Cellosaurus logo
expasy logo

Cellosaurus MCH039 (CVCL_0D92)

[Text version]
Cell line name MCH039
Synonyms MCH 39; MCH39
Accession CVCL_0D92
Resource Identification Initiative To cite this cell line use: MCH039 (RRID:CVCL_0D92)
Comments From: Montreal Children's Hospital cell repository; Montreal; Canada.
Miscellaneous: Cell line no longer available.
Derived from site: In situ; Foreskin, skin; UBERON=UBERON_0001471.
Cell type: Fibroblast of foreskin; CL=CL_1001608.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 11M
Category Finite cell line
Publications

PubMed=3478720; DOI=10.1073/pnas.84.21.7711; PMCID=PMC299370
D.W. Smith, Charles Robert Scriver, Harriet S. Tenenhouse, Olli Simell;
Lysinuric protein intolerance mutation is expressed in the plasma membrane of cultured skin fibroblasts.
Proc. Natl. Acad. Sci. U.S.A. 84:7711-7715(1987)

CLPUB00453
Andrew Pepler Boright;
Prolidase deficiency: studies in human dermal fibroblasts.
Thesis PhD (1988); McGill University Montreal; Montreal; Canada

PubMed=2705457; PMCID=PMC1715628
Andrew Pepler Boright, Charles Robert Scriver, Gerald A. Lancaster, Francis Y.-M. Choy;
Prolidase deficiency: biochemical classification of alleles.
Am. J. Hum. Genet. 44:731-740(1989)

CLPUB00409
Michael Peter Dolenga;
Metabolic studies of prolidase deficiency in cultured human fibroblasts.
Thesis MSc (1991); McGill University Montreal; Montreal; Canada

PubMed=1437403; DOI=10.1203/00006450-199210000-00020
Michael Peter Dolenga, Peter Hechtman;
Prolidase deficiency in cultured human fibroblasts: biochemical pathology and iminodipeptide-enhanced growth.
Pediatr. Res. 32:479-482(1992)

PubMed=1627352; DOI=10.1016/0885-4505(92)90029-x
David S. Rosenblatt, Helena Lue-Shing, A. Arzoumanian, Lawrence Low-Nang, Nora V. Matiaszuk;
Methylenetetrahydrofolate reductase (MR) deficiency: thermolability of residual MR activity, methionine synthase activity, and methylcobalamin levels in cultured fibroblasts.
Biochem. Med. Metab. Biol. 47:221-225(1992)

PubMed=9235907; DOI=10.1074/jbc.272.31.19171
Sumedha Gulati, Zhi-Qiang Chen, Lawrence C. Brody, David S. Rosenblatt, Ruma Banerjee;
Defects in auxiliary redox proteins lead to functional methionine synthase deficiency.
J. Biol. Chem. 272:19171-19175(1997)

CLPUB00662
Lama Yamani;
Studies on transcobalamin in cultured fibroblasts from patients with inborn errors of cobalamin metabolism.
Thesis PhD (2008); McGill University Montreal; Montreal; Canada

CLPUB00668
Natascia Anastasio;
Allelic expression of MMACHC and evidence for genotype-phenotype correlations in cblC disease.
Thesis MSc (2010); McGill University Montreal; Montreal; Canada

Cross-references
Encyclopedic resources Wikidata; Q54904486
Entry history
Entry creation10-Apr-2015
Last entry update29-Jun-2023
Version number9