Cellosaurus cell line PPMI.I.1008.1 (CVCL

Cellosaurus PPMI.I.1008.1 (CVCL_D5M5)

Cross-references
Cell line name	PPMI.I.1008.1
Synonyms	PPMI3411; PPMI_3411; CDIi016-A; FCDI_11295
Accession	CVCL_D5M5
Resource Identification Initiative	To cite this cell line use: PPMI.I.1008.1 (RRID:CVCL_D5M5)
Comments	Part of: Parkinson's Progression Markers Initiative (PPMI) cell line panel. Population: Caucasian, not Hispanic. Omics: Genome sequenced. Omics: Transcriptome analysis by RNAseq. Miscellaneous: PPMI study cohort HC, PPMI study subgroup healthy control. Caution: The PPMI3411 and PPMI_3411 identifiers correspond to an internal donor ID at PPMI. As multiple iPSC clones have been established from the cells of this donor, these identifiers should not be cited in a publication. Note that FujiFilm Cellular Dynamics, Inc (FCDI) and hPSCreg have assigned only a single identifier for all of the PBMC derived clones. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual	CVCL_D5M6 ! PPMI.I.1008.2 CVCL_D5M7 ! PPMI.I.1008.3 CVCL_D5M8 ! PPMI.I.1008.4
Sex of cell	Male
Age at sampling	46Y
Category	Induced pluripotent stem cell
Web pages	https://www.ppmi-info.org/access-data-specimens/download-data https://www.michaeljfox.org/sites/default/files/media/document/2018%20-%20PDTC%20-%20NKP%20Poster%20on%20iPSCs.pdf
Publications	PubMed=34434090; DOI=10.3389/fnmol.2021.734273; PMCID=PMC8381147 Nguyen D., Bharat V., Conradson D.M., Nandakishore P., Wang X.-N. Miro1 impairment in a Parkinson's at-risk cohort. Front. Mol. Neurosci. 14:734273.1-734273.8(2021) PubMed=35895835; DOI=10.1126/scitranslmed.abp8869; PMCID=PMC9809150 Langston R.G., Beilina A., Reed X., Kaganovich A., Singleton A.B., Blauwendraat C., Gibbs J.R., Cookson M.R. Association of a common genetic variant with Parkinson's disease is mediated by microglia. Sci. Transl. Med. 14:eabp8869.1-eabp8869.12(2022) PubMed=36950378; DOI=10.1016/j.xgen.2023.100261; PMCID=PMC10025424 Bressan E., Reed X., Bansal V., Hutchins E.D., Cobb M.M., Webb M.G., Alsop E., Grenn F.P., Illarionova A., Savytska N., Violich I., Broeer S., Fernandes N., Sivakumar R., Beilina A., Billingsley K.J., Berghausen J., Pantazis C.B., Pitz V., Patel D., Daida K., Meechoovet B., Reiman R., Courtright-Lim A., Logemann A., Antone J., Barch M., Kitchen R., Li Y., Dalgard C.L., Rizzu P., Hernandez D.G., Hjelm B.E., Nalls M.A., Gibbs J.R., Finkbeiner S., Cookson M.R., Van Keuren-Jensen K., Craig D.W., Singleton A.B., Heutink P., Blauwendraat C. American Genome Center The Foundational Data Initiative for Parkinson Disease: enabling efficient translation from genetic maps to mechanism. Cell Genom. 3:100261.1-100261.25(2023)
Cell line databases/resources	hPSCreg; CDIi016-A
Biological sample resources	BioSamples; SAMEA115473766
Encyclopedic resources	Wikidata; Q127383156
Entry history
Entry creation	02-May-2024
Last entry update	10-Sep-2024
Version number	2