Mitochondrial DNA disturbances and deregulated expression of oxidative phosphorylation and mitochondrial fusion proteins in sporadic inclusion body myositis.
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A. Zorzano | Á. Díaz-Ramos | J. Montoya | S. Emperador | J. Grau | C. Morén | G. Garrabou | F. Cardellach | M. Guitart-Mampel | J. Milisenda | M. Bano | M. Catalán-García | E. Tobías | P. Moreno | A. Hernando | Jennifer Enrich-Bengoa | D. Juárez | Ingrid González‐Casacuberta
[1] Manish Kumar,et al. Muscle biopsies from human muscle diseases with myopathic pathology reveal common alterations in mitochondrial function , 2016, Journal of neurochemistry.
[2] M. Duchen,et al. Mitochondrial dynamics and quality control in Huntington's disease , 2016, Neurobiology of Disease.
[3] Josep Maria Salanova Grau,et al. Molecular basis of reduced birth weight in smoking pregnant women: mitochondrial dysfunction and apoptosis , 2016, Addiction biology.
[4] Rick B. Vega,et al. Mitochondrial biogenesis and dynamics in the developing and diseased heart , 2015, Genes & development.
[5] W. Engel,et al. Activation of the Unfolded Protein Response in Sporadic Inclusion-Body Myositis but Not in Hereditary GNE Inclusion-Body Myopathy , 2015, Journal of neuropathology and experimental neurology.
[6] Robert W. Taylor,et al. Mitochondrial and inflammatory changes in sporadic inclusion body myositis , 2015, Neuropathology and applied neurobiology.
[7] Ò. Miró,et al. Mitochondrial disturbances in HIV pregnancies , 2015, AIDS (London).
[8] W. Ding,et al. Mitochondrial dynamics and mitochondrial quality control , 2014, Redox biology.
[9] F. Hanisch,et al. Functional relevance of mitochondrial abnormalities in sporadic inclusion body myositis , 2014, Journal of Clinical Neuroscience.
[10] J. Walter,et al. Powering the Immune System: Mitochondria in Immune Function and Deficiency , 2014, Journal of immunology research.
[11] Prashant Mishra,et al. Mitochondrial dynamics and inheritance during cell division, development and disease , 2014, Nature Reviews Molecular Cell Biology.
[12] M. Mirabella,et al. Muscle biopsy features of idiopathic inflammatory myopathies and differential diagnosis , 2014, Autoimmunity Highlights.
[13] H. Houlden,et al. Sporadic inclusion body myositis: the genetic contributions to the pathogenesis , 2014, Orphanet Journal of Rare Diseases.
[14] Josep Maria Salanova Grau,et al. Diagnosis and classification of sporadic inclusion body myositis (sIBM). , 2014, Autoimmunity reviews.
[15] D. Longo,et al. Role of mitofusin 2 (Mfn2) in controlling cellular proliferation , 2014, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[16] Ò. Miró,et al. Study of oxidative, enzymatic mitochondrial respiratory chain function and apoptosis in perinatally HIV-infected pediatric patients , 2013, Drug and chemical toxicology.
[17] R. Artuch,et al. Coenzyme Q₁₀ deficiency in mitochondrial DNA depletion syndromes. , 2013, Mitochondrion.
[18] Ning Li,et al. Mitochondrial Toxicity Studied with the PBMC of Children from the Chinese National Pediatric Highly Active Antiretroviral Therapy Cohort , 2013, PloS one.
[19] K. Kollewe,et al. Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion , 2013, Acta Neuropathologica.
[20] Ò. Miró,et al. Mitochondrial Evolution in HIV-Infected Children Receiving First- or Second-Generation Nucleoside Analogues , 2012, Journal of Acquired Immune Deficiency Syndromes.
[21] V. Pertegato,et al. Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells , 2012, Nature Protocols.
[22] M. Orešič,et al. Mitofusin 2 (Mfn2) links mitochondrial and endoplasmic reticulum function with insulin signaling and is essential for normal glucose homeostasis , 2012, Proceedings of the National Academy of Sciences.
[23] Ò. Miró,et al. The effects of sepsis on mitochondria. , 2012, The Journal of infectious diseases.
[24] S. Ghosh,et al. Mitochondria in innate immune responses , 2011, Nature Reviews Immunology.
[25] E. Ruiz-Pesini,et al. Macular lesion resembling adult‐onset vitelliform macular dystrophy in Kearns–Sayre syndrome with multiple mtDNA deletions , 2010, Clinical & experimental ophthalmology.
[26] W. Engel,et al. Impaired autophagy in sporadic inclusion-body myositis and in endoplasmic reticulum stress-provoked cultured human muscle fibers. , 2010, The American journal of pathology.
[27] T. Prolla,et al. Mitochondrial Fusion Is Required for mtDNA Stability in Skeletal Muscle and Tolerance of mtDNA Mutations , 2010, Cell.
[28] A. Zorzano,et al. Subjects With Early-Onset Type 2 Diabetes Show Defective Activation of the Skeletal Muscle PGC-1α/Mitofusin-2 Regulatory Pathway in Response to Physical Activity , 2009, Diabetes Care.
[29] F L Mastaglia,et al. Sporadic inclusion body myositis: variability in prevalence and phenotype and influence of the MHC. , 2009, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
[30] Marc Liesa,et al. Mitochondrial dynamics in mammalian health and disease. , 2009, Physiological reviews.
[31] G. Tezel. The role of glia, mitochondria, and the immune system in glaucoma. , 2009, Investigative Ophthalmology and Visual Science.
[32] F. Christiansen,et al. Prevalence of sporadic inclusion body myositis and factors contributing to delayed diagnosis , 2008, Journal of Clinical Neuroscience.
[33] D. Chan,et al. Functions and dysfunctions of mitochondrial dynamics , 2007, Nature Reviews Molecular Cell Biology.
[34] F. Muller,et al. Denervation-induced skeletal muscle atrophy is associated with increased mitochondrial ROS production. , 2007, American journal of physiology. Regulatory, integrative and comparative physiology.
[35] Nan Li,et al. [A clinical and pathological analysis of inclusion body myositis]. , 2007, Zhonghua nei ke za zhi.
[36] Jeong W. Pak,et al. Accumulation of mitochondrial DNA deletion mutations in aged muscle fibers: evidence for a causal role in muscle fiber loss. , 2007, The journals of gerontology. Series A, Biological sciences and medical sciences.
[37] Herrero,et al. Deleciones del ADN mitocondrial asociadas al síndrome de Kearns-Sayre , 2006 .
[38] A. Santel. Get the balance right: mitofusins roles in health and disease. , 2006, Biochimica et biophysica acta.
[39] M. Ovize,et al. Link Between Immune Cell Infiltration and Mitochondria‐Induced Cardiomyocyte Death During Acute Cardiac Graft Rejection , 2006, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.
[40] G. Kollberg,et al. Mitochondrial abnormalities in inclusion-body myositis , 2006, Neurology.
[41] J. Murthy,et al. Diagnosis of mitochondrial diseases: clinical and histological study of sixty patients with ragged red fibers. , 2004, Neurology India.
[42] J. Montoya,et al. De Toni-Debré-Fanconi syndrome due to a palindrome-flanked deletion in mitochondrial DNA , 2004, Pediatric Nephrology.
[43] M. Dalakas,et al. Late‐onset muscle weakness in partial phosphofructokinase deficiency , 1996, Neurology.
[44] P. Chinnery,et al. Disturbed mitochondrial dynamics and neurodegenerative disorders , 2015, Nature Reviews Neurology.
[45] M. Rose,et al. International Workshop : Inclusion Body Myositis , 2 – 4 December 2011 , Naarden , The Netherlands , 2013 .
[46] ScienceDirect,et al. The International Journal of Biochemistry , 2013 .
[47] A. Oldfors,et al. Analysis of multiple mitochondrial DNA deletions in inclusion body myositis , 1997, Human mutation.