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TBK1 controls autophagosomal engulfment of polyubiquitinated mitochondria through p62/SQSTM1 phosphorylation

Human molecular genetics, 2015-08, Vol.24 (15), p.4429-4442

2015

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Serine 403 Phosphorylation of p62/SQSTM1 Regulates Selective Autophagic Clearance of Ubiquitinated Proteins

Molecular cell, 2011-10, Vol.44 (2), p.279-289

2011

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Proteomic analysis of heat-stable proteins revealed an increased proportion of proteins with compositionally biased regions

Scientific reports, 2022-03, Vol.12 (1), p.4347-4347, Article 4347

2022

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A Seeding Reaction Recapitulates Intracellular Formation of Sarkosyl-insoluble Transactivation Response Element (TAR) DNA-binding Protein-43 Inclusions

The Journal of biological chemistry, 2011-05, Vol.286 (21), p.18664-18672

2011

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Proteomics-Based Approach Identifies Altered ER Domain Properties by ALS-Linked VAPB Mutation

Scientific reports, 2020-05, Vol.10 (1), p.7610-7610, Article 7610

2020

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Rapamycin-induced oligomer formation system of FRB–FKBP fusion proteins

Journal of bioscience and bioengineering, 2016-07, Vol.122 (1), p.40-46

2016

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pathogenic mechanisms of polyglutamine diseases and current therapeutic strategies

Journal of neurochemistry, 2009-09, Vol.110 (6), p.1737-1765

2009

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The diffuse distribution of Nav1.2 on mid-axonal regions is a marker for unmyelinated fibers in the central nervous system

Neuroscience research, 2022-04, Vol.177, p.145-150

2022

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CELF2 regulates the species-specific alternative splicing of TREM2

Scientific reports, 2020-10, Vol.10 (1), p.17995-17995, Article 17995

2020

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Intranuclear Aggregation of Mutant FUS/TLS as a Molecular Pathomechanism of Amyotrophic Lateral Sclerosis

The Journal of biological chemistry, 2014-01, Vol.289 (2), p.1192-1202

2014

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Non-coding RNA Neat1 and Abhd11os expressions are dysregulated in medium spiny neurons of Huntington disease model mice

Neuroscience research, 2019-10, Vol.147, p.58-63

2019

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ER Dynamics and Derangement in Neurological Diseases

Frontiers in neuroscience, 2018-02, Vol.12, p.91-91

2018

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Phosphorylation of mitochondrial polyubiquitin by PINK1 promotes Parkin mitochondrial tethering

PLoS genetics, 2014-12, Vol.10 (12), p.e1004861-e1004861

2014

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Proteomic analysis of subcellular compartments containing disseminated alpha-synuclein seeds

Neuroscience research, 2021-09, Vol.170, p.341-349

2021

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Mutation-dependent Polymorphism of Cu,Zn-Superoxide Dismutase Aggregates in the Familial Form of Amyotrophic Lateral Sclerosis

The Journal of biological chemistry, 2010-07, Vol.285 (29), p.22221-22231

2010

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Amyloids facilitate DNA transfection in vivo

Neuroscience research, 2022-07, Vol.180, p.99-107

2022

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Biochemical and morphological classification of disease-associated alpha-synuclein mutants aggregates

Biochemical and biophysical research communications, 2019-01, Vol.508 (3), p.729-734

2019

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Nuclear localization of MBNL1: splicing-mediated autoregulation and repression of repeat-derived aberrant proteins

Human molecular genetics, 2015-02, Vol.24 (3), p.740-756

2015

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Complete Loss of Post-translational Modifications Triggers Fibrillar Aggregation of SOD1 in the Familial Form of Amyotrophic Lateral Sclerosis

The Journal of biological chemistry, 2008-08, Vol.283 (35), p.24167-24176

2008

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Preserved proteinase K-resistant core after amplification of alpha-synuclein aggregates: Implication to disease-related structural study

Biochemical and biophysical research communications, 2020-02, Vol.522 (3), p.655-661

2020

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Gene expression profiling in neuronal cells identifies a different type of transcriptome modulated by NF-Y

Scientific reports, 2020-12, Vol.10 (1), p.21714-21714, Article 21714

2020

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Local Unfolding of Cu, Zn Superoxide Dismutase Monomer Determines the Morphology of Fibrillar Aggregates

Journal of molecular biology, 2012-08, Vol.421 (4-5), p.548-560

2012

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Distinct conformations of in vitro and in vivo amyloids of huntingtin-exon1 show different cytotoxicity

Proceedings of the National Academy of Sciences - PNAS, 2009-06, Vol.106 (24), p.9679-9684

2009

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Intracellular localization and splicing regulation of FUS/TLS are variably affected by amyotrophic lateral sclerosis-linked mutations

Nucleic acids research, 2011-04, Vol.39 (7), p.2781

2011

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Functional diversity of protein fibrillar aggregates from physiology to RNA granules to neurodegenerative diseases

Biochimica et biophysica acta, 2013-08, Vol.1832 (8), p.1271-1278

2013

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TBK1 controls autophagosomal engulfment of polyubiquitinated mitochondria through p62/SQSTM1 phosphorylation

Serine 403 Phosphorylation of p62/SQSTM1 Regulates Selective Autophagic Clearance of Ubiquitinated Proteins

Proteomic analysis of heat-stable proteins revealed an increased proportion of proteins with compositionally biased regions

A Seeding Reaction Recapitulates Intracellular Formation of Sarkosyl-insoluble Transactivation Response Element (TAR) DNA-binding Protein-43 Inclusions

Proteomics-Based Approach Identifies Altered ER Domain Properties by ALS-Linked VAPB Mutation

Rapamycin-induced oligomer formation system of FRB–FKBP fusion proteins

pathogenic mechanisms of polyglutamine diseases and current therapeutic strategies

The diffuse distribution of Nav1.2 on mid-axonal regions is a marker for unmyelinated fibers in the central nervous system

CELF2 regulates the species-specific alternative splicing of TREM2

Intranuclear Aggregation of Mutant FUS/TLS as a Molecular Pathomechanism of Amyotrophic Lateral Sclerosis

Non-coding RNA Neat1 and Abhd11os expressions are dysregulated in medium spiny neurons of Huntington disease model mice

ER Dynamics and Derangement in Neurological Diseases

Phosphorylation of mitochondrial polyubiquitin by PINK1 promotes Parkin mitochondrial tethering

Proteomic analysis of subcellular compartments containing disseminated alpha-synuclein seeds

Mutation-dependent Polymorphism of Cu,Zn-Superoxide Dismutase Aggregates in the Familial Form of Amyotrophic Lateral Sclerosis

Amyloids facilitate DNA transfection in vivo

Biochemical and morphological classification of disease-associated alpha-synuclein mutants aggregates

Nuclear localization of MBNL1: splicing-mediated autoregulation and repression of repeat-derived aberrant proteins

Complete Loss of Post-translational Modifications Triggers Fibrillar Aggregation of SOD1 in the Familial Form of Amyotrophic Lateral Sclerosis

Preserved proteinase K-resistant core after amplification of alpha-synuclein aggregates: Implication to disease-related structural study

Gene expression profiling in neuronal cells identifies a different type of transcriptome modulated by NF-Y

Local Unfolding of Cu, Zn Superoxide Dismutase Monomer Determines the Morphology of Fibrillar Aggregates

Distinct conformations of in vitro and in vivo amyloids of huntingtin-exon1 show different cytotoxicity

Intracellular localization and splicing regulation of FUS/TLS are variably affected by amyotrophic lateral sclerosis-linked mutations

Functional diversity of protein fibrillar aggregates from physiology to RNA granules to neurodegenerative diseases

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