Search Results - "Cooper, J Mark"
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Ambroxol improves lysosomal biochemistry in glucocerebrosidase mutation-linked Parkinson disease cells
Published in Brain (London, England : 1878) (01-05-2014)“…Heterozygous GBA gene mutations are the most frequent Parkinson’s disease risk factor. Using Parkinson’s disease patient derived fibroblasts McNeill et al…”
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2
Systemic Exosomal Delivery of shRNA Minicircles Prevents Parkinsonian Pathology
Published in Molecular therapy (04-12-2019)“…The development of new therapies to slow down or halt the progression of Parkinson’s disease is a health care priority. A key pathological feature is the…”
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3
Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy
Published in Human molecular genetics (15-12-2010)“…Mitochondrial dysfunction and perturbed degradation of proteins have been implicated in Parkinson's disease (PD) pathogenesis. Mutations in the Parkin and…”
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4
Lysosomal dysfunction increases exosome-mediated alpha-synuclein release and transmission
Published in Neurobiology of disease (01-06-2011)“…Abstract Alpha-synuclein aggregation plays a central role in Parkinson's disease pathology. Direct transmission of alpha-synuclein from pathologically affected…”
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5
Glial activation precedes alpha-synuclein pathology in a mouse model of Parkinson’s disease
Published in Neuroscience research (01-09-2021)“…[Display omitted] •Microglial cell activation in SNpc precedes alpha-synuclein inclusion formation.•In striatum a significant astrogliosis was observed 90…”
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6
Glucocerebrosidase deficiency in substantia nigra of parkinson disease brains
Published in Annals of neurology (01-09-2012)“…Objective: Mutations in the glucocerebrosidase gene (GBA) represent a significant risk factor for developing Parkinson disease (PD). We investigated the…”
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7
Glucocerebrosidase inhibition causes mitochondrial dysfunction and free radical damage
Published in Neurochemistry international (01-01-2013)“…► Glucocerebrosidase gene mutations are a risk factor for Parkinson’s disease. ► Glucocerebrosidase inhibition causes mitochondrial dysfunction & oxidative…”
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8
G2019S leucine-rich repeat kinase 2 causes uncoupling protein-mediated mitochondrial depolarization
Published in Human molecular genetics (01-10-2012)“…The G2019S leucine rich repeat kinase 2 (LRRK2) mutation is the most common genetic cause of Parkinson's disease (PD), clinically and pathologically…”
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9
Silencing of PINK1 expression affects mitochondrial DNA and oxidative phosphorylation in dopaminergic cells
Published in PloS one (09-03-2009)“…Mitochondrial dysfunction has been implicated in the pathogenesis of Parkinson's disease (PD). Impairment of the mitochondrial electron transport chain (ETC)…”
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10
Intranasal Delivery of pGDNF DNA Nanoparticles Provides Neuroprotection in the Rat 6-Hydroxydopamine Model of Parkinson’s Disease
Published in Molecular neurobiology (01-01-2019)“…Glial cell line-derived neurotrophic factor (GDNF) gene therapy could offer a disease-modifying treatment for Parkinson’s disease (PD). Here, we report that…”
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11
Impaired Mitophagy and Protein Acetylation Levels in Fibroblasts from Parkinson’s Disease Patients
Published in Molecular neurobiology (01-04-2019)“…Parkinson’s disease (PD) is a chronic and progressive neurodegenerative disorder. While most PD cases are idiopathic, the known genetic causes of PD are useful…”
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12
Efficient non-viral ocular gene transfer with compacted DNA nanoparticles
Published in PloS one (20-12-2006)“…The eye is an excellent candidate for gene therapy as it is immune privileged and much of the disease-causing genetics are well understood. Towards this goal,…”
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13
Intranasal delivery of hGDNF plasmid DNA nanoparticles results in long-term and widespread transfection of perivascular cells in rat brain
Published in Nanomedicine (01-02-2019)“…The intranasal route of administration allows large therapeutics to circumvent the blood–brain barrier and be delivered directly to the CNS. Here we examined…”
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14
Comparative analysis of DNA nanoparticles and AAVs for ocular gene delivery
Published in PloS one (18-12-2012)“…Gene therapy is a critical tool for the treatment of monogenic retinal diseases. However, the limited vector capacity of the current benchmark delivery…”
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15
Cell Surface Nucleolin Serves as Receptor for DNA Nanoparticles Composed of Pegylated Polylysine and DNA
Published in Molecular therapy (01-02-2008)“…Compacted DNA nanoparticles deliver transgenes efficiently to the lung following intrapulmonary dosing. Here we show that nucleolin, a protein known to shuttle…”
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16
Systemic exosomal siRNA delivery reduced alpha-synuclein aggregates in brains of transgenic mice
Published in Movement disorders (01-10-2014)Get full text
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17
A partial structural and functional rescue of a retinitis pigmentosa model with compacted DNA nanoparticles
Published in PloS one (24-04-2009)“…Previously we have shown that compacted DNA nanoparticles can drive high levels of transgene expression after subretinal injection in the mouse eye. Here we…”
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18
Extensive Anti-CoA Immunostaining in Alzheimer's Disease and Covalent Modification of Tau by a Key Cellular Metabolite Coenzyme A
Published in Frontiers in cellular neuroscience (15-10-2021)“…Alzheimer's disease (AD) is a neurodegenerative disorder, accounting for at least two-thirds of dementia cases. A combination of genetic, epigenetic and…”
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Relationship between alpha synuclein phosphorylation, proteasomal inhibition and cell death: relevance to Parkinson’s disease pathogenesis
Published in Journal of neurochemistry (01-08-2009)“…Alpha synuclein can be phosphorylated at serine129 (P‐S129), and the presence of highly phosphorylated α‐synuclein in Lewy bodies suggests changes to its…”
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20
Enhancement of airway gene transfer by DNA nanoparticles using a pH-responsive block copolymer of polyethylene glycol and poly- l -lysine
Published in Biomaterials (01-03-2012)“…Abstract Highly compacted DNA nanoparticles, composed of single molecules of plasmid DNA compacted with block copolymers of polyethylene glycol and poly- l…”
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