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Status |
Public on Feb 09, 2016 |
Title |
SNP data from induced Pluripotent Stem cells from Parkinson's Disease patients harbouring G2019S mutations in the LRRK2 gene |
Organism |
Homo sapiens |
Experiment type |
SNP genotyping by SNP array
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Summary |
We have generated human induced Pluripotent Stem cells (hiPSc) using Retroviral virus-mediated delivery of reprogramming factors. hiPSc lines have been screened using SNP array to assess chromosomal stability (alongside the fibroblast lines from which they derived), and validation of the pluripotency of the hiPSc lines is provided by Pluritest assessment of transcriptome datasets, prior to differentiation and downstream assays. Gene expression profiling in patient-derived dopamine neurons identifies candidate therapeutic molecules in Parkinson’s disease.
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Overall design |
human iPSc lines were derived from human dermal fibroblasts from 3 PD LRRK2 G2019S patients and 3 control donors. SNP and gene expression datasets were generated from patient and control lines. Note that iPS OX1-19 and iPS-NHDF-1, also used in the current study, have been published previously so datasets are not given here [GSE45472 PMID:23951090 ; GSE43904 PMID:24586273]
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Contributor(s) |
Sandor C, Robertson P, Lang C, Heger A, Booth H, Vowles J, Witty L, Bowden R, Hu M, Cowley SA, Wade-Martins R, Webber C |
Citation(s) |
28096185 |
Submission date |
Feb 08, 2016 |
Last update date |
Dec 18, 2017 |
Contact name |
Sally A Cowley |
E-mail(s) |
sally.cowley@path.ox.ac.uk
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Phone |
+44 (0) 1865 275600
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Organization name |
University of Oxford
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Department |
Sir William Dunn School of Pathology
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Lab |
James Martin Stem Cell Facility
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Street address |
South Parks Road
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City |
Oxford |
ZIP/Postal code |
OX1 3RE |
Country |
United Kingdom |
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Platforms (1) |
GPL13829 |
Illumina HumanCytoSNP-12 v2.1 BeadChip |
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Samples (8)
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This SubSeries is part of SuperSeries: |
GSE77664 |
Gene expression and SNP genotype data from induced Pluripotent Stem cells from Parkinson's Disease patients harbouring G2019S mutations in the LRRK2 gene |
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Relations |
BioProject |
PRJNA311169 |