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There are 9785 results for: content related to: Mitochondrial DNA (mtDNA) in brain samples from patients with major psychiatric disorders: Gene expression profiles, MtDNA content and presence of the MtDNA common deletion

  1. Transition to Next Generation Analysis of the Whole Mitochondrial Genome: A Summary of Molecular Defects

    Human Mutation

    Volume 34, Issue 6, June 2013, Pages: 882–893, Sha Tang, Jing Wang, Victor Wei Zhang, Fang-Yuan Li, Megan Landsverk, Hong Cui, Cavatina K. Truong, Guoli Wang, Li Chieh Chen, Brett Graham, Fernando Scaglia, Eric S. Schmitt, William J. Craigen and Lee-Jun C. Wong

    Version of Record online : 2 APR 2013, DOI: 10.1002/humu.22307

  2. The human mitochondrial transcriptome and the RNA-binding proteins that regulate its expression

    Wiley Interdisciplinary Reviews: RNA

    Volume 3, Issue 5, September/October 2012, Pages: 675–695, Oliver Rackham, Timothy R. Mercer and Aleksandra Filipovska

    Version of Record online : 9 JUL 2012, DOI: 10.1002/wrna.1128

  3. You have free access to this content
    Complete Mitochondrial Genome Analysis and Clinical Documentation of a Five-Generational Indian Family with Mitochondrial 1555A>G Mutation and Postlingual Hearing Loss

    Annals of Human Genetics

    Volume 78, Issue 3, May 2014, Pages: 217–234, Mahalingam Subathra, Mathiyalagan Selvakumari, Arabandi Ramesh, Rajagopalan Ramakrishnan, Kalpita Rashmi Karan, Manpreet Kaur, Mayakannan Manikandan and C. R. Srikumari Srisailapathy

    Version of Record online : 24 MAR 2014, DOI: 10.1111/ahg.12061

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    Characterization of cis-acting elements in the promoter of the mouse metallothionein-3 gene

    European Journal of Biochemistry

    Volume 267, Issue 6, March 2000, Pages: 1743–1753, Raffaella Faraonio, Pierre Moffatt, Olivier LaRochelle, Hyman M. Schipper, René S-Arnaud and Carl Séguin

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1432-1327.2000.01167.x

  5. Capture of Somatic mtDNA Point Mutations with Severe Effects on Oxidative Phosphorylation in Synaptosome Cybrid Clones from Human Brain

    Human Mutation

    Volume 35, Issue 12, December 2014, Pages: 1476–1484, Matthew McKenzie, Maria Chiotis, Jana Hroudová, Maria I.G. Lopez Sanchez, Sze Chern Lim, Mark J. Cook, Penny McKelvie, Richard G. H. Cotton, Michael Murphy, Justin C. St John and Ian A. Trounce

    Version of Record online : 24 NOV 2014, DOI: 10.1002/humu.22694

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    Genetic aetiology of ophthalmological manifestations in children – a focus on mitochondrial disease-related symptoms

    Acta Ophthalmologica

    Volume 94, Issue 1, February 2016, Pages: 83–91, Paula Widgren, Anri Hurme, Aura Falck, Riikka Keski-Filppula, Anne M Remes, Jukka Moilanen, Kari Majamaa, Marko Kervinen and Johanna Uusimaa

    Version of Record online : 8 OCT 2015, DOI: 10.1111/aos.12897

  7. You have full text access to this OnlineOpen article
    High frequency of mitochondrial DNA mutations in HIV-infected treatment-experienced individuals

    HIV Medicine

    M Li, Y Foli, Z Liu, G Wang, Y Hu, Q Lu, S Selvaraj, W Lam and E Paintsil

    Version of Record online : 22 JUN 2016, DOI: 10.1111/hiv.12390

  8. Role of genetics in resistance to type 1 diabetes

    Diabetes/Metabolism Research and Reviews

    Volume 27, Issue 8, November 2011, Pages: 849–853, Jing Chen, Aaron M. Gusdon and Clayton E. Mathews

    Version of Record online : 8 NOV 2011, DOI: 10.1002/dmrr.1260

  9. New MT-ND1 pathologic mutation for Leber hereditary optic neuropathy

    Clinical & Experimental Ophthalmology

    Volume 42, Issue 9, December 2014, Pages: 856–864, Íñigo Martínez-Romero, M Dolores Herrero-Martín, Laura Llobet, Sonia Emperador, Antonio Martín-Navarro, Bernat Narberhaus, Francisco J Ascaso, Ester López-Gallardo, Julio Montoya and Eduardo Ruiz-Pesini

    Version of Record online : 30 MAY 2014, DOI: 10.1111/ceo.12355

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    Mitochondrial and inflammatory changes in sporadic inclusion body myositis

    Neuropathology and Applied Neurobiology

    Volume 41, Issue 3, April 2015, Pages: 288–303, Karolina A. Rygiel, James Miller, John P. Grady, Mariana C. Rocha, Robert W. Taylor and Doug M. Turnbull

    Version of Record online : 4 MAR 2015, DOI: 10.1111/nan.12149

  11. The role of mitochondrial dysfunction in psychiatric disease

    Developmental Disabilities Research Reviews

    Volume 16, Issue 2, June 2010, Pages: 136–143, Fernando Scaglia

    Version of Record online : 27 AUG 2010, DOI: 10.1002/ddrr.115

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    The transcription factors MTF-1 and USF1 cooperate to regulate mouse metallothionein-I expression in response to the essential metal zinc in visceral endoderm cells during early development

    The EMBO Journal

    Volume 20, Issue 5, March 1, 2001, Pages: 1114–1122, Glen K. Andrews, Dae Kee Lee, Rudravajhala Ravindra, Peter Lichtlen, Mario Sirito, Michele Sawadogo and Walter Schaffner

    Version of Record online : 1 MAR 2001, DOI: 10.1093/emboj/20.5.1114

  13. SNP-finding in pig mitochondrial ESTs

    Animal Genetics

    Volume 39, Issue 2, April 2008, Pages: 193–195, K. Scheibye-Alsing, S. Cirera, M. J. Gilchrist, M. Fredholm and J. Gorodkin

    Version of Record online : 8 FEB 2008, DOI: 10.1111/j.1365-2052.2007.01694.x

  14. Mitochondrial DNA Variation and Heteroplasmy in Monozygotic Twins Clinically Discordant for Multiple Sclerosis

    Human Mutation

    Volume 37, Issue 8, August 2016, Pages: 765–775, Nicole Y.P. Souren, Lisa A. Gerdes, Tania Kümpfel, Pavlo Lutsik, Thomas Klopstock, Reinhard Hohlfeld and Jörn Walter

    Version of Record online : 13 MAY 2016, DOI: 10.1002/humu.23003

  15. Fourier transform IR and Fourier transform Raman spectroscopy studies of metallothionein-III: Amide I band assignments and secondary structural comparison with metallothioneins-I and -II


    Volume 65, Issue 2, 15 October 2002, Pages: 81–88, Yan-Bo Shi, Jiang-Lin Fang, Xiao-Yu Liu, Liang Du and Wen-Xia Tang

    Version of Record online : 21 AUG 2002, DOI: 10.1002/bip.10195

  16. Downregulated expression of metallothionein and its clinicopathological significance in hepatocellular carcinoma

    Hepatology Research

    Volume 37, Issue 10, October 2007, Pages: 820–827, Xia Tao, Jian-Ming Zheng, Ai-Min Xu, Xin-Fang Chen and Shu-Hui Zhang

    Version of Record online : 22 MAY 2007, DOI: 10.1111/j.1872-034X.2007.00113.x

  17. Effects of data incompleteness on the relative performance of parsimony and Bayesian approaches in a supermatrix phylogenetic reconstruction of Mustelidae and Procyonidae (Carnivora)


    Volume 26, Issue 2, April 2010, Pages: 168–194, Mieczyslaw Wolsan and Jun J. Sato

    Version of Record online : 1 SEP 2009, DOI: 10.1111/j.1096-0031.2009.00281.x

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    NADH dehydrogenase subunit 4 variant sequences in childhood acute myeloid leukaemia

    British Journal of Haematology

    Volume 161, Issue 6, June 2013, Pages: 891–895, Michael A. Morgan, Birgit Markus, Malou Hermkens, Frederik Damm, Dirk Reinhardt, Martin Zimmermann, Felicitas Thol, Tania Bunke, Dessislava Bogoeva, Christoph W. M. Reuter, Valerie de Haas, Marry M. van den Heuvel-Eibrink, Christian M. Zwaan and Katarina Reinhardt

    Version of Record online : 25 MAR 2013, DOI: 10.1111/bjh.12298

  19. Whole-Exome Sequencing Identifies a Variant of the Mitochondrial MT-ND1 Gene Associated with Epileptic Encephalopathy: West Syndrome Evolving to Lennox–Gastaut Syndrome

    Human Mutation

    Volume 34, Issue 12, December 2013, Pages: 1623–1627, Aitor Delmiro, Henry Rivera, María Teresa García-Silva, Inés García-Consuegra, Elena Martín-Hernández, Pilar Quijada-Fraile, Rogelio Simón de Las Heras, Ana Moreno-Izquierdo, Miguel Ángel Martín, Joaquín Arenas and Francisco Martínez-Azorín

    Version of Record online : 10 OCT 2013, DOI: 10.1002/humu.22445

  20. Ribozyme-mediated downregulation of human metallothionein IIa induces apoptosis in human prostate and ovarian cancer cell lines

    Molecular Carcinogenesis

    Volume 33, Issue 1, January 2002, Pages: 44–55, Seshadri Tekur and Shuk-Mei Ho

    Version of Record online : 22 JAN 2002, DOI: 10.1002/mc.10017