ID   MCH039
AC   CVCL_0D92
SY   MCH 39; MCH39
DR   Wikidata; Q54904486
RX   CelloPub=CLPUB00409;
RX   CelloPub=CLPUB00453;
RX   CelloPub=CLPUB00662;
RX   CelloPub=CLPUB00668;
RX   PubMed=1437403;
RX   PubMed=1627352;
RX   PubMed=2705457;
RX   PubMed=3478720;
RX   PubMed=9235907;
CC   From: Montreal Children's Hospital cell repository; Montreal; Canada.
CC   Miscellaneous: Cell line no longer available.
CC   Derived from site: In situ; Foreskin, skin; UBERON=UBERON_0001471.
CC   Cell type: Fibroblast of foreskin; CL=CL_1001608.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   11M
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=CLPUB00668;
RA   Anastasio, Natascia
RT   "Allelic expression of MMACHC and evidence for genotype-phenotype
RT   correlations in cblC disease.";
RL   Thesis MSc (2010); McGill University Montreal; Montreal; Canada.
//
RX   CelloPub=CLPUB00662;
RA   Yamani, Lama
RT   "Studies on transcobalamin in cultured fibroblasts from patients with
RT   inborn errors of cobalamin metabolism.";
RL   Thesis PhD (2008); McGill University Montreal; Montreal; Canada.
//
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=1437403; DOI=10.1203/00006450-199210000-00020;
RA   Dolenga, Michael Peter
RA   Hechtman, Peter
RT   "Prolidase deficiency in cultured human fibroblasts: biochemical
RT   pathology and iminodipeptide-enhanced growth.";
RL   Pediatr. Res. 32:479-482(1992).
//
RX   CelloPub=CLPUB00409;
RA   Dolenga, Michael Peter
RT   "Metabolic studies of prolidase deficiency in cultured human
RT   fibroblasts.";
RL   Thesis MSc (1991); McGill University Montreal; Montreal; Canada.
//