Effects of Aging on Mitochondrial DNA Copy Number and Cytochromec Oxidase Gene Expression in Rat Skeletal Muscle, Liver, and Heart

Molecular cloning: A laboratory manual

Deininger, P. L. (1990) · Analytical Biochemistry · doi:10.1016/0003-2697(90)90595-z · Cited by 84,684

tRNA punctuation model of RNA processing in human mitochondria

Ojala, D., Montoya, J., & Attardi, G. M. (1981) · Nature · doi:10.1038/290470a0 · Cited by 2,561

Adaptations of skeletal muscle to endurance exercise and their metabolic consequences

Holloszy, J. O., & Coyle, E. F. (1984) · Journal of Applied Physiology · doi:10.1152/jappl.1984.56.4.831 · Cited by 1,985

The aging process

Harman, D. (1981) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.78.11.7124 · Cited by 1,915

Mitochondrial Genetics: A Paradigm for Aging and Degenerative Diseases?

Wallace, D. C. (1992) · Science · doi:10.1126/science.1533953 · Cited by 1,262

Muscle fiber type composition of the rat hindlimb

Armstrong, R. B., & Phelps, R. O. (1984) · American Journal of Anatomy · doi:10.1002/aja.1001710303 · Cited by 1,004

Cardiovascular regulatory mechanisms in advanced age.

Lakatta, E. G. (1993) · Physiological Reviews · doi:10.1152/physrev.1993.73.2.413 · Cited by 791

Decline in skeletal muscle mitochondrial respiratory chain function: possible factor in ageing

Trounce, I., Byrne, E., & Marzuki, S. (1989) · The Lancet · doi:10.1016/s0140-6736(89)92143-0 · Cited by 730

Effect of age on in vivo rates of mitochondrial protein synthesis in human skeletal muscle

Rooyackers, O. E., Adey, D. B., Ades, P. A., & Nair, K. S. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.26.15364 · Cited by 564

Regulation in Metabolism

Karlson, P. (1974) · Biochemical Education · doi:10.1016/0307-4412(74)90015-6 · Cited by 541

Fiber Type-Specific Differences in Glucose Uptake by Single Fibers From Skeletal Muscles of 9- and 25-Month-Old Rats

MacKrell, J. G., Arias, E. B., & Cartee, G. D. (2012) · The Journals of Gerontology Series A · doi:10.1093/gerona/gls194 · Cited by 25

Mitochondrial DNA deletions and differential mitochondrial DNA content in Rhesus monkeys: Implications for aging

Mao, P., Gallagher, P., Nedungadi, S., Mańczak, M., Shirendeb, U. P., Kohama, S. G., Ferguson, B. M., Park, B. S., & Reddy, P. H. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.10.014 · Cited by 26

Historical perspective of matrix metalloproteases

Pulkoski-Gross, A. E. (2015) · Frontiers in Bioscience-Scholar · doi:10.2741/s429 · Cited by 24

Downregulation of ALAS1 by nicarbazin treatment underlies the reduced synthesis of protoporphyrin IX in shell gland of laying hens

Samiullah, S., Roberts, J. R., & Wu, S. (2017) · Scientific Reports · doi:10.1038/s41598-017-06527-y · Cited by 23

Mitochondrial DNA copy number associates with insulin sensitivity and aerobic capacity, and differs between sedentary, overweight middle-aged males with and without type 2 diabetes

Constantin‐Teodosiu, D., Constantin, D., Pelsers, M. M. A. L., Verdijk, L. B., van Loon, L. J. C., & Greenhaff, P. L. (2019) · International Journal of Obesity · doi:10.1038/s41366-019-0473-2 · Cited by 22

Heterochronic Parabiosis: Old Blood Induces Changes in Mitochondrial Structure and Function of Young Mice

Gonzalez-Armenta, J. L., Li, N., Lee, R.-L., Lu, B., & Molina, A. J. A. (2020) · The Journals of Gerontology Series A · doi:10.1093/gerona/glaa299 · Cited by 23

Sexual Dimorphism in the Alterations of Cardiac Muscle Mitochondrial Bioenergetics Associated to the Ageing Process

Colom, B., Oliver, J., & García-Palmer, F. (2014) · The Journals of Gerontology Series A · doi:10.1093/gerona/glu014 · Cited by 22

Antioxidant pathways in human aged skeletal muscle: relationship with the distribution of type II fibers

Pansarasa, O., Felzani, G., Vecchiet, J., & Marzatico, F. (2002) · Experimental Gerontology · doi:10.1016/s0531-5565(02)00085-2 · Cited by 26

The Age-Sensitive Efficacy of Calorie Restriction on Mitochondrial Biogenesis and mtDNA Damage in Rat Liver

Chimienti, G., Picca, A., Fracasso, F., Russo, F., Orlando, A., Riezzo, G., Leeuwenburgh, C., Pesce, V., & Lezza, A. M. S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041665 · Cited by 24

Increased transcription of mitochondrial genes for Complex I in human platelets during ageing

Pich, M. M., Raule, N., Catani, L., Fagioli, M. E., Faenza, I., Cocco, L., & Lenaz, G. (2004) · FEBS Letters · doi:10.1016/s0014-5793(03)01520-5 · Cited by 22

The “fast” and the “slow” modes of mitochondrial DNA degradation

Shokolenko, I. N., Wilson, G. L., & ALEXEYEV, M. F. (2014) · Mitochondrial DNA Part A · doi:10.3109/19401736.2014.905829 · Cited by 22

Effects of hydrogen peroxide on mitochondrial gene expression of intestinal epithelial cells

Li, J. (2002) · World Journal of Gastroenterology · doi:10.3748/wjg.v8.i6.1117 · Cited by 22

Bioenergetics of the aging heart and skeletal muscles: Modern concepts and controversies

Tepp, K., Timohhina, N., Puurand, M., Klepinin, A., Chekulayev, V., Shevchuk, I., & Kaambre, T. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2016.04.001 · Cited by 21

CYB5R3 overexpression preserves skeletal muscle mitochondria and autophagic signaling in aged transgenic mice

Lopez-Bellón, S., Rodríguez-López, S., González-Reyes, J. A., Burón, M. I., de Cabo, R., & Villalba, J. M. (2022) · GeroScience · doi:10.1007/s11357-022-00574-8 · Cited by 19

Effect of aerobic exercise on mitochondrial DNA and aging

Eluamai, A., & Brooks, K. A. (2013) · Journal of Exercise Science & Fitness · doi:10.1016/j.jesf.2013.03.003 · Cited by 20

Effect of methionine supplementation on mitochondrial genes expression in the breast muscle and liver of broilers

Vesco, A. P. D., Gasparino, E., Neto, A. R. O., Rossi, R. M., Soares, M. A. M., & da Silva, S. C. C. (2012) · Livestock Science · doi:10.1016/j.livsci.2012.11.005 · Cited by 20

The Association of Mitochondrial Content with Prevalent and Incident Type 2 Diabetes

Reiling, E., Ling, C., Uitterlinden, A. G., Riet, E. V. ‘., Welschen, L. M. C., Ladenvall, C., Almgren, P., Lyssenko, V., Nijpels, G., van Hove, E. C., et al. (2010) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2009-1775 · Cited by 20

Bioenergetic Changes during Differentiation of Human Embryonic Stem Cells along the Hepatic Lineage

Hopkinson, B. M., Desler, C., Kalisz, M., Vestentoft, P. S., Rasmussen, L. J., & Bisgaard, H. C. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/5080128 · Cited by 20

A ketogenic diet impacts markers of mitochondrial mass in a tissue specific manner in aged mice

Zhou, Z., Hagopian, K., López-Domínguez, J. A., Kim, K., Jasoliya, M., Roberts, M. N., Cortopassi, G. A., Showalter, M. R., Roberts, B. S., González-Reyes, J. A., et al. (2021) · Aging · doi:10.18632/aging.202834 · Cited by 19

Mitochondrial genomic variation associated with higher mitochondrial copy number: the Cache County Study on Memory Health and Aging

Ridge, P. G., Maxwell, T. J., Foutz, S. J., Bailey, M. H., Corcoran, C. D., Tschanz, J. T., Norton, M. C., Munger, R. G., O’Brien, E., Kerber, R. A., et al. (2014) · BMC Bioinformatics · doi:10.1186/1471-2105-15-s7-s6 · Cited by 19

Potential functionality of β-conglycinin with subunit deficiencies: soy protein may regulate glucose and lipid metabolism

Fu, H., Shan, D., Li, J., Swallah, M. S., Yang, X., Ji, L., Wang, S., Gong, H., Lyu, B., & Yu, H. (2022) · Food & Function · doi:10.1039/d2fo02869g · Cited by 19

Mitochondrial biogenesis in organismal senescence and neurodegeneration

Daskalaki, I., & Tavernarakis, N. (2020) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2020.111345 · Cited by 18

The Aging Athlete: Part 1, ???Boomeritis??? of the Lower Extremity

Prescott, J. W., & Yu, J. S. (2012) · American Journal of Roentgenology · doi:10.2214/ajr.12.8912 · Cited by 19

More from less: Genome skimming for nuclear markers for animal phylogenomics, a case study using decapod crustaceans

Tan, M. H., Gan, H. M., Bracken‐Grissom, H. D., Chan, T., Grandjean, F., & Austin, C. M. (2021) · Journal of Crustacean Biology · doi:10.1093/jcbiol/ruab009 · Cited by 18

Age and Diet Affect Gene Expression Profile in Canine Skeletal Muscle

Middelbos, I. S., Vester, B. M., Karr‐Lilienthal, L. K., Schook, L. B., & Swanson, K. S. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004481 · Cited by 18

Myostatin expression is not altered by insulin deficiency and replacement in streptozotocin-diabetic rat skeletal muscles

Barazzoni, R., Zanetti, M., Bosutti, A., Stebel, M., Cattin, L., Biolo, G., & Guarnieri, G. (2004) · Clinical Nutrition · doi:10.1016/j.clnu.2004.06.007 · Cited by 18

The Mitochondrial Proteomic Signatures of Human Skeletal Muscle Linked to Insulin Resistance

Kruse, R., Sahebekhtiari, N., & Højlund, K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155374 · Cited by 19

Tissue and data archives from irradiation experiments conducted at Argonne National Laboratory over a period of four decades

Wang, Q., Paunesku, T., & Woloschak, G. E. (2010) · Radiation and Environmental Biophysics · doi:10.1007/s00411-010-0270-8 · Cited by 17

Mitochondrial Respiration Is Decreased in Rat Kidney Following Fetal Exposure to a Maternal Low-Protein Diet

Engeham, S., Mdaki, K. S., Jewell, K., Austin, R., Lehner, A. N., & Langley‐Evans, S. C. (2012) · Journal of Nutrition and Metabolism · doi:10.1155/2012/989037 · Cited by 17

Whole-Body Vibration Partially Reverses Aging-Induced Increases in Visceral Adiposity and Hepatic Lipid Storage in Mice

Reijne, A. C., Čiapaitė, J., van Dijk, T. H., Havinga, R., van der Zee, E. A., Groen, A. K., Reijngoud, D., Bakker, B. M., & van Dijk, G. (2016) · PLoS ONE · doi:10.1371/journal.pone.0149419 · Cited by 17

Glucocorticoid receptor is involved in the breed-dependent transcriptional regulation of mtDNA- and nuclear-encoded mitochondria genes in the liver of newborn piglets

Li, R., Zou, H., Jia, Y., & Zhao, R. (2013) · BMC Veterinary Research · doi:10.1186/1746-6148-9-87 · Cited by 16

Fish Models for Exploring Mitochondrial Dysfunction Affecting Neurodegenerative Disorders

Otsuka, T., & Matsui, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24087079 · Cited by 17

Caractéristiques du vieillissement musculaire et effets préventifs de l'exercice régulier

Butler-Browne, G. S., & Bigard, A. X. (2006) · Science & Sports · doi:10.1016/j.scispo.2006.03.005 · Cited by 28

Dietary restriction modulates mitochondrial DNA damage and oxylipin profile in aged rats

Gureev, A. P., Andrianova, N. V., Pevzner, I. B., Zorova, L. D., Chernyshova, E. V., Sadovnikova, I. S., Chistyakov, D. V., Popkov, V. A., Semenovich, D. S., Babenko, V. A., et al. (2022) · FEBS Journal · doi:10.1111/febs.16451 · Cited by 16

Leucine Supplementation in Middle-Aged Male Mice Improved Aging-Induced Vascular Remodeling and Dysfunction via Activating the Sirt1-Foxo1 Axis

Hao, Z., Xu, G., Yuan, M., Tan, R., Xia, Y., Liu, Y., & Yin, X. (2022) · Nutrients · doi:10.3390/nu14183856 · Cited by 17

Quantitative changes in mitochondrial DNA copy number in various tissues of pigs during growth

Xie, Y., Jin, L. G., Chen, X. J., He, M., Wang, Y., Liu, R., Li, M., & Li, X. W. (2015) · Genetics and Molecular Research · doi:10.4238/2015.march.6.12 · Cited by 16

Skeletal muscle from aged American Quarter Horses shows impairments in mitochondrial biogenesis and expression of autophagy markers

Li, C., White-Springer, S. H., Warren, L. K., & Wohlgemuth, S. E. (2017) · Experimental Gerontology · doi:10.1016/j.exger.2017.11.022 · Cited by 16

Comparing Electron Leak in Vertebrate Muscle Mitochondria

Treberg, J. R., Munro, D., Jastroch, M., Quijada‐Rodriguez, A. R., Kutschke, M., & Wiens, L. M. (2018) · Integrative and Comparative Biology · doi:10.1093/icb/icy095 · Cited by 16

Association between the peripartum maternal and fetal telomere lengths and mitochondrial DNA copy numbers and preeclampsia: a prospective case–control study

Zhang, R., Du, J., Xiao, Z., Jiang, Y., Jin, L., & Weng, Q. (2022) · BMC Pregnancy and Childbirth · doi:10.1186/s12884-022-04801-0 · Cited by 17

Molecular Mechanisms for Age-Associated Mitochondrial Deficiency in Skeletal Muscle

Wagatsuma, A., & Sakuma, K. (2012) · Journal of Aging Research · doi:10.1155/2012/768304 · Cited by 15

DNA damage and repair in age-related macular degeneration

Błasiak, J. (2010) · Frontiers in bioscience · doi:10.2741/3789 · Cited by 15

Epigenome-wide association study of mitochondrial genome copy number

Wang, P., Castellani, C. A., Yao, J., Huan, T., Bielak, L. F., Zhao, W., Haessler, J., Joehanes, R., Sun, X., Guo, X., et al. (2021) · Human Molecular Genetics · doi:10.1093/hmg/ddab240 · Cited by 12

Population-level expression variability of mitochondrial DNA-encoded genes in humans

Wang, G., Yang, E., Mandhan, I., Brinkmeyer‐Langford, C., & Cai, J. J. (2014) · European Journal of Human Genetics · doi:10.1038/ejhg.2013.293 · 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

Role of Akirin1 in the regulation of skeletal muscle fiber‐type switch

Rao, V. V., Sangiah, U., Mary, K. A., Akira, S., & Mohanty, A. (2019) · Journal of Cellular Biochemistry · doi:10.1002/jcb.28406 · Cited by 13

Can Proprioceptive Training Enhance Fatigability and Decrease Progression Rate of Sarcopenia in Seniors? A Novel Approach

Mohamed, A. A. (2020) · Current Rheumatology Reviews · doi:10.2174/1573397116666200429113226 · Cited by 13

Long-term cycles of hypoxia and normoxia increase the contents of liver mitochondrial DNA in rats

Luo, Y., Guoshou, L., Chen, Y., Liu, F., Xu, G., Yin, J., & Gao, Y. (2012) · European Journal of Applied Physiology · doi:10.1007/s00421-012-2414-9 · Cited by 13

Sarcopenia of Male Aging

Chow, L. S., & Nair, K. S. (2005) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/j.ecl.2005.07.007 · Cited by 13

Low protein to carbohydrate ratio diet delays onset of Parkinsonism like phenotype in Drosophila melanogaster parkin null mutants

Bajracharya, R., & Ballard, J. W. O. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.10.003 · Cited by 13

Acetyl‐l‐Carnitine Dietary Supplementation to Old Rats Increases Mitochondrial Transcription Factor A Content in Rat Hindlimb Skeletal Muscles

Pesce, V., Fracasso, F., Musicco, C., Lezza, A. M. S., Cantatore, P., & Gadaleta, M. N. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1297.077 · Cited by 13

Aging and diabetes: Mitochondrial dysfunction

Irving, B. A., & Nair, K. S. (2007) · Current Diabetes Reports · doi:10.1007/s11892-007-0039-x · Cited by 13

Association of mitochondrial DNA copy number with self-rated health status

Takahashi, P. Y., Jenkins, G. D., Welkie, B. P., McDonnell, S. K., Evans, J. M., Cerhan, J. R., Olson, J. E., Thibodeau, S. N., Cicek, M. S., & Ryu, E. (2018) · The Application of Clinical Genetics · doi:10.2147/tacg.s167640 · Cited by 13

Method of proof and evidences for the concept that mitochondrial genome is a thrifty genome

Lee, H. K. (2001) · Diabetes Research and Clinical Practice · doi:10.1016/s0168-8227(01)00336-9 · Cited by 13

Nitric oxide promotes energy metabolism and protects mitochondrial DNA in peaches during cold storage

Ren, Y., & Zhu, S. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.970303 · Cited by 12

Altered regulation of energy homeostasis in older rats in response to thyroid hormone administration

Walrand, S., Short, K. R., Heemstra, L. A., Novak, C. M., Levine, J. A., Coenen-Schimke, J. M., & Nair, K. S. (2013) · The FASEB Journal · doi:10.1096/fj.13-239806 · Cited by 12

Apoptosis inducing factor: Cellular protective function in Dictyostelium discoideum

Kadam, A. A., Mehta, D., Jubin, T., Mansuri, M. S., & Begum, R. (2020) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2020.148158 · Cited by 12

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D’Aquila, P., Rango, F. D., Guarasci, F., Mandalà, M., Corsonello, A., Bellizzi, D., & Passarino, G. (2020) · Nutrients · doi:10.3390/nu12020460 · Cited by 12

Familial longevity study reveals a significant association of mitochondrial DNA copy number between centenarians and their offspring

He, Y., Chen, X., Yan, D., Xiao, F., Lin, R., Liao, X.-P., Liu, Y.-W., Pu, S.-Y., Yu, Q., Sun, H., et al. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.07.026 · Cited by 12

Further investigation of mitochondrial biogenesis and gene expression of key regulators in ascites- susceptible and ascites- resistant broiler research lines

Alzahrani, K., Licknack, T. J., Watson, D. L., Anthony, N. B., & Rhoads, D. D. (2019) · PLoS ONE · doi:10.1371/journal.pone.0205480 · Cited by 12

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Heiby, J. C., & Ori‬‬, A. (2022) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2022.100416 · Cited by 11

Effects of larval exposure to the insecticide flumethrin on the development of honeybee (Apis mellifera) workers

Liu, C., Wu, X., Yang, H., Yu, L., & Zhang, Y. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.1054769 · Cited by 10

Investigation of FGF21 mRNA levels and relative mitochondrial DNA copy number levels and their relation in nonalcoholic fatty liver disease: a case-control study

Houshmand, M., Zeinali, V., Hosseini, A., Seifi, A., Danaei, B., & Kamfar, S. (2023) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2023.1203019 · Cited by 11

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Herbst, A. J., Hoang, A. N., Kim, C., Aiken, J. M., McKenzie, D. I., Goldwater, D. S., & Wanagat, J. (2021) · Rejuvenation Research · doi:10.1089/rej.2021.0052 · Cited by 10

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Wu, S., Wu, Y., Chen, J., Zhuang, P., Zhang, Y., & Jiao, J. (2022) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2022.109202 · Cited by 12

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Paula, D. P., & Andow, D. A. (2022) · Neotropical Entomology · doi:10.1007/s13744-022-01011-3 · Cited by 10

Endothelial cells maintain a reduced redox environment even as mitochondrial function declines

CARLISLE, R., Rhoads, C. A., Aw, T. Y., & Harrison, L. (2002) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00092.2002 · Cited by 10

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Zhang, S. B., Maguire, D., Zhang, M., Zhang, Z., Zhang, A., Yin, L., Zhang, L., Huang, L., Vidyasagar, S., Swarts, S. G., et al. (2013) · Radiation Research · doi:10.1667/rr3373.1 · Cited by 9

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Park, J. E., Kim, M. J., Ha, S. K., Hong, S. G., Oh, H. J., Kim, G. A., Park, E., Kang, J. T., Saadeldin, I. M., Jang, G., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041256 · 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

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Solovev, I. A., Shaposhnikov, M. V., & Moskalev, A. (2019) · Healthy ageing and longevity · doi:10.1007/978-3-030-24970-0_6 · Cited by 9

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Sadeesh, E. M., & Malik, A. (2024) · Molecular Biology Reports · doi:10.1007/s11033-024-09815-9 · Cited by 8

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Liu, R.-F., Huang, X., Sun, Q., Hou, Z., Yang, W., Zhang, J., Zhang, P., Huang, L., Lu, Y., & Fu, Q. (2022) · Animals · doi:10.3390/ani12131706 · Cited by 8

Amino acid and protein metabolism in chronic renal failure

Nair, K. S. (2005) · Journal of Renal Nutrition · doi:10.1053/j.jrn.2004.09.026 · Cited by 8

cDNA representational difference analysis used in the identification of genes related to the aging process in rat kidney

Sung, B., Jung, K. J., Song, H. S., Son, M. J., Yu, B. P., & Chung, H. Y. (2005) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2005.03.009 · Cited by 8

Expression of respiratory chain enzyme mRNA and the morphological properties of mitochondria in the masseter muscles of klotho mutant mice

Murata, M., Miwa, Y., & Sato, I. (2009) · Okajimas Folia Anatomica Japonica · doi:10.2535/ofaj.86.93 · Cited by 8

Changes of Mitochondrial DNA Content in the Male Offspring of Protein-Malnourished Rats

Park, H. K., Jin, C. J., Cho, Y. M., Park, D. J., Shin, C. S., Park, K. S., Kim, S. Y., Cho, B. Y., & Lee, H. K. (2004) · Springer eBooks · doi:10.1007/978-3-662-41088-2_21 · Cited by 8

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Witte, S., Boshnakovska, A., Özdemir, M., Chowdhury, A., Rehling, P., & Aich, A. (2023) · Biology Open · doi:10.1242/bio.059844 · Cited by 7

Effect of temperature and salinity on mtDNA copy number of the ridgetail white prawn, Palaemon carinicauda Holthuis, 1950 (Decapoda, Palaemonidae)

Li, Z. H., Zhang, P., Ma, H. K., Xu, W., Sun, J., Yan, B. L., Zhang, Q. Q., & Gao, H. (2018) · Crustaceana · doi:10.1163/15685403-00003816 · Cited by 7

Ninjin'yoeito, a traditional Japanese medicine, attenuates age-related deficits of muscle performance, self-care motivation, and body temperature in C57BL/6 mice

Matsubara, Y., Miyama, Y., Imai, R., Oizumi, H., Miyazaki, S., Haneda, E., Mizuno, K., Omiya, Y., Ikeda, Y., & Mizoguchi, K. (2022) · Bioscience Biotechnology and Biochemistry · doi:10.1093/bbb/zbac052 · Cited by 8

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Santos, A. L., & Sinha, S. (2023) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-031-26576-1_15 · Cited by 8

Mitochondrial Biogenesis in Skeletal Muscle: Exercise and Aging

Damirchi, A., Babaei, P., Gholamali, M., & Ranjbar, K. (2012) · InTech eBooks · doi:10.5772/48411 · Cited by 7

Brain Aging and Performance Plasticity in Honeybees

Münch, D., & Amdam, G. V. (2013) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-415823-8.00037-x · Cited by 7

Insulin downregulates SIRT1 and AMPK activation and is associated with changes in liver fat, but not in inflammation and mitochondrial oxidative capacity, in streptozotocin-diabetic rat

Barazzoni, R., Zanetti, M., Sturnega, M., Stebel, M., Semolic, A., Pirulli, A., Vinci, P., Zentilin, L., Giacca, M., Cattin, L., et al. (2010) · Clinical Nutrition · doi:10.1016/j.clnu.2010.11.001 · Cited by 7

Presequence-Independent Mitochondrial Import of DNA Ligase Facilitates Establishment of Cell Lines with Reduced mtDNA Copy Number

Spadafora, D., Kozhukhar, N., & ALEXEYEV, M. F. (2016) · PLoS ONE · doi:10.1371/journal.pone.0152705 · Cited by 7

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