Mitochondrial quality control: an integrated network of pathways

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

ROS as signalling molecules: Mechanisms that generate specificity in ROS homeostasis

D'Autréaux, B., & Toledano, M. B. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2256 · Cited by 3,642

Mechanisms of mitophagy

Youle, R. J., & Narendra, D. P. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3028 · Cited by 3,273

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

PINK1 Is Selectively Stabilized on Impaired Mitochondria to Activate Parkin

Narendra, D. P., Jin, S. M., Tanaka, A., Suen, D.-F., Gautier, C. A., Shen, J., Cookson, M. R., & Youle, R. J. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000298 · Cited by 2,944

PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1

Geisler, S., Holmström, K. M., Skujat, D., Fiesel, F. C., Rothfuss, O. C., Kahle, P. J., & Springer, W. (2010) · Nature Cell Biology · doi:10.1038/ncb2012 · Cited by 2,835

The Biologic Clock: The Mitochondria?

Harman, D. (1972) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1972.tb00787.x · Cited by 2,026

Mitochondrial fusion and fission in cell life and death

Westermann, B. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3013 · Cited by 2,002

PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy

Matsuda, N., Sato, S., Shiba, K., Okatsu, K., Saisho, K., Gautier, C. A., Sou, Y.-S., Saiki, S., Kawajiri, S., Sato, F., et al. (2010) · Journal of Cell Biology · doi:10.1083/jcb.200910140 · Cited by 1,969

PINK1-dependent recruitment of Parkin to mitochondria in mitophagy

Vives-Bauza, C., Zhou, C., Huang, Y., Cui, M., de Vries, R. L. A., Kim, J., May, J., Tocilescu, M. A., Liu, W., Ko, H. S., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911187107 · Cited by 1,616

The Interplay Between Autophagy and Regulated Necrosis

Zhang, L., Cui, T., & Wang, X. (2022) · Antioxidants and Redox Signaling · doi:10.1089/ars.2022.0110 · Cited by 39

Possible Role of Mitochondrial DNA Mutations in Chronification of Inflammation: Focus on Atherosclerosis

Orekhov, A. N., Nikiforov, N. G., Ivanova, E. A., & Sobenin, I. A. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9040978 · Cited by 37

Mitochondrial biology and dysfunction in secondary mitochondrial disease

Baker, M. J., Crameri, J. J., Thorburn, D. R., Frazier, A. E., & Stojanovski, D. (2022) · Open Biology · doi:10.1098/rsob.220274 · Cited by 39

ZNF32 protects against oxidative stress-induced apoptosis by modulating C1QBP transcription

Li, K., Gao, B., Li, J., Chen, H., Li, Y., Wei, Y., Gong, D., Gao, J., Zhang, J., Tan, W., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.5646 · Cited by 37

A Genome-Wide Longitudinal Transcriptome Analysis of the Aging Model Podospora anserine

Philipp, O., Hamann, A., Servos, J., Werner, A., Koch, I., & Osiewacz, H. D. (2013) · PLoS ONE · doi:10.1371/journal.pone.0083109 · Cited by 36

VAMP7 Regulates Autophagy to Maintain Mitochondrial Homeostasis and to Control Insulin Secretion in Pancreatic β-Cells

Aoyagi, K., Ohara‐Imaizumi, M., Itakura, M., Torii, S., Akimoto, Y., Nishiwaki, C., Nakamichi, Y., Kishimoto, T., Kawakami, H., Harada, A., et al. (2016) · Diabetes · doi:10.2337/db15-1207 · Cited by 36

NIX-mediated mitophagy protects against proteinuria-induced tubular cell apoptosis and renal injury

Xu, D., Chen, P., Wang, B., Wang, Y., Miao, N., Yin, F., Cheng, Q., Zhou, Z., Xie, H., Zhou, L., et al. (2019) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00360.2018 · Cited by 35

Islet Transplantation: Current Limitations and Challenges for Successful Outcomes

Langlois, A., Pinget, M., Kessler, L., & Bouzakri, K. (2024) · Cells · doi:10.3390/cells13211783 · Cited by 42

Mitochondrial ATP-Dependent Proteases—Biological Function and Potential Anti-Cancer Targets

Feng, Y., Nouri, K., & Schimmer, A. D. (2021) · Cancers · doi:10.3390/cancers13092020 · Cited by 35

Mitochondria in autoinflammation: cause, mediator or bystander?

van der Burgh, R., & Boes, M. L. (2015) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2015.03.004 · Cited by 34

Longevity pathways and maintenance of the proteome: the role of autophagy and mitophagy during yeast ageing

Sampaio‐Marques, B., Burhans, W. C., & Ludovico, P. (2014) · Microbial Cell · doi:10.15698/mic2014.04.136 · Cited by 37

Mitochondrial fusion/fission process involved in the improvement of catalpol on high glucose-induced hepatic mitochondrial dysfunction

Xu, Z., Zhang, L., Li, X., Jiang, Z., Sun, L., Zhao, G., Zhou, G., Zhang, H., Shang, J., & Wang, T. (2015) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmv061 · Cited by 34

The Emerging Role of FUNDC1-Mediated Mitophagy in Cardiovascular Diseases

Liu, L., Li, Y., & Chen, Q. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.807654 · Cited by 35

Sleep, mood disorders, and the ketogenic diet: potential therapeutic targets for bipolar disorder and schizophrenia

Choi, J., Kang, J., Kim, T., & Nehs, C. J. (2024) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2024.1358578 · Cited by 37

Mitochondrial Dysfunction as a Biomarker of Illness State in Bipolar Disorder: A Critical Review

Giménez‐Palomo, A., Gracia, H. A., de Juan, O., Olivier, L., Ochandiano, I., Ilzarbe, L., Valentí, M., Stoppa, A., Llach, C.-D., Pacenza, G., et al. (2024) · Brain Sciences · doi:10.3390/brainsci14121199 · Cited by 34

Impaired mitochondrial quality control in Rett Syndrome

Crivellari, I., Pecorelli, A., Cordone, V., Marchi, S., Pinton, P., Hayek, J., Cervellati, C., & Valacchi, G. (2021) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2021.108790 · Cited by 33

Targeting Mitochondrial Oxidative Phosphorylation Eradicates Acute Myeloid Leukemic Stem Cells

Peng, M., Huang, Y., Zhang, L., Zhao, X., & Hou, Y. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.899502 · Cited by 32

VAMP7 Regulates Autophagosome Formation by Supporting Atg9a Functions in Pancreatic β-Cells From Male Mice

Aoyagi, K., Itakura, M., Fukutomi, T., Nishiwaki, C., Nakamichi, Y., Torii, S., Makiyama, T., Harada, A., & Ohara‐Imaizumi, M. (2018) · Endocrinology · doi:10.1210/en.2018-00447 · Cited by 31

Imeglimin mitigates the accumulation of dysfunctional mitochondria to restore insulin secretion and suppress apoptosis of pancreatic β-cells from db/db mice

Aoyagi, K., Nishiwaki, C., Nakamichi, Y., Yamashita, S., Kanki, T., & Ohara‐Imaizumi, M. (2024) · Scientific Reports · doi:10.1038/s41598-024-56769-w · Cited by 32

Quality control of mitochondria during aging: Is there a good and a bad side of mitochondrial dynamics?

Figge, M. T., Osiewacz, H. D., & Reichert, A. S. (2013) · BioEssays · doi:10.1002/bies.201200125 · Cited by 29

With the Help of MOM: Mitochondrial Contributions to Cellular Quality Control

Braun, R. J., & Westermann, B. (2017) · Trends in Cell Biology · doi:10.1016/j.tcb.2017.02.007 · Cited by 29

Power2: The power of yeast genetics applied to the powerhouse of the cell

Rutter, J. P., & Hughes, A. L. (2015) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2014.12.002 · Cited by 30

Drosophila protease ClpXP specifically degrades DmLRPPRC1 controlling mitochondrial mRNA and translation

Matsushima, Y., Hirofuji, Y., Aihara, M., Song, Y., Uchiumi, T., Kaguni, L. S., & Kang, D. (2017) · Scientific Reports · doi:10.1038/s41598-017-08088-6 · Cited by 28

Quality Matters? The Involvement of Mitochondrial Quality Control in Cardiovascular Disease

Lin, K.-L., Chen, S., Lin, K.-J., Liou, C., Chuang, Y., Wang, P., Chuang, J., & Lin, T. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.636295 · Cited by 27

GAGA protein is essential for male germ cell development in Drosophila

Dorogova, N. V., Fedorova, E. V., Bolobolova, E. U., Ogienko, A. A., & Baricheva, E. M. (2014) · genesis · doi:10.1002/dvg.22789 · Cited by 26

Tributyltin induces mitochondrial fission through Mfn1 degradation in human induced pluripotent stem cells

Yamada, S., Asanagi, M., Hirata, N., Itagaki, H., Sekino, Y., & Kanda, Y. (2016) · Toxicology in Vitro · doi:10.1016/j.tiv.2016.04.013 · Cited by 26

The PARK2 gene is involved in the maintenance of pancreatic β-cell functions related to insulin production and secretion

Jin, H., Kim, J., Lee, S., Kim, K., Go, M. J., Lee, J., Lee, H., Song, J., Jeon, B. T., Roh, G. S., et al. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.09.031 · Cited by 26

Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function

Iommarini, L., Peralta, S., Torraco, A., & Díaz, F. (2015) · Mitochondrion · doi:10.1016/j.mito.2015.01.008 · Cited by 28

Reduced mitochondrial fission and impaired energy metabolism in human primary skeletal muscle cells of Megaconial Congenital Muscular Dystrophy

Aksu‐Menges, E., Eylem, C. C., Nemutlu, E., Gizer, M., Korkusuz, P., Topaloğlu, H., Talim, B., & Balcı-Hayta, B. (2021) · Scientific Reports · doi:10.1038/s41598-021-97294-4 · Cited by 25

A new beta cell-specific mitophagy reporter mouse shows that metabolic stress leads to accumulation of dysfunctional mitochondria despite increased mitophagy

Aoyagi, K., Yamashita, S., Akimoto, Y., Nishiwaki, C., Nakamichi, Y., Udagawa, H., Abe, M., Sakimura, K., Kanki, T., & Ohara‐Imaizumi, M. (2022) · Diabetologia · doi:10.1007/s00125-022-05800-8 · Cited by 26

Do we age because we have mitochondria?

Bereiter‐Hahn, J. (2013) · PROTOPLASMA · doi:10.1007/s00709-013-0515-x · Cited by 25

Jian-Pi-Yi-Shen Formula ameliorates chronic kidney disease: involvement of mitochondrial quality control network

Liu, X., Chen, J., Liu, X., Wang, D., Zheng, P., Qi, A., Yi, T., & Li, S. (2018) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-018-2395-2 · Cited by 25

Mitochondria‐Nuclear Crosstalk: Orchestrating mtDNA Maintenance

Darfarin, G., & Pluth, J. M. (2025) · Environmental and Molecular Mutagenesis · doi:10.1002/em.70013 · Cited by 24

Mitochondrial quality control in insulin resistance and diabetes

Wanagat, J., & Hevener, A. L. (2016) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2016.05.007 · Cited by 24

Targeting Mitophagy in Alzheimer’s Disease

Jayatunga, D. P. W., Hone, E., Bharadwaj, P., Garg, M. L., Verdile, G., Guillemin, G. J., & Martins, R. N. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-191258 · Cited by 25

Resistance Exercise Improves Mitochondrial Quality Control in a Rat Model of Sporadic Inclusion Body Myositis

Koo, J., Kang, E., & Cho, J. (2019) · Gerontology · doi:10.1159/000494723 · Cited by 24

Role of sorting nexin PaATG24 in autophagy, aging and development of Podospora anserina

Henkel, V., Schürmanns, L., Brunner, M., Hamann, A., & Osiewacz, H. D. (2020) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2020.111211 · Cited by 23

RCF1-dependent respiratory supercomplexes are integral for lifespan-maintenance in a fungal ageing model

Fischer, F., Filippis, C., & Osiewacz, H. D. (2015) · Scientific Reports · doi:10.1038/srep12697 · Cited by 22

Mitochondrial protein deacetylation by SIRT3 in osteoclasts promotes bone resorption with aging in female mice

Richardson, K. K., Adam, G. O., Ling, W., Warren, A. D., Marques-Carvalho, A., Thostenson, J. D., Krager, K. J., Aykin‐Burns, N., Byrum, S. D., Almeida, M., et al. (2024) · Molecular Metabolism · doi:10.1016/j.molmet.2024.102012 · Cited by 22

LPS-related muscle loss is associated with the alteration of Bacteroidetes abundance, systemic inflammation, and mitochondrial morphology in a weaned piglet model

Yu, J., Zheng, C., Guo, Q., Yin, Y., Duan, Y., & Li, F. (2024) · Science China Life Sciences · doi:10.1007/s11427-023-2552-7 · Cited by 22

Low T3 State Is Correlated with Cardiac Mitochondrial Impairments after Ischemia Reperfusion Injury: Evidence from a Proteomic Approach

Forini, F., Ucciferri, N., Kusmic, C., Nicolini, G., Cecchettini, A., Rocchiccioli, S., Citti, L., & Iervasi, G. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms161125973 · Cited by 21

Mitochondria and Sex-Specific Cardiac Function

Vona, R., Ascione, B., Malorni, W., & Straface, E. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-77932-4_16 · Cited by 22

Administration of Enalapril Started Late in Life Attenuates Hypertrophy and Oxidative Stress Burden, Increases Mitochondrial Mass, and Modulates Mitochondrial Quality Control Signaling in the Rat Heart

Picca, A., Sirago, G., Pesce, V., Lezza, A. M. S., Calvani, R., Bossola, M., Villani, E. R., Landi, F., Leeuwenburgh, C., Carter, C., et al. (2018) · Biomolecules · doi:10.3390/biom8040177 · Cited by 22

A Long-Term Enriched Environment Ameliorates the Accelerated Age-Related Memory Impairment Induced by Gestational Administration of Lipopolysaccharide: Role of Plastic Mitochondrial Quality Control

Zhuang, Z.-Q., Zhang, Z., Zhang, Y., Ge, H.-H., Sun, S., Zhang, P., & Chen, G.-H. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.559182 · Cited by 20

Mitochondrial adaptations to exercise do not require Bcl2‐mediated autophagy but occur with BNIP3/Parkin activation

Ehrlicher, S. E., Stierwalt, H. D., Miller, B. F., Newsom, S. A., & Robinson, M. M. (2020) · The FASEB Journal · doi:10.1096/fj.201902594rr · Cited by 21

Physical exercise elicits UPRmt in the skeletal muscle: The role of c-Jun N-terminal kinase

Gaspar, R. S., Katashima, C. K., Crisol, B., Carneiro, F. S., Sampaio, I. H., Silveira, L. R., da Silva, A. S. R., Cintra, D. E., Pauli, J. R., & Ropelle, E. R. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101816 · Cited by 20

Mitochondrial protein homeostasis

Varabyova, A., Stojanovski, D., & Chacińska, A. (2013) · IUBMB Life · doi:10.1002/iub.1122 · Cited by 19

Protein turnover rates in plant mitochondria

Huang, S., Li, L., Petereit, J., & Millar, A. H. (2020) · Mitochondrion · doi:10.1016/j.mito.2020.04.011 · Cited by 19

Impaired F1Fo-ATP-Synthase Dimerization Leads to the Induction of Cyclophilin D-Mediated Autophagy-Dependent Cell Death and Accelerated Aging

Warnsmann, V., Marschall, L., & Osiewacz, H. D. (2021) · Cells · doi:10.3390/cells10040757 · Cited by 18

The acute and chronic influence of exercise on mitochondrial dynamics in skeletal muscle

Ritenis, E. J., Padilha, C. S., Cooke, M. B., Stathis, C. G., Philp, A., & CAMERA, D. M. (2024) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00311.2024 · Cited by 18

ER Stress-Induced Sphingosine-1-Phosphate Lyase Phosphorylation Potentiates the Mitochondrial Unfolded Protein Response

Yildirim, A. D., Citir, M., Atici, A. E., Veli, Z., Yıldırım, Z., Tufanlı, Ö., Traynor‐Kaplan, A., Schultz, C., & Erbay, E. (2022) · Journal of Lipid Research · doi:10.1016/j.jlr.2022.100279 · Cited by 17

Deficiency of muscle-generated brain-derived neurotrophic factor causes inflammatory myopathy through reactive oxygen species-mediated necroptosis and pyroptosis

Pang, B. P. S., Iu, E. C. Y., Hang, M., Chan, W. S., Tse, M. C. L., Yeung, C. T. Y., Wang, M., Siu, P. M., Lee, C. W., Ye, K., et al. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103418 · Cited by 17

Propionic acid induces mitochondrial dysfunction and affects gene expression for mitochondria biogenesis and neuronal differentiation in SH-SY5Y cell line

Kim, S. A., Jang, E. H., Mun, J. Y., & Choi, H. (2019) · NeuroToxicology · doi:10.1016/j.neuro.2019.09.009 · Cited by 17

Light sheet based volume flow cytometry (VFC) for rapid volume reconstruction and parameter estimation on the go

Kumar, P., Joshi, P., Basumatary, J., & Mondal, P. P. (2022) · Scientific Reports · doi:10.1038/s41598-021-03902-8 · Cited by 17

Methods for mitochondrial health assessment by High Content Imaging System

Panusatid, C., Thangsiriskul, N., & Peerapittayamongkol, C. (2022) · MethodsX · doi:10.1016/j.mex.2022.101685 · Cited by 17

Embryonic Surface Ectoderm-specific Mitofusin 2 Conditional Knockout Induces Congenital Cataracts in Mice

Zhao, J., Wu, X., Wu, D., Yu, Y., Yu, Y., Wang, Y., Fu, Q., Zhang, J., & Yao, K. (2018) · Scientific Reports · doi:10.1038/s41598-018-19849-2 · Cited by 17

Molecular mechanisms of mitochondrial homeostasis regulation in neurons and possible therapeutic approaches for Alzheimer's disease

Ren, J., Xiang, B., Xueling, L., Han, X., Yang, Z., Zhang, M., & Zhang, Y. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e36470 · Cited by 16

Relationship between oxidative stress and lifespan in Daphnia pulex

Ukhueduan, B., Schumpert, C. A., Kim, E., Dudycha, J. L., & Patel, R. C. (2022) · Scientific Reports · doi:10.1038/s41598-022-06279-4 · Cited by 16

Oral combined contraceptives induce liver mitochondrial reactive oxygen species and whole‐body metabolic adaptations in female mice

Fuller, K. N. Z., McCoin, C. S., Stierwalt, H. D., Allen, J., Gandhi, S., Perry, C. G. R., Jambal, P., Shankar, K., & Thyfault, J. P. (2022) · The Journal of Physiology · doi:10.1113/jp283733 · Cited by 17

AMPK signaling pathway as a potential therapeutic target for Parkinson's disease

Athari, S. Z., Farajdokht, F., Keyhanmanesh, ‬., & Mohaddes, G. (2023) · Advanced Pharmaceutical Bulletin · doi:10.34172/apb.2024.013 · Cited by 16

Spatiotemporal Modeling of Mitochondrial Network Architecture

Holt, K. B., Winter, J., Manley, S., & Koslover, E. F. (2024) · PRX Life · doi:10.1103/prxlife.2.043002 · Cited by 17

Superoxide Dismutases in Eukaryotic Microorganisms: Four Case Studies

del Valle, A. D. O. F., & Scheckhuber, C. Q. (2022) · Antioxidants · doi:10.3390/antiox11020188 · Cited by 16

Mitotherapy in doxorubicin induced cardiotoxicity: A promising strategy to reduce the complications of treatment

Maleki, F., Salimi, M., Shirkoohi, R., & Rezaei, M. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.120701 · Cited by 15

The role of mitochondria in cytokine and chemokine signalling during ageing

Kalykaki, M., Rubio‐Tomás, T., & Tavernarakis, N. (2024) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2024.111993 · Cited by 14

Mitochondrial Phospholipid Homeostasis Is Regulated by the i-AAA Protease PaIAP and Affects Organismic Aging

Löser, T., Joppe, A., Hamann, A., & Osiewacz, H. D. (2021) · Cells · doi:10.3390/cells10102775 · Cited by 15

A uvs-5 Strain Is Deficient for a Mitofusin Gene Homologue, fzo1 , Involved in Maintenance of Long Life Span in Neurospora crassa

Kurashima, K., Chae, M. S., Inoue, H., Hatakeyama, S., & Tanaka, S. (2012) · Eukaryotic Cell · doi:10.1128/ec.00226-12 · Cited by 14

Mitochondria organize the cellular proteostatic response and promote cellular senescence

Li, Y., Liu, L., Zhu, Y., & Chen, Q. (2019) · Cell Stress · doi:10.15698/cst2019.04.181 · Cited by 13

Multi-Tissue DNA Methylation Remodeling at Mitochondrial Quality Control Genes According to Diet in Rat Aging Models

D’Aquila, P., Rango, F. D., Guarasci, F., Mandalà, M., Corsonello, A., Bellizzi, D., & Passarino, G. (2020) · Nutrients · doi:10.3390/nu12020460 · Cited by 12

Targeting the Main Sources of Reactive Oxygen Species Production: Possible Therapeutic Implications in Chronic Pain

Cheng, P.-F., Yuan-He, Ge, M.-M., Ye, D., Chen, J.-P., & Wang, J. (2023) · Current Neuropharmacology · doi:10.2174/1570159x22999231024140544 · Cited by 12

Systemic Metabolism and Mitochondria in the Mechanism of Alzheimer’s Disease: Finding Potential Therapeutic Targets

Song, M., & Fan, X. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24098398 · Cited by 11

Polyphenols and Exercise in Mitochondrial Biogenesis: Focus on Age-Related CNS Disorders

Tu, J. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05121-y · Cited by 11

Targeted to neuronal organelles for CNS drug development

Ying, Z., Ye, N., Ma, Q., Chen, F., Li, N., & Zhen, X. (2023) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2023.115025 · Cited by 11

Identification and characterization of a mitochondrial unfolded protein response transcription factor ATFS-1 in Litopenaeus vannamei

Chen, Y.-G., Yue, H., Zhang, Z.-Z., Yuan, F.-H., Bi, H., Yuan, K., Weng, S., He, J., & Chen, Y.-H. (2015) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2015.10.019 · Cited by 10

Simultaneous Ablation of the Catalytic AMPK α-Subunit SNF1 and Mitochondrial Matrix Protease CLPP Results in Pronounced Lifespan Extension

Heinz, D., Krotova, E., Hamann, A., & Osiewacz, H. D. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.616520 · Cited by 11

A Differential Genome-Wide Transcriptome Analysis: Impact of Cellular Copper on Complex Biological Processes like Aging and Development

Servos, J., Hamann, A., Grimm, C., & Osiewacz, H. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049292 · Cited by 10

A Novel High-Content Screening-Based Method for Anti-Trypanosoma cruzi Drug Discovery Using Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes

Portella, D. C. N., Rossi, E. A., Paredes, B. D., Bastos, T. M., Meira, C. S., Nonaka, C. K. V., Silva, D. N., Caria, A. C. I., Moreira, D. R. M., Leite, A. C. L., et al. (2021) · Stem Cells International · doi:10.1155/2021/2642807 · Cited by 9

Bone Marrow Mesenchymal Stem Cells and Their Derived Extracellular Vesicles Attenuate Non-Alcoholic Steatohepatitis-Induced Cardiotoxicity via Modulating Cardiac Mechanisms

El-Derany, M. O., & AbdelHamid, S. G. (2022) · Life · doi:10.3390/life12030355 · Cited by 9

Mitophagy in Alzheimer’s Disease: A Bibliometric Analysis from 2007 to 2022

Wang, H., Yan, X., Zhang, Y., Wang, P., Li, J., & Zhang, X. (2024) · Journal of Alzheimer s Disease Reports · doi:10.3233/adr-230139 · Cited by 9

Do Mitochondrial DNA Mutations Play a Key Role in the Chronification of Sterile Inflammation? Special Focus on Atherosclerosis

Orekhov, A. N., Герасимова, Е. В., Sukhorukov, V. N., Poznyak, A. V., & Nikiforov, N. G. (2020) · Current Pharmaceutical Design · doi:10.2174/1381612826666201012164330 · Cited by 9

Insight into the Interactome of Intramitochondrial PKA Using Biotinylation-Proximity Labeling

Amer, Y. O., & Hébert-Chatelain, É. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21218283 · Cited by 9

Mito–managing ROS & redox to reboot the immune system: Tapping mitochondria & redox management to extend the reach of hematopoietic stem cell transplantation

Mohrin, M. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.01.034 · Cited by 9

Loss of BOSS Causes Shortened Lifespan with Mitochondrial Dysfunction in Drosophila

Kohyama‐Koganeya, A., Kurosawa, M., & Hirabayashi, Y. (2017) · PLoS ONE · doi:10.1371/journal.pone.0169073 · Cited by 9

Parkin in early stage LPS-stimulated BV-2 cells regulates pro-inflammatory response and mitochondrial quality via mitophagy

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