(Q34129760)

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Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorption

scientific article published on August 4, 2010

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Europe PubMed Central

PubMed publication ID

31 July 2017

Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorption (English)

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Europe PubMed Central

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31 July 2017

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inferred from title

hereditary folate malabsorption

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amino acid replacement

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20686069

16 June 2024

Daniel Sanghoon Shin

3

object named as

Daniel Shin

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Europe PubMed Central

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16 June 2024

author name string

Kris Mahadeo

1

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31 July 2017

Ndeye Diop-Bove

2

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Europe PubMed Central

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31 July 2017

Ersin Selcuk Unal

4

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31 July 2017

Juliana Teo

5

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31 July 2017

Rongbao Zhao

6

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31 July 2017

Min-Hwang Chang

7

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31 July 2017

Andreas Fulterer

8

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Europe PubMed Central

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31 July 2017

Michael F. Romero

9

0000-0002-1555-7835

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Europe PubMed Central

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16 June 2024

I. David Goldman

10

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16 June 2024

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20686069

16 June 2024

publication date

4 August 2010

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31 July 2017

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https://europepmc.org/articles/pmc2980313

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Europe PubMed Central

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16 June 2024

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20686069/?tool=EBI

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Europe PubMed Central

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16 June 2024

http://intl-ajpcell.physiology.org/cgi/content/abstract/299/5/C1153

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Europe PubMed Central

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16 June 2024

https://europepmc.org/articles/PMC2980313

online access status

content deliverer

Europe PubMed Central

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20686069

16 June 2024

https://doi.org/10.1152/ajpcell.00113.2010

online access status

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20686069

16 June 2024

https://www.physiology.org/doi/pdf/10.1152/ajpcell.00113.2010

1 reference

10.1152/AJPCELL.00113.2010

https://api.crossref.org/works/10.1152/AJPCELL.00113.2010

16 June 2024

American Journal of Physiology - Cell Physiology

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

299

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Europe PubMed Central

PubMed publication ID

31 July 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

C1153-61

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Membrane topological analysis of the proton-coupled folate transporter (PCFT-SLC46A1) by the substituted cysteine accessibility method

1 reference

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A novel PCFT gene mutation (p.Cys66LeufsX99) causing hereditary folate malabsorption

1 reference

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Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed myelin metabolism

1 reference

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Hypermethylation of the human proton-coupled folate transporter (SLC46A1) minimal transcriptional regulatory region in an antifolate-resistant HeLa cell line

1 reference

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The functional roles of the His247 and His281 residues in folate and proton translocation mediated by the human proton-coupled folate transporter SLC46A1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2980313

28 July 2018

Membrane transporters and folate homeostasis: intestinal absorption and transport into systemic compartments and tissues

1 reference

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28 July 2018

The clinical course and genetic defect in the PCFT gene in a 27-year-old woman with hereditary folate malabsorption

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2980313

28 July 2018

The proton-coupled folate transporter: impact on pemetrexed transport and on antifolates activities compared with the reduced folate carrier

1 reference

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28 July 2018

Entry to "formula tunnel" revealed by SLC4A4 human mutation and structural model

1 reference

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28 July 2018

N-linked glycosylation and its impact on the electrophoretic mobility and function of the human proton-coupled folate transporter (HsPCFT).

1 reference

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28 July 2018

Cloning and functional characterization of the proton-coupled electrogenic folate transporter and analysis of its expression in retinal cell types

1 reference

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28 July 2018

Rodent intestinal folate transporters (SLC46A1): secondary structure, functional properties, and response to dietary folate restriction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2980313

28 July 2018

Pemetrexed: biochemical and cellular pharmacology, mechanisms, and clinical applications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2980313

28 July 2018

Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2980313

28 July 2018

Divalent metal-ion transporter DMT1 mediates both H+ -coupled Fe2+ transport and uncoupled fluxes

1 reference

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28 July 2018

A review of folate receptor alpha cycling and 5-methyltetrahydrofolate accumulation with an emphasis on cell models in vitro

1 reference

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28 July 2018

A prominent low-pH methotrexate transport activity in human solid tumors: contribution to the preservation of methotrexate pharmacologic activity in HeLa cells lacking the reduced folate carrier

1 reference

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28 July 2018

Hereditary folate malabsorption: family report and review of the literature

1 reference

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28 July 2018

Cloning and characterization of a mammalian proton-coupled metal-ion transporter

1 reference

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28 July 2018

Isolated defect of folic acid absorption associated with mental retardation and cerebral calcification

1 reference

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Anticonvulsants, folic acid, and epilepsy

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28 July 2018

Distribution of the folate receptor GP38 in normal and malignant cell lines and tissues

1 reference

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28 July 2018

Cellular localization of the folate receptor: potential role in drug toxicity and folate homeostasis

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Reversible severe combined immunodeficiency phenotype secondary to a mutation of the proton-coupled folate transporter

1 reference

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Congenital null mutations of the FOLR1 gene: a progressive neurologic disease and its treatment

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A family study of congenital malabsorption of folate

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21 January 2018

A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function

1 reference

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21 January 2018

Role of the glutamate 185 residue in proton translocation mediated by the proton-coupled folate transporter SLC46A1.

1 reference

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21 January 2018

Localization of the murine reduced folate carrier as assessed by immunohistochemical analysis

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The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption

1 reference

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21 January 2018

A role for the proton-coupled folate transporter (PCFT-SLC46A1) in folate receptor-mediated endocytosis

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21 January 2018

Mutation of the proton-coupled folate transporter gene (PCFT-SLC46A1) in Turkish siblings with hereditary folate malabsorption

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1 reference

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12 December 2020

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10.1152/AJPCELL.00113.2010

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PMC publication ID

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Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

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Europe PubMed Central

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31 July 2017

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