List of works - Takashi Kurashige

A mutant MATR3 mouse model to explain multisystem proteinopathy

scientific article published on 18 June 2019

Adult-Onset Neuronal Intranuclear Inclusion Disease in Two Female Siblings

scientific article published in March 2017

Anti-HMGCR Antibody-Positive Myopathy Shows Bcl-2-Positive Inflammation and Lymphocytic Accumulations

scientific article published on 01 April 2020

Biallelic mutation of HSD17B4 induces middle age-onset spinocerebellar ataxia

scientific article published on 16 January 2020

C-terminal mutations in SYNE1 are associated with motor neuron disease in patients with SCAR8

scientific article published on 09 May 2019

Clinicopathological features of adult-onset neuronal intranuclear inclusion disease

scientific article published on 25 October 2016

Compound heterozygote mutations in the SIGMAR1 gene in an oldest-old patient with amyotrophic lateral sclerosis

article

Detecting gene mutations in Japanese Alzheimer's patients by semiconductor sequencing

scientific article

Deviation in the recovery of the lower limb and respiratory muscles of patients with polymyositis: a preliminary clinical study

scientific article published on 29 September 2016

Direct effect of radiation on the peripheral nerve in a rat model

scientific article published on 30 January 2014

Elevated urinary β2 microglobulin in the first identified Japanese family afflicted by X-linked myopathy with excessive autophagy.

scientific article published on 11 July 2013

Fiber type-specific expression of low-density lipoprotein receptor-related protein 6 in human skeletal muscles

scientific article published on 23 January 2014

Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia

scientific article published on 07 January 2020

Granulovacuolar degenerations appear in relation to hippocampal phosphorylated tau accumulation in various neurodegenerative disorders.

scientific article

Immunopositivity for ESCRT-III subunit CHMP2B in granulovacuolar degeneration of neurons in the Alzheimer's disease hippocampus.

scientific article published on 24 April 2010

Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patients.

scientific article published on 17 December 2013

Krebs von den Lungen 6 decreased in the serum and muscle of GNE myopathy patients

scientific article published on 22 November 2020

Mitochondrial localization of PABPN1 in oculopharyngeal muscular dystrophy

scientific article published on 20 March 2019

Molecular markers for granulovacuolar degeneration are present in rimmed vacuoles

scientific article

Muscle-dominant wild-type TDP-43 expression induces myopathological changes featuring tubular aggregates and TDP-43-positive inclusions

scientific article published on 18 August 2018

Phosphatidylinositol-4,5-bisphosphate is enriched in granulovacuolar degeneration bodies and neurofibrillary tangles

scientific article

Prevalences of Peripheral Arterial Disease Diagnosed by Computed Tomography Angiography in Patients with Acute Ischemic Stroke.

scientific article

Retinitis pigmentosa prior to familial ALS caused by a homozygous cilia and flagella-associated protein 410 mutation

scientific article published on 20 August 2019

Statins and myotoxic effects associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase autoantibodies: an observational study in Japan

scientific article

Synphilin-1 has neuroprotective effects on MPP-induced Parkinson's disease model cells by inhibiting ROS production and apoptosis

scientific article published on 11 October 2018

The first Japanese case of primary familial brain calcification caused by an MYORG variant

scientific article published on 25 May 2020

[A case of MELAS with G13513A mutation presenting with chronic kidney disease long before stroke-like episodes]

scientific article published on 01 January 2013

[A case of central nervous system lymphomatoid granulomatosis successfully treated with corticosteroids]

scientific article published on 01 January 2012

List of works by Takashi Kurashige

A mutant MATR3 mouse model to explain multisystem proteinopathy

Adult-Onset Neuronal Intranuclear Inclusion Disease in Two Female Siblings

Anti-HMGCR Antibody-Positive Myopathy Shows Bcl-2-Positive Inflammation and Lymphocytic Accumulations

Biallelic mutation of HSD17B4 induces middle age-onset spinocerebellar ataxia

C-terminal mutations in SYNE1 are associated with motor neuron disease in patients with SCAR8

Clinicopathological features of adult-onset neuronal intranuclear inclusion disease

Compound heterozygote mutations in the SIGMAR1 gene in an oldest-old patient with amyotrophic lateral sclerosis

Detecting gene mutations in Japanese Alzheimer's patients by semiconductor sequencing

Deviation in the recovery of the lower limb and respiratory muscles of patients with polymyositis: a preliminary clinical study

Direct effect of radiation on the peripheral nerve in a rat model

Elevated urinary β2 microglobulin in the first identified Japanese family afflicted by X-linked myopathy with excessive autophagy.

Fiber type-specific expression of low-density lipoprotein receptor-related protein 6 in human skeletal muscles

Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia

Granulovacuolar degenerations appear in relation to hippocampal phosphorylated tau accumulation in various neurodegenerative disorders.

Immunopositivity for ESCRT-III subunit CHMP2B in granulovacuolar degeneration of neurons in the Alzheimer's disease hippocampus.

Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patients.

Krebs von den Lungen 6 decreased in the serum and muscle of GNE myopathy patients

Mitochondrial localization of PABPN1 in oculopharyngeal muscular dystrophy

Molecular markers for granulovacuolar degeneration are present in rimmed vacuoles

Muscle-dominant wild-type TDP-43 expression induces myopathological changes featuring tubular aggregates and TDP-43-positive inclusions

Phosphatidylinositol-4,5-bisphosphate is enriched in granulovacuolar degeneration bodies and neurofibrillary tangles

Prevalences of Peripheral Arterial Disease Diagnosed by Computed Tomography Angiography in Patients with Acute Ischemic Stroke.

Retinitis pigmentosa prior to familial ALS caused by a homozygous cilia and flagella-associated protein 410 mutation

Statins and myotoxic effects associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase autoantibodies: an observational study in Japan

Synphilin-1 has neuroprotective effects on MPP-induced Parkinson's disease model cells by inhibiting ROS production and apoptosis

The first Japanese case of primary familial brain calcification caused by an MYORG variant

[A case of MELAS with G13513A mutation presenting with chronic kidney disease long before stroke-like episodes]

[A case of central nervous system lymphomatoid granulomatosis successfully treated with corticosteroids]