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Research Article

Imbalanced oxidant and antioxidant ratio in myotonic dystrophy type 1

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Pages 503-510 | Received 28 Oct 2013, Accepted 22 Jan 2014, Published online: 20 Feb 2014

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Aleksandra Nikolić-Kokić, Dragan Marinković, Stojan Perić, Zorica Stević, Mihajlo B. Spasić, Duško Blagojević & Vidosava Rakocˇević-Stojanović. (2016) Redox imbalance in peripheral blood of type 1 myotonic dystrophy patients. Redox Report 21:5, pages 232-237.
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Mari Carmen Álvarez-Abril, Irma García-Alcover, Jordi Colonques-Bellmunt, Raquel Garijo, Manuel Pérez-Alonso, Rubén Artero & Arturo López-Castel. (2023) Natural Compound Boldine Lessens Myotonic Dystrophy Type 1 Phenotypes in DM1 Drosophila Models, Patient-Derived Cell Lines, and HSALR Mice. International Journal of Molecular Sciences 24:12, pages 9820.
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Selma Gulyurtlu, Monika S. Magon, Patrick Guest, Panagiotis P. Papavasiliou, Kim D. Morrison, Alan R. Prescott & Judith E. Sleeman. (2022) Condensation properties of stress granules and processing bodies are compromised in myotonic dystrophy type 1. Disease Models & Mechanisms 15:7.
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Yuhei Hasuike, Hideki Mochizuki & Masayuki Nakamori. (2022) Expanded CUG Repeat RNA Induces Premature Senescence in Myotonic Dystrophy Model Cells. Frontiers in Genetics 13.
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Yuhei Hasuike, Hideki Mochizuki & Masayuki Nakamori. (2022) Cellular Senescence and Aging in Myotonic Dystrophy. International Journal of Molecular Sciences 23:4, pages 2339.
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Nicola Mosca, Sara Petrillo, Sara Bortolani, Mauro Monforte, Enzo Ricci, Fiorella Piemonte & Giorgio Tasca. (2021) Redox Homeostasis in Muscular Dystrophies. Cells 10:6, pages 1364.
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Gabriele Siciliano, Lucia Chico, Annalisa Lo Gerfo, Costanza Simoncini, Erika Schirinzi & Giulia Ricci. (2020) Exercise-Related Oxidative Stress as Mechanism to Fight Physical Dysfunction in Neuromuscular Disorders. Frontiers in Physiology 11.
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Filiz Koc, Gülüzar Atli, Sule Yildiz Menziletoglu & Sevgul Kose. (2020) Antioxidant imbalance in the erythrocytes of Myotonic dystrophy Type 1 patients. Archives of Biochemistry and Biophysics 680, pages 108230.
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Laura Ludovica Gramegna, Maria Pia Giannoccaro, David Neil Manners, Claudia Testa, Stefano Zanigni, Stefania Evangelisti, Claudio Bianchini, Federico Oppi, Roberto Poda, Patrizia Avoni, Raffaele Lodi, Rocco Liguori & Caterina Tonon. (2018) Mitochondrial dysfunction in myotonic dystrophy type 1. Neuromuscular Disorders 28:2, pages 144-149.
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Elena Campione, Annalisa Botta, Monia Di Prete, Emanuele Rastelli, Manuela Gibellini, Antonio Petrucci, Sergio Bernardini, Giuseppe Novelli, Luca Bianchi, Augusto Orlandi, Roberto Massa & Chiara Terracciano. (2017) Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis. Neuromuscular Disorders 27:2, pages 163-169.
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Aymeric Ravel-Chapuis, Amanda Klein Gunnewiek, Guy Bélanger, Tara E. Crawford Parks, Jocelyn Côté & Bernard J. Jasmin. (2016) Staufen1 impairs stress granule formation in skeletal muscle cells from myotonic dystrophy type 1 patients. Molecular Biology of the Cell 27:11, pages 1728-1739.
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Jin Huang, Chi Zhou, Jun He, Zheng Hu, Wen-chao Guan & Sheng-hong Liu. (2016) Protective effect of reduced glutathione C60 derivative against hydrogen peroxide-induced apoptosis in HEK 293T cells. Journal of Huazhong University of Science and Technology [Medical Sciences] 36:3, pages 356-363.
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Genevieve Ho. (2015) Congenital and childhood myotonic dystrophy: Current aspects of disease and future directions. World Journal of Clinical Pediatrics 4:4, pages 66.
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Bin He, Hai-Ying Tao & Shi-Qing Liu. (2014) Neuroprotective effects of carboxymethylated chitosan on hydrogen peroxide induced apoptosis in Schwann cells. European Journal of Pharmacology 740, pages 127-134.
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