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Distinct genomic copy number in mitochondria of different mammalian organs.
Abstract
This study shows that mitochondria in liver, kidney, heart, and brain of the mouse have a distinct mitochondrial density. It also demonstrates that the mtDNA copy number per mitochondrion is organ-specific. A reliable method of determining mitochondrial density per organ is by stereological analysis of tissue sections while mtDNA quantitation is by the use of radiolabelled mtDNA probe. This is the first study in which a comprehensive examination of mitochondrial density and quantitation of mitochondrial genomes in mouse organs have been done. In summary the variability is not only in mitochondrial density but also in genomic copy number in mitochondria of various tissues.
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“Electron microscopy demonstrates that mitochondrial area is 44% lower in liver than in heart (210) with smaller size, fewer cristae, and lower matrix density.”
From The role of mitochondria in the pathogenesis of type 2 diabetes (2010) · cites this paper as [210]
Citations
Cites
A low-viscosity epoxy resin embedding medium for electron microscopy.
Spurr, A. (1969) · Journal of Ultrastructure Research · doi:10.1016/s0022-5320(69)90033-1 · Cited by 13,268
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
Sequence and gene organization of mouse mitochondrial DNA.
Bibb, M., Etten, R. V., Wright, C. T., Walberg, M. W., & Clayton, D. A. (1981) · Cell · doi:10.1016/0092-8674(81)90300-7 · Cited by 1,619
Replication of animal mitochondrial DNA
Clayton, D. A. (1982) · Cell · doi:10.1016/0092-8674(82)90049-6 · Cited by 1,243
Mitochondrial DNA molecules and virtual number of mitochondria per cell in mammalian cells
Robin, E. D., & Wong, R. J. (1988) · Journal of Cellular Physiology · doi:10.1002/jcp.1041360316 · Cited by 660
The Number of Mitochondrial Deoxyribonucleic Acid Genomes in Mouse L and Human HeLa Cells
Bogenhagen, D. F., & Clayton, D. A. (1974) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)42063-2 · Cited by 526
TRANSCRIPTION OF THE MAMMALIAN MITOCHONDRIAL GENOME
Clayton, D. A. (1984) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.53.070184.003041 · Cited by 446
Williams, R. S. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)67252-7 · Cited by 273
Mitochondrial DNA: Advances, Problems, and Goals
Nass, M. M. K. (1969) · Science · doi:10.1126/science.165.3888.25 · Cited by 212
Mitochondrial DNA I. Preparation and properties of mitochondrial DNA from chick liver
Borst, P., Ruttenberg, G. J. C. M., & Kroon, A. M. (1967) · Biochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis · doi:10.1016/0005-2787(67)90697-1 · Cited by 120
Research works printed but not linked: 2
- Allard C., 1952, Mitochondrial populatin in mammalian cells, Cancer Res., 12, 407
- Tzagoloff A., 1982, Mitochondria
Cited by
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Shadel, G. S., & Clayton, D. A. (1997) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.66.1.409 · Cited by 1,059
Mootha, V. K., Bunkenborg, J., Olsen, J. V., Hjerrild, M., Wisniewski, J. R., Stahl, E., Bolouri, M. S., Ray, H. N., Sihag, S., Kamal, M., et al. (2003) · Cell · doi:10.1016/s0092-8674(03)00926-7 · Cited by 889
Counting with DNA in metabarcoding studies: How should we convert sequence reads to dietary data?
Deagle, B. E., Thomas, A. C., McInnes, J. C., Clarke, L. J., Vesterinen, E. J., Clare, E. L., Kartzinel, T. R., & Eveson, J. P. (2018) · Molecular Ecology · doi:10.1111/mec.14734 · Cited by 884
Mitochondrial dysfunction and molecular pathways of disease
Pieczenik, S. R., & Neustadt, J. O. (2007) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2006.09.008 · Cited by 643
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Bartzokis, G. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.08.007 · Cited by 546
The role of mitochondria in the pathogenesis of type 2 diabetes
Patti, M.-E., & Corvera, S. (2010) · Endocrine Reviews · doi:10.1210/er.2009-0027 · Cited by 551
Is mitochondrial DNA content a potential biomarker of mitochondrial dysfunction?
Malik, A. N., & Czajka, A. (2012) · Mitochondrion · doi:10.1016/j.mito.2012.10.011 · Cited by 507
Regulation of Mitochondrial ATP Production: Ca2+ Signaling and Quality Control
Boyman, L., Karbowski, M., & Lederer, W. J. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2019.10.007 · Cited by 310
Rodríguez-Navarro, J. A., Rodríguez, L., Casarejos, M. J., Solano, R. M., Gómez, A., Perucho, J., Cuervo, A. M., García de Yébenes, J., & Mena, M. A. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2010.05.014 · Cited by 298
Diagnoses of neuronal ceroid‐lipofuscinosis by immunochemical methods
Hosain, S. A., Kaufmann, W. E., Negrin, G., Watkins, P. A., Siakotos, A. N., Palmer, D. N., & Naidu, S. (1995) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320570226 · Cited by 256
Length heteroplasmy in the first hypervariable segment of the human mtDNA control region.
Bendall, K. E., & Sykes, B. C. (1995) · Europe PMC (PubMed Central) · Cited by 233
Mitochondrial DNA polymerase-γ and human disease
Hudson, G., & Chinnery, P. F. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl233 · Cited by 226
Tissue-specific differences in mitochondrial activity and biogenesis
Fernández‐Vizarra, E., Enrı́quez, J. A., Martos, A. P., Montoya, J., & Fernández‐Silva, P. (2010) · Mitochondrion · doi:10.1016/j.mito.2010.09.011 · Cited by 195
Circulating Cell-Free Nucleic Acids: Main Characteristics and Clinical Application
Szilágyi, M., Pös, O., Márton, É., Buglyó, G., Soltész, B., Keserű, J. S., Penyige, A., Szemes, T., & Nagy, B. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186827 · Cited by 201
Metabarcoding a diverse arthropod mock community
Braukmann, T., Ivanova, N. V., Prosser, S. W. J., Elbrecht, V., Steinke, D., Ratnasingham, S., de Waard, J. R., Sones, J. E., Zakharov, E., & Hebert, P. D. N. (2019) · Molecular Ecology Resources · doi:10.1111/1755-0998.13008 · Cited by 199
Mitochondrial function in development and disease
Rossmann, M. P., Dubois, S. M., Agarwal, S., & Zon, L. I. (2021) · Disease Models & Mechanisms · doi:10.1242/dmm.048912 · Cited by 200
Mitochondrial copy number and risk of breast cancer: A pilot study
Shen, J., Platek, M., Mahasneh, A., Ambrosone, C. B., & Zhao, H. (2009) · Mitochondrion · doi:10.1016/j.mito.2009.09.004 · Cited by 162
Mitochondrial Roles and Cytoprotection in Chronic Liver Injury
Esposti, D. D., Hamelin, J., Bosselut, N., Saffroy, R., Sebagh, M., Pommier, A., Martel, C., & Lemoine, A. (2012) · Biochemistry Research International · doi:10.1155/2012/387626 · Cited by 165
Medication‐induced mitochondrial damage and disease
Neustadt, J. O., & Pieczenik, S. R. (2008) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.200700075 · Cited by 158
High‐throughput monitoring of wild bee diversity and abundance via mitogenomics
Tang, M., Hardman, C. J., Ji, Y., Meng, G., Liu, S., Tan, M., Yang, S., Moss, E. D., Wang, J., Yang, C., et al. (2015) · Methods in Ecology and Evolution · doi:10.1111/2041-210x.12416 · Cited by 152
Scaling properties of cell and organelle size
Chan, Y.-H. M., & Marshall, W. F. (2010) · Organogenesis · doi:10.4161/org.6.2.11464 · Cited by 138
Mitochondrial Variability as a Source of Extrinsic Cellular Noise
Johnston, I. G., Gaál, B., das Neves, R. P., Enver, T., Iborra, F. J., & Jones, N. S. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002416 · Cited by 116
Antiviral chemotherapy for the treatment of hepatitis b virus infections
Torresi, J., & LOCARNINI, S. A. (2000) · Gastroenterology · doi:10.1016/s0016-5085(00)70008-4 · Cited by 125
O'Hara, R., Tedone, E., Ludlow, A., Huang, E., Arosio, B., Mari, D., & Shay, J. W. (2019) · Genome Research · doi:10.1101/gr.250480.119 · Cited by 121
Mitochondrial density determines the cellular sensitivity to cisplatin-induced cell death
Qian, W., Nishikawa, M., Haque, A. M., Hirose, M., Mashimo, M., Sato, E. F., & Inoue, M. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00265.2005 · Cited by 122
Human Mitochondrial Diseases: Answering Questions and Questioning Answers
Howell, N. (1998) · International review of cytology · doi:10.1016/s0074-7696(08)61051-7 · Cited by 119
The Evolution of Per-cell Organelle Number
Cole, L. W. (2016) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2016.00085 · Cited by 131
Biju-Duval, C., Ennafaa, H., Dennebouy, N., Monnerot, M., Mignotte, F., Soriguer, R. C., Gaaïed, A. E., Hili, A. E., & Mounolou, J. (1991) · Journal of Molecular Evolution · doi:10.1007/bf02100200 · Cited by 113
Fischel‐Ghodsian, N., Bykhovskaya, Y., Taylor, K. D., Kahen, T., Cantor, R. M., Ehrenman, K., Smith, R. J., & Keithley, E. M. (1997) · Hearing Research · doi:10.1016/s0378-5955(97)00077-4 · Cited by 105
Evidence for aerobic ATP synthesis in isolated myelin vesicles
Ravera, S., Panfoli, I., Calzia, D., Aluigi, M. G., Bianchini, P., Diaspro, A., Mancardi, G., & Morelli, A. M. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.01.009 · Cited by 101
Regeneration in the metazoans: why does it happen?
Alvarado, A. S. (2000) · BioEssays · doi:10.1002/(sici)1521-1878(200006)22:6 · Cited by 342
D’Souza, A. D., Parikh, N. S., Kaech, S. M., & Shadel, G. S. (2007) · Mitochondrion · doi:10.1016/j.mito.2007.08.001 · Cited by 99
Melatonin for the treatment of sepsis: the scientific rationale
Biancatelli, R. M. L. C., Berrill, M., Mohammed, Y. H., & Marik, P. E. (2020) · Journal of Thoracic Disease · doi:10.21037/jtd.2019.12.85 · Cited by 96
Hu, L., Yao, X., & Shen, Y. (2016) · Scientific Reports · doi:10.1038/srep35859 · Cited by 94
Oxidized mitochondrial DNA: a protective signal gone awry
Xian, H., & Karin, M. (2023) · Trends in Immunology · doi:10.1016/j.it.2023.01.006 · Cited by 97
Forensic applications of mitochondrial DNA
Butler, J. M., & Levin, B. C. (1998) · Trends in biotechnology · doi:10.1016/s0167-7799(98)01173-1 · Cited by 92
Mitochondrial off targets of drug therapy
Wallace, K. B. (2008) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2008.04.001 · Cited by 90
The role of mitochondria in rheumatic diseases
Becker, Y. L. C., Duvvuri, B., Fortin, P. R., Lood, C., & Boilard, E. (2022) · Nature Reviews Rheumatology · doi:10.1038/s41584-022-00834-z · Cited by 81
Mitochondrial DNA: cellular genotoxic stress sentinel
Wu, Z., Sainz, A. G., & Shadel, G. S. (2021) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2021.05.004 · Cited by 85
Overcoming the pitfalls of merging dietary metabarcoding into ecological networks
Cuff, J. P., Windsor, F. M., Tercel, M. P. T. G., Kitson, J. J. N., & Evans, D. M. (2021) · Methods in Ecology and Evolution · doi:10.1111/2041-210x.13796 · Cited by 89
Mitochondrial heterogeneity in diseases
Chen, L., Zhou, M., Li, H., Liu, D., Liao, P., Yao, Z., Zhang, C., Zou, W., & Gao, J. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01546-w · Cited by 88
The problem of omnivory: A synthesis on omnivory and DNA metabarcoding
Tercel, M. P. T. G., Symondson, W. O. C., & Cuff, J. P. (2021) · Molecular Ecology · doi:10.1111/mec.15903 · Cited by 80
Recent advances in management of COVID-19: A review
Mouffak, S., Shubbar, Q., Saleh, E., & El‐Awady, R. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.112107 · Cited by 84
Mitochondrial DNA Copy Number and Risk of Oral Cancer: A Report from Northeast India
Mondal, R., Ghosh, S. K., Choudhury, J. H., Singh, S. A., Sinha, K., Hussain, M., Laskar, R. S., Rabha, B., Dey, P., Ganguli, S., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0057771 · Cited by 78
Mitochondrial alterations in photodynamic therapy-resistant cells.
Sharkey, S., Wilson, B. C., Moorehead, R. A., & Singh, G. (1993) · PubMed · Cited by 75
Self-citationThe Fate of Human Sperm-Derived mtDNA in Somatic Cells
Manfredi, G., Thyagarajan, D. E., Papadopoulou, L. C., Pallotti, F., & Schon, E. A. (1997) · The American Journal of Human Genetics · doi:10.1086/514887 · Cited by 74
Fall in circulating mononuclear cell mitochondrial DNA content in human sepsis
Pyle, A., Burn, D. J., Gordon, C., Swan, C., Chinnery, P. F., & Baudouin, S. (2010) · Intensive Care Medicine · doi:10.1007/s00134-010-1823-7 · Cited by 70
Chen, S., Xie, X., Wang, Y., Gao, Y., Xie, X., Yang, J., & Ye, J. (2014) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2014.08.051 · Cited by 70
Mitochondrial Transplantation in Mitochondrial Medicine: Current Challenges and Future Perspectives
D’Amato, M., Morra, F., Meo, I. D., & Tiranti, V. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24031969 · Cited by 72
Botero-Castro, F., Tilak, M., Justy, F., Catzeflis, F. M., Delsuc, F., & Douzery, E. (2013) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2013.07.003 · Cited by 68
Mutational patterns in the breast cancer mitochondrial genome, with clinical correlates
McMahon, S., & LaFramboise, T. (2014) · Carcinogenesis · doi:10.1093/carcin/bgu012 · Cited by 68
Association between mitochondrial DNA content in leukocytes and colorectal cancer risk
Qu, F., Liu, X., Zhou, F., Yang, H., Bao, G., He, X., & Xing, J. (2011) · Cancer · doi:10.1002/cncr.25906 · Cited by 67
Mitochondrial integrity in neurodegeneration
Cowan, K., Anichtchik, O. V., & Luo, S. (2019) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13105 · Cited by 67
The Multiple Levels of Mitonuclear Coregulation
Isaac, R. S., McShane, E., & Churchman, L. S. (2018) · Annual Review of Genetics · doi:10.1146/annurev-genet-120417-031709 · Cited by 63
Reduced oxidative stress increases acute cold stress tolerance in zebrafish
Lu, D., Ma, Q., Sun, S.-X., Zhang, H., Chen, L., Zhang, M., & Du, Z. (2019) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2019.06.009 · Cited by 64
Mitochondrial content of choroid plexus epithelium
Cornford, E. M., Varesi, J. B., Hyman, S., Damian, R. T., & Raleigh, M. J. (1997) · Experimental Brain Research · doi:10.1007/pl00005768 · Cited by 63
Aiken, C., Cindrová‐Davies, T., & Johnson, M. H. (2008) · Reproductive BioMedicine Online · doi:10.1016/s1472-6483(10)60409-9 · Cited by 60
Organ reserve, excess metabolic capacity, and aging
Atamna, H., Tenore, A., Lui, F., & Dhahbi, J. M. (2018) · Biogerontology · doi:10.1007/s10522-018-9746-8 · Cited by 72
Mitochondrial factors in the pathogenesis of diabetes: a hypothesis for treatment.
Lamson, D. W., & Plaza, S. M. (2002) · PubMed · Cited by 57
Hepatic purine and pyrimidine metabolism: implications for antiviral chemotherapy of viral hepatitis
Shaw, T., & LOCARNINI, S. A. (1995) · Liver International · doi:10.1111/j.1600-0676.1995.tb00667.x · Cited by 54
Skeletal Muscle Nucleo-Mitochondrial Crosstalk in Obesity and Type 2 Diabetes
Devarshi, P. P., McNabney, S. M., & Henagan, T. M. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18040831 · Cited by 55
The alterations of mitochondrial DNA in coronary heart disease
Hu, H., Lin, Y., Xu, X., Lin, S., Chen, X., & Wang, S. (2020) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2020.104412 · Cited by 52
Characterization of Myelin Sheath FoF1-ATP Synthase and its Regulation by IF1
Ravera, S., Panfoli, I., Aluigi, M. G., Calzia, D., & Morelli, A. M. (2010) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-010-9112-1 · Cited by 50
Campa, D., Barrdahl, M., Santoro, A., Severi, G., Baglietto, L., Omichessan, H., Tumino, R., Bueno-de-Mesquita, H. B., Peeters, P. H. M., Weiderpass, E., et al. (2018) · Breast Cancer Research · doi:10.1186/s13058-018-0955-5 · Cited by 51
Sun, S., Guo, Z., Fu, H., Zhu, J. X., & Ge, X. (2018) · Environmental Pollution · doi:10.1016/j.envpol.2018.09.072 · Cited by 49
Observation Bias in Metabarcoding
Shaffer, M., Allan, E. A., Cise, A. M. V., Parsons, K. M., Shelton, A. O., & Kelly, R. P. (2025) · Molecular Ecology Resources · doi:10.1111/1755-0998.14119 · Cited by 51
Tricarboxylic acid cycle-sustained oxidative phosphorylation in isolated myelin vesicles
Ravera, S., Bartolucci, M., Calzia, D., Aluigi, M. G., Ramoino, P., Morelli, A. M., & Panfoli, I. (2013) · Biochimie · doi:10.1016/j.biochi.2013.07.003 · Cited by 47
Kirstein, J., & Morimoto, R. I. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22292 · Cited by 52
He, Y., Lu, X., Wu, H., Cai, W., Yang, L.-Q., Xu, L., Sun, H., & Kong, Q. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.01.015 · Cited by 46
Imaging cell morphology and physiology using X-rays
Weinhardt, V., Chen, J.-H., Ekman, A. A., McDermott, G., Gros, M. A. L., & Larabell, C. A. (2019) · Biochemical Society Transactions · doi:10.1042/bst20180036 · Cited by 47
Counting with DNA in metabarcoding studies: how should we convert sequence reads to dietary data?Preprint
Deagle, B. E., Thomas, A. C., McInnes, J. C., Clarket, L. J., Vesterinen, E. J., Clare, E. L., Kartzinel, T. R., & Eveson, J. P. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/303461 · Cited by 45
Hamblet, N. S., & Castora, F. J. (1997) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(97)00158-9 · Cited by 44
Xie, H., Lev, D. C., Gong, Y. Y., Wang, S., Pollock, R. E., Wu, X., & Gu, J. H. (2013) · Carcinogenesis · doi:10.1093/carcin/bgt023 · Cited by 44
Margaryan, A., Noer, C. L., Richter, S. R., Restrup, M. E. M., Bülow‐Hansen, J. L., Leerhøi, F., Langkjær, E., Gopalakrishnan, S., Carøe, C., Gilbert, M. T. P., et al. (2020) · Environmental DNA · doi:10.1002/edn3.138 · Cited by 43
Tissue specific and developmental expression of rat long-and medium-chain acyl-CoA dehydrogenases
Hainline, B. E., Kahlenbeck, D. J., Grant, J., & Strauss, A. W. (1993) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/0167-4781(93)90015-6 · Cited by 43
Hypothesis of an Energetic Function for Myelin
Morelli, A. M., Ravera, S., & Panfoli, I. (2011) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-011-9174-8 · Cited by 41
Lebedeva, M. A., & Shadel, G. S. (2007) · Cell Cycle · doi:10.4161/cc.6.16.4572 · Cited by 40
Photobiomodulation: Evolution and Adaptation
Lipko, N. B. (2022) · Photobiomodulation Photomedicine and Laser Surgery · doi:10.1089/photob.2021.0145 · Cited by 39
Pozzi, A., & Dowling, D. K. (2019) · Genome Biology and Evolution · doi:10.1093/gbe/evz132 · Cited by 41
Mitochondrial DNA Copy Number in Peripheral Blood and Melanoma Risk
Shen, J., Gopalakrishnan, V., Lee, J. E., Fang, S., & Zhao, H. (2015) · PLoS ONE · doi:10.1371/journal.pone.0131649 · Cited by 38
Baek, J. H., Son, H., Jeong, Y., Park, S. W., & Kim, H. J. (2019) · Cells · doi:10.3390/cells8030247 · Cited by 37
Mitochondrial DNA homeostasis impairment and dopaminergic dysfunction: A trembling balance
Manini, A., Abati, E., Comi, G. P., Corti, S. P., & Ronchi, D. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101578 · Cited by 36
Sequence polymorphisms within the human mitochondrial genes MTATP6, MTATP8 and MTND4
Lutz‐Bonengel, S., Schmidt, U. G., Schmitt, T., & Pollak, S. (2003) · International Journal of Legal Medicine · doi:10.1007/s00414-002-0356-1 · Cited by 35
Mitochondrial DNA Copy-Number Variation and Pancreatic Cancer Risk in the Prospective EPIC Cohort
Gentiluomo, M., Katzke, V. A., Kaaks, R., Tjønneland, A. M., Severi, G., Perduca, V., Boutron‐Ruault, M., Weiderpass, E., Ferrari, P., Johnson, T., et al. (2020) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.epi-19-0868 · Cited by 35
Mitochondrial biogenesis in rabbit articular chondrocytes transferred to culture
Mignotte, F., Champagne, A., Froger‐Gaillard, B., Benel, L., Guéride, M., Adolphe, M., & Mounolou, J. (1991) · Biology of the Cell · doi:10.1016/0248-4900(91)90052-o · Cited by 34
Zhu, X., Mao, Y., Huang, T., Yan, C., Yu, F., Du, J., Dai, J., Ma, H., & Jin, G. (2017) · Molecular Carcinogenesis · doi:10.1002/mc.22703 · Cited by 32
Xia, C., Liu, Y., Yang, H., Yang, H., Liu, J., Ma, Y., & Qi, Y. (2017) · Chinese Medical Journal · doi:10.4103/0366-6999.216395 · Cited by 32
Tu, H., Gu, J. H., Meng, Q. H., Kim, J., Davis, J. W., He, Y., Wagar, E. A., Thompson, T. C., Logothetis, C. J., & Wu, X. (2015) · Oncotarget · doi:10.18632/oncotarget.5889 · Cited by 31
Yang, W., Wu, J., Bi, A., Ou-yang, Y.-C., Shen, H., Chirn, G., Zhou, J., Weiss, E., Holman, E. P., & Liao, D. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077016 · Cited by 30
Mitofusin 2: A link between mitochondrial function and substrate metabolism?
Emery, J., & Ortiz, R. M. (2021) · Mitochondrion · doi:10.1016/j.mito.2021.09.003 · Cited by 34
Schulz, S., Lichtmannegger, J., Schmitt, S., Leitzinger, C., Eberhagen, C., Einer, C., Kerth, J., Aichler, M., & Zischka, H. (2015) · Methods in molecular biology · doi:10.1007/978-1-4939-2550-6_7 · Cited by 28
Functional Expression of Electron Transport Chain and FoF1-ATP Synthase in Optic Nerve Myelin Sheath
Bartolucci, M., Ravera, S., Garbarino, G., Ramoino, P., Ferrando, S., Calzia, D., Candiani, S., Morelli, A. M., & Panfoli, I. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1712-0 · Cited by 29
Zhao, S., Yang, Y., Liu, J., Liu, H., Ge, N., Yang, H., Zhang, H., & Xing, J. (2011) · Cancer Science · doi:10.1111/j.1349-7006.2011.01968.x · Cited by 29
Difficulties barcoding in the dark: the case of crustacean stygofauna from eastern Australia
Asmyhr, M. G., & Cooper, S. J. (2012) · Invertebrate Systematics · doi:10.1071/is12032 · Cited by 29
Granquist, S. M., Esparza‐Salas, R., Hauksson, E., Karlsson, O., & Angerbjörn, A. (2018) · Polar Biology · doi:10.1007/s00300-018-2354-x · Cited by 29
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Metadata
- Authors
- Veltri, K. L., Espiritu, M., & Singh, G.
- Affiliations
- McMaster University (CA)
- Corresponding author
- Singh, Gurmit
- ORCID
- Singh, Gurmit
- Venue
- Journal of Cellular Physiology
- Publisher
- Wiley
- Published
- 1990-04
- Volume
- 143
- Issue
- 1
- Pages
- 160-164
- ISSN
- 0021-9541 (ISSN-L)
- 1097-4652
- OpenAlex
- W2030868673
- Cited by
- 242
- References
- 19
- Citations by year
- 2026: 1 · 2025: 6 · 2024: 6 · 2023: 17 · 2022: 9 · 2021: 19 · 2020: 20 · 2019: 19 · 2018: 18 · 2017: 7 · 2016: 6 · 2015: 10 · 2014: 13 · 2013: 13 · 2012: 6
- FWCI
- 0.84
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Cellular Physiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- McMaster University
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Keywords
- mitochondrial density, mitochondrial DNA copy number, mouse organs, liver, kidney, heart, brain, stereology
- MeSH terms
- Animals, Brain, DNA, Mitochondrial, Kidney, Mice, Inbred C57BL, Microscopy, Electron, Mitochondria, Mitochondria, Heart, Mitochondria, Liver, Mice
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