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Cellosaurus CS267BE (CVCL_EG47)

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Cell line name CS267BE
Synonyms Cockayne Syndrome 267 BEthesda; GM11551
Accession CVCL_EG47
Resource Identification Initiative To cite this cell line use: CS267BE (RRID:CVCL_EG47)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Cockayne syndrome type B (NCIt: C135726)
Cockayne syndrome (ORDO: Orphanet_191)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_EG46 ! CS267BE LCL
Sex of cell Female
Age at sampling 16Y
Category Finite cell line
Publications

PubMed=12060391; DOI=10.1046/j.1523-1747.2002.01782.x
Steffen Emmert, Hanoch Slor, David B. Busch, Sima Batko, Roberta B. Albert, Donna M. Coleman, Sikandar G. Khan, Bassam Abu-Libdeh, John Joseph DiGiovanna, Bari Bickel Cunningham, Myung-Moo Lee ...Show all 19 authors... , Jill S. Crollick, Hiroki Inui, Takahiro Ueda, Mohammad Hedayati, Lawrence Grossman, Tala Shahlavi, James Edward Cleaver, Kenneth H. Kraemer; Show fewer authors
Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients.
J. Invest. Dermatol. 118:972-982(2002)

Cross-references
Cell line collections (Providers) Coriell; GM11551
Cell line databases/resources CLO; CLO_0021057
Encyclopedic resources Wikidata; Q54845152
Entry history
Entry creation13-Jul-2016
Last entry update29-Jun-2023
Version number8