Works matching Mitochondrial DNA abnormalities

Results: 680

Sperm telomere length is associated with sperm nuclear DNA integrity and mitochondrial DNA abnormalities among healthy male college students in Chongqing, China.

Published in:

Human Reproduction, 2023, v. 38, n. 6, p. 1036, doi. 10.1093/humrep/dead065

By:

Ling, Xi;
Cui, Haonan;
Chen, Qing;
Yang, Wang;
Zou, Peng;
Yang, Huan;
Zhou, Niya;
Deng, Jiuyang;
Liu, Jinyi;
Cao, Jia;
Ao, Lin

Publication type:

Article

Correction to: Mitochondrial DNA abnormalities provide mechanistic insight and predict reactive oxygen species-stimulating drug efficacy.

Published in:

2021

By:

Zaidieh, Tarek;
Smith, James R.;
Ball, Karen E.;
An, Qian

Publication type:

corrected article

Comparative Study of Mitochondrial DNA Abnormalities in Mesenchymal Stem Cells after Exposure to X-Ray Radiation in Low and Medium Doses.

Published in:

Bulletin of Experimental Biology & Medicine, 2025, v. 178, n. 4, p. 541, doi. 10.1007/s10517-025-06370-6

By:

Dushenko, M. V.;
Abdullaev, S. A.;
Ignatov, M. A.;
Osipov, A. N.

Publication type:

Article

Mitochondrial DNA abnormalities provide mechanistic insight and predict reactive oxygen species-stimulating drug efficacy.

Published in:

2021

By:

Zaidieh, Tarek;
Smith, James R.;
Ball, Karen E.;
An, Qian

Publication type:

journal article

Associations between cigarette smoking and mitochondrial DNA abnormalities in buccal cells.

Published in:

Carcinogenesis, 2008, v. 29, n. 6, p. 1170, doi. 10.1093/carcin/bgn034

By:

Duanjun Tan;
David S. Goerlitz;
Ramona G. Dumitrescu;
Dingfen Han;
Françoise Seillier-Moiseiwitsch;
Stephanie M. Spernak;
Roy Anthony Orden;
Jinguo Chen;
Radoslav Goldman;
Peter G. Shields

Publication type:

Article

Mitochondrial DNA abnormalities provide mechanistic insight and predict reactive oxygen species-stimulating drug efficacy.

Published in:

BMC Cancer, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12885-021-08155-2

By:

Zaidieh, Tarek;
Smith, James R.;
Ball, Karen E.;
An, Qian

Publication type:

Article

Mitochondrial DNA and Disease: Areview.

Published in:

Al-Nahrain Journal of Science, 2024, v. 27, n. 2, p. 81, doi. 10.22401/ANJS.27.2.08

By:

Hussein, Marwa Adel;
Abdulridha, Ruaa Hameed;
Sodani, Ibtisam Jasim;
Al-Ward, Mais Adnan;
Jaafar, May Ridha;
Ibrahim Al-Sammarrie, Hala Khalid;
Neamah, Shahad Emad;
Jawad, Asmaa A.;
Safir, Nadhum Hussen

Publication type:

Article

Mitochondrial Dysfunction in Multiple Sclerosis: A Systematic Review.

Published in:

Acta Medica Iranica, 2019, v. 57, n. 1, p. 5

By:

Saberi, Alia;
Kazemi, Samaneh

Publication type:

Article

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

Published in:

BMC Cardiovascular Disorders, 2002, v. 2, p. 12, doi. 10.1186/1471-2261-2-12

By:

Majamaa-Voltti, Kirsi;
Peuhkurinen, Keijo;
Kortelainen, Marja-Leena;
Hassinen, Ilmo E.;
Majamaa, Kari

Publication type:

Article

Comprehensive analysis of mitochondrial DNA variants, mitochondrial DNA copy number and oxidative damage in psoriatic arthritis.

Published in:

Biomedical Reports, 2023, v. 19, n. 5, p. 1, doi. 10.3892/br.2023.1667

By:

ALWEHAIDAH, MATERAH SALEM;
ALSABBAGH, MANHEL;
AL-KAFAJI, GHADA

Publication type:

Article

ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism.

Published in:

2017

By:

Desai, Radha;
Frazier, Ann E.;
Durigon, Romina;
Patel, Harshil;
Jones, Aleck W.;
Rosa, Ilaria Dalla;
Lake, Nicole J.;
Compton, Alison G.;
Mountford, Hayley S.;
Tucker, Elena J.;
Mitchell, Alice L. R.;
Jackson, Deborah;
Sesay, Abdul;
Di Re, Miriam;
van den Heuvel, Lambert P.;
Burke, Derek;
Francis, David;
Lunke, Sebastian;
McGillivray, George;
Mandelstam, Simone

Publication type:

journal article

Neuropathic Pain as Main Manifestation of POLG -Related Disease: A Case Report.

Published in:

Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.846110

By:

Lang-Orsini, Melanie;
Gonzalez-Perez, Paloma

Publication type:

Article

Genetic characterization of a pentatricopeptide repeat protein gene, orf687 , that restores fertility in the cytoplasmic male-sterile Kosena radish.

Published in:

Plant Journal, 2003, v. 34, n. 4, p. 407, doi. 10.1046/j.1365-313X.2003.01735.x

By:

Koizuka, Nobuya;
Imai, Ritsuko;
Fujimoto, Hideya;
Hayakawa, Takahiko;
Kimura, Yusuke;
Kohno-Murase, Junko;
Sakai, Takako;
Kawasaki, Shinji;
Imamura, Jun

Publication type:

Article

Mitochondria in Human Fertility and Infertility.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 10, p. 8950, doi. 10.3390/ijms24108950

By:

Tesarik, Jan;
Mendoza-Tesarik, Raquel

Publication type:

Article

Extracellular vesicles: opening up a new perspective for the diagnosis and treatment of mitochondrial dysfunction.

Published in:

Journal of Nanobiotechnology, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s12951-024-02750-8

By:

Li, Jiali;
Wang, Tangrong;
Hou, Xiaomei;
Li, Yu;
Zhang, Jiaxin;
Bai, Wenhuan;
Qian, Hui;
Sun, Zixuan

Publication type:

Article

Easing US restrictions on mitochondrial replacement therapy would protect research interests but grease the slippery slope.

Published in:

Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 9, p. 1781, doi. 10.1007/s10815-019-01529-3

By:

Keefe, David L.

Publication type:

Article

Effect of acteoside on the re-localization and abnormal morphology of mitochondria in porcine oocytes during in vitro maturation.

Published in:

Journal of Assisted Reproduction & Genetics, 2016, v. 33, n. 7, p. 939, doi. 10.1007/s10815-016-0729-x

By:

Kim, Keun;
Chun, Ju;
Lee, Kyung-Bon;
Lee, Ji;
Park, Kang-Sun;
Han, Kil;
Lee, Bo;
Kim, Eun;
Kim, Jin;
Kim, Min

Publication type:

Article

Mutation analysis in 16 patients with mtDNA depletionCommunicated by Mark H. PaalmanOnline Citation: Human Mutation, Mutation in Brief #606 (2002) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/606.pdf.

Published in:

Human Mutation, 2003, v. 21, n. 4, p. 453, doi. 10.1002/humu.9135

By:

R. Carrozzo;
B. Bornstein;
S. Lucioli;
Y. Campos;
P. de la Pena;
N. Petit;
C. Dionisi?Vici;
L. Vilarinho;
T. Rizza;
E. Bertini;
R. Garesse;
F.M. Santorelli;
J. Arenas

Publication type:

Article

Mutation analysis in 16 patients with mtDNA depletion (Communicated by Mark H. Paalman) Online Citation: Human Mutation, Mutation in Brief #606 (2002) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/606.pdf).

Published in:

Human Mutation, 2003, v. 21, n. 4, p. 453, doi. 10.1002/humu.9135

By:

R. Carrozzo;
B. Bornstein;
S. Lucioli;
Y. Campos;
P. de la Pena;
N. Petit;
C. Dionisi-Vici;
L. Vilarinho;
T. Rizza;
E. Bertini;
R. Garesse;
F.M. Santorelli;
J. Arenas

Publication type:

Article

Comparison of whole mitochondrial genome variants between hair shafts and reference samples using massively parallel sequencing.

Published in:

International Journal of Legal Medicine, 2020, v. 134, n. 3, p. 853, doi. 10.1007/s00414-019-02205-y

By:

Kim, Bo Min;
Hong, Sae Rom;
Chun, Hein;
Kim, Sangwoo;
Shin, Kyoung-Jin

Publication type:

Article

Expression of the cytoplasmic domain of β1 integrin induces apoptosis in adult rat ventricular myocytes (ARVM) via the involvement of caspase-8 and mitochondrial death pathway.

Published in:

Basic Research in Cardiology, 2006, v. 101, n. 6, p. 485, doi. 10.1007/s00395-006-0602-7

By:

Menon, Bindu;
Krishnamurthy, Prasanna;
Kaverina, Ekaterina;
Johnson, Jennifer N.;
Ross, Robert S.;
Singh, Mahipal;
Singh, Krishna

Publication type:

Article

Mitochondrial genome stability in human: understanding the role of DNA repair pathways.

Published in:

Biochemical Journal, 2021, v. 478, n. 6, p. 1179, doi. 10.1042/BCJ20200920

By:

Dahal, Sumedha;
Raghavan, Sathees C.

Publication type:

Article

Policy update.

Published in:: Biologist, 2017, v. 64, n. 1, p. 8
Publication type:: Article

Mitochondrial genomes and genetic structure of the Kemp's ridley sea turtle (Lepidochelys kempii).

Published in:

Ecology & Evolution (20457758), 2020, v. 10, n. 1, p. 249, doi. 10.1002/ece3.5891

By:

Frandsen, Hilary R.;
Figueroa, Diego F.;
George, Jeff A.

Publication type:

Article

The effects of allospecific mitochondrial genome on the fitness of northern redbelly dace (Chrosomus eos).

Published in:

Ecology & Evolution (20457758), 2018, v. 8, n. 6, p. 3311, doi. 10.1002/ece3.3922

By:

Angers, Bernard;
Leung, Christelle;
Vétil, Romain;
Deremiens, Léo;
Vergilino, Roland

Publication type:

Article

Extensive respiratory chain defects in inhibitory interneurones in patients with mitochondrial disease.

Published in:

Neuropathology & Applied Neurobiology, 2016, v. 42, n. 2, p. 180, doi. 10.1111/nan.12238

By:

Lax, Nichola Z.;
Grady, John;
Laude, Alex;
Chan, Felix;
Hepplewhite, Philippa D.;
Gorman, Grainne;
Whittaker, Roger G.;
Ng, Yi;
Cunningham, Mark O.;
Turnbull, Doug M.

Publication type:

Article

Mitochondrial and inflammatory changes in sporadic inclusion body myositis.

Published in:

Neuropathology & Applied Neurobiology, 2015, v. 41, n. 3, p. 288, doi. 10.1111/nan.12149

By:

Rygiel, Karolina A.;
Miller, James;
Grady, John P.;
Rocha, Mariana C.;
Taylor, Robert W.;
Turnbull, Doug M.

Publication type:

Article

Mitochondrial DNA deletions and depletion within paraspinal muscles.

Published in:

Neuropathology & Applied Neurobiology, 2013, v. 39, n. 4, p. 377, doi. 10.1111/j.1365-2990.2012.01290.x

By:

Campbell, G. R.;
Reeve, A.;
Ziabreva, I.;
Polvikoski, T. M.;
Taylor, R. W.;
Reynolds, R.;
Turnbull, D. M.;
Mahad, D. J.

Publication type:

Article

Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvement.

Published in:

Neuropathology & Applied Neurobiology, 2006, v. 32, n. 4, p. 359, doi. 10.1111/j.1365-2990.2006.00731.x

By:

Betts, J.;
Jaros, E.;
Perry, R. H.;
Schaefer, A. M.;
Taylor, R. W.;
Abdel-All, Z.;
Lightowlers, R. N.;
Turnbull, D. M.

Publication type:

Article

Loss of autophagy promotes murine acetaminophen hepatotoxicity.

Published in:

Journal of Gastroenterology, 2012, v. 47, n. 4, p. 433, doi. 10.1007/s00535-011-0500-0

By:

Igusa, Yuki;
Yamashina, Shunhei;
Izumi, Kousuke;
Inami, Yoshihiro;
Fukada, Hiroo;
Komatsu, Masaaki;
Tanaka, Keiji;
Ikejima, Kenichi;
Watanabe, Sumio

Publication type:

Article

Secondary mutations of mitochondrial DNA in Japanese patients withLeber's hereditary optic neuropathy.

Published in:

Ophthalmic Genetics, 1999, v. 20, n. 3, p. 153, doi. 10.1076/opge.20.3.153.2281

By:

Matsumoto, Masayuki;
Hayasaka, Seiji;
Kadoi, Chiharu;
Hotta, Yoshihiro;
Fujiki, Keiko;
Fujimaki, Takuro;
Takeda, Misako;
Ishida, Nobuo;
Endo, Shinichiro;
Kanai, Atsushi

Publication type:

Article

A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting.

Published in:

2003

By:

Salpietro, Carmelo Damiano;
Briuglia, Silvana;
Merlino, Maria Valeria;
di Bella, Chiara;
Rigoli, Luciana

Publication type:

journal article

Mitochondrial DNA disorders.

Published in:

European Journal of Pediatrics, 2000, v. 159, n. 15, p. S219, doi. 10.1007/PL00014407

By:

Naviaux, Robert K.

Publication type:

Article

Prospects of Germline Nuclear Transfer in Women With Diminished Ovarian Reserve.

Published in:

Frontiers in Endocrinology, 2021, v. 11, p. N.PAG, doi. 10.3389/fendo.2021.635370

By:

Christodoulaki, Antonia;
Boel, Annekatrien;
Tang, Maoxing;
De Roo, Chloë;
Stoop, Dominic;
Heindryckx, Björn

Publication type:

Article

Biallelic NDUFA4 Deletion Causes Mitochondrial Complex IV Deficiency in a Patient with Leigh Syndrome.

Published in:

Genes, 2024, v. 15, n. 4, p. 500, doi. 10.3390/genes15040500

By:

Misceo, Doriana;
Strømme, Petter;
Bitarafan, Fatemeh;
Chawla, Maninder Singh;
Sheng, Ying;
Bach de Courtade, Sandra Monica;
Eide, Lars;
Frengen, Eirik

Publication type:

Article

Mitochondrial Genetic Heterogeneity in Leber's Hereditary Optic Neuropathy: Original Study with Meta-Analysis.

Published in:

Genes, 2021, v. 12, n. 9, p. 1300, doi. 10.3390/genes12091300

By:

Jha, Rajan Kumar;
Dawar, Chhavi;
Hasan, Qurratulain;
Pujar, Akhilesh;
Gupta, Gaurav;
Vishnu, Venugopalan Y.;
Kekunnaya, Ramesh;
Thangaraj, Kumarasamy

Publication type:

Article

Mitochondrial Dynamics: Molecular Mechanisms, Related Primary Mitochondrial Disorders and Therapeutic Approaches.

Published in:

Genes, 2021, v. 12, n. 2, p. 247, doi. 10.3390/genes12020247

By:

Di Nottia, Michela;
Verrigni, Daniela;
Torraco, Alessandra;
Rizza, Teresa;
Bertini, Enrico;
Carrozzo, Rosalba;
Lezza, Angela Maria Serena

Publication type:

Article

Effects of mitoTALENs-Directed Double-Strand Breaks on Plant Mitochondrial Genomes.

Published in:

Genes, 2021, v. 12, n. 2, p. 153, doi. 10.3390/genes12020153

By:

Arimura, Shin-ichi;
Gualberto, José M.;
Molinier, Jean

Publication type:

Article

Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches.

Published in:

Genes, 2021, v. 12, n. 1, p. 112, doi. 10.3390/genes12010112

By:

García-López, Marta;
Arenas, Joaquín;
Gallardo, M. Esther

Publication type:

Article

Mitochondrial Sequencing of Missing Persons DNA Casework by Implementing Thermo Fisher's Precision ID mtDNA Whole Genome Assay.

Published in:

Genes, 2020, v. 11, n. 11, p. 1303, doi. 10.3390/genes11111303

By:

Cuenca, Daniela;
Battaglia, Jessica;
Halsing, Michelle;
Sheehan, Sandra

Publication type:

Article

Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy.

Published in:

Genes, 2020, v. 11, n. 9, p. 1037, doi. 10.3390/genes11091037

By:

Dawod, Phepy G. A.;
Jancic, Jasna;
Marjanovic, Ana;
Brankovic, Marija;
Jankovic, Milena;
Samardzic, Janko;
Potkonjak, Dario;
Djuric, Vesna;
Mesaros, Sarlota;
Novakovic, Ivana;
Abdel Motaleb, Fayda I.;
Kostic, Vladimir S.;
Nikolic, Dejan

Publication type:

Article

Pathogenic Mitochondria DNA Mutations: Current Detection Tools and Interventions.

Published in:

Genes, 2020, v. 11, n. 2, p. 192, doi. 10.3390/genes11020192

By:

Mustafa, Mohd Fazirul;
Fakurazi, Sharida;
Abdullah, Maizaton Atmadini;
Maniam, Sandra

Publication type:

Article

Phylogenetic Analysis and Substitution Rate Estimation of Colonial Volvocine Algae Based on Mitochondrial Genomes.

Published in:

Genes, 2020, v. 11, n. 1, p. 115, doi. 10.3390/genes11010115

By:

Hu, Yuxin;
Xing, Weiyue;
Hu, Zhengyu;
Liu, Guoxiang

Publication type:

Article

Leishmania Mitochondrial Genomes: Maxicircle Structure and Heterogeneity of Minicircles.

Published in:

Genes, 2019, v. 10, n. 10, p. 758, doi. 10.3390/genes10100758

By:

Camacho, Esther;
Rastrojo, Alberto;
Sanchiz, África;
González-de la Fuente, Sandra;
Aguado, Begoña;
Requena, Jose M.

Publication type:

Article

Going Deeper into High and Low Phylogenetic Relationships of Protura.

Published in:

Genes, 2019, v. 10, n. 4, p. 292, doi. 10.3390/genes10040292

By:

Carapelli, Antonio;
Bu, Yun;
Chen, Wan-Jun;
Nardi, Francesco;
Leo, Chiara;
Frati, Francesco;
Luan, Yun-Xia

Publication type:

Article

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

Published in:

Application of Clinical Genetics, 2018, v. 11, p. 121, doi. 10.2147/TACG.S167640

By:

Takahashi, Paul Y;
Jenkins, Gregory D;
Welkie, Benjamin P;
McDonnell, Shannon K;
Evans, Jared M;
Cerhan, James R;
Olson, Janet E;
Thibodeau, Steven N;
Cicek, Mine S;
Ryu, Euijung

Publication type:

Article

Bilateral Progressive Visual Loss in an Epileptic, Mentally Retarded Boy.

Published in:

Middle East African Journal of Ophthalmology, 2011, v. 18, n. 1, p. 67, doi. 10.4103/0974-9233.75892

By:

Guerriero, Silvana;
Vetrugno, Michele;
Ciracì, Lorenza;
Artuso, Lucia;
Dell'Aglio, Rosa;
Petruzzella, Vittoria

Publication type:

Article

Preimplantation genetic diagnosis for mitochondrial DNA disorders: ethical guidance for clinical practice.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 12, p. 1550, doi. 10.1038/ejhg.2009.88

By:

Bredenoord, Annelien;
Dondorp, Wybo;
Pennings, Guido;
de Die-Smulders, Christine;
Smeets, Bert;
de Wert, Guido

Publication type:

Article

mtDNA haplogroup J: a contributing factor of optic neuritis.

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 3, p. 404, doi. 10.1038/sj.ejhg.5200293

By:

Reynier, Pascal;
Penisson-Besnier, Isabelle;
Moreau, Corinne;
Savagner, Frédérique;
Vielle, Bruno;
Emile, Jean;
Dubas, Frédéric;
Malthièry, Yves

Publication type:

Article

LMX1B 17-bp Deletion and A3243G mtDNA Transition in a Previously Described Patient.

Published in:

European Neurology, 2003, v. 49, n. 3, p. 186, doi. 10.1159/000069078

By:

Finsterer, Josef;
Stöllberger, Claudia

Publication type:

Article