Characterization of folate uptake by choroid plexus epithelial cells in a rat primary culture model.
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Biology of the major facilitative folate transporters SLC19A1 and SLC46A1Homocysteine, folate and vitamin B12 in neuropsychiatric diseases: review and treatment recommendationsFolate regulation of axonal regeneration in the rodent central nervous system through DNA methylationMolecular and biochemical characterization of folate transport proteins in retinal Müller cellsTreatments for biomedical abnormalities associated with autism spectrum disorder.L-methylfolate Plus SSRI or SNRI from Treatment Initiation Compared to SSRI or SNRI Monotherapy in a Major Depressive Episode.Cerebral folate receptor autoantibodies in autism spectrum disorder.The human proton-coupled folate transporter: Biology and therapeutic applications to cancer.Choroid plexus transcytosis and exosome shuttling deliver folate into brain parenchyma.The proton-coupled folate transporter: impact on pemetrexed transport and on antifolates activities compared with the reduced folate carrier.Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed myelin metabolism.Reversible severe combined immunodeficiency phenotype secondary to a mutation of the proton-coupled folate transporter.Randomized multicenter investigation of folate plus vitamin B12 supplementation in schizophreniaA P425R mutation of the proton-coupled folate transporter causing hereditary folate malabsorption produces a highly selective alteration in folate binding.A role for the proton-coupled folate transporter (PCFT-SLC46A1) in folate receptor-mediated endocytosis.Use of a novel genetic mouse model to investigate the role of folate in colitis-associated colon cancer.The clinical course and genetic defect in the PCFT gene in a 27-year-old woman with hereditary folate malabsorption.Mutation of the proton-coupled folate transporter gene (PCFT-SLC46A1) in Turkish siblings with hereditary folate malabsorption.The major facilitative folate transporters solute carrier 19A1 and solute carrier 46A1: biology and role in antifolate chemotherapy of cancer.Hijacking solute carriers for proton-coupled drug transport.Metabolic pathology of autism in relation to redox metabolism.Inborn errors of metabolism underlying primary immunodeficiencies.Identification of likely associations between cerebral folate deficiency and complex genetic- and metabolic pathogenesis of autism spectrum disorders by utilization of a pilot interaction modeling approach.Folate nutrition and blood-brain barrier dysfunction.Thyroid dysfunction in children with autism spectrum disorder is associated with folate receptor α autoimmune disorder.The promise and challenges of exploiting the proton-coupled folate transporter for selective therapeutic targeting of cancer.
P2860
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P2860
Characterization of folate uptake by choroid plexus epithelial cells in a rat primary culture model.
description
2007 nî lūn-bûn
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2007年の論文
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2007年学术文章
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2007年学术文章
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2007年学术文章
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2007年学术文章
@zh-my
2007年学术文章
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2007年學術文章
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name
Characterization of folate upt ...... n a rat primary culture model.
@en
Characterization of folate upt ...... n a rat primary culture model.
@nl
type
label
Characterization of folate upt ...... n a rat primary culture model.
@en
Characterization of folate upt ...... n a rat primary culture model.
@nl
prefLabel
Characterization of folate upt ...... n a rat primary culture model.
@en
Characterization of folate upt ...... n a rat primary culture model.
@nl
P2093
P2860
P1476
Characterization of folate upt ...... n a rat primary culture model.
@en
P2093
Andong Qiu
Angela Smith
Barton Kamen
Benedette Makori
I David Goldman
Jan B Wollack
Peter D Cole
Rajeth Koneru
Sonia C Picinich
P2860
P304
P356
10.1111/J.1471-4159.2007.05095.X
P407
P577
2007-12-10T00:00:00Z