AMPK: An Energy-Sensing Pathway with Multiple Inputs and Outputs

WebLogo: A Sequence Logo Generator: Figure 1Preprint

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Resveratrol improves health and survival of mice on a high-calorie diet

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FIMO: scanning for occurrences of a given motif

Grant, C. E., Bailey, T. L., & Noble, W. S. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr064 · Cited by 4,247

AMPK Phosphorylation of Raptor Mediates a Metabolic Checkpoint

Gwinn, D. M., Shackelford, D. B., Egan, D. F., Mihaylova, M. M., Mery, A., Vasquez, D. S., Turk, B. E., & Shaw, R. J. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.03.003 · Cited by 3,849

Antimicrobial Autophagy: A Conserved Innate Immune Response in Drosophila

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Anorexigenic and Orexigenic Hormone Modulation of Mammalian Target of Rapamycin Complex 1 Activity and the Regulation of Hypothalamic Agouti-Related Protein mRNA Expression

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Phosphorylation of ULK1 (hATG1) by AMP-Activated Protein Kinase Connects Energy Sensing to Mitophagy

Egan, D. F., Shackelford, D. B., Mihaylova, M. M., Gelino, S., Kohnz, R. A., Mair, W., Vasquez, D. S., Joshi, A., Gwinn, D. M., Taylor, R., et al. (2011) · Science · doi:10.1126/science.1196371 · Cited by 2,600

Scansite 2.0: proteome-wide prediction of cell signaling interactions using short sequence motifs

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The Structural Basis for 14-3-3:Phosphopeptide Binding Specificity

Yaffe, M. B., Rittinger, K., Volinia, S., Caron, P. R., Aitken, A., Leffers, H. C. B., Gamblin, S. J., Smerdon, S. J., & Cantley, L. C. (1997) · Cell · doi:10.1016/s0092-8674(00)80487-0 · Cited by 1,604

Calmodulin-dependent protein kinase kinase-β is an alternative upstream kinase for AMP-activated protein kinase

Hawley, S. A., Pan, D. A., Mustard, K. J., Ross, L., Bain, J., Edelman, A. M., Frenguelli, B. G., & Hardie, D. G. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.05.009 · Cited by 1,589

Glucose transport across lagomorph jejunum epithelium is modulated by AMP-activated protein kinase under hypoxia

Dengler, F., Rackwitz, R., Pfannkuche, H., & Gäbel, G. (2017) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00436.2017 · Cited by 17

High oleic peanuts improve parameters leading to fatty liver development and change the microbiota in mice intestine

Bimro, E. T., Hovav, R. H., Nyska, A., Assa-Glazer, T., & Madar, Z. (2020) · Food & Nutrition Research · doi:10.29219/fnr.v64.4278 · Cited by 16

Demystifying Chronic Kidney Disease of Unknown Etiology (CKDu): Computational Interaction Analysis of Pesticides and Metabolites with Vital Renal Enzymes

Rajapaksha, H., Pandithavidana, D. R., & Dahanayake, J. N. (2021) · Biomolecules · doi:10.3390/biom11020261 · Cited by 17

A New Insight into an Alternative Therapeutic Approach to Restore Redox Homeostasis and Functional Mitochondria in Neurodegenerative Diseases

Hyun, D., & Lee, J. (2021) · Antioxidants · doi:10.3390/antiox11010007 · Cited by 15

The STIM1 Phosphorylation Saga

Yu, F., & Machaca, K. (2022) · Cell Calcium · doi:10.1016/j.ceca.2022.102551 · Cited by 14

PF ‐06409577 inhibits renal cyst progression by concurrently inhibiting the mTOR pathway and CFTR channel activity

Su, L., Yuan, H., Zhang, H., Wang, R., Fu, K., Yin, L., Ren, Y., Liu, H., Fang, Q., Wang, J., et al. (2022) · FEBS Open Bio · doi:10.1002/2211-5463.13459 · Cited by 14

AMPKα Is Suppressed in Bladder Cancer through Macrophage-Mediated Mechanisms

Kopsiaftis, S., Hegde, P., Taylor, J. A., & Claffey, K. P. (2016) · Translational Oncology · doi:10.1016/j.tranon.2016.07.007 · Cited by 14

Nogo‑B receptor in relevant carcinoma: Current achievements, challenges and aims (Review)

Li, Y., Xie, Y., Wu, D., Long, S.-L., Tang, S., & Mo, Z. (2018) · International Journal of Oncology · doi:10.3892/ijo.2018.4520 · Cited by 14

Low Ouabain Doses and AMP-Activated Protein Kinase as Factors Supporting Electrogenesis in Skeletal Muscle

Васильевна, К. В., Vilchinskaya, N. A., Розломий, В. Л., Shenkman, B. S., & Krivoi, I. I. (2019) · Biochemistry (Moscow) · doi:10.1134/s0006297919090116 · Cited by 14

Glucose Starvation-Induced Rapid Death of Nrf1 α -Deficient, but Not Nrf2-Deficient, Hepatoma Cells Results from Its Fatal Defects in the Redox Metabolism Reprogramming

Zhu, Y., Zheng, Z., Xiang, Y., & Zhang, Y. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/4959821 · Cited by 14

Role of Cardiac AMP-Activated Protein Kinase in a Non-pathological Setting: Evidence From Cardiomyocyte-Specific, Inducible AMP-Activated Protein Kinase α1α2-Knockout Mice

Tokarska-Schlattner, M., Kay, L., Perret, P., Isola, R., Attia, S., Lamarche, F., Tellier, C., Cottet‐Rousselle, C., Uneisi, A., Hininger‐Favier, I., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.731015 · Cited by 13

Exploring Muscle Health Deterioration and Its Determinants Among Community-Dwelling Older Adults

Chao, Y., Fang, W., Chen, W., Peng, T., Yang, W., & Kao, T. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.817044 · Cited by 13

Early life exposure to high fructose diet induces metabolic dysregulation associated with sex-specific cognitive impairment in adolescent rats

Barrett, C. E., Jiang, M., O'Flaherty, B. G., Dias, B. G., Rainnie, D. G., Young, L. J., & Menigoz, A. (2021) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2022.109220 · Cited by 13

Exercise Training Attenuates Acute β-Adrenergic Receptor Activation-Induced Cardiac Inflammation via the Activation of AMP-Activated Protein Kinase

Zhang, M., Alemasi, A., Zhao, M., Xu, W., Zhang, Y., Gao, W. D., Yu, H., & Xiao, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119263 · Cited by 13

Nutritional control of developmental processes

Ferenc, J., & Ikmi, A. (2023) · Development · doi:10.1242/dev.200623 · Cited by 13

Strategy for treating MAFLD: Electroacupuncture alleviates hepatic steatosis and fibrosis by enhancing AMPK mediated glycolipid metabolism and autophagy in T2DM rats

Duan, H., Song, S., Li, R., Hu, S., Zhuang, S., Liu, S., Li, X., & Gao, W. (2024) · Diabetology & Metabolic Syndrome · doi:10.1186/s13098-024-01432-7 · Cited by 16

Kidney-specific genetic deletion of both AMPK α-subunits causes salt and water wasting

Lazo‐Fernandez, Y., Baile, G., Meade, P., Torcal, P., Martínez-Gimeno, L., Ibañez, C. R., Bernal, M. L., Viollet, B., & Gimenez-Lopez, I. (2016) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00169.2016 · Cited by 15

AMP-activated protein kinase in the grass carp Ctenopharyngodon idellus: Molecular characterization, tissue distribution and mRNA expression in response to overwinter starvation stress

Wu, W., Sun, J. H., Ji, H., Yu, H., & Zhou, J. (2020) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2020.110457 · Cited by 13

Mechanisms Underlying the Expansion and Functional Maturation of β-Cells in Newborns: Impact of the Nutritional Environment

Jacovetti, C., & Regazzi, R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042096 · Cited by 14

Tumor protein D52 ( TPD52 ) affects cancer cell metabolism by negatively regulating AMPK

Chen, Y., Peng, C., Tan, W. H., Yu, J., Zayas, J., Peng, Y., Lou, Z., Pei, H., & Wang, L. (2022) · Cancer Medicine · doi:10.1002/cam4.4911 · Cited by 14

The Dual Role of Metformin: Repurposing an Antidiabetic Drug for Cancer Therapy

Barbosa, F., Cunha, A., Barbosa, J., Faria, J., & Queirós, O. (2025) · Applied Sciences · doi:10.3390/app152111576 · Cited by 13

Current insights in molecular characterization of non-alcoholic fatty liver disease and treatment

Che, W., Zhao, M., Li, X., Li, C., Cho, W. C. S., & Yu, S. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1002916 · Cited by 12

Downregulation of miR-137 Facilitates CD4+ T Cell Pyroptosis in Systemic Lupus Erythematosus via Stimulating AMPK Pathway

Gong, A., Mi, L., Wei, F., Zhuang, Y., Song, Y., Pan, C., Zhang, X., Lin, G., Wu, Z., & Liu, Y. (2023) · Journal of Immunology Research · doi:10.1155/2023/1241774 · Cited by 12

Regulation of AMPK activation by extracellular matrix stiffness in pancreatic cancer

Xu, X., Fang, Y., Nowsheen, S., Li, Y., Lou, Z., & Deng, M. (2023) · Genes & Diseases · doi:10.1016/j.gendis.2023.05.022 · Cited by 12

AMPK, a hub for the microenvironmental regulation of bone homeostasis and diseases

Liu, J., Liu, J.-X., Li, R., Zhang, Z., Zhang, X., Xing, S., Sui, B., Jin, F., Ma, B., & Zheng, C. (2024) · Journal of Cellular Physiology · doi:10.1002/jcp.31393 · Cited by 14

PF-06409577 activates AMPK signaling to protect retinal pigment epithelium cells from UV radiation

Li, X., Liu, X., Huang, D., Cao, H.-J., & Wang, J. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.05.003 · Cited by 12

Deletion of AMPK minimizes graft-versus-host disease through an early impact on effector donor T cells

Monlish, D. A., Beezhold, K., Chiaranunt, P., Paz, K. G., Moore, N. J., Dobbs, A. K., Brown, R., Ozolek, J. A., Blazar, B. R., & Byersdorfer, C. A. (2021) · JCI Insight · doi:10.1172/jci.insight.143811 · Cited by 11

β-Aminoisobutyric acid supplementation attenuated salt-sensitive hypertension in Dahl salt-sensitive rats through prevention of insufficient fumarase

Zheng, X., Zhou, L., Jin, Y., Zhao, X., Ahmad, H., Ouyang, Y., Chen, S., Du, J., Chen, X., Chen, L., et al. (2021) · Amino Acids · doi:10.1007/s00726-021-03092-7 · Cited by 12

The Pursuit of Enzyme Activation: A Snapshot of the Gold Rush

Teng, M., Young, D. W., & Tan, Z. (2022) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.2c01291 · Cited by 12

Cell-Free Assays to Measure Effects of Regulatory Ligands on AMPK

Fyffe, F. A., Hawley, S. A., Gray, A., & Hardie, D. G. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7598-3_5 · Cited by 12

Therapeutic Properties of Polyphenols Affect AMPK Molecular Pathway in HyperlipidemiaPreprint

Sotoudeheian, M., Hoseini, S., & Mirahmadi, S. (2023) · Preprints.org · doi:10.20944/preprints202301.0528.v1 · Cited by 12

An In Vitro Gut–Liver–Adipose Axis Model to Evaluate the Anti-Obesity Potential of a Novel Probiotic–Polycosanol Combination

Mulè, S., Galla, R., Parini, F., Botta, M., Ferrari, S., & Uberti, F. (2025) · Foods · doi:10.3390/foods14112003 · Cited by 11

Environmental Pollutant‐Induced Disruption of Lipid Droplet Homeostasis in Aquatic Animals: Molecular Mechanisms and Cross‐Scale Health Effects

Huang, X., Xie, D., & Wang, J. (2025) · Reviews in Aquaculture · doi:10.1111/raq.70086 · Cited by 12

AMP-activated protein kinase-dependent nuclear localization of glyceraldehyde 3-phosphate dehydrogenase in senescent human diploid fibroblasts

Sohn, J. Y., Kwak, H.-J., Rhim, J. H., & Yeo, E. (2022) · Aging · doi:10.18632/aging.203825 · Cited by 11

TRPM7-Mediated Ca2+ Regulates Mussel Settlement through the CaMKKβ-AMPK-SGF1 Pathway

He, J. W., Wang, P., Wang, Z., Feng, D., & Zhang, D. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065399 · Cited by 13

A critical review of ethanol effects on neuronal firing: A metabolic perspective

Popova, D., Sun, J. K., Chow, H., & Hart, R. P. (2024) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.15266 · Cited by 13

Dissolved oxygen and ammonia affect ammonia production via GDH/AMPK signaling pathway and alter flesh quality in Chinese perch (Siniperca chuatsi)

Yang, R., Liu, X., Liu, Y., Tian, Q., Wang, Z., Zhu, D. M., Qian, Z., Yi, Y., Hu, J., Li, Y., et al. (2024) · Fish Physiology and Biochemistry · doi:10.1007/s10695-024-01333-6 · Cited by 11

SF1-specific deletion of the energy sensor AMPKγ2 induces obesity

Freire-Agulleiro, Ó., Estévez‐Salguero, Á., Ferreira, V., Holleman, C. L., García-Currás, J., González‐García, I., Nogueiras, R., Tena‐Sempere, M., García‐Cáceres, C., Diéguez, C., et al. (2024) · Molecular Metabolism · doi:10.1016/j.molmet.2024.102091 · Cited by 11

AMP-activated protein kinase mediates adaptation of glioblastoma cells to conditions of the tumor microenvironment

Lorenz, N. I., Sauer, B., Urban, H., Weinem, J., Parmar, B. S., Zeiner, P. S., Strecker, M., Schulte, D., Mittelbronn, M. G. A., Alekseeva, T., et al. (2025) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-025-03346-2 · Cited by 16

Iron Metabolism and Ferroptosis in Diabetic Kidney Disease

Mu, F., Luo, P., Zhu, Y., Nie, P., Li, B., & Bai, X. (2025) · Cell Biochemistry and Function · doi:10.1002/cbf.70067 · Cited by 11

Osteocalcin Ameliorates CUMS ‐Induced Depressive‐Like Behaviors by Reducing Mitochondrial Damage in Hippocampal Neurons

Chen, H., Mao, J., Wang, M., Zhang, Q., Zheng, R., Zhang, Z., Lv, Q., Liu, Q., Wu, Y., & Ma, X. (2025) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70530 · Cited by 12

Cytokine-Dependent Expression Regulation of ALOX15

Kühn, H., Gehring, T., Schroter, A., & Heydeck, D. (2016) · Journal of Cytokine Biology · doi:10.4172/2576-3881.1000106 · Cited by 11

Multi-Stability and Consequent Phenotypic Plasticity in AMPK-Akt Double Negative Feedback Loop in Cancer Cells

Chedere, A., Hari, K., Kumar, S., Rangarajan, A., & Jolly, M. K. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10030472 · Cited by 11

The Mechanism of Dendrobium officinale as a Treatment for Hyperlipidemia Based on Network Pharmacology and Experimental Validation

Li, L.-Z., Wang, H., Huang, J.-H., Liu, K., Feng, X.-J., Wang, X., Zhu, L.-J., He, X., Zheng, X., Liu, X., et al. (2022) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2022/5821829 · Cited by 11

LKB1 is physiologically required for sleep from Drosophila melanogaster to the Mus musculus

Liu, Z., Jiang, L., Li, C., Li, C., Yang, J., Yu, J., Mao, R., & Rao, Y. (2022) · Genetics · doi:10.1093/genetics/iyac082 · Cited by 11

Targeted Inhibition of Hsp90 in Combination with Metformin Modulates Programmed Cell Death Pathways in A549 Lung Cancer Cells

Hasan, A., Khamjan, N. A., Lohani, M., & Mir, S. S. (2023) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-023-04424-x · Cited by 11

Metformin blocks BIK1-mediated CPK28 phosphorylation and enhances plant immunity

Bao, Y., Zhang, Q., Zhu, H., Pei, Y., Zhao, Y., Li, Y., Ji, P., Du, D., Peng, H. F., Xu, G., et al. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.02.025 · Cited by 13

The stress polarity pathway: AMPK 'GIV'-es protection against metabolic insults

Ghosh, P. (2017) · Aging · doi:10.18632/aging.101179 · Cited by 11

Suppression of gluconeogenic gene transcription by SIK1-induced ubiquitination and degradation of CRTC1

Gao, W., Tang, H.-M. V., Cheng, Y., Chan, C.-P., Chan, C.-P., & Jin, D. (2018) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2018.01.021 · Cited by 11

Energy-Sensing Pathways in Ischemia: The Counterbalance Between AMPK and mTORC

Céspedes-Rubio, Á. E., Villa, M., Benito‐Cuesta, I., Pérez-Álvarez, M. J., Ordóñez‐Gutiérrez, L., & Wandosell, F. G. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666191210152156 · Cited by 11

Are Hippocampal Hypoperfusion and ATP Depletion Prime Movers in the Genesis of Alzheimer’s Disease? A Review of Recent Pertinent Observations from Molecular Biology

Walker, V. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26157328 · Cited by 11

GANT61 Elevates Chemosensitivity to Cisplatin Through Regulating the Hedgehog, AMPK and cAMP Pathways in Ovarian Cancer

Zhu, P., Wang, L., Xu, P., Tan, Q., Wang, Y., Feng, G., & Yuan, L. (2022) · Future Medicinal Chemistry · doi:10.4155/fmc-2021-0310 · Cited by 10

Autoinhibition of ubiquitin-specific protease 8: Insights into domain interactions and mechanisms of regulation

Caba, C., Black, M. K., Liu, Y., DaDalt, A. A., Mallare, J., Fan, L., Harding, R., Wang, Y., Vacratsis, P. O., Huang, R., et al. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.107727 · Cited by 11

Molecular pathways involved in the control of contractile and metabolic properties of skeletal muscle fibers as potential therapeutic targets for Duchenne muscular dystrophy

Bonato, A., Raparelli, G., & Caruso, M. (2024) · Frontiers in Physiology · doi:10.3389/fphys.2024.1496870 · Cited by 10

Affinity Modifications of Porous Microscaffolds Impact Bone Regeneration by Modulating the Delivery Kinetics of Small Extracellular Vesicles

Gao, Y., Yuan, X., Gu, R., Wang, N., Ren, H., Song, R. Y., Wan, Z., Huang, J., Yi, K., Xiong, C., et al. (2025) · ACS Nano · doi:10.1021/acsnano.5c03297 · Cited by 10

Taurine Attenuates Disuse Muscle Atrophy Through Modulation of the xCT-GSH-GPX4 and AMPK-ACC-ACSL4 Pathways

Liu, X., Chen, Y., Zhang, L., Qi, Z., Yang, L., Huang, C., Wang, L., & Lin, D. (2025) · Antioxidants · doi:10.3390/antiox14070847 · Cited by 12

The Role of AMPKα in the Mechanism of Development and Treatment of Heart Failure

Feng, Y., Zhu, Z., He, Y., & Li, X. (2025) · Reviews in Cardiovascular Medicine · doi:10.31083/rcm36391 · Cited by 11

Roles of GTP and Rho GTPases in pancreatic islet beta cell function and dysfunction

Kowluru, A. (2020) · Small GTPases · doi:10.1080/21541248.2020.1815508 · Cited by 10

Impact of heparanase‐2 (Hpa2) on cancer and inflammation: Advances and paradigms

Vlodavsky, I., Hilwi, M., Kayal, Y., Soboh, S., & Ilan, N. (2024) · The FASEB Journal · doi:10.1096/fj.202400286r · Cited by 10

Standardized LC×LC-ELSD Fractionation Procedure for the Identification of Minor Bioactives via the Enzymatic Screening of Natural Extracts

Coulerie, P., Ratinaud, Y., Moco, S., Merminod, L., Pinta, M. N., Boccard, J., Bultot, L., Deák, M., Sakamoto, K., Queiroz, E. F., et al. (2016) · Journal of Natural Products · doi:10.1021/acs.jnatprod.6b00628 · Cited by 10

Regulation of Trypanosoma brucei Acetyl Coenzyme A Carboxylase by Environmental Lipids

Ray, S. S., Wilkinson, C. L., & Paul, K. S. (2018) · mSphere · doi:10.1128/msphere.00164-18 · Cited by 10

PP2A inhibition by LB-100 protects retinal pigment epithelium cells from UV radiation via activation of AMPK signaling

Li, X., Li, S., Dai, C., Li, J., Huang, D., & Wang, J. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.10.077 · Cited by 11

Determination of the Global Pattern of Gene Expression in Yeast Cells by Intracellular Levels of Guanine Nucleotides

Hesketh, A. R., Vergnano, M., & Oliver, S. G. (2019) · mBio · doi:10.1128/mbio.02500-18 · Cited by 10

Expression of messenger RNA encoding two cellular metabolic regulators, AMP-activated protein kinase (AMPK) and O-GlcNAc transferase (OGT), in channel catfish: Their tissue distribution and relationship with changes in food intake

Abernathy, O., Kostner, D. L., Buer, P., Dougherty, M., Schmidtberger, A., Spainhour, R., Leiker, A. J., Vides, M., Teel, B., & Kobayashi, Y. (2019) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2019.04.023 · Cited by 10

l‐ Arginine supplementation of gilts during early gestation modulates energy sensitive pathways in pig conceptuses

Garcia, I. S., Teixeira, S. A., Costa, K. A., Marques, D. B. D., Rodrigues, G. D. A., Costa, T. C., Guimarães, J. D., Otto, P. I., Saraiva, A., Ibelli, A. M. G., et al. (2020) · Molecular Reproduction and Development · doi:10.1002/mrd.23397 · Cited by 10

Berberine inhibits pancreatic intraepithelial neoplasia by inhibiting glycolysis via the adenosine monophosphate -activated protein kinase pathway

Liu, M.-M., Yang, Y., Kang, W., Liu, Y., Tao, X., Li, X., & Pan, Y. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.174680 · Cited by 10

An Inhibitor of Grp94 Inhibits OxLDL-Induced Autophagy and Apoptosis in VECs and Stabilized Atherosclerotic Plaques

Wei, Q., Ren, H., Zhang, J., Yao, W., Zhao, B., & Miao, J. (2021) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2021.757591 · Cited by 10

β-(4-fluorobenzyl) Arteannuin B induced interaction of ATF-4 and C/EBPβ mediates the transition of breast cancer cells from autophagy to senescence

Mir, K. B., Faheem, M. M., Ahmad, S. M., Rasool, J. U., Amin, T., Chakraborty, S., Bhagat, M., Ahmed, Z., Ali, A., & Goswami, A. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.1013500 · Cited by 10

Mitochondria in Health and Disease

Meiliana, A., Dewi, N. M., & Wijaya, A. (2019) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v11i1.779 · Cited by 13

Epithelial–Mesenchymal Transition Suppresses AMPK and Sensitizes Cancer Cells to Pyroptosis under Energy Stress

Liang, M., Li, J. W., Luo, H., Lulu, S., Calbay, O., Shenoy, A. K., Tan, M., Law, B. K., Huang, S., Xiao, T. S., et al. (2022) · Cells · doi:10.3390/cells11142208 · Cited by 9

High-fat diet and palmitate inhibits FNDC5 expression via AMPK-Zfp57 pathway in mouse muscle cells

Guo, Q., Zhang, B., Du, H., Zhu, R., Sun, X., Fan, X., Wei, X., Yang, D., Oh, Y., Fan, L., et al. (2022) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2022.110265 · Cited by 10

Sex-Dimorphic Effects of Hypoglycemia on Metabolic Sensor mRNA Expression in Ventromedial Hypothalamic Nucleus-Dorsomedial Division (VMNdm) Growth Hormone-Releasing Hormone Neurons

Sapkota, S., & Briski, K. P. (2024) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00206 · Cited by 9

Whole-Transcriptome Analysis Sheds Light on the Biological Contexts of Intramuscular Fat Deposition in Ningxiang Pigs

Zhao, J., Gao, H., Fu, Y., Ren, R., Deng, X., Chen, Y., Hou, X., Wang, Q., Song, G., Fan, N., et al. (2024) · Genes · doi:10.3390/genes15050642 · Cited by 9

Precise intracellular uptake and endosomal release of diverse functional mRNA payloads via glutathione-responsive nanogels

Dabas, R., Navaratnam, N., Iino, H., Saidjalolov, S., Matile, S., Carling, D., Rueda, D., & Kamaly, N. (2024) · Materials Today Bio · doi:10.1016/j.mtbio.2024.101425 · Cited by 10

Mechanisms underpinning the effect of exercise on the non-alcoholic fatty liver disease: review

Bekheit, M., Kamera, B. S., Colacino, L., Dropmann, A., Delibegović, M., Almadhoob, F., Hanafy, N. A. N., Bermano, G., & Hammad, S. (2024) · EXCLI journal · doi:10.17179/excli2024-7718 · Cited by 12

Loss of AMPKα2 Impairs Hedgehog-Driven Medulloblastoma Tumorigenesis

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PPARγ Plays an Important Role in Acute Hepatic Ischemia-Reperfusion Injury via AMPK/mTOR Pathway

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