Publications | 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=3863481 Goldman D., Goldin L.R., Rathnagiri P., O'Brien S.J., Egeland J.A., Merril C.R. Twenty-seven protein polymorphisms by two-dimensional electrophoresis of serum, erythrocytes, and fibroblasts in two pedigrees. Am. J. Hum. Genet. 37:898-911(1985) 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) 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=7847674; DOI=10.1111/j.1749-6632.1994.tb44413.x Etcheberrigaray E., Gibson G.E., Alkon D.L. Molecular mechanisms of memory and the pathophysiology of Alzheimer's disease. Ann. N. Y. Acad. Sci. 747:245-255(1994) PubMed=8823375; DOI=10.1111/1523-1747.ep12584287 Moriwaki S.-I., Stefanini M., Lehmann A.R., Hoeijmakers J.H.J., Robbins J.H., Rapin I., Botta E., Tanganelli B., Vermeulen W., Broughton B.C., Kraemer K.H. DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and Cockayne syndrome resemble xeroderma pigmentosum cells. J. Invest. Dermatol. 107:647-653(1996) PubMed=12060391; DOI=10.1046/j.1523-1747.2002.01782.x Emmert S., Slor H., Busch D.B., Batko S., Albert R.B., Coleman D.M., Khan S.G., Abu-Libdeh B., DiGiovanna J.J., Cunningham B.B., Lee M.-M., Crollick J., Inui H., Ueda T., Hedayati M., Grossman L., Shahlavi T., Cleaver J.E., Kraemer K.H. Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients. J. Invest. Dermatol. 118:972-982(2002) 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=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) |