Mitochondrial quality control: an integrated network of pathways

Parkin is recruited selectively to impaired mitochondria and promotes their autophagy

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

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Mechanisms of mitophagy

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Fission and selective fusion govern mitochondrial segregation and elimination by autophagy

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PINK1 Is Selectively Stabilized on Impaired Mitochondria to Activate Parkin

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

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The Biologic Clock: The Mitochondria?

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Mitochondrial fusion and fission in cell life and death

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

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PINK1-dependent recruitment of Parkin to mitochondria in mitophagy

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Mitochondria dysfunction in the pathogenesis of Alzheimer’s disease: Recent advances.

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Mitochondrial dynamics, mitophagy and cardiovascular disease

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Mitochondria as a Target of Environmental Toxicants

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Mitochondrial Dysfunction and Biogenesis in Neurodegenerative diseases: Pathogenesis and Treatment

Golpich, M., Amini, E., Mohamed, Z., Raymond, A. A., Ibrahim, N. M., & Ahmadiani, A. (2016) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12655 · Cited by 555

Drug-induced mitochondrial dysfunction and cardiotoxicity

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Chronic inflammation and the hallmarks of aging

Baechle, J. J., Chen, N., Makhijani, P., Winer, S., Furman, D., & Winer, D. A. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101755 · Cited by 471

Mitochondria: from cell death executioners to regulators of cell differentiation

Kasahara, A., & Scorrano, L. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.08.005 · Cited by 433

Multidimensional proteomics for cell biology

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Parkin and PINK1: much more than mitophagy

Scarffe, L. A., Stevens, D. A., Dawson, V. L., & Dawson, T. M. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.03.004 · Cited by 392

Mitochondrial quality control mechanisms as molecular targets in cardiac ageing

Picca, A., Mankowski, R. T., Burman, J. L., Donisi, L., Js, K., Marzetti, E., & Leeuwenburgh, C. (2018) · Nature Reviews Cardiology · doi:10.1038/s41569-018-0059-z · Cited by 399

Mitochondrial pathways in sarcopenia of aging and disuse muscle atrophy

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Neurobiology, Clinical Presentation, and Treatment of Methamphetamine Use Disorder: A Review

Paulus, M. P., & Stewart, J. L. (2020) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2020.0246 · Cited by 310

AMPK, Mitochondrial Function, and Cardiovascular Disease

Wu, S., & Zou, M.-H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21144987 · Cited by 286

Mitochondrial dysfunction and damage associated molecular patterns (DAMPs) in chronic inflammatory diseases

Dela Cruz, C. S., & Kang, M.-J. (2018) · Mitochondrion · doi:10.1016/j.mito.2017.12.001 · Cited by 255

Oxidative stress and ageing

Birch-Machin, M. A., & Bowman, A. (2016) · British Journal of Dermatology · doi:10.1111/bjd.14906 · Cited by 225

Dysfunctional Mitochondria and Mitophagy as Drivers of Alzheimer’s Disease Pathogenesis

Chakravorty, A., Jetto, C. T., & Manjithaya, R. R. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00311 · Cited by 225

The Role of Mitochondria in the Mechanisms of Cardiac Ischemia-Reperfusion Injury

Kuznetsov, A. V., Javadov, S. A., Margreiter, R., Grimm, M. F., Hagenbuchner, J., & Ausserlechner, M. J. (2019) · Antioxidants · doi:10.3390/antiox8100454 · Cited by 209

Mitochondria, Oxidative Stress and the Kynurenine System, with a Focus on Ageing and Neuroprotection

Sas, K., Szabó, E., & Vécsei, L. (2018) · Molecules · doi:10.3390/molecules23010191 · Cited by 206

Sestrin-2 and BNIP3 regulate autophagy and mitophagy in renal tubular cells in acute kidney injury

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Mitochondrial Energy and Redox Signaling in Plants

Schwarzländer, M., & Finkemeier, I. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2012.5104 · Cited by 199

Loss of mitochondrial peptidase Clpp leads to infertility, hearing loss plus growth retardation via accumulation of CLPX, mtDNA and inflammatory factors

Gispert, S., Parganlija, D., Klinkenberg, M., Dröse, S., Wittig, I., Mittelbronn, M. G. A., Grzmil, P., Koob, S., Hamann, A., Walter, M. J., et al. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt338 · Cited by 194

Dysregulation of mitochondrial dynamics, mitophagy and apoptosis in major depressive disorder: Does inflammation play a role?

Scaini, G., Mason, B. L., Díaz, A. P., Jha, M. K., Soares, J. C., Trivedi, M. H., & Quevedo, J. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01312-w · Cited by 188

The Role of Reactive Oxygen Species in the Life Cycle of the Mitochondrion

Venditti, P., & Meo, S. D. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21062173 · Cited by 176

The Complex Interplay between Mitochondria, ROS and Entire Cellular Metabolism

Kuznetsov, A. V., Margreiter, R., Ausserlechner, M. J., & Hagenbuchner, J. (2022) · Antioxidants · doi:10.3390/antiox11101995 · Cited by 182

Why size matters – balancing mitochondrial dynamics in Alzheimer's disease

DuBoff, B., Feany, M. Β., & Götz, J. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.03.002 · Cited by 168

What is the function of mitochondrial networks? A theoretical assessment of hypotheses and proposal for future research

Hoitzing, H., Johnston, I. G., & Jones, N. S. (2015) · BioEssays · doi:10.1002/bies.201400188 · Cited by 159

Targeting AMPK Signaling as a Neuroprotective Strategy in Parkinson’s Disease

Curry, D. W., Stutz, B., Andrews, Z. B., & Elsworth, J. D. (2018) · Journal of Parkinson s Disease · doi:10.3233/jpd-171296 · Cited by 160

The Role of ClpP Protease in Bacterial Pathogenesis and Human Diseases

Bhandari, V., Wong, K. S., Zhou, J. L., Mabanglo, M. F., Batey, R. A., & Houry, W. A. (2018) · ACS Chemical Biology · doi:10.1021/acschembio.8b00124 · Cited by 157

Mitochondrial ClpP serine protease-biological function and emerging target for cancer therapy

Nouri, K., Feng, Y., & Schimmer, A. D. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-03062-z · Cited by 158

Huntington’s Disease and Mitochondria

Farshbaf, M. J., & Ghaedi, K. (2017) · Neurotoxicity Research · doi:10.1007/s12640-017-9766-1 · Cited by 153

The role of mitochondria in mood disorders: from physiology to pathophysiology and to treatment

Giménez-Palomo, A., Dodd, S., Anmella, G., Carvalho, A. F., Scaini, G., Quevedo, J., Pacchiarotti, I., Vieta, E., & Berk, M. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.546801 · Cited by 140

Mitochondria—hubs for regulating cellular biochemistry: emerging concepts and networks

Anderson, A. J., Jackson, T. D., Stroud, D. A., & Stojanovski, D. (2019) · Open Biology · doi:10.1098/rsob.190126 · Cited by 138

Mitochondrial Dysfunction in Neural Injury

Zhao, X., Lu, M., Yuan, D., Xu, D.-E., Yao, P.-P., Ji, W., Chen, H., Liu, W., Yan, C.-X., Xia, Y., et al. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00030 · Cited by 132

Simultaneous impairment of mitochondrial fission and fusion reduces mitophagy and shortens replicative lifespan

Bernhardt, D., Müller, M., Reichert, A. S., & Osiewacz, H. D. (2015) · Scientific Reports · doi:10.1038/srep07885 · Cited by 125

A mitochondrial FUNDC1/HSC70 interaction organizes the proteostatic stress response at the risk of cell morbidity

Li, Y., Xue, Y., Xu, X., Wang, G., Liu, Y., Wu, H., Li, W., Wang, Y., Chen, Z., Zhang, W., et al. (2018) · The EMBO Journal · doi:10.15252/embj.201798786 · Cited by 117

Muscle-generated BDNF (brain derived neurotrophic factor) maintains mitochondrial quality control in female mice

Ahuja, P., Ng, C. F., Pang, B. P. S., Chan, W. S., Tse, M. C. L., Bi, X., Kwan, H.-L. R., Brobst, D., Herlea-Pana, O., Yang, X., et al. (2022) · Autophagy · doi:10.1080/15548627.2021.1985257 · Cited by 116

Acyldepsipeptide Analogs Dysregulate Human Mitochondrial ClpP Protease Activity and Cause Apoptotic Cell Death

Wong, K. S., Mabanglo, M. F., Seraphim, T. V., Mollica, A., Mao, Y.-Q., Rizzolo, K., Leung, E., Moutaoufik, M. T., Hoell, L., Phanse, S., et al. (2018) · Cell chemical biology · doi:10.1016/j.chembiol.2018.05.014 · Cited by 116

Mitochondrial hyperpolarization during chronic complex I inhibition is sustained by low activity of complex II, III, IV and V

Forkink, M., Manjeri, G. R., Liemburg-Apers, D. C., Nibbeling, E. A. R., Blanchard, M. G., Wojtala, A., Smeitink, J. A. M., Wieckowski, M. R., Willems, P. H. G. M., & Koopman, W. J. H. (2014) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2014.04.008 · Cited by 106

Mitochondrial Dysfunction in Primary Ovarian Insufficiency

Tiosano, D., Mears, J. A., & Buchner, D. A. (2019) · Endocrinology · doi:10.1210/en.2019-00441 · Cited by 106

Oxidative stress-a key emerging impact factor in health, ageing, lifestyle and aesthetics

Kandola, K., Bowman, A., & Birch‐Machin, M. A. (2015) · International Journal of Cosmetic Science · doi:10.1111/ics.12287 · Cited by 103

Mitochondrial and Nuclear DNA Damage and Repair in Age-Related Macular Degeneration

Błasiak, J., Głowacki, S., Kauppinen, A., & Kaarniranta, K. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms14022996 · Cited by 100

PINK1-dependent phosphorylation of PINK1 and Parkin is essential for mitochondrial quality control

Zhuang, N., Li, L., Chen, S., & Wang, T. (2016) · Cell Death and Disease · doi:10.1038/cddis.2016.396 · Cited by 96

Identification of potential mitochondrial CLPXP protease interactors and substrates suggests its central role in energy metabolism

Fischer, F., Langer, J. D., & Osiewacz, H. D. (2015) · Scientific Reports · doi:10.1038/srep18375 · Cited by 98

Mitochondria and Aging—The Role of Exercise as a Countermeasure

Nilsson, M. I., & Tarnopolsky, M. A. (2019) · Biology · doi:10.3390/biology8020040 · Cited by 92

The disruption of mitochondrial axonal transport is an early event in neuroinflammation

Errea, O., Moreno, B., González-Franquesa, A., García-Rovés, P. M., & Villoslada, P. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0375-8 · Cited by 91

Irisin exhibits neuroprotection by preventing mitochondrial damage in Parkinson’s disease

Zhang, X., Xu, S., Hu, Y. H., Liu, Q., Liu, C., Chai, H., Luo, Y., Jin, L., & Li, S. (2023) · npj Parkinson s Disease · doi:10.1038/s41531-023-00453-9 · Cited by 97

The Mitochondrial Rhomboid Protease PARL Is Regulated by PDK2 to Integrate Mitochondrial Quality Control and Metabolism

Shi, G., & McQuibban, G. A. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.01.029 · Cited by 82

Chaperone-Independent Peripheral Quality Control of CFTR by RFFL E3 Ligase

Okiyoneda, T., Veit, G., Sakai, R., Aki, M., Fujihara, T., Higashi, M., Susuki-Miyata, S., Miyata, M., Fukuda, N., Yoshida, A., et al. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.02.001 · Cited by 83

AMPK activation serves a critical role in mitochondria quality control via modulating mitophagy in the heart under chronic hypoxia

Zhang, H., Liu, B., Li, T., Zhu, Y. K., Luo, G.-P., Jiang, Y., Tang, F., Zhao, J., & Xiao, Y. (2017) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2017.3213 · Cited by 80

Mitochondrial transfer between cell crosstalk – An emerging role in mitochondrial quality control

Liu, Y., Fu, T., Li, G., Li, B., Luo, G., Li, N., & Geng, Q. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.102038 · Cited by 81

Redox signalling and mitochondrial stress responses; lessons from inborn errors of metabolism

Olsen, R. K. J., Cornelius, N., & Gregersen, N. (2015) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-015-9861-5 · Cited by 83

Mitochondrial dysfunction as a critical event in the pathophysiology of bipolar disorder

Scaini, G., Andrews, T., Lima, C. N. D. C., Benevenuto, D., STRECK, E. L., & Quevedo, J. (2020) · Mitochondrion · doi:10.1016/j.mito.2020.12.002 · Cited by 77

Degradation Rate of Mitochondrial Proteins in Arabidopsis thaliana Cells

Nelson, C. J., Li, L., Jacoby, R. P., & Millar, A. H. (2013) · Journal of Proteome Research · doi:10.1021/pr400304r · Cited by 76

Morphological and bioenergetic demands underlying the mitophagy in post-mitotic neurons: the pink–parkin pathway

Amadoro, G., Corsetti, V., Florenzano, F., Atlante, A., Bobba, A., Nicolin, V., Nori, S. L., & Calissano, P. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00018 · Cited by 77

Calcineurin suppresses AMPK-dependent cytoprotective autophagy in cardiomyocytes under oxidative stress

He, H., Liu, X., Lv, L., Liang, H., Leng, B., Zhao, D., Zhang, Y., Du, Z., Chen, X., Li, S., et al. (2014) · Cell Death and Disease · doi:10.1038/cddis.2013.533 · Cited by 77

Astragaloside IV ameliorates diabetic nephropathy by modulating the mitochondrial quality control network

Liu, X., Wang, W., Song, G., Wei, X., Zeng, Y., Han, P., Wang, D., Shao, M., Wu, J., Sun, H., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0182558 · Cited by 75

Multi-target-directed therapeutic strategies for Alzheimer's disease: controlling amyloid-β aggregation, metal ion homeostasis, and enzyme inhibition

Yoo, J., Lee, J., Ahn, B., Han, J., & Lim, M. H. (2025) · Chemical Science · doi:10.1039/d4sc06762b · Cited by 78

Mitochondria: key players in the neurotoxic effects of amphetamines

Barbosa, D. J., Capela, J. P., Feio‐Azevedo, R., Gomes, A., Bastos, M. D. L., & Carvalho, F. D. (2015) · Archives of Toxicology · doi:10.1007/s00204-015-1478-9 · Cited by 70

Adiponectin modulates oxidative stress-induced mitophagy and protects C2C12 myoblasts against apoptosis

Ren, Y., Li, Y., Yan, J., Ma, M., Zhou, D., Xue, Z., Zhang, Z., Liu, H., Yang, H., Jia, L., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-03319-2 · Cited by 70

The mitochondrial unfolded protein response in mammalian physiology

Mottis, A., Jovaisaite, V., & Auwerx, J. H. (2014) · Mammalian Genome · doi:10.1007/s00335-014-9525-z · Cited by 70

Mitochondrial MsrB2 serves as a switch and transducer for mitophagy

Lee, S. H., Lee, S., Du, J., Jain, K., Ding, M., Kadado, A. J., Atteya, G. A., Jaji, Z., Tyagi, T., Kim, W., et al. (2019) · EMBO Molecular Medicine · doi:10.15252/emmm.201910409 · Cited by 67

Mitophagy and Its Contribution to Metabolic and Aging-Associated Disorders

Liu, L., Liao, X., Wu, H., Li, Y., Zhu, Y., & Chen, Q. (2020) · Antioxidants and Redox Signaling · doi:10.1089/ars.2019.8013 · Cited by 69

Human CLPP reverts the longevity phenotype of a fungal ClpP deletion strain

Fischer, F., Weil, A. C., Hamann, A., & Osiewacz, H. D. (2013) · Nature Communications · doi:10.1038/ncomms2397 · Cited by 67

Emerging role of transcription factor EB in mitochondrial quality control

Wang, S., Chen, Y., Li, X., Zhang, W., Liu, Z., Wu, M., Pan, Q., & Liu, H. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110272 · Cited by 64

Mitochondrial Quality Control: Its Role in Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)

Shin, S., Kim, J., Lee, J., Kim, J., & Oh, C. (2023) · Journal of Obesity & Metabolic Syndrome · doi:10.7570/jomes23054 · Cited by 71

The Tricky Connection between Extracellular Vesicles and Mitochondria in Inflammatory-Related Diseases

Mambro, T. D., Pellielo, G., Agyapong, E. D., Carinci, M., Chianese, D., Giorgi, C., Morciano, G., Patergnani, S., Pinton, P., & Rimessi, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24098181 · Cited by 68

Tom70 Is Essential for PINK1 Import into Mitochondria

Kato, H., Lu, Q., Rapaport, D., & Kozjak‐Pavlovic, V. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058435 · Cited by 64

Defective insulin signaling and mitochondrial dynamics in diabetic cardiomyopathy

Westermeier, F., Navarro-Márquez, M., López‐Crisosto, C., Bravo-Sagua, R., Quiroga, C., Bustamante, M., Verdejo, H., Ricardo Zalaquett, S., Ibacache, M. E., Parra, V., et al. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2015.02.005 · Cited by 63

Control of mitochondrial integrity in ageing and disease

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Mutation or knock-down of 17β-hydroxysteroid dehydrogenase type 10 cause loss of MRPP1 and impaired processing of mitochondrial heavy strand transcripts

Deutschmann, A. J., Amberger, A., Zavadil, C., Steinbeißer, H., Mayr, J. A., Feichtinger, R. G., Oerum, S., Yue, W. W., & Zschocke, J. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu072 · Cited by 61

Antagonistic functions of LMNA isoforms in energy expenditure and lifespan

López‐Mejía, I. C., de Toledo, M., Chavey, C., Lapasset, L., Cavelier, P., Herrera, C. L., Chébli, K., Fort, P., Béranger, G. E., Fajas, L., et al. (2014) · EMBO Reports · doi:10.1002/embr.201338126 · Cited by 61

The interplay between mitochondria and autophagy and its role in the aging process

Schiavi, A., & Ventura, N. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.02.015 · Cited by 61

Genetic and cellular modifiers of oxidative stress: What can we learn from fatty acid oxidation defects?

Olsen, R. K. J., Cornelius, N., & Gregersen, N. (2013) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2013.10.007 · Cited by 58

Mitophagy receptors sense stress signals and couple mitochondrial dynamic machinery for mitochondrial quality control

Wu, H., Wei, H., Sehgal, S. A., Liu, L., & Chen, Q. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.03.030 · Cited by 58

Mitochondrial Quality Control: A Pathophysiological Mechanism and Therapeutic Target for Stroke

Yang, M., He, Y. T., Deng, S., Xiao, L., Tian, M., Xin, Y., Lu, C., Zhao, F., & Gong, Y. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.786099 · Cited by 56

What are the 100 most cited fungal genera?

Bhunjun, C. S., Chen, Y. J., Phukhamsakda, C., Boekhout, T., Groenewald, J. Z., McKenzi, E. H. C., Francisco, E. C., Frisvad, J. C., Groenewald, M., Hurdeal, V. G., et al. (2024) · Studies in Mycology · doi:10.3114/sim.2024.108.01 · Cited by 58

A-Kinase Anchoring Protein 1: Emerging Roles in Regulating Mitochondrial Form and Function in Health and Disease

Liu, Y., Merrill, R. A., & Strack, S. (2020) · Cells · doi:10.3390/cells9020298 · Cited by 59

Mitochondrial protein quality control in health and disease

Baker, M. J., Palmer, C. S., & Stojanovski, D. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12430 · Cited by 60

Identification of autophagy as a longevity-assurance mechanism in the aging modelPodospora anserina

Knuppertz, L., Hamann, A., Pampaloni, F., Stelzer, E. H. K., & Osiewacz, H. D. (2014) · Autophagy · doi:10.4161/auto.28148 · Cited by 57

Lack of FTSH4 Protease Affects Protein Carbonylation, Mitochondrial Morphology, and Phospholipid Content in Mitochondria of Arabidopsis: New Insights into a Complex Interplay

Smakowska, E., Skibior, R., Czarna, M., Kołodziejczak, M., Kwaśniak-Owczarek, M., Parys, K., Funk, C., & Jańska, H. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.00370 · Cited by 51

Disturbed mitochondrial quality control involved in hepatocytotoxicity induced by silica nanoparticles.

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Mitophagy: Basic Mechanism and Potential Role in Kidney Diseases

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Short‐chain acyl‐CoA dehydrogenase deficiency: from gene to cell pathology and possible disease mechanisms

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Inhibition of PI3K/mTOR increased the sensitivity of hepatocellular carcinoma cells to cisplatin via interference with mitochondrial‐lysosomal crosstalk

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Mitochondrial translation and dynamics synergistically extend lifespan in C. elegans through HLH-30

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Live imaging of alterations in cellular morphology and organelles during cornification using an epidermal equivalent model

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Alcohol induces mitochondrial redox imbalance in alveolar macrophages

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Inhibition of the mitochondria-shaping protein Opa1 restores sensitivity to Gefitinib in a lung adenocarcinomaresistant cell line

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Mitochondrial‐targeted nitroxides disrupt mitochondrial architecture and inhibit expression of peroxiredoxin 3 and FOXM1 in malignant mesothelioma cells

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Cellular consequences of oxidative stress in riboflavin responsive multiple acyl-CoA dehydrogenation deficiency patient fibroblasts

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Mitochondrion-mediated cell death: dissecting yeast apoptosis for a better understanding of neurodegeneration

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Mitochondrial Determinants of Anti-Cancer Drug-Induced Cardiotoxicity

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LONP1-mediated mitochondrial quality control safeguards metabolic shifts in heart development

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Tauroursodeoxycholic Acid Enhances Mitochondrial Biogenesis, Neural Stem Cell Pool, and Early Neurogenesis in Adult Rats

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Plant mitochondrial retrograde signaling: post-translational modifications enter the stage

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Regulation and Quantification of Cellular Mitochondrial Morphology and Content

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Role of Mitochondria-Cytoskeleton Interactions in the Regulation of Mitochondrial Structure and Function in Cancer Stem Cells

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Mitochondrial quality control pathways as determinants of metabolic health

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Impaired quality control of mitochondria: Aging from a new perspective

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Mitochondria as a Key Player in Aging

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Autophagic responses compensate mitochondrial impairments

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