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Loss of Tmem106b exacerbates FTLD pathologies and causes motor deficits in progranulin‐deficient mice

EMBO reports, 2020-10, Vol.21 (10), p.e50197-n/a

2020

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TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia

Journal of neurochemistry, 2013-09, Vol.126 (6), p.781-791

2013

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Investigating the Pathogenic Interplay of Alpha-Synuclein, Tau, and Amyloid Beta in Lewy Body Dementia: Insights from Viral-Mediated Overexpression in Transgenic Mouse Models

Biomedicines, 2023-10, Vol.11 (10), p.2863

2023

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Poly(GR) impairs protein translation and stress granule dynamics in C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis

Nature medicine, 2018-08, Vol.24 (8), p.1136-1142

2018

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Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS

Acta neuropathologica, 2013-12, Vol.126 (6), p.829-844

2013

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Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress

Acta neuropathologica, 2014-10, Vol.128 (4), p.505-524

2014

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(Patho-)physiological relevance of PINK1-dependent ubiquitin phosphorylation

EMBO reports, 2015-09, Vol.16 (9), p.1114-1130

2015

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Aberrant deposition of stress granule-resident proteins linked to C9orf72-associated TDP-43 proteinopathy

Molecular neurodegeneration, 2019-02, Vol.14 (1), p.9-15, Article 9

2019

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Phosphorylated tau sites that are elevated in Alzheimer's disease fluid biomarkers are visualized in early neurofibrillary tangle maturity levels in the post mortem brain

Alzheimer's & dementia, 2023-03, Vol.19 (3), p.1029-1040

2023

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Microglial lysosome dysfunction contributes to white matter pathology and TDP-43 proteinopathy in GRN-associated FTD

Cell reports (Cambridge), 2021-08, Vol.36 (8), p.109581-109581, Article 109581

2021

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Perry Syndrome: A Distinctive Type of TDP-43 Proteinopathy

Journal of neuropathology and experimental neurology, 2017-08, Vol.76 (8), p.676-682

2017

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Galactosylceramidase deficiency and pathological abnormalities in cerebral white matter of Krabbe disease

Neurobiology of disease, 2022-11, Vol.174, p.105862-105862, Article 105862

2022

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Wild-type human TDP-43 expression causes TDP-43 phosphorylation, mitochondrial aggregation, motor deficits, and early mortality in transgenic mice

The Journal of neuroscience, 2010-08, Vol.30 (32), p.10851-10859

2010

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Hexanucleotide Repeat Expansions in c9FTD/ALS and SCA36 Confer Selective Patterns of Neurodegeneration In Vivo

Cell reports (Cambridge), 2020-05, Vol.31 (5), p.107616-107616, Article 107616

2020

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Poly(GR) interacts with key stress granule factors promoting its assembly into cytoplasmic inclusions

Cell reports (Cambridge), 2023-08, Vol.42 (8), p.112822-112822, Article 112822

2023

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Loss of Tmem106b leads to cerebellum Purkinje cell death and motor deficits

Brain pathology (Zurich, Switzerland), 2021-05, Vol.31 (3), p.e12945-n/a

2021

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Reduced orexin immunoreactivity in Perry syndrome and multiple system atrophy

Parkinsonism & related disorders, 2017-09, Vol.42, p.85-89

2017

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p62 Pathology Model in the Rat Substantia Nigra with Filamentous Inclusions and Progressive Neurodegeneration

PloS one, 2017-01, Vol.12 (1), p.e0169291

2017

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Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies

Acta neuropathologica communications, 2023-07, Vol.11 (1), p.109-109, Article 109

2023

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Tau exhibits unique seeding properties in globular glial tauopathy

Acta neuropathologica communications, 2019-03, Vol.7 (1), p.36-36, Article 36

2019

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Publisher Correction to: Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies

Acta neuropathologica communications, 2023-07, Vol.11 (1), p.117-117, Article 117

2023

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Transactivation Response DNA-Binding Protein 43 Microvasculopathy in Frontotemporal Degeneration and Familial Lewy Body Disease

Journal of neuropathology and experimental neurology, 2009-11, Vol.68 (11), p.1167-1176

2009

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Neonatal AAV delivery of alpha-synuclein induces pathology in the adult mouse brain

Acta neuropathologica communications, 2017-06, Vol.5 (1), p.51-51, Article 51

2017

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Plasma PolyQ-ATXN3 Levels Associate With Cerebellar Degeneration and Behavioral Abnormalities in a New AAV-Based SCA3 Mouse Model

Frontiers in cell and developmental biology, 2022-03, Vol.10, p.863089-863089

2022

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Loss of Tmem106b exacerbates FTLD pathologies and causes motor deficits in progranulin‐deficient mice

TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia

Investigating the Pathogenic Interplay of Alpha-Synuclein, Tau, and Amyloid Beta in Lewy Body Dementia: Insights from Viral-Mediated Overexpression in Transgenic Mouse Models

Poly(GR) impairs protein translation and stress granule dynamics in C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis

Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS

Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress

(Patho-)physiological relevance of PINK1-dependent ubiquitin phosphorylation

Aberrant deposition of stress granule-resident proteins linked to C9orf72-associated TDP-43 proteinopathy

Phosphorylated tau sites that are elevated in Alzheimer's disease fluid biomarkers are visualized in early neurofibrillary tangle maturity levels in the post mortem brain

Microglial lysosome dysfunction contributes to white matter pathology and TDP-43 proteinopathy in GRN-associated FTD

Perry Syndrome: A Distinctive Type of TDP-43 Proteinopathy

Galactosylceramidase deficiency and pathological abnormalities in cerebral white matter of Krabbe disease

Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease

Wild-type human TDP-43 expression causes TDP-43 phosphorylation, mitochondrial aggregation, motor deficits, and early mortality in transgenic mice

Hexanucleotide Repeat Expansions in c9FTD/ALS and SCA36 Confer Selective Patterns of Neurodegeneration In Vivo

Poly(GR) interacts with key stress granule factors promoting its assembly into cytoplasmic inclusions

Loss of Tmem106b leads to cerebellum Purkinje cell death and motor deficits

Reduced orexin immunoreactivity in Perry syndrome and multiple system atrophy

p62 Pathology Model in the Rat Substantia Nigra with Filamentous Inclusions and Progressive Neurodegeneration

Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies

Tau exhibits unique seeding properties in globular glial tauopathy

Publisher Correction to: Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies

Transactivation Response DNA-Binding Protein 43 Microvasculopathy in Frontotemporal Degeneration and Familial Lewy Body Disease

Neonatal AAV delivery of alpha-synuclein induces pathology in the adult mouse brain

Plasma PolyQ-ATXN3 Levels Associate With Cerebellar Degeneration and Behavioral Abnormalities in a New AAV-Based SCA3 Mouse Model

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