Mitochondrial Medicine for Aging and Neurodegenerative Diseases

The Amyloid Hypothesis of Alzheimer’s Disease: Progress and Problems on the Road to Therapeutics

Hardy, J., & Selkoe, D. J. (2002) · Science · doi:10.1126/science.1072994 · Cited by 13,864

Sequence and organization of the human mitochondrial genome

Anderson, S., Bankier, A. T., Barrell, B. G., de Bruijn, M. H. L., Coulson, A. R., Drouin, J., Eperon, I. C., Nierlich, D. P., Roe, B. A., Sanger, F., et al. (1981) · Nature · doi:10.1038/290457a0 · Cited by 9,740

Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease

Polymeropoulos, M. H., Lavedan, C., Leroy, E., Ide, S. E., Dehejia, A., Dutra, A., Pike, B., Root, H., Rubenstein, J., Boyer, R., et al. (1997) · Science · doi:10.1126/science.276.5321.2045 · Cited by 8,240

A JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS

Lindemann, L., Jaeschke, G., Michalon, A., Vieira, E., Honer, M., Spooren, W., Porter, R., Hartung, T., Kolczewski, S., Büttelmann, B., et al. (1909) · JAMA · doi:10.1001/jama.1909.02550020033007 · Cited by 7,889

Mitochondrial Dysfunction and Oxidative Stress in Neurodegenerative Diseases

Lin, M. T., & Beal, M. F. (2006) · Nature · doi:10.1038/nature05292 · Cited by 6,455

Alzheimer's Disease: Genes, Proteins, and Therapy

Selkoe, D. J. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.2.741 · Cited by 6,063

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

Kitada, T., Asakawa, S., Hattori, N., Matsumine, H., Yamamura, Y., Minoshima, S., Yokochi, M., Mizuno, Y., & Shimizu, N. (1998) · Nature · doi:10.1038/33416 · Cited by 5,227

Chronic Parkinsonism in Humans Due to a Product of Meperidine-Analog Synthesis

Langston, J. W., Ballard, P., Tetrud, J. W., & Irwin, I. (1983) · Science · doi:10.1126/science.6823561 · Cited by 4,914

Motor Neuron Degeneration in Mice that Express a Human Cu,Zn Superoxide Dismutase Mutation

Gurney, M. E., Pu, H., Chiu, A. Y., Dal Canto, M. C., Polchow, C. Y., Alexander, D. D., Caliendo, J., Hentati, A., Kwon, Y. W., Deng, H.-X., et al. (1994) · Science · doi:10.1126/science.8209258 · Cited by 4,143

Association of apolipoprotein E allele ϵ4 with late‐onset familial and sporadic Alzheimer's disease

Saunders, A. M., Strittmatter, W. J., Schmechel, D., St. George-Hyslop, P. H., Pericak-Vance, M. A., Joo, S. H., Rosi, B. L., Gusella, J. F., Crapper-MacLachlan, D. R., Alberts, M. J., et al. (1993) · Neurology · doi:10.1212/wnl.43.8.1467 · Cited by 3,786

Toxicity, recovery, and resilience in a 3D dopaminergic neuronal in vitro model exposed to rotenone

Harris, G., Eschment, M., Orozco, S. P., McCaffery, J. M., Maclennan, R., Severín, D., Leist, M., Kleensang, A., Pamies, D., Maertens, A., et al. (2018) · Archives of Toxicology · doi:10.1007/s00204-018-2250-8 · Cited by 42

Suppression of Mitochondrial Oxidative Phosphorylation and TCA Enzymes in Discrete Brain Regions of Mice Exposed to High Fluoride: Amelioration by Panax ginseng (Ginseng) and Lagerstroemia speciosa (Banaba) Extracts

Basha, P. M., & Saumya, S. M. (2013) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-013-9912-0 · Cited by 41

Micronutrients/miRs/ATP networking in mitochondria: Clinical intervention with ferroptosis, cuproptosis, and calcium burden

Panda, S. P., & Kesharwani, A. (2023) · Mitochondrion · doi:10.1016/j.mito.2023.05.003 · Cited by 41

A partial reduction of VDAC1 enhances mitophagy, autophagy, synaptic activities in a transgenic Tau mouse model

Vijayan, M., Alvir, R. V., Alvir, R. V., Bunquin, L. E., Pradeepkiran, J. A., & Reddy, P. H. (2022) · Aging Cell · doi:10.1111/acel.13663 · Cited by 40

Mechanisms associated with the dysregulation of mitochondrial function due to lead exposure and possible implications on the development of Alzheimer’s disease

Bandaru, L. J. M., Ayyalasomayajula, N., Murumulla, L., & Challa, S. (2022) · BioMetals · doi:10.1007/s10534-021-00360-7 · Cited by 39

Targeted Interception of Signaling Reactive Oxygen Species in the Vascular Endothelium

Han, J., Shuvaev, V. V., & Muzykantov, V. R. (2012) · Therapeutic Delivery · doi:10.4155/tde.11.151 · Cited by 39

Protective Role of Capsaicin in Neurological Disorders: An Overview

Tyagi, S., Shekhar, N., & Thakur, A. K. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03549-5 · Cited by 37

Proteomic Profile of Mouse Brain Aging Contributions to Mitochondrial Dysfunction, DNA Oxidative Damage, Loss of Neurotrophic Factor, and Synaptic and Ribosomal Proteins

Li, Y., Yu, H., Chen, C., Li, S., Zhang, Z., Xu, H., Zhu, F., Liu, J., Spencer, P. S., Dai, Z., et al. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/5408452 · Cited by 37

Toxicity of Neurons Treated with Herbicides and Neuroprotection by Mitochondria-Targeted Antioxidant SS31

Reddy, T. P., Mańczak, M., Calkins, M. J., Mao, P., Reddy, A. P., Shirendeb, U. P., Park, B. S., & Reddy, P. H. (2011) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph8010203 · Cited by 36

Testosterone ameliorates age-related brain mitochondrial dysfunction

Yan, W., Zhang, T., Kang, Y., Zhang, G., Ji, X., Feng, X., & Shi, G. (2021) · Aging · doi:10.18632/aging.203153 · Cited by 35

Cognitive impairment, genomic instability and trace elements

Meramat, A. A., Rajab, N. F., Shahar, S., & Sharif, R. (2014) · The journal of nutrition health & aging · doi:10.1007/s12603-014-0489-1 · Cited by 35

Aging Influences Cardiac Mitochondrial Gene Expression and Cardiovascular Function following Hemorrhage Injury

Jian, B., Yang, S., Chen, D., Zou, L., Chatham, J. C., Chaudry, I. H., & Raju, R. P. (2010) · Molecular Medicine · doi:10.2119/molmed.2010.00195 · Cited by 33

Renovascular disease induces mitochondrial damage in swine scattered tubular cells

Nargesi, A. A., Zhu, X.-Y., Conley, S. M., Woollard, J. R., Saadiq, I. M., Lerman, L. O., & Eirin, A. (2019) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00276.2019 · Cited by 32

Targeting Infectious Agents as a Therapeutic Strategy in Alzheimer’s Disease

Fülöp, T., Munawara, U., Larbi, A., Desroches, M., Rodrigues, S., Catanzaro, M., Guidolin, A., Khalil, A., Bernier, F., Barron, A. E., et al. (2020) · CNS Drugs · doi:10.1007/s40263-020-00737-1 · Cited by 32

Potential Retinal Biomarkers in Alzheimer’s Disease

García-Bermúdez, M. Y., Vohra, R., Freude, K., van Wijngaarden, P., Martin, K. R. G., Thomsen, M. S., Aldana, B. I., & Kolko, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242115834 · Cited by 30

Mitochondrial Deficits With Neural and Social Damage in Early-Stage Alzheimer’s Disease Model Mice

Misrani, A., Tabassum, S., Huo, Q., Tabassum, S., Jiang, J., Ahmed, A., Chen, X., Zhou, J., Zhang, J., Liu, S., et al. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.748388 · Cited by 29

Reduced VDAC1, Maintained Mitochondrial Dynamics and Enhanced Mitochondrial Biogenesis in a Transgenic Tau Mouse Model of Alzheimer’s Disease

Vijayan, M., & Reddy, P. H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158561 · Cited by 29

The oligosaccharide portion of ganglioside GM1 regulates mitochondrial function in neuroblastoma cells

Fazzari, M., Audano, M., Lunghi, G., Biase, E. D., Loberto, N., Mauri, L., Mitro, N., Sonnino, S., & Chiricozzi, E. (2020) · Glycoconjugate Journal · doi:10.1007/s10719-020-09920-4 · Cited by 29

Downregulation of Pink1 influences mitochondrial fusion–fission machinery and sensitizes to neurotoxins in dopaminergic cells

Rojas-Charry, L., Cookson, M., Niño, A., Arboleda, H., & Arboleda, G. (2014) · NeuroToxicology · doi:10.1016/j.neuro.2014.04.007 · Cited by 29

Evaluation of respiratory chain activity in lymphocytes of patients with Alzheimer disease

Feldhaus, P., Fraga, D. B., Ghedim, F. V., De Luca, R. D., Bruna, T. D., Heluany, M., Matos, M. P., Ferreira, G. K., Jeremias, I. C., Heluany, C., et al. (2011) · Metabolic Brain Disease · doi:10.1007/s11011-011-9253-y · Cited by 27

Mitochondrial Dynamics in Brain Cells During Normal and Pathological Aging

Sukhorukov, V. S., Baranich, T. I., Egorova, A. V., Akateva, A. V., Okulova, K. M., Ryabova, M. S., Skvortsova, K. A., Dmitriev, O. V., Mudzhiri, N. M., Воронков, Д. Н., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252312855 · Cited by 27

Early Cellular, Molecular, Morphological and Behavioral Changes in the Humanized Amyloid-Beta-Knock-In Mouse Model of Late-Onset Alzheimer’s Disease

Kshirsagar, S., Alvir, R. V., Hindle, A., Kumar, S., Vijayan, M., Pradeepkiran, J. A., Reddy, A. P., Ramasubramanian, B., & Reddy, P. H. (2022) · Cells · doi:10.3390/cells11040733 · Cited by 27

Enabling Mitochondrial Uptake of Lipophilic Dications Using Methylated Triphenylphosphonium Moieties

Ong, H. C., Hu, Z., Coimbra, J. T. S., Ramos, M. J., Kon, O. L., Xing, B., Yeow, E. K. L., Fernandes, P. A., & Garcı́a, F. (2019) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.8b03380 · Cited by 27

Suppressing inflammatory cascade by cyclo-oxygenase inhibitors attenuates quinolinic acid induced Huntington's disease-like alterations in rats

Kalonia, H., & Kumar, A. (2011) · Life Sciences · doi:10.1016/j.lfs.2011.02.020 · Cited by 26

Mitochondrial DNA deletions and differential mitochondrial DNA content in Rhesus monkeys: Implications for aging

Mao, P., Gallagher, P., Nedungadi, S., Mańczak, M., Shirendeb, U. P., Kohama, S. G., Ferguson, B. M., Park, B. S., & Reddy, P. H. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.10.014 · Cited by 26

Electrochemically Reduced Water Protects Neural Cells from Oxidative Damage

Kashiwagi, T., Yan, H., Hamasaki, T., Kinjo, T., Nakamichi, N., Teruya, K., Kabayama, S., & Shirahata, S. (2014) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2014/869121 · Cited by 26

RALBP1 in Oxidative Stress and Mitochondrial Dysfunction in Alzheimer’s Disease

Awasthi, S., Hindle, A., Sawant, N. A., George, M., Vijayan, M., Kshirsagar, S., Morton, H., Bunquin, L. E., Palade, P., Lawrence, J. J., et al. (2021) · Cells · doi:10.3390/cells10113113 · Cited by 25

Fucoidan Improves D-Galactose-Induced Cognitive Dysfunction by Promoting Mitochondrial Biogenesis and Maintaining Gut Microbiome Homeostasis

Xu, Y., Xue, M., Li, J., Ma, Y., Wang, Y., Zhang, H., & Liang, H. (2024) · Nutrients · doi:10.3390/nu16101512 · Cited by 25

Neuroprotective effects of 5-(4-hydroxy-3-dimethoxybenzylidene)-thiazolidinone in MPTP induced Parkinsonism model in mice

Ren, Z., Yang, N., Ji, C., Zheng, J., Wang, T., Liu, Y., & Zuo, P. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.01.030 · Cited by 25

Mitochondria-Targeted Molecules as Potential Drugs to Treat Patients With Alzheimer's Disease

Reddy, A. P., & Reddy, P. H. (2017) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2016.12.010 · Cited by 25

Dietary interventions designed to protect the perinatal brain from hypoxic-ischemic encephalopathy – Creatine prophylaxis and the need for multi-organ protection

Ellery, S. J., Dickinson, H., McKenzie, M., & Walker, D. W. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2015.11.002 · Cited by 23

Resveratrol in Neurodegeneration, in Neurodegenerative Diseases, and in the Redox Biology of the Mitochondria

Danışman, B., Kelek, S. E., & Aslan, M. (2023) · Psychiatry and Clinical Psychopharmacology · doi:10.5152/pcp.2023.23633 · Cited by 23

Mitochondrially-Targeted Therapeutic Strategies for Alzheimer’s Disease

Onyango, I. G., Bennett, J. P., & Stokin, G. B. (2021) · Current Alzheimer Research · doi:10.2174/1567205018666211208125855 · Cited by 22

In vitro mitochondrial failure and oxidative stress mimic biochemical features of Alzheimer disease

Selvatici, R., Marani, L., Marino, S., & Siniscalchi, A. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.05.005 · Cited by 22

Effect of restorative treatment on mutans streptococci and IgA antibodies.

Gregory, R. L., el-Rahman, A. M., & Avery, D. R. (1998) · PubMed · Cited by 22

Microglia-Synapse Pathways: Promising Therapeutic Strategy for Alzheimer’s Disease

Xie, J., Wang, H., Lin, T., & Bi, B. (2017) · BioMed Research International · doi:10.1155/2017/2986460 · Cited by 22

Alkyl vs. aryl modifications: a comparative study on modular modifications of triphenylphosphonium mitochondrial vectors

Ong, H. C., Coimbra, J. T. S., Kwek, G., Ramos, M. J., Xing, B., Fernandes, P. A., & Garcı́a, F. (2021) · RSC Chemical Biology · doi:10.1039/d1cb00099c · Cited by 21

Palm vitamin E reduces locomotor dysfunction and morphological changes induced by spinal cord injury and protects against oxidative damage

Zadeh-Ardabili, P. M., Rad, S. K., Rad, S. K., Khaza’ai, H., Sanusi, J., & Zadeh, M.-A.-R. H. (2017) · Scientific Reports · doi:10.1038/s41598-017-14765-3 · Cited by 21

Cytotoxicity and Mitochondrial Effects of Phenolic and Quinone-Based Mitochondria-Targeted and Untargeted Antioxidants on Human Neuronal and Hepatic Cell Lines: A Comparative Analysis

Fernandes, C., Videira, A. J. C., Veloso, C. D., Benfeito, S., Soares, P., Martins, J. D., Gonçalves, B., Duarte, J. F. S., Santos, A. M. S., Oliveira, P. J., et al. (2021) · Biomolecules · doi:10.3390/biom11111605 · Cited by 20

Dictyostelium discoideum as a Model for Investigating Neurodegenerative Diseases

Haver, H. N., & Scaglione, K. M. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.759532 · Cited by 20

Apoptosis inducing factor deficiency causes reduced mitofusion 1 expression and patterned Purkinje cell degeneration

Chung, S., Calafiore, M., Plane, J. M., Pleasure, D., & Deng, W. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2010.10.016 · Cited by 20

More Ulam for Your Brain: A Review on the Potential Role of Ulam in Protecting Against Cognitive Decline

You, Y. X., Shahar, S., Haron, H., & Yahya, H. M. (2018) · Sains Malaysiana · doi:10.17576/jsm-2018-4711-15 · Cited by 19

Mitophagy pathways and Alzheimer's disease: From pathogenesis to treatment

Pan, X.-J., Misrani, A., Tabassum, S., & Yang, L. (2021) · Mitochondrion · doi:10.1016/j.mito.2021.04.007 · Cited by 18

ARE/Nrf2 Transcription System Involved in Carotenoid, Polyphenol, and Estradiol Protection from Rotenone-Induced Mitochondrial Oxidative Stress in Dermal Fibroblasts

Darawsha, A., Trachtenberg, A., & Sharoni, Y. (2024) · Antioxidants · doi:10.3390/antiox13081019 · Cited by 19

The Underlying Role of Mitophagy in Different Regulatory Mechanisms of Chronic Obstructive Pulmonary Disease

Liu, J., Zhang, M., & Qu, Y.-Q. (2020) · International Journal of COPD · doi:10.2147/copd.s265728 · Cited by 18

Elevated [Ca 2+ ] i Levels Occur with Decreased Calpain Activity in Aged Fibroblasts and Their Reversal by Energy-Rich Compounds: New Paradigm for Alzheimer's Disease Prevention

Nguyen, H. T., Sawmiller, D. R., Markov, O., & Chen, M. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-131001 · Cited by 17

Experimental lung injury promotes alterations in energy metabolism and respiratory mechanics in the lungs of rats: prevention by exercise

da Cunha, M. J., da Cunha, A. A., Scherer, E. B. S., Machado, F. R., Loureiro, S. O., Jaenisch, R. B., Guma, F. T. C. R., Lago, P. D., & Wyse, Â. T. D. S. (2013) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-013-1944-8 · Cited by 17

Changes in neuromuscular function in elders: Novel techniques for assessment of motor unit loss and motor unit remodeling with aging

Verschueren, A., Palminha, C., Delmont, É., & Attarian, S. (2022) · Revue Neurologique · doi:10.1016/j.neurol.2022.03.019 · Cited by 16

Fluorescence microscopic platforms imaging mitochondrial abnormalities in neurodegenerative diseases

Wang, Y., Wang, P., & Li, C. (2023) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2023.114841 · Cited by 13

The impact of obesity on mitochondrial dysfunction during pregnancy

de Oliveira, M. P., da Silva, L. E., Fernandes, B. B., da Silva, M. R., Pistóia, D. G., Cichella, T. D. S., Jacinto, L. B., Spuldaro, K. M., Iser, B. P. M., & Rezin, G. T. (2025) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2025.112463 · Cited by 13

Neurodegenerative and Fatiguing Illnesses, Infections and Mitochondrial Dysfunction: Use of Natural Supplements to Improve Mitochondrial Function.

Nicolson, G. L., Settineri, R. A., & Ellithorpe, R. R. (2014) · Functional Foods in Health and Disease · doi:10.31989/ffhd.v4i1.26 · Cited by 13

The Mitochondrial Italian Human Proteome Project Initiative (mt-HPP)

Urbani, A., & Canio, M. D. (2013) · Molecular BioSystems · doi:10.1039/c3mb70065h · Cited by 12

An investigation into closed-loop treatment of neurological disorders based on sensing mitochondrial dysfunction

Adams, S. D., Kouzani, A. Z., Tye, S. J., Bennet, K. E., & Berk, M. (2018) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/s12984-018-0349-z · Cited by 12

Esculetin Provides Neuroprotection against Mutant Huntingtin-Induced Toxicity in Huntington’s Disease Models

Pruccoli, L., Breda, C., Teti, G., Falconi, M., Giorgini, F., & Tarozzi, A. (2021) · Pharmaceuticals · doi:10.3390/ph14101044 · Cited by 12

Mitsugumin 53 promotes mitochondrial autophagy through regulating Ambra1 expression in C2C12 myoblast cells

Lijie, G., Yueyue, Z., Zhu, N., Ling, W., Xuan, W., & Weijie, Y. (2019) · Cell Biology International · doi:10.1002/cbin.11097 · Cited by 12

Interplay Between Aging and Glial Cell Dysfunction: Implications for CNS Health

García‐Domínguez, M. (2025) · Life · doi:10.3390/life15101498 · Cited by 12

Gain of PITRM1 peptidase in cortical neurons affords protection of mitochondrial and synaptic function in an advanced age mouse model of Alzheimer’s disease

Du, F., Yu, Q., Yan, S., Zhang, Z., Vangavaragu, J. R., Chen, D., Yan, S. S., & Yan, S. S. (2021) · Aging Cell · doi:10.1111/acel.13368 · Cited by 11

Development of high-affinity fluorinated ligands for cannabinoid subtype 2 receptor, and in vitro evaluation of a radioactive tracer for imaging

Modemann, D. J., Mahardhika, A. B., Yamoune, S., Kreyenschmidt, A.-K., Maaß, F., Kremers, S., Breunig, C., Sahlmann, C., Bucerius, J. A., Stalke, D., et al. (2022) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2022.114138 · Cited by 11

Emerging Promise of Therapeutic Approaches Targeting Mitochondria in Neurodegenerative Disorders

Rahman, M. M., Tumpa, M. A. A., Rahaman, M. S., Islam, F., Sutradhar, P. R., Ahmed, M., Alghamdi, B. S. A., Hafeez, A., Alexiou, A. T., Perveen, A., et al. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230316150559 · Cited by 11

Existing and emerging mitochondrial-targeting therapies for altering Parkinson's disease severity and progression

Pienaar, I. S., & Chinnery, P. F. (2012) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2012.08.010 · Cited by 11

Putting bioactivation reactions to work: Targeting antioxidants to mitochondria

Anders, M. W. (2010) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2010.10.004 · Cited by 10

Novel Approaches of Oxidative Stress Mechanisms in the Multiple Sclerosis Pathophysiology and Therapy

Adamczyk, B., Niedziela, N., & Adamczyk-Sowa, M. H. (2017) · Codon Publications eBooks · doi:10.15586/codon.multiplesclerosis.2017.ch10 · Cited by 10

Alzheimer’s Disease: The Effect of Nrf2 Signaling Pathway on Cell Death Caused by Oxidative Stress

Abraki, S. B., & Chavoshinezhad, S. (2015) · The Neuroscience Journal of Shefaye Khatam · doi:10.18869/acadpub.shefa.3.1.145 · Cited by 10

Dimebon as a Potential Therapy for Alzheimer's Disease

Doody, R. S. (2009) · CNS Spectrums · doi:10.1017/s1092852900024913 · Cited by 10

Mitochondrial Defects and Oxidative Stress in Alzheimer Disease

Abraki, S. B., & Chavoshinezhad, S. (2014) · The Neuroscience Journal of Shefaye Khatam · doi:10.18869/acadpub.shefa.2.1.85 · Cited by 9

Cross Talks between CNS and CVS Diseases: An Alliance to Annihilate

Chib, S., Devi, S., Chalotra, R., Mittal, N., Singh, T. G., Kumar, P., & Singh, R. (2024) · Current Cardiology Reviews · doi:10.2174/011573403x278550240221112636 · Cited by 7

Decoding synaptic imbalance in neurodegenerative diseases: From pathological analysis to targeted intervention

Li, X., Wan, R., Zhao, Y., Wu, Y., Chen, X., Li, Q., & Luo, C. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103028 · Cited by 7

Tuning the Fire: Context-Dependent Mitochondrial ROS Signaling, Mitohormesis, and Redox-Modulating Interventions

Charidemou, E., Andreou, E. P., & Papaneophytou, C. P. (2026) · Biomolecules · doi:10.3390/biom16060867 · Cited by 7

Mitochondrial dysfunction mediates neuronal cell response to DMMB photodynamic therapy

Gomes, R. D. A. N., Marmolejo-Garza, A., Haan, F.-J., Mitchell, T., Chen, T., Mauthe, M., Parisotto, Y. F., Murakami, M. M., Marie, S. K. N., Baptista, M. S., et al. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2022.119429 · Cited by 7

Effects of Elamipretide on Autophagy in Renal Cells of Pigs with Metabolic Syndrome

Hong, S., Ghandriz, R., Siddiqi, S., Zhu, X., Saadiq, I. M., Jordan, K. L., Tang, H. J., Ali, K. A., Lerman, A., Eirin, A., et al. (2022) · Cells · doi:10.3390/cells11182891 · Cited by 7

The Bacterial Toxin CNF1 Protects Human Neuroblastoma SH-SY5Y Cells against 6-Hydroxydopamine-Induced Cell Damage: The Hypothesis of CNF1-Promoted Autophagy as an Antioxidant Strategy

Travaglione, S., Loizzo, S., Vona, R., Ballan, G., Rivabene, R., Giordani, D., Guidotti, M., Dupuis, M. L., Maroccia, Z., Baiula, M., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21093390 · Cited by 7

The protection of acute spinal cord injury by subarachnoid space injection of Danshen in animal models

Yu, Y.-G., Yang, J. M., Cheng, X., Shang, W., Zhao, B., Zhao, F., Chen, Z., & Zhen-hua, H. (2018) · Journal of Spinal Cord Medicine · doi:10.1080/10790268.2018.1468583 · Cited by 7

Decreased mitochondrial DNA copy number in children with cerebral palsy quantified by droplet digital PCR

Lu, B., Fanyong, Z., Xing, W., Lin, L., Huo, J., Tan, C., Zhu, L., & Liu, Z. (2020) · Clinica Chimica Acta · doi:10.1016/j.cca.2020.01.018 · Cited by 7

Mitochondrial Dysfunction and Chronic Disease: Treatment with Membrane Lipid Replacement and Other Natural Supplements

Nicolson, G. L., Ferreira, G., Settineri, R. A., Ellithorpe, R. R., Breeding, P. C., & Ash, M. E. (2018) · Springer eBooks · doi:10.1007/978-3-319-73344-9_22 · Cited by 6

Neurodegenerative diseases

Gupta, A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820122-0.00004-2 · Cited by 6

Establishment of a novel cellular model for Alzheimer's disease in vitro studies

El-Araby, R. E., Wasif, K., Johnson, R., Tu, Q., Aboushousha, T., Zhu, Z. X., & Chen, J. (2024) · Experimental Neurology · doi:10.1016/j.expneurol.2024.114820 · Cited by 5

Targeting cellular batteries for the therapy of neurological diseases

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Stable knockdown of Drp1 improves retinoic acid-BDNF-induced neuronal differentiation through global transcriptomic changes and results in reduced phosphorylation of ERK1/2 independently of DUSP1 and 6

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