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Antisense Proline-Arginine RAN Dipeptides Linked to C9ORF72-ALS/FTD Form Toxic Nuclear Aggregates that Initiate In Vitro and In Vivo Neuronal Death

Neuron (Cambridge, Mass.), 2014-12, Vol.84 (6), p.1213-1225

2014

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A fruitful endeavor: Modeling ALS in the fruit fly

Brain research, 2015-05, Vol.1607, p.47-74

2015

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Function and dysfunction of GEMIN5: understanding a novel neurodevelopmental disorder

Neural regeneration research, 2024-11, Vol.19 (11), p.2377-2386

2024

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RNA Binding Antagonizes Neurotoxic Phase Transitions of TDP-43

Neuron (Cambridge, Mass.), 2019-04, Vol.102 (2), p.321-338.e8

2019

Volltextzugriff (PDF)

Methods to assay Drosophila behavior

Journal of visualized experiments, 2012-03 (61)

2012

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HDAC6 controls autophagosome maturation essential for ubiquitin-selective quality-control autophagy

The EMBO journal, 2010-03, Vol.29 (5), p.969-980

2010

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Autophagy Dysregulation in ALS: When Protein Aggregates Get Out of Hand

Frontiers in molecular neuroscience, 2017-08, Vol.10, p.263-263

2017

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Low-level overexpression of wild type TDP-43 causes late-onset, progressive neurodegeneration and paralysis in mice

PloS one, 2022-02, Vol.17 (2), p.e0255710

2022

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Stress granules at the intersection of autophagy and ALS

Brain research, 2016-10, Vol.1649 (Pt B), p.189-200

2016

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Matrin-3 dysfunction in myopathy and motor neuron degeneration

Neural regeneration research, 2022-03, Vol.17 (3), p.575-576

2022

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Downregulation of microRNA-9 in iPSC-derived neurons of FTD/ALS patients with TDP-43 mutations

PloS one, 2013-10, Vol.8 (10), p.e76055-e76055

2013

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NUP62 localizes to ALS/FTLD pathological assemblies and contributes to TDP-43 insolubility

Nature communications, 2022-06, Vol.13 (1), p.3380-17, Article 3380

2022

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Interactions between ALS-linked FUS and nucleoporins are associated with defects in the nucleocytoplasmic transport pathway

Nature neuroscience, 2021-08, Vol.24 (8), p.1077

2021

Volltextzugriff (PDF)

Artificial intelligence and leukocyte epigenomics: Evaluation and prediction of late-onset Alzheimer's disease

PloS one, 2021-03, Vol.16 (3), p.e0248375-e0248375

2021

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Prevalence of antibiotic resistance in commensal Escherichia coli among the children in rural hill communities of Northeast India

PloS one, 2018-06, Vol.13 (6), p.e0199179-e0199179

2018

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Nucleocytoplasmic Proteomic Analysis Uncovers eRF1 and Nonsense-Mediated Decay as Modifiers of ALS/FTD C9orf72 Toxicity

Neuron (Cambridge, Mass.), 2020-04, Vol.106 (1), p.90-107.e13

2020

Volltextzugriff (PDF)

Defective Proteasome Delivery of Polyubiquitinated Proteins by Ubiquilin-2 Proteins Containing ALS Mutations

PloS one, 2015-06, Vol.10 (6), p.e0130162

2015

Volltextzugriff (PDF)

Protein arginine methyltransferase 6 enhances polyglutamine-expanded androgen receptor function and toxicity in spinal and bulbar muscular atrophy

Neuron (Cambridge, Mass.), 2015-01, Vol.85 (1), p.88-100

2015

Volltextzugriff (PDF)

Mutations in TGM6 induce the unfolded protein response in SCA35

Human molecular genetics, 2017-10, Vol.26 (19), p.3749-3762

2017

Volltextzugriff (PDF)

Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome

PLoS genetics, 2010-12, Vol.6 (12), p.e1001240

2010

Volltextzugriff (PDF)

Caprylic triglyceride as a novel therapeutic approach to effectively improve the performance and attenuate the symptoms due to the motor neuron loss in ALS disease

PloS one, 2012-11, Vol.7 (11), p.e49191-e49191

2012

Volltextzugriff (PDF)

Optogenetic TDP-43 nucleation induces persistent insoluble species and progressive motor dysfunction in vivo

Neurobiology of disease, 2020-12, Vol.146, p.105078-105078, Article 105078

2020

Volltextzugriff (PDF)

Basal autophagy is required for promoting dendritic terminal branching in Drosophila sensory neurons

PloS one, 2018-11, Vol.13 (11), p.e0206743

2018

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Muscleblind acts as a modifier of FUS toxicity by modulating stress granule dynamics and SMN localization

Nature communications, 2019-12, Vol.10 (1), p.5583-20, Article 5583

2019

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Huntingtin-mediated axonal transport requires arginine methylation by PRMT6

Cell reports (Cambridge), 2021-04, Vol.35 (2), p.108980-108980, Article 108980

2021

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Antisense Proline-Arginine RAN Dipeptides Linked to C9ORF72-ALS/FTD Form Toxic Nuclear Aggregates that Initiate In Vitro and In Vivo Neuronal Death

A fruitful endeavor: Modeling ALS in the fruit fly

Function and dysfunction of GEMIN5: understanding a novel neurodevelopmental disorder

RNA Binding Antagonizes Neurotoxic Phase Transitions of TDP-43

Methods to assay Drosophila behavior

HDAC6 controls autophagosome maturation essential for ubiquitin-selective quality-control autophagy

Autophagy Dysregulation in ALS: When Protein Aggregates Get Out of Hand

Low-level overexpression of wild type TDP-43 causes late-onset, progressive neurodegeneration and paralysis in mice

Stress granules at the intersection of autophagy and ALS

Matrin-3 dysfunction in myopathy and motor neuron degeneration

Downregulation of microRNA-9 in iPSC-derived neurons of FTD/ALS patients with TDP-43 mutations

NUP62 localizes to ALS/FTLD pathological assemblies and contributes to TDP-43 insolubility

Interactions between ALS-linked FUS and nucleoporins are associated with defects in the nucleocytoplasmic transport pathway

Artificial intelligence and leukocyte epigenomics: Evaluation and prediction of late-onset Alzheimer's disease

Prevalence of antibiotic resistance in commensal Escherichia coli among the children in rural hill communities of Northeast India

Nucleocytoplasmic Proteomic Analysis Uncovers eRF1 and Nonsense-Mediated Decay as Modifiers of ALS/FTD C9orf72 Toxicity

Defective Proteasome Delivery of Polyubiquitinated Proteins by Ubiquilin-2 Proteins Containing ALS Mutations

Protein arginine methyltransferase 6 enhances polyglutamine-expanded androgen receptor function and toxicity in spinal and bulbar muscular atrophy

Mutations in TGM6 induce the unfolded protein response in SCA35

Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome

Caprylic triglyceride as a novel therapeutic approach to effectively improve the performance and attenuate the symptoms due to the motor neuron loss in ALS disease

Optogenetic TDP-43 nucleation induces persistent insoluble species and progressive motor dysfunction in vivo

Basal autophagy is required for promoting dendritic terminal branching in Drosophila sensory neurons

Muscleblind acts as a modifier of FUS toxicity by modulating stress granule dynamics and SMN localization

Huntingtin-mediated axonal transport requires arginine methylation by PRMT6

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