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   CelloPub=CLPUB00453;
RA   Boright A.P.;
RT   "Prolidase deficiency: studies in human dermal fibroblasts.";
RL   Thesis PhD (1988); McGill University Montreal; Montreal; Canada.
//
RX   CelloPub=CLPUB00661;
RA   Fraser J.;
RT   "Collagen metabolism by fibroblasts from normals and individuals with
RT   osteogenesis imperfecta.";
RL   Thesis PhD (1980); McGill University Montreal; Montreal; Canada.
//
RX   PubMed=1627352; DOI=10.1016/0885-4505(92)90029-x;
RA   Rosenblatt D.S., Lue-Shing H., Arzoumanian A., Low-Nang L.,
RA   Matiaszuk N.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   PubMed=2705457; PMCID=PMC1715628;
RA   Boright A.P., Scriver C.R., Lancaster G.A., Choy F.Y.-M.;
RT   "Prolidase deficiency: biochemical classification of alleles.";
RL   Am. J. Hum. Genet. 44:731-740(1989).
//
RX   PubMed=3478720; DOI=10.1073/pnas.84.21.7711; PMCID=PMC299370;
RA   Smith D.W., Scriver C.R., Tenenhouse H.S., Simell O.;
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=6221880; DOI=10.3109/03008208309015011;
RA   Fraser J., Lancaster G.A., Scriver C.R.;
RT   "Secreted collagen ratios in normal human and osteogenesis imperfecta
RT   skin fibroblasts.";
RL   Connect. Tissue Res. 11:57-67(1983).
//
RX   PubMed=7909321; DOI=10.1172/JCI117166; PMCID=PMC294249;
RA   Qureshi A.A., Crane A.M., Matiaszuk N.V., Rezvani I., Ledley F.D.,
RA   Rosenblatt D.S.;
RT   "Cloning and expression of mutations demonstrating intragenic
RT   complementation in mut0 methylmalonic aciduria.";
RL   J. Clin. Invest. 93:1812-1819(1994).
//
RX   PubMed=9235907; DOI=10.1074/jbc.272.31.19171;
RA   Gulati S., Chen Z.-Q., Brody L.C., Rosenblatt D.S., Banerjee R.;
RT   "Defects in auxiliary redox proteins lead to functional methionine
RT   synthase deficiency.";
RL   J. Biol. Chem. 272:19171-19175(1997).
//