ID   GM00038
AC   CVCL_7271
SY   GM0038; GM-38; GM 38; Gm 38; GM38; GM00038A; GM0038A; GM00038B; GM00038C
DR   CLO; CLO_0025187
DR   EFO; EFO_0004921
DR   Coriell; GM00038
DR   GEO; GSM88289
DR   GEO; GSM88307
DR   GEO; GSM88290
DR   GEO; GSM88308
DR   GEO; GSM88291
DR   GEO; GSM88309
DR   GEO; GSM992926
DR   GEO; GSM992927
DR   GEO; GSM3124635
DR   Wikidata; Q54835996
RX   CelloPub=CLPUB00387;
RX   CelloPub=CLPUB00447;
RX   CelloPub=CLPUB00600;
RX   CelloPub=CLPUB00720;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=656543;
RX   PubMed=2897722;
RX   PubMed=6409440;
RX   PubMed=6843573;
RX   PubMed=7380831;
RX   PubMed=7779715;
RX   PubMed=9650596;
RX   PubMed=12665480;
RX   PubMed=15268757;
RX   PubMed=17668376;
RX   PubMed=19329487;
RX   PubMed=30567591;
CC   Population: African American.
CC   Omics: Transcriptome analysis by microarray.
CC   Omics: Transcriptome analysis by 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   9Y
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 29-06-23; Version: 21
//
RX   CelloPub=CLPUB00387;
RA   Coriell L.L., Greene A.E., Mulivor R.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) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda (1980).
//
RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//
RX   CelloPub=CLPUB00600;
RA   Coriell L.L., Greene A.E., Mulivor R.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) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-168; National Institutes of Health; Bethesda (1979).
//
RX   CelloPub=CLPUB00720;
RA   Greene A.E., Mulivor R.A.;
RT   "1986/1987 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 13th edition. October 1986.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 87-2011; pp.1-549; National Institutes of Health; Bethesda (1986).
//
RX   DOI=10.5962/bhl.title.4090;
RA   Coriell L.L., Greene A.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) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977).
//
RX   PubMed=656543; DOI=10.1016/S0006-3495(78)85487-3;
RA   Ehmann U.K., Cook K.H., Friedberg E.C.;
RT   "The kinetics of thymine dimer excision in ultraviolet-irradiated
RT   human cells.";
RL   Biophys. J. 22:249-264(1978).
//
RX   PubMed=2897722; DOI=10.1002/tcm.1770080104;
RA   Nagasawa H., Burke M.J., Little F.F., McCone E.F., Chan G.L.,
RA   Little J.B.;
RT   "Multiple abnormalities in the ultraviolet light response of cultured
RT   fibroblasts derived from patients with the basal cell nevus syndrome.";
RL   Teratog. Carcinog. Mutagen. 8:25-33(1988).
//
RX   PubMed=6409440; DOI=10.1093/carcin/4.7.911;
RA   Smith P.J., Greene M.H., Adams D., Paterson M.C.;
RT   "Abnormal responses to the carcinogen 4-nitroquinoline 1-oxide of
RT   cultured fibroblasts from patients with dysplastic nevus syndrome and
RT   hereditary cutaneous malignant melanoma.";
RL   Carcinogenesis 4:911-916(1983).
//
RX   PubMed=6843573; DOI=10.1016/0027-5107(83)90054-4;
RA   Nagasawa H., Little J.B.;
RT   "Comparison of kinetics of X-ray-induced cell killing in normal,
RT   ataxia telangiectasia and hereditary retinoblastoma fibroblasts.";
RL   Mutat. Res. 109:297-308(1983).
//
RX   PubMed=7380831; DOI=10.1016/S0021-9258(19)70683-8;
RA   Daddona P.E., Frohman M.A., Kelley W.N.;
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=7779715; DOI=10.1038/bjc.1995.237;
RA   Mirzayans R., Aubin R.A., Bosnich W., Blattner W.A., Paterson M.C.;
RT   "Abnormal pattern of post-gamma-ray DNA replication in radioresistant
RT   fibroblast strains from affected members of a cancer-prone family with
RT   Li-Fraumeni syndrome.";
RL   Br. J. Cancer 71:1221-1230(1995).
//
RX   PubMed=9650596; DOI=10.2307/3579639;
RA   Enns L., Barley R.D.C., Paterson M.C., Mirzayans R.;
RT   "Radiosensitivity in ataxia telangiectasia fibroblasts is not
RT   associated with deregulated apoptosis.";
RL   Radiat. Res. 150:11-16(1998).
//
RX   PubMed=12665480; DOI=10.1096/fj.02-0851com;
RA   Tuo J.-S., Jaruga P., Rodriguez H., Bohr V.A., Dizdaroglu M.;
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   PubMed=15268757; DOI=10.1111/j.1474-9728.2004.00105.x;
RA   Csoka A.B., English S.B., Simkevich C.P., Ginzinger D.G., Butte A.J.,
RA   Schatten G.P., Rothman F.G., Sedivy J.M.;
RT   "Genome-scale expression profiling of Hutchinson-Gilford progeria
RT   syndrome reveals widespread transcriptional misregulation leading to
RT   mesodermal/mesenchymal defects and accelerated atherosclerosis.";
RL   Aging Cell 3:235-243(2004).
//
RX   PubMed=17668376; DOI=10.1086/519248;
RA   Prandini P., Deutsch S., Lyle R., Gagnebin M., Delucinge-Vivier C.,
RA   Delorenzi M., Gehrig C., Descombes P., Sherman S.L.,
RA   Dagna-Bricarelli F., Baldo C., Novelli A., Dallapiccola B.,
RA   Antonarakis S.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).
//
RX   PubMed=19329487; DOI=10.1073/pnas.0902113106;
RA   Nardo T., Oneda R., Spivak G., Vaz B., Mortier L., Thomas P.,
RA   Orioli D., Laugel V., Stary A., Hanawalt P.C., Sarasin A.,
RA   Stefanini M.;
RT   "A UV-sensitive syndrome patient with a specific CSA mutation reveals
RT   separable roles for CSA in response to UV and oxidative DNA damage.";
RL   Proc. Natl. Acad. Sci. U.S.A. 106:6209-6214(2009).
//
RX   PubMed=30567591; DOI=10.1186/s13059-018-1599-6;
RA   Fleischer J.G., Schulte R., Tsai H.H., Tyagi S., Ibarra A.,
RA   Shokhirev M.N., Huang L., Hetzer M.W., Navlakha S.;
RT   "Predicting age from the transcriptome of human dermal fibroblasts.";
RL   Genome Biol. 19:221.1-221.8(2018).
//