Ichizo NISHINO

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May Christine MalicdanNHGRIPreverjeni e-poštni naslov na mail.nih.gov
Akinori URUHA（漆葉章典）Tokyo Metropolitan Neurological Hospital, Department of NeurologyPreverjeni e-poštni naslov na tmhp.jp
Shigeaki SuzukiDepartment of Neurology, Keio University School of MedicinePreverjeni e-poštni naslov na keio.jp
Michio HiranoProfessor of NeurologyPreverjeni e-poštni naslov na columbia.edu
Kevin P CampbellChair, Molecular Physiology and Biophysics, Howard Hughes Medical Institute, Carver College ofPreverjeni e-poštni naslov na uiowa.edu
Antonella SpinazzolaUCL Institute of NeurologyPreverjeni e-poštni naslov na ucl.ac.uk
Naomichi MatsumotoYokohama City UniversityPreverjeni e-poštni naslov na yokohama-cu.ac.jp
Olivier BenvenisteProfesseur de Médecine Interne et Immunologie Clinique, Sorbonne UniversitéPreverjeni e-poštni naslov na aphp.fr
Volker StraubNewcastle UniversityPreverjeni e-poštni naslov na ncl.ac.uk
laporte jocelynIGBMC (Inserm, Cnrs, Strasbourg University)Preverjeni e-poštni naslov na igbmc.fr
Takahiro YonekawaPostdoctoral fellow, The University of IowaPreverjeni e-poštni naslov na uiowa.edu
Carolyn SueProfessor and Kinghorn Chair, University of New South Wales, SydneyPreverjeni e-poštni naslov na neura.edu.au
Daniel J. KlionskyUniversity of MichiganPreverjeni e-poštni naslov na umich.edu
Daniel MicheleUniversity of MichiganPreverjeni e-poštni naslov na umich.edu
Shinji MiuraUniversity of Shizuoka, School of Food and Nutritional Sciences 静岡県立大学食品栄養科学部Preverjeni e-poštni naslov na u-shizuoka-ken.ac.jp
Haluk TopalogluPreverjeni e-poštni naslov na hacettepe.edu.tr
Jin NakaharaDepartment of Neurology, Keio University School of MedicinePreverjeni e-poštni naslov na a6.keio.jp
Nigel LAINGNeurogenetics, University of Western Australia, Harry Perkins Institute of Medical ResearchPreverjeni e-poštni naslov na uwa.edu.au
Alan H. Beggs, PhDProfessor of Pediatrics, Harvard Medical School, Director The Manton CenterPreverjeni e-poštni naslov na enders.tch.harvard.edu
Anthony AmatoPreverjeni e-poštni naslov na partners.org

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Ichizo NISHINO

Director, Department of Neuromuscular Research, National Institute of Neuroscience, NCNP

Preverjeni e-poštni naslov na ncnp.go.jp - Domača stran

myopathy muscular dystrophy muscle pathology autophagy mitochondria


Naslov Razvrsti po navedbah Razvrsti po letniku Razvrsti po naslovu	Navedeno Navedeno	Leto
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	13913*	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	1149	2010
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	1098	2000
Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder I Nishino, A Spinazzola, M Hirano Science 283 (5402), 689-692, 1999	1042	1999
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	887	2002
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	705	2004
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	688	1999
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	615	2007
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	499	2018
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	457	2009
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	398	2000
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	363	2011
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	349	2019
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	334	2016
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	313	2001
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	303	2004
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	291	2002
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	284	2014
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	278	2002
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	270	2002

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