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Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice

Nature (London), 2017-04, Vol.544 (7650), p.367-371

2017

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Antisense therapies for movement disorders

Movement disorders, 2019-08, Vol.34 (8), p.1112-1119

2019

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Staufen1 links RNA stress granules and autophagy in a model of neurodegeneration

Nature communications, 2018-09, Vol.9 (1), p.3648-14, Article 3648

2018

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Potassium channel dysfunction underlies Purkinje neuron spiking abnormalities in spinocerebellar ataxia type 2

Human molecular genetics, 2017-10, Vol.26 (20), p.3935-3945

2017

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Cellular and circuit mechanisms underlying spinocerebellar ataxias

The Journal of physiology, 2016-08, Vol.594 (16), p.4653-4660

2016

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Trials for Cerebellar Ataxias: From Cellular Models to Human Therapies

1, 2023

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Control of innate immunity and lipid biosynthesis in neurodegeneration

Frontiers in molecular neuroscience, 2024-07, Vol.17, p.1402055

2024

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Deep cerebellar stimulation reduces ataxic motor symptoms in the shaker rat

Annals of neurology, 2019-05, Vol.85 (5), p.681-690

2019

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Antisense-Therapie neurologischer Erkrankungen

Nervenarzt, 2019-08, Vol.90 (8), p.781-786

Pulst, Stefan‑M.

2019

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Correction: Generation of SNCA Cell Models Using Zinc Finger Nuclease (ZFN) Technology for Efficient High-Throughput Drug Screening

PloS one, 2021-08, Vol.16 (8), p.e0256366-e0256366

2021

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Ataxin-2 regulates RGS8 translation in a new BAC-SCA2 transgenic mouse model

PLoS genetics, 2015-04, Vol.11 (4), p.e1005182-e1005182

2015

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Deranged Calcium Signaling and Neurodegeneration in Spinocerebellar Ataxia Type 2

The Journal of neuroscience, 2009-07, Vol.29 (29), p.9148-9162

2009

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Gene co-expression network analysis for identifying modules and functionally enriched pathways in SCA2

Human molecular genetics, 2017-08, Vol.26 (16), p.3069-3080

2017

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Neural selectivity, efficiency, and dose equivalence in deep brain stimulation through pulse width tuning and segmented electrodes

Brain stimulation, 2020-07, Vol.13 (4), p.1040-1050

2020

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Protein kinase C activity is a protective modifier of Purkinje neuron degeneration in cerebellar ataxia

Human molecular genetics, 2018-04, Vol.27 (8), p.1396-1410

2018

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Repeat Associated Non-AUG Translation (RAN Translation) Dependent on Sequence Downstream of the ATXN2 CAG Repeat

PloS one, 2015-06, Vol.10 (6), p.e0128769

2015

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Familial clustering of ALS in a population-based resource

Neurology, 2014-01, Vol.82 (1), p.17-22

2014

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Receptor protein tyrosine phosphatases control Purkinje neuron firing

Cell cycle (Georgetown, Tex.), 2020-01, Vol.19 (2), p.153-159

2020

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Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human

Nature genetics, 2000-09, Vol.26 (1), p.44-50

2000

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Dystonia and ataxia progression in spinocerebellar ataxias

Parkinsonism & related disorders, 2017-12, Vol.45, p.75-80

2017

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Repolarization matters: Mutations in the Kv4.3 potassium channel cause SCA19/22

Annals of neurology, 2012-12, Vol.72 (6), p.829-831

2012

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Generation of SNCA Cell Models Using Zinc Finger Nuclease (ZFN) Technology for Efficient High-Throughput Drug Screening

PloS one, 2015-08, Vol.10 (8), p.e0136930

2015

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Degenerative ataxias, from genes to therapies: The 2015 Cotzias Lecture

Neurology, 2016-06, Vol.86 (24), p.2284-2290

Pulst, Stefan M

2016

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The Initial Symptom and Motor Progression in Spinocerebellar Ataxias

Cerebellum (London, England), 2017-06, Vol.16 (3), p.615-622

2017

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Generation and characterization of Sca2 (ataxin-2) knockout mice

Biochemical and biophysical research communications, 2006-01, Vol.339 (1), p.17-24

2006

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Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice

Antisense therapies for movement disorders

Staufen1 links RNA stress granules and autophagy in a model of neurodegeneration

Potassium channel dysfunction underlies Purkinje neuron spiking abnormalities in spinocerebellar ataxia type 2

Cellular and circuit mechanisms underlying spinocerebellar ataxias

Trials for Cerebellar Ataxias: From Cellular Models to Human Therapies

Control of innate immunity and lipid biosynthesis in neurodegeneration

Deep cerebellar stimulation reduces ataxic motor symptoms in the shaker rat

Antisense-Therapie neurologischer Erkrankungen

Correction: Generation of SNCA Cell Models Using Zinc Finger Nuclease (ZFN) Technology for Efficient High-Throughput Drug Screening

Ataxin-2 regulates RGS8 translation in a new BAC-SCA2 transgenic mouse model

Deranged Calcium Signaling and Neurodegeneration in Spinocerebellar Ataxia Type 2

Gene co-expression network analysis for identifying modules and functionally enriched pathways in SCA2

Neural selectivity, efficiency, and dose equivalence in deep brain stimulation through pulse width tuning and segmented electrodes

Protein kinase C activity is a protective modifier of Purkinje neuron degeneration in cerebellar ataxia

Repeat Associated Non-AUG Translation (RAN Translation) Dependent on Sequence Downstream of the ATXN2 CAG Repeat

Familial clustering of ALS in a population-based resource

Receptor protein tyrosine phosphatases control Purkinje neuron firing

Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human

Dystonia and ataxia progression in spinocerebellar ataxias

Repolarization matters: Mutations in the Kv4.3 potassium channel cause SCA19/22

Generation of SNCA Cell Models Using Zinc Finger Nuclease (ZFN) Technology for Efficient High-Throughput Drug Screening

Degenerative ataxias, from genes to therapies: The 2015 Cotzias Lecture

The Initial Symptom and Motor Progression in Spinocerebellar Ataxias

Generation and characterization of Sca2 (ataxin-2) knockout mice

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