2022
DOI: 10.1016/j.dib.2022.107958
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Transcriptome datasets of neural progenitors and neurons differentiated from induced pluripotent stem cells of healthy donors and Parkinson's disease patients with mutations in the PARK2 gene

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Cited by 7 publications
(10 citation statements)
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“…At the same time, samples of healthy donors and donors with PD behave similarly without clusters. All mature neurons from set51 [ 36 ] were located in the area of the neuronal progenitors, as well as some PD neurons from set32 [ 37 ]. Perhaps some differences in the expression profile can be explained by the fact that the meaning of the concept of “mature neurons” is somewhat different for different authors.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…At the same time, samples of healthy donors and donors with PD behave similarly without clusters. All mature neurons from set51 [ 36 ] were located in the area of the neuronal progenitors, as well as some PD neurons from set32 [ 37 ]. Perhaps some differences in the expression profile can be explained by the fact that the meaning of the concept of “mature neurons” is somewhat different for different authors.…”
Section: Resultsmentioning
confidence: 99%
“…According to the expression signature, mature neurons were produced by all protocols except set51 [ 36 ]. Set32 [ 37 ] also demonstrates maturity despite its location on the PCA. The DAn signature is not consistent among the datasets.…”
Section: Resultsmentioning
confidence: 99%
“…In an experiment, neural progenitors and terminally differentiated neurons were derived from iPSCs lines from three healthy donors and three PD patients. At the end, a comparative transcriptome analysis of all patients was conducted to demonstrate how PARK2 can contribute to the pathogenesis (29).…”
Section: Parkinson's Diseasementioning
confidence: 99%
“…Studying dysregulated genes in DA neurons is crucial for deepening our understanding of the molecular mechanisms underlying PD. Using powerful tools like high throughput RNA sequencing, attempts have been made to identify dysregulated genes in the disease state by comparing gene expression patterns in healthy versus PD-afflicted DA neurons [4][5][6][7][8][9][10] . Analyzing the postmortem brain tissue from PD patients provides a direct view of gene expression patterns in affected DA neurons [4][5][6] .…”
Section: Introductionmentioning
confidence: 99%
“…This approach offers a unique opportunity to study gene expression patterns in DA neurons specific to PD patients. CRISPR/Cas9 and other gene editing technologies have also enabled researchers to introduce or correct gene mutations associated with PD in cellular or animal models to investigate the direct impact of specific gene dysregulation on DA neuron function and survival 5 . Despite the differences in their genetic basis, some common pathways and mechanisms may contribute to the degeneration of DA neurons in both familial and sporadic PD.…”
Section: Introductionmentioning
confidence: 99%