Defective high-affinity thiamine transporter leads to cell death in thiamine-responsive megaloblastic anemia syndrome fibroblasts.
about
Cloning of the human thiamine transporter, a member of the folate transporter familyPancreatic beta cells and islets take up thiamin by a regulated carrier-mediated process: studies using mice and human pancreatic preparationsVitamin B1 (thiamine) uptake by human retinal pigment epithelial (ARPE-19) cells: mechanism and regulationImpact of the reduced folate carrier on the accumulation of active thiamin metabolites in murine leukemia cells.Thiamine intestinal transport and related issues: recent aspects.Does early treatment prevent deafness in thiamine-responsive megaloblastic anaemia syndrome?Glucose stimulates protein modification by O-linked GlcNAc in pancreatic beta cells: linkage of O-linked GlcNAc to beta cell death.A novel homozygous SLC19A2 mutation in a Portuguese patient with diabetes mellitus and thiamine-responsive megaloblastic anaemia.A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex IRelative contribution of THTR-1 and THTR-2 in thiamin uptake by pancreatic acinar cells: studies utilizing Slc19a2 and Slc19a3 knockout mouse models.The impact of thiamine treatment in the diabetes mellitus.Enteropathogenic Escherichia coli inhibits intestinal vitamin B1 (thiamin) uptake: studies with human-derived intestinal epithelial Caco-2 cellsTreatment of genetic defects of thiamine transport and metabolism.A novel mutation in the SLC19A2 gene in a Tunisian family with thiamine-responsive megaloblastic anaemia, diabetes and deafness syndrome.Disruption of thiamine uptake and growth of cells by feline leukemia virus subgroup A.Thiamine responsive megaloblastic anemia syndrome associated with patent ductus arteriosus: First case report from Kashmir Valley of the Indian subcontinentReduced folate carrier transports thiamine monophosphate: an alternative route for thiamine delivery into mammalian cells.Functional role of specific amino acid residues in human thiamine transporter SLC19A2: mutational analysis.Leber's congenital amaurosis as the retinal degenerative phenotype in thiamine responsive megaloblastic anemia: a case report.Thiamine withdrawal can lead to diabetic ketoacidosis in thiamine responsive megaloblastic anemia: report of two siblings.Cochlear implant and thiamine-responsive megaloblastic anemia syndrome.Metabolic impairment elicits brain cell type-selective changes in oxidative stress and cell death in culture.
P2860
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P2860
Defective high-affinity thiamine transporter leads to cell death in thiamine-responsive megaloblastic anemia syndrome fibroblasts.
description
1999 nî lūn-bûn
@nan
1999 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի մարտին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Defective high-affinity thiami ...... c anemia syndrome fibroblasts.
@ast
Defective high-affinity thiami ...... c anemia syndrome fibroblasts.
@en
type
label
Defective high-affinity thiami ...... c anemia syndrome fibroblasts.
@ast
Defective high-affinity thiami ...... c anemia syndrome fibroblasts.
@en
prefLabel
Defective high-affinity thiami ...... c anemia syndrome fibroblasts.
@ast
Defective high-affinity thiami ...... c anemia syndrome fibroblasts.
@en
P2093
P2860
P356
P1476
Defective high-affinity thiami ...... c anemia syndrome fibroblasts.
@en
P2093
P2860
P304
P356
10.1172/JCI3895
P407
P577
1999-03-01T00:00:00Z