| Cell line name |
79RD27 |
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| Accession |
CVCL_A0EU |
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| Resource Identification Initiative |
To cite this cell line use: 79RD27 (RRID:CVCL_A0EU) |
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| Comments |
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620. |
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| Disease |
Nijmegen breakage syndrome (NCIt: C4692)
Nijmegen breakage syndrome (ORDO: Orphanet_647) |
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| Species of origin |
Homo sapiens (Human)
(NCBI Taxonomy: 9606) |
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| Sex of cell |
Male |
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| Age at sampling |
Age unspecified |
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| Category |
Finite cell line |
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| Publications | PubMed=3248383; DOI=10.1159/000132673
Nicolaas G.J. Jaspers, Richard A. Gatti, Carla C. Baan, Peter C.M.L. Linssen, Dirk Bootsma;
Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients.
Cytogenet. Cell Genet. 49:259-263(1988) PubMed=3337113; PMCID=PMC1715319
Nicolaas G.J. Jaspers, Rob Desire F.M. Taalman, Carla C. Baan;
Patients with an inherited syndrome characterized by immunodeficiency, microcephaly, and chromosomal instability: genetic relationship to ataxia telangiectasia.
Am. J. Hum. Genet. 42:66-73(1988) DOI=10.1007/978-1-4757-5016-4_9
Nicolaas G.J. Jaspers, Len Roza, Wim Vermeulen, Andre P.M. Eker, Rob Desire F.M. Taalman, Jan Hendrik Jozef Hoeijmakers, Dirk Bootsma;
In vitro correction of cells from patients with mutagen hypersensitivity.
(In book chapter) DNA damage and repair; Castellani, Amleto (eds.); pp.73-82; Springer; Boston; USA (1989) |
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| Cross-references |
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| Encyclopedic resources |
Wikidata; Q108819759
|
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| Entry history |
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| Entry creation | 23-Sep-2021 |
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| Last entry update | 29-Jun-2023 |
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| Version number | 5 |
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