Publications by authors named "Michinori Funato"

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Establishment of human Leber's hereditary optic neuropathy model using iPSC-derived retinal organoids.
Kota Aoshima, Yuya Takagi, Michinori Funato, Yoshiki Kuse, Shinsuke Nakamura

Front Cell Neurosci· September 2025

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Establishment of vascularized human retinal organoids from induced pluripotent stem cells.
Satoshi Inagaki, Shinsuke Nakamura, Yoshiki Kuse, Kota Aoshima, Michinori Funato

Stem Cells· March 2025

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Safety and efficacy of viltolarsen treatment in patients with Duchenne muscular dystrophy: A retrospective study with 3-year follow-up.
Michinori Funato, Reina Iwata, Toru Ando, Motohiro Takeuchi, Yohei Horibe, Takashi Funato

Brain Dev· February 2025

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Urinary titin reflects the severity of walking ability, muscle strength, and muscle and cardiac damage in patients with Becker muscular dystrophy.
Hiroyuki Awano, Yoshinori Nambu, Kayo Osawa, Taku Shirakawa, Tsuyoshi Matsumura, Michinori Funato

Clin Chim Acta· January 2025

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Association of the immunogenicity of intramuscular SARS-CoV-2 mRNA vaccination with computed tomography muscle images in patients with muscular disorders.
Tomoaki Naka, Michinori Funato, Kunihiko Yasuda, Takahiro Nakayama, Satoshi Kuru

Front Immunol· January 2025

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Threshold dose of cow's milk in sensitization to casein higher than those of casein and β-lactoglobulin in children with cow's milk allergy.
Yukiko Otsuka, Hideyuki Morita, Yuka Kimura, Rikako Mori, Kumiko Miyazaki, Michinori Funato

Asian Pac J Allergy Immunol· December 2024

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Later efficacy of nusinersen treatment in adult patients with spinal muscular atrophy: A retrospective case study with a median 4-year follow-up.
Michinori Funato, Atsunari Kino, Reina Iwata, Misaki Yumioka, Kohei Yamashita

Brain Dev· January 2024

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Efficacy of 5% sofpironium bromide gel in Duchenne muscular dystrophy with palmoplantar hyperhidrosis: A retrospective case study.
Michinori Funato, Reina Iwata, Masami Iimoto

J Dermatol· January 2024

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Intellectual disability and abnormal cortical neuron phenotypes in patients with Bloom syndrome.
Hideo Kaneko, Chizuru Kawase, Junko Seki, Yasuhiro Ikawa, Akihiro Yachie, Michinori Funato

J Hum Genet· May 2023

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Development of an osteosarcoma model with MYCN amplification and TP53 mutation in hiPS cell-derived neural crest cells.
Kyosuke Mukae, Hisanori Takenobu, Yuki Endo, Masayuki Haruta, Tianyuan Shi, Michinori Funato

Cancer Sci· May 2023

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Immunogenicity of SARS-CoV-2 mRNA intramuscular vaccination in patients with muscular disorders.
Ryousuke Kasai, Michinori Funato, Kanako Maruta, Kunihiko Yasuda, Hiroshi Minatsu

Front Immunol· February 2023

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RNA-seq analysis, targeted long-read sequencing and in silico prediction to unravel pathogenic intronic events and complicated splicing abnormalities in dystrophinopathy.
Mariko Okubo, Satoru Noguchi, Tomonari Awaya, Motoyasu Hosokawa, Nobue Tsukui, Michinori Funato

Hum Genet· January 2023

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Efficacy of interferential current transcutaneous electrical sensory stimulation through the neck skin for treating dysphagia in children with disabilities: A case series.
Michinori Funato, Kanako Maruta, Mitsuru Yano, Mitsue Kai, Yaeko Umezawa

SAGE Open Med Case Rep· January 2023

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Cohesinopathy presenting with microtia, facial palsy, and hearing loss caused by STAG1 pathogenic variant.
Michinori Funato, Tomoko Uehara, Yuki Okada, Hideo Kaneko, Kenjiro Kosaki

Congenit Anom (Kyoto)· March 2022

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Duchenne muscular dystrophy diagnosis using fibroblast-derived myotube cells.
Yuki Okada, Michinori Funato, Shin'ichi Takeda, Hideo Kaneko

Pediatr Int· January 2022

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Noonan syndrome-like phenotype in a patient with heterozygous ERF truncating variant.
Mamiko Yamada, Michinori Funato, Goro Kondo, Hisato Suzuki, Tomoko Uehara

Congenit Anom (Kyoto)· November 2021

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A web-based questionnaire survey on the influence of coronavirus disease-19 on the care of patients with muscular dystrophy.
Tsuyoshi Matsumura, Hiroto Takada, Michio Kobayashi, Takashi Nakajima, Katsuhisa Ogata, Michinori Funato

Neuromuscul Disord· September 2021

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Study Protocol for a Multicenter, Open-Label, Single-Arm Study of Tranilast for Cardiomyopathy of Muscular Dystrophy.
Tsuyoshi Matsumura, Hiroya Hashimoto, Masahiro Sekimizu, Akiko M Saito, Yuko Iwata, Michinori Funato

Kurume Med J· July 2021

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Characteristics of Li-Fraumeni Syndrome in Japan; A Review Study by the Special Committee of JSHT.
Michinori Funato, Yukiko Tsunematsu, Fumito Yamazaki, Chieko Tamura, Tadashi Kumamoto

Cancer Sci· May 2021

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Viltolarsen in Japanese Duchenne muscular dystrophy patients: A phase 1/2 study.
Hirofumi Komaki, Yasuhiro Takeshima, Tsuyoshi Matsumura, Shiro Ozasa, Michinori Funato

Ann Clin Transl Neurol· December 2020

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Phosphoethanolamine Elevation in Plasma of Spinal Muscular Atrophy Type 1 Patients.
Mawaddah Ar Rochmah, Yogik Onky Silvana Wijaya, Nur Imma Fatimah Harahap, Chisato Tode, Atsuko Takeuchi, Michinori Funato

Kobe J Med Sci· April 2020

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Early phase 2 trial of TAS-205 in patients with Duchenne muscular dystrophy.
Hirofumi Komaki, Yoshihiro Maegaki, Tsuyoshi Matsumura, Kazuhiro Shiraishi, Hiroyuki Awano, Michinori Funato

Ann Clin Transl Neurol· February 2020

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The Protective Effects of Levetiracetam on a Human iPSCs-Derived Spinal Muscular Atrophy Model.
Shiori Ando, Michinori Funato, Kazuki Ohuchi, Satoshi Inagaki, Arisu Sato

Neurochem Res· July 2019

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Notch Signaling Mediates Astrocyte Abnormality in Spinal Muscular Atrophy Model Systems.
Kazuki Ohuchi, Michinori Funato, Yuta Yoshino, Shiori Ando, Satoshi Inagaki

Sci Rep· March 2019

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