Human mitochondrial DNA: roles of inherited and somatic mutations

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

The metabolism of tumors in the body

Warburg, O., Wind, F., & Negelein, E. (1927) · Journal of General Physiology · doi:10.1085/jgp.8.6.519 · Cited by 4,416

Mitochondrial DNA and human evolution

Cann, R. L., Stoneking, M., & Wilson, A. C. (1987) · Nature · doi:10.1038/325031a0 · Cited by 3,100

Succinate links TCA cycle dysfunction to oncogenesis by inhibiting HIF-α prolyl hydroxylase

Selak, M. A., Armour, S. M., MacKenzie, E. D., Boulahbel, H., Watson, D. G., Mansfield, K. D., Pan, Y., Simon, M. C., Thompson, C. B., & Gottlieb, E. (2005) · Cancer Cell · doi:10.1016/j.ccr.2004.11.022 · Cited by 2,108

On the origin of mitosing cells

Sagan, L. (1967) · Journal of Theoretical Biology · doi:10.1016/0022-5193(67)90079-3 · Cited by 1,870

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

Holt, I. J., Harding, A. E., & MORGAN-HUGHES, J. A. (1988) · Nature · doi:10.1038/331717a0 · Cited by 1,860

Human Cells Lacking mtDNA: Repopulation with Exogenous Mitochondria by Complementation

King, M. P., & Attardi, G. M. (1989) · Science · doi:10.1126/science.2814477 · Cited by 1,685

Mitochondrial Respiratory-Chain Diseases

DiMauro, S., & Schon, E. A. (2003) · New England Journal of Medicine · doi:10.1056/nejmra022567 · Cited by 1,672

Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer

The Multiple Leiomyoma Consortium (2002) · Nature Genetics · doi:10.1038/ng849 · Cited by 1,635

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

Bender, A., Krishnan, K. J., Morris, C. M., Taylor, G. A., Reeve, A. K., Perry, R. H., Jaros, E., Hersheson, J. S., Betts, J., Klopstock, T., et al. (2006) · Nature Genetics · doi:10.1038/ng1769 · Cited by 1,570

The Mitochondrial DNA Control Region Might Have Useful Diagnostic and Prognostic Biomarkers for Thyroid Tumors

Bircan, R., Gözü, H. I., Ulu, E. M. K., Sarıkaya, Ş., Gul, A. E., Şirin, D. Y., Özçelik, S., & Aral, C. (2019) · Experimental and Clinical Endocrinology & Diabetes · doi:10.1055/a-0869-7355 · Cited by 2

A novel mitochondrial m.4414T>C MT-TM gene variant causing progressive external ophthalmoplegia and myopathy

Hellebrekers, D. M. E. I., Blakely, E. L., Hendrickx, A. T. M., Hardy, S. A., Hopton, S., Falkous, G., de Coo, I. F. M., Smeets, H. J. M., van der Beek, N. M. E., & Taylor, R. W. (2019) · Neuromuscular Disorders · doi:10.1016/j.nmd.2019.08.005 · Cited by 2

Molecular genetic analysis of leucine tRNA in relevance to type 2 diabetes mellitus

Khan, N. M., Ullah, H., Raziq, A., Khan, A. A., & Khan, M. W. (2020) · Clinical Diabetology · doi:10.5603/dk.2020.0018 · Cited by 2

Mitonuclear interactions affect locomotor activity and sleep in Drosophila melanogasterPreprint

Anderson, L. G., Camus, M. F., Monteith, K. M., Salminen, T. S., & Vale, P. F. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.30.464953 · Cited by 2

A new marker of human aging: heteroplasmy level of mitochondrial genome mutations

Синёв, В. В., Ryzhkova, A. I., Sazonova, M. D., Дорощук, Н. А., Kirichenko, T. V., Карагодин, В. П., Orekhov, A. N., Sobenin, I. A., & Sazonova, M. A. (2021) · Zhurnal «Patologicheskaia fiziologiia i eksperimental`naia terapiia» · doi:10.25557/0031-2991.2021.02.4-9 · Cited by 1

The anti-aging mechanism of Berberine associated with metabolic control

Guo, X., Xiong, X., Lijun, Z., Zhong, G., & Zhu, X. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-823679-6.00020-5 · Cited by 1

The three-parent baby: Medicolegal, forensic and ethical concerns

Chitara, N., Krishan, K., & Kanchan, T. (2024) · Medicine Science and the Law · doi:10.1177/00258024241266566 · Cited by 1

Advanced maternal reproductive age elevates myopia risk in offspring

Qi, J., Lin, J., Zhang, K., Zhang, P., Chen, C., Lü, Y., & Zhu, X. (2025) · British Journal of Ophthalmology · doi:10.1136/bjo-2025-327367 · Cited by 1

Mitochondrial Base Editing of the m.8993T>G Mutation Restores Bioenergetics and Neural Differentiation in Patient iPSCs

Yin, L., Yin, A., & Jones, M. A. (2025) · Genes · doi:10.3390/genes16111298 · Cited by 1

Evaluation of MASSARRAY technique in detecting mitochondrial disease mutations

Chetu, N., Onsod, P., Rerkamnuaychoke, B., Siriboonpiputtana, T., & Chareonsirisuthigul, T. (2026) · Clinica Chimica Acta · doi:10.1016/j.cca.2026.120820 · Cited by 1

Clinical Validation of Digital PCR for Precise m.3243A>G Heteroplasmy Quantification in Early‐Onset Diabetes

Kong, X., Bei, L., Gao, P., Lu, L., Zhu, H., Jiang, Y., Zhao, M., Liu, Y., Wang, G., Li, M., et al. (2026) · Journal of Diabetes Research · doi:10.1155/jdr/9298888 · Cited by 1

From Pharmacodynamic Biomarker to Evaluating Treatment Response: Biomarkers in Primary Mitochondrial Diseases

Stern, S., Crisamore, K., Patton, J., Schuck, R. N., & Pacanowski, M. A. (2026) · Clinical and Translational Science · doi:10.1111/cts.70634 · Cited by 1

Gene Therapy Tools for Diseases Caused by Mutations of the Mitochondrial Genome

Simonov, V., & Rastorguev, S. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27125517 · Cited by 2

Mitochondrial genome alterations in cancer: From mutations and epigenetics to targeted therapiesack

Shetty, S., Padmasali, N. M., Adiga, D., & Kabekkodu, S. P. (2026) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2026.154218 · Cited by 1

The pro-tumorigenic functions of cancer-associated adipocytes are dependent on the mitochondrial chaperone tumor necrosis factor receptor-associated protein 1

Yoon, N. G., Kim, S.-Y., Jung, S., Kwon, K., Yeom, S. A., Park, H., Lee, J. H., Ryu, J., Lee, G. Y., Kang, M.-C., et al. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-026-02861-8 · Cited by 1

Consenso libero ed informato: la Convenzione di Oviedo nell'articolato contesto storico e giuridico delle fonti / Free and informed consent: the Oviedo Convention in the articulated historical and legal context of the sources

Angelis, F. D. (2016) · Medicina e Morale · doi:10.4081/mem.2016.428 · Cited by 1

Mitochondrial G8292A and C8794T mutations in patients with Niemann‑Pick disease type C

Masserrat, A., Sharifpanah, F., Akbari, L., Tonekaboni, S. H., Karimzadeh, P., Asharafi, M. R., Mazouei, S., Sauer, H., & Houshmand, M. (2018) · Biomedical Reports · doi:10.3892/br.2018.1095 · Cited by 1

Sapiens mtDNA circular long-range numerical meta-structures are highly correlated with mtDNA diseases mutations

Perez, J. C. (2017) · SDRP Journal of Cellular and Molecular Physiology · doi:10.25177/jcmp.1.1.5 · Cited by 1

The implications of mitochondria in doxorubicin treatment of cancer in the context of traditional and modern medicine

Souza, L. D. C. M., Chen, M., Ikeno, Y., Salvadori, D. M. F., & Bai, Y. (2020) · Traditional Medicine and Modern Medicine · doi:10.1142/s2575900020300076 · Cited by 1

Verso una proposta eticamente accettabile nella prevenzione delle malattie del DNA mitocondriale / Towards an ethically acceptable proposal in the prevention of mitochondrial DNA-associated diseases

Gómez‐Tatay, L., Hernández‐Andreu, J. M., & Aznar, J. (2016) · Medicina e Morale · doi:10.4081/mem.2016.425 · Cited by 1

Trabecular Meshwork and Intraocular Pressure Dynamics: Oxidative Stress‐Induced Changes

Hohberger, B., Welge-Lüßen, U.-C., & Yu, A. (2016) · InTech eBooks · doi:10.5772/66138 · Cited by 1

Modelling the redox imbalance in Dominant Optic Atrophy: the case of respiratory Complex I

Merabet, N., Bordeneuve, J., & Davezac, N. (2017) · IFAC-PapersOnLine · doi:10.1016/j.ifacol.2017.08.255 · Cited by 1

Einführung in die Genetik

Wessner, B., & Katschinka, G. (2017) · Springer eBooks · doi:10.1007/978-3-7091-1591-6_1 · Cited by 1

Nuclear regulation of mitochondrial functions during oocyte development

Wang, T., & Yang, W. (2020) · Biocell · doi:10.32604/biocell.2020.014708 · Cited by 1

Mitochondria, Chloroplasts, Peroxisomes

(2016) · Elsevier eBooks · doi:10.1016/b978-0-323-34126-4.00019-0 · Cited by 1

Transferência de citoplasma submetido ao estresse oxidativo como modelo para o estudo da herança de doenças mitocondriais

Machado, T. S. (2014) · doi:10.11606/d.10.2014.tde-12012015-085943 · Cited by 1

Combination of mitochondrial tRNA and OXPHOS mutation reduces lifespan and physical condition in aged micePreprint

Reichart, G., Mayer, J., Tokay, T., Lange, F., Johne, C., Baltrusch, S., Tiedge, M., Fuellen, G., Ibrahim, S. M., & Köhling, R. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/233593 · Cited by 1

The mitochondrial DNA control region might have useful diagnostic and prognostic biomarkers for thyroid tumors

Bircan, R., Gözü, H. I., Ulu, E. M. K., Sarıkaya, Ş., Şirin, D. Y., Özçelik, S., & Aral, C. (2018) · Endocrine Abstracts · doi:10.1530/endoabs.56.p1149 · Cited by 1

Diabetic conditions induce intolerance to accumulation of pathogenic mitochondrial DNAsPreprint

Ogasawara, E., Katada, S., Mito, T., Hayashi, J., & Nakada, K. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/790956 · Cited by 2

Multiple distinct evolutionary mechanisms govern the dynamics of selfish mitochondrial genomesPreprint

Gitschlag, B. L., Pereira, C. V., Held, J. P., McCandlish, D. M., & Patel, M. R. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.04.08.487647 · Cited by 1

Exposome du cancer : reprogrammation métabolique du cancer du poumon par les nitrosamines spécifiques de la fumée de tabac

Sarlak, S. (2021) · theses.fr (ABES) · doi:10.70675/2e2c5420z3a1fz49c3zb548z8e72b24a52b2 · Cited by 1

Instabilidade do Genoma Mitocondrial em Adenoma e Adenocarcinoma Colorretal.

de Araújo, L. F. (2013) · doi:10.11606/d.17.2013.tde-13062013-084134

Mitochondrial DNA haplogroup-dependence of drugs and xenobiotics toxicity

Strobbe, D. (2014) · Padua@research (University of Padova)

Avaliação da relação entre haplogrupo mitocondrial e ancestralidade genômica no desenvolvimento de insuficiência cardíaca em amostra brasileira

Cardena, M. M. S. G. (2013) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.5.2013.tde-18102013-151616

Analysis of the mitochondrial DNA of Schizophrenia patients by next generation sequencing

Balada, M. R. (2014) · RIUVic (UVic-UCC)

Mitochondrial tRNA Thr A15951G mutation may not be associated with Leber’s Hereditary Optic Neuropathy

Zhang, X., Yu, S., Tu, Y., & Huang, W. (2015) · Mitochondrial DNA Part A · doi:10.3109/19401736.2015.1022763

functional analyses of variants of human SCO1, a mitochondrial metallochaperone

Pan, M. (2013) · University Library - University of Saskatchewan (University of Saskatchewan)

Mating type specific roles during the sexual cycle of Phycomyces blakesleeanus

Shakya, V. P. S. (2014) · MOspace Institutional Repository (University of Missouri)

The Molecular Mechanisms Underlying the Cytochrome C Oxidase Dysfunction-Induced Accelerated Apoptosis

Schüll, S. (2014) · Kölner Universitäts PublikationsServer (Universität zu Köln)

Mutations of mitochondrial genome and atherosclerosis: Possible mechanistic relationship

Sobenin, I. A., Bobryshev, Y. V., Romanenko, E. B., & Orekhov, A. N. (2014)

Mitochondrial hearing loss mutations in Northern Finnish preterm and term-born babies

Soini, H. K. (2016)

Multilevel Approaches to Schizophrenia and Other Psychotic Disorders: The Biobehavioral Interface

Walker, E. F., Ryan, A. T., Goines, K., Novacek, D. M., Goulding, S. M., Brasfield, J. L., MacDonald, A. N., & Trotman, H. D. (2016) · Wiley eBooks · doi:10.1002/9781119125556.devpsy322

Fifty Years After Huxley: The Roadmap of Reproductive Medicine Revisited and Updated: The 2015 SRI-Pardi Distinguished Scientist Plenary Lecture of the Society for Reproductive Investigation

Adashi, E. Y. (2015) · Reproductive Sciences · doi:10.1177/1933719115605740

Clinical and genotypic aspects of mitochondrial disease

Gorman, G. S. (2015)

The role of mitochondria in innate immunity and inflammation

Widdrington, J. D. (2016)

Author Response: Do High mtDNA Copy Numbers Truly Prevent LHON Manifestations?

Bianco, A., & Petruzzella, V. (2017) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.17-22545

Nutrigenómica humana: efectos de los alimentos o sus componentes sobre la expresión RNA Human Nutrigenomics: Effects of Food or Food Components on RNA Expression

Vargas-Hernández, J. E. (2016)

MITOCHONDRIAL DNA- REVOLUTIONARY EVOLUTION

Nayak, V. N., Honnappa, A., Shrestha, P., & Lakshmanan, N. (2017) · Journal of Evidence Based Medicine and Healthcare · doi:10.18410/jebmh/2017/714

Mitochondria Remodeling in Cancer

Dornfeld, K. J., & Skildum, A. J. (2018) · Springer eBooks · doi:10.1007/978-3-319-73344-9_9

Response to Finsterer and Zarrouk-Mahjoub

Sambuughin, N., Smith, J. K., O’Connor, F., & Deuster, P. A. (2018) · Molecular Genetics and Metabolism Reports · doi:10.1016/j.ymgmr.2018.08.004

Single fiber proteomics of respiratory chain defects in mitochondrial disordersPreprint

Murgia, M., Tan, J., Geyer, P. E., Doll, S., Mann, M., & Klopstock, T. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/421750

Estudo do papel da proteína p53 em reparo por excisão de bases em mitocôndrias de células de mamíferos

Godoy, F. A. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.85.2018.tde-21062018-090338

Over Expression of NOS2 in Ragged-red Fibers from Patients with Mitochondrial Disorders due to Mutations in mtDNA

Guglielmi, V., Marini, M., Tomelleri, G., & Vattemi, G. N. A. (2018) · Annals of Behavioral Neuroscience · doi:10.18314/abne.v1i1.863

[Corrigendum] Mitochondrial G8292A and C8794T mutations in patients with Niemann‑Pick disease type C

Masserrat, A., Sharifpanah, F., Akbari, L., Tonekaboni, S. H., Karimzadeh, P., Asharafi, M. R., Mazrouei, S., Sauer, H., & Houshmand, M. (2018) · Biomedical Reports · doi:10.3892/br.2018.1156

Estudo do metabolismo energético com base na instabilidade do genoma mitocondrial no melanoma

de Araújo, L. F. (2018) · doi:10.11606/t.17.2018.tde-23042018-153436

Impact of San-mediated Signaling on Glioblastoma and Neuroblastoma Metabolism

Silva, M. R. (2018) · FIU - Digital Commons (Florida International University) · doi:10.25148/etd.fidc006885

Możliwości przywracania i utrzymania jakości mitochondriów w oocytach ssaków

Gąsior, Ł., & Polański, Z. (2018) · Kosmos · doi:10.36921/kos.2018_2434

Mitochondria: Muscle Morphology

Sciacco, M., Fagiolari, G., Tironi, R., Peverelli, L., & Moggio, M. G. (2019) · Springer eBooks · doi:10.1007/978-3-030-05517-2_2

Genomic Instability: DNA Repair and Cancer

Carlos, A. R. (2019) · Learning materials in biosciences · doi:10.1007/978-3-030-11812-9_5

Ultrasmall signal-amplified Ag2Se–imide hybrid fluorescence nanodots for the detection of trace DNA in mitochondria

Wang, G., Wang, K., Zhu, L., Guo, Y., Liu, J., Ma, X., Yang, H., & Yang, L. (2019) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2019.126752

Skeletal muscle, exercise and activity in pulmonary hypertension

Sithamparanathan, S. (2018)

Mitochondrial Therapy for Disease Treatment and Prevention: What’s New?

Tesařík, J. (2019) · American Journal of Biomedical Science & Research · doi:10.34297/ajbsr.2019.04.000767

Perfil proteômico da lesão renal aguda induzida por isquemia e reperfusão

Malagrino, P. A. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2019.tde-23082019-141951

Papel de la isoforma mitocondrial de FASTK en la modulación de la fagocitosis no opsónica de bacterias por los macrófagos

Río, A. G.-D. (2019) · UVaDOC UVaDOC University of Valladolid Documentary Repository (University of Valladolid) · doi:10.35376/10324/36270

Leucodistrofias e leucoencefalopatias genéticas em adultos: caracterização clínica, molecular e de neuroimagem

de Paiva, A. R. B. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2019.tde-16102019-142301

a Circulating cell free mitochondrial DNA copy number variation in neurodegenerative disease

Lowes, H. (2018)

Genetic ablation of the mitochondrial ribosome in Plasmodium falciparum sensitizes the human malaria parasite to antimalarial drugs targeting mitochondrial functionsPreprint

Ling, L., Maruthi, M., Munro, J. T., Dass, S., Mather, M. W., Riscoe, M. K., Llinás, M., Zhou, J., & Ke, H. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.01.14.906198

The Involvement of Anti-Oxidative Response and Mitochondrial Dynamics in the Pathogenesis of Friedreich’s Ataxia: Relevance to the Development of Future Therapeutics

Chiang, S. (2019) · The Sydney eScholarship Repository (The University of Sydney)

Mitofusinas em oócitos murinos: seus papéis na fertilidade e na herança mitocondrial

Machado, T. S. (2020) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.10.2020.tde-19062019-105614

Constitutive activation of the PI3K-Akt-mTORC1 pathway sustains the m.3243A>G mtDNA mutationPreprint

Chung, C.-Y., Singh, K., Kotiadis, V. N., Valdebenito, G. E., Ahn, J. H., Topley, E., Tan, J., Andrews, W. D., Bilanges, B., Pitceathly, R. D. S., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.18.159103

Epigenetic features of mitochondrial DNA

Yasukawa, T., Matsuda, S., & Kang, D. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819656-4.00003-6

Targeting Alzheimer's disease neuronal mitochondria as a therapeutic approach

Onyango, I. G., & Stokin, G. B. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819621-2.00015-2

Mitochondrial DNA Variants in Autism Spectrum Disorder: A Systematic ReviewPreprint

Liao, X., & Li, Y. (2020) · Research Square · doi:10.21203/rs.3.rs-131427/v1

Mitochondrial microsatellite genomic instability and brafv600e mutation in central nervous system tumors

Radzak, S. M. A. (2020) · Universiti Sains Malaysia Institutional Repository (Universiti Sains Malaysia)

A New Deletion of Mitochondrial DNA of a BALB/c Mouse

Antipova, V. N. (2021) · Russian Journal of Genetics · doi:10.1134/s1022795421020022

Erkenntnisse zu und aus Krankheiten. Eukaryotengifte als Impulsgeber für die Zellbiologie

Plattner, H. (2021) · Springer eBooks · doi:10.1007/978-3-662-62118-9_14

Técnicas de substituição de DNA mitocondrial para reduzir a transmissão da Síndrome de Leigh

de Fraga, A. G., & Lazzari, V. M. (2021) · Clinical & Biomedical Research · doi:10.22491/2357-9730.105256

Alterations of non-coding RNA expression and mitochondrial biogenesis in colorectal cancer tissue: Possible crosstalk with macrophage polarization

El-Tahan, R. A., Youssry, S., Michel, T. N., Salman, M. S. K., Kamel, M. A. E.-N., & Eweda, S. M. (2021) · Gene Reports · doi:10.1016/j.genrep.2021.101344

An Innovative Data Analysis Strategy For Accurate NGS Detection of Tumor mtDNA MutationsPreprint

Guo, S., Zhou, K., Yuan, Q., Su, L., Ji, X., Gu, X., Guo, X., & Xing, J. (2020) · Research Square · doi:10.21203/rs.3.rs-46773/v1

Mitochondrial Genome (mtDNA) and Human Diseases

Davidson, R. L. (2021) · Science Insights · doi:10.15354/si.21.re201

Follicular Fluid Steroid Levels and Mitochondrial Function from Exosomes Predict Embryonic DevelopmentPreprint

Yu, L., Liu, M., Xu, S., Wang, Z., Liu, T., Zhou, J., Zhang, D., Dong, X., Pan, B., Wang, B., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1456333/v1

Investigação do papel de Alquiladenina DNA glicosilase (AAG) no reparo de bases alquiladas no DNA mitocondrial de camundongos

Alves, R. B. (2021) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.46.2021.tde-17012022-172119

Acute Liver Failure

Álvarez, F., & Jouvet, P. A. (2021) · Springer eBooks · doi:10.1007/978-3-030-79132-2_2

Mitochondriopathie

Arnemann, J. (2018) · Springer eBooks · doi:10.1007/978-3-662-49054-9_3531-1

Mitochondrial disorders due to mutations in the nuclear genome

Chinnery, P. F., & Horváth, R. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-813955-4.00028-3

Mitochondriale DNA

Arnemann, J. (2019) · Springer Reference Medizin · doi:10.1007/978-3-662-48986-4_3530

Mitochondriale DNA

Arnemann, J. (2018) · Springer eBooks · doi:10.1007/978-3-662-49054-9_3530-1

Faculty Opinions recommendation of Mitochondrial DNA: the overlooked oncogenome?

Klymkowsky, M. W. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736145727.793565296

Mitochondriopathie

Arnemann, J. (2019) · Springer Reference Medizin · doi:10.1007/978-3-662-48986-4_3531

Caracterização do estímulo da produção mitocondrial de H2O2 por inibição parcial do Complexo I da cadeia respiratória

Michelini, L. G. B. (2014) · doi:10.47749/t/unicamp.2014.927804

Follicular fluid steroid levels and mitochondrial function from exosomes predict embryonic developmentPreprint

Yu, L., Liu, M., Xu, S., Wang, Z., Liu, T., Zhou, J., Zhang, D., Dong, X., Pan, B., Wang, B., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1456333/v2

Basics and Terminology

(2022) · Wiley eBooks · doi:10.1002/9781119847212.ch1

A Bioinformatics pipeline for variant discovery from Targeted Next Generation Sequencing of the human mitochondrial genome

Jayasekera, L., Senanayake, K., Ranasinghe, R., & Tennekoon, K. H. (2022) · EMBnet journal · doi:10.14806/ej.28.0.1007

Patterns of somatic mutations in normal cells

Manders, F. (2023) · Utrecht University Repository (Utrecht University) · doi:10.33540/1622

Comparative Analysis of Tyrosine tRNA (MT-TY) Gene Mutation Related to Lung Cancer Patients from District Peshawar, Khyber-Pakhtunkhwa, Pakistan During 2020-2022

Abbas, Z., Aslam, S., Nabeel, M., & Habib, F. Z. (2023) · Pakistan BioMedical Journal · doi:10.54393/pbmj.v6i08.928

Genetic analysis and multimodal imaging identify novel mtDNA 12148T>C leading to multisystem dysfunction with tissue-specific heteroplasmyPreprint

Belle, K. C., Kreymerman, A., Vadgama, N., Ji, M. H., Randhawa, S., Caicedo, J., Wong, M. Y., Muscat, S. P., Gifford, C. A., Lee, R. T., et al. (2023) · medRxiv · doi:10.1101/2023.11.03.23297854

Erkenntnisse zu und aus Krankheiten. Eukaryotengifte als Impulsgeber für die Zellbiologie

Plattner, H. (2023) · Springer eBooks · doi:10.1007/978-3-662-66740-8_14

The UPR ER governs the cell-specific response of human dopaminergic neurons to mitochondrial stressPreprint

Heneine, J., Sauty-Colace, C., Zhu, C., Galet, B., Guégan, J., Lejeune, F., Gareau, T., Asfogo, N., Pardanaud-Glavieux, C., Corti, O., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.17.599325

Vinca alkaloids in breast cancer treatment

Mishra, Y., & Mishra, V. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-29913-1.00012-8

Hematopoietic stem cell transplantation for neuromyelitis optica spectrum disorder. Can immune tolerance be reestablished?

Burt, R. K., Burman, J., Greco, R., & ROSE, J. W. (2024) · Handbook of clinical neurology · doi:10.1016/b978-0-323-90242-7.00009-2

Mitochondrial DNA mutations in human disease

Greaves, L. C., & Taylor, R. W. (2006) · IUBMB Life · doi:10.1080/15216540600686888 · Cited by 88

Mitochondrial DNA mutations and related human diseases

Du, W. (2007)

A Mitochondrial Paradigm for Metabolic and Degenerative Diseases, Aging, and Cancer

Wallace, D. C. (2008) · The FASEB Journal · doi:10.1096/fasebj.22.1_supplement.249.2 · Cited by 2

The contribution of mitochondrial DNA alterations to aging, cancer, and neurodegeneration

Picca, A., Guerra, F., Calvani, R., Coelho‐Júnior, H. J., Leeuwenburgh, C., Bucci, C., & Marzetti, E. (2023) · Experimental Gerontology · doi:10.1016/j.exger.2023.112203 · Cited by 43

Mitochondrial DNA and disease

Greaves, L. C., Reeve, A. K., Taylor, R. W., & Turnbull, D. M. (2011) · The Journal of Pathology · doi:10.1002/path.3028 · Cited by 317