受强制性开放获取政策约束的文章 - Jun Mitsui了解详情
无法在其他位置公开访问的文章：2 篇
Two distinct mechanisms of augmented antitumor activity by modulation of immunostimulatory/inhibitory signals
J Mitsui, H Nishikawa, D Muraoka, L Wang, T Noguchi, E Sato, S Kondo, ...
Clinical Cancer Research 16 (10), 2781-2791, 2010
强制性开放获取政策： Howard Hughes Medical Institute
Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in Japan
M Yamada, M Tanaka, M Takagi, S Kobayashi, Y Taguchi, S Takashima, ...
Neurology 82 (8), 705-712, 2014
强制性开放获取政策： US National Institutes of Health
可在其他位置公开访问的文章：12 篇
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
E Sidransky, MA Nalls, JO Aasly, J Aharon-Peretz, G Annesi, ER Barbosa, ...
New England Journal of Medicine 361 (17), 1651-1661, 2009
强制性开放获取政策： US National Institutes of Health
Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy
Multiple-System Atrophy Research Collaboration
New England Journal of Medicine 369 (3), 233-244, 2013
强制性开放获取政策： US National Institutes of Health, German Research Foundation
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
KL Williams, S Topp, S Yang, B Smith, JA Fifita, ST Warraich, KY Zhang, ...
Nature communications 7 (1), 11253, 2016
强制性开放获取政策： US National Institutes of Health, Australian Research Council, National …
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19
Y Takahashi, Y Fukuda, J Yoshimura, A Toyoda, K Kurppa, H Moritoyo, ...
The American Journal of Human Genetics 93 (5), 900-905, 2013
强制性开放获取政策： US National Institutes of Health
Variants associated with Gaucher disease in multiple system atrophy
J Mitsui, T Matsukawa, H Sasaki, I Yabe, M Matsushima, A Dürr, A Brice, ...
Annals of clinical and translational neurology 2 (4), 417-426, 2015
强制性开放获取政策： US National Institutes of Health, German Research Foundation
The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement
H Ishiura, W Sako, M Yoshida, T Kawarai, O Tanabe, J Goto, Y Takahashi, ...
The American Journal of Human Genetics 91 (2), 320-329, 2012
强制性开放获取政策： National Health and Medical Research Council, Australia
The pathogenesis linked to coenzyme Q10 insufficiency in iPSC-derived neurons from patients with multiple-system atrophy
FK Nakamoto, S Okamoto, J Mitsui, T Sone, M Ishikawa, Y Yamamoto, ...
Scientific reports 8 (1), 14215, 2018
强制性开放获取政策： Wellcome Trust
Amnionless-mediated glycosylation is crucial for cell surface targeting of cubilin in renal and intestinal cells
T Udagawa, Y Harita, K Miura, J Mitsui, KL Ode, S Morishita, S Urae, ...
Scientific Reports 8 (1), 2351, 2018
强制性开放获取政策： US National Institutes of Health
Generation of D1-1 TALEN isogenic control cell line from Dravet syndrome patient iPSCs using TALEN-mediated editing of the SCN1A gene
Y Tanaka, T Sone, N Higurashi, T Sakuma, S Suzuki, M Ishikawa, ...
Stem Cell Research 28, 100-104, 2018
强制性开放获取政策： US National Institutes of Health
Muscle transcriptomics shows overexpression of cadherin 1 in inclusion body myositis
C Ikenaga, H Date, M Kanagawa, J Mitsui, H Ishiura, J Yoshimura, ...
Annals of neurology 91 (3), 317-328, 2022
强制性开放获取政策： US National Institutes of Health
SNP haplotype mapping in a small ALS family
KAD Krueger, S Tsuji, Y Fukuda, Y Takahashi, J Goto, J Mitsui, H Ishiura, ...
PLoS One 4 (5), e5687, 2009
强制性开放获取政策： US National Institutes of Health
Genome-wide association study identifies a new susceptibility locus in PLA2G4C for Multiple System Atrophy
Y Nakahara, J Mitsui, H Date, KJ Porto, Y Hayashi, A Yamashita, ...
medRxiv, 2023.05. 02.23289328, 2023
强制性开放获取政策： US National Institutes of Health
出版信息和资助信息由计算机程序自动确定