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Cellosaurus ND34391 (CVCL_F202)

[Text version]
Cell line name ND34391
Synonyms ND34391*E; ND34391*H
Accession CVCL_F202
Resource Identification Initiative To cite this cell line use: ND34391 (RRID:CVCL_F202)
Comments Population: Caucasian.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Gene amplification; HGNC; 11138; SNCA; Triplication; Zygosity=Heterozygous (NHCDR=ND34391).
Disease Parkinson disease 4, autosomal dominant (NCIt: C198604)
Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_F204 (ND27760)
Sex of cell Female
Age at sampling 55Y
Category Induced pluripotent stem cell
Publications

PubMed=26651604; DOI=10.1016/j.stemcr.2015.11.004
Schwab A.J., Ebert A.D.
Neurite aggregation and calcium dysfunction in iPSC-derived sensory neurons with Parkinson's disease-related LRRK2 G2019S mutation.
Stem Cell Reports 5:1039-1052(2015)

PubMed=27264186; DOI=10.1016/j.celrep.2016.05.022
Lin L., Goke J., Cukuroglu E., Dranias M.R., VanDongen A.M.J., Stanton L.W.
Molecular features underlying neurodegeneration identified through in vitro modeling of genetically diverse Parkinson's disease patients.
Cell Rep. 15:2411-2426(2016)

Cross-references
Cell line collections (Providers) Coriell; ND34391 - Discontinued
NHCDR; ND34391
Cell line databases/resources SKIP; SKIP001366
SKIP; SKIP004681
Encyclopedic resources Wikidata; Q54929775
Entry history
Entry creation22-Oct-2012
Last entry update30-Jan-2024
Version number21