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Cellosaurus HVRDi016-A (CVCL_WS09)

[Text version]
Cell line name HVRDi016-A
Synonyms PNN 1-38 (SMA); PNN1-38
Accession CVCL_WS09
Resource Identification Initiative To cite this cell line use: HVRDi016-A (RRID:CVCL_WS09)
Comments From: Harvard University; Boston; USA.
Disease Werdnig-Hoffmann disease (NCIt: C98670)
Proximal spinal muscular atrophy type 1 (ORDO: Orphanet_83330)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 1Y6M
Category Induced pluripotent stem cell
Publications

PubMed=28178525; DOI=10.1016/j.celrep.2017.01.035
Rodriguez-Muela N., Litterman N.K., Norabuena E.M., Mull J.L., Galazo M.J., Sun C.-C., Ng S.-Y., Makhortova N.R., White A., Lynes M.M., Chung W.K., Davidow L.S., Macklis J.D., Rubin L.L.
Single-cell analysis of SMN reveals its broader role in neuromuscular disease.
Cell Rep. 18:1484-1498(2017)

Cross-references
Cell line databases/resources hPSCreg; HVRDi016-A
Biological sample resources BioSamples; SAMEA12598003
Encyclopedic resources Wikidata; Q94310009
Entry history
Entry creation05-Jul-2019
Last entry update21-Mar-2023
Version number5