Therapeutic approach for myotonic dystrophy: Recent advances in translational research von Nakamori, Masayuki

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Targeting Expanded Repeats by Small Molecules in Repeat Expansion Disorders von Nakamori, Masayuki, Mochizuki, Hideki

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Cellular Senescence and Aging in Myotonic Dystrophy von Hasuike, Yuhei, Mochizuki, Hideki, Nakamori, Masayuki

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Nucleic Acid–Based Therapeutics for Parkinson’s Disease von Nakamori, Masayuki, Junn, Eunsung, Mochizuki, Hideki, Mouradian, M. Maral

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Modulating RNA secondary and tertiary structures by mismatch binding ligands von Murata, Asako, Nakamori, Masayuki, Nakatani, Kazuhiko

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Amido-bridged nucleic acid (AmNA)-modified antisense oligonucleotides targeting α-synuclein as a novel therapy for Parkinson’s disease von Uehara, Takuya, Choong, Chi-Jing, Nakamori, Masayuki, Hayakawa, Hideki, Nishiyama, Kumiko, Kasahara, Yuuya, Baba, Kousuke, Nagata, Tetsuya, Yokota, Takanori, Tsuda, Hiroshi, Obika, Satoshi, Mochizuki, Hideki

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Targeting nuclear RNA for in vivo correction of myotonic dystrophy von Wheeler, Thurman M., Leger, Andrew J., Pandey, Sanjay K., MacLeod, A. Robert, Nakamori, Masayuki, Cheng, Seng H., Wentworth, Bruce M., Bennett, C. Frank, Thornton, Charles A.

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The Dimeric Form of 1,3‐Diaminoisoquinoline Derivative Rescued the Mis‐splicing of Atp2a1 and Clcn1 Genes in Myotonic Dystrophy Type 1 Mouse Model von Matsumoto, Jun, Nakamori, Masayuki, Okamoto, Tatsumasa, Murata, Asako, Dohno, Chikara, Nakatani, Kazuhiko

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Splicing biomarkers of disease severity in myotonic dystrophy von Nakamori, Masayuki, Sobczak, Krzysztof, Puwanant, Araya, Welle, Steve, Eichinger, Katy, Pandya, Shree, Dekdebrun, Jeannne, Heatwole, Chad R., McDermott, Michael P., Chen, Tian, Cline, Melissa, Tawil, Rabi, Osborne, Robert J., Wheeler, Thurman M., Swanson, Maurice S., Moxley III, Richard T., Thornton, Charles A.

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Alternative splicing of clathrin heavy chain contributes to the switch from coated pits to plaques von Moulay, Gilles, Lainé, Jeanne, Lemaître, Mégane, Nakamori, Masayuki, Nishino, Ichizo, Caillol, Ghislaine, Mamchaoui, Kamel, Julien, Laura, Dingli, Florent, Loew, Damarys, Bitoun, Marc, Leterrier, Christophe, Furling, Denis, Vassilopoulos, Stéphane

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Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy von Freyermuth, Fernande, Rau, Frédérique, Kokunai, Yosuke, Linke, Thomas, Sellier, Chantal, Nakamori, Masayuki, Kino, Yoshihiro, Arandel, Ludovic, Jollet, Arnaud, Thibault, Christelle, Philipps, Muriel, Vicaire, Serge, Jost, Bernard, Udd, Bjarne, Day, John W., Duboc, Denis, Wahbi, Karim, Matsumura, Tsuyoshi, Fujimura, Harutoshi, Mochizuki, Hideki, Deryckere, François, Kimura, Takashi, Nukina, Nobuyuki, Ishiura, Shoichi, Lacroix, Vincent, Campan-Fournier, Amandine, Navratil, Vincent, Chautard, Emilie, Auboeuf, Didier, Horie, Minoru, Imoto, Keiji, Lee, Kuang-Yung, Swanson, Maurice S., de Munain, Adolfo Lopez, Inada, Shin, Itoh, Hideki, Nakazawa, Kazuo, Ashihara, Takashi, Wang, Eric, Zimmer, Thomas, Furling, Denis, Takahashi, Masanori P., Charlet-Berguerand, Nicolas

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Disrupted prenatal RNA processing and myogenesis in congenital myotonic dystrophy von Thomas, James D, Sznajder, Łukasz J, Bardhi, Olgert, Aslam, Faaiq N, Anastasiadis, Zacharias P, Scotti, Marina M, Nishino, Ichizo, Nakamori, Masayuki, Wang, Eric T, Swanson, Maurice S

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Expanded CUG Repeat RNA Induces Premature Senescence in Myotonic Dystrophy Model Cells von Hasuike, Yuhei, Mochizuki, Hideki, Nakamori, Masayuki

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Analysis of splicing abnormalities in the white matter of myotonic dystrophy type 1 brain using RNA sequencing von Yoshizumi, Kazuki, Nishi, Masamitsu, Igeta, Masataka, Nakamori, Masayuki, Inoue, Kimiko, Matsumura, Tsuyoshi, Fujimura, Harutoshi, Jinnai, Kenji, Kimura, Takashi

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A Dimeric 2,9‐Diamino‐1,10‐phenanthroline Derivative Improves Alternative Splicing in Myotonic Dystrophy Type 1 Cell and Mouse Models von Li, Jinxing, Nakamori, Masayuki, Matsumoto, Jun, Murata, Asako, Dohno, Chikara, Kiliszek, Agnieszka, Taylor, Katarzyna, Sobczak, Krzysztof, Nakatani, Kazuhiko

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Pharmacotherapy alleviates pathological changes in human direct reprogrammed neuronal cell model of myotonic dystrophy type 1 von Eltahir, Mougina K, Nakamori, Masayuki, Hattori, Satoshi, Kimura, Takashi, Mochizuki, Hideki, Nagano, Seiichi

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CAG repeat-binding small molecule improves motor coordination impairment in a mouse model of Dentatorubral–pallidoluysian atrophy von Hasuike, Yuhei, Tanaka, Hana, Gall-Duncan, Terence, Mehkary, Mustafa, Nakatani, Kazuhiko, Pearson, Christopher E., Tsuji, Shoji, Mochizuki, Hideki, Nakamori, Masayuki

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Bidirectional transcription stimulates expansion and contraction of expanded (CTG)•(CAG) repeats von NAKAMORI, Masayuki, PEARSON, Christopher E, THORNTON, Charles A

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Pentamidine reverses the splicing defects associated with myotonic dystrophy von Warf, M. Bryan, Nakamori, Masayuki, Matthys, Catherine M, Thornton, Charles A, Berglund, J. Andrew

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Antineutrophil cytoplasmic antibody-associated vasculitis with predominant truncal muscle weakness: a retrospective case series von Nemoto, Joe, Nishihara, Hideaki, Yasuhi, Taro, Sato, Ryota, Koga, Michiaki, Kanda, Takashi, Nakamori, Masayuki

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