(Q37133626)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18400692%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

review article

1 reference

title

Apical transporters for neutral amino acids: physiology and pathophysiology (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18400692%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18400692%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

author name string

Stefan Bröer

series ordinal

1

1 reference

18 August 2017

publication date

1 April 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18400692%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18400692%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

volume

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18400692%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

page(s)

95-103

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18400692%20AND%20SRC:MED&resulttype=core&format=json

H+/amino acid transporter 1 (PAT1) is the imino acid carrier: An intestinal nutrient/drug transporter in human and rat.

5 January 2020

cites work

1 reference

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Newborn urine screening programme in the province of Quebec: an update of 30 years' experience

21 January 2018

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Further evidence for allelic heterogeneity in Hartnup disorder.

21 January 2018

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Persistence of the common Hartnup disease D173N allele in populations of European origin.

21 January 2018

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The generalized aminoaciduria seen in patients with hepatocyte nuclear factor-1alpha mutations is a feature of all patients with diabetes and is associated with glucosuria.

21 January 2018

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Characterization of mouse amino acid transporter B0AT1 (slc6a19).

21 January 2018

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The SLC36 family: proton-coupled transporters for the absorption of selected amino acids from extracellular and intracellular proteolysis

21 January 2018

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A cluster of proton/amino acid transporter genes in the human and mouse genomes

21 January 2018

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Functional characterization of two novel mammalian electrogenic proton-dependent amino acid cotransporters

21 January 2018

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The molecular basis of neutral aminoacidurias

21 January 2018

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Molecular cloning of mouse amino acid transport system B0, a neutral amino acid transporter related to Hartnup disorder

21 January 2018

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The orphan transporter v7-3 (slc6a15) is a Na+-dependent neutral amino acid transporter (B0AT2)

21 January 2018

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Amino acid transport across mammalian intestinal and renal epithelia

21 January 2018

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The SLC6 orphans are forming a family of amino acid transporters.

21 January 2018

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Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine

21 January 2018

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Essential role for collectrin in renal amino acid transport

21 January 2018

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A nonsense polymorphism (Y319X) of the solute carrier family 6 member 18 (SLC6A18) gene is not associated with hypertension and blood pressure in Japanese

21 January 2018

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Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT

21 January 2018

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Low and high affinity amino acid H+-cotransporters for cellular import of neutral and charged amino acids.

21 January 2018

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Substrate specificity and transport mode of the proton-dependent amino acid transporter mPAT2.

21 January 2018

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Identification of a chloride ion binding site in Na+/Cl -dependent transporters.

21 January 2018

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The structure of human 4F2hc ectodomain provides a model for homodimerization and electrostatic interaction with plasma membrane

21 January 2018

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The HNF-1 target collectrin controls insulin exocytosis by SNARE complex formation

21 January 2018

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Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder

21 January 2018

1 reference

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Molecular cloning of the mouse IMINO system: an Na+- and Cl--dependent proline transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

The emerging role of PDZ adapter proteins for regulation of intestinal ion transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Sodium-coupled neutral amino acid (System N/A) transporters of the SLC38 gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Intestinal absorption of amino acids and peptides

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Lysine transport across the small intestine. Stimulating and inhibitory effects of neutral amino acids.

21 January 2018

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Homozygosity mapping to chromosome 5p15 of a gene responsible for Hartnup disorder

21 January 2018

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Lysinuric protein intolerance: mechanisms of pathophysiology

21 January 2018

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The genetics of heteromeric amino acid transporters

21 January 2018

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Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome

21 January 2018

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Iminoaciduria: a benign renal tubular defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Hypertension and impaired glycine handling in mice lacking the orphan transporter XT2

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Luminal kidney and intestine SLC6 amino acid transporters of B0AT-cluster and their tissue distribution in Mus musculus

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Identification and characterization of a lysosomal transporter for small neutral amino acids

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

SWISS-MODEL: An automated protein homology-modeling server

21 January 2018

1 reference

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Renal tubular transport of proline, hydroxyproline, and glycine. 3. Genetic basis for more than one mode of transport in human kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Neonatal iminoglycinuria: evidence that the prolinuria originates in selective deficiency of transport activity in the proximal nephron

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Genetic aspects of renal tubular transport: diversity and topology of carriers

21 January 2018

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New renal tubular amino-acid transport system and a new hereditary disorder of amino-acid metabolism.

21 January 2018

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Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19

21 January 2018

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Assignment of the gene coding for the human high-affinity glutamate transporter EAAC1 to 9p24: potential role in dicarboxylic aminoaciduria and neurodegenerative disorders

21 January 2018

1 reference

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Characterization of a branched-chain amino-acid transporter SBAT1 (SLC6A15) that is expressed in human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Identification of mammalian proline transporter SIT1 (SLC6A20) with characteristics of classical system imino

21 January 2018

1 reference

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Deciphering the mechanisms of intestinal imino (and amino) acid transport: the redemption of SLC36A1.

21 January 2018

1 reference

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H+-coupled nutrient, micronutrient and drug transporters in the mammalian small intestine

21 January 2018

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H(+)/solute-induced intracellular acidification leads to selective activation of apical Na(+)/H(+) exchange in human intestinal epithelial cells

21 January 2018

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Sequential amino acid exchange across b(0,+)-like system in chicken brush border jejunum.

21 January 2018

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The angiotensin-converting enzyme gene family: genomics and pharmacology

21 January 2018

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ACEH/ACE2 is a novel mammalian metallocarboxypeptidase and a homologue of angiotensin-converting enzyme insensitive to ACE inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Neurotransmitter transporter family cDNAs in a rat midbrain library: 'orphan transporters' suggest sizable structural variations

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Surprising versatility of Na+-glucose cotransporters: SLC5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Crystal structure of a bacterial homologue of Na+/Cl--dependent neurotransmitter transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Collectrin, a collecting duct-specific transmembrane glycoprotein, is a novel homolog of ACE2 and is developmentally regulated in embryonic kidneys

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Collectrin, a homologue of ACE2, its transcriptional control and functional perspectives.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007

Mechanism of chloride interaction with neurotransmitter:sodium symporters.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00045.2007