The DOI matches its Crossref record; 232 of the 234 references it cites were found in a registry or an index.
Cell Biology of the Mitochondrion
Open accessAbstract
Mitochondria are best known for harboring pathways involved in ATP synthesis through the tricarboxylic acid cycle and oxidative phosphorylation. Major advances in understanding these roles were made with Caenorhabditiselegans mutants affecting key components of the metabolic pathways. These mutants have not only helped elucidate some of the intricacies of metabolism pathways, but they have also served as jumping off points for pharmacology, toxicology, and aging studies. The field of mitochondria research has also undergone a renaissance, with the increased appreciation of the role of mitochondria in cell processes other than energy production. Here, we focus on discoveries that were made using C. elegans, with a few excursions into areas that were studied more thoroughly in other organisms, like mitochondrial protein import in yeast. Advances in mitochondrial biogenesis and membrane dynamics were made through the discoveries of novel functions in mitochondrial fission and fusion proteins. Some of these functions were only apparent through the use of diverse model systems, such as C. elegans. Studies of stress responses, exemplified by mitophagy and the mitochondrial unfolded protein response, have also benefitted greatly from the use of model organisms. Recent developments include the discoveries in C. elegans of cell autonomous and nonautonomous pathways controlling the mitochondrial unfolded protein response, as well as mechanisms for degradation of paternal mitochondria after fertilization. The evolutionary conservation of many, if not all, of these pathways ensures that results obtained with C. elegans are equally applicable to studies of human mitochondria in health and disease.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“Mitochondria are the principal source of ATP, which is formed by oxidative phosphorylation following electron flow through highly integrated protein complexes; however, mitochondria are also involved in many other functions as well, which, among others, include apoptosis, protein synthesis, and fatty acid oxidation [14,15].”
From Mitochondrial Oxidative and Nitrosative Stress and Alzheimer Disease (2020) · cites this paper as [14]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
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
Flagged first, then by citations
2 of the 234 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Mitochondrial proteins: from biogenesis to functional networks
Pfanner, N., Warscheid, B., & Wiedemann, N. (2019) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0092-0 · Cited by 1,028
Lactate in the Regulation of Tumor Microenvironment and Therapeutic Approaches
de la Cruz-López, K. G., Castro-Muñoz, L. J., Reyes-Hernández, D. O., García-Carrancá, A., & Manzo-Merino, J. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.01143 · Cited by 940
“Normal cells (except erythrocytes and skeletal muscle cells during high intensity exercise) depend on OXPHOS for ATP production from glucose; on the contrary, cancer cells obtain their ATP by glycolysis and the final conversion of glucose to lactate (40).”
BackgroundThe role of metabolism in chondrocyte dysfunction and the progression of osteoarthritis
Zheng, L., Zhang, Z., Sheng, P., & Mobasheri, A. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101249 · Cited by 767
History and progress of hypotheses and clinical trials for Alzheimer’s disease
Liu, P.-P., Xie, Y., Meng, X.-Y., & Kang, J.-S. (2019) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-019-0063-8 · Cited by 723
Mitochondrial dysfunction in neurodegenerative disorders
Klemmensen, M. M., Borrowman, S. H., Pearce, C., Pyles, B., & Chandra, B. (2024) · Neurotherapeutics · doi:10.1016/j.neurot.2023.10.002 · Cited by 396
Mitochondria: Central Organelles for Melatonin′s Antioxidant and Anti-Aging Actions
Reiter, R., Tan, D., Rosales-Corral, S., Galano, A., Zhou, X., & Xu, B. (2018) · Molecules · doi:10.3390/molecules23020509 · Cited by 393
Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context
Morgenstern, M., Peikert, C. D., Lübbert, P., Suppanz, I., Klemm, C., Alka, O., Steiert, C., Naumenko, N., Schendzielorz, A. B., Melchionda, L., et al. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.11.001 · Cited by 326
OrthoList 2: A New Comparative Genomic Analysis of Human and Caenorhabditis elegans Genes
Kim, W., Underwood, R. S., Greenwald, I., & Shaye, D. D. (2018) · Genetics · doi:10.1534/genetics.118.301307 · Cited by 324
mTORC1 as a Regulator of Mitochondrial Functions and a Therapeutic Target in Cancer
de la Cruz-López, K. G., Toledo-Guzmán, M. E., Sánchez, E. O., & Carrancá, A. G. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.01373 · Cited by 223
Targeting multiple signaling pathways: the new approach to acute myeloid leukemia therapy
Carter, J. L., Hege-Hurrish, K., Yang, J., Kalpage, H. A., Su, Y., Edwards, H. J., Hüttemann, M., Taub, J. W., & Ge, Y. (2020) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-020-00361-x · Cited by 230
Barrera, M.-J., Aguilera, S., Castro, I., Carvajal, P., Jara, D., Molina, C., González, S., & González, M.-J. (2021) · Autoimmunity Reviews · doi:10.1016/j.autrev.2021.102867 · Cited by 213
Mitochondrial Functionality in Male Fertility: From Spermatogenesis to Fertilization
Park, Y.-J., & Pang, M. (2021) · Antioxidants · doi:10.3390/antiox10010098 · Cited by 225
Iske, J., Seyda, M., Heinbokel, T., Maenosono, R., Minami, K., Nian, Y., Quante, M., Falk, C. S., Azuma, H., Martin, F., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-18039-x · Cited by 211
Wang, K., Zhao, Z., & Wu, J. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.109182 · Cited by 181
Shenoy, S. (2020) · Inflammation Research · doi:10.1007/s00011-020-01389-z · Cited by 179
Yan, W., Diao, S., & Fan, Z. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02194-z · Cited by 167
Inigo, J. R., & Chandra, D. (2022) · Journal of Hematology & Oncology · doi:10.1186/s13045-022-01317-0 · Cited by 160
The Role of Mitochondria in Cardiovascular Diseases
Poznyak, A. V., Ivanova, E. A., Sobenin, I. A., Yet, S., & Orekhov, A. N. (2020) · Biology · doi:10.3390/biology9060137 · Cited by 158
Mitochondria, spermatogenesis, and male infertility – An update
Singh, V., Singh, K. K., & Rajender, S. (2020) · Mitochondrion · doi:10.1016/j.mito.2020.06.003 · Cited by 149
Wan, M., Liu, Z., Li, T., Chen, H., Wang, Q., Chen, T., Tao, Y., & Mao, C. (2021) · Angewandte Chemie International Edition · doi:10.1002/anie.202104304 · Cited by 135
Dysregulated energy metabolism impairs chondrocyte function in osteoarthritis
Wu, X., Liyanage, C., Plan, M. R., Stark, T., McCubbin, T., Barrero, R. A., Batra, J., Crawford, R., Xiao, Y., & Prasadam, I. (2022) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2022.11.004 · Cited by 135
Wang, J., Gao, S., Wang, S., Xu, Z., & Wei, L. (2018) · International Journal of Nanomedicine · doi:10.2147/ijn.s165699 · Cited by 134
Tumor Microenvironment: Lactic Acid Promotes Tumor Development
Gao, Y., Zhou, H., Liu, G., Wu, J., Yuan, Y., & Shang, A. (2022) · Journal of Immunology Research · doi:10.1155/2022/3119375 · Cited by 143
Molecular Mechanisms and Regulation of Mammalian Mitophagy
Choubey, V., Zeb, A., & Kaasik, A. (2021) · Cells · doi:10.3390/cells11010038 · Cited by 128
Mitochondrial Biogenesis, Mitochondrial Dynamics, and Mitophagy in the Maturation of Cardiomyocytes
Ding, Q., Qi, Y., & Tsang, S. Y. (2021) · Cells · doi:10.3390/cells10092463 · Cited by 128
Yang, F., Liao, J., Yu, W., Qiao, N., Guo, J., Han, Q., Li, Y., Hu, L., Pan, J., & Tang, Z. (2020) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2020.124888 · Cited by 114
Mitochondria Related Cell Death Modalities and Disease
Tian, C., Liu, Y., Li, Z., Zhu, P., & Zhao, M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.832356 · Cited by 113
MitoSegNet: Easy-to-use Deep Learning Segmentation for Analyzing Mitochondrial Morphology
Fischer, C. A., Besora-Casals, L., Rolland, S. G. M., Haeussler, S., Singh, K., Duchen, M. R., Conradt, B., & Marr, C. (2020) · iScience · doi:10.1016/j.isci.2020.101601 · Cited by 104
Cheng, X.-Y., Biswas, S., Li, J., Mao, C.-J., Chechneva, O. V., Chen, J., Li, K., Li, J., Zhang, J.-R., Liu, C., et al. (2020) · Translational Neurodegeneration · doi:10.1186/s40035-020-00190-6 · Cited by 108
Insights into Disease-Associated Tau Impact on Mitochondria
Szabo, L., Eckert, A., & Grimm, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21176344 · Cited by 107
Huang, T., Jiang, H., Zhao, Y. H., He, J., Cheng, H., & Martyniuk, C. J. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.151177 · Cited by 103
Mitochondrial Dysfunction in Cardiovascular Diseases: Potential Targets for Treatment
Yang, J., Guo, Q., Feng, X., Liu, Y., & Zhou, Y. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.841523 · Cited by 105
Xu, H., & Yang, F. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-02233-0 · Cited by 114
Mitochondria as central hubs in synaptic modulation
Duarte, F. V., Ciampi, D., & Duarte, C. B. (2023) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-04814-8 · Cited by 109
Mitochondrial Transplantation as a Novel Therapeutic Strategy for Mitochondrial Diseases
Park, A., Oh, M., Lee, S. H., Oh, K., Lee, E., Lee, S.-W., Bae, K., Han, B., & Kim, W. Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094793 · Cited by 97
Seizure-Induced Oxidative Stress in Status Epilepticus: Is Antioxidant Beneficial?
Lin, T., Chen, S., Lin, K.-J., & Chuang, Y. (2020) · Antioxidants · doi:10.3390/antiox9111029 · Cited by 96
Human Skeletal Muscle Mitochondrial Adaptations Following Resistance Exercise Training
Parry, H. A., Roberts, M. D., & Kavazis, A. N. (2020) · International Journal of Sports Medicine · doi:10.1055/a-1121-7851 · Cited by 99
Scheffer, D. D. L., Garcia, A. A., Lee, L., Mochly‐Rosen, D., & Ferreira, J. C. B. (2022) · Antioxidants and Redox Signaling · doi:10.1089/ars.2021.0145 · Cited by 96
Mitochondrial Oxidative and Nitrosative Stress and Alzheimer Disease
Butterfield, D. A., & Boyd-Kimball, D. (2020) · Antioxidants · doi:10.3390/antiox9090818 · Cited by 85
Down the Iron Path: Mitochondrial Iron Homeostasis and Beyond
Dietz, J. V., Fox, J. L., & Khalimonchuk, O. (2021) · Cells · doi:10.3390/cells10092198 · Cited by 98
Cardiac Aging: From Basic Research to Therapeutics
Yan, M., Sun, S., Xu, K., Huang, X., Dou, L., Pang, J., Tang, W., Shen, T., & Li, J. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/9570325 · Cited by 86
Hua, X., Liang, G., Chao, J., & Wang, D. (2024) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2024.134598 · Cited by 77
Mitochondria as multifaceted regulators of ferroptosis
Guo, J., Zhou, Y., Liu, D., Wang, M., Wu, Y., Tang, D., & Liu, X. (2022) · Life Metabolism · doi:10.1093/lifemeta/loac035 · Cited by 83
Lin, D., Huang, Y.-W., Ho, C., Hung, P., Hsu, M., Wang, T.-J., Wu, T., Lee, T., Huang, Z.-D., Chang, P.-C., et al. (2019) · Cells · doi:10.3390/cells8010065 · Cited by 74
Orekhov, A. N., Poznyak, A. V., Sobenin, I. A., Nikifirov, N. N., & Ivanova, E. A. (2019) · Current Neuropharmacology · doi:10.2174/1570159x17666191118125018 · Cited by 76
Lu, T., Zhang, Z., Bi, Z., Lan, T., Zeng, H., Liu, Y., Mo, F., Yang, J., Chen, S., He, X., et al. (2023) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2022-005430 · Cited by 71
Mitochondrial dysfunction: a new molecular mechanism of intervertebral disc degeneration
Song, C., Xu, Y., Peng, Q., Chen, R., Zhou, D., Cheng, K., Cai, W., Liu, T., Huang, C., Fu, Z., et al. (2023) · Inflammation Research · doi:10.1007/s00011-023-01813-0 · Cited by 78
Madireddy, S., & Madireddy, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031844 · Cited by 76
Mechanical forces on cellular organelles
Feng, Q., & Kornmann, B. (2018) · Journal of Cell Science · doi:10.1242/jcs.218479 · Cited by 61
Transcranial Photobiomodulation For The Management Of Depression: Current Perspectives
Askalsky, P., & Iosifescu, D. V. (2019) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s188906 · Cited by 63
Revisiting the role of melatonin in human melanocyte physiology: A skin context perspective
Sevilla, A., Chéret, J., Slominski, R. M., Slominski, A. T., & Paus, R. (2022) · Journal of Pineal Research · doi:10.1111/jpi.12790 · Cited by 65
Yang, F., Ye, X.-J., Chen, M., Li, H., Wang, Y., Zhong, M.-Y., Zhong, C.-S., Zeng, B., Xu, L., He, X., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.632606 · Cited by 64
Magnani, N., Marchini, T., Calabró, V., Álvarez, S., & Evelson, P. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.568305 · Cited by 67
Yang, L., He, T., Xiong, F., Chen, X., Fan, X., Jin, S., & Geng, Z. (2020) · BMC Genomics · doi:10.1186/s12864-020-6713-y · Cited by 61
Chen, Y., Hamidu, S., Yang, X., Yan, Y., Wang, Q., Li, L., Oduro, P. K., & Li, Y. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.880421 · Cited by 62
Sex differences in renal mitochondrial function: a hormone-gous opportunity for research
Sultanova, R. F., Schibalski, R. S., Yankelevich, I. A., Stadler, K., & Ilatovskaya, D. V. (2020) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00320.2020 · Cited by 58
Shin, N., Cuenca, L., Karthikraj, R., Kannan, K., & Colaiácovo, M. P. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1007975 · Cited by 57
Jiang, W., Zhao, H., Zhang, L., Wu, B., & Zha, Z. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.109629 · Cited by 57
Insights into the New Cancer Therapy through Redox Homeostasis and Metabolic Shifts
Hyun, D. (2020) · Cancers · doi:10.3390/cancers12071822 · Cited by 58
Liu, J., Li, L., Yang, Y., Hong, B., Chen, X., Xie, Q., & Han, H. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00599 · Cited by 50
Qı, L., Dong, Y., Chao, H., Zhao, P., Ma, S., & Li, G. (2023) · Chemosphere · doi:10.1016/j.chemosphere.2023.137751 · Cited by 57
Status of Mitochondrial Oxidative Phosphorylation during the Development of Heart Failure
Bhullar, S. K., & Dhalla, N. S. (2023) · Antioxidants · doi:10.3390/antiox12111941 · Cited by 59
Fan, H., Lee, H.-F., Yue, C.-T., & Chi, C. (2021) · Life · doi:10.3390/life11111111 · Cited by 51
Takeichi, Y., Miyazawa, T., Sakamoto, S., Hanada, Y., Wang, L., Gotoh, K., Uchida, K., Katsuhara, S., Sakamoto, R., Ishihara, T., et al. (2021) · Diabetologia · doi:10.1007/s00125-021-05488-2 · Cited by 51
Mitochondrial dysfunction and pancreatic islet β‑cell failure (Review)
Sha, W., Hu, F., & Bu, S. (2020) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2020.9396 · Cited by 53
Liu, D., Wang, Q., He, W., Chen, X., Wei, Z., & Huang, K. (2020) · Chemosphere · doi:10.1016/j.chemosphere.2020.126464 · Cited by 53
Neurotoxicity and underlying cellular changes of 21 mitochondrial respiratory chain inhibitors
Delp, J., Cediel-Ulloa, A., Suciu, I., Kranaster, R., van Vugt‐Lussenburg, B. M. A., Kos, V. M., van der Stel, W., Carta, G., Bennekou, S. H., Jennings, P., et al. (2021) · Archives of Toxicology · doi:10.1007/s00204-020-02970-5 · Cited by 50
Mitoepigenetics and Its Emerging Roles in Cancer
Dong, Z., Pu, L., & Cui, H. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00004 · Cited by 51
The role of mitochondria in the resistance of melanoma to PD-1 inhibitors
Du, F., Yang, L.-H., Liu, J., Wang, J., Fan, L., Duangmano, S., Liu, H., Liu, M., Wang, J., Zhong, X., et al. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04200-9 · Cited by 47
Redox signaling and skeletal muscle adaptation during aerobic exercise
Zhou, Y., Zhang, X., Baker, J. S., Davison, G. W., & Yan, X. (2024) · iScience · doi:10.1016/j.isci.2024.109643 · Cited by 52
Fang, C., Di, S., Yu, Y., Qi, P., Wang, X., & Jin, Y. (2024) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2024.134357 · Cited by 48
Loussouarn, C., Pers, Y., Bony, C., Jørgensen, C., & Noël, D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.623973 · Cited by 47
Ceramides and mitochondrial homeostasis
Ding, S. Z., Li, G., Fu, T., Zhang, T., Lu, X., Li, N., & Geng, Q. (2024) · Cellular Signalling · doi:10.1016/j.cellsig.2024.111099 · Cited by 50
Senolytic therapeutics: An emerging treatment modality for osteoarthritis
Ansari, M. M., Ghosh, M., Lee, D., & Son, Y. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102275 · Cited by 49
Ferreira, A. F. F., Binda, K. H., Singulani, M. P., Pereira, C. P. M., Ferrari, G. D., Alberici, L. C., Real, C. C., & Britto, L. R. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112607 · Cited by 46
Lin, J., Zheng, X.-Q., Zhang, Z., Zhuge, J., Shao, Z., Huang, C., Jin, J., Chen, X., Chen, Y., Wu, Y., et al. (2021) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2021.01.002 · Cited by 46
Chang, X., Zhang, T., Dong, L., Meng, Q., Yan, P., Luo, D., Wang, X., & Zhou, X. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/6659240 · Cited by 45
RetractedMitochondrial dysfunction and potential mitochondrial protectant treatments in tendinopathy
Zhang, X.-Y., Eliasberg, C. D., & Rodeo, S. (2021) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14599 · Cited by 39
Assessment of mitochondrial dysfunction and implications in cardiovascular disorders
Li, Y., Ma, Y., Dang, Q., Fan, X., Han, C., Xu, S., & Li, P. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.120834 · Cited by 43
Polyphenols and Metabolites Enhance Survival in Rodents and Nematodes—Impact of Mitochondria
Dilberger, B., Passon, M., Asseburg, H., Silaidos, C. V., Schmitt, F., Schmiedl, T., Schieber, A., & Eckert, G. P. (2019) · Nutrients · doi:10.3390/nu11081886 · Cited by 43
Yen, C., Ruter, D. L., Turner, C. D., Pang, S., & Curran, S. P. (2020) · eLife · doi:10.7554/elife.52899 · Cited by 42
Goretzki, A., Lin, Y., & Schülke, S. (2021) · Allergy · doi:10.1111/all.14843 · Cited by 42
Current progress with mammalian models of mitochondrial DNA disease
Stewart, J. B. (2020) · Journal of Inherited Metabolic Disease · doi:10.1002/jimd.12324 · Cited by 40
Immune Metabolism of IL-4-Activated B Cells and Th2 Cells in the Context of Allergic Diseases
Lin, Y., Goretzki, A., & Schülke, S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.790658 · Cited by 40
Li, C., Zhu, Y., Liu, W., Xiang, W., He, S., Hayashi, T., Mizuno, K., Hattori, S., Fujisaki, H., & Ikejima, T. (2023) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2023.109553 · Cited by 39
Lu, J., Li, H., Yu, D., Zhao, P., & Liu, Y. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1171506 · Cited by 37
Mitochondrion: A bridge linking aging and degenerative diseases
Zhang, L., Wu, J., Zhu, Z., He, Y., & Fang, R. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121666 · Cited by 38
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. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04767-3 · Cited by 37
Bargelloni, L., Babbucci, M., Ferraresso, S., Papetti, C., Vitulo, N., Carraro, R., Pauletto, M., Santovito, G., Lucassen, M., Mark, F. C., et al. (2019) · Communications Biology · doi:10.1038/s42003-019-0685-y · Cited by 34
Mitochondrial disease, mitophagy, and cellular distress in methylmalonic acidemia
Luciani, A., Denley, M. C. S., Govers, L. P., Sorrentino, V., & Froese, D. S. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03934-3 · Cited by 41
Lv, W., Jiang, J., Li, Y., Fu, L., Meng, F., & Li, J. (2020) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2020.104522 · Cited by 35
Lithium and the Interplay Between Telomeres and Mitochondria in Bipolar Disorder
Lundberg, M., Millischer, V., Backlund, L., Martinsson, L., Stenvinkel, P., Sellgren, C. M., Lavebratt, C., & Schalling, M. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.586083 · Cited by 38
Indole-3-acetic acid improves the hepatic mitochondrial respiration defects by PGC1a up-regulation
Zhang, C., Fu, Q., Shao, K., Liu, L., Ma, X., Zhang, F., Zhang, X., Meng, L., Yan, C., & Zhao, X. (2022) · Cellular Signalling · doi:10.1016/j.cellsig.2022.110442 · Cited by 36
Kumar, N. (2022) · Current Molecular Medicine · doi:10.2174/1566524022666220408104047 · Cited by 34
Pan, D., Lindau, C., Lagies, S., Wiedemann, N., & Kammerer, B. (2018) · Metabolomics · doi:10.1007/s11306-018-1352-x · Cited by 33
Ferroptosis-Driven Nanotherapeutics to Reverse Drug Resistance in Tumor Microenvironment
Zhu, L., Meng, D., Wang, X., & Chen, X. (2022) · ACS Applied Bio Materials · doi:10.1021/acsabm.2c00199 · Cited by 35
Leuthner, T. C., Benzing, L., Kohrn, B. F., Bergemann, C. M., Hipp, M. J., Hershberger, K. A., Mello, D. F., Sokolskyi, T., Stevenson, K., Merutka, I. R., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac666 · Cited by 34
Silencing of KCNA1 suppresses the cervical cancer development via mitochondria damage
Liu, L., Chen, Y., Zhang, Q., & Li, C. (2019) · Channels · doi:10.1080/19336950.2019.1648627 · Cited by 33
Shaping Up Mitochondria in Diabetic Nephropathy
Mise, K., Galvan, D. L., & Danesh, F. R. (2020) · Kidney360 · doi:10.34067/kid.0002352020 · Cited by 33
Mitochondrial-induced Epigenetic Modifications: From Biology to Clinical Translation
Sharma, J., Kumari, R., Bhargava, A., Tiwari, R. R., & Mishra, P. K. (2020) · Current Pharmaceutical Design · doi:10.2174/1381612826666200826165735 · Cited by 32
Metadata
- Authors
- van der Bliek, A. M., Sedensky, M. M., & Morgan, P. G.
- Affiliations
- Department of Biological Chemistry, Jonsson Comprehensive Cancer Center and Molecular Biology Institute, David Geffen School of Medicine at UCLA, Los Angeles, California 90024
- University of Washington (US)
- Department of Anesthesiology and Pain Medicine, University of Washington and Center for Developmental Therapeutics, Seattle Children’s Research Institute, Washington 98101
- ORCID
- Sedensky, Margaret M
- Venue
- Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2017-10-25
- Volume
- 207
- Issue
- 3
- Pages
- 843-871
- ISSN
- 0016-6731 (ISSN-L)
- 1943-2631
- PMC
- PMC5676242
- OpenAlex
- W2765579241
- Cited by
- 388
- References
- 234
- Citations by year
- 2026: 22 · 2025: 45 · 2024: 44 · 2023: 58 · 2022: 60 · 2021: 59 · 2020: 62 · 2019: 26 · 2018: 11
- FWCI
- 2.53
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- Genetics (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Institutes of Health
- National Institute of General Medical Sciences (U01GM109764, R01GM118514, R01GM105696)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Keywords
- mitochondria, TCA cycle, oxidative phosphorylation, mitochondrial protein import, mitochondrial biogenesis, mitochondrial fission, mitochondrial fusion, mitophagy, mitochondrial unfolded protein response, stress response, aging
- MeSH terms
- Animals, Organelle Biogenesis, Citric Acid Cycle, Electron Transport, Mitochondria
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review