Characterization of Zebrafish Models of Marinesco-Sjögren Syndrome

由 Kawahara, Genri, Hayashi, Yukiko K.
發表在 PLoS One (2016)

Dysferlinopathy Fibroblasts Are Defective in Plasma Membrane Repair

由 Matsuda, Chie, Kiyosue, Kazuyuki, Nishino, Ichizo, Goto, Yuichi, Hayashi, Yukiko K.
發表在 PLoS Curr (2015)

2 Month‐Old Male with Hypotonia

由 Tanboon, Jantima, Viravan, Sorawit, Hayashi, Yukiko K., Nishino, Ichizo, Sangruchi, Tumtip
發表在 Brain Pathol (2015)

The psychoactive drug 25B-NBOMe recapitulates rhabdomyolysis in zebrafish larvae

由 Kawahara, Genri, Maeda, Hideyuki, Kikura-Hanajiri, Ruri, Yoshida, Ken-ichi, Hayashi, Yukiko K.
發表在 Forensic Toxicol (2017)

Treatment with the anti-IL-6 receptor antibody attenuates muscular dystrophy via promoting skeletal muscle regeneration in dystrophin-/utrophin-deficient mice

由 Wada, Eiji, Tanihata, Jun, Iwamura, Akira, Takeda, Shin’ichi, Hayashi, Yukiko K., Matsuda, Ryoichi
發表在 Skelet Muscle (2017)

Chromosome 4q;10q translocations; Comparison with different ethnic populations and FSHD patients

由 Matsumura, Tsuyoshi, Goto, Kanako, Yamanaka, Gaku, Lee, Je Hyeon, Zhang, Cheng, Hayashi, Yukiko K, Arahata, Kiichi
出版 2002

Deficiency of emerin contributes differently to the pathogenesis of skeletal and cardiac muscles in Lmna(H222P/H222P) mutant mice

由 Wada, Eiji, Kato, Megumi, Yamashita, Kaori, Kokuba, Hiroko, Liang, Wen-Chen, Bonne, Gisèle, Hayashi, Yukiko K.
發表在 PLoS One (2019)

A 31‐Year‐Old Man with Slowly Progressive Limb Muscle Weakness and Respiratory Insufficiency

由 Uruha, Akinori, Hayashi, Yukiko K., Mori‐Yoshimura, Madoka, Oya, Yasushi, Kanai, Masahiro, Murata, Miho, Nishino, Ichizo
發表在 Brain Pathol (2017)

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

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

Peracetylated N-Acetylmannosamine, a Synthetic Sugar Molecule, Efficiently Rescues Muscle Phenotype and Biochemical Defects in Mouse Model of Sialic Acid-deficient Myopathy

由 Malicdan, May Christine V., Noguchi, Satoru, Tokutomi, Tomoharu, Goto, Yu-ichi, Nonaka, Ikuya, Hayashi, Yukiko K., Nishino, Ichizo
出版 2012

Rimmed Vacuoles in Becker Muscular Dystrophy Have Similar Features with Inclusion Myopathies

由 Momma, Kazunari, Noguchi, Satoru, Malicdan, May Christine V., Hayashi, Yukiko K., Minami, Narihiro, Kamakura, Keiko, Nonaka, Ikuya, Nishino, Ichizo
出版 2012

A nationwide survey on Marinesco-Sjögren syndrome in Japan

由 Goto, Masahide, Okada, Mari, Komaki, Hirofumi, Sugai, Kenji, Sasaki, Masayuki, Noguchi, Satoru, Nonaka, Ikuya, Nishino, Ichizo, Hayashi, Yukiko K
出版 2014

Nationwide patient registry for GNE myopathy in Japan

由 Mori-Yoshimura, Madoka, Hayashi, Yukiko K, Yonemoto, Naohiro, Nakamura, Harumasa, Murata, Miho, Takeda, Shin’ichi, Nishino, Ichizo, Kimura, En
出版 2014

Inflammatory myopathy with anti-signal recognition particle antibodies: case series of 100 patients

由 Suzuki, Shigeaki, Nishikawa, Atsuko, Kuwana, Masataka, Nishimura, Hiroaki, Watanabe, Yurika, Nakahara, Jin, Hayashi, Yukiko K., Suzuki, Norihiro, Nishino, Ichizo
發表在 Orphanet J Rare Dis (2015)

Sialyllactose ameliorates myopathic phenotypes in symptomatic GNE myopathy model mice

由 Yonekawa, Takahiro, Malicdan, May Christine V., Cho, Anna, Hayashi, Yukiko K., Nonaka, Ikuya, Mine, Toshiki, Yamamoto, Takeshi, Nishino, Ichizo, Noguchi, Satoru
出版 2014

Aberrant myokine signaling in congenital myotonic dystrophy

由 Nakamori, Masayuki, Hamanaka, Kohei, Thomas, James D., Wang, Eric T., Hayashi, Yukiko K., Takahashi, Masanori P., Swanson, Maurice S., Nishino, Ichizo, Mochizuki, Hideki
發表在 Cell Rep (2017)

Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan

由 Okubo, Mariko, Goto, Kanako, Komaki, Hirofumi, Nakamura, Harumasa, Mori-Yoshimura, Madoka, Hayashi, Yukiko K., Mitsuhashi, Satomi, Noguchi, Satoru, Kimura, En, Nishino, Ichizo
發表在 Orphanet J Rare Dis (2017)

Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy)

由 Nakamura, Harumasa, Kimura, En, Mori-Yoshimura, Madoka, Komaki, Hirofumi, Matsuda, Yu, Goto, Kanako, Hayashi, Yukiko K, Nishino, Ichizo, Takeda, Shin‘ichi, Kawai, Mitsuru
出版 2013

Milder forms of muscular dystrophy associated with POMGNT2 mutations

由 Endo, Yukari, Dong, Mingrui, Noguchi, Satoru, Ogawa, Megumu, Hayashi, Yukiko K., Kuru, Satoshi, Sugiyama, Kenji, Nagai, Shigehiro, Ozasa, Shiro, Nonaka, Ikuya, Nishino, Ichizo
發表在 Neurol Genet (2015)

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

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