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Cellosaurus GM01142 (CVCL_F129)

[Text version]
Cell line name GM01142
Synonyms GM-1142; GM1142; GM01142A; AG01142; AG-1142; AG 1142; AG1142
Accession CVCL_F129
Secondary accession CVCL_V542
Resource Identification Initiative To cite this cell line use: GM01142 (RRID:CVCL_F129)
Comments Omics: CNV analysis.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Sporadic retinoblastoma (NCIt: C42596)
Retinoblastoma (ORDO: Orphanet_790)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_F128 (GM03022)
Originate from same individual CVCL_F130 ! GM01484
Sex of cell Female
Age at sampling 2Y3M
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)

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=7471105
Weichselbaum R.R., Nove J., Little J.B.
X-ray sensitivity of fifty-three human diploid fibroblast cell strains from patients with characterized genetic disorders.
Cancer Res. 40:920-925(1980)

PubMed=7471106
Arlett C.F., Harcourt S.A.
Survey of radiosensitivity in a variety of human cell strains.
Cancer Res. 40:926-932(1980)

PubMed=7253718; DOI=10.1016/0047-6374(81)90027-0
Das N.K., Murphy D.G.
The National Institute on Aging repository cell cultures.
Mech. Ageing Dev. 16:1-17(1981)

PubMed=7329430; DOI=10.1016/0027-5107(81)90059-2
Nove J., Nichols W.W., Weichselbaum R.R., Little J.B.
Abnormalities of human chromosome 13 and in vitro radiosensitivity; a study of 19 fibroblast strains.
Mutat. Res. 84:157-167(1981)

PubMed=7338842; DOI=10.1269/jrr.22.472
Fujiwara Y., Miyazaki N., Kano Y., Takahashi T., Kaneko A.
X-ray, UV and chemical mutagen sensitivities of skin fibroblasts from patients with familial and chromosome 13q- retinoblastomas.
J. Radiat. Res. 22:472-476(1981)

PubMed=6600729; DOI=10.1080/09553008314550171
Arlett C.F., Priestley A.
Defective recovery from potentially lethal damage in some human fibroblast cell strains.
Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med. 43:157-167(1983)

PubMed=3762576; DOI=10.1016/0165-7992(86)90133-8
Wang Y.-Y., Parks W.C., Wigle J.C., Maher V.M., McCormick J.J.
Fibroblasts from patients with inherited predisposition to retinoblastoma exhibit normal sensitivity to the mutagenic effects of ionizing radiation.
Mutat. Res. 175:107-114(1986)

PubMed=2973075; DOI=10.2307/3577479
Fertil B., Deschavanne P.J., Debieu D., Malaise E.-P.
Correlation between PLD repair capacity and the survival curve of human fibroblasts in exponential growth phase: analysis in terms of several parameters.
Radiat. Res. 116:74-88(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=23665875; DOI=10.1534/g3.113.006577
Tang Z.-Y., Berlin D.S., Toji L.H., Toruner G.A., Beiswanger C.M., Kulkarni S., Martin C.L., Emanuel B.S., Christman M., Gerry N.P.
A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds.
G3 (Bethesda) 3:1143-1149(2013)

Cross-references
Cell line collections (Providers) Coriell; AG01142 - Discontinued
Coriell; GM01142
JCRB; KURB2682
Cell line databases/resources CLO; CLO_0030240
Biological sample resources BioSample; SAMN00803660
Encyclopedic resources Wikidata; Q54836665
Entry history
Entry creation22-Oct-2012
Last entry update29-Jun-2023
Version number20