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Cellosaurus HGMDFN090 (CVCL_1Y94)

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Cell line name HGMDFN090
Accession CVCL_1Y94
Resource Identification Initiative To cite this cell line use: HGMDFN090 (RRID:CVCL_1Y94)
Comments Part of: Progeria Research Foundation cell lines.
Miscellaneous: Cell line no longer available.
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)
Hierarchy Children:
CVCL_2A13 (HGMDFN090 iPS1B)CVCL_2A14 (HGMDFN090 iPS1C)CVCL_DP41 (HGMDFSV40T090)
Originate from same individual CVCL_YU37 ! HGMDFN717
CVCL_1Z29 ! HGMLBV010
Sex of cell Female
Age at sampling 37Y10M
Category Finite cell line
Publications

PubMed=16126733; DOI=10.1093/hmg/ddi326
Michael W. Glynn, Thomas W. Glover;
Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition.
Hum. Mol. Genet. 14:2959-2969(2005)

PubMed=19958786; DOI=10.1016/j.mad.2009.11.006; PMCID=PMC2837844
Gabriela Viteri, Youn Wook Chung, Earl Reece Stadtman;
Effect of progerin on the accumulation of oxidized proteins in fibroblasts from Hutchinson Gilford progeria patients.
Mech. Ageing Dev. 131:2-8(2010)

Cross-references
Encyclopedic resources Wikidata; Q54887288
Entry history
Entry creation22-Sep-2015
Last entry update29-Jun-2023
Version number8