Cell Biology of the Mitochondrion

Oxyl radicals, redox-sensitive signalling cascades and antioxidants

Genestra, M. (2007) · Cellular Signalling · doi:10.1016/j.cellsig.2007.04.009 · Cited by 4,930

Mitochondrial Fission, Fusion, and Stress

Youle, R. J., & van der Bliek, A. M. (2012) · Science · doi:10.1126/science.1219855 · Cited by 3,674

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

Phosphorylation of ULK1 (hATG1) by AMP-Activated Protein Kinase Connects Energy Sensing to Mitophagy

Egan, D. F., Shackelford, D. B., Mihaylova, M. M., Gelino, S., Kohnz, R. A., Mair, W., Vasquez, D. S., Joshi, A., Gwinn, D. M., Taylor, R., et al. (2011) · Science · doi:10.1126/science.1196371 · Cited by 2,600

Assessing mitochondrial dysfunction in cells

Brand, M. D., & Nicholls, D. G. (2011) · Biochemical Journal · doi:10.1042/bj20110162 · Cited by 2,436

The Roles of PINK1, Parkin, and Mitochondrial Fidelity in Parkinson’s Disease

Pickrell, A. M., & Youle, R. J. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.007 · Cited by 2,310

Mitochondrial form and function

Friedman, J. R., & Nunnari, J. (2014) · Nature · doi:10.1038/nature12985 · Cited by 1,803

Production of Reactive Oxygen Species by Mitochondria

Chen, Q., Vazquez, E. J., Moghaddas, S., Hoppel, C. L., & Lesnefsky, E. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m304854200 · Cited by 1,616

Mitochondrial Dynamics in the Regulation of Nutrient Utilization and Energy Expenditure

Liesa, M., & Shirihai, O. S. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.03.002 · Cited by 1,341

Metabolic regulation of mitochondrial dynamics

Mishra, P., & Chan, D. C. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201511036 · Cited by 1,143

Nanomedicine-based therapeutic strategies for cerebral ischemia–reperfusion injury: from blood–brain barrier penetration to precision targeting

Guo, X., Liu, G., Liu, Y., Jin, M., Zihao, Y. O. N. G., Li, F., Tang, S., Xie, L., Huang, C., Mu, Q., et al. (2026) · European journal of medical research · doi:10.1186/s40001-026-04073-w · Cited by 2

Mitochondrial homeostasis imbalance-triggered PANoptosis in traumatic brain and spinal cord injury: from mechanism to therapeutic strategies

Ye, Y., Feng, Z., Huang, P., Su, X., Lu, C., Yang, Y., Li, L., Wang, J., & Li, X. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104257 · Cited by 2

Modulation of the mitochondrial function with polyphenols and other natural bioactive compounds to treat obesity

Gibert‐Ramos, A., Baselga‐Escudero, L., & Crescenti, A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819621-2.00026-7 · Cited by 2

Characterization and Phylogenetic Analysis of the Complete Mitochondrial Genome of Aythya marila

Zhang, L., Xia, T., Gao, X., Yang, X., Sun, G., Zhao, C., Liu, G., & Zhang, H. (2023) · Genes · doi:10.3390/genes14061205 · Cited by 2

Mitochondrial Genomic Evidence of Selective Constraints in Small-Bodied Terrestrial Cetartiodactyla

Mei, X., Wang, X., Wu, X., Liu, G., Chen, Y., Zhou, S., Shang, Y., Liu, Z., Yang, X., Sha, W., et al. (2024) · Animals · doi:10.3390/ani14101434 · Cited by 3

PRR34-AS1 promotes mitochondrial division and glycolytic reprogramming in hepatocellular carcinoma cells through upregulation of MIEF2

Yang, X., Feng, H., Kim, J., Ti, G., Wang, L., Wang, K., & Song, D. (2024) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2024083 · Cited by 2

Predicting T Cell Mitochondria Hijacking from Tumor Single-Cell RNA Sequencing Data with MitoR

Jiang, A., Lyu, C., & Zhao, Y. (2025) · Mathematics · doi:10.3390/math13040673 · Cited by 2

Translation of bioenergetics therapies

Bhatti, G. K., Gupta, A., Reddy, P. H., & Bhatti, J. S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819621-2.00022-x · Cited by 2

Assessment of Mitochondrial Dysfunctions After Sirtuin Inhibition

Marx, C., Marx-Blümel, L., Sonnemann, J., & Wang, Z. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2788-4_18 · Cited by 2

MITOL dysfunction causes dwarfism with anterior pituitary hypoplasia

Matsuno, K., Nagashima, S., Shiiba, I., Taniwaka, K., Takeda, K., Tokuyama, T., Ito, N., Matsushita, N., Fukuda, T., Ishido, S., et al. (2020) · The Journal of Biochemistry · doi:10.1093/jb/mvaa050 · Cited by 2

Pharmacological agents affecting mitophagy and inflammation

Borisov, E. E., Bezsonov, E. E., Lyukmanov, D., Poggio, P., Moschetta, D., & Valerio, V. (2022) · Vessel Plus · doi:10.20517/2574-1209.2022.20 · Cited by 3

Loss of flavin adenine dinucleotide (FAD) impairs sperm function and male reproductive advantage in C. elegansPreprint

Yen, C.-A., Ruter, D. L., Turner, C. D., Pang, S., & Curran, S. P. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/456863 · Cited by 2

Mitochondrial Transplantation in the Eye: A Review and Evaluation of Surgical ApproachesPreprint

Cakir, B., Yeh, T.-C., Lin, C., Wu, M.-R., Boilard, É., Pelletier, M., Singh, A., Breton, Y., Patel, S. P., Benson, T., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.06.716722 · Cited by 3

Assessing Mitochondrial Function in Sciatic Nerve by High-Resolution Respirometry

Formiga-Jr, M. A., & Camacho-Pereira, J. (2022) · Journal of Visualized Experiments · doi:10.3791/63690 · Cited by 1

Approaches for drug delivery to the mitochondria

Goyal, M., Parvathaneni, V., & Gupta, V. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-85041-4.00005-6 · Cited by 1

Bioactive peptide PDBSN improves mitochondrial function and suppresses oxidative stress in human adipose cells

Shen, H., Lei, Y. H., Xie, W., Ma, T., Li, B., Gao, Q., Chen, B., Dai, B., & Qin, D. (2023) · Adipocyte · doi:10.1080/21623945.2023.2278213 · Cited by 1

The Mitochondrial Distribution and Morphology Family 33 Gene FgMDM33 Is Involved in Autophagy and Pathogenesis in Fusarium graminearum

Lv, W., Tu, Y., Xu, T., You, Z., Chen, J., Yang, N., & Wang, Y. (2024) · Journal of Fungi · doi:10.3390/jof10080579 · Cited by 1

Puerarin alleviates LPS-induced endothelial cells injury via SIRT1-mediated mitochondrial homeostasis signaling

Chang, X., Cheng, M., Li, Y., & Zhou, X. (2024) · Journal of Holistic Integrative Pharmacy · doi:10.1016/j.jhip.2024.08.004 · Cited by 1

Effects of mating system and adaptedness on the evolution of fitness and mtDNA copy number in mitonuclear mismatched C. elegans

Dietz, Z. P., Banerji, D., Sullins, J. A., Bever, B. W., Christy, S. F., Bergthorsson, U., Katju, V., & Estes, S. (2025) · Heredity · doi:10.1038/s41437-025-00786-6 · Cited by 1

In Vitro Activity of Pterocarpanquinone LQB-118 on Trypanosoma cruzi and Its Impact on Parasite Bioenergetics

Azevedo, B. F., Brito, A. C. S., Vilarim, J. A., Ventura, B. D., Mendes, M. A. P., dos Santos, R. F., Dutra, P. M. L., Torres, E. J. L., Costa, P. R. R., Netto, C. D., et al. (2025) · ACS Omega · doi:10.1021/acsomega.5c02858 · Cited by 1

Nuclear Magnetic Resonance-Based Metabolomics Reveals Systemic Metabolic Disarray in the Transition from Acute Kidney Injury To Chronic Kidney Disease

Wang, L., Wang, X., Zou, T., Su, F., Yao, Y., & Gu, J. (2025) · Phenomics · doi:10.1007/s43657-025-00276-z · Cited by 1

Otoprotective Effects of Resveratrol and Melatonin in Noise-Exposed Wistar Rats

Novanta, G. G. R., Zica, A. C. O., de Andrade, R. R., Kückelhaus, S. A. S., Kückelhaus, C. D. S., Serra, L. S. M., & Sampaio, A. L. L. (2025) · Noise and Health · doi:10.4103/nah.nah_84_25 · Cited by 1

Resistance to Anti-PD-1 Immunotherapy in Cutaneous Melanoma: The Role of Mitochondrial Metabolism and Therapeutic Perspectives

de Melo, V. C., Sales, G. S., de Moura, J. L. N., Bagatini, M. D., & da Silva, G. B. (2026) · Clinical bioenergetics · doi:10.3390/clinbioenerg2020008 · Cited by 1

Light‐Inducible Bispecific DNAzymes Reveal Mitochondrial Fe 2+ /Fe 3+ Dynamics During Ferroptosis

Shi, Y., Wang, R., Wang, J., Xing, H., Zhang, J., Jiang, J.-H., & Wu, Z. (2026) · Angewandte Chemie International Edition · doi:10.1002/anie.7378442 · Cited by 1

Mitochondrial abnormalities in neurological disorders

Ferreira, A. F. F., Singulani, M. P., & de Britto, L. R. G. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822416-8.00012-9 · Cited by 1

Mitochondrial Inherited Disorders and their Correlation with Neurodegenerative Diseases

Gushi, S., & Balis, V. (2023) · Endocrine Metabolic & Immune Disorders - Drug Targets · doi:10.2174/0118715303250271231018103202 · Cited by 1

Isoliquiritin can cause mitochondrial dysfunction and regulate Nrf2 to affect the development of mouse oocytes

Sun, Z., Jiao, A., Zhao, Y., Han, T., Zhang, H., & Gao, Q. (2024) · Food and Chemical Toxicology · doi:10.1016/j.fct.2024.114445 · Cited by 1

Differentiating Compromised Mitochondria of Lung Cancer Cells from Mitochondria in Healthy Cells

Sharma, B., Shafaee, Z., Twelker, K., Bhatia, N. D., Agriantonis, G., Dave, J., Mestre, J., Ghanta, H., Arora, S., & Whittington, J. (2024) · Journal of Biomedical Research & Environmental Sciences · doi:10.37871/jbres1900 · Cited by 1

The POLG Variant c.678G>C; p.(Gln226His) Is Associated with Mitochondrial Abnormalities in Fibroblasts Derived from a Patient Compared to a First-Degree Relative

Mantey, I., Langerscheidt, F., Cakmak, C., Baba, N., Burghardt, K., Karakaya, M., & Zempel, H. (2025) · Genes · doi:10.3390/genes16020198 · Cited by 2

The immune response and autophagy of Macrobrachium rosenbergii against Aeromonas veronii infection

Zhou, L., Cai, X. T., Dong, Q., Yin, J., Liu, Y., Gao, X., Jiang, Q., Zhang, Y., & Zhang, X. (2025) · Comparative Biochemistry and Physiology Part D Genomics and Proteomics · doi:10.1016/j.cbd.2025.101488 · Cited by 1

Mitochondrial Genome and Phylogenetic Analysis of Rhinogobius virgigena

Zhan, Y.-J., Hu, W., Zhang, K.-R., & Sun, C. (2025) · Biochemical Genetics · doi:10.1007/s10528-025-11171-7 · Cited by 1

Novel Mitochondria-Targeted Triphenylphosphonium Conjugates of Linear β-Phosphorylated Nitrones: Preparation, 31P NMR Mitochondrial Distribution, EPR Spin Trapping Reporting, and Site-Directed Antiapoptotic Properties

Petrocchi, C., Laurent, S., Culcasi, M., & Pietri, S. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1262-0_5 · Cited by 1

The medicinal chemistry of mitochondrial dysfunction: a critical overview of efforts to modulate mitochondrial health

Lee, M. T. W., Mahy, W., & Rackham, M. D. (2021) · RSC Medicinal Chemistry · doi:10.1039/d1md00113b · Cited by 1

Las mitocondrias: sus funciones, las relaciones con otros organelos, la supervivencia celular y la medicina mitocondrial

Olvera-Sánchez, S., Gómez-Chang, E., Flores-Herrera, Ó., & Martínez, F. (2023) · TIP Revista Especializada en Ciencias Químico-Biológicas · doi:10.22201/fesz.23958723e.2023.547 · Cited by 1

High-Fat Diet Enhances Triglyceride Recycling, Impairs UCP1-Mediated Thermogenic Activity, and Causes Insulin Resistance in Rat Brown Adipocytes

Eira, D. D., & Pereira, D. J. (2019) · YorkSpace (York University) · Cited by 1

Impact of the influenza protein PB1-F2 on the biochemical composition of human epithelial cells revealed by synchrotron Fourier transform infrared spectromicroscopy

Leymarie, O., Goffic, R. L., Jamme, F., & Chevalier, C. (2019) · Journal of Spectral Imaging · doi:10.1255/jsi.2019.a18

Using the NIH symptom science model to understand fatigue and mitochondrial bioenergetics

Shen, Q., Mahoney, D. E., Peltzer, J. N., Rahman, F. K., Krueger, K. J., Hiebert, J. B., & Pierce, J. D. (2020) · Journal of Nursing · doi:10.7243/2056-9157-7-2

ROS-based lethality of C. elegans mitochondrial electron transport mutants grown on E. coli siderophore iron release mutantsPreprint

Govindan, J. A., Jayamani, E., & Ruvkun, G. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/707968

Synergistic Effect of Saikosaponin a and Albiflorin Against Corticosterone-Induced Neuro-Injury in PC12 Cells via Regulation of TCA Cycle, Purine Metabolism, and Glutamate MetabolismPreprint

Xiao, L., Hou, R., Shi, H. S., Qin, X., Wu, Y., Wu, X., Tian, J., Gao, X., Du, G., & Zhou, Y. (2021) · Research Square · doi:10.21203/rs.3.rs-159289/v1

Global profiles of a cetylated proteins in the brains of scrapie agents 139A- and ME7-infected mice collected at mid-early, mid-late and terminal stagePreprint

Shi, Q., Chen, D., Maimaitiming, A., Xiao, K., Gao, L., Yang, X., Wu, Y.-Z., Chen, C., & Dong, X. (2020) · doi:10.21203/rs.3.rs-17989/v1

Skeletal muscle weakness and mitochondrial dysfunction in the osteogenesis imperfecta murine (oim) model

Gremminger, V. L. (2021) · MOspace Institutional Repository (University of Missouri) · doi:10.32469/10355/85774

Mechanisms by which mild impairment of mitochondrial function increases stress resistance and lifespan

Liontis, T. (2020) · eScholarship@McGill (McGill) · doi:10.82308/42346

Mitonuclear Mismatch is Associated with Increased Male Frequency, Outcrossing, and Male Sperm Size in Experimentally-Evolved C. elegans

Bever, B. W. (2021) · doi:10.15760/etd.7661

三大国家資格から税理士、警察官、理容師、保育士、大工まで 医者、弁護士、会計士……70職業の給与比較 (特集 日本人の給料 全公開!)

松崎, 隆. (2005) · プレジデント

Geriatrik Popülasyonda Kardiyak Fizyoloji de Yaş Alır mı?

Karadüz, E. G., & Yurdalan, S. U. (2021) · Geriatrik Bilimler Dergisi · doi:10.47141/geriatrik.1022619 · Cited by 1

Cancer therapy, immunotherapy, photothermal therapy

Liddle, G. M., Wei, J., & Hartmann, J. X. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-823033-6.00028-4

The Kidney and Cardiovascular Disease

Fadem, S. Z. (2022) · Springer eBooks · doi:10.1007/978-3-030-93528-3_3

Mitochondrial transfer restores the proliferation of injured endometrial stromal cellPreprint

Chen, L., Zhu, J., Chen, Y., Zhu, M., Wang, Q., & Zhang, J. (2022) · Research Square · doi:10.21203/rs.3.rs-1360187/v1

Concepts | Mitochondrial Dynamics

Scorrano, L., & Verma, V. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819460-7.00194-8

Discussion on the Treatment of Chronic Heart Failure by Spleen-Strengthening and Qi-Invigorating Therapy Based on the “Spleen-Mitochondria in TCM”

董, 莹. (2022) · Traditional Chinese Medicine · doi:10.12677/tcm.2022.116188

JoVE Video Dataset

Yang, E. J.-N., Boldogh, I. R., Ji, H., Pon, L. A., & Swayne, T. C. (2023) · doi:10.3791/65428-v

Efficacy of creatine nitrate supplementation on redox status and mitochondrial function in pectoralis major muscle of preslaughter transported broilers

Xu, J., Xing, T., Li, J., Zhang, L., & Gao, F. (2023) · Animal Biotechnology · doi:10.1080/10495398.2023.2249957

Intermembrane space-localized twin Cx 9 C motif-containing TbTim15 is an essential subunit of the single mitochondrial inner membrane protein translocase of trypanosomesPreprint

von Känel, C., Oeljeklaus, S., Wenger, C., Stettler, P., Harsman, A., Warscheid, B., & Schneider, A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.31.578135

N-acetylcysteine may improve endometrial receptivity by modulating endometrial stromal cells in goats

Fu, K., Chen, X., Tian, X., Tang, W., Gong, T., Zhang, Y., & Ji, T. (2024) · Archives animal breeding/Archiv für Tierzucht · doi:10.5194/aab-67-361-2024

Role of oxidative stress and mitochondria dysfunction in Diabetes mellitus disease

Ojo, O. A., Ilomuanya, C. S., Iyobhebhe, M. E., Rotimi, D. E., Ojo, A. B., Odesanmi, O. E., Obasanmi, E. T., & Nwonuma, C. O. (2024) · International Conference on Science, Engineering and Business for Driving Sustainable Development Goals (SEB4SDG) · doi:10.1109/seb4sdg60871.2024.10630230

Mitochondrial quality control and the microphthalmia/transcription factor E (MiTF/TFE) family

Agostini, F., & Raimundo, N. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15260-3.00003-x

The effect of succinate containing crystalloid solution on the inflammatory response in intensive care of community-acquired pneumonia in children: a prospective open comparative study

Lazarev, V. V., Анчутин, П. Е., Быков, М. В., Смирнов, Д. А., Pchelicnceva, T. A., Frolov, N. S., Makhachilaeva, K. M., & Golubev, B. I. (2025) · Annals of critical care · doi:10.21320/1818-474x-2025-1-123-133

Dose Modeling for Mitochondrial Transplantation in Barrier-Limited TissuesPreprint

Walker, M., Orlando, G., Asthana, A., Oniscu, G. C., & Levitt, M. R. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.08.663384

Muscle physiology and insect flight

Schnorrer, F., & Avellaneda, J. (2025) · Elsevier eBooks · doi:10.1016/b978-0-323-95424-2.00055-8

Supplemental use of melatonin to protect against oxidative stress induced by intensive athletic training and competition

Cui, Y., Liu, X., & Reiter, R. J. (2025) · Pharmacological Research - Reports · doi:10.1016/j.prerep.2025.100069

Additional file 1 of Identification of key genes and pathways associated with feed efficiency of native chickens based on transcriptome data via bioinformatics analysis

Yang, L., He, T., Xiong, F., Chen, X., Fan, X., Jin, S., & Geng, Z. (2020) · Figshare · doi:10.6084/m9.figshare.12109578

Additional file 2 of Human iPSCs derived astrocytes rescue rotenone-induced mitochondrial dysfunction and dopaminergic neurodegeneration in vitro by donating functional mitochondria

Cheng, X.-Y., Biswas, S., Li, J., Mao, C.-J., Chechneva, O., Chen, J., Li, K., Li, J., Zhang, J.-R., Liu, C.-F., et al. (2020) · Figshare · doi:10.6084/m9.figshare.12518825

Additional file 3 of Human iPSCs derived astrocytes rescue rotenone-induced mitochondrial dysfunction and dopaminergic neurodegeneration in vitro by donating functional mitochondria

Cheng, X.-Y., Biswas, S., Li, J., Mao, C.-J., Chechneva, O., Chen, J., Li, K., Li, J., Zhang, J.-R., Liu, C.-F., et al. (2020) · Figshare · doi:10.6084/m9.figshare.12518831

Additional file 1 of Human iPSCs derived astrocytes rescue rotenone-induced mitochondrial dysfunction and dopaminergic neurodegeneration in vitro by donating functional mitochondria

Cheng, X.-Y., Biswas, S., Li, J., Mao, C.-J., Chechneva, O., Chen, J., Li, K., Li, J., Zhang, J.-R., Liu, C.-F., et al. (2020) · Figshare · doi:10.6084/m9.figshare.12518816

Additional file 6 of Identification of key genes and pathways associated with feed efficiency of native chickens based on transcriptome data via bioinformatics analysis

Yang, L., He, T., Xiong, F., Chen, X., Fan, X., Jin, S., & Geng, Z. (2020) · Figshare · doi:10.6084/m9.figshare.12109611

Additional file 4 of Human iPSCs derived astrocytes rescue rotenone-induced mitochondrial dysfunction and dopaminergic neurodegeneration in vitro by donating functional mitochondria

Cheng, X.-Y., Biswas, S., Li, J., Mao, C.-J., Chechneva, O., Chen, J., Li, K., Li, J., Zhang, J.-R., Liu, C.-F., et al. (2020) · Figshare · doi:10.6084/m9.figshare.12518837

Additional file 1 of Nicotinamide mononucleotide as a therapeutic agent to alleviate multi-organ failure in sepsis

Cao, T., Ni, R., Ding, W., Ji, X., Fan, G., Zhang, Z., & Peng, T. (2024) · Figshare · doi:10.6084/m9.figshare.26650398

Additional file 1 of Decreased Vascular Bundle 1 affects mitochondrial and plant development in rice

Zhang, L., Feng, P., Deng, Y., Yin, W., Wan, Y., Lei, T., He, G., & Wang, N. (2021) · Figshare · doi:10.6084/m9.figshare.13642292

Additional file 1 of UPRmt activation improves pathological alterations in cellular models of mitochondrial diseases

Suárez-Rivero, J. M., Pastor‐Maldonado, C. J., Povea-Cabello, S., Álvarez-Córdoba, M., Villalón-García, I., Talaverón-Rey, M., Suárez-Carrillo, A., Munuera-Cabeza, M., Reche-López, D., Cilleros-Holgado, P., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19785695

Mitochondria, apoptosis, and necrosis

Şenol, H. B., Yılmaz, E. A., & Özdemir, Ö. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-24836-8.00002-x

Mesenchymal stem cells and the rescue of mitochondrial damage in different disease models (Review)

Tran, C., & Nguyen, V. (2025) · World Academy of Sciences Journal · doi:10.3892/wasj.2025.419

Mitochondria: Origin, structure, and function

Mehjabin, S., Akanda, M. K. M., & Akhter, N. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-40535-8.00003-x

Étude des liens entre les acteurs de la dynamique mitochondriale et l'apoptose dans la dégénérescence musculaire dystrophinedépendante chez Caenorhabditis elegans

Scholtes, C. (2018) · theses.fr (ABES) · doi:10.70675/b1d429a3z14ebz4af9zaf96zb280790106d4

Évaluation de la perfusion viscérale et anastomotique par réalité augmentée basée sur la fluorescence

Seeliger, B. (2019) · theses.fr (ABES) · doi:10.70675/4e77927fzf930z4451z9deazf89581812487

Les cœlomocytes régulent le métabolisme lipidique intestinal et l’extension de la durée de vie en réponse à la restriction alimentaire à travers la lipase LIPL-5 chez Caenorhabditis elegans

Buis, A. (2018) · theses.fr (ABES) · doi:10.70675/ff48ee42zf635z4e66z8f4dz4ffa4f5334ad

Rôle du transporteur mitochondrial UCP2 dans la leucémie

Sancerni, T. (2019) · theses.fr (ABES) · doi:10.70675/c0f1a3a3z992az4717zb426z210e51dadf82

Assessing the risk of resistance selection towards QiI fungicides in Zymoseptoria tritici

Fouché, G. (2021) · theses.fr (ABES) · doi:10.70675/b2bddc22z76f0z4d08z950cz2b03da999efa

Lin28a induit la reprogrammation du métabolisme énergétique des chondrocytes pour régénérer le cartilage

Bouchemla, Z. (2023) · doi:10.70675/f4162315z2c94z404ezb198zaaa068d79125

Quantitative reconstruction of neuronal mitochondrial network in neurites and somata in rat hippocampus and prefrontal cortex

Wang, L., Li, L., Liu, J., Wang, Z., Liu, J., Chang, S., Yuan, J., Chen, X., Xie, Q., Shen, L., et al. (2026) · Frontiers in Physiology · doi:10.3389/fphys.2026.1735677

Iron dyshomeostasis in neuropsychiatric disorders

Cheng, M., Ma, J., Yang, Y., Cao, M., Zhang, E., Feng, B., Wang, Q., & Du, Z. J. (2026) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2026.1771423

MitoSafe hypothesis: safeguarding mitochondrial morphology and innate immunity

Haggerty, N., Nakamura, K., Sesaki, H., & Iijima, M. (2026) · Trends in Cell Biology · doi:10.1016/j.tcb.2026.04.007

Light‐Inducible Bispecific DNAzymes Reveal Mitochondrial Fe 2+ /Fe 3+ Dynamics During Ferroptosis

Shi, Y., Wang, R., Wang, J., Xing, H., Zhang, J., Jiang, J.-H., & Wu, Z. (2026) · Angewandte Chemie · doi:10.1002/ange.7378442

The pseudokinase domain PK1 of UNC-89/obscurin is required for mitochondrial morphology and function in C. elegans

Matsunaga, Y., Ghazal, N., Heim, A., Dorendorf, T., Qadota, H., Wang, Y., Mayer, T. U., Mayans, O. M., Kwong, J. Q., & Benian, G. M. (2026) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-026-09733-2

The m6A reader YTHDF1 modulates adipocyte mitochondrial remodeling and diet-induced adiposity through translational control of NOD1

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