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Development of a large-bore plasma window with an indirectly heated hollow cathode

Journal of applied physics, 2023-09, Vol.134 (9)

2023

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On-demand generation and characterization of a microwave time-bin qubit

npj quantum information, 2020-04, Vol.6 (1), Article 34

2020

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Generation of stationary high-density cascade arc plasma and application to plasma windows

Japanese Journal of Applied Physics, 2023-09, Vol.62 (SL), p.SL1009

2023

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Atelocollagen-mediated local and systemic applications of myostatin-targeting siRNA increase skeletal muscle mass

Gene therapy, 2008-08, Vol.15 (15), p.1126-1130

2008

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Molecular interaction of caveolin-3 and nNOS: Implication in the pathogenesis of limb-girdle muscular dystrophy 1C

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S236-S236

2015

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MELAS, a first-ever tRNA modification disorder is alleviated by taurine supplementation therapy

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S210-S210

2016

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Taurine supplemental therapy in prevention of stroke-like episodes in MELAS

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S313-S313

2015

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Exploring Chronic Drug Effects on Microengineered Human Liver Cultures Using Global Gene Expression Profiling

Toxicological sciences, 2017-06, Vol.157 (2), p.387-398

2017

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Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus

The Journal of biological chemistry, 1994-05, Vol.269 (19), p.13729-13732

1994

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27. The 6-min walk test as a parameter of the fatigability in Kennedy’s disease

Clinical neurophysiology, 2012-06, Vol.123 (6), p.e24-e24

2012

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69. Followup needle electromyography findings in parkinson’s disease patients with dropped head syndrome after steroid therapy

Clinical neurophysiology, 2012-06, Vol.123 (6), p.e36-e36

2012

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Reduced amplitude of the sural nerve sensory action potential in PARK2 patients

Neurology, 2005-08, Vol.65 (3), p.459

2005

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Muscular fatigue and decremental response to repetitive nerve stimulation in X-linked spinobulbar muscular atrophy

European journal of neurology, 2009-01, Vol.16 (1), p.76-80

2009

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Inhibitors of the TGF-beta superfamily and their clinical applications

Mini reviews in medicinal chemistry, 2006-11, Vol.6 (11), p.1255

2006

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G.P.49 Muscle-specific overexpression of caveolin 3 causes muscle atrophy, but not muscular dystrophy

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.834-834

2012

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Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activity

Human molecular genetics, 2001-02, Vol.10 (3), p.173-178

2001

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P13-15 Active myopathy in neck extensor muscles in parkinsonism patients with dropped head syndrome

Clinical neurophysiology, 2010, Vol.121, p.S182-S182

2010

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Fast Readout and Reset of a Superconducting Qubit Coupled to a Resonator with an Intrinsic Purcell Filter

Physical review applied, 2022-04, Vol.17 (4), Article 044016

2022

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Comparison of the sensitivities of plantar nerve conduction techniques for early detection of diabetic sensory polyneuropathy

Electromyography and clinical neurophysiology, 2010-09, Vol.50 (6), p.269

2010

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Theory of chemical bonds in metalloenzymes V: Hybrid-DFT studies of the inorganic [8Fe-7S] core

International journal of quantum chemistry, 2006, Vol.106 (15), p.3288-3302

2006

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T.P.5.10 Introduction of wound-healing MRL-MpJ phenotype improves skeletal muscle pathology in mdx mouse

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.619-619

2009

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In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes

Gene therapy, 1996-11, Vol.3 (11), p.965

1996

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Transgenic expression of a myostatin inhibitor derived from follistatin increases skeletal muscle mass and ameliorates dystrophic pathology in mdx mice

The FASEB journal, 2008-02, Vol.22 (2), p.477-487

2008

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P3.22 Reprogrammed fibroblasts as a feasible source of cell-based therapy for muscular dystrophy

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.647-647

2010

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D.P.3.13 A small-molecule inhibitor targeting transforming growth factor-β type I receptor kinase ameliorates muscular atrophy in a mouse model of caveolin-3-deficient muscular dystrophy

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.768-769

2008

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Development of a large-bore plasma window with an indirectly heated hollow cathode

On-demand generation and characterization of a microwave time-bin qubit

Generation of stationary high-density cascade arc plasma and application to plasma windows

Atelocollagen-mediated local and systemic applications of myostatin-targeting siRNA increase skeletal muscle mass

Molecular interaction of caveolin-3 and nNOS: Implication in the pathogenesis of limb-girdle muscular dystrophy 1C

MELAS, a first-ever tRNA modification disorder is alleviated by taurine supplementation therapy

Taurine supplemental therapy in prevention of stroke-like episodes in MELAS

Exploring Chronic Drug Effects on Microengineered Human Liver Cultures Using Global Gene Expression Profiling

Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus

27. The 6-min walk test as a parameter of the fatigability in Kennedy’s disease

69. Followup needle electromyography findings in parkinson’s disease patients with dropped head syndrome after steroid therapy

Reduced amplitude of the sural nerve sensory action potential in PARK2 patients

Muscular fatigue and decremental response to repetitive nerve stimulation in X-linked spinobulbar muscular atrophy

Inhibitors of the TGF-beta superfamily and their clinical applications

G.P.49 Muscle-specific overexpression of caveolin 3 causes muscle atrophy, but not muscular dystrophy

Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activity

P13-15 Active myopathy in neck extensor muscles in parkinsonism patients with dropped head syndrome

Fast Readout and Reset of a Superconducting Qubit Coupled to a Resonator with an Intrinsic Purcell Filter

Comparison of the sensitivities of plantar nerve conduction techniques for early detection of diabetic sensory polyneuropathy

Theory of chemical bonds in metalloenzymes V: Hybrid-DFT studies of the inorganic [8Fe-7S] core

T.P.5.10 Introduction of wound-healing MRL-MpJ phenotype improves skeletal muscle pathology in mdx mouse

In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes

Transgenic expression of a myostatin inhibitor derived from follistatin increases skeletal muscle mass and ameliorates dystrophic pathology in mdx mice

P3.22 Reprogrammed fibroblasts as a feasible source of cell-based therapy for muscular dystrophy

D.P.3.13 A small-molecule inhibitor targeting transforming growth factor-β type I receptor kinase ameliorates muscular atrophy in a mouse model of caveolin-3-deficient muscular dystrophy

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