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

Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation

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Bioconductor: open software development for computational biology and bioinformatics

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mTOR Signaling in Growth Control and Disease

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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

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Metabolic Reprogramming: A Cancer Hallmark Even Warburg Did Not Anticipate

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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

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

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

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c-Myc steers translation in lymphoma

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Activation of nemo-like kinase in diamond blackfan anemia suppresses early erythropoiesis by preventing mitochondrial biogenesis

Wilkes, M., Shibuya, A., Liu, Y., Mark, K., Mercado, J., Saxena, M., Sathianathen, R. S., Kim, H., Glader, B., Kenny, P., et al. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.107542 · Cited by 7

Postnatal and Juvenile Fluoxetine Treatment Evokes Sex-Specific, Opposing Effects on Mood-Related Behavior, Gene Expression, Mitochondrial Function, and Dendritic Architecture in the Rat Medial Prefrontal Cortex

Ghai, U., Chachra, P., Mendon, S., Janakiraman, B., Fanibunda, S. E., Sarkar, A., Gohil, D., Jayaprasad, A. B., Kukkemane, K., Singh, V. K., et al. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.04.026 · Cited by 7

Translational control of leukemic metabolism and disease progression

Mercier, F., Gife, V., Aloyz, R. S., & Hulea, L. (2025) · Trends in Cell Biology · doi:10.1016/j.tcb.2025.04.006 · Cited by 6

Modulation of mitochondrial quality control through autophagic pathway in familial Alzheimer's disease

Limone, A., Napoli, C., Rosa, G. D., Bagnoli, S., Izzo, A., Procaccini, C., Matarese, G., Nacmias, B., Lavecchia, A., & Sarnataro, D. (2025) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2025.120019 · Cited by 5

Skeletal Muscle HSF1 Alleviates Age‐Associated Sarcopenia and Mitochondrial Function Decline via SIRT3‐PGC1α Axis

Zhang, J., Hu, M., Wu, X., Guo, M., Ma, Y., Qiu, J., Wang, S., Cao, Y., Zhong, Y., Chen, F., et al. (2025) · Advanced Science · doi:10.1002/advs.202510368 · Cited by 6

4E-BP inhibition ameliorates heart failure through translational upregulation of SERCA2a and modulation of mitochondrial redox signaling in cardiomyocytes

Gao, J., Lan, T., Xu, X., Guo, H., Wang, S., Zhang, P., Polunovsky, V. A., Sonenberg, N., Bitterman, P. B., Bache, R. J., et al. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104089 · Cited by 5

More than a number: Incorporating the aged phenotype to improve in vitro and in vivo modeling of neurodegenerative disease

Carr, L. M., Mustafa, S., Care, A., & Collins‐Praino, L. E. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.04.023 · Cited by 5

Reduced bioenergetics and mitochondrial fragmentation in human primary cytotrophoblasts induced by an EGFR-targeting chemical mixture

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Blocking tumor-intrinsic MNK1 kinase restricts metabolic adaptation and diminishes liver metastasis

Preston, S. E. J., Dahabieh, M. S., González, R. E. F., Gonçalves, C., Richard, V. R., Leibovitch, M., Dakin, E., Papadopoulos, T., Naranjo, C. L., McCallum, P. A., et al. (2024) · Science Advances · doi:10.1126/sciadv.adi7673 · Cited by 6

The role of mitochondrial mRNA translation in cellular communication

Zilio, E., Schlegel, T., Zaninello, M., & Rugarli, E. I. (2025) · Journal of Cell Science · doi:10.1242/jcs.263753 · Cited by 5

Crosstalk between degradation and bioenergetics: how autophagy and endolysosomal processes regulate energy production

Pabon, A., Bhupana, J. N., & Wong, C. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-02095 · Cited by 6

A system-level model reveals that transcriptional stochasticity is required for hematopoietic stem cell differentiation

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Characterisation of bioenergetic pathways and related regulators by multiple assays in human tumour cells

Jéney, A., Hujber, Z., Szoboszlai, N., Fullár, A., Oláh, J., Pap, É., Márk, Á., Kriston, C., Kralovánszky, J., Kovalszky, I., et al. (2016) · Cancer Cell International · doi:10.1186/s12935-016-0281-x · Cited by 5

Nucleus to Mitochondria: Lost in Transcription, Found in Translation

St‐Pierre, J., & Topisirović, I. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.06.003 · Cited by 5

Conceptualizing Eukaryotic Metabolic Sensing and Signaling

Laxman, S. (2017) · Journal of the Indian Institute of Science · doi:10.1007/s41745-016-0013-1 · Cited by 5

Effects of Feeding Time on Markers of Muscle Metabolic Flexibility Following Acute Aerobic Exercise in Trained Mice Undergoing Time Restricted Feeding

Persinger, A., Butawan, M. B., Faietti, M., Pryke, A., Rose, K., van der Merwe, M., Bloomer, R. J., & Puppa, M. (2021) · Nutrients · doi:10.3390/nu13051717 · Cited by 5

Characterization of Chinese hamster ovary cells with disparate chromosome numbers: Reduction of the amount of mRNA relative to total protein

Yamano, N., Ogata, N., Tanaka, S., Onitsuka, M., & Ōmasa, T. (2019) · Journal of Bioscience and Bioengineering · doi:10.1016/j.jbiosc.2019.06.012 · Cited by 5

Comparative profiles of DNA methylation and differential gene expression in osteocytic areas from aged and young mice

Yu, W., Fu, J., Wu, W., & Wu, J. (2020) · Cell Biochemistry and Function · doi:10.1002/cbf.3539 · Cited by 6

eIF3 associates with 80S ribosomes to promote translation elongation, mitochondrial homeostasis, and muscle healthPreprint

Lin, Y., Li, F., Huang, L., Duan, H., Fang, J., Sun, L., Xing, X., Tian, G., Cheng, Y., Yang, X., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/651240 · Cited by 5

Reprogrammed mRNA translation drives resistance to therapeutic targeting of ribosome biogenesisPreprint

Kusnadi, E. P., Trigos, A., Cullinane, C. M., Goode, D. L., Larsson, O. S., Devlin, J. R., Chan, K. T., Souza, D. P. D., McConville, M. J., McArthur, G. A., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/847723 · Cited by 5

FMRP drives mRNP targets into translationally silenced complexes

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Mitochondrial metabolism: Critical mechanisms underpinning normal hematopoietic stem cell and acute myeloid leukemia stem cell function

Yu, H., & Yan, L. (2025) · Gene · doi:10.1016/j.gene.2025.149685 · Cited by 6

Deciphering the critical roles of the AMPK/mTOR signaling pathway in cancer cell metabolism (Review)

Alasadi, A., Fadhil, N. M., & Chen, S. (2025) · World Academy of Sciences Journal · doi:10.3892/wasj.2025.391 · Cited by 7

Targeting TRAF3IP2 disrupts cellular energetics through inhibition of NAMPT in triple negative breast cancer

Willingham, K., Izadpanah, A., Rashad, Y., Reilich, A., Daneshimehr, F., Braun, S. E., Alt, E., & Izadpanah, R. (2025) · Scientific Reports · doi:10.1038/s41598-025-29057-4 · Cited by 4

SARS-CoV-2 directly infects the inner ear and causes hearing dysfunction

Liu, X., Zong, Y., Liu, K., Shi, X., Zhao, Z., Shan, C., & Sun, Y. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117251 · Cited by 4

Metabolic support of trained immune responses in myeloid cells

Jarit-Cabanillas, A., Dunphy, G., Virga, F., den Bossche, J. V., & Sancho, D. (2026) · eLife · doi:10.7554/elife.108814 · Cited by 4

The intersection between metabolism and translation through a subcellular lens.

Santoro, M. M. (2025) · Trends in Cell Biology · doi:10.1016/j.tcb.2025.05.003 · Cited by 6

Light-dark dependent changes in chloroplast and mitochondrial activity in Chlamydomonas reinhardtii

Dhawan, G., & Rao, B. J. (2025) · Frontiers in Plant Science · doi:10.3389/fpls.2025.1622214 · Cited by 4

Targeting LARP1 to mitigate aging in lens epithelial cells: mechanistic insights into mitochondrial dysfunction

Qi, H., Sun, L., Chai, J., Ma, J., Yu, H., Xia, M., & Hu, X. (2025) · Experimental Eye Research · doi:10.1016/j.exer.2025.110582 · Cited by 4

Dual roles of mTOR in skeletal muscle adaptation: coordinating hypertrophic and mitochondrial biogenesis pathways for exercise-induced chronic disease management

Zhao, Y.-C. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1635219 · Cited by 6

Translational Control by 4E-BP1/2 Suppressor Proteins Regulates Mitochondrial Biosynthesis and Function during CD8+ T Cell Proliferation

Dimitriou, I. D., Meiri, D., Jitkova, Y., Elford, A. R., Koritzinsky, M., Schimmer, A. D., Ohashi, P. S., Sonenberg, N., & Rottapel, R. K. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2101090 · Cited by 4

Mitochondrial proteostasis and cellular health: insights from chaperones and autophagy

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Cyclic GMP-AMP Synthase (cGAS) Deletion Promotes Less Prominent Inflammatory Macrophages and Sepsis Severity in Catheter-Induced Infection and LPS Injection Models

Suksamai, C., Kaewduangduen, W., Phuengmaung, P., Sae‐khow, K., Charoensappakit, A., Udomkarnjananun, S., Lotinun, S., Kueanjinda, P., & Leelahavanichkul, A. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26115069 · Cited by 4

Adaptive Benefits of Storage Strategy and Dual AMPK/TOR Signaling in Metabolic Stress Response

Pfeuty, B., & Thommen, Q. (2016) · PLoS ONE · doi:10.1371/journal.pone.0160247 · Cited by 4

Primary methods of adaptation of muscle fibers to physical activity and the ways of their implementation

Gallyamutdinov, R. V., Kashtanov, A. D., Kustavinova, E. V., Kartashkina, N. L., & YATSKOVSKII, A. N. (2020) · Operativnaâ hirurgiâ i kliničeskaâ anatomiâ (Pirogovskij naučnyj žurnal) · doi:10.17116/operhirurg2019304128 · Cited by 4

Immature symbiotic system between horizontally transmitted green algae and brown hydra

Miyokawa, R., Kanaya, H. J., Itoh, T. Q., Kobayakawa, Y., & Kusumi, J. (2021) · Scientific Reports · doi:10.1038/s41598-021-82489-6 · Cited by 4

Regulation of Mitochondrial Biogenesis in Human Skeletal Muscles Induced by Aerobic Exercise and Disuse

Bokov, R. O., & Popov, D. V. (2022) · Human Physiology · doi:10.1134/s0362119722030033 · Cited by 4

Peptide- and Protein-Level Combined Strategy for Analyzing Newly Synthesized Proteins by Integrating Tandem Orthogonal Proteolysis with Cleavable Bioorthogonal Tagging

Meng, P., Shao, Y., Xiong, Y., Zhang, L. J., Bao, H., & Lu, H. (2022) · Analytical Chemistry · doi:10.1021/acs.analchem.2c01537 · Cited by 4

Native-state proteomics of Parvalbumin interneurons identifies novel molecular signatures and metabolic vulnerabilities to early Alzheimer’s disease pathologyPreprint

Kumar, P., Goettemoeller, A. M., Espinosa‐García, C., Tobin, B. R., Tfaily, A., Nelson, R. S., Natu, A., Dammer, E. B., Santiago, J. V., Malepati, S., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.17.541038 · Cited by 4

Development of an Engineered Bacterial Endophyte: Promoting Plant Growth Through Pyrroloquinoline Quinone (PQQ) Synthesis

Fang, T., Lo, S.-C., Yu, Y.-N., Sou, N., Hung, S.-H. W., Peng, J.-H., Chiang, E. I., & Huang, C. (2025) · Microorganisms · doi:10.3390/microorganisms13020293 · Cited by 3

ESRRA (estrogen related receptor, alpha) induces ribosomal protein RPLP1-mediated adaptive hepatic translation during prolonged starvation

Tripathi, M., Gauthier, K. C., Sandireddy, R., Zou, J., Gupta, P. S., Sakthivel, S., Jiemin, N., Arul, K., Tikno, K., Park, S.-H., et al. (2025) · Autophagy · doi:10.1080/15548627.2025.2465183 · Cited by 5

Cannabidiolic Acid Rescues Deficits in Hippocampal Long-Term Potentiation in Models of Alzheimer’s Disease: An Electrophysiological and Proteomic Analysis

Gil, B., Sullivan, M., Scaife, C., Glennon, J. C., & Herron, C. E. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26104944 · Cited by 3

Premature aging and neuropathic behaviours induced by an acute low-dose exposure to a sarin surrogate

Champault, A., Leterrier, S., Bel, R., Knoertzer, J., Soyer, A., Goutal, S., Baati, R., François, S., Tournier, N., Bo, G. D., et al. (2025) · Toxicology · doi:10.1016/j.tox.2025.154327 · Cited by 3

Proposed Mechanistic Axis of Infections and mTOR Hyperactivation: A Multidisciplinary Review of Immune, Rheumatologic, and Psychiatric Links

Baldelli, G. F., & Buonsenso, D. (2025) · Children · doi:10.3390/children12121603 · Cited by 3

Mechanometabolism instructs hematopoietic stem cell specification

Horton, P. D., Syed, A., Winkler, M., Vaidya, A. B., Rariden, M., Arora, N., Zhou, Y., Kobayashi, M., Yoshimoto, M., Lee, H. J., et al. (2025) · The Journal of Experimental Medicine · doi:10.1084/jem.20250607 · Cited by 3

Impact of oxytosis on the cross‐talk of mTORC with mitochondrial proteins in drug‐resistant cancer stem cells

Pandrangi, S. L., Chittineedi, P., Manthari, R. K., & Suhruth, B. (2024) · Journal of Cellular Physiology · doi:10.1002/jcp.31421 · Cited by 3

Tumor-intrinsic and immune-related features associated with treatment failure in human papillomavirus-related oropharyngeal cancer

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. (2025) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djaf053 · Cited by 3

Testes-specific protease 50 heightens stem-like properties and improves mitochondrial function in colorectal cancer

Gao, F., Liu, S., Sun, Y., Yu, C., Zheng, L., Sun, L., Wang, G., Sun, Y., Bao, Y., Song, Z., et al. (2025) · Life Sciences · doi:10.1016/j.lfs.2025.123560 · Cited by 3

The mTOR Complexes in Cancer Cell Metabolism

Lynch, T. P., Moloughney, J. G., & Jacinto, E. (2016) · Cancer drug discovery and develogment/Cancer drug discovery and development · doi:10.1007/978-3-319-34211-5_2 · Cited by 3

Post-transcriptional regulation of mitochondrial function

Schatton, D., & Rugarli, E. I. (2017) · Current Opinion in Physiology · doi:10.1016/j.cophys.2017.12.008 · Cited by 3

Effects of perfluoroundecanoic acid on the function of Leydig cells in adult male rats

Xin, X. L., Chen, H., Tian, F., Li, J., Yan, H., Yu, Y., Ma, F., Li, H., Wang, Y., Li, X., et al. (2022) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2022.115903 · Cited by 3

Effects of Phosphatidic Acid on Mammalian Target of Rapamycin (mTOR) and Metabolic Pathways in Bivalve Mollusk Sinonovacula constricta

Liao, K., Zhang, Q., Qiu, Y., Zhu, Y., Liu, Y., Huang, H., Chen, D., Ma, B., Zhang, L., Ran, Z., et al. (2023) · Aquaculture Research · doi:10.1155/2023/6666946 · Cited by 4

Significance of quantitative analyses of the impact of heterogeneity in mitochondrial content and shape on cell differentiation

Agarwala, S., Dhabal, S., & Mitra, K. (2024) · Open Biology · doi:10.1098/rsob.230279 · Cited by 3

IRX5 suppresses osteogenic differentiation of hBMSCs by inhibiting protein synthesis

Jiang, B., Zheng, J., Yao, H., Wang, Y., Song, F., & Huang, C. (2024) · Journal of Cellular Physiology · doi:10.1002/jcp.31286 · Cited by 3

Nonessential amino acid is not nonessential in geriatric patients: implications for maxillofacial wound healing and bone repair

Kim, S. (2025) · Maxillofacial Plastic and Reconstructive Surgery · doi:10.1186/s40902-025-00465-w · Cited by 3

Beyond blood flow: the multifaceted role of AMPK in regulating fetal growth at high altitudes

Julian, C. G. (2025) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2024.0173 · Cited by 3

Metabolic abnormalities induced by mitochondrial dysfunction in skeletal muscle of the renal carcinoma Eker (TSC2+/−) rat model

Aizawa, Y., Shirai, T., Kobayashi, T., Hino, O., Tsujii, Y., Inoue, H., Kazami, M., Tadokoro, T., Suzuki, T., Kobayashi, K., et al. (2016) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2016.1165603 · Cited by 3

RNA G-quadruplex dynamic steers the crosstalk between protein synthesis and energy metabolismPreprint

Dumas, L., Shin, S., Rigaud, Q., Cargnello, M., Suárez, B. H., Herviou, P., Saint‐Laurent, N., Leduc, M., Gall, M. L., Monchaud, D., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.29.577192 · Cited by 3

Translational control of microglial inflammatory and neurodegenerative responsesPreprint

Bermudez, S., Choi, J., Vogel, J. W., Kim, S., Mahmood, N., Zhu, V. Y., Cozachenco, D., Yaqubi, M., Zhou, L., Stratton, J. A., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.06.587750 · Cited by 3

Impact of Rapamycin on Longevity: Updated Insights

Sanati, M., Afshari, A. R., Aminyavari, S., Banach, M., & Sahebkar, A. (2024) · Archives of Medical Science · doi:10.5114/aoms/191565 · Cited by 3

RSK1 and RSK2 modulate the translatome of glioblastoma cells in an isoform-specific and mTORC1 independent manner

Roffé, M., Nascimento, D. P., Nunes, P. B. C., Soares, L. C., Alves, A. H., Hamraghani, A., Almasi, Y., Djaoud, Z., Hajj, G. N. M., Martins, V. R., et al. (2025) · Neuro-Oncology Advances · doi:10.1093/noajnl/vdaf144 · Cited by 2

Lignin-Derived Oligomers as Promising mTOR Inhibitors: Insights from Dynamics Simulations

Gabellone, S., Carotenuto, G., Arcieri, M., Bottoni, P., Sbanchi, G., Castrignanò, T., Piccinino, D., Liverani, C., & Saladino, R. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26178728 · Cited by 3

Lighting Up Arginine Metabolism Dynamics in Neural Differentiation through Ratiometric Fluorescence Imaging

Jin, Y., Mei, Y., Zhao, Y., & Tian, Y. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c05685 · Cited by 2

S100A10 knockdown exacerbates phenylephrine-induced cardiomyocyte hypertrophy via modulating mitochondrial oxidative phosphorylation

Xu, F., Chen, Y., Xu, M., Li, D., Lu, Y., Zhang, M., Li, J., Li, W., & Guo, Y. (2025) · Frontiers in Genetics · doi:10.3389/fgene.2025.1610008 · Cited by 2

mTOR-siRNA-conjugated and Gboxin-loaded micelles for mitochondrial dysfunction-driven synergistic glioblastoma therapy

Chen, Z., Yang, Q., Fan, M., Chai, T., Liu, Y., Xia, X., Ismail, M., & Zheng, M. (2025) · Biomaterials · doi:10.1016/j.biomaterials.2025.123902 · Cited by 4

Ribosome Homeostasis Regulated by SETD2 Preserves Intestinal Epithelial Barrier

Rao, H., Wang, A., Xu, Y., Feng, W., Ma, C., Wang, Z., Zhang, W., Su, W., Xiuying, X. I. A. O., Gao, W., et al. (2026) · Advanced Science · doi:10.1002/advs.202508168 · Cited by 2

Loss of the translational repressor 4E-BP1 promotes skin carcinogenesis

Zhou, Y., Dou, H., Liu, Y., Wang, J., Ding, X., & Huang, T. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1742429 · Cited by 2

Obesity disrupts ILC2 metabolic and functional homeostasis by inhibiting mTORC1 signaling

Hu, L., Wang, D., Chen, Y., Qiu, J., Wang, H., Zhang, Y., Zhang, M. H., Su, X., Qiu, J., Sun, J., et al. (2026) · Cellular and Molecular Immunology · doi:10.1038/s41423-026-01389-9 · Cited by 2

Recent advances in traditional Chinese medicine-mediated regulation of microglial metabolic reprogramming in neurological disease therapy

Wu, Z., Lv, F., Shao, S., Chen, Y., Weng, N., & Xia, Y. (2026) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2026.121355 · Cited by 2

Molecular mechanisms and recent advances in cellular senescence

Hussain, A., Tatar, M., & Gong, R. (2026) · Cell & Bioscience · doi:10.1186/s13578-026-01596-x · Cited by 2

mTOR and post-translational modifications rely on mitochondrion as the arsenal for cellular metabolism regulation

Zhuge, C.-C., Chen, S. J., & Chin, Y. E. (2015) · Science China Life Sciences · doi:10.1007/s11427-015-4909-1 · Cited by 2

Mitotic CDK1 and 4E-BP1 II: A single phosphomimetic mutation in 4E-BP1 induces glucose intolerance in mice

Cao, S., Jurczak, M. J., Shuda, Y., Sun, R., Shuda, M., Chang, Y., & Moore, P. S. (2023) · PLoS ONE · doi:10.1371/journal.pone.0282914 · Cited by 2

Structure and Signalling Function of the B-Cell Antigen Receptor and Its Coreceptors

Reth, M. G., Kläsener, K., Nitschke, L., & Gold, M. R. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95895-0.00003-9 · Cited by 2

Tumor Necrosis Factor Receptor-2 Signals Clear-Cell Renal Carcinoma Proliferation via Phosphorylated 4E Binding Protein-1 and Mitochondrial Gene Translation

Al‐Lamki, R. S., Tolkovsky, A. M., Alawwami, M., Lu, W., Field, S. F., Wang, J., Pober, J. S., & Bradley, J. R. (2024) · American Journal Of Pathology · doi:10.1016/j.ajpath.2024.02.019 · Cited by 2

JR-AB2-011 induces fast metabolic changes independent of mTOR complex 2 inhibition in human leukemia cells

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TORC1 Regulates Thermotolerance via Modulating Metabolic Rate and Antioxidant Capacity in Scallop Argopecten irradians irradians

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