Works by Nonaka, Ikuya

Results: 136

Sarcolemmopathy: Muscular Dystrophies with Cell Membrane Defects.

Published in:

Brain Pathology, 2001, v. 11, n. 2, p. 218, doi. 10.1111/j.1750-3639.2001.tb00394.x

By:

Ozawa, Eijiro;
Nishino, Ichizo;
Nonaka, Ikuya

Publication type:

Article

Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model.

Published in:

Nature Medicine, 2009, v. 15, n. 6, p. 690, doi. 10.1038/nm.1956

By:

Malicdan, May Christine V.;
Noguchi, Satoru;
Hayashi, Yukiko K.;
Nonaka, Ikuya;
Nishino, Ichizo

Publication type:

Article

Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA.

Published in:

Nature Medicine, 2001, v. 7, n. 8, p. 934, doi. 10.1038/90976

By:

Nakada, Kazuto;
Inoue, Kimiko;
Ono, Tomoko;
Isobe, Kotoyo;
Ogura, Atsuo;
Goto, Yu-ichi;
Nonaka, Ikuya;
Hayashi, Jun-Ichi

Publication type:

Article

Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes.

Published in:

Nature Genetics, 2000, v. 26, n. 2, p. 176, doi. 10.1038/82826

By:

Inoue, Kimiko;
Nakada, Kazuto;
Ogura, Atsuo;
Isobe, Kotoyo;
Goto, Yu-ichi;
Nonaka, Ikuya;
Hayashi, Jun-Ichi

Publication type:

Article

Fatal cerebral hemorrhage in mitochondrial encephalomyopathy.

Published in:

Journal of Neurology, 2006, v. 253, n. 4, p. 529, doi. 10.1007/s00415-005-0010-1

By:

Kato, Haruhisa;
Uchigata, Masanobu;
Iijima, Mutsumi;
Shimizu, Seeichiro;
Nonaka, Ikuya;
Goto, Yuichi

Publication type:

Article

High-density areas on muscle CT in childhood-onset Pompe disease are caused by excess calcium accumulation.

Published in:

2010

By:

Ishigaki, Keiko;
Mitsuhashi, Satomi;
Kuwatsuru, Ryohei;
Murakami, Terumi;
Shishikura, Keiko;
Suzuki, Haruko;
Hirayama, Yoshito;
Nonaka, Ikuya;
Osawa, Makiko

Publication type:

Report

Congenital myotonic dystrophy can show congenital fiber type disproportion pathology.

Published in:

Acta Neuropathologica, 2010, v. 119, n. 4, p. 481, doi. 10.1007/s00401-010-0660-7

By:

Tominaga, Kayo;
Hayashi, Yukiko K.;
Goto, Kanako;
Minami, Narihiro;
Noguchi, Satoru;
Nonaka, Ikuya;
Miki, Tetsuro;
Nishino, Ichizo

Publication type:

Article

Ultrastructural detection of DNA fragmentation in myonuclei of fatal reducing body myopathy.

Published in:

Acta Neuropathologica, 2004, v. 107, n. 5, p. 439, doi. 10.1007/s00401-004-0831-5

By:

Ikezoe, Koji;
Nakagawa, Masahiro;
Osoegawa, Manabu;
Kira, Jun-ichi;
Nonaka, Ikuya

Publication type:

Article

Dysferlin expression in tubular aggregates: their possible relationship to endoplasmic reticulum stress.

Published in:

Acta Neuropathologica, 2003, v. 105, n. 6, p. 603, doi. 10.1007/s00401-003-0686-1

By:

Ikezoe, Koji;
Furuya, Hirokazu;
Ohyagi, Yasumasa;
Osoegawa, Manabu;
Nishino, Ichizo;
Nonaka, Ikuya;
Kira, Jun-ichi

Publication type:

Article

Apoptosis is suspended in muscle of mitochondrial encephalomyopathies.

Published in:

Acta Neuropathologica, 2002, v. 103, n. 6, p. 531, doi. 10.1007/s00401-001-0502-8

By:

Ikezoe, Koji;
Nakagawa, Masahiro;
Yan, Chuanzhu;
Kira, Jun-ichi;
Goto, Yu-ichi;
Nonaka, Ikuya

Publication type:

Article

Apoptotic muscle fiber degeneration in distal myopathy with rimmed vacuoles.

Published in:

Acta Neuropathologica, 2001, v. 101, n. 1, p. 9, doi. 10.1007/s004010000249

By:

Yan, Chuanzhu;
Ikezoe, Koji;
Nonaka, Ikuya

Publication type:

Article

Expression of MyoD and myogenin in dystrophic mice, mdx and dy, during regeneration.

Published in:

Acta Neuropathologica, 2000, v. 99, n. 6, p. 619, doi. 10.1007/s004010051172

By:

Jin, Yuko;
Murakami, Nobuyuki;
Saito, Yoko;
Goto, Yu-ichi;
Koishi, Kyoko;
Nonaka, Ikuya

Publication type:

Article

Nebulin is normally expressed in nemaline myopathy.

Published in:

Acta Neuropathologica, 1999, v. 97, n. 5, p. 433, doi. 10.1007/s004010051011

By:

Imoto, C.;
Kimura, Sumiko;
Kawai, Mitsuru;
Nonaka, Ikuya

Publication type:

Article

Fiber-type-dependent expression of adenovirus-mediated transgene in mouse skeletal muscle fibers.

Published in:

Acta Neuropathologica, 1998, v. 96, n. 3, p. 228, doi. 10.1007/s004010050888

By:

Hagiwara, Y.;
Ishii, A.;
Nonaka, Ikuya;
Kikuchi, Tateki;
Takeda, Shin’ichi

Publication type:

Article

Apoptotic nuclear degeneration in Marinesco-Sjögren syndrome.

Published in:

Acta Neuropathologica, 1997, v. 94, n. 5, p. 410, doi. 10.1007/s004010050727

By:

Suzuki, Y.;
Murakami, Nobuyuki;
Goto, Yu-ichi;
Orimo, Satoshi;
Komiyama, Atsushi;
Kuroiwa, Yoshiyuki;
Nonaka, Ikuya

Publication type:

Article

Basement membrane abnormality in merosin-negative congenital muscular dystrophy.

Published in:

Acta Neuropathologica, 1996, v. 91, n. 4, p. 332, doi. 10.1007/s004010050433

By:

Osari, Shin-ichi;
Kobayashi, Osamu;
Yamashita, Yushiro;
Matsuishi, Toyojiro;
Goto, Michiyo;
Tanabe, Yuzo;
Migita, Takuo;
Nonaka, Ikuya

Publication type:

Article

Dystrophin-positive muscle fibers following C2 myoblast transplantation into mdx nude mice.

Published in:

Acta Neuropathologica, 1995, v. 90, n. 6, p. 592, doi. 10.1007/BF00318571

By:

Hagiwara, Yasuko;
Mizuno, Yuji;
Takemitsu, Masakazu;
Matsuzaki, Tetsuya;
Nonaka, Ikuya;
Ozawa, Eijiro

Publication type:

Article

Reducing bodies in distal myopathy with rimmed vacuole formation.

Published in:

Acta Neuropathologica, 1995, v. 89, n. 1, p. 109, doi. 10.1007/BF00294268

By:

Kiyomoto, Beatriz;
Murakami, Nobuyuki;
Kishibayashi, Jun;
Sunohara, Nobuhiko;
Nonaka, Ikuya

Publication type:

Article

Muscle fiber degeneration in distal myopathy with rimmed vacuole formation.

Published in:

Acta Neuropathologica, 1995, v. 89, n. 1, p. 29, doi. 10.1007/BF00294256

By:

Murakami, Nobuyuki;
Ihara, Yasuo;
Nonaka, Ikuya

Publication type:

Article

Dystrophin-related protein in skeletal muscles in neuromuscular disorders: immunohistochemical study.

Published in:

Acta Neuropathologica, 1993, v. 85, n. 3, p. 256, doi. 10.1007/BF00227719

By:

Takemitsu, Masakazu;
Nonaka, Ikuya;
Sugita, Hideo

Publication type:

Article

CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations.

Published in:

Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01084-4

By:

Ogasawara, Masashi;
Iida, Aritoshi;
Kumutpongpanich, Theerawat;
Ozaki, Ayami;
Oya, Yasushi;
Konishi, Hirofumi;
Nakamura, Akinori;
Abe, Ryuta;
Takai, Hiroshi;
Hanajima, Ritsuko;
Doi, Hiroshi;
Tanaka, Fumiaki;
Nakamura, Hisayoshi;
Nonaka, Ikuya;
Wang, Zhaoxia;
Hayashi, Shinichiro;
Noguchi, Satoru;
Nishino, Ichizo

Publication type:

Article

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

Published in:

PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0052002

By:

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

Publication type:

Article

Unfolded protein response and aggresome formation in hereditary reducing-body myopathy.

Published in:

Muscle & Nerve, 2007, v. 35, n. 3, p. 322, doi. 10.1002/mus.20691

By:

Liewluck, Teerin;
Hayashi, Yukiko K.;
Ohsawa, Maki;
Kurokawa, Rumi;
Fujita, Masako;
Noguchi, Satoru;
Nonaka, Ikuya;
Nishino, Ichizo

Publication type:

Article

Negative result in search for human alpha-dystrobrevin deficiency.

Published in:

Muscle & Nerve, 2003, v. 28, n. 3, p. 387, doi. 10.1002/mus.10441

By:

Harumi Ishikawa;
Ikuya Nonaka;
Ichizo Nishino

Publication type:

Article

A new form of muscular dystrophy with mitochondrial structural abnormalities.

Published in:

2001

By:

Ikemoto-Tsuchiya, Kaori;
Nishino, Ichizo;
Kawai, Motoharu;
Morimatsu, Mitsunori;
Nonaka, Ikuya;
Ikemoto-Tsuchiya, K;
Nishino, I;
Kawai, M;
Morimatsu, M;
Nonaka, I

Publication type:

Case Study

Transforming growth factor-β2 is elevated in skeletal muscle disorders.

Published in:

Muscle & Nerve, 1999, v. 22, n. 7, p. 889, doi. 10.1002/(SICI)1097-4598(199907)22:7<889::AID-MUS12>3.0.CO;2-B

By:

Murakami, Nobuyuki;
McLennan, Ian S.;
Nonaka, Ikuya;
Koishi, Kyoko;
Baker, Christina;
Hammond-Tooke, Graeme

Publication type:

Article

Effective adenovirus-mediated gene expression in adult murine skeletal muscle.

Published in:

1999

By:

Ishii, Akiko;
Hagiwara, Yasuko;
Saito, Yoko;
Yamamoto, Kanji;
Yuasa, Katsutoshi;
Sato, Yumi;
Arahata, Kiichi;
Shoji, Shin'ichi;
Nonaka, Ikuya;
Saito, Izumu;
Nabeshima, Yo-ichi;
Takeda, Shin'ichi;
Ishii, A;
Hagiwara, Y;
Saito, Y;
Yamamoto, K;
Yuasa, K;
Sato, Y;
Arahata, K;
Shoji, S

Publication type:

journal article

Mitochondrial abnormalities in selenium-deficient myopathy.

Published in:

1998

By:

Osaki, Yasushi;
Nishino, Ichizo;
Murakami, Nobuyuki;
Matsubayashi, Kozo;
Tsuda, Keisuke;
Yokoyama, Yu-Ichi;
Morita, Masanori;
Onishi, Saburo;
Goto, Yu-Ichi;
Nonaka, Ikuya;
Osaki, Y;
Nishino, I;
Murakami, N;
Matsubayashi, K;
Tsuda, K;
Yokoyama, Y I;
Morita, M;
Onishi, S;
Goto, Y I;
Nonaka, I

Publication type:

journal article

A new congenital muscular dystrophy with mitochondrial structural abnormalities.

Published in:

1998

By:

Nishino, Ichizo;
Kobayashi, Osamu;
Goto, Yu-ichi;
Kurihara, Mana;
Kumagai, Komei;
Fujita, Takehisa;
Hashimoto, Kiyoshi;
Horai, Satoshi;
Nonaka, Ikuya;
Nishino, I;
Kobayashi, O;
Goto, Y;
Kurihara, M;
Kumagai, K;
Fujita, T;
Hashimoto, K;
Horai, S;
Nonaka, I

Publication type:

journal article

Myoclonus epilepsy associated with ragged-red fibers: A G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA<sup>Lys</sup> in two families.

Published in:

Muscle & Nerve, 1997, v. 20, n. 3, p. 271, doi. 10.1002/(SICI)1097-4598(199703)20:3<271::AID-MUS2>3.0.CO;2-8

By:

Ozawa, Matsuko;
Nishino, Ichizo;
Horai, Satoshi;
Nonaka, Ikuya;
Goto, Yu-Ichi

Publication type:

Article

The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS).

Published in:

1996

By:

Nishino, Ichizo;
Komatsu, Mikio;
Kodama, Soichi;
Horai, Satoshi;
Nonaka, Ikuya;
Goto, Yu-Ichi;
Nishino, I;
Komatsu, M;
Kodama, S;
Horai, S;
Nonaka, I;
Goto, Y

Publication type:

journal article

Deficiency of laminin α2-Chain mRNA in muscle in a patient with merosin-negative congenital muscular dystrophy.

Published in:

Muscle & Nerve, 1995, v. 18, n. 9, p. 1027, doi. 10.1002/mus.880180918

By:

Hayashi, Yukiko K.;
Koga, Ritsuko;
Tsukahara, Toshifumi;
Ishii, Hiroko;
Matsuishi, Toyojiro;
Yamashita, Yushiro;
Nonaka, Ikuya;
Arahata, Kiichi

Publication type:

Article

Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.

Published in:

Muscle & Nerve, 1995, v. 18, n. S14, p. S113, doi. 10.1002/mus.880181423

By:

Mita, Shuji;
Tokunaga, Makoto;
Kumamoto, Toshihide;
Uchino, Makoto;
Nonaka, Ikuya;
Ando, Masayuki

Publication type:

Article

The molecular genetic basis of myophosphorylase deficiency (McArdle's disease).

Published in:

Muscle & Nerve, 1995, v. 18, n. S14, p. S23, doi. 10.1002/mus.880181407

By:

Tsujino, Seiichi;
Shanske, Sara;
Nonaka, Ikuya;
DiMauro, Salvatore

Publication type:

Article

Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): Immunocytochemical and genetic analyses.

Published in:

Muscle & Nerve, 1995, v. 18, n. S13, p. S56, doi. 10.1002/mus.880181312

By:

Arahata, Kiichi;
Ishihara, Tadayuki;
Fukunaga, Hidetoshi;
Orimo, Satoshi;
Lee, Je Hyeon;
Goto, Kanako;
Nonaka, Ikuya

Publication type:

Article

Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD).

Published in:

Muscle & Nerve, 1995, v. 18, n. S13, p. S27, doi. 10.1002/mus.880181307

By:

Lee, Je Hyeon;
Goto, Kanako;
Sahashi, Ko;
Nonaka, Ikuya;
Matsuda, Chie;
Arahata, Kiichi

Publication type:

Article

Chloroquine treated rat: A possible model for alzheimer's disease.

Published in:

Muscle & Nerve, 1995, v. 18, n. 1, p. 123, doi. 10.1002/mus.880180120

By:

Murakami, Nobuyuki;
Nonaka, Ikuya;
Ihara, Yasuo

Publication type:

Article

Expression of utrophin (dystrophin-related protein) and dystrophin-associated glycoproteins in muscles from patients with Duchenne muscular dystrophy.

Published in:

Muscle & Nerve, 1994, v. 17, n. 2, p. 206, doi. 10.1002/mus.880170212

By:

Mizuno, Yuji;
Yoshida, Mikiharu;
Nonaka, Ikuya;
Hirai, Shunsaku;
Ozawa, Eijiro

Publication type:

Article

'All-or-none' cytochrome C oxidase positivity in mitochondria in chronic progressive external ophthalmoplegia: An ultrastructural-cytochemical study.

Published in:

Muscle & Nerve, 1993, v. 16, n. 2, p. 206, doi. 10.1002/mus.880160215

By:

Matsuoka, Taro;
Goto, Yu-Ichi;
Nonaka, Ikuya

Publication type:

Article

An experimental model of mitochondrial myopathy: Germanium-induced myopathy and coenzyme Q<sub>10</sub> administration.

Published in:

Muscle & Nerve, 1992, v. 15, n. 11, p. 1258, doi. 10.1002/mus.880151107

By:

Wu, Chien-Ming;
Matsuoka, Taro;
Takemitsu, Masakazu;
Goto, Yu-Ichi;
Nonaka, Ikuya

Publication type:

Article

Segmental cytochrome c-oxidase deficiency in CPEO: Teased muscle fiber analysis.

Published in:

Muscle & Nerve, 1992, v. 15, n. 2, p. 209, doi. 10.1002/mus.880150213

By:

Matsuoka, Taro;
Goto, Yu-Ichi;
Hasegawa, Hitomi;
Nonaka, Ikuya

Publication type:

Article

Muscle histology in becker muscular dystrophy.

Published in:

Muscle & Nerve, 1991, v. 14, n. 11, p. 1067, doi. 10.1002/mus.880141105

By:

Kaido, Misako;
Arahata, Kiichi;
Hoffman, Eric P.;
Nonaka, Ikuya;
Sugita, Hideo

Publication type:

Article

α-Glucosidase isoenzymes in normal and acid maltase-deficient human skeletal muscles.

Published in:

Muscle & Nerve, 1988, v. 11, n. 4, p. 365, doi. 10.1002/mus.880110413

By:

Usuki, Fusako;
Ishiura, Shoichi;
Nonaka, Ikuya;
Sugita, Hideo

Publication type:

Article

Immunohistochemical localization of AMP deaminase in rimmed vacuoles in human skeletal muscle.

Published in:

Muscle & Nerve, 1987, v. 10, n. 9, p. 790, doi. 10.1002/mus.880100904

By:

Higuchi, Itsuro;
Ishiura, Shoichi;
Nonaka, Ikuya;
Sugita, Hideo

Publication type:

Article

Localization of calcium-activated neutral protease (CANP) in the peripheral nerve.

Published in:

1985

By:

Kamakura, Keiko;
Ishiura, Shoichi;
Fujita, Takehisa;
Nonaka, Ikuya;
Sugita, Hideo;
Kamakura, K;
Ishiura, S;
Fujita, T;
Nonaka, I;
Sugita, H

Publication type:

journal article

An electron microscopical study of the T-system in biopsied muscles from fukuyama type congenital muscular dystrophy.

Published in:

Muscle & Nerve, 1984, v. 7, n. 8, p. 629, doi. 10.1002/mus.880070806

By:

Miike, Teruhisa;
Ohtani, Yoshinobu;
Tamari, Hideo;
Ishitsu, Takateru;
Nonaka, Ikuya

Publication type:

Article

Regenerative capability of skeletal muscle in chicken muscular dystrophy.

Published in:

Muscle & Nerve, 1984, v. 7, n. 5, p. 400, doi. 10.1002/mus.880070510

By:

Nonaka, Ikuya;
Fujita, Takehisa;
Sugita, Hideo

Publication type:

Article

Malignant hyperthermia and related neuromuscular diseases: Caffeine contracture of the skinned muscle fibers.

Published in:

Muscle & Nerve, 1983, v. 6, n. 7, p. 510, doi. 10.1002/mus.880060707

By:

Takagi, Akio;
Sunohara, Nobuhiko;
Ishihara, Tadayuki;
Nonaka, Ikuya;
Sugita, Hideo

Publication type:

Article

Letters to the editor.

Published in:

Muscle & Nerve, 1983, v. 6, n. 1, p. 75, doi. 10.1002/mus.880060113

By:

Olney, Richard K.;
Miller, Robert G.;
Nonaka, Ikuya;
Sugita, Hideo;
Olson, Norman D.

Publication type:

Article

In vivo administration of a thiol protease inhibitor, E-64-C, to hereditary dystrophic chicken.

Published in:

Muscle & Nerve, 1982, v. 5, n. 9, p. 738, doi. 10.1002/mus.880050914

By:

Sugita, Hideo;
Kimura, Masaaki;
Tarumoto, Yasuo;
Tamai, Masaharu;
Hanada, Kazunori;
Ishiura, Shoichi;
Nonaka, Ikuya;
Ohzeki, Masahiro;
Imahori, Kazutomo

Publication type:

Article