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Cellosaurus ND50050 (CVCL_RY35)

[Text version]
Cell line name ND50050
Accession CVCL_RY35
Resource Identification Initiative To cite this cell line use: ND50050 (RRID:CVCL_RY35)
Comments Population: Caucasian; Greek.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 11138; SNCA; Simple; p.Ala53Thr (c.157G>A); ClinVar=VCV000014007; Zygosity=Heterozygous (from parent cell line).
Disease Parkinson disease 1, autosomal dominant (NCIt: C198602)
Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_RY33 (ND40996)
Children:
CVCL_RY36 (ND50085)CVCL_RY37 (ND50086)
Sex of cell Female
Age at sampling 51Y
Category Induced pluripotent stem cell
Publications

PubMed=34831478; DOI=10.3390/cells10113256
Vogiatzis S., Celestino M., Trevisan M., Magro G., Del Vecchio C., Erdengiz D., Palu G., Parolin C., Maguire-Zeiss K., Calistri A.
Lentiviral vectors expressing chimeric NEDD4 ubiquitin ligases: an innovative approach for interfering with alpha-synuclein accumulation.
Cells 10:3256.1-3256.21(2021)

Cross-references
Cell line collections (Providers) NHCDR; ND50050
Encyclopedic resources Wikidata; Q54930272
Entry history
Entry creation14-May-2018
Last entry update05-Oct-2023
Version number10