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Cellosaurus GM03348 (CVCL_7382)

[Text version]
Cell line name GM03348
Synonyms GM3348; GM-03348; GM 03348; GM 3348; GM 3348A; GM3348A; GM03348C; GM03348D; GMO3348E; C3448; IMR-3348
Accession CVCL_7382
Resource Identification Initiative To cite this cell line use: GM03348 (RRID:CVCL_7382)
Comments Part of: ENCODE project common cell types; tier 3.
Omics: Transcriptome analysis by RNAseq.
Derived from site: In situ; Groin, skin; UBERON=UBERON_8410021.
Cell type: Fibroblast of skin; CL=CL_0002620.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 10Y
Category Finite cell line
Web pages http://genome.ucsc.edu/ENCODE/protocols/cell/human/FibroblGM03348_Crawford_protocol.pdf
Publications

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=6280044; DOI=10.1002/mus.880050215
Pena S.D.J.
Giant axonal neuropathy: an inborn error of organization of intermediate filaments.
Muscle Nerve 5:166-172(1982)

PubMed=6574472; DOI=10.1073/pnas.80.10.3086
Kent C.
Increased rate of cell-substratum detachment of fibroblasts from patients with Duchenne muscular dystrophy.
Proc. Natl. Acad. Sci. U.S.A. 80:3086-3090(1983)

PubMed=6689020; DOI=10.1016/S0021-9258(17)43873-7
de Wet W.J., Chu M.-L., Prockop D.J.
The mRNAs for the pro-alpha 1(I) and pro-alpha 2(I) chains of type I procollagen are translated at the same rate in normal human fibroblasts and in fibroblasts from two variants of osteogenesis imperfecta with altered steady state ratios of the two mRNAs.
J. Biol. Chem. 258:14385-14389(1983)

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=2445735; DOI=10.1016/S0021-9258(18)47730-7
Lin P.-Y., Gruenstein E.
Identification of a defective cAMP-stimulated Cl- channel in cystic fibrosis fibroblasts.
J. Biol. Chem. 262:15345-15347(1987)

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=8650226; DOI=10.1073/pnas.93.12.6101
Zhao H.G., Li H.-H., Bach G., Schmidtchen A., Neufeld E.F.
The molecular basis of Sanfilippo syndrome type B.
Proc. Natl. Acad. Sci. U.S.A. 93:6101-6105(1996)

PubMed=29125828; DOI=10.1242/dmm.030536
Napierala J.S., Li Y.-J., Lu Y., Lin K., Hauser L.A., Lynch D.R., Napierala M.
Comprehensive analysis of gene expression patterns in Friedreich's ataxia fibroblasts by RNA sequencing reveals altered levels of protein synthesis factors and solute carriers.
Dis. Model. Mech. 10:1353-1369(2017)

Cross-references
Cell line collections (Providers) Coriell; GM03348 - Discontinued
Cell line databases/resources CLO; CLO_0016536
Biological sample resources BioSample; SAMN00808363
BioSample; SAMN03253068
ENCODE; ENCBS285AAA
ENCODE; ENCBS558ENC
ENCODE; ENCBS559ENC
Encyclopedic resources Wikidata; Q54838016
Gene expression databases GEO; GSM1008563
GEO; GSM1008568
GEO; GSM1008564
Entry history
Entry creation04-Apr-2012
Last entry update29-Jun-2023
Version number25