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

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

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

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

The Hormetic Effect of Metformin: “Less Is More”?

Panfoli, I., Puddu, A., Bertola, N., Ravera, S., & Maggi, D. C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126297 · Cited by 29

In Cold Blood: Compositional Bias and Positive Selection Drive the High Evolutionary Rate of Vampire Bats Mitochondrial Genomes

Botero-Castro, F., Tilak, M., Justy, F., Catzeflis, F. M., Delsuc, F., & Douzery, E. (2018) · Genome Biology and Evolution · doi:10.1093/gbe/evy120 · Cited by 29

Results of the 2003–2004 GEP-ISFG collaborative study on mitochondrial DNA: Focus on the mtDNA profile of a mixed semen-saliva stain

Crespillo, M., Paredes, M. R., Prieto, L., Montesino, M., Salas, A., Albarrán, C., Álvarez‐Iglesias, V., Amorin, A., Berniell‐Lee, G., Brehm, A., et al. (2005) · Forensic Science International · doi:10.1016/j.forsciint.2005.09.005 · Cited by 26

All together now: Limitations and recommendations for the simultaneous analysis of all eukaryotic soil sequences

Jurburg, S. D., Keil, P., Singh, B. K., & Chase, J. M. (2021) · Molecular Ecology Resources · doi:10.1111/1755-0998.13401 · Cited by 28

Association of Mitochondrial DNA Copy Number and Telomere Length with Prevalent and Incident Cancer and Cancer Mortality in Women: A Prospective Swedish Population-Based Study

Li, Y., Sundquist, K., Wang, X., Zhang, N., Hedelius, A., Sundquist, J., & Memon, A. A. (2021) · Cancers · doi:10.3390/cancers13153842 · Cited by 26

Lower mitochondrial DNA copy number in peripheral blood leukocytes increases the risk of endometrial cancer

Sun, Y., Zhang, L., Ho, S. S., Wu, X., & Gu, J. H. (2015) · Molecular Carcinogenesis · doi:10.1002/mc.22373 · Cited by 25

Mitochondrial DNA copy number in whole blood and glioma risk: A case control study

Shen, J., Song, R., Lu, Z., & Zhao, H. (2016) · Molecular Carcinogenesis · doi:10.1002/mc.22453 · Cited by 25

Alignment-free approaches for predicting novel Nuclear Mitochondrial Segments (NUMTs) in the human genome

Li, W., Freudenberg, J., & Freudenberg, J. (2019) · Gene · doi:10.1016/j.gene.2018.12.040 · Cited by 25

Association of leukocyte mitochondrial DNA content with glioma risk: evidence from a Chinese case–control study

Zhang, J., Li, D., Qu, F., Chen, Y., Li, G., Jiang, H., Huang, X., Yang, H., & Xing, J. (2014) · BMC Cancer · doi:10.1186/1471-2407-14-680 · Cited by 24

Effect of methanol and Me2SO exposure on mitochondrial activity and distribution in stage III ovarian follicles of zebrafish (Danio rerio)

Zampolla, T., Spikings, E. C., Zhang, T., & Rawson, D. M. (2009) · Cryobiology · doi:10.1016/j.cryobiol.2009.07.002 · Cited by 24

Five non-mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes phenotype adult patients with m.3243A>G mutation after kidney transplantation: follow-up and review of the literature

de Laat, P., van Engelen, N., Wetzels, J. F. M., Smeitink, J. A. M., & Janssen, M. C. H. (2019) · Clinical Kidney Journal · doi:10.1093/ckj/sfz020 · Cited by 23

Loss of the antioxidant enzyme CuZnSOD (Sod1) mimics an age-related increase in absolute mitochondrial DNA copy number in the skeletal muscle

Masser, D. R., Clark, N. W., Remmen, H. V., & Freeman, W. M. (2016) · AGE · doi:10.1007/s11357-016-9930-1 · Cited by 24

Target enrichment of metazoan mitochondrial DNA with hybridization capture probes

Sevigny, J. L., Leasi, F., Simpson, S., Domênico, M. D., Jörger, K. M., Norenburg, J. L., & Thomas, W. K. (2020) · Ecological Indicators · doi:10.1016/j.ecolind.2020.106973 · Cited by 23

Support of Nerve Conduction by Respiring Myelin Sheath: Role of Connexons

Ravera, S., Bartolucci, M., Adriano, E., Garbati, P., Ferrando, S., Ramoino, P., Calzia, D., Morelli, A. M., Balestrino, M., & Panfoli, I. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9216-0 · Cited by 23

Perinatal maturation of rat kidney mitochondria

Prieur, B., Cordeau‐Lossouarn, L., Rötig, A., Bismuth, J., Geloso, J. P., & Delaval, E. (1995) · Biochemical Journal · doi:10.1042/bj3050675 · Cited by 23

Why to compare absolute numbers of mitochondria

Schmitt, S., Schulz, S., Schropp, E.-M., Eberhagen, C., Simmons, A., Beisker, W., Aichler, M., & Zischka, H. (2014) · Mitochondrion · doi:10.1016/j.mito.2014.06.005 · Cited by 22

Increased leukocyte mitochondrial DNA copy number is associated with oral premalignant lesions: an epidemiology study

He, Y., Gong, Y., Gu, J. H., Lee, J. J., Lippman, S. M., & Wu, X. (2014) · Carcinogenesis · doi:10.1093/carcin/bgu093 · Cited by 22

Selective DNA amplification regulates transcript levels in plant mitochondria

Muise, R. C., & Hauswirth, W. W. (1995) · Current Genetics · doi:10.1007/bf00315776 · Cited by 22

Properties of porcine white adipose tissue and liver mitochondrial subpopulations

Koekemoer, T., & Oelofsen, W. (2001) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/s1357-2725(01)00064-4 · Cited by 22

Myelination increases chemical energy support to the axon without modifying the basic physicochemical mechanism of nerve conduction

Ravera, S., Morelli, A. M., & Panfoli, I. (2020) · Neurochemistry International · doi:10.1016/j.neuint.2020.104883 · Cited by 21

Evaluation of the Acquisition of the Aerobic Metabolic Capacity by Myelin, during its Development

Ravera, S., Bartolucci, M., Garbati, P., Ferrando, S., Calzia, D., Ramoino, P., Balestrino, M., Morelli, A. M., & Panfoli, I. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9575-6 · Cited by 20

Mitochondrial DNA copy number in peripheral blood cell and hypertension risk among mining workers: a case–control study in Chinese coal miners

Lei, L., Guo, J., Shi, X., Zhang, G., Kang, H., Sun, C., Huang, J. L., & Wang, T. (2017) · Journal of Human Hypertension · doi:10.1038/jhh.2017.30 · Cited by 19

Avoiding Extinction: Recent Advances in Understanding Mechanisms of Mitochondrial DNA Purifying Selection in the Germline

Jeedigunta, S. P., Minenkova, A. V., Palozzi, J. M., & Hurd, T. R. (2021) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-121420-081805 · Cited by 19

Phenotype instability of hepatocyte-like cells produced by direct reprogramming of mesenchymal stromal cells

Orge, I. D., Gadd, V. L., Barouh, J. L., Rossi, E. A., Carvalho, R. H., Smith, I. P., Allahdadi, K. J., Paredes, B. D., Silva, D. N., Damasceno, P. K. F., et al. (2020) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-01665-z · Cited by 19

Mitochondrial DNA copy number in peripheral blood leukocytes is associated with biochemical recurrence in prostate cancer patients in African Americans

Xu, J., CHANG, W.-S., Tsai, C.-W., Bau, D., Davis, J. W., Thompson, T. C., Logothetis, C. J., & Gu, J. H. (2019) · Carcinogenesis · doi:10.1093/carcin/bgz139 · Cited by 18

Mitochondria in Early Life

He, L., & Maheshwari, A. (2022) · Current Pediatric Reviews · doi:10.2174/1573396319666221221110728 · Cited by 17

A Cell Culture Model of BK Polyomavirus Persistence, Genome Recombination, and Reactivation

Zhao, L., & Imperiale, M. J. (2021) · mBio · doi:10.1128/mbio.02356-21 · Cited by 18

Emerging methods for and novel insights gained by absolute quantification of mitochondrial DNA copy number and its clinical applications

Li, B., Kalinowski, P., Kim, B., Pauls, A. D., & Poburko, D. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107995 · Cited by 19

Spectrum of mitochondrial genome instability and implication of mitochondrial haplogroups in Korean patients with acute myeloid leukemia

Kim, H. R., Kang, M.-G., Lee, Y. E., Na, B. R., Noh, M. S., Yang, S. H., Shin, J. H., & Shin, M.-G. (2018) · Blood Research · doi:10.5045/br.2018.53.3.240 · Cited by 18

Identification of Biochemical and Molecular Markers of Early Aging in Childhood Cancer Survivors

Ravera, S., Vigliarolo, T., Bruno, S., Morandi, F., Marimpietri, D., Sabatini, F., Dagnino, M., Petretto, A., Bartolucci, M., Muraca, M., et al. (2021) · Cancers · doi:10.3390/cancers13205214 · Cited by 17

Circulating Cell-Free mtDNA Content as a Non-invasive Prognostic Biomarker in HCC Patients Receiving TACE and Traditional Chinese Medicine

Zhou, G., Li, Y., Li, S., Liu, H., Xu, F., Lai, X., Zhang, Q., Xu, J., & Wan, S. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.719451 · Cited by 17

Quantifying compartment‐associated variations of protein abundance in proteomics data

Parca, L., Beck, M., Bork, P., & Ori‬‬, A. (2018) · Molecular Systems Biology · doi:10.15252/msb.20178131 · Cited by 16

Bioenergetics: the evolutionary basis of progressive kidney disease

Chevalier, R. L. (2023) · Physiological Reviews · doi:10.1152/physrev.00029.2022 · Cited by 17

Optical spectroscopy for in-vitro differentiation of pediatric neoplastic and epileptogenic brain lesions

Lin, W., Sandberg, D. I., Bhatia, S., Johnson, M. D., Morrison, G., & Ragheb, J. R. (2009) · Journal of Biomedical Optics · doi:10.1117/1.3080144 · Cited by 16

Oligodendrocyte N-Methyl-d-aspartate Receptor Signaling: Insights into Its Functions

Cao, N., & Yao, Z. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8408-8 · Cited by 16

Mitochondrial gene expression in different organs of Hoplobatrachus rugulosus from China and Thailand under low-temperature stress

Jin, W.-T., Guan, J.-Y., Dai, X.-Y., Wu, G.-J., Zhang, L., Storey, K. B., Zhang, J., Zheng, R., & Yu, D. (2022) · BMC Zoology · doi:10.1186/s40850-022-00128-7 · Cited by 15

Blood from a turnip: tissue origin of low-coverage shotgun sequencing libraries affects recovery of mitogenome sequences

Barker, F. K., Oyler‐McCance, S. J., & Tomback, D. F. (2013) · Mitochondrial DNA · doi:10.3109/19401736.2013.840588 · Cited by 15

Identification of horse, donkey and pig ingredients by species-specific ERA-based methods to assess the authenticity of meat products

Zhou, C., Liu, L., Xiang, J., Fu, Q., Wang, J., Wang, K., Sun, X., Ai, L., Sun, X., & Wang, J. (2023) · Food Bioscience · doi:10.1016/j.fbio.2023.102827 · Cited by 14

Biochemical properties of porcine white adipose tissue mitochondria and relevance to fatty acid oxidation

Koekemoer, T., & Oelofsen, W. (2001) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/s1096-4959(01)00398-0 · Cited by 14

Mitochondrial DNA copy number mediated the associations between perfluoroalkyl substances and breast cancer incidence: A prospective case-cohort study

Feng, Y., You, Y., Li, M., Guan, X., Fu, M., Wang, C., Xiao, Y., He, M., & Guo, H. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.173767 · Cited by 13

Mitochondrial DNA copy number is modulated by genetic variation in the signal transducer and activator of transcription 3 (STAT3)

Gianotti, T. F., Castaño, G. O., Gemma, C., Burgueño, A. L., Rosselli, M. S., Pirola, C. J., & Sookoian, S. C. (2011) · Metabolism · doi:10.1016/j.metabol.2010.12.008 · Cited by 13

Paranodal Schwann cell mitochondria in spinal roots of the cat. An ultrastructural morphometric analysis

Rydmark, M., Berthold, C., & Gatzinsky, K. P. (1998) · Journal of Neurocytology · doi:10.1023/a:1006995205504 · Cited by 12

Hepatic Progenitor Cell Lines from Allyl Alcohol‐Treated Adult Rats Are Derived from γ‐Irradiated Mouse STO Cells

Zhang, M., Sell, S., & Leffert, H. L. (2003) · Stem Cells · doi:10.1634/stemcells.21-4-449 · Cited by 12

A novel mitochondrial DNA missense mutation at G3421A in a family with maternally inherited diabetes and deafness

Chen, F. L., Liu, Y., Song, X. Y., Hu, H., Xu, H., Zhang, X. M., Shi, J. H., Hu, J., Shen, Y., Lu, B., et al. (2006) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2006.07.006 · Cited by 11

Metabolism and DNA repair shape a specific modification pattern in mitochondrial DNA

Pawar, T., Bjørås, M., Klungland, A., & Eide, L. (2017) · Mitochondrion · doi:10.1016/j.mito.2017.09.002 · Cited by 10

Association between pre-diagnostic leukocyte mitochondrial DNA copy number and survival among colorectal cancer patients

Yang, K., Forman, M. R., Graham, B. H., Monahan, P. O., Giovannucci, E. L., Vivo, I. D., Chan, A. T., & Nan, H. (2020) · Cancer Epidemiology · doi:10.1016/j.canep.2020.101778 · Cited by 11

Mitochondrial Dynamics during Development

Maheshwari, A., He, L., & Tronstad, K. J. (2023) · Newborn · doi:10.5005/jp-journals-11002-0053 · Cited by 10

Forecasting Cell Death Dose-Response from Early Signal Transduction Responses In Vitro

Vrana, J. A., Currie, H. N., Han, A. A., & Boyd, J. W. (2014) · Toxicological Sciences · doi:10.1093/toxsci/kfu089 · Cited by 10

Statistical Mitogenome Assembly with RepeaTs

Alqahtani, F., & Măndoiu, I. (2020) · Journal of Computational Biology · doi:10.1089/cmb.2019.0505 · Cited by 12

PCR-select subtraction for characterization of messages differentially expressed in brown compared with white adipose tissue

Kajimoto, K., Daikoku, T., Kita, F., Yamazaki, N., Kataoka, M., Baba, Y., Terada, H., & Shinohara, Y. (2003) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2003.08.006 · Cited by 10

α-Linolenic acid promotes testosterone synthesis by improving mitochondrial function in primary rooster Leydig cells

Chang, X., Li, D., Guo, Y. X., Sheng, X., Wang, X., Xing, K., Xiao, L., Lv, X., Long, C., & Qi, X. (2024) · Theriogenology · doi:10.1016/j.theriogenology.2024.10.026 · Cited by 9

Geometries of vasculature bifurcation can affect the level of trophic damage during formation of a brain ischemic lesion

Nartsissov, Y. R. (2017) · Biochemical Society Transactions · doi:10.1042/bst20160418 · Cited by 9

Social affiliation predicts mitochondrial DNA copy number in female rhesus macaques

Debray, R., Snyder‐Mackler, N., Kohn, J. N., Wilson, M. E., Barreiro, L. B., & Tung, J. (2019) · Biology Letters · doi:10.1098/rsbl.2018.0643 · Cited by 10

Calcium Regulation of Mitochondrial Metabolism

Mannella, C. A., Swietach, P., & Boyman, L. (2025) · Annual Review of Physiology · doi:10.1146/annurev-physiol-052424-082740 · Cited by 8

Clinical utility of whole genome sequencing for the detection of mitochondrial genome mutations

Husami, A., Slone, J. D., Brown, J., Bromwell, M., Valencia, C. A., & Huang, T. (2020) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2020.03.001 · Cited by 8

Mitochondrial DNA analysis of the putative skeletal remains of Sieur de Marle: Genetic support for anthropological assessment of biogeographic ancestry

Ambers, A., Elwick, K. E., Cropper, E., Brandhagen, M. D., Jones, B. M., Durst, J. J., Gilmore, K. K., Bruseth, J. E., & Gill-King, H. (2021) · Forensic Science International · doi:10.1016/j.forsciint.2021.110682 · Cited by 8

Selection of stable reference genes for quantitative real‐time PCR in the Varroa mite, Varroa destructor

Lee, J.-H., Kim, Y. H., Kim, K., Kim, D., Lee, S. H., & Kim, S. (2022) · Archives of Insect Biochemistry and Physiology · doi:10.1002/arch.21905 · Cited by 8

SMART2: Multi-library Statistical Mitogenome Assembly with Repeats

Alqahtani, F., & Măndoiu, I. (2020) · Lecture notes in computer science · doi:10.1007/978-3-030-46165-2_15 · Cited by 8

Immunocytochemical Localization of Mitochondrial Single-Stranded DNA-Binding Protein in Mitochondria-rich Cells of Normal and Neoplastic Human Tissue

Müller-Höcker, J., Schäfer, S., & Li, K. (2001) · Applied immunohistochemistry & molecular morphology · doi:10.1097/00129039-200109000-00013 · Cited by 8

Biomaterial design strategies for enhancing mitochondrial transplantation therapy

Kang, S., Zhang, Y., Li, H., Peng, S., Lyu, D., Zhou, C., Ding, S., Feng, Z., Huang, P., Zhang, C., et al. (2025) · BMEMat · doi:10.1002/bmm2.70046 · Cited by 8

High leukocyte mitochondrial DNA copy number contributes to poor prognosis in breast cancer patients

Zhang, W., Lin, S., Zeng, B., Chen, X., Chen, L., Chen, M., Guo, W., Lin, Y., Yu, L., Hou, J., et al. (2023) · BMC Cancer · doi:10.1186/s12885-023-10838-x · Cited by 7

Evaluation of critical design parameters for RT‐qPCR‐based analysis of multiple dUTPase isoform genes in mice

Rácz, G. A., Nagy, N. T., Gál, Z., Pintér, T., Hiripi, L., & Vértessy, B. G. (2019) · FEBS Open Bio · doi:10.1002/2211-5463.12654 · Cited by 7

Lifespan Development, Instability, and Waddington’s Epigenetic Landscape

Hollar, D. (2016) · Springer eBooks · doi:10.1007/978-3-319-25325-1_16 · Cited by 6

Exploring the Role of Cell-Free Nucleic Acids and Peritoneal Dialysis: A Narrative Review

Morisi, N., Virzì, G. M., Ferrarini, M., Alfano, G., Zanella, M., Ronco, C., & Donati, G. (2024) · Genes · doi:10.3390/genes15050553 · Cited by 8

Mitochondrial DNA Copy Number Variations in Gastrointestinal Tract Cancers: Potential Players

Alikhani, M., Touati, E., Karimipoor, M., Vosough, M., & Mohammadi, M. (2021) · Journal of Gastrointestinal Cancer · doi:10.1007/s12029-021-00707-w · Cited by 5

Mitochondrial Abundance and Function Differ Across Muscle Within Species

Yen, C., Bodmer, J. S., Wicks, J. C., Zumbaugh, M. D., Persia, M. E., Shi, T. H., & Gerrard, D. E. (2024) · Metabolites · doi:10.3390/metabo14100553 · Cited by 5

Measure quantity of mitochondrial DNA in aged bones or calculate it from nuclear DNA quantitative PCR results?

Obal, M., Zupanc, T., & Pajnič, I. Z. (2023) · International Journal of Legal Medicine · doi:10.1007/s00414-023-03074-2 · Cited by 6

Functional foods and cognition

Scholey, A. B., Camfield, D., Owen, L., Pipingas, A., & Stough, C. K. K. (2011) · Elsevier eBooks · doi:10.1533/9780857092557.2.277 · Cited by 5

In Vitro and In Vivo Structure–Property Relationship of 68Ga-Labeled Schiff Base Derivatives for Functional Myocardial PET Imaging

Thews, O., Zimny, M., Eppard, E., Piel, M., Bausbacher, N., Nagel, V., & Rösch, F. (2014) · Molecular Imaging and Biology · doi:10.1007/s11307-014-0750-3 · Cited by 5

A mechanism for the loss of cytochrome P-450 in primary mouse hepatocytes

Singh, G., & Veltri, K. L. (1991) · Molecular and Cellular Biochemistry · doi:10.1007/bf00233120 · Cited by 5

Mitochondrial DNA Mutations, Pathogenicity and Inheritance

Houshmand, M. (2003) · Gothenburg University Publications Electronic Archive (Gothenburg University) · Cited by 5

Hypothalamic and amygdalar cell lines differ markedly in mitochondrial rather than nuclear encoded gene expression

Dalwadi, D. A., & Uht, R. M. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-413 · Cited by 4

Exercise and the Mitochondria

Gidlund, E. (2019) · Springer eBooks · doi:10.1007/978-3-030-04816-7_3 · Cited by 4

Tissue-specific heteroplasmy segregation is accompanied by a sharp mtDNA decline in Caenorhabditis elegans soma

Tsyba, N., Feng, G., Grub, L. K., Held, J. P., Strozak, A. M., Burkewitz, K., & Patel, M. R. (2023) · iScience · doi:10.1016/j.isci.2023.106349 · Cited by 4

Tissue specificity of energy metabolism in mitochondria

Moreno‐Loshuertos, R., & Fernández‐Silva, P. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819621-2.00001-2 · Cited by 4

Mitochondrial genome deletions in the brain and their role in neurodegenerative diseases

Merril, C. R., & Zullo, S. (1995) · International Review of Psychiatry · doi:10.3109/09540269509022989 · Cited by 4

Effects of differentiation of embryonal carcinoma cells (P19) on mitochondrial DNA content in vitro

Singh, G., & Veltri, K. L. (1991) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/bf02631286 · Cited by 4

Mitochondria in smooth muscle cells of viscera

Gabella, G. (2018) · Journal of Smooth Muscle Research · doi:10.1540/jsmr.54.51 · Cited by 3

Mitochondrial Dysfunction and Cancer

한유선, 제갈명은, & Kim, Y. J. (2019) · JoLS Journal of Life Sciences · doi:10.5352/jls.2019.29.9.1034 · Cited by 3

Accumulated mtDNA mutations are linked to specific impairments in NADH-linked respiration

Franczak, E., Montgomery, M. M., Terwilliger, Z. S., Aruleba, R. T., Krassovskaia, P. M., Boykov, I. N., Hagen, J. T., Pacheco, E. A., Chrest, B. R., Zeczycki, T. N., et al. (2026) · iScience · doi:10.1016/j.isci.2026.115184 · Cited by 2

Mitochondrial DNA copy number is not associated with fatigue status in Primary Sjögren’s Syndrome

de Menezes, E. C. S., Brown, A. E., Bowman, S., Mirza, K., Newton, J. L., Ng, W., & Elson, J. L. (2018) · Fatigue Biomedicine Health & Behavior · doi:10.1080/21641846.2018.1486799 · Cited by 2

Metabolomics in the Study of Human Mitochondrial Diseases

Sebaa, R., Harper, M., Altassan, R., Al‐Owain, M. A., & Rahman, A. M. A. (2023) · Springer eBooks · doi:10.1007/978-981-99-5162-8_7 · Cited by 2

Tissue‐specific differences in Ca2+ sensitivity of the mitochondrial permeability transition pore (PTP). Experiments in male rat liver and heart

Ricardez-García, C., Reyes‐Becerril, M., Mosqueda-Martínez, E., Méndez-Romero, O. A., Ruiz‐Ramírez, A., & Uribe‐Carvajal, S. (2024) · Physiological Reports · doi:10.14814/phy2.16056 · Cited by 2

Utility of melatonin on brain injury, synaptic transmission, and energy metabolism in rats with sepsis

Ates, G., Tamer, Ş., Özkök, E., Yorulmaz, H., Gündoğan, G. İ., Aksu, A., & Balkıs, N. Ç. (2024) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-024-03337-8 · Cited by 2

Current Methods for the Prevention of Transmission of Mitochondrial DNA Diseases

Turner, K. A. (2014) · Journal of Molecular and Genetic Medicine · doi:10.4172/1747-0862.1000127 · Cited by 2

Mitochondrial DNA Dosage Effects in Triploid Grass Carp

Anderson, J. (2010) · North American Journal of Aquaculture · doi:10.1577/a09-052.1 · Cited by 2

Mitochondrial Biogenesis and Quality Control

Mears, J. A. (2014) · Advances in photosynthesis and respiration · doi:10.1007/978-94-017-8742-0_24 · Cited by 2

Statistical Mitogenome Assembly with Repeats

Alqahtani, F., & Măndoiu, I. (2018) · IEEE International Conference on Computational Advances in Bio and Medical Sciences · doi:10.1109/iccabs.2018.8542062 · Cited by 2

Mitochondria as the memory of preconditioning.

Zerimech, S., Nguyen, H., & Baltan, S. (2021) · PubMed · Cited by 2

Quantitative mitochondrial DNA copy number determination using droplet digital PCR with single cell resolution: a focus on aging and cancerPreprint

O’Hara, R. A., Tedone, E., Ludlow, A. T., Huang, E. E., Arosio, B., Mari, D., & Shay, J. W. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/579789 · Cited by 2

Mitochondrial lipidome's fatty acid profile and peroxidation index are programmed tissue-specific traits

Mota‐Martorell, N., Fernàndez‐Bernal, A., Sol, J., Santacreu-Vilaseca, M., Juanes-Casado, A., Portero‐Otín, M., Jové, M., & Pamplona, R. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103850 · Cited by 1

Inter- and intraspecific variability in the copy number of mitochondria in rodents from different elevations of the Ethiopian Highlands

Pavlíčková, B., Bryjová, A., Žák, J., Boratyński, Z., Lavrenchenko, L. A., & Bryja, J. (2025) · Folia Zoologica · doi:10.25225/jvb.25063 · Cited by 1

Role of Mitochondria in Epilepsy

Houshmand, M. (2011) · InTech eBooks · doi:10.5772/19547 · Cited by 1

Physiopathologie des maladies mitochondriales

Lombès, A., Auré, K., & Jardel, C. (2015) · Biologie Aujourd hui · doi:10.1051/jbio/2015014 · Cited by 1

Herbal Extracts and Cognition in Adulthood and Ageing

Camfield, D., Owen, L., Pipingas, A., Stough, C. K. K., & Scholey, A. B. (2012) · doi:10.1007/978-1-137-00689-9_15 · Cited by 2

SMART: Statistical Mitogenome Assembly with RepeatsPreprint

Alqahtani, F., & Măndoiu, I. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/795633 · Cited by 1

Sequence variation characteristics of D-loop, rRNA, tRNA, and polypeptide coding region of bovine mitochondrial DNA

Wu, J. (1995) · doi:10.31274/rtd-180813-10138 · Cited by 1

RNA Chimeras as a Gene Signature of Breast Cancer

Liao, D. J. (2013) · Defense Technical Information Center (DTIC) · doi:10.21236/ada582144

Bovine mammary interleukin-8 receptor expression and genetic association with Streptococcus uberis based mastitis.

Siebert, L. J. (2013)

NRTIs’ effect on the sequence of mitochondrial DNA HV 2 in HIV infected patients

Wu, Y., Chen, X., Shi, Y., Wu, H., Chen, D., Sun, Y., & Zhang, F. (2010) · Frontiers of Medicine · doi:10.1007/s11684-010-0038-1

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

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 62

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 52

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

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

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