Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity by Zewen Gao, Ye Chen, Min-Xin Guan

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Mitochondrial DNA mutations in etiopathogenesis of male infertility by Monis Bilal Shamsi, Rakesh Kumar, Audesh Bhatt, R.N.K Bamezai, Rajeev Kumar, Narmada P Gupta, T K Das, Rima Dada

Subjects: “…Mitochondrion and mitochondrial DNA mutations…”
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The mitochondrial disease associated protein Ndufaf2 is dispensable for Complex-1 assembly but critical for the regulation of oxidative stress by Julia S. Schlehe, Marion S.M. Journel, Kelsey P. Taylor, Katherine D. Amodeo, Matthew J. LaVoie

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Pathogenic mitochondrial DNA variants are associated with response to anti-VEGF therapy in ovarian cancer PDX models by Daniele Boso, Ilaria Piga, Chiara Trento, Sonia Minuzzo, Eleonora Angi, Luisa Iommarini, Elisabetta Lazzarini, Leonardo Caporali, Claudio Fiorini, Luigi D’Angelo, Monica De Luise, Ivana Kurelac, Matteo Fassan, Anna Maria Porcelli, Filippo Navaglia, Ilaria Billato, Giovanni Esposito, Giuseppe Gasparre, Chiara Romualdi, Stefano Indraccolo

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Mitochondria and Brain Disease: A Comprehensive Review of Pathological Mechanisms and Therapeutic Opportunities by Vicente Javier Clemente-Suárez, Laura Redondo-Flórez, Ana Isabel Beltrán-Velasco, Domingo Jesús Ramos-Campo, Pedro Belinchón-deMiguel, Ismael Martinez-Guardado, Athanasios A. Dalamitros, Rodrigo Yáñez-Sepúlveda, Alexandra Martín-Rodríguez, José Francisco Tornero-Aguilera

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Single-cell lineage tracing by endogenous mutations enriched in transposase accessible mitochondrial DNA by Jin Xu, Kevin Nuno, Ulrike M Litzenburger, Yanyan Qi, M Ryan Corces, Ravindra Majeti, Howard Y Chang

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Pathogenic Mitochondrial DNA Mutation Load Inversely Correlates with Malignant Features in Familial Oncocytic Parathyroid Tumors Associated with Hyperparathyroidism-Jaw Tumor Syndr... by Monica De Luise, Luisa Iommarini, Lorena Marchio, Greta Tedesco, Camelia Alexandra Coadă, Andrea Repaci, Daniela Turchetti, Maria Lucia Tardio, Nunzio Salfi, Uberto Pagotto, Ivana Kurelac, Anna Maria Porcelli, Giuseppe Gasparre

Subjects: “…mitochondrial DNA mutations…”
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Results of Mitochondrial DNA Sequence Analysis in Patients with Clinically Diagnosed Leber’s Hereditary Optic Neuropathy by Haluk Esgin, Sadık Altan Özal, Hakan Gürkan

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Functional Mitochondria in Health and Disease by Patries M. Herst, Patries M. Herst, Matthew R. Rowe, Georgia M. Carson, Georgia M. Carson, Michael V. Berridge

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Exploring haematopoietic stem cell dynamics through mitochondrial mutation profiling by Yongming Xia, Ruixiu Chen, Shiwei Duan

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Papillary thyroid carcinoma tall cell variant shares accumulation of mitochondria, mitochondrial DNA mutations, and loss of oxidative phosphorylation complex I integrity with oncoc... by Oleksiy Tsybrovskyy, Monica De Luise, Dario deBiase, Leonardo Caporali, Claudio Fiorini, Giuseppe Gasparre, Valerio Carelli, Dominik Hackl, Larisa Imamovic, Silke Haim, Manuel Sobrinho‐Simões, Giovanni Tallini

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Possible Role of Mitochondrial Transfer RNA Gene 5816 A > G Genetic Polymorphism (m.5816A > G) in a 3-Year-Old Child with Dystonia: Report of a Case by Sumei Wang, Minglu Liang, Jiehui Ma, Sheng Huang, Lili Fan, Feng Zhu, Dan Sun

Subjects: “…mitochondrial DNA mutation…”
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Mitochondrial DNA Alterations in Glioblastoma and Current Therapeutic Targets by Maher Kurdi, Ahmed Bamaga, Alaa Alkhotani, Thamer Alsharif, Ghada A Abdel-Hamid, Mohamed E Selim, Taghreed Alsinani, Ahmed Albeshri, Adnan Badahdah, Mazen Basheikh, Saleh Baeesa

Subjects: “…mitochondrial dna mutation…”
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A Mitochondrial DNA A8701G Mutation Associated with Maternally Inherited Hypertension and Dilated Cardiomyopathy in a Chinese Pedigree of a Consanguineous Marriage by Ye Zhu, Xiang Gu, Chao Xu

Subjects: “…Dilated Cardiomyopathy; Hypertension; Mitochondria; Mitochondrial DNA Mutation…”
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Identification of a new human mtDNA polymorphism (A14290G) in the NADH dehydrogenase subunit 6 gene by M. Houshmand, T. Mahmoudi, M. Shafa Shariat Panahi, Y. Seyedena, S. Saber, M. Ataei

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Heteroplasmic Variants of Mitochondrial DNA in Atherosclerotic Lesions of Human Aortic Intima by Igor A. Sobenin, Andrey V. Zhelankin, Zukhra B. Khasanova, Vasily V. Sinyov, Lyudmila V. Medvedeva, Maria O. Sagaidak, Vsevolod J. Makeev, Kira I. Kolmychkova, Anna S. Smirnova, Vasily N. Sukhorukov, Anton Y. Postnov, Andrey V. Grechko, Alexander N. Orekhov

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Mitochondrial DNA Mutations in Grade II and III Glioma Cell Lines Are Associated with Significant Mitochondrial Dysfunction and Higher Oxidative Stress by Nor Azian Abdul Murad, Rahman Jamal, Bee Hong Soon, Bee Hong Soon, Sue-Mian Then, Sue-Mian Then, Azizi Abu Bakar, Farizal Fadzil, Jegan Thanabalan, Mohd S. Mohd Haspani, Charng Jeng Toh, Azmi Mohd Tamil, Roslan Harun, Wan Z. Wan Ngah

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Mitochondrial DNA mutations in Korean patients with Leber’s hereditary optic neuropathy by Hee Kyung Yang, Moon-Woo Seong, Jeong-Min Hwang

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An Asp to Strike Out Cancer? Therapeutic Possibilities Arising from Aspartate’s Emerging Roles in Cell Proliferation and Survival by Iiro Taneli Helenius, Hanumantha Rao Madala, Jing-Ruey Joanna Yeh

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Leber's hereditary optic neuropathy with complete visual recovery - the first report by Kalezić Tanja, Maraš Željko, Karamarković Nemanja, Jeremić Miroslav, Bila Mladen

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