(Q35128236)

6 August 2017

title

Impaired nutrient signaling and body weight control in a Na+ neutral amino acid cotransporter (Slc6a19)-deficient mouse (English)

1 reference

6 August 2017

Angelika Bröer

1

1 reference

6 August 2017

Torsten Juelich

2

1 reference

6 August 2017

Jessica M Vanslambrouck

3

1 reference

6 August 2017

Nadine Tietze

4

1 reference

6 August 2017

Peter S Solomon

5

1 reference

6 August 2017

Jeff Holst

6

1 reference

6 August 2017

Charles G Bailey

7

1 reference

6 August 2017

John E J Rasko

8

1 reference

6 August 2017

Stefan Bröer

9

1 reference

6 August 2017

language of work or name

English

0 references

publication date

2 June 2011

1 reference

Journal of Biological Chemistry

6 August 2017

published in

1 reference

6 August 2017

volume

286

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6 August 2017

issue

30

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6 August 2017

page(s)

26638-26651

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Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria

6 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Angiotensin-converting enzyme 2 (ACE2) in disease pathogenesis

13 July 2018

1 reference

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Physiology and function of the tight junction

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

ATF4-dependent transcription mediates signaling of amino acid limitation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Orphan transporter SLC6A18 is renal neutral amino acid transporter B0AT3

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

The role of the neutral amino acid transporter B0AT1 (SLC6A19) in Hartnup disorder and protein nutrition.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Amino acid transport across mammalian intestinal and renal epithelia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Essential role for collectrin in renal amino acid transport

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Characterization of carnosine uptake and its physiological function in human intestinal epithelial Caco-2 cells.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

A signaling role of glutamine in insulin secretion

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Glutamate transporter EAAC-1-deficient mice develop dicarboxylic aminoaciduria and behavioral abnormalities but no neurodegeneration

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Intestinal absorption of amino acids and peptides

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

The Hartnup phenotype: Mendelian transport disorder, multifactorial disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Renal imino acid and glycine transport system ontogeny and involvement in developmental iminoglycinuria.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

A protein complex in the brush-border membrane explains a Hartnup disorder allele

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Tmem27: a cleaved and shed plasma membrane protein that stimulates pancreatic beta cell proliferation

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Steady-state kinetic characterization of the mouse B(0)AT1 sodium-dependent neutral amino acid transporter.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Characterization of mouse amino acid transporter B0AT1 (slc6a19).

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Reconstitution into liposomes of the glutamine/amino acid transporter from renal cell plasma membrane: functional characterization, kinetics and activation by nucleotides.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Growth hormone and epidermal growth factor together enhance amino acid transport systems B0,+ and A in remnant small intestine after massive enterectomy

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143628

Deletion of Nicotinamide Nucleotide Transhydrogenase: A New Quantitive Trait Locus Accounting for Glucose Intolerance in C57BL/6J Mice

27 September 2018

1 reference

12 December 2020

Isolation of renal proximal tubular brush-border membranes

1 reference

12 December 2020

Na(+)-dependent neutral amino acid transporter ATB(0) is a rabbit epithelial cell brush-border protein

1 reference

12 December 2020

Phenylalanine uptake in isolated renal brush border vesicles

1 reference

12 December 2020

Transport of amino acids in renal brush border membrane vesicles. Uptake of the neutral amino acid L-alanine

1 reference

12 December 2020

Multiple transport pathways for neutral amino acids in rabbit jejunal brush border vesicles

1 reference

12 December 2020

Genetic mapping of hph2, a mutation affecting amino acid transport in the mouse

1 reference

12 December 2020

A candidate mouse model for Hartnup disorder deficient in neutral amino acid transport

1 reference

12 December 2020

Identifiers

DOI

10.1074/JBC.M111.241323

1 reference

6 August 2017

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6 August 2017

1 reference