AMP-activated protein kinase: also regulated by ADP?

Role of AMP-Activated Protein Kinase in Mechanism of Metformin Action

Zhou, G., Myers, R., Li, Y., Chen, Y., Shen, X., Fenyk-Melody, J., Wu, M., Ventre, J., Doebber, T., Fujii, N., et al. (2001) · Journal of Clinical Investigation · doi:10.1172/jci13505 · Cited by 5,652

Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan

Howitz, K. T., Bitterman, K. J., Cohen, H. Y., Lamming, D. W., Lavu, S., Wood, J. G., Zipkin, R. E., Chung, P., Kisielewski, A., Zhang, L.-L., et al. (2003) · Nature · doi:10.1038/nature01960 · Cited by 3,796

Hudson et al.

Anderson, E. N. (1977) · eScholarship (California Digital Library) · Cited by 2,567

AMP-activated/SNF1 protein kinases: conserved guardians of cellular energy

Hardie, D. G. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2249 · Cited by 2,261

Evidence that metformin exerts its anti-diabetic effects through inhibition of complex 1 of the mitochondrial respiratory chain

OWEN, M. R., DORAN, E., & HALESTRAP, A. P. (2000) · Biochemical Journal · doi:10.1042/bj3480607 · Cited by 2,157

The Kinase LKB1 Mediates Glucose Homeostasis in Liver and Therapeutic Effects of Metformin

Shaw, R. J., Lamia, K. A., Vasquez, D., Koo, S.-H., Bardeesy, N., DePinho, R. A., Montminy, M., & Cantley, L. C. (2005) · Science · doi:10.1126/science.1120781 · Cited by 1,950

Complexes between the LKB1 tumor suppressor, STRADα/β and MO25α/β are upstream kinases in the AMP-activated protein kinase cascade

Hawley, S. A., Boudeau, J., Reid, J. L., Mustard, K. J., Udd, L., Mäkelä, T. P., Alessi, D. R., & Hardie, D. G. (2003) · Journal of Biology · doi:10.1186/1475-4924-2-28 · Cited by 1,694

AMPK in Health and Disease

Steinberg, G. R., & Kemp, B. E. (2009) · Physiological Reviews · doi:10.1152/physrev.00011.2008 · Cited by 1,672

LKB1 is the upstream kinase in the AMP-activated protein kinase cascade

Woods, A., Johnstone, S. R., Dickerson, K., Leiper, F. C., Fryer, L. G. D., Neumann, D., Schlattner, U., Wallimann, T., Carlson, M., & Carling, D. (2003) · Current Biology · doi:10.1016/j.cub.2003.10.031 · Cited by 1,650

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

AMPK Signalling Pathway: A Potential Strategy for the Treatment of Heart Failure with Chinese Medicine

Liu, C., Guo, X., Zhou, Y., & Wang, H. (2023) · Journal of Inflammation Research · doi:10.2147/jir.s441597 · Cited by 25

NBM-T-BMX-OS01, an Osthole Derivative, Sensitizes Human Lung Cancer A549 Cells to Cisplatin through AMPK-Dependent Inhibition of ERK and Akt Pathway

Chen, T.-J., Zhou, Y.-F., Ning, J.-J., Yang, T., Ren, H., Li, Y., Zhang, S., & Chen, M.-W. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000430264 · Cited by 24

Mice lacking AMP-activated protein kinase α1 catalytic subunit have increased bone remodelling and modified skeletal responses to hormonal challenges induced by ovariectomy and intermittent PTH treatment

Jeyabalan, J., Shah, M., Viollet, B., Roux, J. P., Chavassieux, P., Korbonits, M., & Chenu, C. (2012) · Journal of Endocrinology · doi:10.1530/joe-12-0184 · Cited by 24

Spinosad induces autophagy of Spodoptera frugiperda Sf9 cells and the activation of AMPK/mTOR signaling pathway

Yang, M., Hao, Y., Gao, J., Zhang, Y., Xu, W., & Tao, L. (2017) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2017.02.008 · Cited by 24

AMPK synergizes with the combined treatment of 1′‐acetoxychavicol acetate and sodium butyrate to upregulate phase II detoxifying enzyme activities

Yaku, K., Matsui‐Yuasa, I., Konishi, Y., & Kojima‐Yuasa, A. (2013) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201200809 · Cited by 23

Dealing with Stress: Defective Metabolic Adaptation in Chronic Obstructive Pulmonary Disease Pathogenesis

Michaeloudes, C., Bhavsar, P. K., Mumby, S. E., Chung, K. F., & Adcock, I. M. (2017) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201702-153aw · Cited by 24

Japanese quince (Chaenomeles japonica L.) fruit polyphenolic extract modulates carbohydrate metabolism in HepG2 cells via AMP-activated protein kinase

Zakłos‐Szyda, M., & Pietrzyk, N. (2018) · Acta Biochimica Polonica · doi:10.18388/abp.2017_1604 · Cited by 22

AMP-activated protein kinase regulates alternative pre-mRNA splicing by phosphorylation of SRSF1

Matsumoto, E., Akiyama, K., Saito, T., Matsumoto, Y., Kobayashi, K., Inoue, J., Yamamoto, Y., & Suzuki, T. (2020) · Biochemical Journal · doi:10.1042/bcj20190894 · Cited by 22

Roundup-Induced AMPK/mTOR-Mediated Autophagy in Human A549 Cells

Hao, Y., Xu, W., Gao, J., Zhang, Y., Yang, Y., & Tao, L. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.9b04679 · Cited by 22

Purine metabolite and energy charge analysis of Trypanosoma brucei cells in different growth phases using an optimized ion-pair RP-HPLC/UV for the quantification of adenine and guanine pools

Graven, P., Tambalo, M., Scapozza, L., & Perozzo, R. (2014) · Experimental Parasitology · doi:10.1016/j.exppara.2014.03.006 · Cited by 22

Determining AMPK Activation via the Lysosomal v-ATPase-Ragulator-AXIN/LKB1 Axis

Zhang, C., Li, M., Zong, Y., & Lin, S. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7598-3_25 · Cited by 23

Stachydrine Mediates Rapid Vascular Relaxation: Activation of Endothelial Nitric Oxide Synthase Involving AMP-Activated Protein Kinase and Akt Phosphorylation in Vascular Endothelial Cells

Xie, X., Yang, C., Cui, Q., Ma, W., Liu, J., Yao, Q., Zhang, Z., Xiao, L., & Wang, N. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.9b03501 · Cited by 20

Skeletal muscle AMP-activated protein kinase γ1H151R overexpression enhances whole body energy homeostasis and insulin sensitivity

Schönke, M., Myers, M. G., Zierath, J. R., & Björnholm, M. (2015) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00195.2015 · Cited by 17

Adenosine Monophosphate-Activated Protein Kinase (AMPK) as a Diverse Therapeutic Target: A Computational Perspective

Ramesh, M., Vepuri, S. B., Oosthuizen, F., & Soliman, M. E. S. (2015) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-015-1911-9 · Cited by 17

AMPK Wars: the VMH Strikes Back, Return of the PVH

López, M. (2018) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2018.01.004 · Cited by 17

Downregulation of glucose-energy metabolism via AMPK signaling pathway in granulosa cells of diminished ovarian reserve patients

Zhu, Q., Du, J., Li, Y., Qin, X. Y., He, R., Ma, H., & Liang, X. (2024) · Gene · doi:10.1016/j.gene.2024.148979 · Cited by 16

Hernandezine, a natural herbal alkaloid, ameliorates type 2 diabetes by activating AMPK in two mouse models

Bai, J., Zhang, S., Cao, J., Sun, H., Mang, Z., Shen, W. L., & Li, H. (2022) · Phytomedicine · doi:10.1016/j.phymed.2022.154366 · Cited by 15

A Functional Signature Ontology (FUSION) screen detects an AMPK inhibitor with selective toxicity toward human colon tumor cells

Das, B., Neilsen, B. K., Fisher, K. W., Gehring, D., Hu, Y., Volle, D. J., Kim, H. S., McCall, J. L., Kelly, D. L., MacMillan, J. B., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-22090-6 · Cited by 16

ULK1-regulated AMP sensing by AMPK and its application for the treatment of chronic kidney disease

Yanagi, T., Kikuchi, H., Takeuchi, K., Susa, K., Mori, T., Chiga, M., Yamamoto, K., Furukawa, A., Kanazawa, T., Kato, Y., et al. (2024) · Kidney International · doi:10.1016/j.kint.2024.08.024 · Cited by 14

Characterizing region-specific glucose metabolic profile of the rodent brain using Seahorse XFe96 analyzer

Wang, L., Chaudhari, K., Winters, A., Sun, Y., Liu, R., & Yang, S.-H. (2022) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x221077341 · Cited by 14

Genetically Encoded Fluorescent Biosensors to Explore AMPK Signaling and Energy Metabolism

Pelosse, M., Cottet‐Rousselle, C., Grichine, A., Berger, I., & Schlattner, U. (2016) · Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions · doi:10.1007/978-3-319-43589-3_20 · Cited by 17

Measurement of AMP-Activated Protein Kinase Activity and Expression in Response to Ghrelin

Lim, C. T., Lolli, F., Thomas, J., Kola, B., & Korbonits, M. (2012) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/b978-0-12-381272-8.00017-9 · Cited by 14

Ion Channel Regulation by the LKB1-AMPK Signalling Pathway: The Key to Carotid Body Activation by Hypoxia and Metabolic Homeostasis at the Whole Body Level

Evans, A. M., Peers, C., Wyatt, C. N., Kumar, P., & Hardie, D. G. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-4584-1_11 · Cited by 13

Contraction-induced signaling: evidence of convergent cascades in the regulation of muscle fatty acid metabolism

Turcotte, L. P., & Abbott, M. J. (2012) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y2012-124 · Cited by 15

Lessons from Nature: Sources and Strategies for Developing AMPK Activators for Cancer Chemotherapeutics

Arkwright, R. T., Deshmukh, R. R., Adapa, N., Stevens, R. A., Zonder, E., Zhang, Z., Farshi, P., Ahmed, R. S. I., El-Banna, H. A., Chan, T. H., et al. (2015) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1871520615666141216145417 · Cited by 15

Liver Kinase B1 Expression Promotes Phosphatase Activity and Abrogation of Receptor Tyrosine Kinase Phosphorylation in Human Cancer Cells

Okon, I. S., Coughlan, K. A., & Zou, M. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.500934 · Cited by 11

Liraglutide Inhibits Hepatitis C Virus Replication Through an AMP Activated Protein Kinase Dependent Mechanism

Lee, M., Chen, W., Hsu, W., Chen, S., & Lee, J. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20184569 · Cited by 12

Systems Level Regulation of Cardiac Energy Fluxes Via Metabolic Cycles: Role of Creatine, Phosphotransfer Pathways, and AMPK Signaling

Saks, V. A., Schlattner, U., Tokarska-Schlattner, M., Wallimann, T., Bagur, R., Zorman, S., Pelosse, M., Santos, P. D. D., Boucher, F. R., Käämbre, T., et al. (2013) · Springer series in biophysics · doi:10.1007/978-3-642-38505-6_11 · Cited by 13

Kinase signalling adaptation supports dysfunctional mitochondria in disease

Skalka, G., Tsakovska, M., & Murphy, D. J. (2024) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2024.1354682 · Cited by 12

Flavonoids’ Dual Benefits in Gastrointestinal Cancer and Diabetes: A Potential Treatment on the Horizon?

AL-Ishaq, R. K., Mazuráková, A., Kubatka, P., & Büsselberg, D. (2022) · Cancers · doi:10.3390/cancers14246073 · Cited by 13

Metabolomics Dysfunction in Replicative Senescence of Periodontal Ligament Stem Cells Regulated by AMPK Signaling Pathway

Hu, M., Liu, R., Chen, X., Yan, S., Gao, J. P., Zhang, Y., Wu, D., Sun, L., Jia, Z., Sun, G., et al. (2024) · Stem Cells and Development · doi:10.1089/scd.2024.0112 · Cited by 9

Floralozone regulates MiR-7a-5p expression through AMPKα2 activation to improve cognitive dysfunction in vascular dementia

Song, Y., Li, S., Chao, C.-Y., Shuang-Guo, Chen, G.-Z., Wang, S., Zhang, M., Yin, Y.-L., & Li, P. (2024) · Experimental Neurology · doi:10.1016/j.expneurol.2024.114748 · Cited by 9

A Gene Expression High-Throughput Screen (GE-HTS) for Coordinated Detection of Functionally Similar Effectors in Cancer

Rao, C., Huisman, D. H., Vieira, H. M., Frodyma, D. E., Neilsen, B. K., Chakraborty, B., Hight, S. K., White, M. A., Fisher, K. W., & Lewis, R. E. (2020) · Cancers · doi:10.3390/cancers12113143 · Cited by 8

Rationale for investigating metformin as a protectant against statin-associated muscle symptoms

Elsaid, O., Taylor, B. A., Zaleski, A. L., Panza, G. A., & Thompson, P. D. (2017) · Journal of clinical lipidology · doi:10.1016/j.jacl.2017.06.019 · Cited by 9

The mammalian AMP‐activated protein kinase complex mediates glucose regulation of gene expression in the yeast Saccharomyces cerevisiae

Tian, Y., Bendrioua, L., Carmena, D., García‐Salcedo, R., Dahl, P. J., Carling, D., & Hohmann, S. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.04.039 · Cited by 8

Hypoxia improves self-renew and migration of urine-derived stem cells by upregulating autophagy and mitochondrial function through ERK signal pathway

Hu, C., Sun, Y., Li, W., & Bi, Y. (2023) · Mitochondrion · doi:10.1016/j.mito.2023.09.001 · Cited by 7

ATP sensitive bi-quinoline activator of the AMP-activated protein kinase

Scott, J. W., Oakhill, J. S., Ling, N. X. Y., Langendorf, C. G., Foitzik, R. C., Kemp, B. E., & Issinger, O. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.11.130 · Cited by 7

Effect of A-769662, a direct AMPK activator, on Tlr-4 expression and activity in mice heart tissue.

Rameshrad, M., Maleki‐Dizaji, N., Soraya, H., Toutounchi, N. S., Barzegari, A., & Garjani, A. (2016) · Europe PMC (PubMed Central) · doi:10.22038/ijbms.2016.7917 · Cited by 6

Context-dependent AMPK activation distinctly regulates TAp73 stability and transcriptional activity

Li, D., Dulloo, I., & Sabapathy, K. (2018) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-018-0020-y · Cited by 5

Niclosamide activates the AMP-activated protein kinase complex containing the β2 subunit independently of AMP

Suzuki, T., Kojima, M., Matsumoto, Y., Kobayashi, K., Inoue, J., & Yamamoto, Y. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.09.071 · Cited by 6

Markers of Hypoxia and Metabolism Correlate With Cell Differentiation in Retina and Lens Development

Gardiner, T. A., Branagh, T., Tipping, N., & McDonald, D. (2022) · Frontiers in Ophthalmology · doi:10.3389/fopht.2022.867326 · Cited by 5

Mice with low levels of Shc proteins display reduced glycolytic and increased gluconeogenic activities in liver

Hagopian, K., Kim, K., Lopez-Dominguez, J. A., Tomilov, A. A., Cortopassi, G. A., & Ramsey, J. J. (2016) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2016.06.021 · Cited by 5

Cellular energy sensors: AMPK and beyond

López, M., & Diéguez, C. (2014) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2014.11.007 · Cited by 4

Regulation of autophagy: Insights into O-GlcNAc modification mechanisms

Liu, C., Wang, X., Xu, S., Liu, M., & Cao, X. (2025) · Life Sciences · doi:10.1016/j.lfs.2025.123547 · Cited by 4

AMP-Activated Protein Kinase: A Metabolic Stress Sensor in the Heart

Pelosse, M., Tokarska-Schlattner, M., & Schlattner, U. (2015) · Springer eBooks · doi:10.1007/978-3-319-15263-9_10 · Cited by 4

Compartmentalization in cardiomyocytes modulates creatine kinase and adenylate kinase activities

Birkedal, R., Branovets, J., & Vendelin, M. (2024) · FEBS Letters · doi:10.1002/1873-3468.14994 · Cited by 4

Higher AMPK activation in mouse oxidative compared with glycolytic muscle does not correlate with LKB1 or CaMKKβ expression

Bernasconi, R., Soodla, K., Sirp, A., Zovo, K., Kuhtinskaja, M., Lukk, T., Vendelin, M., & Birkedal, R. (2024) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00261.2024 · 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

5-Aminoimidazole-4-carboxyamide-1-β-D-ribofranoside stimulates the ratenhancer of split- and hairy-related protein-2gene via atypical protein kinase C lambda

Komatsu, Y., Yanagisawa, Y., Moriizumi, M., Tsuchiya, Y., Yokouchi, H., Otsuka, H., Aoyagi, M., Tsukada, A., Kanai, Y., Haneishi, A., et al. (2015) · The Journal of Biochemistry · doi:10.1093/jb/mvv116 · Cited by 4

Small molecules as activators in medicinal chemistry (2000–2016)

Hameed, A., al‐Rashida, M., Alharthy, R. D., Uroos, M., Mughal, E. U., Ali, S. A., & Khan, K. M. (2017) · Expert Opinion on Therapeutic Patents · doi:10.1080/13543776.2017.1349103 · Cited by 6

Novel AMP-activated protein kinase activators and their potential for mitigating renal injury and fibrosis

Harley, G., & Mount, P. F. (2025) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/j.jpet.2025.103741 · Cited by 3

YAP upregulates AMPKα1 to induce cancer cell senescence

Zhan, Y., Wu, G., Fan, X., Fu, Z., Ni, Y., Sun, B., Chen, H., Chen, T., & Wang, X. (2024) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2024.106559 · Cited by 3

Reproductive senescence and energetic metabolism of human luteinized granulosa cells: is it all about ATP? A prospective cohort and critical view

Cecchino, G. N., Pacheco, A., & García-Velasco, J. A. (2020) · Gynecological Endocrinology · doi:10.1080/09513590.2020.1810656 · Cited by 3

MCT1-mediated transport of valeric acid promotes porcine preimplantation embryo development by improving mitochondrial function and inhibiting the autophagic AMPK-ULK1 pathway

Zhang, X.-L., An, Z.-Y., Lu, G.-J., Zhang, T., Liu, C., Liu, M.-Q., Qing-xin, W., Quan, L., & Kang, J. (2024) · Theriogenology · doi:10.1016/j.theriogenology.2024.05.037 · Cited by 3

Topsentinol L Trisulfate, a Marine Natural Product That Targets Basal-like and Claudin-Low Breast Cancers

El-Chaar, N. N., Smith, T. E., Shrestha, G., Piccolo, S., Harper, M. K., Wagoner, R. M. V., Lu, Z., Venancio, A. R., Ireland, C. M., Bild, A. H., et al. (2021) · Marine Drugs · doi:10.3390/md19010041 · Cited by 3

Cytopathological Outcomes of Knocking down Expression of Mitochondrial Complex II Subunits in Dictyostelium discoideum

Lay, S. T., Pearce, X. G., Sanislav, O., Fisher, P. R., & Annesley, S. J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23095039 · Cited by 3

Deciphering the modulatory role of short-chain fatty acids in Parkinson’s disease via phosphorylation-dependent signaling mechanisms

Liu, J., & Su, R. (2026) · PeerJ · doi:10.7717/peerj.20688 · Cited by 2

Ampk alpha2 T172 activation dictates exercise performance and energy transduction in skeletal muscle

Montalvo, R. N., Li, X., Many, G. M., Sagendorf, T. J., Yu, Q., Shen, W., Wase, N. V., Burgardt, A. R., Zhang, T., Gritsenko, M., et al. (2026) · Science Advances · doi:10.1126/sciadv.aeb3338 · Cited by 5

Redox‐Guided Metabolic Control in Cancer: Integration of the Reactive Oxygen Species–AMP‐Activated Protein Kinase–Sirtuin Axis in Tumour Adaptation and Therapy

Singh, F. (2026) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.70851 · Cited by 1

A sequential, RNA-derived, modified adenosine pathway safeguards cellular metabolismPreprint

Ogawa, A., Watanabe, S. P., Kawakami, T., Tsai, A. Y., Fuse, J., Araki, K., Sawa, S., Inaba, K., & Wei, F. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.23.595515 · Cited by 1

A D. melanogaster parkin mutant larval model of Parkinson's Disease

Vincent, A. (2013) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)

The AMPK signalling pathway in cancer and DNA damage

Dandapani, M. (2013) · Discovery Research Portal (University of Dundee)

Mechanisms of vascular protection in chronic inflammatory disease

Thornton, C. C. (2014) · Spiral (Imperial College London) · doi:10.25560/26595

Molecular Regulators of Metabolism and Cardiometabolic Disease

Sukmawati, I. R., & Wijaya, A. (2012) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v4i3.173

in Human Cancer Cells Receptor Tyrosine Kinase Phosphorylation Phosphatase Activity and Abrogation of

Zou, M., Okon, I. S., & Coughlan, K. A. (2014)

Nutritional Regulation of Inflammation in Obesity and Diabetes

Wang, X., & Liu, J. (2020) · Royal Society of Chemistry eBooks · doi:10.1039/9781839160608-00071

Reciprocal Regulation of AMPK-SIRT1 Complex Control of Colorectal Cancer Cell Metastasis by MetforminPreprint

Zhou, P., Li, D., Qiu, Z., Zeng, D., Wei, Q., Li, X., Ran, J., Chen, D., & Li, J. (2020) · Research Square · doi:10.21203/rs.3.rs-125336/v1

Characterisation of organic osmolytes and biomarkers of smoltification in the Atlantic salmon (Salmo salar)

Dagen, C. A. (2020) · St Andrews Research Repository (St Andrews Research Repository) · doi:10.17630/sta/31

Metabolism Regulates Phenotype of Inner Annulus Fibrosus Cells Within Tissue Engineered Constructs

Matadar, R. (2020) · TSpace (University of Toronto)

Plant-derived molecules for the prevention and treatment of mitochondria-related diseases

Asghari, M. H., Moloudizargari, M., & Abdollahi, M. R. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821562-3.00002-2

Untersuchungen zur Bedeutung des mitochondrialen CLPXP-Komplexes für den Energie-Metabolismus von Podospora anserina

Heinz, D. (2021) · Publication Server of Goethe University Frankfurt am Main (Goethe University Frankfurt) · doi:10.21248/gups.65210

Impacto da via de sinalização AMPK na modulação da resposta imune antitumoral por linfócitos T CD4>sup<+>/sup< e CD8>sup<+>/sup<

Feitosa, A. C. M. (2020) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2020.tde-18122019-110528

Mitogenic and Metabolic signals regulate mTOR complex 1 function to control GSK3β nuclear program

Bautista, S. J. (2021) · doi:10.32920/ryerson.14654061.v1 · Cited by 1

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

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

Lifelong creatine deficiency leads to augmented sarcoplasmic reticulum calcium release but not heart failure

Branovets, J., Laasmaa, M., Stolova, J., Shen, X. M., Rätsepso, T., Bernasconi, R., Soodla, K., Balodis, M. J., Grahv, C., Hendrikson, E., et al. (2025) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00106.2025

Electron transport chain disruption leads to failure of glucose derepression via the Snf1/AMPK pathwayPreprint

Lewis, A. G., Smith, J. R., Smardz, M., Sandoval, C. M., Suzuki, S. W., Bennett, B. D., & Gibney, P. A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.06.687039

AMP-activated protein kinase regulation of myeloid antigen presenting cell activity.

Carroll, K. (2013) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/215

Mitochondrial mutations

Mahdi, A. G. M., & Mahdi, B. M. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-24836-8.00007-9

Effets du GSK773, un activateur de l'AMPK, sur le métabolisme et la différenciation de cellules musculaires déficitaires en carnitine palmitoyl tranférase 2 (CPT2)

Boufroura, F.-Z. (2018) · theses.fr (ABES) · doi:10.70675/195ee703z9398z4cbbz80e9za6af972cf0f6

Biochemical characterization of mTORC1 regulation by glutamine metabolism

Bodineau, C. (2020) · theses.fr (ABES) · doi:10.70675/9d5aaabdz81bdz4118zb3edze237bdd8dee0

Identification des mécanismes moléculaires de l'hépatoprotection du foie de rat isolé

Papegay, B. (2020) · theses.fr (ABES) · doi:10.70675/260c1dcdz52cbz45d9zb4daz69157a0bf853

Macrophage autophagy in allergic diseases: Regulatory mechanisms, immune crosstalk, and therapeutic implications

Fan, K., Gu, Z., & Wang, Y. (2026) · International Immunopharmacology · doi:10.1016/j.intimp.2026.117112

Oxidative inhibition of AMPKα2 by 4-hydroxynonenal in human atherosclerotic lesions

Li, S., Zhang, X., Zhang, G. Q., Yang, H., Deng, J., & Zou, M. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104314

The AMPK signaling pathway in cell metabolism and human diseases

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