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UnknownPost-mortem ventricular cerebrospinal fluid cell-free-mtDNA in neurodegenerative disease.
Not available
S-EPMC7499424 | biostudies-literature
UnknownThe Role of Nerve Growth Factor in Maintaining Proliferative Capacity, Colony-Forming Efficiency, and the Limbal Stem Cell Phenotype.
Not available
S-EPMC6334532 | biostudies-literature
UnknownReduced mitochondrial DNA copy number is a biomarker of Parkinson's disease.
Not available
S-EPMC4759605 | biostudies-literature
UnknownSomatic mtDNA variation is an important component of Parkinson's disease.
Not available
S-EPMC4759607 | biostudies-literature
UnknownGlucocerebrosidase mutations alter the endoplasmic reticulum and lysosomes in Lewy body disease.
Not available
S-EPMC3494984 | biostudies-literature
UnknownReduced cerebrospinal fluid mitochondrial DNA is a biomarker for early-stage Parkinson's disease.
Not available
S-EPMC6551217 | biostudies-literature
ProteomicsAltered ceramide metabolism is a feature in the extracellular vesicle mediated spread of alpha-synuclein in sporadic and GBA-linked Lewy body disease
Mutations in glucocerebrosidase (GBA) are the most prevalent genetic risk factor for Lewy body disorders (LBD) – collectively Parkinson’s disease, Parkinson’s disease dementia and dementia with Lewy bodies. Despite this genetic association, it remains unclear how GBA mutation contributes to the susc...
ORGANISM(S): Homo sapiens (Human) 
2021-11-02 | PXD026980 | Pride
Exosomes Alpha-synuclein Ceramide Inflammation Lewy body disease Extracellular vesicles Glucocerebrosidase 
UnknownDementia with Lewy bodies: an update and outlook.
Not available
S-EPMC6341685 | biostudies-literature
TranscriptomicsPRPF8 CLIP seq for iPSC, kidney organoid, retinal organoid, and retinal epithelium derived from c.6926A>C RPE with Retinitis Pigmentosa patients and CRISPR/Cas9 corrected
Retinitis Pigmentosa is a group of inherited eye disorders characterized by progressive degeneration of photoreceptor cells in the retina, leading to vision loss and eventual blindness. One of the known genetic mutations associated with RP is the c.6926A>C mutation in the RPE (retinal pigment epithe...
ORGANISM(S): Homo sapiens 
2024-03-13 | E-MTAB-13171 | biostudies-arrayexpress
UnknownComplement modulation reverses pathology in Y402H-retinal pigment epithelium cell model of age-related macular degeneration by restoring lysosomal function.
Not available
S-EPMC7695639 | biostudies-literature
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