ID   HGMDFN090
AC   CVCL_1Y94
DR   Wikidata; Q54887288
RX   PubMed=16126733;
RX   PubMed=19958786;
CC   Part of: Progeria Research Foundation cell lines.
CC   Miscellaneous: Cell line no longer available.
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_YU37 ! HGMDFN717
OI   CVCL_1Z29 ! HGMLBV010
SX   Female
AG   37Y10M
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 29-06-23; Version: 8
//
RX   PubMed=16126733; DOI=10.1093/hmg/ddi326;
RA   Glynn M.W., Glover T.W.;
RT   "Incomplete processing of mutant lamin A in Hutchinson-Gilford
RT   progeria leads to nuclear abnormalities, which are reversed by
RT   farnesyltransferase inhibition.";
RL   Hum. Mol. Genet. 14:2959-2969(2005).
//
RX   PubMed=19958786; DOI=10.1016/j.mad.2009.11.006;
RA   Viteri G., Chung Y.W., Stadtman E.R.;
RT   "Effect of progerin on the accumulation of oxidized proteins in
RT   fibroblasts from Hutchinson Gilford progeria patients.";
RL   Mech. Ageing Dev. 131:2-8(2010).
//