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Cellosaurus GM00969 (CVCL_7311)

[Text version]
Cell line name GM00969
Synonyms GM0969; GM-969; GM 969; GM00969A; GM 969A; GM0969B; GM00969C; C4
Accession CVCL_7311
Resource Identification Initiative To cite this cell line use: GM00969 (RRID:CVCL_7311)
Comments Population: Caucasian.
Omics: miRNA expression profiling.
Omics: Transcriptome analysis by microarray.
Omics: Transcriptome analysis by RNAseq.
Derived from sampling site: Skin. Cell type=Fibroblast.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_DR05 (CHOPWT1.1)CVCL_DR06 (CHOPWT1.2)CVCL_DR07 (CHOPWT1.3)
Sex of cell Female
Age at sampling 2Y
Category Finite cell line
Publications

DOI=10.5962/bhl.title.4090
Coriell L.L., Greene A.E.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 4th edition. October 1977.
(In) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977)

CLPUB00600
Coriell L.L., Greene A.E., Mulivor R.A.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 6th edition. October 1979.
(In) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-168; National Institutes of Health; Bethesda (1979)

CLPUB00387
Coriell L.L., Greene A.E., Mulivor R.A.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 7th edition. October 1980.
(In) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda (1980)

PubMed=7380831; DOI=10.1016/S0021-9258(19)70683-8
Daddona P.E., Frohman M.A., Kelley W.N.
Human adenosine deaminase and its binding protein in normal and adenosine deaminase-deficient fibroblast cell strains.
J. Biol. Chem. 255:5681-5687(1980)

PubMed=6458814; DOI=10.1073/pnas.78.10.6451
Scudiero D.A., Meyer S.A., Clatterbuck B.E., Tarone R.E., Robbins J.H.
Hypersensitivity to N-methyl-N'-nitro-N-nitrosoguanidine in fibroblasts from patients with Huntington disease, familial dysautonomia, and other primary neuronal degenerations.
Proc. Natl. Acad. Sci. U.S.A. 78:6451-6455(1981)

PubMed=6726265; DOI=10.1136/jnnp.47.4.391
Robbins J.H., Scudiero D.A., Otsuka F., Tarone R.E., Brumback R.A., Wirtschafter J.D., Polinsky R.J., Barrett S.F., Moshell A.N., Scarpinato R.G., Ganges M.B., Nee L.E., Meyer S.A., Clatterbuck B.E.
Hypersensitivity to DNA-damaging agents in cultured cells from patients with Usher's syndrome and Duchenne muscular dystrophy.
J. Neurol. Neurosurg. Psych. 47:391-398(1984)

CLPUB00720
Greene A.E., Mulivor R.A.
1986/1987 catalog of cell lines. NIGMS human genetic mutant cell repository. 13th edition. October 1986.
(In) Institute for Medical Research (Camden, N.J.) NIH 87-2011; pp.1-549; National Institutes of Health; Bethesda (1986)

PubMed=3745952; DOI=10.1111/1523-1747.ep12285424
Sephel G.C., Davidson J.M.
Elastin production in human skin fibroblast cultures and its decline with age.
J. Invest. Dermatol. 86:279-285(1986)

PubMed=2837086
Winkler J.K., Suttle D.P.
Analysis of UMP synthase gene and mRNA structure in hereditary orotic aciduria fibroblasts.
Am. J. Hum. Genet. 43:86-94(1988)

CLPUB00447
Mulivor R.A., Suchy S.F.
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992)

PubMed=12665480; DOI=10.1096/fj.02-0851com
Tuo J., Jaruga P., Rodriguez H., Bohr V.A., Dizdaroglu M.
Primary fibroblasts of Cockayne syndrome patients are defective in cellular repair of 8-hydroxyguanine and 8-hydroxyadenine resulting from oxidative stress.
FASEB J. 17:668-674(2003)

PubMed=17668376; DOI=10.1086/519248
Prandini P., Deutsch S., Lyle R., Gagnebin M., Delucinge-Vivier C., Delorenzi M., Gehrig C., Descombes P., Sherman S.L., Dagna-Bricarelli F., Baldo C., Novelli A., Dallapiccola B., Antonarakis S.E.
Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance.
Am. J. Hum. Genet. 81:252-263(2007)

PubMed=19896956; DOI=10.1016/j.mrfmmm.2009.10.013
Wilson P.F., Nham P.B., Urbin S.S., Hinz J.M., Jones I.M., Thompson L.H.
Inter-individual variation in DNA double-strand break repair in human fibroblasts before and after exposure to low doses of ionizing radiation.
Mutat. Res. 683:91-97(2010)

PubMed=26831110; DOI=10.1073/pnas.1525665113
Iovino S., Burkart A.M., Warren L., Patti M.-E., Kahn C.R.
Myotubes derived from human-induced pluripotent stem cells mirror in vivo insulin resistance.
Proc. Natl. Acad. Sci. U.S.A. 113:1889-1894(2016)

PubMed=30567591; DOI=10.1186/s13059-018-1599-6
Fleischer J.G., Schulte R., Tsai H.H., Tyagi S., Ibarra A., Shokhirev M.N., Huang L., Hetzer M.W., Navlakha S.
Predicting age from the transcriptome of human dermal fibroblasts.
Genome Biol. 19:221.1-221.8(2018)

Cross-references
Cell line collections Coriell; GM00969
Cell line databases/resources CLO; CLO_0029504
Encyclopedic resources Wikidata; Q54836570
Gene expression databases GEO; GSM1316971
GEO; GSM1317008
GEO; GSM3124626
Entry history
Entry creation04-Apr-2012
Last entry update21-Mar-2023
Version number21