Clinical Utility of Synthesized 18-Lead Electrocardiography von Yamamoto, Tetsushi, Awano, Hiroyuki, Ogawa, Shuichiro, Matsuo, Masafumi

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Mutation spectrum of the dystrophin gene in 442 Duchenne Becker muscular dystrophy cases from one Japanese referral center von Takeshima, Yasuhiro, Yagi, Mariko, Okizuka, Yo, Awano, Hiroyuki, Zhang, Zhujun, Yamauchi, Yumiko, Nishio, Hisahide, Matsuo, Masafumi

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Exon skipping induced by nonsense/frameshift mutations in DMD gene results in Becker muscular dystrophy von Okubo, Mariko, Noguchi, Satoru, Hayashi, Shinichiro, Nakamura, Harumasa, Komaki, Hirofumi, Matsuo, Masafumi, Nishino, Ichizo

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An Antisense Oligonucleotide against a Splicing Enhancer Sequence within Exon 1 of the MSTN Gene Inhibits Pre-mRNA Maturation to Act as a Novel Myostatin Inhibitor von Maeta, Kazuhiro, Farea, Manal, Nishio, Hisahide, Matsuo, Masafumi

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A novel splice variant of the human MSTN gene encodes a myostatin‐specific myostatin inhibitor von Maeta, Kazuhiro, Farea, Manal, Nishio, Hisahide, Matsuo, Masafumi

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Cellular senescence-mediated exacerbation of Duchenne muscular dystrophy von Sugihara, Hidetoshi, Teramoto, Naomi, Nakamura, Katsuyuki, Shiga, Takanori, Shirakawa, Taku, Matsuo, Masafumi, Ogasawara, Masashi, Nishino, Ichizo, Matsuwaki, Takashi, Nishihara, Masugi, Yamanouchi, Keitaro

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Dystrophin Dp71ab is monoclonally expressed in human satellite cells and enhances proliferation of myoblast cells von Farea, Manal, Rani, Abdul Qawee Mahyoob, Maeta, Kazuhiro, Nishio, Hisahide, Matsuo, Masafumi

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Contribution of Rare Variants of the SLC22A12 Gene to the Missing Heritability of Serum Urate Levels von Misawa, Kazuharu, Hasegawa, Takanori, Mishima, Eikan, Jutabha, Promsuk, Ouchi, Motoshi, Kojima, Kaname, Kawai, Yosuke, Matsuo, Masafumi, Anzai, Naohiko, Nagasaki, Masao

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Establishment of a highly sensitive sandwich ELISA for the N-terminal fragment of titin in urine von Maruyama, Nobuhiro, Asai, Tsuyoshi, Abe, Chiaki, Inada, Akari, Kawauchi, Takeshi, Miyashita, Kazuya, Maeda, Masahiro, Matsuo, Masafumi, Nabeshima, Yo-ichi

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Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome von Horinouchi, Tomoko, Nozu, Kandai, Yamamura, Tomohiko, Minamikawa, Shogo, Omori, Takashi, Nakanishi, Keita, Fujimura, Junya, Ashida, Akira, Kitamura, Mineaki, Kawano, Mitsuhiro, Shimabukuro, Wataru, Kitabayashi, Chizuko, Imafuku, Aya, Tamagaki, Keiichi, Kamei, Koichi, Okamoto, Kenjirou, Fujinaga, Shuichiro, Oka, Masafumi, Igarashi, Toru, Miyazono, Akinori, Sawanobori, Emi, Fujimaru, Rika, Nakanishi, Koichi, Shima, Yuko, Matsuo, Masafumi, Ye, Ming Juan, Nozu, Yoshimi, Morisada, Naoya, Kaito, Hiroshi, Iijima, Kazumoto

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Diagnostic and clinical significance of the titin fragment in urine of Duchenne muscular dystrophy patients von Awano, Hiroyuki, Matsumoto, Masaaki, Nagai, Masashi, Shirakawa, Taku, Maruyama, Nobuhiro, Iijima, Kazumoto, Nabeshima, Yo-ichi, Matsuo, Masafumi

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Contributions of Japanese patients to development of antisense therapy for DMD von Matsuo, Masafumi, Takeshima, Yasuhiro, Nishio, Hisahide

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Successful skipping of abnormal pseudoexon by antisense oligonucleotides in vitro for a patient with beta-propeller protein-associated neurodegeneration von Yamada, Mamiko, Maeta, Kazuhiro, Suzuki, Hisato, Kurosawa, Ryo, Takenouchi, Toshiki, Awaya, Tomonari, Ajiro, Masahiko, Takeuchi, Atsuko, Nishio, Hisahide, Hagiwara, Masatoshi, Miya, Fuyuki, Matsuo, Masafumi, Kosaki, Kenjiro

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Mortality Rates for Extremely Low Birth Weight Infants Born in Japan in 2005 von Itabashi, Kazuo, Horiuchi, Takeshi, Kusuda, Satoshi, Kabe, Kazuhiko, Itani, Yasufumi, Nakamura, Takashi, Fujimura, Masanori, Matsuo, Masafumi

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Challenges of supplementary treatment for neurodegenerative diseases von Matsuo, Masafumi

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Rbfox2 mediates exon 11 inclusion in insulin receptor pre-mRNA splicing in hepatoma cells von Nakura, Takahito, Ozoe, Atsufumi, Narita, Yuka, Matsuo, Masafumi, Hakuno, Fumihiko, Kataoka, Naoyuki, Takahashi, Shin-Ichiro

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Antisense Oligonucleotide-Mediated Exon-skipping Therapies: Precision Medicine Spreading from Duchenne Muscular Dystrophy von Matsuo, Masafumi

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Interleukin-1beta (IL-1β)-induced Notch ligand Jagged1 suppresses mitogenic action of IL-1β on human dystrophic myogenic cells von Nagata, Yuki, Kiyono, Tohru, Okamura, Kikuo, Goto, Yu-Ichi, Matsuo, Masafumi, Ikemoto-Uezumi, Madoka, Hashimoto, Naohiro

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Human Dystrophin Dp71ab Enhances the Proliferation of Myoblasts Across Species But Not Human Nonmyoblast Cells von Farea, Manal, Maeta, Kazuhiro, Nishio, Hisahide, Matsuo, Masafumi

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Dravet syndrome and hemorrhagic shock and encephalopathy syndrome associated with an intronic deletion of SCN1A von Hanafusa, Hiroaki, Yamaguchi, Hiroshi, Kondo, Hidehito, Nagasaka, Miwako, Juan Ye, Ming, Oikawa, Shizuka, Tokumoto, Shoichi, Tomioka, Kazumi, Nishiyama, Masahiro, Morisada, Naoya, Matsuo, Masafumi, Nozu, Kandai, Nagase, Hiroaki

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