ID GM01177 AC CVCL_JB60 SY GM-1177; GM1177; AG01177; AG-1177; AG 1177; AG1177; WG0360; WG360 DR Coriell; AG01177 DR Coriell; GM01177 DR Wikidata; Q54836688 RX CelloPub=CLPUB00387; RX DOI=10.5962/bhl.title.4090; RX PubMed=7176709; RX PubMed=7253718; CC From: Montreal Children's Hospital cell repository; Montreal; Canada. CC Discontinued: Coriell; AG01177; probable. CC Discontinued: Coriell; GM01177; probable. CC Derived from site: In situ; Skin; UBERON=UBERON_0002097. CC Cell type: Fibroblast of skin; CL=CL_0002620. DI NCIt; C34951; Progeria DI ORDO; Orphanet_740; Hutchinson-Gilford progeria syndrome OX NCBI_TaxID=9606; ! Homo sapiens (Human) SX Male AG 9Y CA Finite cell line DT Created: 15-05-17; Last updated: 29-06-23; Version: 9 // RX DOI=10.5962/bhl.title.4090; RA Coriell, Lewis Lemon RA Greene, Arthur E. RT "The human genetic mutant cell repository: list of genetic variants, RT chromosomal aberrations and normal cell cultures submitted to the RT repository. 4th edition. October 1977."; RL (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977). // RX PubMed=7253718; DOI=10.1016/0047-6374(81)90027-0; RA Das, Nirmal K. RA Murphy, Donald G. RT "The National Institute on Aging repository cell cultures."; RL Mech. Ageing Dev. 16:1-17(1981). // RX PubMed=7176709; DOI=10.1016/0047-6374(82)90061-6; RA Tollefsbol, Trygve O. RA Zaun, M. Rebecca RA Gracy, Robert W. RT "Increased lability of triosephosphate isomerase in progeria and RT Werner's syndrome fibroblasts."; RL Mech. Ageing Dev. 20:93-101(1982). // RX CelloPub=CLPUB00387; RA Coriell, Lewis Lemon RA Greene, Arthur E. RA Mulivor, Richard A. RT "The human genetic mutant cell repository: list of genetic variants, RT chromosomal aberrations and normal cell cultures submitted to the RT repository. 7th edition. October 1980."; RL (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda; USA (1980). //