Yan, X., Ji, Q., & Zhang, H. (2026) · MedComm · doi:10.1002/mco2.70938 · Cited by 1

Stress Response of Nutrient-Starved Cardiovascular Cells

Pulakat, L., & Gavini, M. P. (2019) · Springer eBooks · doi:10.1007/978-3-319-55387-0_23 · Cited by 1

The accelerated organ senescence and proteotoxicity in thyrotoxicosis mice

Qin, F., Xia, W., Feng, Z., Tan, Y., Zhang, Y., Liu, D., & Zhang, G. (2023) · Journal of Cellular Physiology · doi:10.1002/jcp.31108 · Cited by 1

Impaired Mitochondrial Function and Marrow Failure in Patients Carrying a Variant of the SRSF4 Gene

Miano, M., Bertola, N., Grossi, A., Dell’Orso, G., Regis, S., Rusmini, M., Uva, P., Vozzi, D., Fioredda, F., Palmisani, E., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25042083 · Cited by 1

mTOR-related linc-PMB promotes mitochondrial biogenesis via stabilizing SIRT1 mRNA through binding to the HuR protein

Chen, Q., Zhang, H., Wang, D., Liao, W., Liu, Y., Cai, Y., Wang, S., & Yu, M. (2024) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2024236 · Cited by 2

Integration of transcriptome and immunophenotyping data highlights differences in the pathogenetic kinetics of B cells across immune-mediated disease

Izuka, S., Komai, T., Itamiya, T., Ota, M., Yamada, S., Nagafuchi, Y., Shoda, H., Matsuki, K., Yamamoto, K., Okamura, T., et al. (2025) · RMD Open · doi:10.1136/rmdopen-2024-005310 · Cited by 1

The PI3K-mTOR Pathway

Thomas, H. E., Veiga, S. R., Thomas, G., & Kozma, S. C. (2015) · Springer eBooks · doi:10.1007/978-2-8178-0492-7_2 · Cited by 1

Eukaryotic initiation factor 4E binding protein family members are widely expressed in fish tissues: Cloning and distribution of 4E-BPs in Schizothorax prenanti

Lin, F., Yuan, D., Chen, D., & Li, Z. (2016) · Agri Gene · doi:10.1016/j.aggene.2016.10.001 · Cited by 1

Mechanistic Target of Rapamycin

McKee-Muir, O. C., & Russell, R. C. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-812146-7.00009-3 · Cited by 2

Mitochondrial protease and human disease

Binjiao, Z., Zhang, Y., Yang, J., & Lü, B. (2023) · Scientia Sinica Vitae · doi:10.1360/ssv-2023-0102 · Cited by 1

Geração de linhagens celulares HEK293 knockdown para as proteínas p53, ATM, mTOR e PGC1α e estudo do papel de p53 na resposta ao estresse oxidativo provocado por azul de metileno

Dias, G. C. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.46.2014.tde-29042014-143702 · Cited by 1

Nutrient-induced Mitochondrial Activation (NiMA): A Novel Lysosome-to-Mitochondria Signaling Pathway Disrupted by Amyloid-- OligomersPreprint

Norambuena, A., Wallrabe, H. K., Cao, R., Wang, D. B., Silva, A., Švindrych, Z., Periasamy, A., Hu, S., Kim, D. Y., Tanzi, R. E., et al. (2018) · SSRN Electronic Journal · doi:10.2139/ssrn.3188445 · Cited by 1

Study on the Role of SIRT2 in Stem Cell Aging and Chronic Inflammation

Luo, H. (2017) · eScholarship (California Digital Library) · Cited by 1

Adaptive translational pausing is a hallmark of the cellular response to severe environmental stressPreprint

Jobava, R., Mao, Y., Guan, B., Krokowski, D., Shu, E., Hu, D., Chukwurah, E., Wu, J., Gao, Z., Zagore, L. L., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.10.334375 · Cited by 1

Translational and HIF11-Dependent Metabolic Reprograming Underpin Oncometabolome Plasticity and Synergy Between Oncogenic Kinase Inhibitors and BiguanidesPreprint

Hulea, L., Gravel, S., Morita, M., Cargnello, M., Uchenunu, O., Im, Y. K., McLaughlan, S., Larsson, O. S., Ohh, M., Ferreira, T., et al. (2018) · SSRN Electronic Journal · doi:10.2139/ssrn.3155732 · Cited by 1

Adipose mitochondrial metabolism controls body growth by modulating cytokine and insulin signalingPreprint

Sriskanthadevan-Pirahas, S., Turingan, M. J., Chahal, J. S., Thorson, E., & Grewal, S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.04.12.439566 · Cited by 1

Esrra regulates Rplp1-mediated translation of lysosome proteins suppressed in non-alcoholic steatohepatitis and reversed by alternate day fastingPreprint

Tripathi, M., Gauthier, K. C., Sandireddy, R., Zhou, J., Gupta, P. S., Sakthivel, S., Teo, W. W., Naing, Y. T., Arul, K., Tikno, K., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.16.468891 · Cited by 1

Overexpression of TPT1-AS1 and SAMMSON and down expression of LINC00961 associated with Advanced Grades of Gastric CancerPreprint

Amini, M. A., Karimi, J., Khodadadi, I., Tavilani, H., Talebi, S. S., & Afshar, B. (2020) · doi:10.21203/rs.3.rs-22694/v1 · Cited by 1

B/T cell crosstalk and aberrant inflammatory IgG exacerbate autoimmune intestinal inflammationPreprint

Gadjalova, I., Heinze, J. M., Goess, M. C., Hofmann, J. I., Albers, J. J., Spallek, R., Blissenbach, B., Buck, A., Weber, M.-C., Scherer, E., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.12.507066 · Cited by 1

TREM2 Alteration Increases AD Biomarkers and is Associated with Key Genes with 5xFAD Mice Model Analysis on MODEL-AD DatabasePreprint

Budyak, E. I., Kwon, J., Messenger, E. J., Maharjan, S., & Koothur, J. J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.06.552135 · Cited by 1

mTOR Modulation Induces Selective Perturbations in Histone Methylation Which Influence the Anti-Proliferative Effects of mTOR InhibitorsPreprint

Kim, H., Lebeau, B., Papadopoli, D. J., Jovanović, P., Russo, M. D. S. T., Avizonis, D. Z., Morita, M., Afzali, F., Ursini‐Siegel, J., Postovit, L.-M. M., et al. (2023) · SSRN Electronic Journal · doi:10.2139/ssrn.4631549 · Cited by 1

AFG3L2-mediated proteolysis restricts mitochondrial biogenesis and gene expression in hypoxiaPreprint

Chandragiri, S., Grotehans, N., Lasarzewski, Y., Patrón, M., MacVicar, T., Ohba, Y., Hermans, S., Rugarli, E. I., Nolte, H., & Langer, T. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.27.615438 · Cited by 1

Cortical organoids reveal human-specific roles of METTL5 in neurodevelopment via regulation of CHCHD2Preprint

Turkalj, E. M., Kuljanishvili, M., Kang, G., Liu, I., Ghent, C. M., Soriano, C. W., Keyhanvar, N., Brody, D., Oldham, M., & Vissers, C. B. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.13.664555 · Cited by 1

Nutrient/TOR signaling controls Mitochondrial transcription factor A (TFAM) to regulate organismal growth in DrosophilaPreprint

Sriskanthadevan-Pirahas, S., Sharma, A., Khan, S., & Grewal, S. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.08.693086 · Cited by 1

Enhanced mTORC1 signaling and Protein Synthesis in Parkinson’s Disease Pathogenesis Disease Pathogenesis

Khan, M. R., Yin, X., Kang, S.-U., Mitra, J., Wang, H., Brahmachari, S., Karuppagounder, S. S., Kimura, Y., Jhaldiyal, A., Kim, H. H., et al. (2022) · doi:10.1101/2022.10.03.510455

Mitochondrial ETF insufficiency drives neoplastic growth by selectively optimizing cancer bioenergetics

Papadopoli, D., Palia, R., Jovanovic, P., Tabariès, S., Ciccolini, E., Sabourin, V., Igelmann, S., McLaughlan, S., Zhan, L., Kim, H., et al. (2026) · eLife · doi:10.7554/elife.106587.3 · Cited by 1

Canagliflozin Potently Activates AMPK and Inhibits the Growth and Survival of Cancer Cells

Villani, L. A. (2015) · MacSphere (McMaster University) · doi:10.71548/8610

Metabolic Peculiarities of the Stem Cell Entity

Ivanović, Z., & Vlaski‐Lafarge, M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800540-8.00006-5

Life on the Edge: Determinants of Selective Neuronal Vulnerability in Parkinson’s Disease

Surmeier, D. J., Zampese, E., Galtieri, D. J., & Schumacker, P. T. (2016) · Springer eBooks · doi:10.1007/978-3-319-28637-2_6

MASTER 2 « SCIENCES, TECHNOLOGIES, SANTE » MENTION « NUTRITION ET SCIENCES DES ALIMENTS » (NSA )

Lyon, V., Attaix, D., & Bruhat, A. (2015)

Flawed Phospholipid Formation or Faulty Fatty Acid Oxidation: Determining the Cause of Mitochondrial Dysfunction in Hearts Lacking ACSL1

Grevengoed, T. J. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/g7gj-eb34

mTOR: Pumping Nutrients into Tubules

Inoki, K. (2016) · Journal of the American Society of Nephrology · doi:10.1681/asn.2016080924

Role of Occludin in the Regulation of Epithelial Tight Junctions

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

A ativação constitutiva de mTORC1 em adipócitos aumenta a capacidade oxidativa mitocondrial e reduz a adiposidade visceral em camundongos.

Magdalon, J. (2017) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2017.tde-19012017-155521

VIRAL REGULATION OF CAP-DEPENDENT MESSENGER RNA TRANSLATION INHIBITOR 4E-BP1 DURING MITOSIS

Velásquez, C. (2017) · D-Scholarship@Pitt (University of Pittsburgh)

Stress Response of Nutrient-Starved Cardiovascular Cells

Pulakat, L., & Gavini, M. P. (2017) · Springer eBooks · doi:10.1007/978-3-319-40007-5_23-1

Exercise preconditioning and TFAM overexpression diminish skeletal muscle atrophy.

Theilen, N. T. (2018) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/2986 · Cited by 1

Molecular Mechanisms of Postmeal Regulation of Muscle Anabolism

Bacquer, O. L. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-810422-4.00003-8

Identificação de vias moduladas por microRNAs na diferenciação celular e manutenção da pluripotência em células humanas

Lima, I. M. D. S. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.17.2018.tde-17042018-154038

Could Antibiotics Be Therapeutic Agents in Alzheimer’s Disease?

Gómez, O., Pintado, C., Rodríguez-Pérez, M., & Burgos‐Ramos, E. (2019) · Frontiers in clinical drug research. Alzheimer disorders · doi:10.2174/9789811401893119080005

mTOR under stress

Heberle, A. M. (2019) · University of Groningen research database (University of Groningen / Centre for Information Technology)

Lysosomal and mitochondrial crosstalk: the role of lysosomal signaling on mitochondrial biogenesis and function

Yambire, K. F. (2018) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7142

Metabolic reprogramming supports microglial survival and immune function

York, E. M. (2021) · cIRcle (University of British Columbia) · doi:10.14288/1.0379730

Potentiating Immune Cells Function During Inflammation and Virus Infection by Modulating Metabolism

Almutairi, S. M. (2020) · uO Research (University of Ottawa) · doi:10.20381/ruor-24391

Mitochondria Controlled mTORC1 Activation Compartmentalizes Translation Initiation Factor eIF4E to Augment Intracellular Trafficking and Extracellular Export of miRNA in Mammalian CellsPreprint

Chatterjee, S., Chakrabarty, Y., Banerjee, S., Ghosh, S., & Bhattacharyya, S. (2020) · bioRxiv · doi:10.1101/2020.05.20.105601

Tissue-specific Stem Cells

Patra, S. S. (2020) · doi:10.37421/2168-9547.2020.09.250

Tumor metabolic reprogramming in therapeutic resistance

Siegel, P. M., & Ursini‐Siegel, J. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821310-0.00005-x · Cited by 1

Up-Regulation of TPT1-AS1 and SAMMSON and Down-Regulation of LINC00961 Long Non-Coding RNAs (lncRNAs) as Potential Tumor Markers in Gastric Cancer

Amini, M. A., Khodadadi, I., Tayebinia, H., Talebi, S. S., Afshar, B., & Karimi, J. (2021) · مجله پزشکی بالینی ابن سینا · doi:10.52547/ajcm.27.4.201

MITOCHONDRIAL DISEASE THERAPY

Khajuria, K., Khajuria, V., & Sawhney, V. (2021) · Asian Journal of Pharmaceutical and Clinical Research · doi:10.22159/ajpcr.2021.v14i5.41046

mTORC2 is the Primary Target for Simvastatin-Associated Toxicity in C2C12 Cells and in Mouse Skeletal MusclePreprint

Sanvee, G. M., Hitzfeld, L., Bouitbir, J., & Krähenbühl, S. (2021) · Research Square · doi:10.21203/rs.3.rs-565395/v1

Regulation | mTOR and its Substrates

Proud, C. G., & Xie, J. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819460-7.00001-3

Proteome dynamics under proteotoxic stress and disease

Klann, K. (2021) · Publication Server of Goethe University Frankfurt am Main (Goethe University Frankfurt) · doi:10.21248/gups.60905

The impact of the integrated stress response on DNA replication

Choo, J. A. M. Y. (2020) · doi:10.53846/goediss-7917

Environmental Signaling through the Target of Rapamycin Complex 1 (TORC1) and the Regulation of Epigenetic Mechanisms

Workman, J. (2016) · doi:10.21007/etd.cghs.2016.0577

Faculty Opinions recommendation of A novel lysosome-to-mitochondria signaling pathway disrupted by amyloid-β oligomers.

Nairn, A. C., & Leslie, S. N. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734280180.793553827

Faculty Opinions recommendation of Prosapip1-Dependent Synaptic Adaptations in the Nucleus Accumbens Drive Alcohol Intake, Seeking, and Reward.

Russo, S. J., & Han, M. (2017) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.731077746.793537883

mGluR5 Modulation as a Treatment for Parkinson’s Disease

Farmer, K. (2018) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2018-14442

Faculty Opinions recommendation of Somatic mutations in early metazoan genes disrupt regulatory links between unicellular and multicellular genes in cancer.

Clairambault, J. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735161470.793575404

EIF4A inhibition targets bioenergetic homeostasis in AML and synergizes with cytarabine and venetoclaxPreprint

Fooks, K., Galicia-Vázquez, G., Schcolnik‐Cabrera, A., Gife, V., Nouhi, Z., Poon, W. W. L., Luo, V. M., Aloyz, R. S., Orthwein, A., Hulea, L., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1696855/v1

mTORC1: Upstream and Downstream

Yao, Y., & Inoki, K. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00182-6

Early-Onset Diabetes Mellitus in Chromosome 8p11.2 Deletion Syndrome Combined With Becker Muscular Dystrophy - A Case Report

Cao, C., Wang, X., & Zhao, X. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.914863

mTORC2 em adipócitos é essencial para o aumento da capacidade termogênica induzida pelo frio e melhora da sensibilidade à insulina induzida pelo frio e ingestão de dieta rica em ácidos graxos ômega 3.

Castro, É. (2021) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2021.tde-14012022-182538

Wat1/mLst8, a TOR complex protein regulates mitochondrial integrity and calcium ion homeostasis in fission yeast S. pombePreprint

Anjum, S., Srivastava, S., Panigrahi, L., Ansari, U. A., Trivedi, A. K., & Ahmed, S. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.27.534337

SPTF-3/SP1 orchestrates mitochondrial biogenesis upon ribosomal stress and acute starvationPreprint

Hemerling, J. C., Pavlenko, V., Herholz, M., Baumann, L. C., Zečić, A., Kukat, A., Popović, M., Szczepanowska, K., Cores, E. C., Vílchez, D., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.18.553493 · Cited by 1

The Role of eIF2B Localisation in Cell-specific Stress Responses

Hanson, F. M. (2023) · Sheffield Hallam University · doi:10.7190/shu-thesis-00555

Translational control contribution to human neuronal gene expression

Lins, É. M. (2021) · doi:10.47749/t/unicamp.2021.1246427

Fluoxetine treatment during postnatal and juvenile temporal epochs evokes diametrically opposing changes in anxio-depressive behaviors, gene expression, mitochondrial function, and neuronal architecture in the medial prefrontal cortexPreprint

Ghai, U., Chachra, P., Fanibunda, S. E., Mendon, S., Bhaskaran, A., Sarkar, A., Kukkemane, K., Singh, V. K., & Vaidya, V. A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.29.573529

Regulation of Megalin and Clathrin-Mediated Endocytosis by Amp-Activated Protein Kinase

Leshchyshyn, N. (2024) · doi:10.32920/25234420.v1

The nutrient-sensing Rag-GTPase complex in B cells controls humoral immunity via TFEB/TFE3-dependent mitochondrial fitnessPreprint

Zhu, X., Wu, Y., Li, Y., Zhou, X., Watzlawik, J. O., Chen, Y., Raybuck, A. L., Billadeau, D. D., Shapiro, V. S., Springer, W., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.26.582122

Onco-Circuit Addiction and Onco-Nutrient mTORC1 Signaling Vulnerability in a Model of Aggressive T Cell MalignancyPreprint

Wang, X., Cornish, A. E., Do, M., Brunner, J. S., Hsu, T.-W., Xu, Z., Malik, I., Edwards, C., Capistrano, K. J., Zhang, X., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.03.587917

Rag-GTPase-TFEB/TFE3 axis controls B cell mitochondrial fitness and humoral immunity independent of mTORC1Preprint

Zeng, H., Zhu, X., Wu, Y., Li, Y., Zhou, X., Watzlawik, J. O., Chen, Y. M., Raybuck, A. L., Billadeau, D. D., Shapiro, V. S., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-3957355/v1

Structural and Dynamical Analyses of Apo and Cap-binding eIF4E: An in silico StudyPreprint

Hasegawa, K., Burzachiello, J., Connolly, L., Kementzidis, G., Niu, Z., Papadopoulos, E., Aktas, B. H., & Deng, Y. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.18.594816

Redox Regulation in Hematology and Stem Cell Research

Mushtaq, I., Hussain, K., Ishtiaq, A., & Murtaza, I. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15717-2.00114-1

Human tau promotes Warburg effect-like glycolytic metabolism under acute hyperglycemia conditions through modulating the homeostasis of protein-membrane associationPreprint

Yao, J., Fu, Z., Li, K., Zheng, J., Chen, Z., Xu, J., Lai, G., Huang, Y., Huang, J., You, G., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.20.599836

mTORC1 Signaling Inhibition Modulates Mitochondrial Function in Frataxin DeficiencyPreprint

Lehmer, M. K., & Zoncu, R. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.06.606942 · Cited by 1

Momordica charantia Extract Treatment Extends the Healthy Lifespan of Aging Mice via the Bitter Taste Receptor/mTOR Pathway

Hiramoto, K., & Oikawa, H. (2024) · Journal of Ageing and Longevity · doi:10.3390/jal4040021

The PHD3-FOXO3 axis modulates the interferon type I response in microglia aggravating Alzheimer’s disease progressionPreprint

Sánchez-García, M. A., Lara-Ureña, N., March‐Díaz, R., Luis, C. O. S., Quiñones-Cañete, S., Barba-Reyes, J. M., Cabello-Rivera, D., Muñoz-Cabello, A. M., Mora-Romero, B., Romero‐Molina, C., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.01.616066

Comprehending the Rationale for Repurposing Type 2 Diabetes Mellitus Medicines for Alzheimer's Disease Patients Via Gene Networks Studies and its Associated Molecular Pathways

Yadav, R., Mani, R. J., Kumar, A. H. S., Ahmad, S., & Katare, D. P. (2024) · Biomedical & Pharmacology Journal · doi:10.13005/bpj/2990 · Cited by 1

Association of oropharyngeal cancer recurrence with tumor-intrinsic and immune-mediated sequelae of reduced genomic instabilityPreprint

Sannigrahi, M. K., Raghav, L., Rich, D. J., Schrank, T. P., Califano, J. A., Lukens, J. N., Sun, L., Morgan, I. M., Cohen, R. B., Lin, A., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.31.621311

Mitochondrial ETF insufficiency drives neoplastic growth by selectively optimizing cancer bioenergeticsPreprint

Papadopoli, D., Palia, R., Jovanovic, P., Tabariès, S., Ciccolini, E., Sabourin, V., Igelmann, S., Mclaughlan, S., Zhan, L., Kim, H., et al. (2026) · eLife · doi:10.7554/elife.106587

Mechanism of Alcohol-Mediated CyPD Regulation in mPTP-Dependent Myocardial Injury

胡, 彬. (2025) · Advances in Clinical Medicine · doi:10.12677/acm.2025.1551560

The translational inhibitor 4EBP/Thor is required for Drosophila adaptation to hypoxia

Sorianello, E., Katz, M., Acevedo, J. M., Melani, M., Perez-Perri, J. I., & Wappner, P. (2025) · Scientific Reports · doi:10.1038/s41598-025-94457-5 · Cited by 1

Mitochondria and redox homeostasis - the backseat drivers in glioma

Patrick, S., & Sen, E. (2025) · Free Radical Research · doi:10.1080/10715762.2025.2548479

Assessing the Safety and Efficacy of Non-vitamin K Antagonist Oral Anticoagulants in Solid-Organ Transplant Recipients: A Comprehensive Analysis of a Transplant Center.

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Additional file 1 of Mitochondrial defects in the respiratory complex I contribute to impaired translational initiation via ROS and energy homeostasis in SMA motor neurons

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Additional file 2 of Ventilator-induced lung injury results in oxidative stress response and mitochondrial swelling in a mouse model

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