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Where and how alpha‐synuclein pathology spreads in Parkinson’s disease

Neuropathology, 2020-10, Vol.40 (5), p.415-425

Wakabayashi, Koichi

2020

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Neuropathology of Lewy body disease: Clinicopathological crosstalk between typical and atypical cases

Neuropathology, 2020-02, Vol.40 (1), p.30-39

2020

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Role of the Keap1/Nrf2 pathway in neurodegenerative diseases

Pathology international, 2015-05, Vol.65 (5), p.210-219

2015

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Neuropathology of Multiple System Atrophy, a Glioneuronal Degenerative Disease

Cerebellum (London, England), 2024-02, Vol.23 (1), p.2-12

2024

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Sigma-1 receptor is involved in degradation of intranuclear inclusions in a cellular model of Huntington's disease

Neurobiology of disease, 2015-02, Vol.74, p.25-31

2015

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The Lewy body in Parkinson's disease: Molecules implicated in the formation and degradation of α-synuclein aggregates

Neuropathology, 2007-10, Vol.27 (5), p.494-506

2007

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Trehalose intake and exercise upregulate a glucose transporter, GLUT8, in the brain

Biochemical and biophysical research communications, 2019-06, Vol.514 (3), p.672-677

2019

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Cabergoline, a long-acting dopamine agonist, attenuates L-dopa-induced dyskinesia without L-dopa sparing in a rat model of Parkinson’s disease

Neuroscience research, 2022-05, Vol.178, p.93-97

2022

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Autophagy Is a Common Degradation Pathway for Bunina Bodies and TDP-43 Inclusions in Amyotrophic Lateral Sclerosis

Journal of neuropathology and experimental neurology, 2019-10, Vol.78 (10), p.910-921

2019

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Is amyotrophic lateral sclerosis a prion-like disorder? A case report

Neurological sciences, 2023-07, Vol.44 (7), p.2587-2589

2023

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Praja1 RING‐finger E3 ubiquitin ligase is a common suppressor of neurodegenerative disease‐associated protein aggregation

Neuropathology, 2022-12, Vol.42 (6), p.488-504

2022

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Alteration of autophagosomal proteins (LC3, GABARAP and GATE-16) in Lewy body disease

Neurobiology of disease, 2011-09, Vol.43 (3), p.690-697

2011

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Involvement of the peripheral nervous system in synucleinopathies, tauopathies and other neurodegenerative proteinopathies of the brain

Acta neuropathologica, 2010-07, Vol.120 (1), p.1-12

2010

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Cellular pathology in multiple system atrophy

Neuropathology, 2006-08, Vol.26 (4), p.338-345

2006

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Immunoreactivity of myelin‐associated oligodendrocytic basic protein in Lewy bodies

Neuropathology, 2019-08, Vol.39 (4), p.279-285

2019

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Alteration of mitochondrial protein PDHA1 in Lewy body disease and PARK14

Biochemical and biophysical research communications, 2017-08, Vol.489 (4), p.439-444

2017

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Degeneration of Cardiac Sympathetic Nerve Begins in the Early Disease Process of Parkinson's Disease

Brain pathology (Zurich, Switzerland), 2007-01, Vol.17 (1), p.24-30

2007

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A mouse model of adult-onset multiple system atrophy

Neurobiology of disease, 2019-07, Vol.127, p.339-349

2019

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Case report: Adult-onset neuronal intranuclear inclusion disease with an amyotrophic lateral sclerosis phenotype

Frontiers in neuroscience, 2022-08, Vol.16

2022

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Identification of multiple system atrophy mimicking Parkinson's disease or progressive supranuclear palsy

Brain (London, England : 1878), 2021-05, Vol.144 (4), p.1138-1151

2021

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Alteration of Upstream Autophagy-Related Proteins (ULK1, ULK2, Beclin1, VPS34 and AMBRA1) in Lewy Body Disease

Brain pathology (Zurich, Switzerland), 2016-05, Vol.26 (3), p.359-370

2016

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Accumulation of Nonfibrillar TDP-43 in the Rough Endoplasmic Reticulum Is the Early-Stage Pathology in Amyotrophic Lateral Sclerosis

Journal of neuropathology and experimental neurology, 2022-04, Vol.81 (4), p.271-281

2022

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The AAA-ATPase VPS4 regulates extracellular secretion and lysosomal targeting of α-synuclein

PloS one, 2011-12, Vol.6 (12), p.e29460-e29460

2011

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Sulforaphane Increase Mitochondrial Biogenesis-Related Gene Expression in the Hippocampus and Suppresses Age-Related Cognitive Decline in Mice

International journal of molecular sciences, 2022-07, Vol.23 (15), p.8433

2022

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YOD1 attenuates neurogenic proteotoxicity through its deubiquitinating activity

Neurobiology of disease, 2018-04, Vol.112, p.14-23

2018

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Where and how alpha‐synuclein pathology spreads in Parkinson’s disease

Neuropathology of Lewy body disease: Clinicopathological crosstalk between typical and atypical cases

Role of the Keap1/Nrf2 pathway in neurodegenerative diseases

Neuropathology of Multiple System Atrophy, a Glioneuronal Degenerative Disease

Sigma-1 receptor is involved in degradation of intranuclear inclusions in a cellular model of Huntington's disease

The Lewy body in Parkinson's disease: Molecules implicated in the formation and degradation of α-synuclein aggregates

Trehalose intake and exercise upregulate a glucose transporter, GLUT8, in the brain

Cabergoline, a long-acting dopamine agonist, attenuates L-dopa-induced dyskinesia without L-dopa sparing in a rat model of Parkinson’s disease

Autophagy Is a Common Degradation Pathway for Bunina Bodies and TDP-43 Inclusions in Amyotrophic Lateral Sclerosis

Is amyotrophic lateral sclerosis a prion-like disorder? A case report

Praja1 RING‐finger E3 ubiquitin ligase is a common suppressor of neurodegenerative disease‐associated protein aggregation

Alteration of autophagosomal proteins (LC3, GABARAP and GATE-16) in Lewy body disease

Involvement of the peripheral nervous system in synucleinopathies, tauopathies and other neurodegenerative proteinopathies of the brain

Cellular pathology in multiple system atrophy

Immunoreactivity of myelin‐associated oligodendrocytic basic protein in Lewy bodies

Alteration of mitochondrial protein PDHA1 in Lewy body disease and PARK14

Degeneration of Cardiac Sympathetic Nerve Begins in the Early Disease Process of Parkinson's Disease

A mouse model of adult-onset multiple system atrophy

Case report: Adult-onset neuronal intranuclear inclusion disease with an amyotrophic lateral sclerosis phenotype

Identification of multiple system atrophy mimicking Parkinson's disease or progressive supranuclear palsy

Alteration of Upstream Autophagy-Related Proteins (ULK1, ULK2, Beclin1, VPS34 and AMBRA1) in Lewy Body Disease

Accumulation of Nonfibrillar TDP-43 in the Rough Endoplasmic Reticulum Is the Early-Stage Pathology in Amyotrophic Lateral Sclerosis

The AAA-ATPase VPS4 regulates extracellular secretion and lysosomal targeting of α-synuclein

Sulforaphane Increase Mitochondrial Biogenesis-Related Gene Expression in the Hippocampus and Suppresses Age-Related Cognitive Decline in Mice

YOD1 attenuates neurogenic proteotoxicity through its deubiquitinating activity

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