Диссертация (1140070), страница 30
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Nat Rev Mol Cell Biol. 2011 Jan; 12(1): 14-20.93. Mick DU, Vukotic M, Piechura H, Meyer HE, Warscheid B, Deckers M, Rehling P (2010).Coa3 and Cox14 are essential for negative feed- back regulation of COX1 translation in mitochondria.J Cell Biol 191, 141–154.94. MITOMAP: A Human Mitochondrial Genome Database. http://www.mitomap.org201295. Munteanu I., Zhou H., Hargreaves I. et al. Investigating mitochondria in cell culture modelsof core myopathies. Neuromuscular Disorders 2012; 22: 7–35.96. Nadaj-Pakleza A.A., Dorobek M., Nestorowicz K., Ryniewicz B., Szmidt-Sałkowska E.,Kamińska AM. Muscle pathology in 31 patients with calpain 3 gene mutations.
Neurol Neurochir Pol.2013 May-Jun; 47(3): 214-22.97. Nahirny A. Elevated Intracellular Ca2+ Alters Mitochondrial Protein Import and theAccumulation of Intramitochondrial Proteins in Neurons. A thesis submitted in conformity with therequirements for the degree of Master of Science. 201198. Nesbitt V., Pitceathly R.D., Turnbull D.M., Taylor R.W., Sweeney M.G., Mudanohwo E.E.,Rahman S., Hanna M.G., McFarland R. The UK MRC Mitochondrial Disease Patient Cohort Study:clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis andmanagement. J Neurol Neurosurg Psychiatry.
2013 Aug 84(8):936-8.99. Old, S. L. & Johnson, M. A. Methods of microphotometric assay of succinatedehydrogenase and cytochrome c oxidase activities for use on human skeletal muscle. Histochem J 21,545–555 (1989).100. Oldfors, A., Larsson, N.-G., Lindberg, C. & Holme, E. Mitochondrial DNA deletions ininclusion body myositis.
Brain 116, 325–336 (1993). 101. Ott M., Herrmann J.M. Co-translational membrane insertion of mitochondrially encodedproteins. Biochim Biophys Acta. 2010 Jun; 1803(6): 767-75.102. Payne B.A., Wilson I.J., Yu-Wai-Man P. et al. Universal heteroplasmy of humanmitochondrial DNA. Human Molecular Genetics 2013; 22: 2: 384-390.103. Percival J.M., Siegel M.P., Knowels G.
et al. Defects in mitochondrial localization andATP synthesis in the mdx mouse model of Duchenne muscular dystrophy are not alleviated by PDE5inhibition. Hum Mol Genet. 2013 Jan 1; 22(1): 153–167.104. Phadke M., Lokeshwar M. R., Bhutada S., Tampi Ch., Saxena R., Kohli S., Shah K. N.Kearns Sayre Syndrome—Case Report with Review of Literature. Indian J Pediatr (May 2012) 79(5):650–654105. Pitceathly, R. D. & McFarland, R.
Mitochondrial myopathies in adults and children:management and therapy development. Curr Opin Neurol 27, 576–582 (2014). 106. Poyton R.O., Ball K.A., Castello P.R. Mitochondrial generation of free radicals andhypoxic signaling.Trends Endocrinol Metab. 2009 Sep; 20(7): 332-40.177107. Reeve, A. K. et al. Nature of mitochondrial DNA deletions in substantia nigra neurons. AmJ Hum Genet 82, 228–235 (2008).108. Rocha MC, Grady JP, Grünewald A, Vincent A, Dobson PF, Taylor RW, Turnbull DM,Rygiel KA.
A novel immuno uorescent assay to investigate oxidative phosphorylation de ciency inmitochondrial myopathy: understanding mechanisms and improving diagnosis. Sci Rep. 2015 Oct 15;5: 15037. doi: 10.1038/srep15037.109. Romero N.B., Bevilacqua J.A., Oldfors A.
et al.: Sporadic centronuclear myopathy withmuscle pseudohypertrophy, neutropenia, and necklace fibres due to a DNM2 mutation. NeuromusculDisord. 21: 148 2011 author reply 148–149.110. Sabatelli P., Palma E., Angelin A. et al. Critical evaluation of the use of cell cultures forinclusion in clinical trials of patients affected by collagen VI myopathies. J Cell Physiol 2012; 227:2927-2935.111.
Schmidt O., Pfanner N., Meisinger C. Mitochondrial protein import: from proteomics tofunctional mechanisms. Nature Rev. Mol. Cell Biol. 11, 655–667 (2010).112. Schon EA, Dimauro S, Hirano M. Human mitochondrial DNA: roles of inherited andsomatic mutations. Nature Reviews Genetics 2012; 13: 878–90.113. Sciacco M. & Bonilla E.
Cytochemistry and immunocytochemistry of mitochondria intissue sections. Methods Enzymol 264, 509–521 (1996). 114. Sewry C.A., Jimenez-Mallebrera C., Muntoni F. Congenital myopathies. Curr Opin Neurol2008; 21: 569–575.115. Siskova Z., D.J. Mahad, C. Pudney, G. Campbell, M. Cadogan, A. Asuni, et al.Morphological and functional abnormalities in mitochondria associated with synaptic degeneration inprion disease.
Am J Pathol, 177 (2010), pp. 1411–1421116. Soto I.C., Fontanesi F, Myera RS, Hamel P, Barrientos A (2012a). A heme- sensingmechanism in the translational regulation of mitochondrial cytochrome c oxidase biogenesis. CellMetabol 16, 801–813.117. Stadhouders A and Sengers R (1987). Morphological observations in Skeletal muscle frompatients with a mitochondrial myopathy. Journal of Inherited Metabolic Disease 10 62-80.118.
Sueoka E, Sueoka-Aragane N, Sato A, Ide M, Nakamura H, Sotomaru Y, Taya C,Yonekawa H, Kitagawa T, Kubota Y, Kimura S, Nakachi K, Tanimoto K (2013) Development oflymphoprolifer- ative diseases by hypoxia inducible factor-1alpha is associated with prolongedlymphocyte survival. PLoS One 8(4): e57833. doi: 10. 1371/journal.pone.0057833.119. Sutendra G, Dromparis P, Kinnaird A, Stenson TH, Haromy A, Parker JM, McMurtry MS,Michelakis ED (2013) Mitochondrial activation by inhibition of PDKII suppresses HIF1a signalingand angiogenesis in cancer. Oncogene 32(13): 1638–1650.
doi: 10.1038/ onc.2012.198.120. Swalwell H, Kirby DM, Blakely EL, Mitchell A, Salemi R, Sugiana C, et al. Respiratorychain complex I deficiency caused by mitochondrial DNA mutations. Eur J Hum Genet 2011; 19:769–75.121. Tanji K., Bonilla E. Light microscopic methods to visualize mitochondria on tissuesections. Methods. 2008 Dec; 46(4): 274-80.178122.
Tawfik V.L., White R.E., Giffard R. Glial Cells, Inflammation and Heat Shock Proteins inCerebral Ischemia. "Advances in the Preclinical Study of Ischemic Stroke", ISBN 978-953-51-0290-8,2012, стр 177-192.123. Tinelli E., Pereira J.A., Suter U. Muscle-specific function of the centronuclear myopathyand Charcot-Marie-Tooth neuropathy-associated dynamin 2 is required for proper lipid metabolism,mitochondria, muscle fibers, neuromuscular junctions and peripheral nerves. Hum Mol Genet 2013;22: 21: 441729.124. Tomita S, Kihira Y, Imanishi M, Fukuhara Y, Imamura Y, Ishizawa K, Ikeda Y, TsuchiyaK, Tamaki T (2011) Pathophysiological response to hypoxia—from the molecular mechanisms ofmalady to drug discovery: inflammatory responses of hypoxia-inducible factor 1al- pha (HIF-1alpha)in T cells observed in development of vascular remodeling.
J Pharmacol Sci 115(4): 433–439.125. Tuppen HA, Blakely EL, Turnbull DM, et al.: Mitochondrial DNA mutations and humandisease. Biochim Biophys Acta. 1797:113-128 2010.126. Voloboueva LA, Duan M, Ouyang Y, Emery JF, Stoy C and Giffard RG. Overexpressionof mitochondrial Hsp70/Hsp75 protects astrocytes against ischemic injury in vitro. J Cereb BloodFlow Metab 28: 5: 1009-1016, 2008.127.
Voos W., Martin H., Krimmer T., Pfanner N. Mechanisms of protein translocation intomitochondria. Biochim Biophys Acta 1422: 235–254, 1999.128. Wanschit J., Nakano S., Goudeau B. et al. Myofibrillar (desmin-related) myopathy:Clinico-pathological spectrum in 3 cases and review of the literature. Clin Neuropathol 2002; 21: 220231.129. Wiesner R.J., Hornung T.V., Garman J.D. et al.
Stimulation of Mitochondrial GeneExpression and Proliferation of Mitochondria Following Impairment of Cellular Energy Transfer byInhibition of the Phosphocreatine Circuit in Rat Hearts // J. Bioenerg. Biomembr. 1999. Vol. 31. P.559—567.130. Williamson CL, Dabkowski ER, Dillmann WH, Hollander JM. Mitochondria protectionfrom hypoxia/reoxygenation injury with mitochondria heat shock protein 70 overexpression. Am JPhysiol Heart Circ Physiol 294: H249–H256, 2008.131.
Xu, L., Voloboueva, L. A., Ouyang, Y., Emery, J. F.& Giffard, R. G. (2009).Overexpression of mitochondrial Hsp70/Hsp75 in rat brain protects mitochondria, reduces oxidativestress, and protects from focal ischemia. J Cereb Blood Flow Metab, Vol. 29, No. 2, pp. 365-374.132. Yatsuga S., Povalko N., Nishioka J., Katayama K., Kakimoto N., Matsuishi T. et al..MELAS: a nationwide prospective cohort study of 96 patients in Japan. Biochim Biophys Acta.
2012;1820(5):619-24.133. Yoshida M., Ozawa E. Glycoprotein complex anchoring dystrophin to sarcolemma.Journal of biochemistry.1990; 108(5):748–52.134. Zeviani M., Di Donato S. Mitochondrial disorders. Brain. 2004; 127(10):2153-72.doi:10.1093/brain/awh259.135. Zhao L, Yang YF, Gao YB, Wang SM, Wang LF, Zuo HY, Dong J, Xu XP, Su ZT, ZhouHM, Zhu LL, Peng RY. Upregulation of HIF-1α via activation of ERK and PI3K pathway mediatedprotective response to microwave-induced mitochondrial injury in neuron-like cells. Mol Neurobiol.2014 Dec; 50(3):1024-34.179136. Zierz CM, Joshi PR, Zierz S. Frequencies of myohistological mitochondrial changes inpatients with mitochondrial DNA deletions and the common m.3243A>G point mutation.Neuropathology.
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