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Cellosaurus PSMDFN387 (CVCL_YU44)

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Cell line name PSMDFN387
Accession CVCL_YU44
Resource Identification Initiative To cite this cell line use: PSMDFN387 (RRID:CVCL_YU44)
Comments Part of: Progeria Research Foundation cell lines.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 36Y5M
Category Finite cell line
STR profile Source(s): PubMed=27920058

Markers:
AmelogeninX
CSF1PO10,11
D2S133817,24
D3S135814,15
D5S81811,13
D7S8208,11
D8S117914
D13S31711,12
D16S53911,12
D18S5112,15
D19S43314
D21S1128,31.2
FGA21,23
TH016,9.3
TPOX11,12
vWA16,17

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Web pages Provider; PRF; -; https://www.progeriaresearch.org/available-cell-lines/
Publications

PubMed=27920058; DOI=10.1136/jmedgenet-2016-104295; PMCID=PMC5384422
Daniel Z. Bar, Martin F. Arlt, Joan F. Brazier, Wendy E. Norris, Susan E. Campbell, Peter S. Chines, Delphine Larrieu, Stephen Philip Jackson, Francis Sellers Collins, Thomas W. Glover, Leslie Beth Gordon;
A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome.
J. Med. Genet. 54:212-216(2017)

Cross-references
Encyclopedic resources Wikidata; Q98128681
Entry history
Entry creation12-Mar-2020
Last entry update10-Apr-2025
Version number6