Allele-specific Gene Silencing of Mutant mRNA Restores Cellular Function in Ullrich Congenital Muscular Dystrophy Fibroblasts

Por Noguchi, Satoru, Ogawa, Megumu, Kawahara, Genri, Malicdan, May Christine, Nishino, Ichizo
Publicado em 2014

Muscle Weakness and Fibrosis Due to Cell Autonomous and Non-cell Autonomous Events in Collagen VI Deficient Congenital Muscular Dystrophy

Por Noguchi, Satoru, Ogawa, Megumu, Malicdan, May Christine, Nonaka, Ikuya, Nishino, Ichizo
Publicado no EBioMedicine (2016)

Emerin-Lacking Mice Show Minimal Motor and Cardiac Dysfunctions with Nuclear-Associated Vacuoles

Por Ozawa, Ritsuko, Hayashi, Yukiko K., Ogawa, Megumu, Kurokawa, Rumi, Matsumoto, Hiroshi, Noguchi, Satoru, Nonaka, Ikuya, Nishino, Ichizo
Publicado em 2006

Congenital muscular dystrophy with fatty liver and infantile-onset cataract caused by TRAPPC11 mutations: broadening of the phenotype

Por Liang, Wen-Chen, Zhu, Wenhua, Mitsuhashi, Satomi, Noguchi, Satoru, Sacher, Michael, Ogawa, Megumu, Shih, Hsiang-Hung, Jong, Yuh-Jyh, Nishino, Ichizo
Publicado no Skelet Muscle (2015)

Milder forms of muscular dystrophy associated with POMGNT2 mutations

Por Endo, Yukari, Dong, Mingrui, Noguchi, Satoru, Ogawa, Megumu, Hayashi, Yukiko K., Kuru, Satoshi, Sugiyama, Kenji, Nagai, Shigehiro, Ozasa, Shiro, Nonaka, Ikuya, Nishino, Ichizo
Publicado no Neurol Genet (2015)

A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRI

Por MURAKAMI, Terumi, HAYASHI, Yukiko K., OGAWA, Megumu, NOGUCHI, Satoru, CAMPBELL, Kevin P., TOGAWA, Masami, INOUE, Takehiko, OKA, Akira, OHNO, Kousaku, NONAKA, Ikuya, NISHINO, Ichizo
Publicado em 2008

Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy

Por Hayashi, Yukiko K., Matsuda, Chie, Ogawa, Megumu, Goto, Kanako, Tominaga, Kayo, Mitsuhashi, Satomi, Park, Young-Eun, Nonaka, Ikuya, Hino-Fukuyo, Naomi, Haginoya, Kazuhiro, Sugano, Hisashi, Nishino, Ichizo
Publicado em 2009