ID   MCH070
AC   CVCL_U493
SY   MCH 70; MCH70
DR   Wikidata; Q54904502
RX   CelloPub=CLPUB00409;
RX   PubMed=1437403;
RX   PubMed=9235907;
RX   PubMed=17331252;
WW   https://web.archive.org/web/20070627165036/http://www.cellbank.mcgill.ca:80/cgi-bin/cellbank/allnormals.cgi
CC   From: Montreal Children's Hospital cell repository; Montreal; Canada.
CC   Omics: Transcriptome analysis by microarray.
CC   Derived from site: In situ; Abdomen, skin; UBERON=UBERON_0001416.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   19Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 11
//
RX   CelloPub=CLPUB00409;
RA   Dolenga M.P.;
RT   "Metabolic studies of prolidase deficiency in cultured human
RT   fibroblasts.";
RL   Thesis MSc (1991); McGill University Montreal; Montreal; Canada.
//
RX   PubMed=1437403; DOI=10.1203/00006450-199210000-00020;
RA   Dolenga M.P., Hechtman P.;
RT   "Prolidase deficiency in cultured human fibroblasts: biochemical
RT   pathology and iminodipeptide-enhanced growth.";
RL   Pediatr. Res. 32:479-482(1992).
//
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).
//
RX   PubMed=17331252; DOI=10.1186/1471-2156-8-6; PMCID=PMC1810559;
RA   Leung C.L., Pang Y.-H., Shu C., Goryunov D., Liem R.K.H.;
RT   "Alterations in lipid metabolism gene expression and abnormal lipid
RT   accumulation in fibroblast explants from giant axonal neuropathy
RT   patients.";
RL   BMC Genet. 8:6.1-6.12(2007).
//