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 misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977) PubMed=6458814; DOI=10.1073/pnas.78.10.6451; PMCID=PMC349057 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=6220707; DOI=10.1016/0006-291x(83)90361-3 Chua C.C., Geiman D.E., Ladda R.L. Detection of an Mr 200,000 glycoprotein in the culture medium of skin fibroblasts from patients with Huntington disease. Biochem. Biophys. Res. Commun. 111:690-699(1983) PubMed=6621576; DOI=10.1016/0027-5107(83)90010-6 Tarone R.E., Scudiero D.A., Robbins J.H. Statistical methods for in vitro cell survival assays. Mutat. Res. 111:79-96(1983) PubMed=6726265; DOI=10.1136/jnnp.47.4.391; PMCID=PMC1027781 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. Psychiatry 47:391-398(1984) PubMed=2897722; DOI=10.1002/tcm.1770080104 Nagasawa H., Burke M.J., Little F.F., McCone E.F., Chan G.L., Little J.B. Multiple abnormalities in the ultraviolet light response of cultured fibroblasts derived from patients with the basal cell nevus syndrome. Teratog. Carcinog. Mutagen. 8:25-33(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 misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992) PubMed=8643543; DOI=10.1073/pnas.93.10.5146; PMCID=PMC39422 Parshad R., Sanford K.K., Price F.M., Melnick L.K., Nee L.E., Schapiro M.B., Tarone R.E., Robbins J.H. Fluorescent light-induced chromatid breaks distinguish Alzheimer disease cells from normal cells in tissue culture. Proc. Natl. Acad. Sci. U.S.A. 93:5146-5150(1996) 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=24555846; DOI=10.1186/gb-2014-15-2-r37; PMCID=PMC4053980 Wagner J.R., Busche S., Ge B., Kwan T., Pastinen T., Blanchette M. The relationship between DNA methylation, genetic and expression inter-individual variation in untransformed human fibroblasts. Genome Biol. 15:R37.1-R37.17(2014) PubMed=25326100; DOI=10.15252/msb.20145114; PMCID=PMC4299376 Adoue V., Schiavi A., Light N., Almlof J.C., Lundmark P., Ge B., Kwan T., Caron M., Ronnblom L., Wang C., Chen S.-H., Goodall A.H., Cambien F., Deloukas P., Ouwehand W.H., Syvanen A.-C., Pastinen T. Allelic expression mapping across cellular lineages to establish impact of non-coding SNPs. Mol. Syst. Biol. 10:754-754(2014) |