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Pituitary Adenylate Cyclase-Activating Polypeptide (PACAP) Enhances Hippocampal Synaptic Plasticity and Improves Memory Performance in Huntington’s Disease

Molecular neurobiology, 2018-11, Vol.55 (11), p.8263-8277

2018

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The expanding clinical profile of anti-AMPA receptor encephalitis

Neurology, 2010-03, Vol.74 (10), p.857-859

2010

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Deficits in coordinated neuronal activity and network topology are striatal hallmarks in Huntington's disease

BMC biology, 2020-05, Vol.18 (1), p.58-58, Article 58

2020

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Imbalance of p75NTR/TrkB protein expression in Huntington’s disease: implication for neuroprotective therapies

Cell death & disease, 2013-04, Vol.4 (4), p.e595-e595

2013

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Long-term memory deficits in Huntington's disease are associated with reduced CBP histone acetylase activity

Human molecular genetics, 2012-03, Vol.21 (6), p.1203-1216

2012

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Imbalance of p75(NTR)/TrkB protein expression in Huntington's disease: implication for neuroprotective therapies

Cell death & disease, 2013-04, Vol.4, p.e595

2013

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BDNF regulation under GFAP promoter provides engineered astrocytes as a new approach for long-term protection in Huntington's disease

Gene therapy, 2010-10, Vol.17 (10), p.1294-1308

2010

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Brain-derived neurotrophic factor modulates the severity of cognitive alterations induced by mutant huntingtin: Involvement of phospholipaseCγ activity and glutamate receptor expression

Neuroscience, 2009-02, Vol.158 (4), p.1234-1250

2009

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Neuroprotection by GDNF-secreting stem cells in a Huntington's disease model: optical neuroimage tracking of brain-grafted cells

Gene therapy, 2007-01, Vol.14 (2), p.118-128

2007

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Parkin loss of function contributes to RTP801 elevation and neurodegeneration in Parkinson’s disease

Cell death & disease, 2014-08, Vol.5 (8), p.e1364-e1364

2014

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B10 Nuclear Lamina Is Differentially Altered In Huntington’s Disease Brain Regions

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (Suppl 1), p.A12-A12

2014

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PH domain leucine-rich repeat protein phosphatase 1 contributes to maintain the activation of the PI3K Akt pro-survival pathway in Huntington's disease striatum

Cell death and differentiation, 2010-02, Vol.17 (2), p.324-335

2010

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Brain‐Derived Neurotrophic Factor, Neurotrophin‐3, and Neurotrophin‐4/5 Prevent the Death of Striatal Projection Neurons in a Rodent Model of Huntington's Disease

Journal of neurochemistry, 2000-11, Vol.75 (5), p.2190-2199

2000

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Long-Term Expression of Erythropoietin from Myoblasts Immobilized in Biocompatible and Neovascularized Microcapsules

Molecular therapy, 2005-08, Vol.12 (2), p.283-289

2005

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Effect of glatiramer acetate (Copaxone ®) on the immunophenotypic and cytokine profile and BDNF production in multiple sclerosis: A longitudinal study

Neuroscience letters, 2006-10, Vol.406 (3), p.270-275

2006

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B22 Normalisation Of Aberrant P75NTR Levels Prevents Hippocampal Synaptic And Cognitive Deficits And Ameliorates Cortico-striatal Dysfunction In Huntington Disease

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (Suppl 1), p.A16-A17

2014

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The dopaminergic stabilizer, (−)-OSU6162, rescues striatal neurons with normal and expanded polyglutamine chains in huntingtin protein from exposure to free radicals and mitochondrial toxins

Brain research, 2012-06, Vol.1459, p.100-112

2012

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Neuroprotection by neurotrophins and GDNF family members in the excitotoxic model of Huntington’s disease

Brain research bulletin, 2002-04, Vol.57 (6), p.817-822

2002

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Les conflits d’archives: France, Espagne, Méditerranée

2022

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Cellular and molecular mechanisms involved in the selective vulnerability of striatal projection neurons in Huntington's disease

Histology and histopathology, 2006-11, Vol.21 (11), p.1217

2006

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Association between BDNF Val66Met polymorphism and age at onset in Huntington disease

Neurology, 2005-09, Vol.65 (6), p.964-965

2005

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Analysis of antibodies to neuronal surface antigens in adult opsoclonus–myoclonus

Journal of neuroimmunology, 2008-05, Vol.196 (1), p.188-191

2008

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Cyclin-Dependent Kinase 5 Dysfunction Contributes to Depressive-like Behaviors in Huntington’s Disease by Altering the DARPP-32 Phosphorylation Status in the Nucleus Accumbens

Biological psychiatry (1969), 2019-08, Vol.86 (3), p.196-207

2019

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Porous anodic oxides on titanium and on a Ti–W alloy

Corrosion science, 2008-02, Vol.50 (2), p.548-553

2008

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Bone morphogenetic protein-6 is a neurotrophic factor for calbindin-positive striatal neurons

Journal of neuroscience research, 2002-12, Vol.70 (5), p.638-644

2002

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Pituitary Adenylate Cyclase-Activating Polypeptide (PACAP) Enhances Hippocampal Synaptic Plasticity and Improves Memory Performance in Huntington’s Disease

The expanding clinical profile of anti-AMPA receptor encephalitis

Deficits in coordinated neuronal activity and network topology are striatal hallmarks in Huntington's disease

Imbalance of p75NTR/TrkB protein expression in Huntington’s disease: implication for neuroprotective therapies

Long-term memory deficits in Huntington's disease are associated with reduced CBP histone acetylase activity

Imbalance of p75(NTR)/TrkB protein expression in Huntington's disease: implication for neuroprotective therapies

BDNF regulation under GFAP promoter provides engineered astrocytes as a new approach for long-term protection in Huntington's disease

Brain-derived neurotrophic factor modulates the severity of cognitive alterations induced by mutant huntingtin: Involvement of phospholipaseCγ activity and glutamate receptor expression

Neuroprotection by GDNF-secreting stem cells in a Huntington's disease model: optical neuroimage tracking of brain-grafted cells

Parkin loss of function contributes to RTP801 elevation and neurodegeneration in Parkinson’s disease

B10 Nuclear Lamina Is Differentially Altered In Huntington’s Disease Brain Regions

PH domain leucine-rich repeat protein phosphatase 1 contributes to maintain the activation of the PI3K Akt pro-survival pathway in Huntington's disease striatum

Brain‐Derived Neurotrophic Factor, Neurotrophin‐3, and Neurotrophin‐4/5 Prevent the Death of Striatal Projection Neurons in a Rodent Model of Huntington's Disease

Long-Term Expression of Erythropoietin from Myoblasts Immobilized in Biocompatible and Neovascularized Microcapsules

Effect of glatiramer acetate (Copaxone ®) on the immunophenotypic and cytokine profile and BDNF production in multiple sclerosis: A longitudinal study

B22 Normalisation Of Aberrant P75NTR Levels Prevents Hippocampal Synaptic And Cognitive Deficits And Ameliorates Cortico-striatal Dysfunction In Huntington Disease

The dopaminergic stabilizer, (−)-OSU6162, rescues striatal neurons with normal and expanded polyglutamine chains in huntingtin protein from exposure to free radicals and mitochondrial toxins

Neuroprotection by neurotrophins and GDNF family members in the excitotoxic model of Huntington’s disease

Les conflits d’archives: France, Espagne, Méditerranée

Cellular and molecular mechanisms involved in the selective vulnerability of striatal projection neurons in Huntington's disease

Association between BDNF Val66Met polymorphism and age at onset in Huntington disease

Analysis of antibodies to neuronal surface antigens in adult opsoclonus–myoclonus

Cyclin-Dependent Kinase 5 Dysfunction Contributes to Depressive-like Behaviors in Huntington’s Disease by Altering the DARPP-32 Phosphorylation Status in the Nucleus Accumbens

Porous anodic oxides on titanium and on a Ti–W alloy

Bone morphogenetic protein-6 is a neurotrophic factor for calbindin-positive striatal neurons

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