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Shaping the Nrf2-ARE-related pathways in Alzheimer's and Parkinson's diseases

Ageing research reviews, 2019-09, Vol.54, p.100942-100942, Article 100942

2019

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Dysfunctional synapse in Alzheimer's disease – A focus on NMDA receptors

Neuropharmacology, 2014-01, Vol.76, p.16-26

2014

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Mitochondrial Dysfunction in Huntington’s Disease

Polyglutamine Disorders, 2018, Vol.1049, p.59-83

2018

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Insulin and IGF-1 improve mitochondrial function in a PI-3K/Akt-dependent manner and reduce mitochondrial generation of reactive oxygen species in Huntington’s disease knock-in striatal cells

Free radical biology & medicine, 2014-09, Vol.74, p.129-144

2014

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Comparative Mitochondrial-Based Protective Effects of Resveratrol and Nicotinamide in Huntington’s Disease Models

Molecular neurobiology, 2017-09, Vol.54 (7), p.5385-5399

2017

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c-Src regulates Nrf2 activity through PKCδ after oxidant stimulus

Biochimica et biophysica acta. Molecular cell research, 2019-04, Vol.1866 (4), p.686-698

2019

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The NAD+-dependent deacetylase SIRT2 attenuates oxidative stress and mitochondrial dysfunction and improves insulin sensitivity in hepatocytes

Human molecular genetics, 2017-11, Vol.26 (21), p.4105-4117

2017

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Mitochondrial Ca2+ handling in Huntington's and Alzheimer's diseases – Role of ER-mitochondria crosstalk

Biochemical and biophysical research communications, 2017-02, Vol.483 (4), p.1069-1077

2017

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Alpha-synuclein-induced oxidative stress correlates with altered superoxide dismutase and glutathione synthesis in human neuroblastoma SH-SY5Y cells

Archives of toxicology, 2017-03, Vol.91 (3), p.1245-1259

2017

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Linking alpha-synuclein phosphorylation to reactive oxygen species formation and mitochondrial dysfunction in SH-SY5Y cells

Molecular and cellular neuroscience, 2014-09, Vol.62, p.51-59

2014

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Microbial BMAA elicits mitochondrial dysfunction, innate immunity activation, and Alzheimer’s disease features in cortical neurons

Journal of neuroinflammation, 2020-11, Vol.17 (1), p.1-18, Article 332

2020

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The Sigma-1 Receptor Mediates Pridopidine Rescue of Mitochondrial Function in Huntington Disease Models

Neurotherapeutics, 2021-04, Vol.18 (2), p.1017-1038

2021

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Mechanistic perspectives on differential mitochondrial-based neuroprotective effects of several carnitine forms in Alzheimer’s disease in vitro model

Archives of toxicology, 2021-08, Vol.95 (8), p.2769-2784

2021

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Revisiting Mitochondrial Function and Metabolism in Pluripotent Stem Cells: Where Do We Stand in Neurological Diseases?

Molecular neurobiology, 2017-04, Vol.54 (3), p.1858-1873

2017

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Aβ and NMDAR activation cause mitochondrial dysfunction involving ER calcium release

Neurobiology of aging, 2015-02, Vol.36 (2), p.680-692

2015

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Histone Deacetylase Inhibitors Protect Against Pyruvate Dehydrogenase Dysfunction in Huntington's Disease

The Journal of neuroscience, 2017-03, Vol.37 (10), p.2776-2794

2017

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Impaired transcription in Alzheimer's disease: key role in mitochondrial dysfunction and oxidative stress

Journal of Alzheimer's disease, 2013-01, Vol.34 (1), p.115-131

2013

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IGF-1 Intranasal Administration Rescues Huntington's Disease Phenotypes in YAC128 Mice

Molecular neurobiology, 2014-06, Vol.49 (3), p.1126-1142

2014

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Mitochondrial dysfunction and reactive oxygen species in excitotoxicity and apoptosis: Implications for the pathogenesis of neurodegenerative diseases

Neurochemical research, 2003-10, Vol.28 (10), p.1563-1574

2003

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Glutathione redox cycle dysregulation in Huntington’s disease knock-in striatal cells

Free radical biology & medicine, 2012-11, Vol.53 (10), p.1857-1867

2012

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Assessing Mitochondrial Function in In Vitro and Ex Vivo Models of Huntington's Disease

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.415

2018

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Activation of IGF-1 and Insulin Signaling Pathways Ameliorate Mitochondrial Function and Energy Metabolism in Huntington’s Disease Human Lymphoblasts

Molecular neurobiology, 2015-02, Vol.51 (1), p.331-348

2015

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Mitochondrial and redox modifications in early stages of Huntington's disease

Redox biology, 2022-10, Vol.56, p.102424-102424, Article 102424

2022

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Valosin-containing protein (VCP/p97) is an activator of wild-type ataxin-3

PloS one, 2012-09, Vol.7 (9), p.e43563

2012

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Shaping the Nrf2-ARE-related pathways in Alzheimer's and Parkinson's diseases

Dysfunctional synapse in Alzheimer's disease – A focus on NMDA receptors

Mitochondrial Dysfunction in Huntington’s Disease

Insulin and IGF-1 improve mitochondrial function in a PI-3K/Akt-dependent manner and reduce mitochondrial generation of reactive oxygen species in Huntington’s disease knock-in striatal cells

Comparative Mitochondrial-Based Protective Effects of Resveratrol and Nicotinamide in Huntington’s Disease Models

c-Src regulates Nrf2 activity through PKCδ after oxidant stimulus

The NAD+-dependent deacetylase SIRT2 attenuates oxidative stress and mitochondrial dysfunction and improves insulin sensitivity in hepatocytes

Mitochondrial Ca2+ handling in Huntington's and Alzheimer's diseases – Role of ER-mitochondria crosstalk

Alpha-synuclein-induced oxidative stress correlates with altered superoxide dismutase and glutathione synthesis in human neuroblastoma SH-SY5Y cells

Linking alpha-synuclein phosphorylation to reactive oxygen species formation and mitochondrial dysfunction in SH-SY5Y cells

Microbial BMAA elicits mitochondrial dysfunction, innate immunity activation, and Alzheimer’s disease features in cortical neurons

The Sigma-1 Receptor Mediates Pridopidine Rescue of Mitochondrial Function in Huntington Disease Models

Mechanistic perspectives on differential mitochondrial-based neuroprotective effects of several carnitine forms in Alzheimer’s disease in vitro model

Revisiting Mitochondrial Function and Metabolism in Pluripotent Stem Cells: Where Do We Stand in Neurological Diseases?

Aβ and NMDAR activation cause mitochondrial dysfunction involving ER calcium release

Histone Deacetylase Inhibitors Protect Against Pyruvate Dehydrogenase Dysfunction in Huntington's Disease

Impaired transcription in Alzheimer's disease: key role in mitochondrial dysfunction and oxidative stress

IGF-1 Intranasal Administration Rescues Huntington's Disease Phenotypes in YAC128 Mice

Mitochondrial dysfunction and reactive oxygen species in excitotoxicity and apoptosis: Implications for the pathogenesis of neurodegenerative diseases

Glutathione redox cycle dysregulation in Huntington’s disease knock-in striatal cells

Assessing Mitochondrial Function in In Vitro and Ex Vivo Models of Huntington's Disease

Activation of IGF-1 and Insulin Signaling Pathways Ameliorate Mitochondrial Function and Energy Metabolism in Huntington’s Disease Human Lymphoblasts

Mitochondrial and redox modifications in early stages of Huntington's disease

Neuronal cell-based high-throughput screen for enhancers of mitochondrial function reveals luteolin as a modulator of mitochondria-endoplasmic reticulum coupling

Valosin-containing protein (VCP/p97) is an activator of wild-type ataxin-3

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