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Balachandar Vellingiri, Dhivya Venkatesan, Mahalaxmi Iyer, Gomathi Mohan, Padmavathi Krishnan, Krothapalli Sai Krishna, Sangeetha R, Arul Narayanasamy, Abilash Valsala Gopalakrishnan, Nachimuthu Senthil Kumar & Mohana Devi Subramaniam. (2023) Concurrent Assessment of Oxidative Stress and MT-ATP6 Gene Profiling to Facilitate Diagnosis of Autism Spectrum Disorder (ASD) in Tamil Nadu Population. Journal of Molecular Neuroscience 73:4-5, pages 214-224.
Crossref
Crossref
Seyta Ley‐Ngardigal & Giulia Bertolin. (2021) Approaches to monitor ATP levels in living cells: where do we stand?. The FEBS Journal 289:24, pages 7940-7969.
Crossref
Crossref
Ramesh Bhat Y. 2022. Common Pediatric Diseases: an Updated Review. Common Pediatric Diseases: an Updated Review
452
479
.
Naoko Kumagai-Takei, Suni Lee, Bandaru Srinivas, Yurika Shimizu, Nagisa Sada, Kei Yoshitome, Tatsuo Ito, Yasumitsu Nishimura & Takemi Otsuki. (2020) The Effects of Asbestos Fibers on Human T Cells. International Journal of Molecular Sciences 21:19, pages 6987.
Crossref
Crossref
Kathryn Cimdins, Hayley S. Waugh, Vicki Chrysostomou, M. Isabel G. Lopez Sanchez, Vanessa A. Johannsen, Mark J. Cook, Jonathan G. Crowston, Andrew F. Hill, James A. Duce, Ashley I. Bush & Ian A. Trounce. (2019) Amyloid Precursor Protein Mediates Neuronal Protection from Rotenone Toxicity. Molecular Neurobiology 56:8, pages 5471-5482.
Crossref
Crossref
Julien Beyrath, Mina Pellegrini, Herma Renkema, Lisanne Houben, Svetlana Pecheritsyna, Peter van Zandvoort, Petra van den Broek, Akkiz Bekel, Pierre Eftekhari & Jan A. M. Smeitink. (2018) KH176 Safeguards Mitochondrial Diseased Cells from Redox Stress-Induced Cell Death by Interacting with the Thioredoxin System/Peroxiredoxin Enzyme Machinery. Scientific Reports 8:1.
Crossref
Crossref
KAI YUAN, WEI LIANG & JIWEI ZHANG. (2015) A comprehensive analysis of differentially expressed genes and pathways in abdominal aortic aneurysm. Molecular Medicine Reports 12:2, pages 2707-2714.
Crossref
Crossref
Mohamed Salama & Wael M.Y. Mohamed. (2015) NDUFA12L mitochondrial complex-I assembly factor: Implications for taupathies. Applied & Translational Genomics 5, pages 37-39.
Crossref
Crossref
Guiyuan Chen, Jie Dai, Shirui Tan, Shengke Meng, Zhongjian Liu, Meizhang Li, Qinghua Cui & Min Yu. (2014) MTERF1 regulates the oxidative phosphorylation activity and cell proliferation in HeLa cells. Acta Biochimica et Biophysica Sinica 46:6, pages 512-521.
Crossref
Crossref
Elise Hacioglu, Ayse Banu Demir & Ahmet Koc. (2012) Identification of respiratory chain gene mutations that shorten replicative life span in yeast. Experimental Gerontology 47:2, pages 149-153.
Crossref
Crossref
Vittoria Petruzzella, Anna Maria Sardanelli, Salvatore Scacco, Damiano Panelli, Francesco Papa, Raffaella Trentadue & Sergio Papa. 2012. Advances in Mitochondrial Medicine. Advances in Mitochondrial Medicine
371
384
.
Saskia Koene, Peter H. G. M. Willems, Peggy Roestenberg, Werner J. H. Koopman & Jan A. M. Smeitink. (2010) Mouse models for nuclear DNA‐encoded mitochondrial complex I deficiency. Journal of Inherited Metabolic Disease 34:2, pages 293-307.
Crossref
Crossref
Cynthia N. Perry, Chengqun Huang, Wayne Liu, Najib Magee, Raquel Sousa Carreira & Roberta A. Gottlieb. (2011) Xenotransplantation of Mitochondrial Electron Transfer Enzyme, Ndi1, in Myocardial Reperfusion Injury. PLoS ONE 6:2, pages e16288.
Crossref
Crossref
S. Koene & J. Smeitink. (2009) Mitochondrial medicine: entering the era of treatment. Journal of Internal Medicine 265:2, pages 193-209.
Crossref
Crossref
Marju Gruno, Nadezhda Peet, Andres Tein, Riina Salupere, Meeli Sirotkina, Julio Valle, Ants Peetsalu & Enn K. Seppet. (2008) Atrophic gastritis: deficient complex I of the respiratory chain in the mitochondria of corpus mucosal cells. Journal of Gastroenterology 43:10, pages 780-788.
Crossref
Crossref
Werner J.H. Koopman, Sjoerd Verkaart, Sjenet E. van Emst-de Vries, Sander Grefte, Jan A.M. Smeitink, Leo G.J. Nijtmans & Peter H.G.M. Willems. (2008) Mitigation of NADH: Ubiquinone oxidoreductase deficiency by chronic Trolox treatment. Biochimica et Biophysica Acta (BBA) - Bioenergetics 1777:7-8, pages 853-859.
Crossref
Crossref
Claude A. Piantadosi & Hagir B. Suliman. (2008) Transcriptional Regulation of SDHa Flavoprotein by Nuclear Respiratory Factor-1 Prevents Pseudo-hypoxia in Aerobic Cardiac Cells. Journal of Biological Chemistry 283:16, pages 10967-10977.
Crossref
Crossref
Aijaz A. Wani, Sajad H. Ahanger, Sharmila A. Bapat, Ashraf Y. Rangrez, Nitin Hingankar, C. G. Suresh, Shama Barnabas, Milind S. Patole & Yogesh S. Shouche. (2007) Analysis of Mitochondrial DNA Sequences in Childhood Encephalomyopathies Reveals New Disease-Associated Variants. PLoS ONE 2:9, pages e942.
Crossref
Crossref
Sjoerd Verkaart, Werner J.H. Koopman, Julia Cheek, Sjenet E. van Emst-de Vries, Lambertus W.P.J. van den Heuvel, Jan A.M. Smeitink & Peter H.G.M. Willems. (2007) Mitochondrial and cytosolic thiol redox state are not detectably altered in isolated human NADH:ubiquinone oxidoreductase deficiency. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1772:9, pages 1041-1051.
Crossref
Crossref
Werner J. H. Koopman, Sjoerd Verkaart, Henk Jan Visch, Sjenet van Emst-de Vries, Leo G. J. Nijtmans, Jan A. M. Smeitink & Peter H. G. M. Willems. (2007) Human NADH:ubiquinone oxidoreductase deficiency: radical changes in mitochondrial morphology?. American Journal of Physiology-Cell Physiology 293:1, pages C22-C29.
Crossref
Crossref
Ali-Reza Moslemi & Niklas Darin. (2007) Molecular genetic and clinical aspects of mitochondrial disorders in childhood. Mitochondrion 7:4, pages 241-252.
Crossref
Crossref
S. Papa, V. Petruzzella & S. Scacco. 2007. Handbook of Neurochemistry and Molecular Neurobiology. Handbook of Neurochemistry and Molecular Neurobiology
93
118
.
Takao YagiByoung Boo SeoEiko Nakamaru-OgisoMathieu MarellaJennifer Barber-SinghTetsuo YamashitaMou-Chieh KaoAkemi Matsuno-Yagi. (2006) Can a Single Subunit Yeast NADH Dehydrogenase (Ndi1) Remedy Diseases Caused by Respiratory Complex I Defects?. Rejuvenation Research 9:2, pages 191-197.
Crossref
Crossref
Byoung Boo Seo, Eiko Nakamaru-Ogiso, Terence R. Flotte, Akemi Matsuno-Yagi & Takao Yagi. (2006) In Vivo Complementation of Complex I by the Yeast Ndi1 Enzyme. Journal of Biological Chemistry 281:20, pages 14250-14255.
Crossref
Crossref
Takao Yagi, Byoung Boo Seo, Eiko Nakamaru-Ogiso, Mathieu Marella, Jennifer Barber-Singh, Tetsuo Yamashita & Akemi Matsuno-Yagi. (2006) Possibility of transkingdom gene therapy for Complex I diseases. Biochimica et Biophysica Acta (BBA) - Bioenergetics 1757:5-6, pages 708-714.
Crossref
Crossref
Michio Hirano & Clotilde Lagier-Tourenne. 2005. Neurogenetics. Neurogenetics
256
283
.
Sergey I. Zhadanov, Vasily V. Atamanov, Nikolay I. Zhadanov, Oleg V. Oleinikov, Ludmila P. Osipova & Theodore G. Schurr. (2005) A novel mtDNA ND6 gene mutation associated with LHON in a Caucasian family. Biochemical and Biophysical Research Communications 332:4, pages 1115-1121.
Crossref
Crossref
Mou-Chieh Kao, Salvatore Di Bernardo, Eiko Nakamaru-Ogiso, Hideto Miyoshi, Akemi Matsuno-Yagi & Takao Yagi. (2005)
Characterization of the Membrane Domain Subunit NuoJ (ND6) of the NADH-Quinone Oxidoreductase from
Escherichia coli
by Chromosomal DNA Manipulation
. Biochemistry 44:9, pages 3562-3571.
Crossref
Crossref
Eric A. Schon. (2004) Complements of the house. Journal of Clinical Investigation 114:6, pages 760-762.
Crossref
Crossref
Byoung Boo SeoEiko Nakamaru-OgisoPedro CruzTerence R. FlotteTakao YagiAkemi Matsuno-Yagi. (2004) Functional Expression of the Single Subunit NADH Dehydrogenase in Mitochondria In Vivo: A Potential Therapy for Complex I Deficiencies. Human Gene Therapy 15:9, pages 887-895.
Crossref
Crossref