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Corrigendum: Depotentiation depends on IP3 receptor activation sustained by synaptic inputs after LTP induction

Learning & memory (Cold Spring Harbor, N.Y.), 2023-05, Vol.30 (5-6), p.124-124

2023

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Preventing social isolation: Otsuchi town after the Great East Japan Earthquake

Environmental hazards, 2022-10, Vol.21 (5), p.379-399

2022

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The Role of HECT-Type E3 Ligase in the Development of Cardiac Disease

International journal of molecular sciences, 2021-06, Vol.22 (11), p.6065

2021

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Synaptic plasticity in hippocampal CA1 neurons of mice lacking inositol-1,4,5-trisphosphate receptor-binding protein released with IP3 (IRBIT)

Learning & memory (Cold Spring Harbor, N.Y.), 2022-04, Vol.29 (4), p.110-119

2022

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Decreased Psoas Muscle Computed Tomography Value Predicts Poor Outcome in Peripheral Artery Disease

Circulation Journal, 2018/11/24, Vol.82(12), pp.3069-3075

2018

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Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body Myositis

Annals of neurology, 2022-03, Vol.91 (3), p.317-328

2022

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Depotentiation depends on IP3 receptor activation sustained by synaptic inputs after LTP induction

Learning & memory (Cold Spring Harbor, N.Y.), 2020-02, Vol.27 (2), p.52-66

2020

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Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALS

Journal of neurology, neurosurgery and psychiatry, 2019-05, Vol.90 (5), p.537-542

2019

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Evaluation of a simple activity measurement method in rats

Journal of Physical Therapy Science, 2023, Vol.35(9), pp.633-637

2023

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A Farnesyltransferase Inhibitor Restores Cognitive Deficits in Tsc2 +/- Mice through Inhibition of Rheb1

The Journal of neuroscience, 2022-03, Vol.42 (12), p.2598-2612

2022

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Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutation

Neurobiology of aging, 2018-01, Vol.61, p.255.e9-255.e16

2018

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Expanded clinical spectrum of oculopharyngodistal myopathy type 1

Muscle & nerve, 2022-12, Vol.66 (6), p.679-685

2022

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The TRK-Fused Gene Is Mutated in Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement

American journal of human genetics, 2012-08, Vol.91 (2), p.320-329

2012

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A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55)

Journal of medical genetics, 2012-12, Vol.49 (12), p.777-784

2012

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The association between microRNA-21 and hypertension-induced cardiac remodeling

PloS one, 2020-02, Vol.15 (2), p.e0226053-e0226053

2020

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Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes

Brain (London, England : 1878), 2014-09, Vol.137 (Pt 9), p.2444-2455

2014

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Anti-LGI1 Encephalitis Developing Immunoglobulin Responsive Orthostatic Hypotension after Remission

Internal Medicine, 2021/09/15, Vol.60(18), pp.3021-3024

2021

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Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing

Bioinformatics, 2014-03, Vol.30 (6), p.815-822

2014

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Perceptions of Residents in Relation to Smartphone Applications to Promote Understanding of Radiation Exposure after the Fukushima Accident: A Cross-Sectional Study within and outside Fukushima Prefecture

Journal of radiation protection and research, 2022-06, Vol.47 (2), p.67-76

2022

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Prominent Spasticity and Hyperreflexia of the Legs in a Nepalese Patient with Friedreich Ataxia

Internal Medicine, 2019/10/01, Vol.58(19), pp.2865-2869

2019

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Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese population

Journal of human genetics, 2021-03, Vol.66 (3), p.237-241

2021

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Mutations in KCND3 cause spinocerebellar ataxia type 22

Annals of neurology, 2012-12, Vol.72 (6), p.859-869

2012

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Prior Activation of Inositol 1,4,5-Trisphosphate Receptors Suppresses the Subsequent Induction of Long-Term Potentiation in Hippocampal CA1 Neurons

Learning & memory (Cold Spring Harbor, N.Y.), 2016-05, Vol.23 (5), p.208-220

2016

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Expression profile analysis in cells overexpressing DRPLA cDNA to explore the roles of DRPLAp as a transcriptional coregulator

Neurology and clinical neuroscience, 2022-07, Vol.10 (4), p.210-217

2022

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Potent functional uncoupling between STIM1 and Orai1 by dimeric 2-aminodiphenyl borinate analogs

Cell calcium (Edinburgh), 2014-12, Vol.56 (6), p.482-492

2014

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Corrigendum: Depotentiation depends on IP3 receptor activation sustained by synaptic inputs after LTP induction

Preventing social isolation: Otsuchi town after the Great East Japan Earthquake

The Role of HECT-Type E3 Ligase in the Development of Cardiac Disease

Synaptic plasticity in hippocampal CA1 neurons of mice lacking inositol-1,4,5-trisphosphate receptor-binding protein released with IP3 (IRBIT)

Decreased Psoas Muscle Computed Tomography Value Predicts Poor Outcome in Peripheral Artery Disease

Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body Myositis

Depotentiation depends on IP3 receptor activation sustained by synaptic inputs after LTP induction

Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALS

Evaluation of a simple activity measurement method in rats

A Farnesyltransferase Inhibitor Restores Cognitive Deficits in Tsc2 +/- Mice through Inhibition of Rheb1

Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutation

Expanded clinical spectrum of oculopharyngodistal myopathy type 1

The TRK-Fused Gene Is Mutated in Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement

A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55)

The association between microRNA-21 and hypertension-induced cardiac remodeling

Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes

Anti-LGI1 Encephalitis Developing Immunoglobulin Responsive Orthostatic Hypotension after Remission

Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing

Perceptions of Residents in Relation to Smartphone Applications to Promote Understanding of Radiation Exposure after the Fukushima Accident: A Cross-Sectional Study within and outside Fukushima Prefecture

Prominent Spasticity and Hyperreflexia of the Legs in a Nepalese Patient with Friedreich Ataxia

Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese population

Mutations in KCND3 cause spinocerebellar ataxia type 22

Prior Activation of Inositol 1,4,5-Trisphosphate Receptors Suppresses the Subsequent Induction of Long-Term Potentiation in Hippocampal CA1 Neurons

Expression profile analysis in cells overexpressing DRPLA cDNA to explore the roles of DRPLAp as a transcriptional coregulator

Potent functional uncoupling between STIM1 and Orai1 by dimeric 2-aminodiphenyl borinate analogs

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