Keywords: ABC; ATP-binding cassette; AHUI; aqueous humor uptake index; AUC; area under the curve; BAB; blood-aqueous barrier; BBB; blood-brain barrier; BCRP; breast cancer resistance protein; BRB; blood-retinal barrier; BUI; brain uptake index; MATE1; multidrug and
مقالات ISI (ترجمه نشده)
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Keywords: AICA; 5-aminoimidazole-4-carboxamide; AICARFTase; 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase; CA; carbonic anhydrase; CBE; CI-HCO3â exchanger; CHO; Chinese hamster ovary; FR; folate receptor; GARFTase; β-glycinamide ribonucleotide
Human proton coupled folic acid transporter is a monodisperse oligomer in the lauryl maltose neopentyl glycol solubilized state
Keywords: PCFT; Substrate binding assay; Negative stain EM; Size exclusion chromatography; Oligomeric state;
The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption
Keywords: Proton-coupled folate transporter; PCFT; SLC46A1; Reduced folate carrier; RFC; SLC19A1; Folate receptors; FRα; Folates; Folic acid; Methotrexate; Pemetrexed; Hereditary folate malabsorption; HFM; Cerebral folate deficiency; CFD; 5-Formyltetrahydrofolate
Genetic animal models to decipher the pathogenic effects of vitamin B12 and folate deficiency
Keywords: Vitamin B12; Folate; Methyl donor deficiency; Pathogenesis; Genetic animal models; B12; vitamin B12; SAM; S-adenosylmethionine; SAH; S-adenosylhomocysteine; HCY; homocysteine; KO; knock-out; ES cells; embryonic stem cells; OCM; one-carbon metabolism; NTD;
Redox cycling metals: Pedaling their roles in metabolism and their use in the development of novel therapeutics
Keywords: AC; adenylyl cyclase; AI; anemia of inflammation; cdks; cyclin-dependent kinases; bFGF; basic fibroblast growth factor; BpT; 2-benzoylpyridine thiosemicarbazone; Bp4eT; 2-benzoylpyridine 4-ethyl-3-thiosemicarbazone; Bp44mT; 2-benzoylpyridine 4,4-dimethyl-
Transcriptional regulation of PCFT by KLF4, HNF4α, CDX2 and C/EBPα: Implication in its site-specific expression in the small intestine
Keywords: PCFT; Gene expression; Transcriptional regulation; Intestine; KLF4; HNF4α; CDX2; C/EBPα;
Folate and thiamine transporters mediated by facilitative carriers (SLC19A1-3 and SLC46A1) and folate receptors
Keywords: RFC; reduced folate carrier; PCFT; proton-coupled folate transporter; ThTr1; thiamine transporter-1; ThTr2; thiamine transporter-2; FOLR1; folate receptor 1 or FRα; FOLR2; folate receptor 2 or FRβ; CSF; cerebrospinal fluid; HFM; hereditary folate malabs
Spatial and temporal expression of folate-related transporters and metabolic enzymes during mouse placental development
Keywords: Mthfr; Methionine synthase; Slc46a1; PCFT; Rfc1; Trophoblast giant cells; Glycogen trophoblast cells5-methyl-THF, 5-methyl-tetrahydrofolate; C-TGC, canal trophoblast giant cell; E, embryonic day; EPC, ectoplacental cone; Folr, folate receptor; GlyT cells,
Prevalence of a Loss-of-Function Mutation in the Proton-Coupled Folate Transporter Gene (PCFT-SLC46A1) Causing Hereditary Folate Malabsorption in Puerto Rico
Keywords: HFM; Hereditary folate malabsorption; PCFT; Proton-Coupled Folate Transporter; PCR; Polymerase chain reaction;
Vulnerability of the cysteine-less proton-coupled folate transporter (PCFT-SLC46A1) to mutational stress associated with the substituted cysteine accessibility method
Keywords: CL; Cysteine-less; HA; hemagglutinin; MTX; methotrexate; PCFT; the proton-coupled folate transporter; HFM; hereditary folate malabsorption; SCAM; substituted cysteine accessibility method; Proton-coupled folate transporter; Hereditary folate malabsorption
A novel PCFT gene mutation (p.Cys66LeufsX99) causing hereditary folate malabsorption
Keywords: Hereditary folate malabsorption; PCFT; SLC46A1; Frameshift mutation; Anemia;
Hereditary folate malabsorption: A positively charged amino acid at position 113 of the proton-coupled folate transporter (PCFT/SLC46A1) is required for folic acid binding
Keywords: HFM, hereditary folate malabsorption; PCFT, proton-coupled folate transporter; FA, folic acid; MTX, methotrexateHereditary folate malabsorption; Folates; Intestinal folate transport; PCFT; Loss-of-function mutations
Reversible severe combined immunodeficiency phenotype secondary to a mutation of the proton-coupled folate transporter
Keywords: Hereditary folate malabsorption; PCFT; Folic acid; Severe combined immunodeficiency; Recent thymic emigrants
PCFT/SLC46A1 promoter methylation and restoration of gene expression in human leukemia cells
Keywords: Folates; Antifolates; PCFT; Promoter; Gene expression; Methylation