Works by Sunada, Yoshihide

Results: 57

Temporal lobe epilepsy associated with GAD autoimmunity.

Published in:

2017

By:

Obata, Atsushi;
Kutoku, Yumiko;
Sunada, Yoshihide;
Okauchi, Seizo;
Kimura, Tomohiko;
Hirukawa, Hidenori;
Tanabe, Akihito;
Kinoshita, Tomoe;
Kohara, Kenji;
Tatsumi, Fuminori;
Shimoda, Masashi;
Kamei, Shinji;
Nakanishi, Shuhei;
Mune, Tomoatsu;
Kaku, Kohei;
Kaneto, Hideaki

Publication type:

Letter

Becker Muscular Dystrophy Accompanied by Anti-HMGCR Antibody-positive Immune-mediated Necrotizing Myopathy.

Published in:

Internal Medicine, 2023, v. 62, n. 9, p. 1345, doi. 10.2169/internalmedicine.0202-22

By:

Asami Munekane;
Yutaka Ohsawa;
Mariko Okubo;
Taiji Nagai;
Hirotake Nishimura;
Ichizo Nishino;
Yoshihide Sunada

Publication type:

Article

A Novel PRPS1 Mutation in a Japanese Patient with CMTX5 .

Published in:

Internal Medicine, 2022, v. 61, n. 11, p. 1749, doi. 10.2169/internalmedicine.8029-21

By:

Shunichi Shirakawa;
Tatsufumi Murakami;
Akihiro Hashiguchi;
Hiroshi Takashima;
Hiroshi Hasegawa;
Kimiyoshi Ichida;
Yoshihide Sunada

Publication type:

Article

Maximal Multistage Shuttle Run Test-induced Myalgia in a Patient with Muscle Phosphorylase B Kinase Deficiency.

Published in:

Internal Medicine, 2022, v. 61, n. 8, p. 1241, doi. 10.2169/internalmedicine.8137-21

By:

Asami Munekane;
Yutaka Ohsawa;
Tokiko Fukuda;
Hirotake Nishimura;
Shin-ichiro Nishimatsu;
Hideo Sugie;
Yoshihiko Saito;
Ichizo Nishino;
Yoshihide Sunada

Publication type:

Article

Fukuyama-type congenital muscular dystrophy (FCMD) and α-dystroglycanopathy.

Published in:

Congenital Anomalies, 2003, v. 43, n. 2, p. 97, doi. 10.1111/j.1741-4520.2003.tb01033.x

By:

Toda, Tatsushi;
Kobayashi, Kazuhiro;
Takeda, Satoshi;
Sasaki, Junko;
Kurahashi, Hiroki;
Kano, Hiroki;
Tachikawa, Masaji;
Wang, Fan;
Nagai, Yoshitaka;
Taniguchi, Kiyomi;
Taniguchi, Mariko;
Sunada, Yoshihide;
Terashima, Toshio;
Endo, Tamao;
Matsumura, Kiichiro

Publication type:

Article

VEGF 164 gene transfer by electroporation improves diabetic sensory neuropathy in mice.

Published in:

Journal of Gene Medicine, 2006, v. 8, n. 6, p. 773, doi. 10.1002/jgm.893

By:

Murakami, Tatsufumi;
Arai, Makiko;
Sunada, Yoshihide;
Nakamura, Akihiro

Publication type:

Article

Muscular dystrophy associated with β-dystroglycan deficiency.

Published in:

Annals of Neurology, 1996, v. 40, n. 6, p. 925, doi. 10.1002/ana.410400617

By:

Salih, Mustafa A. M.;
Sunada, Yoshihide;
Al-Nasser, M.;
Ozo, C. O.;
Al-Turaiki, M. H. S.;
Akbar, Maksood;
Campbell, Kevin P.

Publication type:

Article

Clinical heterogeneity of adhalin deficiency.

Published in:

1996

By:

Morandi, Lucia;
Barresi, Rita;
Di Blasi, Claudia;
Jung, Daniel;
Sunada, Yoshihide;
Confalonieri, Valeria;
Dworzak, Federica;
Mantegazza, Renato;
Antozzi, Carlo;
Jarre, Laura;
Pini, Antonella;
Gobbi, Giuseppe;
Bianchi, Carlo;
Cornelio, Ferdinando;
Campbell, Kevin P.;
Mora, Marina;
Morandi, L;
Barresi, R;
Di Blasi, C;
Jung, D

Publication type:

journal article

Inherited amyloid polyneuropathy type IV (gelsolin variant) in a Japanese family.

Published in:

Annals of Neurology, 1993, v. 33, n. 1, p. 57, doi. 10.1002/ana.410330110

By:

Sunada, Yoshihide;
Shimizu, Teruo;
Nakase, Hirofumi;
Ohta, Shigeo;
Asaoka, Tetsuo;
Amano, Shiro;
Sawa, Mitsuru;
Kagawa, Yasuo;
Kanazawa, Ichiro;
Mannen, Toru

Publication type:

Article

Transgenic expression of a myostatin inhibitor derived from follistatin increases skeletal muscle mass and ameliorates dystrophic pathology in mdx mice.

Published in:

FASEB Journal, 2008, v. 22, n. 2, p. 477, doi. 10.1096/fj.07-8673com

By:

Nakatani, Masashi;
Takehara, Yuka;
Sugino, Hiromu;
Matsumoto, Mitsuru;
Hashimoto, Osamu;
Hasegawa, Yoshihisa;
Murakami, Tatsuya;
Uezumi, Akiyoshi;
Takeda, Shin'ichi;
Noji, Sumihare;
Sunada, Yoshihide;
Tsuchida, Kunihiro

Publication type:

Article

Treatment consensus for management of polymyositis and dermatomyositis among rheumatologists, neurologists and dermatologists.

Published in:

Journal of Dermatology (John Wiley & Sons, Inc.), 2019, v. 46, n. 1, p. e1, doi. 10.1111/1346-8138.14604

By:

Kohsaka, Hitoshi;
Mimori, Tsuneyo;
Kanda, Takashi;
Shimizu, Jun;
Sunada, Yoshihide;
Fujimoto, Manabu;
Kawaguchi, Yasushi;
Jinnin, Masatoshi;
Muro, Yoshinao;
Ishihara, Shoichiro;
Tomimitsu, Hiroyuki;
Ohta, Akiko;
Sumida, Takayuki

Publication type:

Article

Fukuyama-type congenital muscular dystrophy (FCMD) and oc-dystroglycanopathy.

Published in:

Clinical Genetics, 1993, v. 43, n. 2, p. 97, doi. 10.1111/j.1399-0004.1993.tb04427.x

By:

Toda, Tatsushi;
Kobayashi, Kazuhiro;
Takeda, Satoshi;
Sasaki, Junko;
Kurahashi, Hiroki;
Kano, Hiroki;
Tachikawa, Masaji;
Wang, Fan;
Nagai, Yoshitaka;
Taniguchi, Kiyomi;
Taniguchi, Mariko;
Sunada, Yoshihide;
Terashima, Toshio;
Endo, Tamao;
Matsumura, Kiichiro

Publication type:

Article

Three-dimensional MR imaging of brain surface anomalies in fukuyama-type congenital muscular dystrophy.

Published in:

Muscle & Nerve, 1995, v. 18, n. 5, p. 508, doi. 10.1002/mus.880180506

By:

Toda, Tatsushi;
Watanabe, Toshiaki;
Matsumura, Kiichiro;
Sunada, Yoshihide;
Yamada, Hiroki;
Nakano, Imaharu;
Mannen, Toru;
Kanazawa, Ichiro;
Shimizu, Teruo

Publication type:

Article

Involvement of Wnt4 signaling during myogenic proliferation and differentiation of skeletal muscle.

Published in:

Developmental Dynamics, 2007, v. 236, n. 10, p. 2800, doi. 10.1002/dvdy.21327

By:

Takata, Haruyuki;
Terada, Kumiko;
Oka, Hiroaki;
Sunada, Yoshihide;
Moriguchi, Takahiko;
Nohno, Tsutomu

Publication type:

Article

Social problems in daily life of patients with dementia.

Published in:

Geriatrics & Gerontology International, 2019, v. 19, n. 2, p. 113, doi. 10.1111/ggi.13554

By:

Terada, Seishi;
Nakashima, Makoto;
Wakutani, Yosuke;
Nakata, Kenji;
Kutoku, Yumiko;
Sunada, Yoshihide;
Kondo, Keiko;
Ishizu, Hideki;
Yokota, Osamu;
Maki, Yohko;
Hattori, Hideyuki;
Yamada, Norihito

Publication type:

Article

Haplotype analysis in gelsoiin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan.

Published in:

Human Mutation, 1995, v. 6, n. 1, p. 60, doi. 10.1002/humu.1380060112

By:

Paunio, Tiina;
Sunada, Yoshihide;
Kiuru, Sari;
Makishita, Hideo;
Ikeda, Shu-Ichi;
Weissenbach, Jean;
Palo, Jorma;
Peltonen, Leena

Publication type:

Article

Current status and problems of driving in elderly with cognitive decline in Okayama.

Published in:

Kawasaki Medical Journal, 2023, v. 49, p. 69, doi. 10.11482/KMJ-E202349069

By:

Yumiko KUTOKU;
Masahito MIHARA;
Mariko YASUDA;
Hidetoshi TANI;
Yumi AKAMATSU;
Misaki NAKAHATA;
Yoshika MIYAKE;
Yoshihide SUNADA

Publication type:

Article

Clinical value of abnormal median-normal sural sensory response pattern for the early diagnosis of acute oropharyngeal palsy: a comparison of recent and previous cases.

Published in:

Kawasaki Medical Journal, 2021, v. 47, p. 21, doi. 10.11482/KMJ-E202147021

By:

Katsumi KUROKAWA;
Keisuke TACHIYAMA;
Masahiro SONOO;
Haruki YAMADA;
Shoji HEMMI;
Koichi TOMODA;
Yoshihide SUNADA

Publication type:

Article

Atelocollagen-mediated systemic administration of myostatin-targeting siRNA improves muscular atrophy in caveolin-3-deficient mice.

Published in:

Development, Growth & Differentiation, 2011, v. 53, n. 1, p. 48, doi. 10.1111/j.1440-169X.2010.01221.x

By:

Kawakami, Emi;
Kinouchi, Nao;
Adachi, Taro;
Ohsawa, Yutaka;
Ishimaru, Naozumi;
Ohuchi, Hideyo;
Sunada, Yoshihide;
Hayashi, Yoshio;
Tanaka, Eiji;
Noji, Sumihare

Publication type:

Article

Biochemical and pathological changes result from mutated Caveolin-3 in muscle.

Published in:

Skeletal Muscle, 2018, v. 8, n. 1, p. N.PAG, doi. 10.1186/s13395-018-0173-y

By:

González Coraspe, José Andrés;
Weis, Joachim;
Anderson, Mary E.;
Münchberg, Ute;
Lorenz, Kristina;
Buchkremer, Stephan;
Carr, Stephanie;
Zahedi, René Peiman;
Brauers, Eva;
Michels, Hannah;
Sunada, Yoshihide;
Lochmüller, Hanns;
Campbell, Kevin P.;
Freier, Erik;
Hathazi, Denisa;
Roos, Andreas

Publication type:

Article

Treatment consensus for management of polymyositis and dermatomyositis among rheumatologists, neurologists and dermatologists.

Published in:

Neurology & Clinical Neuroscience, 2019, v. 7, n. 1, p. 3, doi. 10.1111/ncn3.12223

By:

Kohsaka, Hitoshi;
Mimori, Tsuneyo;
Kanda, Takashi;
Shimizu, Jun;
Sunada, Yoshihide;
Fujimoto, Manabu;
Kawaguchi, Yasushi;
Jinnin, Masatoshi;
Muro, Yoshinao;
Ishihara, Shoichiro;
Tomimitsu, Hiroyuki;
Ohta, Akiko;
Sumida, Takayuki

Publication type:

Article

Proteinuria in neuronal intranuclear inclusion disease.

Published in:

Neurology & Clinical Neuroscience, 2018, v. 6, n. 2, p. 51, doi. 10.1111/ncn3.12182

By:

Fukai, Yuta;
Yorimitsu, Daisuke;
Nishimura, Hirotake;
Kutoku, Yumiko;
Sasaki, Tamaki;
Kashihara, Naoki;
Ohsawa, Yutaka;
Sunada, Yoshihide

Publication type:

Article

Spuriously Large Subcortex Infarct due to Confluent Smaller Lesions: A Diffusion-Weighted MRI/CT Study.

Published in:

European Neurology, 2005, v. 54, n. 3, p. 161, doi. 10.1159/000090106

By:

Wada, Kuniyasu;
Kimura, Kazumi;
Iguchi, Yasuyuki;
Inoue, Takeshi;
Matsumoto, Noriko;
Shibasaki, Kensaku;
Ueno, Yuji;
Sunada, Yoshihide

Publication type:

Article

A simplified and sensitive method to identify Alzheimer's disease biomarker candidates using patient-derived induced pluripotent stem cells (iPSCs).

Published in:

Journal of Biochemistry, 2017, v. 162, n. 6, p. 391, doi. 10.1093/jb/mvx058

By:

Keiro Shirotani;
Kazuya Matsuo;
Sumio Ohtsuki;
Takeshi Masuda;
Masashi Asai;
Yumiko Kutoku;
Yutaka Ohsawa;
Yoshihide Sunada;
Takayuki Kondo;
Haruhisa Inoue;
Nobuhisa Iwata

Publication type:

Article

Development of sensory neuropathy in streptozotocin‐induced diabetic mice.

Published in:

Brain & Behavior, 2013, v. 3, n. 1, p. 35, doi. 10.1002/brb3.111

By:

Murakami, Tatsufumi;
Iwanaga, Takayuki;
Ogawa, Yoshinao;
Fujita, Yoshiaki;
Sato, Eiji;
Yoshitomi, Hironori;
Sunada, Yoshihide;
Nakamura, Akihiro

Publication type:

Article

Alterations of ATG4A and LC3B in neurons derived from Alzheimer's disease patients.

Published in:

Genes to Cells, 2023, v. 28, n. 4, p. 319, doi. 10.1111/gtc.13010

By:

Shirotani, Keiro;
Watanabe, Kaori;
Hatta, Daisuke;
Kutoku, Yumiko;
Ohsawa, Yutaka;
Sunada, Yoshihide;
Kondo, Takayuki;
Inoue, Haruhisa;
Iwata, Nobuhisa

Publication type:

Article

A novel method to measure sensory nerve conduction of the posterior antebrachial cutaneous nerve.

Published in:

Muscle & Nerve, 2022, v. 66, n. 2, p. 202, doi. 10.1002/mus.27645

By:

Hemmi, Shoji;
Kurokawa, Katsumi;
Nagai, Taiji;
Asano, Akio;
Murakami, Tatsufumi;
Mihara, Masahito;
Sunada, Yoshihide

Publication type:

Article

Acute inflammatory demyelinating polyneuropathy following Ciguatera poisoning.

Published in:

Muscle & Nerve, 2022, v. 65, n. 4, p. E16, doi. 10.1002/mus.27486

By:

Kurokawa, Katsumi;
Sonoo, Masahiro;
Yamamoto, Tetsuya;
Yamada, Haruki;
Hemmi, Shoji;
Tomoda, Koichi;
Sunada, Yoshihide

Publication type:

Article

Anatomical variations of the superficial branch of the radial nerve and the dorsal branch of the ulnar nerve: A detailed electrophysiological study.

Published in:

2021

By:

Hemmi, Shoji;
Kurokawa, Katsumi;
Nagai, Taiji;
Okamoto, Toshio;
Asano, Akio;
Murakami, Tatsufumi;
Mihara, Masahito;
Sunada, Yoshihide

Publication type:

journal article

Variations in the distal branches of the superficial fibular sensory nerve.

Published in:

2017

By:

Hemmi, Shoji;
Kurokawa, Katsumi;
Nagai, Taiji;
Kushida, Ryutaro;
Okamoto, Toshio;
Murakami, Tatsufumi;
Sunada, Yoshihide

Publication type:

journal article

Whole plantar nerve conduction study with disposable strip electrodes.

Published in:

2016

By:

Hemmi, Shoji;
Kurokawa, Katsumi;
Nagai, Taiji;
Okamoto, Toshio;
Murakami, Tatsufumi;
Sunada, Yoshihide

Publication type:

journal article

A novel method to measure sensory nerve conduction of the supraclavicular nerve.

Published in:

Muscle & Nerve, 2014, v. 50, n. 6, p. 1005, doi. 10.1002/mus.24335

By:

Hemmi, Shoji;
Kurokawa, Katsumi;
Nagai, Taiji;
Murakami, Tatsufumi;
Sunada, Yoshihide

Publication type:

Article

Magnetic resonance imaging diagnosis of panniculitis in dermatomyositis.

Published in:

Muscle & Nerve, 2010, v. 41, n. 1, p. 151, doi. 10.1002/mus.21537

By:

Hemmi, Shoji;
Kushida, Ryutaro;
Nishimura, Hirotake;
Murakami, Tatsufumi;
Sunada, Yoshihide

Publication type:

Article

Tongue fasciculations in chronic inflammatory demyelinating polyradiculoneuropathy.

Published in:

Muscle & Nerve, 2008, v. 38, n. 4, p. 1341, doi. 10.1002/mus.21108

By:

Hemmi, Shoji;
Kutoku, Yumiko;
Inoue, Ken;
Murakami, Tatsufumi;
Sunada, Yoshihide

Publication type:

Article

Simple and novel method to measure distal sensory nerve conduction of the medial plantar nerve.

Published in:

Muscle & Nerve, 2007, v. 36, n. 3, p. 307, doi. 10.1002/mus.20814

By:

Hemmi, Shoji;
Inoue, Ken;
Murakami, Tatsufumi;
Sunada, Yoshihide

Publication type:

Article

Full-length dystrophin cDNA transfer into skeletal muscle of adult mdx mice by electroporation.

Published in:

Muscle & Nerve, 2003, v. 27, n. 2, p. 237, doi. 10.1002/mus.10283

By:

Murakami, Tatsufumi;
Nishi, Toru;
Kimura, En;
Goto, Tomoaki;
Maeda, Yasushi;
Ushio, Yukitaka;
Uchino, Makoto;
Sunada, Yoshihide

Publication type:

Article

A low amyloidogenic E61K transthyretin mutation may cause familial amyloid polyneuropathy.

Published in:

Journal of Neurochemistry, 2021, v. 156, n. 6, p. 957, doi. 10.1111/jnc.15162

By:

Murakami, Tatsufumi;
Yokoyama, Takeshi;
Mizuguchi, Mineyuki;
Toné, Shigenobu;
Takaku, Shizuka;
Sango, Kazunori;
Nishimura, Hirotake;
Watabe, Kazuhiko;
Sunada, Yoshihide

Publication type:

Article

Schwann cells contribute to neurodegeneration in transthyretin amyloidosis.

Published in:

Journal of Neurochemistry, 2015, v. 134, n. 1, p. 66, doi. 10.1111/jnc.13068

By:

Murakami, Tatsufumi;
Sango, Kazunori;
Watabe, Kazuhiko;
Niimi, Naoko;
Takaku, Shizuka;
Li, Zhenghua;
Yamamura, Ken‐ichi;
Sunada, Yoshihide

Publication type:

Article

Calcium dysregulation contributes to neurodegeneration in FTLD patient iPSC-derived neurons.

Published in:

Scientific Reports, 2016, p. 34904, doi. 10.1038/srep34904

By:

Imamura, Keiko;
Sahara, Naruhiko;
Kanaan, Nicholas M.;
Tsukita, Kayoko;
Kondo, Takayuki;
Kutoku, Yumiko;
Ohsawa, Yutaka;
Sunada, Yoshihide;
Kawakami, Koichi;
Hotta, Akitsu;
Yawata, Satoshi;
Watanabe, Dai;
Hasegawa, Masato;
Trojanowski, John Q.;
Lee, Virginia M.-Y.;
Suhara, Tetsuya;
Higuchi, Makoto;
Inoue, Haruhisa

Publication type:

Article

Endoplasmic reticulum stress response in P104L mutant caveolin-3 transgenic mice.

Published in:

Human Molecular Genetics, 2011, v. 20, n. 15, p. 2975, doi. 10.1093/hmg/ddr201

By:

Kuga, Atsushi;
Ohsawa, Yutaka;
Okada, Tadashi;
Kanda, Fumio;
Kanagawa, Motoi;
Toda, Tatsushi;
Sunada, Yoshihide

Publication type:

Article

The Inhibitory Core of the Myostatin Prodomain: Its Interaction with Both Type I and II Membrane Receptors, and Potential to Treat Muscle Atrophy.

Published in:

PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0133713

By:

Ohsawa, Yutaka;
Takayama, Kentaro;
Nishimatsu, Shin-ichiro;
Okada, Tadashi;
Fujino, Masahiro;
Fukai, Yuta;
Murakami, Tatsufumi;
Hagiwara, Hiroki;
Itoh, Fumiko;
Tsuchida, Kunihiro;
Hayashi, Yoshio;
Sunada, Yoshihide

Publication type:

Article

<i>SLC25A13</i> Gene Analysis in Citrin Deficiency: Sixteen Novel Mutations in East Asian Patients, and the Mutation Distribution in a Large Pediatric Cohort in China.

Published in:

PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0074544

By:

Song, Yuan-Zong;
Zhang, Zhan-Hui;
Lin, Wei-Xia;
Zhao, Xin-Jing;
Deng, Mei;
Ma, Yan-Li;
Guo, Li;
Chen, Feng-Ping;
Long, Xiao-Ling;
He, Xiang-Ling;
Sunada, Yoshihide;
Soneda, Shun;
Nakatomi, Akiko;
Dateki, Sumito;
Ngu, Lock-Hock;
Kobayashi, Keiko;
Saheki, Takeyori

Publication type:

Article

Local Applications of Myostatin-siRNA with Atelocollagen Increase Skeletal Muscle Mass and Recovery of Muscle Function

Published in:

PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0064719

By:

Kawakami, Emi;
Kawai, Nobuhiko;
Kinouchi, Nao;
Mori, Hiroyo;
Ohsawa, Yutaka;
Ishimaru, Naozumi;
Sunada, Yoshihide;
Noji, Sumihare;
Tanaka, Eiji

Publication type:

Article

Overexpression of P104L mutant caveolin-3 in mice develops hypertrophic cardiomyopathy with enhanced contractility in association with increased endothelial nitric oxide synthase activity.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 2, p. 151, doi. 10.1093/hmg/ddh014

By:

Yutaka Ohsawa;
Haruhiro Toko;
Masashi Katsura;
Kazue Morimoto;
Haruki Yamada;
Yaeko Ichikawa;
Tatsufumi Murakami;
Seitaro Ohkuma;
Issei Komuro;
Yoshihide Sunada

Publication type:

Article

Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 12, p. 1449, doi. 10.1093/hmg/ddg153

By:

Takeda, Satoshi;
Kondo, Mari;
Sasaki, Junko;
Kurahashi, Hiroki;
Kano, Hiroki;
Arai, Ken;
Misaki, Kazuyo;
Fukui, Takehiko;
Kobayashi, Kazuhiro;
Tachikawa, Masaji;
Imamura, Michihiro;
Nakamura, Yusuke;
Shimizu, Teruo;
Murakami, Tatsufumi;
Sunada, Yoshihide;
Fujikado, Takashi;
Matsumura, Kiichiro;
Terashima, Toshio;
Toda, Tatsushi

Publication type:

Article

Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activity.

Published in:

Human Molecular Genetics, 2001, v. 10, n. 3, p. 173, doi. 10.1093/hmg/10.3.173

By:

Sunada, Yoshihide

Publication type:

Article

Dystroglycan Is Essential for Early Embryonic Development: Disruption of Reichert's Membrane in Dag1-Null Mice.

Published in:

Human Molecular Genetics, 1997, v. 6, n. 6, p. 831, doi. 10.1093/hmg/6.6.831

By:

Williamson, Roger A.;
Henry, Michael D.;
Daniels, Karla J.;
Hrstka, Ronald F.;
Lee, Jane C.;
Sunada, Yoshihide;
Ibraghimov-Beskrovnaya, Oxana;
Campbell, Kevin P.

Publication type:

Article

Mild Congenital Muscular Dystrophy in Two Patients with an Internally Deleted Laminin α2-Chain.

Published in:

Human Molecular Genetics, 1997, v. 6, n. 5, p. 747, doi. 10.1093/hmg/6.5.747

By:

Allamand, Valérie;
Sunada, Yoshihide;
Salih, Mustafa A. M.;
Straub, Volker;
Ozo, O.;
Al-Turaiki, M. H. S.;
Akbar, Maksood;
Kolo, Timo;
Colognato, Holly;
Zhang, Xu;
Sorokin, Lydia M.;
Yurchenco, Peter D.;
Tryggvason, Karl;
Campbell, Kevin P.

Publication type:

Article

Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy.

Published in:

Human Molecular Genetics, 1995, v. 4, n. 8, p. 1245

By:

Wells, Dominic J.;
Wells, Kim E.;
Asante, Emmanuel A.;
Turner, Gaynor;
Sunada, Yoshihide;
Campbell, Kevin P.;
Walsh, Frank S.;
Dickson, George

Publication type:

Article

Identification of a novel mutant transcript of laminin α2 chain gene responsible for muscular dystrophy and dysmyelination in dy mice.

Published in:

Human Molecular Genetics, 1995, v. 4, n. 6, p. 1055

By:

Sunada, Yoshihide;
Bernier, Suzanne M.;
Utani, Atsushi;
Yamada, Yoshihiko;
Campbell, Kevin P.

Publication type:

Article