ID MCH024 AC CVCL_0F57 SY MCH 24; MCH24 DR Wikidata; Q54904484 RX CelloPub=CLPUB00453; RX CelloPub=CLPUB00661; RX PubMed=1627352; RX PubMed=2705457; RX PubMed=3478720; RX PubMed=6221880; RX PubMed=7909321; RX PubMed=9235907; CC From: Montreal Children's Hospital cell repository; Montreal; Canada. CC Population: Caucasian. CC Miscellaneous: Cell line no longer available. CC Derived from site: In situ; Skin; UBERON=UBERON_0002097. CC Cell type: Fibroblast of skin; CL=CL_0002620. OX NCBI_TaxID=9606; ! Homo sapiens (Human) SX Male AG 2Y CA Finite cell line DT Created: 10-04-15; Last updated: 29-06-23; Version: 9 // RX PubMed=2705457; PMCID=PMC1715628; RA Boright, Andrew Pepler RA Scriver, Charles Robert RA Lancaster, Gerald A. RA Choy, Francis Y.-M. RT "Prolidase deficiency: biochemical classification of alleles."; RL Am. J. Hum. Genet. 44:731-740(1989). // RX CelloPub=CLPUB00453; RA Boright, Andrew Pepler RT "Prolidase deficiency: studies in human dermal fibroblasts."; RL Thesis PhD (1988); McGill University Montreal; Montreal; Canada. // RX PubMed=1627352; DOI=10.1016/0885-4505(92)90029-x; RA Rosenblatt, David S. RA Lue-Shing, Helena RA Arzoumanian, A. RA Low-Nang, Lawrence RA Matiaszuk, Nora V. RT "Methylenetetrahydrofolate reductase (MR) deficiency: thermolability RT of residual MR activity, methionine synthase activity, and RT methylcobalamin levels in cultured fibroblasts."; RL Biochem. Med. Metab. Biol. 47:221-225(1992). // RX CelloPub=CLPUB00661; RA Fraser, Judith RT "Collagen metabolism by fibroblasts from normals and individuals with RT osteogenesis imperfecta."; RL Thesis PhD (1980); McGill University Montreal; Montreal; Canada. // RX PubMed=6221880; DOI=10.3109/03008208309015011; RA Fraser, Judith RA Lancaster, Gerald A. RA Scriver, Charles Robert RT "Secreted collagen ratios in normal human and osteogenesis imperfecta RT skin fibroblasts."; RL Connect. Tissue Res. 11:57-67(1983). // RX PubMed=9235907; DOI=10.1074/jbc.272.31.19171; RA Gulati, Sumedha RA Chen, Zhi-Qiang RA Brody, Lawrence C. RA Rosenblatt, David S. RA Banerjee, Ruma RT "Defects in auxiliary redox proteins lead to functional methionine RT synthase deficiency."; RL J. Biol. Chem. 272:19171-19175(1997). // RX PubMed=3478720; DOI=10.1073/pnas.84.21.7711; PMCID=PMC299370; RA Smith, D.W. RA Scriver, Charles Robert RA Tenenhouse, Harriet S. RA Simell, Olli RT "Lysinuric protein intolerance mutation is expressed in the plasma RT membrane of cultured skin fibroblasts."; RL Proc. Natl. Acad. Sci. U.S.A. 84:7711-7715(1987). // RX PubMed=7909321; DOI=10.1172/JCI117166; PMCID=PMC294249; RA Qureshi, Amber A. RA Crane, Ana M. RA Matiaszuk, Nora V. RA Rezvani, Iraj RA Ledley, Fred D. RA Rosenblatt, David S. RT "Cloning and expression of mutations demonstrating intragenic RT complementation in mut0 methylmalonic aciduria."; RL J. Clin. Invest. 93:1812-1819(1994). //