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

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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

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Srebf1c preserves hematopoietic stem cell function and survival as a switch of mitochondrial metabolism

Lu, Y., Zhang, Z., Wang, S., Qi, Y., Chen, F., Xu, Y., Shen, M., Chen, M., Chen, N., Yang, L., et al. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2022.01.011 · Cited by 15

Mechanistic insights into cancer drug resistance through optogenetic PI3K signaling hyperactivation

Ueda, Y., Miura, Y., Tomishige, N., Sugimoto, N., Murase, M., Kawamura, G., Sasaki, N., Ishiwata, T., & Ozawa, T. (2022) · Cell chemical biology · doi:10.1016/j.chembiol.2022.10.002 · Cited by 14

Molecular biology and novel therapeutics for IDH mutant gliomas: The new era of IDH inhibitors

Kitagawa, Y., Kobayashi, A., Cahill, D. P., Wakimoto, H., & Tanaka, S. (2024) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2024.189102 · Cited by 13

Mitochondrial translation is the primary determinant of secondary mitochondrial complex I deficiencies

Čunátová, K., Vrbacký, M., Puertas-Frias, G., Alán, L., Vanišová, M., Saucedo-Rodríguez, M. J., Houštěk, J., Fernández‐Vizarra, E., Neužil, J., Pecinová, A., et al. (2024) · iScience · doi:10.1016/j.isci.2024.110560 · Cited by 14

Unraveling the roles and mechanisms of mitochondrial translation in normal and malignant hematopoiesis

Liu, L., Shao, M., Huang, Y., Qian, P., & Huang, H. (2024) · Journal of Hematology & Oncology · doi:10.1186/s13045-024-01615-9 · Cited by 14

Stereochemical and structural effects of (2R,6R)-hydroxynorketamine on the mitochondrial metabolome in PC-12 cells

Faccio, A. T., Rupérez, F. J., Singh, N., Angulo, S., Tavares, M. F. M., Bernier, M., Barbas, C., & Wainer, I. W. (2018) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2018.03.008 · Cited by 13

Metabolomics analysis highlights Yashtimadhu (Glycyrrhiza glabra L.)‐mediated neuroprotection in a rotenone‐induced cellular model of Parkinson's disease by restoring the mTORC1‐AMPK1 axis in autophagic regulation

Karthikkeyan, G., Behera, S. K., Upadhyay, S. S., Pervaje, R., Prasad, T. S. K., & Modi, P. K. (2022) · Phytotherapy Research · doi:10.1002/ptr.7449 · Cited by 15

EIF4EBP1 is transcriptionally upregulated by MYCN and associates with poor prognosis in neuroblastoma

Voeltzke, K., Scharov, K., Funk, C. M., Kahler, A., Picard, D. J., Hauffe, L., Orth, M. F., Remke, M., Esposito, I., Kirchner, T., et al. (2022) · Cell Death Discovery · doi:10.1038/s41420-022-00963-0 · Cited by 14

CLUH controls astrin-1 expression to couple mitochondrial metabolism to cell cycle progression

Schatton, D., Pietro, G. D., Szczepanowska, K., Veronese, M., Marx, M., Braunöhler, K., Barth, E., Müller, S., Giavalisco, P., Langer, T., et al. (2022) · eLife · doi:10.7554/elife.74552 · Cited by 14

mTORC1 alters the expression of glycolytic genes by regulating KPNA2 abundances

Chen, X., Zhu, Y., Wang, Z., Zhu, H., Pan, Q., Su, S., Dong, Y., Li, L., Zhang, H., Wu, L., et al. (2016) · Journal of Proteomics · doi:10.1016/j.jprot.2016.01.021 · Cited by 15

Mitochondrial translation factors reflect coordination between organelles and cytoplasmic translation via mTOR signaling: Implication in disease

Cao, X., & Qin, Y. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.04.010 · Cited by 15

The role of mTOR-mediated signals during haemopoiesis and lineage commitment

Malik, N., Sansom, O. J., & Michie, A. M. (2018) · Biochemical Society Transactions · doi:10.1042/bst20180141 · Cited by 13

Nutrigenomics and Epigenetic Regulation in Poultry: DNA-Based Mechanisms Linking Diet to Performance and Health

Naeem, M., & Fatima, A. (2025) · DNA · doi:10.3390/dna5040060 · Cited by 13

mTORC1 Regulates the Metabolic Switch of Postnatal Cardiomyocytes During Regeneration

Paltzer, W. G., Aballo, T. J., Bae, J., Flynn, C. G. K., Wanless, K. N., Hubert, K. A., Nuttall, D. J., Perry, C., Nahlawi, R., Ge, Y., et al. (2023) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2023.12.004 · Cited by 13

The integrated stress response suppresses PINK1-dependent mitophagy by preserving mitochondrial import efficiency

Yang, M., Mo, Z., Walsh, K., Liu, W., Irahal, I. N., Arnoult, D., & Guo, X. (2026) · Nature Communications · doi:10.1038/s41467-026-71630-6 · Cited by 17

Carbon fluxes rewiring in engineered E. coli via reverse tricarboxylic acid cycle pathway under chemolithotrophic condition

Peng, J.-H., Lo, S.-C., Yu, Y.-N., Yang, Y., Chen, Y.-C., Tsai, A.-I., Wu, D.-Y., Huang, C.-H., Su, T.-T., Huang, C.-C., et al. (2025) · Journal of Biological Engineering · doi:10.1186/s13036-025-00489-w · Cited by 14

FXR1a-associated microRNP: A driver of specialized non-canonical translation in quiescent conditions

Bukhari, S. I. A., & Vasudevan, S. (2016) · RNA Biology · doi:10.1080/15476286.2016.1265197 · Cited by 14

Epilepsy in a melanocyte-lineage mTOR hyperactivation mouse model: A novel epilepsy model

Yang, F., Yang, L., Wataya‐Kaneda, M., Teng, L., & Katayama, I. (2020) · PLoS ONE · doi:10.1371/journal.pone.0228204 · Cited by 12

Novel mTORC1 Inhibitors Kill Glioblastoma Stem Cells

Sandoval, J. A., Tomilov, A. A., Datta, S., Allen, S. A., OʼDonnell, R. T., Sears, T. K., Woolard, K., Kovalskyy, D., Angelastro, J. M., & Cortopassi, G. A. (2020) · Pharmaceuticals · doi:10.3390/ph13120419 · Cited by 13

BAD regulates mammary gland morphogenesis by 4E-BP1-mediated control of localized translation in mouse and human models

Githaka, J. M., Tripathi, N., Kirschenman, R. D., Patel, N., Pandya, V., Kramer, D. A., Montpetit, R., Zhu, L. F., Sonenberg, N., Fahlman, R. P., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-23269-8 · Cited by 14

Clinical, neuroradiological, and molecular characterization of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder

Accogli, A., Lin, S., Severino, M., Kim, S.-H., Huang, K., Rocca, C., Landsverk, M., Zaki, M. S., Al-Maawali, A. A., Srinivasan, V. M., et al. (2023) · Genetics in Medicine · doi:10.1016/j.gim.2023.100938 · Cited by 14

Lysosomes as hubs of metabolic sensing and cellular homeostasis

Jain, A., & Zoncu, R. (2026) · Molecular Cell · doi:10.1016/j.molcel.2026.01.011 · Cited by 15

Aqueous Nyctanthes arbortristis and doxorubicin conjugated gold nanoparticles synergistically induced mTOR-dependent autophagy-mediated ferritinophagy in paclitaxel-resistant breast cancer stem cells

Chittineedi, P., Pandrangi, S. L., Mosquera, J. A. N., Llaguno, S. N. S., & Mohiddin, G. J. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1201319 · Cited by 12

Purinosomes and Purine Metabolism in Mammalian Neural Development: A Review

Yamada, S., Mizukoshi, T., Sato, A., & Sakakibara, S. (2024) · ACTA HISTOCHEMICA ET CYTOCHEMICA · doi:10.1267/ahc.24-00027 · Cited by 12

LARP1, an RNA-binding protein, participates in ovarian cancer cell survival by regulating mitochondrial oxidative phosphorylation in response to the influence of the PI3K/mTOR pathway

Ma, J., Dong, D., Qi, H., Li, J., Yu, H., Hu, X., Sun, L., & Shen, L. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2024.167453 · Cited by 12

Alpha-synuclein Fibrils Inhibit Activation of the BDNF/ERK Signaling Loop in the mPFC to Induce Parkinson's Disease-like Alterations with Depression

Ma, Z., Xu, Y., Lian, P., Wu, Y., Liu, K., Zhang, Z., Tang, Z., Yang, X., & Cao, X. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01323-x · Cited by 12

Rapamycin-mediated mTOR inhibition impairs silencing of sex chromosomes and the pachytene piRNA pathway in the mouse testis

Zhu, Z.-P., Yue, Q., Xie, J., Zhang, S., He, W., Bai, S., Tian, S., Zhang, Y., Xiong, M., Sun, Z., et al. (2019) · Aging · doi:10.18632/aging.101740 · Cited by 13

Zishen Huoxue Recipe Protecting Mitochondrial Function of Hypoxic/Reoxygenated Myocardial Cells through mTORC1 Signaling Pathway

Liu, R., Chang, X., Li, J., & Shunyu, Y. (2020) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2020/8327307 · Cited by 12

Inhibition of mTOR signaling protects human glioma cells from hypoxia-induced cell death in an autophagy-independent manner

Divé, I., Klann, K., Michaelis, J. B., Heinzen, D., Steinbach, J. P., Münch, C., & Ronellenfitsch, M. W. (2022) · Cell Death Discovery · doi:10.1038/s41420-022-01195-y · Cited by 13

PGC-1s shape epidermal physiology by modulating keratinocyte proliferation and terminal differentiation

Gravel, S., Khalifa, Y. B., McGuirk, S., St‐Louis, C., Laurin, K. M., Lavallée, E., Benas, D., Desbouis, S., Amaral, F., D’Amours, D., et al. (2023) · iScience · doi:10.1016/j.isci.2023.106314 · Cited by 12

Elongation factor 1A1 regulates metabolic substrate preference in mammalian cells

Wilson, R. B., Kozlov, A. M., Tehrani, H. H., Twumasi-Ankrah, J. S., Chen, Y. J., Borrelli, M. J., Sawyez, C. G., Maini, S., Shepherd, T. G., Cumming, R. C., et al. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.105684 · Cited by 12

mTOR inhibitors for treatment of low-risk prostate cancer

Liss, M. A., Rickborn, L., DiGiovanni, J., Bacich, D. J., deGraffenried, L. A., Parihar, M., Thompson, I. M., & Sharp, Z. D. (2018) · Medical Hypotheses · doi:10.1016/j.mehy.2018.06.004 · Cited by 12

Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys

Capristo, M., Dotto, V. D., Tropeano, C. V., Fiorini, C., Caporali, L., Morgia, C. L., Valentino, M. L., Montopoli, M., Carelli, V., & Maresca, A. (2022) · Molecular Medicine · doi:10.1186/s10020-022-00519-z · Cited by 11

Metabolic Regulation of Copper Toxicity during Marine Mussel Embryogenesis

Young, T., Gale, S. L., Ragg, N. L. C., Sander, S. G., Burritt, D. J., Benedict, B., Le, D. V., Villas-Bôas, S. G., & Alfaro, A. C. (2023) · Metabolites · doi:10.3390/metabo13070838 · Cited by 11

The absence of the ribosomal protein Rpl2702 elicits the MAPK-mTOR signaling to modulate mitochondrial morphology and functions

Liu, L., Wu, Y., Liu, P., Zhu, M., Guang, S., Wang, F., Liu, X., Yao, X., He, J., & Fu, C. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103174 · Cited by 11

Differential cell type-specific function of the aryl hydrocarbon receptor and its repressor in diet-induced obesity and fibrosis

Graelmann, F. J., Gondorf, F., Majlesain, Y., Niemann, B., Klepac, K., Gosejacob, D., Gottschalk, M., Mayer, M., Iriady, I., Hatzfeld, P., et al. (2024) · Molecular Metabolism · doi:10.1016/j.molmet.2024.101963 · Cited by 11

Glutamine and serum starvation alters the ATP production, oxidative stress, and abundance of mitochondrial RNAs in extracellular vesicles produced by cancer cells

Bugajová, M., Raudenská, M., Hánělová, K., Navrátil, J., Gumulec, J., Petrlak, F., Vičar, T., Hrachovinová, Š., Masařík, M., Kalfeřt, D., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-73943-2 · Cited by 11

DOCK8 gene mutation alters cell subsets, BCR signaling, and cell metabolism in B cells

Gu, H., Xie, M., Zhao, S., Luo, X., Huang, Y., Lü, Y., Guan, F., Lei, J., & Liu, C. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-07180-w · Cited by 11

Osteocyte connexin hemichannels and prostaglandin E 2 release dictate bone marrow mesenchymal stromal cell commitment

Zhang, J., Acosta, F. M., Wang, X., Zhao, D., Zhang, L., Hua, R., Guo, Q., Zhong, L., Qin, L., Riquelme, M. A., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2412144122 · Cited by 14

Ablation of collagen VI leads to the release of platelets with altered function

Abbonante, V., Gruppi, C., Battiston, M., Zulian, A., Buduo, C. A. D., Chrisam, M., Sereni, L. P., Laurent, P.-A., Semplicini, C., Lombardi, E., et al. (2021) · Blood Advances · doi:10.1182/bloodadvances.2020002671 · Cited by 11

Angiotensin II Regulates Mitochondrial mTOR Pathway Activity Dependent on Acyl-CoA Synthetase 4 in Adrenocortical Cells

Helfenberger, K. E., Argentino, G. F., Benzo, Y., Herrera, L. M., Finocchietto, P. V., & Poderoso, C. (2022) · Endocrinology · doi:10.1210/endocr/bqac170 · Cited by 12

Autophagy: Molecular Insight and Role in Plant Programmed Cell Death and Defense Mechanism.

Khan, M. S., & Hemalatha, S. (2015) · Cited by 11

Novel metabolic signatures of compound heterozygous Szt2 variants in a case of early‐onset of epileptic encephalopathy

Uittenbogaard, M. N., Gropman, A. L., Brantner, C. A., & Chiaramello, A. (2018) · Clinical Case Reports · doi:10.1002/ccr3.1868 · Cited by 11

Too Sweet for Autophagy: Hexokinase Inhibition of mTORC1 Activates Autophagy

Kundu, M. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.02.009 · Cited by 11

Antimalarial drug artesunate is effective against chemoresistant anaplastic thyroid carcinoma via targeting mitochondrial metabolism

Ma, L., & Fei, H. (2020) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-020-09824-w · Cited by 11

The interplay between DNA damage response and mitochondrial dysfunction in radiotherapy

Yang, S., Li, Y., Zhang, J., Shen, A., Hu, B., & Yan, J. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1642100 · Cited by 16

The role of dysregulated mRNA translation machinery in cancer pathogenesis and therapeutic value of ribosome-inactivating proteins

Jia, W., Yuan, J., Li, S., & Cheng, B. (2023) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2023.189018 · Cited by 9

Regulation of TSC2 lysosome translocation and mitochondrial turnover by TSC2 acetylation status

Marqués, P., Burillo, J., González-Blanco, C., Jiménez, B., García, G., García-Aguilar, A., Iglesias-Fortes, S., Lockwood, Á. C., & Guillén, C. (2024) · Scientific Reports · doi:10.1038/s41598-024-63525-7 · Cited by 10

Chemical Probes for Studying the Eukaryotic Translation Initiation Factor 4E (eIF4E)-Regulated Translatome in Cancer

O’Rourke, R. L., & Garner, A. L. (2025) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.4c00674 · Cited by 11

Inactivation of the PHD3-FOXO3 axis blunts the type I interferon response in microglia and ameliorates Alzheimer’s disease progression

Sánchez-García, M. A., Lara-Ureña, N., March‐Díaz, R., Luis, C. O. S., Quiñones-Cañete, S., Mora-Romero, B., Cabello-Rivera, D., Cabello-Rivera, D., Romero‐Molina, C., Romero‐Molina, C., et al. (2025) · Science Advances · doi:10.1126/sciadv.adu2244 · Cited by 10

Interplay between SERCA, 4E-BP, and eIF4E in the Drosophila heart

Santalla, M., García, A., MATTIAZZI, A. R., Valverde, C. A., Schiemann, R., Paululat, A., Hernández, G., Meyer, H., & Ferrero, P. (2022) · PLoS ONE · doi:10.1371/journal.pone.0267156 · Cited by 10

BRIX1 promotes ribosome synthesis and enhances glycolysis by selected translation of GLUT1 in colorectal cancer

Jiang, C., Sun, L., Wen, S., Tian, Y., Xu, C., Xu, Q., & Xue, H. (2024) · The Journal of Gene Medicine · doi:10.1002/jgm.3632 · Cited by 10

Targeted inhibition of mRNA translation initiation factors as a novel therapeutic strategy for mature B-cell neoplasms

Taylor, J., Yeomans, A., & Packham, G. (2020) · Exploration of Targeted Anti-tumor Therapy · doi:10.37349/etat.2020.00002 · Cited by 11

Cyclopamine and Rapamycin Synergistically Inhibit mTOR Signalling in Mouse Hepatocytes, Revealing an Interaction of Hedgehog and mTor Signalling in the Liver

Spormann, L., Rennert, C., Kolbe, E., Ott, F., Lossius, C., Lehmann, R., Gebhardt, R., Berg, T., & Matz‐Soja, M. (2020) · Cells · doi:10.3390/cells9081817 · Cited by 10

Circadian Rheb oscillation alters the dynamics of hepatic mTORC1 activity and mitochondrial morphology

Yuan, Q., Chen, M., Yang, W., & Xiao, B. (2020) · FEBS Letters · doi:10.1002/1873-3468.14009 · Cited by 10

Autophagy: A Novel Horizon for Hair Cell Protection

Liu, C., Zheng, Z., Wang, P., He, S., & He, Y. (2021) · Neural Plasticity · doi:10.1155/2021/5511010 · Cited by 10

Restoration of Normal Cerebral Oxygen Consumption with Rapamycin Treatment in a Rat Model of Autism–Tuberous Sclerosis

CHI, O. Z., Wu, C., Liu, X., Rah, K. H., Jacinto, E., & Weiss, H. R. (2015) · NeuroMolecular Medicine · doi:10.1007/s12017-015-8359-5 · Cited by 11

(TORC)ing up purine biosynthesis

Ma, E. H., & Jones, R. G. (2016) · Science · doi:10.1126/science.aaf1929 · Cited by 10

Rapamycin-Induced Feedback Activation of eIF4E-EIF4A Dependent mRNA Translation in Pancreatic Cancer

Nguyen, T. U., Hector, H., Pederson, E. N., Lin, J., Ouyang, Z., Wendel, H., & Singh, K. (2023) · Cancers · doi:10.3390/cancers15051444 · Cited by 10

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

Zhu, X., Wu, Y., Li, Y., Zhou, X., Watzlawik, J. O., Chen, Y. M., Raybuck, A. L., Billadeau, D. D., Shapiro, V. S., Springer, W., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-54344-5 · Cited by 9

Metabolic Reprogramming and Adaption in Breast Cancer Progression and Metastasis

Zuo, Q., & Kang, Y. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-70875-6_17 · Cited by 9

Glutaminase as a metabolic target of choice to counter acquired resistance to Palbociclib by colorectal cancer cells

Tarrado‐Castellarnau, M., Foguet, C., Tarragó‐Celada, J., Palobart, M., Hernández-Carro, C., Perarnau, J., Zodda, E., Polat, I. H., Marín, S., Suárez‐Bonnet, A., et al. (2025) · Oncogene · doi:10.1038/s41388-025-03495-w · Cited by 12

Bacillus coagulans (species of lactic acid-forming Bacillus bacteria) ameliorates azoxymethane and dextran sodium sulfate-induced colon cancer in mice

Hiramoto, K., Kubo, S., Tsuji, K., Sugiyama, D., Iizuka, Y., & Hamano, H. (2023) · Journal of Functional Foods · doi:10.1016/j.jff.2023.105406 · Cited by 9

Long-term dietary DHA intervention prevents telomere attrition and lipid disturbance in telomerase-deficient male mice

Chen, J., Wu, S., Wu, Y., Zhuang, P., Zhang, Y., & Jiao, J. (2023) · European Journal of Nutrition · doi:10.1007/s00394-023-03120-0 · Cited by 9

A ketogenic diet alters mTOR activity, systemic metabolism and potentially prevents collagen degradation associated with chronic alcohol consumption in mice

Willemse, L., Terburgh, K., & Louw, R. (2023) · Metabolomics · doi:10.1007/s11306-023-02006-w · Cited by 9

Biofactors regulating mitochondrial function and dynamics in podocytes and podocytopathies

Hejazian, S. M., Ardalan, M., Khatibi, S. M. H., Saadat, Y. R., Barzegari, A., Gueguen, V., Meddahi‐Pellé, A., Anagnostou, F., Vahed, S. Z., & Pavon‐Djavid, G. (2023) · Journal of Cellular Physiology · doi:10.1002/jcp.31110 · Cited by 9

Chronic AMPK inactivation slows SHH medulloblastoma progression by inhibiting mTORC1 signaling and depleting tumor stem cells

Malawsky, D. S., Dismuke, T., Liu, H., Castellino, E., Brenman, J. E., Dasgupta, B., Tikunov, A. P., & Gershon, T. R. (2023) · iScience · doi:10.1016/j.isci.2023.108443 · Cited by 9

Aberrant miR-29 is a predictive feature of severe phenotypes in pediatric Crohn’s disease

Shumway, A. J., Shanahan, M. T., Hollville, É., Chen, K., Beasley, C., Villanueva, J., Albert, S., Lian, G., Cure, M. R., Schaner, M. R., et al. (2024) · JCI Insight · doi:10.1172/jci.insight.168800 · Cited by 9

Evolution of TOR and Translation Control

Fonseca, B. D., Graber, T. E., Hoang, H., González, A., Soukas, A. A., Hernández, G., Alain, T., Swift, S. L., Weisman, R., Meyer, C., et al. (2016) · Springer eBooks · doi:10.1007/978-3-319-39468-8_15 · Cited by 9

High-resolution genomic profiling of thyroid lesions uncovers preferential copy number gains affecting mitochondrial biogenesis loci in the oncocytic variants.

Kurelac, I., de Biase, D., Calabrese, C., Ceccarelli, C., Ng, C. K. Y., Lim, R. S., Mackay, A. G., Weigelt, B., Porcelli, A. M., Reis-Filho, J. S., et al. (2015) · Europe PMC (PubMed Central) · Cited by 9

Systemic PTEN-Akt1-mTOR pathway activity in patients with normal tension glaucoma and ocular hypertension: A case series

Lascaratos, G., Chau, K., Zhu, H., Gkotsi, D., Kamal, D., Gout, I. T., Luthert, P. J., Schapira, A. H. V., & Garway‐Heath, D. F. (2017) · Mitochondrion · doi:10.1016/j.mito.2017.05.003 · Cited by 9

Neurotrophin‐3 stimulates stem Leydig cell proliferation during regeneration in rats

Yu, Y., Li, Z., Ma, F., Chen, Q., Lin, L., Xu, Q., Li, Y., Xin, X. L., Pan, P., Huang, T., et al. (2020) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.15886 · Cited by 9

OASL enhances mRNA translation and reprograms lipid metabolism to promote cancer progression

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Nutritional Strategies and Aging: Current Evidence and Future Directions

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