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Ichizo NISHINO
Ichizo NISHINO
Director, Department of Neuromuscular Research, National Institute of Neuroscience, NCNP
Verified email at ncnp.go.jp - Homepage
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Cited by
Cited by
Year
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
13548*2021
Adiponectin and AdipoR1 regulate PGC-1α and mitochondria by Ca2+ and AMPK/SIRT1
M Iwabu, T Yamauchi, M Okada-Iwabu, K Sato, T Nakagawa, M Funata, ...
Nature 464 (7293), 1313-1319, 2010
11192010
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)
I Nishino, J Fu, K Tanji, T Yamada, S Shimojo, T Koori, M Mora, JE Riggs, ...
Nature 406 (6798), 906-910, 2000
10762000
Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder
I Nishino, A Spinazzola, M Hirano
Science 283 (5402), 689-692, 1999
10381999
Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophies
DE Michele, R Barresi, M Kanagawa, F Saito, RD Cohn, JS Satz, J Dollar, ...
Nature 418 (6896), 417-421, 2002
8772002
Skeletal muscle Foxo1 (Fkhr) transgenic mice have less skeletal muscle mass, down-regulated type I (Slow twitch/red muscle) fiber genes, and impaired glycemic control*[Boxs]
Y Kamei, S Miura, M Suzuki, Y Kai, J Mizukami, T Taniguchi, K Mochida, ...
Journal of Biological Chemistry 279 (39), 41114-41123, 2004
6932004
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
LC Papadopoulou, CM Sue, MM Davidson, K Tanji, I Nishino, JE Sadlock, ...
Nature genetics 23 (3), 333-337, 1999
6831999
Distinctive patterns of microRNA expression in primary muscular disorders
I Eisenberg, A Eran, I Nishino, M Moggio, C Lamperti, AA Amato, ...
Proceedings of the National Academy of Sciences 104 (43), 17016-17021, 2007
6062007
224th ENMC International Workshop:: Clinico-sero-pathological classification of immune-mediated necrotizing myopathies Zandvoort, The Netherlands, 14–16 October 2016
Y Allenbach, AL Mammen, O Benveniste, W Stenzel, A Amato, A Aussey, ...
Neuromuscular disorders 28 (1), 87-99, 2018
4512018
Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy
YK Hayashi, C Matsuda, M Ogawa, K Goto, K Tominaga, S Mitsuhashi, ...
The Journal of clinical investigation 119 (9), 2623-2633, 2009
4482009
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations
I Nishino, A Spinazzola, A Papadimitriou, S Hammans, I Steiner, CD Hahn, ...
Annals of Neurology: Official Journal of the American Neurological …, 2000
3942000
Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy
C Fugier, AF Klein, C Hammer, S Vassilopoulos, Y Ivarsson, A Toussaint, ...
Nature medicine 17 (6), 720-725, 2011
3512011
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease
H Ishiura, S Shibata, J Yoshimura, Y Suzuki, W Qu, K Doi, MA Almansour, ...
Nature genetics 51 (8), 1222-1232, 2019
3272019
Clinical features and prognosis in anti-SRP and anti-HMGCR necrotising myopathy
Y Watanabe, A Uruha, S Suzuki, J Nakahara, K Hamanaka, K Takayama, ...
Journal of Neurology, Neurosurgery & Psychiatry 87 (10), 1038-1044, 2016
3142016
The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle
C Matsuda, YK Hayashi, M Ogawa, M Aoki, K Murayama, I Nishino, ...
Human molecular genetics 10 (17), 1761-1766, 2001
3072001
LARGE can functionally bypass α-dystroglycan glycosylation defects in distinct congenital muscular dystrophies
R Barresi, DE Michele, M Kanagawa, HA Harper, SA Dovico, JS Satz, ...
Nature medicine 10 (7), 696-703, 2004
3012004
Clinicopathological features of genetically confirmed Danon disease
K Sugie, A Yamamoto, K Murayama, SJ Oh, M Takahashi, M Mora, ...
Neurology 58 (12), 1773-1778, 2002
2852002
Identification and characterization of PDGFRα+ mesenchymal progenitors in human skeletal muscle
A Uezumi, S Fukada, N Yamamoto, M Ikemoto-Uezumi, M Nakatani, ...
Cell death & disease 5 (4), e1186-e1186, 2014
2782014
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy
I Nishino, S Noguchi, K Murayama, A Driss, K Sugie, Y Oya, T Nagata, ...
Neurology 59 (11), 1689-1693, 2002
2752002
Altered thymidine metabolism due to defects of thymidine phosphorylase
A Spinazzola, R Marti, I Nishino, AL Andreu, A Naini, S Tadesse, I Pela, ...
Journal of Biological Chemistry 277 (6), 4128-4133, 2002
2692002
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