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Inhibition of HDAC6 activity protects dopaminergic neurons from alpha-synuclein toxicity

Scientific reports, 2020-04, Vol.10 (1), p.6064, Article 6064

2020

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In vivo imaging of brain glutamate defects in a knock-in mouse model of Huntington's disease

NeuroImage (Orlando, Fla.), 2016-10, Vol.139, p.53-64

2016

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Mutant huntingtin alters Tau phosphorylation and subcellular distribution

Human molecular genetics, 2015-01, Vol.24 (1), p.76-85

2015

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The striatal kinase DCLK3 produces neuroprotection against mutant huntingtin

Brain (London, England : 1878), 2018-05, Vol.141 (5), p.1434-1454

2018

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Loss of the thyroid hormone-binding protein Crym renders striatal neurons more vulnerable to mutant huntingtin in Huntington's disease

Human molecular genetics, 2015-03, Vol.24 (6), p.1563-1573

2015

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CLN7/MFSD8 may be an important factor for SARS-CoV-2 cell entry

iScience, 2022-10, Vol.25 (10), p.105082-105082, Article 105082

2022

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Neuroinflammation in Gaucher disease, neuronal ceroid lipofuscinosis, and commonalities with Parkinson’s disease

Brain research, 2022-04, Vol.1780, p.147798-147798, Article 147798

2022

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Rescue of α-synuclein aggregation in Parkinson’s patient neurons by synergistic enhancement of ER proteostasis and protein trafficking

Neuron (Cambridge, Mass.), 2022-02, Vol.110 (3), p.436-451.e11

2022

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Contribution of Neuroepigenetics to Huntington's Disease

Frontiers in human neuroscience, 2017-01, Vol.11, p.17-17

2017

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Possible involvement of self-defense mechanisms in the preferential vulnerability of the striatum in Huntington's disease

Frontiers in cellular neuroscience, 2014-09, Vol.8, p.295-295

2014

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Contribution of Neuroepigenetics to Huntington’s Disease

Frontiers in human neuroscience, 2017-01, Vol.11

2017

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Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder

Human molecular genetics, 2012-09, Vol.21 (18), p.4030-4037

2012

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Identification of a conserved gene signature associated with an exacerbated inflammatory environment in the hippocampus of aging rats

Hippocampus, 2017-04, Vol.27 (4), p.435-449

2017

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High throughput screening for inhibitors of REST in neural derivatives of human embryonic stem cells reveals a chemical compound that promotes expression of neuronal genes

Stem cells (Dayton, Ohio), 2013-09, Vol.31 (9), p.1816-1828

2013

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The striatal long noncoding RNA Abhd11os is neuroprotective against an N-terminal fragment of mutant huntingtin in vivo

Neurobiology of aging, 2015-03, Vol.36 (3), p.1601.e7-1601.e16

2015

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Biological features of herpes simplex virus type 1 latency in mice according to experimental conditions and type of neurones

Investigative ophthalmology & visual science, 2014-12, Vol.55 (12), p.7761-7774

2014

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B40 In vivo imaging of brain glutamate defects in a knock-in mouse model of huntington’s disease

Journal of neurology, neurosurgery and psychiatry, 2016-09, Vol.87 (Suppl 1), p.A23-A23

2016

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The striatal long noncoding RNA Abhd11os is neuroprotective against an N-terminal fragment of mutant huntingtin in vivo

Neurobiology of aging, 2015-03, Vol.36 (3), p.1601.e7-1601.e16

2015

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Inhibition of HDAC6 activity protects dopaminergic neurons from alpha-synuclein toxicity

The mechanism of sirtuin 2-mediated exacerbation of alpha-synuclein toxicity in models of Parkinson disease

In vivo imaging of brain glutamate defects in a knock-in mouse model of Huntington's disease

Mutant huntingtin alters Tau phosphorylation and subcellular distribution

The striatal kinase DCLK3 produces neuroprotection against mutant huntingtin

Loss of the thyroid hormone-binding protein Crym renders striatal neurons more vulnerable to mutant huntingtin in Huntington's disease

CLN7/MFSD8 may be an important factor for SARS-CoV-2 cell entry

Correction: The mechanism of sirtuin 2-mediated exacerbation of alpha-synuclein toxicity in models of Parkinson disease

Neuroinflammation in Gaucher disease, neuronal ceroid lipofuscinosis, and commonalities with Parkinson’s disease

Rescue of α-synuclein aggregation in Parkinson’s patient neurons by synergistic enhancement of ER proteostasis and protein trafficking

Contribution of Neuroepigenetics to Huntington's Disease

Possible involvement of self-defense mechanisms in the preferential vulnerability of the striatum in Huntington's disease

Contribution of Neuroepigenetics to Huntington’s Disease

Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder

Identification of a conserved gene signature associated with an exacerbated inflammatory environment in the hippocampus of aging rats

High throughput screening for inhibitors of REST in neural derivatives of human embryonic stem cells reveals a chemical compound that promotes expression of neuronal genes

The striatal long noncoding RNA Abhd11os is neuroprotective against an N-terminal fragment of mutant huntingtin in vivo

Biological features of herpes simplex virus type 1 latency in mice according to experimental conditions and type of neurones

B40 In vivo imaging of brain glutamate defects in a knock-in mouse model of huntington’s disease

The striatal long noncoding RNA Abhd11os is neuroprotective against an N-terminal fragment of mutant huntingtin in vivo

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