Distinct genomic copy number in mitochondria of different mammalian organs.

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 · see citing works

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 9,640 · see citing works

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 · see citing works

Replication of animal mitochondrial DNA

Clayton, D. A. (1982) · Cell · doi:10.1016/0092-8674(82)90049-6 · Cited by 1,236 · see citing works

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 656 · see citing works

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 · see citing works

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 · see citing works

Mitochondrial gene expression in mammalian striated muscle. Evidence that variation in gene dosage is the major regulatory event.

Williams, R. S. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)67252-7 · Cited by 273 · see citing works

Mitochondrial DNA: Advances, Problems, and Goals

Nass, M. M. K. (1969) · Science · doi:10.1126/science.165.3888.25 · Cited by 212 · see citing works

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 122 · see citing works

Cells and organelles

Novikoff, A. B., & Holtzman, E. (1984) · Cited by 117 · see citing works

Deoxyribonucleic acid in isolated rat-liver mitochondria

Nass, S., Nass, M. M. K., & Hennix, U. (1965) · Biochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis · doi:10.1016/0005-2787(65)90189-9 · Cited by 107 · see citing works

MITOCHONDRIAL DNA FROM PROTOZOA

Suyama, Y., & Preer, J. R. (1965) · Genetics · doi:10.1093/genetics/52.5.1051 · Cited by 97 · see citing works

Mitochondrial population in mammalian cells. I. Description of a counting technic and preliminary results on rat liver in different physiological and pathological conditions.

Allard, C., MATHIEU, R., de Lamirande, G., & Cantero, A. (1952) · PubMed · Cited by 94 · see citing works

The isolation and some properties of rat liver mitochondrial deoxyribonucleic acid.

Schneider, W., & Kuff, E. L. (1965) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.54.6.1650 · Cited by 76 · see citing works

Biosynthesis of DNA by Isolated Mitochondria: Incorporation of Thymidine Triphosphate-2-C 14

Parsons, P. G., & Simpson, M. V. (1967) · Science · doi:10.1126/science.155.3758.91 · Cited by 75 · see citing works

DNA From Plant Mitochondria

Suyama, Y., & Bonner, W. D. (1966) · PLANT PHYSIOLOGY · doi:10.1104/pp.41.3.383 · Cited by 72 · see citing works

A possible cellular mechanism of cisplatin-induced nephrotoxicity

Singh, G. (1989) · Toxicology · doi:10.1016/0300-483x(89)90105-4 · Cited by 68 · see citing works

The differentiation of animal mitochondria during development

POLLAK, J. K., & Sutton, R. (1980) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(80)80073-9 · Cited by 49 · see citing works

MITOCHONDRIAL DNA MAINTENANCE IN VERTEBRATES

Shadel, G. S., & Clayton, D. A. (1997) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.66.1.409 · Cited by 1,059 · see citing works

Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria.

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 · see citing works

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 834 · see citing works

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 638 · see citing works

Alzheimer's disease as homeostatic responses to age-related myelin breakdown

Bartzokis, G. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.08.007 · Cited by 546 · see citing works

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 · see citing works

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 499 · see citing works

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 309 · see citing works

Trehalose ameliorates dopaminergic and tau pathology in parkin deleted/tau overexpressing mice through autophagy activation

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 · see citing works

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 · see citing works

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 · see citing works

Mitochondrial DNA polymerase-γ and human disease

Hudson, G., & Chinnery, P. F. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl233 · Cited by 221 · see citing works

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 · see citing works

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 193 · see citing works

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 189 · see citing works

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 191 · see citing works

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 · see citing works

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 159 · see citing works

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 · see citing works

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 144 · see citing works

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 127 · see citing works

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 · see citing works

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 124 · see citing works

Quantitative mitochondrial DNA copy number determination using droplet digital PCR with single-cell resolution

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 · see citing works

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 119 · see citing works

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 118 · see citing works

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 116 · see citing works

Mitochondrial DNA evolution in lagomorphs: Origin of systematic heteroplasmy and organization of diversity in European rabbits

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 · see citing works

Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations

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 · see citing works

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 · see citing works

Nuclear targeting signal recognition: a key control point in nuclear transport?

Jans, D. A., Xiao, C.-Y., & Lam, M. H. C. (2000) · BioEssays · doi:10.1002/(sici)1521-1878(200006)22:6 · Cited by 519 · see citing works

Convergence of multiple signaling pathways is required to coordinately up-regulate mtDNA and mitochondrial biogenesis during T cell activation

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 · see citing works

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 95 · see citing works

Altered mitochondrial DNA copy number contributes to human cancer risk: evidence from an updated meta-analysis

Hu, L., Yao, X., & Shen, Y. (2016) · Scientific Reports · doi:10.1038/srep35859 · Cited by 94 · see citing works

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 94 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 83 · see citing works

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 · see citing works

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 85 · see citing works

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 · see citing works

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 81 · see citing works

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 · see citing works

Mitochondrial alterations in photodynamic therapy-resistant cells.

Sharkey, S., Wilson, B. C., Moorehead, R. A., & Singh, G. (1993) · PubMed · Cited by 75 · see citing works

The 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 · see citing works

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 · see citing works

Association between leukocyte mitochondrial DNA content and risk of coronary heart disease: A case-control study

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 · see citing works

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 70 · see citing works

Next-generation sequencing and phylogenetic signal of complete mitochondrial genomes for resolving the evolutionary history of leaf-nosed bats (Phyllostomidae)

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 · see citing works

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 · see citing works

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 · see citing works

Mitochondrial integrity in neurodegeneration

Cowan, K., Anichtchik, O. V., & Luo, S. (2019) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13105 · Cited by 65 · see citing works

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 65 · see citing works

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 63 · see citing works

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 · see citing works

Variations in mouse mitochondrial DNA copy number from fertilization to birth are associated with oxidative stress

Aiken, C., Cindrová‐Davies, T., & Johnson, M. H. (2008) · Reproductive BioMedicine Online · doi:10.1016/s1472-6483(10)60409-9 · Cited by 60 · see citing works

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 60 · see citing works

Mitochondrial factors in the pathogenesis of diabetes: a hypothesis for treatment.

Lamson, D. W., & Plaza, S. M. (2002) · PubMed · Cited by 57 · see citing works

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 · see citing works

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 · see citing works

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 51 · see citing works

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 · see citing works

Mitochondrial DNA copy number variation, leukocyte telomere length, and breast cancer risk in the European Prospective Investigation into Cancer and Nutrition (EPIC) study

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 50 · see citing works

Integrated metabolomic and transcriptomic analysis of brain energy metabolism in the male Oriental river prawn (Macrobrachium nipponense) in response to hypoxia and reoxygenation

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 · see citing works

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 · see citing works

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 · see citing works

Caenorhabditis elegans as a model system to study intercompartmental proteostasis: Interrelation of mitochondrial function, longevity, and neurodegenerative diseases

Kirstein, J., & Morimoto, R. I. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22292 · Cited by 49 · see citing works

Mitochondrial DNA content contributes to healthy aging in Chinese: a study from nonagenarians and centenarians

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 · see citing works

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 45 · see citing works

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 · see citing works

Elevated levels of the Kearns–Sayre syndrome mitochondrial DNA deletion in temporal cortex of Alzheimer's patients

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 · see citing works

Reduced mitochondrial DNA copy number in peripheral blood leukocytes increases the risk of soft tissue sarcoma

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 · see citing works

Mitochondrial genomes of Danish vertebrate species generated for the national DNA reference database, DNAmark

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 · see citing works

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 · see citing works

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 · see citing works

Cell Cycle- and Ribonucleotide Reductase-Driven Changes in mtDNA Copy Number Influence mtDNA Inheritance Without Compromising Mitochondrial Gene Expression

Lebedeva, M. A., & Shadel, G. S. (2007) · Cell Cycle · doi:10.4161/cc.6.16.4572 · Cited by 40 · see citing works

Photobiomodulation: Evolution and Adaptation

Lipko, N. B. (2022) · Photobiomodulation Photomedicine and Laser Surgery · doi:10.1089/photob.2021.0145 · Cited by 37 · see citing works

The Genomic Origins of Small Mitochondrial RNAs: Are They Transcribed by the Mitochondrial DNA or by Mitochondrial Pseudogenes within the Nucleus (NUMTs)?

Pozzi, A., & Dowling, D. K. (2019) · Genome Biology and Evolution · doi:10.1093/gbe/evz132 · Cited by 38 · see citing works

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 · see citing works

Chronological Aging Standard Curves of Telomere Length and Mitochondrial DNA Copy Number in Twelve Tissues of C57BL/6 Male Mouse

Baek, J. H., Son, H., Jeong, Y., Park, S. W., & Kim, H. J. (2019) · Cells · doi:10.3390/cells8030247 · Cited by 36 · see citing works

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 · see citing works

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 · see citing works

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 34 · see citing works

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 · see citing works

High mitochondrial DNA copy number was associated with an increased gastric cancer risk in a Chinese population

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 · see citing works

Reference Intervals of Mitochondrial DNA Copy Number in Peripheral Blood for Chinese Minors and Adults

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 · see citing works

Mitochondrial DNA copy number in peripheral blood leukocytes and the aggressiveness of localized prostate cancer

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 · see citing works

Possible Formation of Mitochondrial-RNA Containing Chimeric or Trimeric RNA Implies a Post-Transcriptional and Post-Splicing Mechanism for RNA Fusion

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 31 · see citing works

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 32 · see citing works

A Protocol for the Parallel Isolation of Intact Mitochondria from Rat Liver, Kidney, Heart, and Brain

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 · see citing works

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 · see citing works

Association of mitochondrial DNA content in peripheral blood leukocyte with hepatitis B virus‐related hepatocellular carcinoma in a Chinese Han population

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 · see citing works

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 · see citing works

Fish consumption of harbour seals (Phoca vitulina) in north western Iceland assessed by DNA metabarcoding and morphological analysis

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 · see citing works

The unresolved role of mitochondrial DNA in Parkinson's disease: An overview of published studies, their limitations, and future prospects

Müller-Nedebock, A. C., Brennan, R. R., Venter, M., Pienaar, I. S., van der Westhuizen, F. H., Elson, J. L., Ross, O. A., & Bardien, S. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.104495 · Cited by 29 · see citing works

Mitochondrial DNA deletion and sarcopenia

Shah, V. O., Scariano, J., Waters, D. L., Qualls, C., Morgan, M., Pickett, G., Gasparovic, C., Dokładny, K., Moseley, P. L., & Raj, D. S. (2009) · Genetics in Medicine · doi:10.1097/gim.0b013e31819307a2 · Cited by 28 · see citing works

Extramitochondrial energy production in platelets

Ravera, S., Signorello, M. G., Bartolucci, M., Ferrando, S., Manni, L., Caicci, F., Calzia, D., Panfoli, I., Morelli, A. M., & Leoncini, G. (2018) · Biology of the Cell · doi:10.1111/boc.201700025 · Cited by 28 · see citing works

D-loop mutations in mitochondrial DNA: link with mitochondrial DNA depletion?

Barthélémy, C., de Baulny, H. O., & Lombès, A. (2002) · Human Genetics · doi:10.1007/s00439-002-0708-4 · Cited by 28 · see citing works

Mitochondrial DNA Mutation and Depletion Are Associated with Decline of Fertility and Motility of Human Sperm

Wei, Y., & Kao, S. (2000) · Zoological studies · Cited by 27 · see citing works

An in Situ Atlas of Mitochondrial DNA in Mammalian Tissues Reveals High Content in Stem and Proliferative Compartments

Chen, J., Zheng, Q., Peiffer, L. B., Hicks, J. L., Haffner, M. C., Rosenberg, A. Z., Levi, M., Wang, X. X., Özbek, B., Valle, J. A. B.-D., et al. (2020) · American Journal Of Pathology · doi:10.1016/j.ajpath.2020.03.018 · Cited by 26 · see citing works

Regional variation in mitochondrial DNA copy number in mouse brain

Fuke, S., Kubota‐Sakashita, M., Kasahara, T., Shigeyoshi, Y., & Kato, T. (2010) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2010.11.016 · Cited by 65 · see citing works

Mitochondrial genome copy number variation across tissues in mice and humans

Rath, S. P., Gupta, R., Todres, E. Z., Wang, H., Jourdain, A. A., Ardlie, K., Calvo, S. E., & Mootha, V. K. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2402291121 · Cited by 47 · see citing works

Tissue-specific mtDNA abundance from exome data and its correlation with mitochondrial transcription, mass and respiratory activity

D'Erchia, A. M., Atlante, A., Gadaleta, G., Pavesi, G., Chiara, M., De Virgilio, C., Manzari, C., Mastropasqua, F., Prazzoli, G. M., Picardi, E., et al. (2015) · Mitochondrion · doi:10.1016/j.mito.2014.10.005 · Cited by 197 · see citing works

Stereological examination of the mitochondrial configuration in selected rat's organs.

Cieciura, L., Rydzynski, K., & Klitończyk, W. (1979) · PubMed