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Structures of the Wild-Type and S59L Mutant CHCHD10 Proteins Important in Amyotrophic Lateral Sclerosis–Frontotemporal Dementia

ACS chemical neuroscience, 2022-04, Vol.13 (8), p.1273-1280

2022

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Frontotemporal Dementia-Related V57E Mutation Impairs Mitochondrial Function and Alters the Structural Properties of CHCHD10

ACS chemical neuroscience, 2023-06, Vol.14 (11), p.2134-2145

2023

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Mitochondrial CHCHD2: Disease-Associated Mutations, Physiological Functions, and Current Animal Models

Frontiers in aging neuroscience, 2021-04, Vol.13, p.660843-660843

2021

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CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

Neurobiology of aging, 2015-04, Vol.36 (4), p.1767.e3-1767.e6

2015

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A novel CHCHD10 mutation implicates a Mia40‐dependent mitochondrial import deficit in ALS

EMBO molecular medicine, 2018-06, Vol.10 (6), p.1-n/a

2018

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Editorial: Molecular links between mitochondrial damage and human neurodegenerative disorders, volume II

Frontiers in cell and developmental biology, 2024-04, Vol.12, p.1417802-1417802

Imai, Yuzuru

2024

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Mitochondria, a Key Target in Amyotrophic Lateral Sclerosis Pathogenesis

Genes, 2023-10, Vol.14 (11), p.1981

2023

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Mutation analysis of CHCHD2 and CHCHD10 in Italian patients with mitochondrial myopathy

Neurobiology of aging, 2018-06, Vol.66, p.181.e1-181.e2

2018

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Modulation of synaptic plasticity, motor unit physiology, and TDP-43 pathology by CHCHD10

Acta neuropathologica communications, 2022-07, Vol.10 (1), p.95-95, Article 95

2022

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CHCHD10 mutations in patients with amyotrophic lateral sclerosis in mainland China

Neurobiology of aging, 2017-06, Vol.54, p.214.e7-214.e10

2017

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The identification of high-performing antibodies for Coiled-coil-helix-coiled-coil-helix domain containing protein 10 (CHCHD10) for use in Western Blot, immunoprecipitation and immunofluorescence [version 1; peer review: 1 approved, 1 approved with reservations]

F1000 research, 2023, Vol.12, p.403

2023

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Identification of CHCHD10 Mutation in Chinese Patients with Alzheimer Disease

Molecular neurobiology, 2017-09, Vol.54 (7), p.5243-5247

2017

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Genetic Features of MAPT, GRN, C9orf72 and CHCHD10 Gene Mutations in Chinese Patients with Frontotemporal Dementia

Current Alzheimer research, 2017-01, Vol.14 (10), p.1102

2017

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The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patients

Neurobiology of aging, 2015-10, Vol.36 (10), p.2908.e17-2908.e18

2015

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Disruption of Mitophagy Flux through the PARL-PINK1 Pathway by CHCHD10 Mutations or CHCHD10 Depletion

Cells (Basel, Switzerland), 2023-12, Vol.12 (24), p.2781

2023

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Meta-analysis of the association between CHCHD10 Pro34Ser variant and the risk of amyotrophic lateral sclerosis

Neurological sciences, 2021-02, Vol.42 (2), p.625-631

2021

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The identification of high-performing antibodies for Coiled-coil-helix-coiled-coil-helix domain containing protein 10 (CHCHD10) for use in Western Blot, immunoprecipitation and immunofluorescence [version 2; peer review: 2 approved, 1 approved with reservations]

F1000 research, 2023, Vol.12, p.403

2023

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Genetic analysis of CHCHD2 and CHCHD10 in Italian patients with Parkinson’s disease

Neurobiology of aging, 2017-05, Vol.53, p.193.e7-193.e8

2017

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Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66Val

Acta neurologica Scandinavica, 2016-05, Vol.133 (5), p.361-366

2016

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Mitochondrial dynamism and the pathogenesis of Amyotrophic Lateral Sclerosis

Frontiers in cellular neuroscience, 2015-02, Vol.9, p.31-31

2015

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Mutation Screening of the CHCHD10 Gene in Chinese Patients with Amyotrophic Lateral Sclerosis

Molecular neurobiology, 2017-07, Vol.54 (5), p.3189-3194

2017

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CHCHD10 is not a frequent causative gene in Chinese ALS patients

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2016-08, Vol.17 (5-6), p.458-460

2016

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Functional annotation of heart enriched mitochondrial genes GBAS and CHCHD10 through guilt by association

Biochemical and biophysical research communications, 2010-11, Vol.402 (2), p.203-208

2010

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Letter to the Editor on a paper by Hsiao C-T, Tsai P-C, Liao Y-C, Lee Y-C, Soong B-W. C9ORF72 repeat expansion is not a significant cause of late-onset cerebellar ataxia syndrome. J Neurol Sci 2014;347:322–324

Journal of the neurological sciences, 2015-04, Vol.351 (1), p.196-197

2015

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Spontaneous activity in electromyography may differentiate certain benign lower motor neuron disease forms from amyotrophic lateral sclerosis

Journal of the neurological sciences, 2015-08, Vol.355 (1), p.143-146

2015

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Structures of the Wild-Type and S59L Mutant CHCHD10 Proteins Important in Amyotrophic Lateral Sclerosis–Frontotemporal Dementia

Frontotemporal Dementia-Related V57E Mutation Impairs Mitochondrial Function and Alters the Structural Properties of CHCHD10

Mitochondrial CHCHD2: Disease-Associated Mutations, Physiological Functions, and Current Animal Models

CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

A novel CHCHD10 mutation implicates a Mia40‐dependent mitochondrial import deficit in ALS

Editorial: Molecular links between mitochondrial damage and human neurodegenerative disorders, volume II

Mitochondria, a Key Target in Amyotrophic Lateral Sclerosis Pathogenesis

Mutation analysis of CHCHD2 and CHCHD10 in Italian patients with mitochondrial myopathy

Modulation of synaptic plasticity, motor unit physiology, and TDP-43 pathology by CHCHD10

CHCHD10 mutations in patients with amyotrophic lateral sclerosis in mainland China

The identification of high-performing antibodies for Coiled-coil-helix-coiled-coil-helix domain containing protein 10 (CHCHD10) for use in Western Blot, immunoprecipitation and immunofluorescence [version 1; peer review: 1 approved, 1 approved with reservations]

Identification of CHCHD10 Mutation in Chinese Patients with Alzheimer Disease

Genetic Features of MAPT, GRN, C9orf72 and CHCHD10 Gene Mutations in Chinese Patients with Frontotemporal Dementia

The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patients

Disruption of Mitophagy Flux through the PARL-PINK1 Pathway by CHCHD10 Mutations or CHCHD10 Depletion

Meta-analysis of the association between CHCHD10 Pro34Ser variant and the risk of amyotrophic lateral sclerosis

The identification of high-performing antibodies for Coiled-coil-helix-coiled-coil-helix domain containing protein 10 (CHCHD10) for use in Western Blot, immunoprecipitation and immunofluorescence [version 2; peer review: 2 approved, 1 approved with reservations]

Genetic analysis of CHCHD2 and CHCHD10 in Italian patients with Parkinson’s disease

Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66Val

Mitochondrial dynamism and the pathogenesis of Amyotrophic Lateral Sclerosis

Mutation Screening of the CHCHD10 Gene in Chinese Patients with Amyotrophic Lateral Sclerosis

CHCHD10 is not a frequent causative gene in Chinese ALS patients

Functional annotation of heart enriched mitochondrial genes GBAS and CHCHD10 through guilt by association

Letter to the Editor on a paper by Hsiao C-T, Tsai P-C, Liao Y-C, Lee Y-C, Soong B-W. C9ORF72 repeat expansion is not a significant cause of late-onset cerebellar ataxia syndrome. J Neurol Sci 2014;347:322–324

Spontaneous activity in electromyography may differentiate certain benign lower motor neuron disease forms from amyotrophic lateral sclerosis

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