Ichizo NISHINO
Ichizo NISHINO
Director, Department of Neuromuscular Research, National Institute of Neuroscience, NCNP
Verified email at ncnp.go.jp - Homepage
TitleCited byYear
Guidelines for the use and interpretation of assays for monitoring autophagy
DJ Klionsky, FC Abdalla, H Abeliovich, RT Abraham, A Acevedo-Arozena, ...
Autophagy 8 (4), 445-544, 2012
5573*2012
Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes
DJ Klionsky, H Abeliovich, P Agostinis, DK Agrawal, G Aliev, DS Askew, ...
Autophagy 4 (2), 151-175, 2008
23142008
Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder
I Nishino, A Spinazzola, M Hirano
Science 283 (5402), 689-692, 1999
8571999
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, 2000
7822000
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, 2002
7642002
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, 2010
6812010
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, 1999
5721999
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
Y Kamei, S Miura, M Suzuki, Y Kai, J Mizukami, T Taniguchi, K Mochida, ...
Journal of Biological Chemistry 279 (39), 41114-41123, 2004
5052004
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
4382007
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
3202000
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
3012009
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, 2004
2622004
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
2532001
Molecular features of the CAG repeats and clinical manifestation of Machado—Joseph disease
H Maruyama, S Nakamura, Z Matsuyama, T Sakai, M Doyu, G Sobue, ...
Human molecular genetics 4 (5), 807-812, 1995
2221995
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
2182002
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
2172002
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
2162002
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, 2011
2062011
Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNASer (UCN) gene
CM Sue, K Tanji, G Hadjigeorgiou, AL Andreu, I Nishino, S Krishna, ...
Neurology 52 (9), 1905-1905, 1999
1961999
Allogeneic stem cell transplantation corrects biochemical derangements in MNGIE
M Hirano, R Marti, C Casali, S Tadesse, T Uldrick, B Fine, DM Escolar, ...
Neurology 67 (8), 1458-1460, 2006
1682006
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