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Transsynaptic modulation of presynaptic short-term plasticity in hippocampal mossy fiber synapses

Nature communications, 2021-05, Vol.12 (1), p.2912-2912, Article 2912

2021

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Mesoporous BaTiO3/TiO2 Double Layer for Electron Transport in Perovskite Solar Cells

Journal of physical chemistry. C, 2016-07, Vol.120 (26), p.13995-14000

2016

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The Current State of Charcot-Marie-Tooth Disease Treatment

Genes, 2023-07, Vol.14 (7), p.1391

2023

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Subcellular patch-clamp techniques for single-bouton stimulation and simultaneous pre- and postsynaptic recording at cortical synapses

Nature protocols, 2021-06, Vol.16 (6), p.2947-2967

2021

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Effective silicon production from SiCl4 source using hydrogen radicals generated and transported at atmospheric pressure

Science and technology of advanced materials, 2020-01, Vol.21 (1), p.482-491

2020

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Clinical diversity caused by novel IGHMBP2 variants

Journal of human genetics, 2017-06, Vol.62 (6), p.599-604

2017

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Elderly patients with suspected Charcot-Marie-Tooth disease should be tested for the TTR gene for effective treatments

Journal of human genetics, 2022-06, Vol.67 (6), p.353-362

2022

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Developmental changes in Ca2+ channel subtypes regulating endocytosis at the calyx of Held

The Journal of physiology, 2014-08, Vol.592 (16), p.3495-3510

2014

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Neuron-specific knockdown of Drosophila HADHB induces a shortened lifespan, deficient locomotive ability, abnormal motor neuron terminal morphology and learning disability

Experimental cell research, 2019-06, Vol.379 (2), p.150-158

2019

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Perovskite-type SrTiO3, CaTiO3 and BaTiO3 porous film electrodes for dye-sensitized solar cells

Journal of the Ceramic Society of Japan, 2014-01, Vol.122 (1428), p.728-731

2014

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Adipose Mitochondrial Biogenesis Is Suppressed in db/db and High-Fat Diet–Fed Mice and Improved by Rosiglitazone

Diabetes (New York, N.Y.), 2007-07, Vol.56 (7), p.1751-1760

2007

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Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes

Journal of neurology, 2022-08, Vol.269 (8), p.4129-4140

2022

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The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins

Internal Medicine, 2020/01/15, Vol.59(2), pp.277-283

2020

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An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese families

Journal of human genetics, 2022-07, Vol.67 (7), p.399-403

2022

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Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosis

Journal of neurology, 2011-11, Vol.258 (11), p.1998-2008

2011

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Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implications

Acta neuropathologica communications, 2024-08, Vol.12 (1), p.136-14

2024

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Genetic and clinical features of cerebellar ataxia with RFC1 biallelic repeat expansions in Japan

Frontiers in neurology, 2022-08, Vol.13, p.952493-952493

2022

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Bilateral striatal necrosis caused by a founder mitochondrial 14459G > A mutation in two independent Japanese families

Journal of the neurological sciences, 2017-07, Vol.378, p.177-181

2017

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Distinct modes of endocytotic presynaptic membrane and protein uptake at the calyx of Held terminal of rats and mice

eLife, 2016-05, Vol.5

2016

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Combinatorial screening of halide perovskite thin films and solar cells by mask-defined IR laser molecular beam epitaxy

Science and technology of advanced materials, 2017-01, Vol.18 (1), p.307-315

2017

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Clinical variability associated with intronic FGF14 GAA repeat expansion in Japan

Annals of clinical and translational neurology, 2024-01, Vol.11 (1), p.96-104

2024

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Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible

Biomedicines, 2022-06, Vol.10 (7), p.1546

2022

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Clinical and mutational spectrum of Japanese patients with recessive variants in SH3TC2

Journal of human genetics, 2018-03, Vol.63 (3), p.281-287

2018

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Transsynaptic modulation of presynaptic short-term plasticity in hippocampal mossy fiber synapses

Mesoporous BaTiO3/TiO2 Double Layer for Electron Transport in Perovskite Solar Cells

The Current State of Charcot-Marie-Tooth Disease Treatment

Subcellular patch-clamp techniques for single-bouton stimulation and simultaneous pre- and postsynaptic recording at cortical synapses

Effective silicon production from SiCl4 source using hydrogen radicals generated and transported at atmospheric pressure

Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy

Clinical diversity caused by novel IGHMBP2 variants

Elderly patients with suspected Charcot-Marie-Tooth disease should be tested for the TTR gene for effective treatments

Developmental changes in Ca2+ channel subtypes regulating endocytosis at the calyx of Held

Neuron-specific knockdown of Drosophila HADHB induces a shortened lifespan, deficient locomotive ability, abnormal motor neuron terminal morphology and learning disability

Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2

Perovskite-type SrTiO3, CaTiO3 and BaTiO3 porous film electrodes for dye-sensitized solar cells

Adipose Mitochondrial Biogenesis Is Suppressed in db/db and High-Fat Diet–Fed Mice and Improved by Rosiglitazone

Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes

The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins

An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese families

Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosis

Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implications

Genetic and clinical features of cerebellar ataxia with RFC1 biallelic repeat expansions in Japan

Bilateral striatal necrosis caused by a founder mitochondrial 14459G > A mutation in two independent Japanese families

Distinct modes of endocytotic presynaptic membrane and protein uptake at the calyx of Held terminal of rats and mice

Combinatorial screening of halide perovskite thin films and solar cells by mask-defined IR laser molecular beam epitaxy

Clinical variability associated with intronic FGF14 GAA repeat expansion in Japan

Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible

Clinical and mutational spectrum of Japanese patients with recessive variants in SH3TC2

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