Dystrophin Dp116: A Yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene

por Matsuo, Masafumi, Awano, Hiroyuki, Matsumoto, Masaaki, Nagai, Masashi, Kawaguchi, Tatsuya, Zhang, Zhujun, Nishio, Hisahide
Publicado 2017

2′-O-Methyl RNA/Ethylene-Bridged Nucleic Acid Chimera Antisense Oligonucleotides to Induce Dystrophin Exon 45 Skipping

por Lee, Tomoko, Awano, Hiroyuki, Yagi, Mariko, Matsumoto, Masaaki, Watanabe, Nobuaki, Goda, Ryoya, Koizumi, Makoto, Takeshima, Yasuhiro, Matsuo, Masafumi
Publicado 2017

DMD transcripts in CRL-2061 rhabdomyosarcoma cells show high levels of intron retention by intron-specific PCR amplification

por Niba, Emma Tabe Eko, Yamanaka, Ryo, Rani, Abdul Qawee Mahyoob, Awano, Hiroyuki, Matsumoto, Masaaki, Nishio, Hisahide, Matsuo, Masafumi
Publicado 2017

Incidence and Neonatal Risk factors of Short Stature and Growth Hormone treatment in Japanese Preterm Infants Born Small for Gestational Age

por Matsumoto, Masaaki, Nagano, Nobuhiko, Awano, Hiroyuki, Ohyama, Shohei, Fujioka, Kazumichi, Iwatani, Sota, Urakami, Tatsuhiko, Iijima, Kazumoto, Morioka, Ichiro
Publicado 2019

SUN-064 Diversity of Endocrine Function in Patients with CHARGE Association

por Uehara, Erika, Nagata, Tomohiro, Terashita, Shintaro, Matsumoto, Masaaki, Yamaguchi, Tomoe, Ota, Tomoko, Yoshii, Keisuke, Naiki, Yasuhiro, Horikawa, Reiko
Publicado 2020

In silico and in vitro analyses of the pathological relevance of the R258H mutation of hepatocyte nuclear factor 4α identified in maturity‐onset diabetes of the young type 1

por Sugawara, Kenji, Nomura, Kazuhiro, Okada, Yuko, Sugano, Aki, Matsumoto, Masaaki, Takarada, Toru, Takeuchi, Atsuko, Awano, Hiroyuki, Hirota, Yushi, Nishio, Hisahide, Takaoka, Yutaka, Ogawa, Wataru
Publicado 2018

Safe administration of sotrovimab to a COVID-19 patient with acute phase type 1 diabetes mellitus

por Tanaka, Haruna, Matsumoto, Masaaki, Hong, Sung Won, Mitsuboshi, Akari, Nagai, Masashi, Yoshino, Go, Otake, Shogo, Matsuo, Susumu, Yamada, Hiroyuki, Kurosawa, Hiroshi, Kasai, Masashi, Ozaki, Kayo
Publicado 2023

Treatment of a case of severe insulin resistance as a result of a PIK3R1 mutation with a sodium–glucose cotransporter 2 inhibitor

por Hamaguchi, Tetsushi, Hirota, Yushi, Takeuchi, Takehito, Nakagawa, Yasushi, Matsuoka, Atsuko, Matsumoto, Masaaki, Awano, Hiroyuki, Iijima, Kazumoto, Cha, Pei Chieng, Satake, Wataru, Toda, Tatsushi, Ogawa, Wataru
Publicado 2018

Cardiac Dysfunction in Duchenne Muscular Dystrophy Is Less Frequent in Patients With Mutations in the Dystrophin Dp116 Coding Region Than in Other Regions

por Yamamoto, Tetsushi, Awano, Hiroyuki, Zhang, Zhujun, Sakuma, Mio, Kitaaki, Shoko, Matsumoto, Masaaki, Nagai, Masashi, Sato, Itsuko, Imanishi, Takamitsu, Hayashi, Nobuhide, Matsuo, Masafumi, Iijima, Kazumoto, Saegusa, Jun
Publicado 2018

Detection of Dystrophin Dp71 in Human Skeletal Muscle Using an Automated Capillary Western Assay System

por Kawaguchi, Tatsuya, Niba, Emma Tabe Eko, Rani, Abdul Qawee Mahyoob, Onishi, Yoshiyuki, Koizumi, Makoto, Awano, Hiroyuki, Matsumoto, Masaaki, Nagai, Masashi, Yoshida, Shinobu, Sakakibara, Sachiko, Maeda, Naoyuki, Sato, Osamu, Nishio, Hisahide, Matsuo, Masafumi
Publicado 2018