ID GM00969 AC CVCL_7311 SY GM0969; GM-969; GM 969; GM00969A; GM 969A; GM0969B; GM00969C; GM00969F; C4 DR CLO; CLO_0029504 DR Coriell; GM00969 DR GEO; GSM1316971 DR GEO; GSM1317008 DR GEO; GSM3124626 DR Wikidata; Q54836570 RX CelloPub=CLPUB00387; RX CelloPub=CLPUB00447; RX CelloPub=CLPUB00600; RX CelloPub=CLPUB00720; RX DOI=10.5962/bhl.title.4090; RX PubMed=2837086; RX PubMed=3745952; RX PubMed=6458814; RX PubMed=6726265; RX PubMed=7380831; RX PubMed=12665480; RX PubMed=17668376; RX PubMed=19896956; RX PubMed=26831110; RX PubMed=30567591; CC Population: Caucasian. CC Omics: Transcriptomics; Microarray. CC Omics: Transcriptomics; miRNA profiling; Microarray. CC Omics: Transcriptomics; RNAseq. CC Derived from site: In situ; Skin; UBERON=UBERON_0002097. CC Cell type: Fibroblast of skin; CL=CL_0002620. OX NCBI_TaxID=9606; ! Homo sapiens (Human) SX Female AG 2Y CA Finite cell line DT Created: 04-04-12; Last updated: 10-04-25; Version: 24 CH CVCL_C9IZ ! CBRCULi011-A CH CVCL_DR05 ! CHOPWT1.1 CH CVCL_DR06 ! CHOPWT1.2 CH CVCL_DR07 ! CHOPWT1.3 // RX PubMed=7380831; DOI=10.1016/S0021-9258(19)70683-8; RA Daddona, Peter E. RA Frohman, Michael A. RA Kelley, William Nimmons RT "Human adenosine deaminase and its binding protein in normal and RT adenosine deaminase-deficient fibroblast cell strains."; RL J. Biol. Chem. 255:5681-5687(1980). // RX PubMed=6458814; DOI=10.1073/pnas.78.10.6451; PMCID=PMC349057; RA Scudiero, Dominic A. RA Meyer, Sharon A. RA Clatterbuck, Brian E. RA Tarone, Robert E. RA Robbins, Jay H. RT "Hypersensitivity to N-methyl-N'-nitro-N-nitrosoguanidine in RT fibroblasts from patients with Huntington disease, familial RT dysautonomia, and other primary neuronal degenerations."; RL Proc. Natl. Acad. Sci. U.S.A. 78:6451-6455(1981). // RX PubMed=30567591; DOI=10.1186/s13059-018-1599-6; PMCID=PMC6300908; RA Fleischer, Jason G. RA Schulte, Roberta RA Tsai, Hsiao H. RA Tyagi, Swati RA Ibarra, Arkaitz RA Shokhirev, Maxim N. RA Huang, Ling RA Hetzer, Martin W. RA Navlakha, Saket RT "Predicting age from the transcriptome of human dermal fibroblasts."; RL Genome Biol. 19:221.1-221.8(2018). // RX DOI=10.5962/bhl.title.4090; RA Coriell, Lewis Lemon RA Greene, Arthur E. RT "The human genetic mutant cell repository: list of genetic variants, RT chromosomal aberrations and normal cell cultures submitted to the RT repository. 4th edition. October 1977."; RL (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977). // RX PubMed=12665480; DOI=10.1096/fj.02-0851com; RA Tuo, Jing-Sheng RA Jaruga, Pawel RA Rodriguez, Henry RA Bohr, Vilhelm A. RA Dizdaroglu, Miral RT "Primary fibroblasts of Cockayne syndrome patients are defective in RT cellular repair of 8-hydroxyguanine and 8-hydroxyadenine resulting RT from oxidative stress."; RL FASEB J. 17:668-674(2003). // RX CelloPub=CLPUB00600; RA Coriell, Lewis Lemon RA Greene, Arthur E. RA Mulivor, Richard A. RT "The human genetic mutant cell repository: list of genetic variants, RT chromosomal aberrations and normal cell cultures submitted to the RT repository. 6th edition. October 1979."; RL (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-168; National Institutes of Health; Bethesda; USA (1979). // RX PubMed=19896956; DOI=10.1016/j.mrfmmm.2009.10.013; RA Wilson, Paul F. RA Nham, Peter B. RA Urbin, Salustra S. RA Hinz, John M. RA Jones, Irene M. RA Thompson, Lawrence H. RT "Inter-individual variation in DNA double-strand break repair in human RT fibroblasts before and after exposure to low doses of ionizing RT radiation."; RL Mutat. Res. 683:91-97(2010). // RX CelloPub=CLPUB00447; RA Mulivor, Richard A. RA Suchy, Sharon F. RT "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell RT repository. 16th edition. October 1992."; RL (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992). // RX PubMed=6726265; DOI=10.1136/jnnp.47.4.391; PMCID=PMC1027781; RA Robbins, Jay H. RA Scudiero, Dominic A. RA Otsuka, Fujio RA Tarone, Robert E. RA Brumback, Roger Alan RA Wirtschafter, Jonathan D. RA Polinsky, Ronald J. RA Barrett, Susanna F. RA Moshell, Alan N. RA Scarpinato, Ronald G. RA Ganges, Mary Bruce RA Nee, Linda E. RA Meyer, Sharon A. RA Clatterbuck, Brian E. RT "Hypersensitivity to DNA-damaging agents in cultured cells from RT patients with Usher's syndrome and Duchenne muscular dystrophy."; RL J. Neurol. Neurosurg. Psychiatry 47:391-398(1984). // RX PubMed=2837086; PMCID=PMC1715274; RA Winkler, Janet K. RA Suttle, D. Parker RT "Analysis of UMP synthase gene and mRNA structure in hereditary orotic RT aciduria fibroblasts."; RL Am. J. Hum. Genet. 43:86-94(1988). // RX CelloPub=CLPUB00387; RA Coriell, Lewis Lemon RA Greene, Arthur E. RA Mulivor, Richard A. RT "The human genetic mutant cell repository: list of genetic variants, RT chromosomal aberrations and normal cell cultures submitted to the RT repository. 7th edition. October 1980."; RL (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda; USA (1980). // RX PubMed=26831110; DOI=10.1073/pnas.1525665113; PMCID=PMC4763759; RA Iovino, Salvatore RA Burkart, Alison M. RA Warren, Laura RA Patti, Mary-Elizabeth RA Kahn, Carl Ronald RT "Myotubes derived from human-induced pluripotent stem cells mirror in RT vivo insulin resistance."; RL Proc. Natl. Acad. Sci. U.S.A. 113:1889-1894(2016). // RX CelloPub=CLPUB00720; RA Greene, Arthur E. RA Mulivor, Richard A. RT "1986/1987 catalog of cell lines. NIGMS human genetic mutant cell RT repository. 13th edition. October 1986."; RL (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 87-2011; pp.1-549; National Institutes of Health; Bethesda; USA (1986). // RX PubMed=3745952; DOI=10.1111/1523-1747.ep12285424; RA Sephel, Gregory Charles RA Davidson, Jeffrey M. RT "Elastin production in human skin fibroblast cultures and its decline RT with age."; RL J. Invest. Dermatol. 86:279-285(1986). // RX PubMed=17668376; DOI=10.1086/519248; PMCID=PMC1950802; RA Prandini, Paola RA Deutsch, Samuel RA Lyle, Robert RA Gagnebin, Maryline RA Delucinge-Vivier, Celine RA Delorenzi, Mauro RA Gehrig, Corinne RA Descombes, Patrick RA Sherman, Stephanie L. RA Dagna-Bricarelli, Franca RA Baldo, Chiara RA Novelli, Antonio RA Dallapiccola, Bruno RA Antonarakis, Stylianos E. RT "Natural gene-expression variation in Down syndrome modulates the RT outcome of gene-dosage imbalance."; RL Am. J. Hum. Genet. 81:252-263(2007). //