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Cholinergic system changes of falls and freezing of gait in Parkinson's disease

Annals of neurology, 2019-04, Vol.85 (4), p.538-549

2019

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The Nuclear Envelope as a Signaling Node in Development and Disease

Developmental cell, 2009-11, Vol.17 (5), p.626-638

2009

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A critical evaluation of the Braak staging scheme for Parkinson's disease

Annals of neurology, 2008-11, Vol.64 (5), p.485-491

2008

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LRRK2 Parkinson disease mutations enhance its microtubule association

Human molecular genetics, 2012-02, Vol.21 (4), p.890-899

2012

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Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia

Cerebellum (London, England), 2017-04, Vol.16 (2), p.577-594

2017

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Loss of the Dystonia-Associated Protein TorsinA Selectively Disrupts the Neuronal Nuclear Envelope

Neuron (Cambridge, Mass.), 2005-12, Vol.48 (6), p.923-932

2005

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Regional vesicular acetylcholine transporter distribution in human brain: A [18F]fluoroethoxybenzovesamicol positron emission tomography study

Journal of comparative neurology (1911), 2018-12, Vol.526 (17), p.2884-2897

2018

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Neuronal Nuclear Membrane Budding Occurs during a Developmental Window Modulated by Torsin Paralogs

Cell reports (Cambridge), 2016-09, Vol.16 (12), p.3322-3333

2016

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Discussion of Research Priorities for Gait Disorders in Parkinson's Disease

Movement disorders, 2022-02, Vol.37 (2), p.253-263

2022

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Hepatocytes Deficient in Nuclear Envelope Protein Lamina-associated Polypeptide 1 are an Ideal Mammalian System to Study Intranuclear Lipid Droplets

Journal of lipid research, 2022-10, Vol.63 (10), p.100277-100277, Article 100277

2022

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molecular mechanism underlying the neural-specific defect in torsinA mutant mice

Proceedings of the National Academy of Sciences - PNAS, 2010-05, Vol.107 (21), p.9861-9866

2010

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TorsinA controls TAN line assembly and the retrograde flow of dorsal perinuclear actin cables during rearward nuclear movement

The Journal of cell biology, 2017-03, Vol.216 (3), p.657-674

2017

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Lamina-Associated Polypeptide-1 Interacts with the Muscular Dystrophy Protein Emerin and Is Essential for Skeletal Muscle Maintenance

Developmental cell, 2013-09, Vol.26 (6), p.591-603

2013

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The WD40 domain is required for LRRK2 neurotoxicity

PloS one, 2009-12, Vol.4 (12), p.e8463

2009

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Cerebellothalamocortical pathway abnormalities in torsinA DYT1 knock-in mice

Proceedings of the National Academy of Sciences - PNAS, 2011-04, Vol.108 (16), p.6638-6643

2011

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Targeting the pedunculopontine nucleus in Parkinson's disease: Time to go back to the drawing board

Movement disorders, 2018-12, Vol.33 (12), p.1871-1875

2018

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A motif within the armadillo repeat of Parkinson's-linked LRRK2 interacts with FADD to hijack the extrinsic death pathway

Scientific reports, 2018-02, Vol.8 (1), p.3455-17, Article 3455

2018

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TorsinB overexpression prevents abnormal twisting in DYT1 dystonia mouse models

eLife, 2020-03, Vol.9

2020

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Mislocalization to the Nuclear Envelope: An Effect of the Dystonia-Causing TorsinA Mutation

Proceedings of the National Academy of Sciences - PNAS, 2004-01, Vol.101 (3), p.847-852

2004

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Reply to: “Letter on Discussion of Gait Research”

Movement disorders, 2022-06, Vol.37 (6), p.1328-1328

2022

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Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neurons

eLife, 2015-06, Vol.4, p.e08352

2015

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CNS critical periods: implications for dystonia and other neurodevelopmental disorders

JCI insight, 2021-02, Vol.6 (4)

2021

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Forebrain knock-out of torsinA reduces striatal free-water and impairs whole-brain functional connectivity in a symptomatic mouse model of DYT1 dystonia

Neurobiology of disease, 2017-10, Vol.106, p.124-132

2017

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A cell autonomous torsinA requirement for cholinergic neuron survival and motor control

eLife, 2018-08, Vol.7

2018

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The Nuclear Envelope: An Intriguing Focal Point for Neurogenetic Disease

Neurotherapeutics, 2014-10, Vol.11 (4), p.764-772

2014

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Cholinergic system changes of falls and freezing of gait in Parkinson's disease

The Nuclear Envelope as a Signaling Node in Development and Disease

A critical evaluation of the Braak staging scheme for Parkinson's disease

LRRK2 Parkinson disease mutations enhance its microtubule association

Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia

Loss of the Dystonia-Associated Protein TorsinA Selectively Disrupts the Neuronal Nuclear Envelope

Regional vesicular acetylcholine transporter distribution in human brain: A [18F]fluoroethoxybenzovesamicol positron emission tomography study

Neuronal Nuclear Membrane Budding Occurs during a Developmental Window Modulated by Torsin Paralogs

Discussion of Research Priorities for Gait Disorders in Parkinson's Disease

Hepatocytes Deficient in Nuclear Envelope Protein Lamina-associated Polypeptide 1 are an Ideal Mammalian System to Study Intranuclear Lipid Droplets

molecular mechanism underlying the neural-specific defect in torsinA mutant mice

TorsinA controls TAN line assembly and the retrograde flow of dorsal perinuclear actin cables during rearward nuclear movement

Lamina-Associated Polypeptide-1 Interacts with the Muscular Dystrophy Protein Emerin and Is Essential for Skeletal Muscle Maintenance

The WD40 domain is required for LRRK2 neurotoxicity

Cerebellothalamocortical pathway abnormalities in torsinA DYT1 knock-in mice

Targeting the pedunculopontine nucleus in Parkinson's disease: Time to go back to the drawing board

A motif within the armadillo repeat of Parkinson's-linked LRRK2 interacts with FADD to hijack the extrinsic death pathway

TorsinB overexpression prevents abnormal twisting in DYT1 dystonia mouse models

Mislocalization to the Nuclear Envelope: An Effect of the Dystonia-Causing TorsinA Mutation

Reply to: “Letter on Discussion of Gait Research”

Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neurons

CNS critical periods: implications for dystonia and other neurodevelopmental disorders

Forebrain knock-out of torsinA reduces striatal free-water and impairs whole-brain functional connectivity in a symptomatic mouse model of DYT1 dystonia

A cell autonomous torsinA requirement for cholinergic neuron survival and motor control

The Nuclear Envelope: An Intriguing Focal Point for Neurogenetic Disease

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