Mitophagy: mechanisms, pathophysiological roles, and analysis

Autophagy: Renovation of Cells and Tissues

Mizushima, N., & Komatsu, M. (2011) · Cell · doi:10.1016/j.cell.2011.10.026 · Cited by 6,615

A role for mitochondria in nlrp3 inflammasome activation

Zhou, R., Yazdi, A. S., Menu, P., & Tschopp, J. (2011) · Nature · doi:10.1038/nature09663 · Cited by 5,602

Autophagy: process and functionPreprint

Mizushima, N. (2007) · Genes & Development · doi:10.1101/gad.1599207 · Cited by 4,104

Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1α

Lagouge, M., Argmann, C., Gerhart-Hines, Z., Meziane, H., Lerin, C., Daussin, F., Messadeq, N., Milne, J., Lambert, P., Elliott, P., et al. (2006) · Cell · doi:10.1016/j.cell.2006.11.013 · Cited by 4,057

Parkin is recruited selectively to impaired mitochondria and promotes their autophagy

Narendra, D., Tanaka, A., Suen, D.-F., & Youle, R. J. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200809125 · Cited by 4,026

Autophagy regulates lipid metabolism

Singh, R., Kaushik, S., Wang, Y., Xiang, Y., Novak, I., Komatsu, M., Tanaka, K., Cuervo, A. M., & Czaja, M. J. (2009) · Nature · doi:10.1038/nature07976 · Cited by 3,975

Loss of autophagy in the central nervous system causes neurodegeneration in mice

Komatsu, M., Waguri, S., Chiba, T., Murata, S., Iwata, J.-I., Tanida, I., Ueno, T., Koike, M., Uchiyama, Y., Kominami, E., et al. (2006) · Nature · doi:10.1038/nature04723 · Cited by 3,500

Fission and selective fusion govern mitochondrial segregation and elimination by autophagy

Twig, G., Elorza, A., Molina, A. J. A., Mohamed, H., Wikstrom, J. D., Walzer, G., Stiles, L., Haigh, S. E., Katz, S., Las, G., et al. (2008) · The EMBO Journal · doi:10.1038/sj.emboj.7601963 · Cited by 3,082

Autophagy proteins regulate innate immune responses by inhibiting the release of mitochondrial DNA mediated by the NALP3 inflammasome

Nakahira, K., Haspel, J. A., Rathinam, V. A. K., Lee, S.-J., Dolinay, T., Lam, H. C., Englert, J. A., Rabinovitch, M., Cernadas, M., Kim, H. P., et al. (2011) · Nature Immunology · doi:10.1038/ni.1980 · Cited by 3,049

Deformation and diagenetic histories around foreland thrust faults

Roberts, G. P. (1990) · Durham e-Theses (Durham University) · Cited by 4

The RAB27A effector SYTL5 regulates mitophagy and mitochondrial metabolism

Lapão, A., Johnson, L. S., Trachsel-Moncho, L., Rodgers, S. J., Singh, S., NG, M. M., Nakken, S., Eskelinen, E., & Simonsen, A. (2025) · eLife · doi:10.7554/elife.105541.3 · Cited by 4

Therapeutic potential of KATP channels in the attenuation of Parkinson's disease pathogenesis and progression – A review

Gundi, B., Ho, H. L., Zhang, X., He, A., Xin, D., Ferreira, A. F. F., de Britto, L. R. G., Feng, Z., & Sun, H. (2025) · Neurochemistry International · doi:10.1016/j.neuint.2025.106091 · Cited by 3

Ethanol, acetaldehyde, lipopolysaccharide, and neutrophil extracellular traps: four‐pronged attack on gut epithelial barrier in alcohol use disorder

Mak, K. M., Ding, S. Y., & Jain, C. L. (2025) · The Anatomical Record · doi:10.1002/ar.70084 · Cited by 3

The multifaceted functions of selective autophagy in cancer: molecular basis, consequences, and clinical prospects

Jiang, M., Zhang, K., Li, M., Tian, Y., Wang, T., Rodríguez, R. A., Lin, Z., Meng, J., Li, C., Wang, Z., et al. (2026) · Molecular Cancer · doi:10.1186/s12943-026-02615-8 · Cited by 4

Targeting mitochondria in triple-negative breast cancer: Emerging therapeutic and drug development strategies

Yuan, Z., Mu, D., Chen, X., Yang, Q., Zhang, J., & Zhang, L. J. (2026) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2026.189591 · Cited by 5

Microglial mitochondria transfer to astrocytes via GPNMB-enriched extracellular vesicles alleviates cognitive deficits in tauopathy mice

Liang, C., Zhou, Y., Zhuang, K., Wang, S., Zhong, L., Can, D., Lei, A., Li, H., Zhang, J., & Leng, L. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02317-w · Cited by 3

TRPML1 loss disrupts lysosome–mitochondria homeostasis and sensitizes MDA-MB-231 triple-negative breast cancer cells to chemotherapy

Syeda, A. K. R., Almasi, S., Benson, C. J., Kennedy, B. E., Yoast, R. E., Emrich, S. M., Delima-Baril, A., Slade, L., Pakkiriswami, S., Vijayan, V. V., et al. (2026) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2026.113596 · Cited by 4

Revealing the protective role of mitophagy for liver injury via a promising dual-channel activated fluorescent probe

Li, L., Guo, D., Wang, C., Wu, T., Lu, D., Shao, M., Wen, L., Zhu, Q., Zhu, L., Li, Y., et al. (2024) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2024.136459 · Cited by 3

Diagnosis of mitochondrial defects: livestock diseases

Schilling-Tóth, B. M., Kiss, D. S., Németh, K., Ondrašovičová, S., Jócsák, G., Bartha, T., & Tóth, I. (2025) · Animal Diseases · doi:10.1186/s44149-025-00195-6 · Cited by 3

Mitochondrial Degradation, Autophagy and Neurodegenerative Disease

Otten, E. G., Manni, D., & Korolchuk, V. I. (2016) · Springer eBooks · doi:10.1007/978-3-319-28637-2_11 · Cited by 3

Mitophagy Decreases in the Peripheral Vestibular System of Aged C57BL/6J Mice

Cho, S. I., Jo, E.-R., & Lee, S. M. (2023) · In Vivo · doi:10.21873/invivo.13426 · Cited by 4

The ketogenic diet and hypoxia promote mitophagy in the context of glaucoma

Morgan, A. B., Fan, Y., & Inman, D. M. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1409717 · Cited by 3

Astaxanthin Prevents Dysregulation of Mitochondrial Dynamics in Rat Brain Mitochondria Induced by Isoproterenol

Krestinin, R. R., Baburina, Y. L., Odinokova, I. V., Sotnikova, L. D., & Krestinina, O. V. (2024) · BIOPHYSICS · doi:10.1134/s000635092470009x · Cited by 3

Excess Fructose Intake Activates Hyperinsulinemia and Mitogenic MAPK Pathways in Association With Cellular Stress, Inflammation, and Apoptosis in the Pancreas of Rats

Güney, C., Alçığır, M. E., & Akar, F. (2025) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.70048 · Cited by 3

Mitophagy

Mijaljica, D., Prescott, M., & Devenish, R. J. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405528-5.00005-5 · Cited by 3

Time-Lapse Video Microscopy for Assessment of EYFP-Parkin Aggregation as a Marker for Cellular Mitophagy

Sante, G. D., Casimiro, M. C., Pestell, T. G., & Pestell, R. G. (2016) · Journal of Visualized Experiments · doi:10.3791/53657 · Cited by 3

The role of mitophagy in selected neurodegenerative diseases

Osuch, B., Kucharska, T., Chmielewska, N., Maciejak, P., Szyndler, J., & Płaźnik, A. (2019) · Postępy Psychiatrii i Neurologii · doi:10.5114/ppn.2019.86258 · Cited by 3

Autophagy Driven Extracellular Vesicles in the Leukaemic Microenvironment

Horton, R. H., Wileman, T., & Rushworth, S. A. (2020) · Current Cancer Drug Targets · doi:10.2174/1568009620666200428111051 · Cited by 3

Assessing Chondrocyte Status by Immunofluorescence-Mediated Localization of Parkin Relative to Mitochondria

ANSARI, M. Y. K., & Haqqi, T. M. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-1119-7_15 · Cited by 3

University of Alabama at Birmingham Nathan Shock Center: comparative energetics of aging

Austad, S. N., Buford, T. W., Allison, D. B., Ballinger, S. W., Brown, A. W., Carter, C. S., Darley-Usmar, V. M., Hartman, J. L., Nagy, T. R., Smith, D. L., et al. (2021) · GeroScience · doi:10.1007/s11357-021-00414-1 · Cited by 3

Role of AMP-activated protein kinase and sirtuins as antiaging proteins

Ramu, M., Vishal, S. S., & Gogia, N. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90235-9.00015-x · Cited by 3

Interplay of autophagy, apoptosis, and senescence in primary biliary cholangitis

Kouroumalis, E., Tsomidis, I., & Voumvouraki, A. (2023) · Exploration of Digestive Diseases · doi:10.37349/edd.2023.00028 · Cited by 3

Towards Tissue-Specific Stem Cell Therapy for the Intervertebral Disc: PPARδ Agonist Increases the Yield of Human Nucleus Pulposus Progenitor Cells in Expansion

Zhang, X., Guerrero, J., Croft, A. S., Oswald, K. A. C., Albers, C. E., Häckel, S., & Gantenbein, B. (2021) · Surgeries · doi:10.3390/surgeries2010008 · Cited by 3

Mitochondrial Function and Neurodegenerative Diseases

Wilkins, H. M., Weidling, I., Koppel, S., Wang, X., von Schulze, A., & Swerdlow, R. H. (2018) · The Molecular and Cellular Basis of Neurodegenerative Diseases · doi:10.1016/b978-0-12-811304-2.00013-4 · Cited by 2

The Role of Autophagy and Mitophagy in Mitochondrial Diseases

Paz, M. V., Cotán, D., Cordero, M. D., Garrido‐Maraver, J., Oropesa-Ávila, M., de la Mata, M., Pavón, A. D., Alcocer‐Gómez, E., de Lavera, I., & Alcázar, J. A. S. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802937-4.00008-9 · Cited by 1

Mito-kaede photoactivation and chase experiment for mitophagy: optimizing flux measurement via fluid exchange system

Morinaga, H., Sugawara, Y., Kitagawa, Y., Chen, J., Yasuda, N., Ogata, H., Yamaguchi, Y., Kaneki, M., Martyn, J. A. J., & Yasuhara, S. (2024) · BioTechniques · doi:10.1080/07366205.2024.2372955 · Cited by 2

The intracellular agent of Q fever, Coxiella burnetii , alters human alveolar macrophage metabolism and mitochondrial physiology

Adhvaryu, H., Huang, L., Long, C. M., & Voth, D. E. (2025) · mBio · doi:10.1128/mbio.01436-25 · Cited by 2

Sphingolipid and methionine metabolism in aging

Adebayo, D., Obaseki, E., Vasudeva, K., Aboumourad, M., Sleiman, A., Bandyopadhyay, S., Kreinbring, L., & Hariri, H. H. (2025) · Journal of Cell Science · doi:10.1242/jcs.264026 · Cited by 2

Stress at the gates: Mitochondrial import dysfunctions, response pathways, and therapeutic potential

Calais, H., & Bertolin, G. (2025) · Mitochondrion · doi:10.1016/j.mito.2025.102107 · Cited by 3

Restoring autophagy flux by rolipram attenuates ototoxicity in Hearing loss

Vijayakumar, K. A., Jang, C. H., & Cho, G.-W. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.178473 · Cited by 2

Investigating the Potential Role of Capsaicin in Facilitating the Spread of Coxsackievirus B3 via Extracellular Vesicles

Chatterjee, S., Kordbacheh, R., Tilley, H., Briordy, D., Waldron, R. T., Cutts, W. D., Aleman, J., Cook, A., Dhanji, R., Wong, L.-Y. R., et al. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27020661 · Cited by 2

The spatiotemporal dynamics of MAMs: mechanisms, pathologies, and therapeutic rewiring

Xu, D., Huang, Y., Zhang, X., Liu, B., Wang, M., Li, Y., & Peng, Z. (2026) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-026-00887-y · Cited by 2

Ageing was never a singular problem in biology: implications for mechanisms, measurements and interventions

Chmielewski, P. P. (2026) · Biogerontology · doi:10.1007/s10522-026-10436-x · Cited by 2

Mitochondrial resilience: a convergent framework for pathogenesis and neuroprotection in Parkinson’s disease

Arias-Carrión, Ó., Guerra‐Crespo, M., Soto-Rojas, L. O., Valle, Y., Ortega‐Robles, E., & Ortuño‐Sahagún, D. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1886917 · Cited by 2

A New Cofilin-Dependent Mechanism for the Regulation of Brain Mitochondria Biogenesis and Degradation

Kovaleva, T. F., Maksimova, N. S., Pchelin, P. V., Pershin, V. I., Tkachenko, N. M., Gainullin, M., & Mukhina, I. V. (2020) · Современные технологии в медицине · doi:10.17691/stm2020.12.1.01 · Cited by 2

Moving Beyond the Ice Age in Heart Transplant Procurement

Jaiswal, A., & Baran, D. A. (2024) · Transplantation · doi:10.1097/tp.0000000000005170 · Cited by 2

Cell Biology and Regulation of Adult and Aging Leydig Cell Steroidogenesis

Papadopoulos, V., Garza, S., & Zirkin, B. R. (2025) · Springer eBooks · doi:10.1007/978-3-031-96376-6_4 · Cited by 2

Mitochondrial Dysfunction in Metabolic Disorders

Murtaza, G., Tariq, M., & Shawahna, R. (2020) · Emerging contaminants and associated treatment technologies · doi:10.1007/978-3-030-45923-9_3 · Cited by 2

Pharmacological efficacy and potential of the use of nitazoxanide, a thiazolide drug with a wide spectrum of action

Rusanovsky, V. V., Savelyeva, A. A., Tadtaeva, Z. G., Astudin, E. S., Krivoshein, A. E., Akimov, A. A., & Kuritsina, N. A. (2024) · Reviews on Clinical Pharmacology and Drug Therapy · doi:10.17816/rcf624703 · Cited by 2

Pathology Deterioration in a Pure β-zero Thalassemia Heterozygote After mRNA COVID-19 Vaccination: A Case Report and Literature Review

Kyriakopoulos, A. M., & Seneff, S. (2024) · International Journal of Vaccine Theory Practice and Research · doi:10.56098/y768gc33 · Cited by 2

Regulation of mitophagy and mitochondrial biogenesis by monocarbonyl analogues of curcumin in the cerebral cortex of rats in experimental Alzheimer’s disease

Поздняков, Д. И., & Вихорь, А. А. (2024) · S S Korsakov Journal of Neurology and Psychiatry · doi:10.17116/jnevro2024124091109 · Cited by 2

Monitoring of Atg5-Independent Mitophagy

Arakawa, S., Honda, S., Torii, S., Tsujioka, M., & Shimizu, S. (2017) · Methods in molecular biology · doi:10.1007/7651_2017_16 · Cited by 2

The Critical Role of Mitochondria in Drug-Induced Liver Injury

Decker, C. W., Casian, J. G., Nguyen, K. T., Horton, L. A., Rao, M. P., Silkwood, K. H., & Han, D. (2017) · Springer eBooks · doi:10.1007/978-3-319-58106-4_8 · Cited by 2

Role of Horizontal Gene Transfer in Cancer Progression

Abril, A. G., & Notario, V. (2019) · Springer eBooks · doi:10.1007/978-3-030-21862-1_17 · Cited by 3

Impaired mitochondrial bioenergetics and signaling pathways

Bhatti, J. S., Pahwa, P., Reddy, P. H., & Bhatti, G. K. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819621-2.00002-4 · Cited by 2

Energy metabolism and behavioral parameters in female mice subjected to obesity and offspring deprivation stress

da Cruz, K. L. D. O., Salla, D. H., de Oliveira, M. P., da Silva, L. E., Vedova, L. M. D., Mendes, T. F., Bressan, C. B. C., da Silva, M. R., Santos, S. M. L., Soares, H. J., et al. (2023) · Behavioural Brain Research · doi:10.1016/j.bbr.2023.114526 · Cited by 2

Dexmedetomidine protects against sepsis-induced lung injury through autophagy and Smad2/3 signaling pathway.

Liu, Z., Xu, J., Zhao, Y., Wan, Y., Guo, R., Long, C., Liu, J., Yao, X., & Yin, W. (2024) · PubMed Central · doi:10.22038/ijbms.2023.73479.15964 · Cited by 2

Atg32 Confers Selective Mitochondrial Sequestration as a Cargo for Autophagy

Kurihara, Y., & Kanki, T. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405528-5.00010-9 · Cited by 2

Mitochondrial DNA dynamics during fruiting body formation in Grifola frondosa

Numata, F., Kawaguchi, N., Yamada, C., Ota, Y., Chen, F.-C., Hayashi, M., Shimomura, N., Yamaguchi, T., & Aimi, T. (2019) · Mycoscience · doi:10.1016/j.myc.2019.01.003 · Cited by 2

High Dose Tigecycline-Induced Mitochondrial Dysfunction-Associated Acute Metabolic Acidosis: A Retrospective Study

Hasan, M. J., Rabbani, R., Bachar, S. C., & Huq, S. M. R. (2019) · Journal of Molecular and Genetic Medicine · Cited by 2

Aggregation induced emission (AIE) materials for mitochondria imaging

Deshmukh, S. U., Biradar, M. R., Kharat, K. R., & Bhosale, S. V. (2021) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2021.06.016 · Cited by 2

Elucidating Mechanisms of Benzo[a]pyrene Mediated Apoptotic and Autophagic Cell Death and its Prevention with Phytotherapeutics

Das, D. N. (2015) · Cited by 2

The RAB27A effector SYTL5 regulates mitophagy and mitochondrial metabolismPreprint

Lapão, A., Johnson, L. S., Trachsel-Moncho, L., Singh, S., Ng, M. Y. W., Nakken, S., Eskelinen, E., & Simonsen, A. (2025) · eLife · doi:10.7554/elife.105541.1 · Cited by 2

Mitochondrial Dysfunction in Skin and Ocular Surface Disease: An Interdisciplinary Review

Memar, O. M. (2019) · American Journal of Biomedical Science & Research · doi:10.34297/ajbsr.2019.01.000538 · Cited by 1

Intergenomic and epistatic interactions control free radical mediated pancreatic β-cell damage

Chen, J., Li, R., Knapp, S., Zhu, G., Whitener, R. L., Leiter, E. H., & Mathews, C. E. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.994501 · Cited by 1

The Role of Autophagy in Heart Disease

Mohiuddin, O., Abraham, S., Zhang, H., & Ruiz‐Velasco, A. (2024) · International Journal of Drug Discovery and Pharmacology · doi:10.53941/ijddp.2024.100021 · Cited by 1

A red-emitting, microenvironment-insensitive fluorophore for lysosome-specific imaging in live cells

Mansuri, S., Ojha, S., & Kanvah, S. (2025) · Journal of Materials Chemistry B · doi:10.1039/d5tb00296f · Cited by 1

Styryl benzoxazolium salts as environment-sensitive mitochondrial probes for imaging ferroptosis

Cheerala, V. S. K., Mansuri, S., Sarkar, P., Rajput, D., & Kanvah, S. (2025) · Organic & Biomolecular Chemistry · doi:10.1039/d5ob01181g · Cited by 1

Neurodegenerative features of damage to Deiters neurons in the lateral vestibular nucleus of mice after vestibular stimulation

Mikheeva, I. B., Zhuikova, N. S., Chernomorets, I. Y., Pavlik, L. L., & Arkhipov, V. I. (2025) · Neuroscience Letters · doi:10.1016/j.neulet.2025.138363 · Cited by 1

Autophagy cargo profiles in skeletal muscle during starvation and exercise

Farhan, M., Lyu, S., Nguyen, T. P., Zhang, D., Liang, H., Zhou, Y., An, Y., Wang, J., Yang, H., Du, G., et al. (2025) · Autophagy Reports · doi:10.1080/27694127.2025.2593060 · Cited by 1

A Tetrahedral DNA Framework-Based Mitochondrial Anchoring System Promotes Diabetic Wound Healing via Mitophagy and Mitostress Regulation

Yao, Y., Zhang, T., Li, Y., Zhang, G., Gao, Y., Lin, Y., Gao, S., & Cai, X. (2025) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.5c19661 · Cited by 1

Autophagy–Actin Crosstalk: Implications for Cellular Homeostasis and Disease

Fierti, A. O., Rozsa, R. G., Potu, A., Tajammal, A., & Li, H. (2026) · Cells · doi:10.3390/cells15080665 · Cited by 1

Divergent Role of ULK1 to Balance Mitochondrial Homeostasis and Bioenergetics in Ovarian Cancer Spheroids

Webb, J. D., Borrelli, M. J., Valdés, Y. R., & Shepherd, T. G. (2026) · Cancers · doi:10.3390/cancers18111746 · Cited by 1

Selective Disposal of Insoluble Protein Aggregates

Seneci, P. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800186-8.00005-5 · Cited by 1

Voghera Sweet Pepper Regulates Cell Death Pathways in an Aging In Vitro Model

Gola, F., Casali, C., Gaiaschi, L., Roda, E., Milanesi, G., Luca, F. D., & Bottone, M. G. (2025) · Nutrients · doi:10.3390/nu17132147 · Cited by 1

STING Signaling Pathway as a Target for Neuroprotective Therapy in Parkinson’s Disease

Usenko, T. S. (2025) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093025030019 · Cited by 1

Chondroitin Sulfate A-Selenium Nanoparticles Activate Autophagy Through the AMPK-mTOR Pathway to Alleviate Oxidative Stress and Mitochondrial Dysfunction to Repair Kashin-Beck Disease Chondrocytes

Deng, H., Qiao, L., Jiang, Y., Amhare, A. F., & Han, J. (2025) · Biological Trace Element Research · doi:10.1007/s12011-025-04732-9 · Cited by 1

A Comprehensive Review on Pulmonary Fibrosis (PF): Histological Spectrum, Diagnosis, Risk Factors, Pathogenesis, Molecular Pathophysiology, and Current Treatment Options

Sadek, M. A., ElBishbishy, R. M., Lotfy, R. M., Fayez, N., Sayed, G. A., El‐Shiekh, R. A., & Hal, D. M. (2025) · Chemistry & Biodiversity · doi:10.1002/cbdv.202500981 · Cited by 2

Mitochondrial Dysfunction as a Pathophysiological Bridge between Metabolic Dysfunction-Associated Fatty Liver Disease and Chronic Kidney Disease

You, C., Yin, A., Xia, J., Zhang, L., Wang, X., & Hou, Y. (2025) · Biocell · doi:10.32604/biocell.2025.072971 · Cited by 1

Grass carp ( Ctenopharyngodon idella ) resist heat stress by maintaining mitochondrial quality and enhancing energy production

Zhang, X., Yan, X., Li, P., Wang, C., Zhang, C., Ji, H., & Yu, H. (2025) · Journal of Fish Biology · doi:10.1111/jfb.70320 · Cited by 1

The Estrogen–Mitochondria Axis in Bipolar Disorder: From Fluctuating Hormones to Failing Bioenergetics

Zachos, K. A., Behravan, K., Demyati, J., & Andreazza, A. C. (2026) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2026.100723 · Cited by 1

Thioredoxin protects against diabetic hearing loss by regulating TOMM22 mediated mitochondrial autophagy in hair cells and inhibiting microglial M1 polarization

Zhong, S., (62933), M. X., Wang, Q., Wang, S., Li, X., Guo, Y., & Kong, H. (2026) · Scientific Reports · doi:10.1038/s41598-026-44909-3 · Cited by 1

High-throughput sequencing reveals microRNA-mediated osmoregulation in Litopenaeus vannamei under freshwater stress

Zhou, B., Liu, H., Dai, X., Fu, Y., & Li, Y. (2026) · Aquaculture Reports · doi:10.1016/j.aqrep.2026.103554 · Cited by 1

A Pyrazole-Based Small Molecule, KB3409, Restores Mitochondrial Function via VCP Activation and RCN2-Dependent Ca2+ Regulation

Lee, Y. J., Yoon, J. H., Lim, H., Song, E. S., Park, J. H., Kim, D., Yang, J.-E., So, M. K., Kim, M., Song, J., et al. (2026) · Antioxidants · doi:10.3390/antiox15081006 · Cited by 1

Dinámica mitocondrial en las enfermedades neurodegenerativas

Alarcón‐Aguilar, A., Maycotte, P., Cortés-Hernández, P., López‐Díazguerrero, N. E., & Königsberg, M. (2019) · Gaceta Médica de México · doi:10.24875/gmm.18004337 · Cited by 1

Study of the mechanism underlying the role of PINK1/Parkin in the formic acid‐induced autophagy of PC12 cells

Chen, N., Yan, J., Hu, Y., Hao, L., Liu, H., & Yang, H. (2023) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.13833 · Cited by 1

Involvement of Mitochondrial Dysfunction in FOXG1 Syndrome

Bjerregaard, V. A., Levy, A. M., Batz, M. S., Salehi, R., Hildonen, M., Hammer, T. B., Møller, R. S., Desler, C., & Tümer, Z. (2023) · Genes · doi:10.3390/genes14020246 · Cited by 1

Therapeutic Insights into α-Lipoic Acid and Thymoquinone for Neurodegenerative Diseases

Khanq, I., & Bist, R. (2024) · International Journal of Health Sciences and Research · doi:10.52403/ijhsr.20240567 · Cited by 2

Antisecretory Factor 16 (AF16): A Promising Avenue for the Treatment of Traumatic Brain Injury—An In Vitro Model Approach

Vahrmeijer, N., Kriel, J., Harrington, B. M., Staden, A. D. P. V., Vlok, A. J., Engelbrecht, L., du Toit, A., & Loos, B. (2024) · Journal of Molecular Neuroscience · doi:10.1007/s12031-024-02268-6 · Cited by 1

DMT1 Maintains Iron Homeostasis to Regulate Mitochondrial Function in Porcine Oocytes

Zhang, J., Lan, M., Shang, J., Lai, X., Li, L., Duan, T., Xu, R., Chen, K., & Duan, X. (2024) · Journal of Cellular Physiology · doi:10.1002/jcp.31494 · Cited by 1

Mitochondrial dynamics in neurodegenerative diseases

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