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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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

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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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mTORC2 is an important target for simvastatin-associated toxicity in C2C12 cells and mouse skeletal muscle – Roles of Rap1 geranylgeranylation and mitochondrial dysfunction

Sanvee, G. M., Hitzfeld, L., Bouitbir, J., & Krähenbühl, S. (2021) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114750 · Cited by 25

Cap-dependent translation initiation monitored in living cells

Gandin, V., English, B. P., Freeman, M., Leroux, L., Preibisch, S., Walpita, D., Jaramillo, M., & Singer, R. H. (2022) · Nature Communications · doi:10.1038/s41467-022-34052-8 · Cited by 24

Mechanism of progression of diabetic kidney disease mediated by podocyte mitochondrial injury

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Sr-Incorporated Bioactive Glass Remodels the Immunological Microenvironment by Enhancing the Mitochondrial Function of Macrophage via the PI3K/AKT/mTOR Signaling Pathway

Qiu, H., Xiong, H., Zheng, J., Peng, Y., Wang, C., Hu, Q. C., Zhao, F., & Chen, K. (2024) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.4c00228 · Cited by 24

Adipose mitochondrial metabolism controls body growth by modulating systemic cytokine and insulin signaling

Sriskanthadevan-Pirahas, S., Turingan, M. J., Chahal, J. S., Thorson, E., Khan, S., Tinwala, A. Q., & Grewal, S. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110802 · Cited by 24

Pilot study evaluating everolimus molecular mechanisms in tuberous sclerosis complex and focal cortical dysplasia

Leitner, D., Kanshin, E., Askenazi, M., Siu, Y., Friedman, D. J., Devore, S., Jones, D. R., Ueberheide, B. M., Wısnıewskı, T., & Devinsky, O. (2022) · PLoS ONE · doi:10.1371/journal.pone.0268597 · Cited by 23

Insulinemic potential of diet and risk of total and subtypes of breast cancer among US females

Romanos-Nanclares, A., Tabung, F. K., Willett, W. C., ROSNER, B. A., Holmes, M. D., Chen, W. Y., Tamimi, R. M., & Eliassen, A. H. (2022) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/nqac284 · Cited by 26

Spatiotemporal Regulation of De Novo and Salvage Purine Synthesis during Brain Development

Mizukoshi, T., Yamada, S., & Sakakibara, S. (2023) · eNeuro · doi:10.1523/eneuro.0159-23.2023 · Cited by 23

Autophagy is a signature of a signaling network that maintains hematopoietic stem cells

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PRL2 links magnesium flux and sex-dependent circadian metabolic rhythms

Uetani, N., Hardy, S., Gravel, S., Kießling, S., Pietrobon, A., Wong, N. N., Chénard, V., Cermakian, N., St‐Pierre, J., & Tremblay, M. L. (2017) · JCI Insight · doi:10.1172/jci.insight.91722 · Cited by 30

Mitochondrial pathway is involved in the protective effects of alpha-ketoglutarate on hydrogen peroxide induced damage to intestinal cells

Jiang, Q., Liu, G., Wang, X., Hou, Y., Duan, Y., Wu, G., Yin, Y., & Kang, Y. (2017) · Oncotarget · doi:10.18632/oncotarget.20426 · Cited by 23

Garcimultiflorone K inhibits angiogenesis through Akt/eNOS- and mTOR-dependent pathways in human endothelial progenitor cells

Yang, C., Chen, C., Lin, C., Chen, Y., Lin, C., Chi, C., Chen, Y.-J., Liu, S., Chang, T., Tang, C., et al. (2019) · Phytomedicine · doi:10.1016/j.phymed.2019.152911 · Cited by 23

Changes in the Turnover of the Cellular Proteome during Metabolic Reprogramming: A Role for mtROS in Proteostasis

García-Aguilar, A., Martínez‐Reyes, I., & Cuezva, J. M. (2019) · Journal of Proteome Research · doi:10.1021/acs.jproteome.9b00239 · Cited by 24

Loss of coordination between basic cellular processes in human aging

Leote, A. C., Lopes, F. J. C. C., & Beyer, A. (2024) · Nature Aging · doi:10.1038/s43587-024-00696-y · Cited by 28

The role of m6A modification during macrophage metabolic reprogramming in human diseases and animal models

Wang, H., Xu, P., Yin, K., & Wang, S. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1521196 · Cited by 22

The role of mTOR signaling pathway in systemic lupus erythematosus and systemic vasculitis

Michailidou, D., Gartshteyn, Y., Askanase, A., & Perl, A. (2025) · Autoimmunity Reviews · doi:10.1016/j.autrev.2025.103910 · Cited by 26

Nuclear-Encoded Mitochondrial mRNAs: A Powerful Force in Axonal Growth and Development

Gale, J. R., Aschrafi, A., Gioio, A. E., & Kaplan, B. B. (2017) · The Neuroscientist · doi:10.1177/1073858417714225 · Cited by 23

Co-ingestion of protein or a protein hydrolysate with carbohydrate enhances anabolic signaling, but not glycogen resynthesis, following recovery from prolonged aerobic exercise in trained cyclists

Cogan, K. E., Evans, M., Iuliano, E., Melvin, A., Susta, D., Neff, K., VITO, G. D., & Egan, B. (2017) · European Journal of Applied Physiology · doi:10.1007/s00421-017-3775-x · Cited by 22

Death by lipids: The role of small nucleolar RNAs in metabolic stress

Schaffer, J. E. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.aw120.011105 · Cited by 21

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

Joelsson, J. P., Ásbjarnarson, Á., Sigurðsson, S., Kricker, J. A., Valdimarsdóttir, B., Thorarinsdottir, H., Starradottir, E., Guðjónsson, Þ., Ingþórsson, S., & Kárason, S. (2022) · Laboratory Animal Research · doi:10.1186/s42826-022-00133-4 · Cited by 25

Uptake of Tumor-Derived Microparticles Induces Metabolic Reprogramming of Macrophages in the Early Metastatic Lung

Kersten, K., You, R., Liang, S., Tharp, K. M., Pollack, J. L., Weaver, V. M., Krummel, M. F., & Headley, M. B. (2022) · Cell Reports · doi:10.1016/j.celrep.2023.112582 · Cited by 23

Transferrin receptor is necessary for proper oligodendrocyte iron homeostasis and development

Cheli, V. T., González, D. A. S., Wan, R., Rosenblum, S. L., Denaroso, G., Angeliu, C. G., Smith, Z. I., Wang, C., & Paez, P. M. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1383-22.2023 · Cited by 21

The consequences of increased 4E-BP1 in polycystic kidney disease

Holditch, S. J., Brown, C. N., Atwood, D. J., Pokhrel, D., Brown, S., Lombardi, A. M., Nguyen, K. N., Hill, R. C., Lanaspa, M. A., Hopp, K., et al. (2019) · Human Molecular Genetics · doi:10.1093/hmg/ddz244 · Cited by 21

Cardiac mitochondrial function depends on BUD23 mediated ribosome programming

Baxter, M. D., Voronkov, M., Poolman, T. M., Galli, G. L. J., Pinali, C., Goosey, L. C., Knight, A., Krakowiak, K., Maidstone, R. J., Iqbal, M., et al. (2020) · eLife · doi:10.7554/elife.50705 · Cited by 19

Raptor is critical for increasing the mitochondrial proteome and skeletal muscle force during hypertrophy

Baraldo, M., Nogara, L., Dumitras, A. G., Dondjang, A. H. T., Geremia, A., Scalabrin, M., Türk, C., Tellkamp, F., Zentilin, L., Giacca, M., et al. (2021) · The FASEB Journal · doi:10.1096/fj.202101054rr · Cited by 23

Hepatocyte growth factor protects pulmonary endothelial barrier against oxidative stress and mitochondria-dependent apoptosis

Meng, S., Xia, F., Xu, J., Zhang, X., Xue, M., Gu, M., Guo, F., Huang, Y., Qiu, H., & Yang, Y. (2022) · Chinese Medical Journal · doi:10.1097/cm9.0000000000001916 · Cited by 21

Left‐right asymmetry in the light of TOR: An update on what we know so far

Tena, T. C., Burkhalter, M. D., & Philipp, M. (2015) · Biology of the Cell · doi:10.1111/boc.201400094 · Cited by 20

Inhibition of mTOR reduces lipotoxic cell death in primary macrophages through an autophagy-independent mechanism

He, L., Weber, K., Diwan, A., & Schilling, J. D. (2016) · Journal of Leukocyte Biology · doi:10.1189/jlb.3a1015-463r · Cited by 21

The Effect of Inulin on Lifespan, Related Gene Expression and Gut Microbiota in InRp5545/TM3 Mutant Drosophila melanogaster: A Preliminary Study

Dong, Y., Sun, H., Yang, W., Ma, S., Du, B., & Xu, H. (2019) · Nutrients · doi:10.3390/nu11030636 · Cited by 20

Smaug1 membrane-less organelles respond to AMPK and mTOR and affect mitochondrial function

Fernández-Álvarez, A. J., Thomas, M. G., Pascual, M. L., Habif, M., Pimentel, J., Corbat, A. A., Pessoa, J., Spina, P. E. L., Boscaglia, L., Plessis, A., et al. (2021) · Journal of Cell Science · doi:10.1242/jcs.253591 · Cited by 20

Ribosome Quality Control mitigates the cytotoxicity of ribosome collisions induced by 5-Fluorouracil

Chatterjee, S., Naeli, P., Onar, O., Simms, N., Garzia, A., Hackett, A. P., Coyle, K., Snell, P. H., McGirr, T., Sawant, T. N., et al. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae849 · Cited by 18

Targeting mitochondrial complex I of CD177+ neutrophils alleviates lung ischemia-reperfusion injury

Wu, J., Gao, P., Yang, C., Zhuang, F., Luo, Y., Wen, F., Zhang, P., Wang, L., Xie, H., Dai, C., et al. (2025) · Cell Reports Medicine · doi:10.1016/j.xcrm.2025.102140 · Cited by 22

Ribosome profiling in mouse hippocampus: plasticity-induced regulation and bidirectional control by TSC2 and FMRP

Hien, A., Molinaro, G., Liu, B., Huber, K. M., & Richter, J. D. (2020) · Molecular Autism · doi:10.1186/s13229-020-00384-9 · Cited by 20

l-Arginine Alleviates Hydrogen Peroxide–Induced Oxidative Damage in Ovine Intestinal Epithelial Cells by Regulating Apoptosis, Mitochondrial Function, and Autophagy

Zhang, H., Liu, X., Fan, Y., Yu, Y., Loor, J. J., Loor, J. J., Peng, A., & Wang, H. (2020) · Journal of Nutrition · doi:10.1093/jn/nxaa428 · Cited by 20

Contribution of Energy Dysfunction to Impaired Protein Translation in Neurodegenerative Diseases

Liu, Y., & Chern, Y. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.668500 · Cited by 20

A human-based multi-gene signature enables quantitative drug repurposing for metabolic disease

Timmons, J. A., Anighoro, A., Brogan, R. J., Stahl, J., Wahlestedt, C., Farquhar, D. G., Taylor‐King, J. P., Volmar, C., Kraus, W. E., & Phillips, S. M. (2021) · eLife · doi:10.7554/elife.68832 · Cited by 21

The development and function of human monocyte-derived dendritic cells regulated by metabolic reprogramming

Zhao, Y., Gao, C., Liu, L., Wang, L., & Song, Z. (2023) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiad062 · Cited by 20

Icariside II, a natural mTOR inhibitor, disrupts aberrant energy homeostasis via suppressing mTORC1-4E-BP1 axis in sarcoma cells

Zhang, C., Yang, L., Geng, Y., An, F., Xia, Y., Guo, C., Luo, J., Zhang, L., Guo, Q., & Kong, L. (2016) · Oncotarget · doi:10.18632/oncotarget.8538 · Cited by 20

Cancer: Linking Powerhouses to Suicidal Bags

Martínez-Carreres, L., Nasrallah, A., & Fajas, L. (2017) · Frontiers in Oncology · doi:10.3389/fonc.2017.00204 · Cited by 21

Hepatic DNAJB9 Drives Anabolic Biasing to Reduce Steatosis and Obesity

Sun, F., Liao, Y., Qu, X., Xiao, X., Hou, S., Chen, Z., Huang, H., Li, P., & Fu, S. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.043 · Cited by 21

The opposing roles of the mTOR signaling pathway in different phases of human umbilical cord blood-derived CD34+ cell erythropoiesis

Liu, Q., Luo, L., Ren, C., Zou, M., Yang, S., Cai, B., Wu, L., Wang, Y., Fu, S., Xu, H., et al. (2020) · Stem Cells · doi:10.1002/stem.3268 · Cited by 20

Targeting spermine metabolism to overcome immunotherapy resistance in pancreatic cancer

Yang, H., Zhang, X., Zhang, S., Yang, Y., Chen, Y., Jiang, Y., Lu, Q., Liu, L., Lao, M., Du, W., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-63146-2 · Cited by 19

Mitochondrial genotype alters the impact of rapamycin on the transcriptional response to nutrients in Drosophila

Santiago, J., Boylan, J. M., Lemieux, F. A., Gruppuso, P. A., Sanders, J. A., & Rand, D. M. (2021) · BMC Genomics · doi:10.1186/s12864-021-07516-2 · Cited by 18

mTOR Signaling in the Inner Ear as Potential Target to Treat Hearing Loss

Cortada, M., Levano, S., & Bodmer, D. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126368 · Cited by 21

Eukaryotic translation initiation factor 4E binding protein 1 (EIF4EBP1) expression in glioblastoma is driven by ETS1- and MYBL2-dependent transcriptional activation

Hauffe, L., Picard, D. J., Musa, J., Remke, M., Grünewald, T. G. P., Rotblat, B., Reifenberger, G., & Leprivier, G. (2022) · Cell Death Discovery · doi:10.1038/s41420-022-00883-z · Cited by 17

Emerging Mechanisms of Skeletal Muscle Homeostasis and Cachexia: The SUMO Perspective

Khan, B., Gand, L. V., Amrute‐Nayak, M., & Nayak, A. (2023) · Cells · doi:10.3390/cells12040644 · Cited by 19

Protein Turnover in Skeletal Muscle: Looking at Molecular Regulation towards an Active Lifestyle

Ferreira, R. P., & Duarte, J. A. (2023) · International Journal of Sports Medicine · doi:10.1055/a-2044-8277 · Cited by 23

Counteracting oxidative phosphorylation-mediated resistance of melanomas to MAPK pathway inhibition

McQuade, J. L., & Gopal, Y. V. (2015) · Molecular & Cellular Oncology · doi:10.4161/23723556.2014.991610 · Cited by 19

Chemical genomics approach to identify genes associated with sensitivity to rapamycin in the fission yeast Schizosaccharomyces pombe

Doi, A., Fujimoto, A., Sato, S., Uno, T., Kanda, Y., Asami, K., Tanaka, Y., Kita, A., Satoh, R., & Sugiura, R. (2015) · Genes to Cells · doi:10.1111/gtc.12223 · Cited by 19

Early Trypanosoma cruzi Infection Triggers mTORC1-Mediated Respiration Increase and Mitochondrial Biogenesis in Human Primary Cardiomyocytes

Libisch, G., Faral‐Tello, P., Garg, N. J., Radí, R., Piacenza, L., & Robello, C. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01889 · Cited by 19

Exercise training increases CISD family protein expression in murine skeletal muscle and white adipose tissue

Yokokawa, T., Kido, K., Suga, T., Sase, K., Isaka, T., Hayashi, T., & Fujita, S. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.10.101 · Cited by 19

Glial Cell Line–Derived Neurotrophic Factor Enhances Autophagic Flux in Mouse and Rat Hepatocytes and Protects Against Palmitate Lipotoxicity

Mwangi, S. M., Li, G., Ye, L., Liu, Y., Reichardt, F., Yeligar, S. M., Hart, C. M., Czaja, M. J., & Srinivasan, S. (2019) · Hepatology · doi:10.1002/hep.30541 · Cited by 19

Translation of Human β-Actin mRNA is Regulated by mTOR Pathway

Eliseeva, I. A., Vasilieva, M., & Ovchinnikov, L. P. (2019) · Genes · doi:10.3390/genes10020096 · Cited by 18

The mTOR Inhibitor Rapamycin Prevents General Anesthesia-Induced Changes in Synaptic Transmission and Mitochondrial Respiration in Late Postnatal Mice

Ju, X., Ryu, M. J., Cui, J., Lee, Y., Park, S., Hong, B., Yoo, S., Lee, W. H., Shin, Y. S., Yoon, S.-H., et al. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00004 · Cited by 19

Immunoglobulin expression in the endoplasmic reticulum shapes the metabolic fitness of B lymphocytes

Jumaa, H., Cagánová, M., McAllister, E. J., Hoenig, L., He, X., Saltukoglu, D., Brenker, K., Köhler, M., Leben, R., Hauser, A. E., et al. (2020) · Life Science Alliance · doi:10.26508/lsa.202000700 · Cited by 19

Macrophage mitochondrial bioenergetics and tissue invasion are boosted by an Atossa‐Porthos axis in Drosophila

Emtenani, S., Martin, E. T., Gyoergy, A., Bicher, J., Genger, J., Köcher, T., Akhmanova, M., Guarda, M., Roblek, M., Bergthaler, A., et al. (2022) · The EMBO Journal · doi:10.15252/embj.2021109049 · Cited by 15

Nutrient Sensor mTOR and OGT: Orchestrators of Organelle Homeostasis in Pancreatic β-Cells

Esch, N., Jo, S., Moore, M., & Alejandro, E. U. (2020) · Journal of Diabetes Research · doi:10.1155/2020/8872639 · Cited by 18

PTEN Regulates Mitochondrial Biogenesis via the AKT/GSK-3β/PGC-1α Pathway in Autism

Feng, C., Chen, Y., Zhang, Y., Yan, Y., Yang, M., Gui, H., & Wang, M. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.04.010 · Cited by 19

MTOR modulation induces selective perturbations in histone methylation which influence the anti-proliferative effects of mTOR inhibitors

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. (2024) · iScience · doi:10.1016/j.isci.2024.109188 · Cited by 17

Malonate induces the assembly of cytoplasmic stress granules

Fu, X., Gao, X., Ge, L., Cui, X., Su, C., Yang, W., Sun, X., Zhang, W., Yao, Z., Yang, X., et al. (2015) · FEBS Letters · doi:10.1002/1873-3468.12049 · Cited by 18

mTOR regulates PRMT1 expression and mitochondrial mass through STAT1 phosphorylation in hepatic cell

Zhang, X., Li, L., Li, Y., Li, Z., Zhai, W., Sun, Q., Yang, X., Roth, M., & Lu, S. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2021.119017 · Cited by 18

Isoform-resolved mRNA profiling of ribosome load defines interplay of HIF and mTOR dysregulation in kidney cancer

Sugimoto, Y., & Ratcliffe, P. J. (2022) · Nature Structural & Molecular Biology · doi:10.1038/s41594-022-00819-2 · Cited by 18

The mTORC1‐eIF4F axis controls paused pluripotency

Xu, X., Ahmed, T., Wang, L., Cao, X., Zhang, Z., Wang, M., Lv, Y., Kanwal, S., Tariq, M., Lin, R., et al. (2021) · EMBO Reports · doi:10.15252/embr.202153081 · Cited by 18

Accumulation of branched-chain amino acids deteriorates the neuroinflammatory response of Müller cells in diabetic retinopathy via leucine/Sestrin2-mediated sensing of mTOR signaling

Gong, Q., Wang, J., Luo, D., Xu, Y., Zhang, R., Li, X., Yin, Z., Fang, J., & Wang, H.-Y. (2024) · Acta Diabetologica · doi:10.1007/s00592-024-02349-3 · Cited by 17

RNA G-quadruplexes control mitochondria-localized mRNA translation and energy metabolism

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. (2025) · Nature Communications · doi:10.1038/s41467-025-58118-5 · Cited by 21

PI3K/AKT/mTOR signaling pathway modulation by circular RNAs in breast cancer progression

Fath, M. K., Masouleh, R. A., Afifi, N., Loghmani, S., Tamimi, P., Fazeli, A., Mousavian, S. A., Falsafi, M. M., & Barati, G. (2022) · Pathology - Research and Practice · doi:10.1016/j.prp.2022.154279 · Cited by 17

Emerging implications for ribosomes in proximity to mitochondria

Cohen, B., Golani‐Armon, A., & Arava, Y. (2023) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2023.01.003 · Cited by 15

Lineage-specific changes in mitochondrial properties during neural stem cell differentiation

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Mechanisms coupling the mTOR pathway to chronic obstructive pulmonary disease (COPD) pathogenesis

Goyal, A., Chopra, V., Garg, K., & Sharma, S. (2025) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2024.12.005 · Cited by 17

Metabolomics Analyses of Cancer Cells in Controlled Microenvironments

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A comprehensive characterization of the impact of mycophenolic acid on the metabolism of Jurkat T cells

Fernández-Ramos, A. A., Marchetti, C., Poindessous, V., Antonio, S., Petitgas, C., Ceballos-Picot, I., Laurent‐Puig, P., Bortoli, S., Loriot, M., & Pallet, N. (2017) · Scientific Reports · doi:10.1038/s41598-017-10338-6 · Cited by 18

Apomorphine rescues reactive oxygen species-induced apoptosis of fibroblasts with mitochondrial disease

Miyauchi, A., Kouga, T., Jimbo, E. F., Matsuhashi, T., Abe, T., Yamagata, T., & Osaka, H. (2019) · Mitochondrion · doi:10.1016/j.mito.2019.07.006 · Cited by 18

Injury-induced Autophagy Delays Axonal Regeneration after Optic Nerve Damage in Adult Zebrafish

Beckers, A., Vanhunsel, S., Dyck, A. V., Bergmans, S., Masin, L., & Moons, L. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.07.009 · Cited by 17

Omics analyses of a somatic Trp53 R245W/+ breast cancer model identify cooperating driver events activating PI3K/AKT/mTOR signaling

Yu, X., Zhang, Y., Xiong, S., McDaniel, J. M., Sun, C., Chau, G. P., Gencel‐Augusto, J., Chachad, D., Morrissey, R. L., Rao, X., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2210618119 · Cited by 16

An investigation of nutrient-dependent mRNA translation in Drosophila larvae

Nagarajan, S., & Grewal, S. (2014) · Biology Open · doi:10.1242/bio.20149407 · Cited by 19

Mitochondria link metabolism and epigenetics in haematopoiesis

Schell, J. C., & Rutter, J. P. (2017) · Nature Cell Biology · doi:10.1038/ncb3540 · Cited by 18

Tumor-derived vesicles in immune modulation: focus on signaling pathways

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Decoding the interactions and functions of non-coding RNA with artificial intelligence

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