(Q44686498)

5 December 2017

title

Tyrosine residues affecting sodium stimulation of carnitine transport in the OCTN2 carnitine/organic cation transporter (English)

1 reference

5 December 2017

author name string

Cristina Amat di San Filippo

series ordinal

1

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5 December 2017

Nicola Longo

series ordinal

2

1 reference

5 December 2017

language of work or name

English

0 references

publication date

9 December 2003

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Journal of Biological Chemistry

5 December 2017

published in

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5 December 2017

volume

279

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5 December 2017

issue

8

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5 December 2017

page(s)

7247-7253

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Primary and secondary alterations of neonatal carnitine metabolism.

5 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

cDNA sequence, transport function, and genomic organization of human OCTN2, a new member of the organic cation transporter family

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Molecular and functional identification of sodium ion-dependent, high affinity human carnitine transporter OCTN2

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency: lack of genotype-phenotype correlation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Phenotype and genotype variation in primary carnitine deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Functional characteristics and tissue distribution pattern of organic cation transporter 2 (OCTN2), an organic cation/carnitine transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Studies on functional sites of organic cation/carnitine transporter OCTN2 (SLC22A5) using a Ser467Cys mutant protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

A missense mutation in the OCTN2 gene associated with residual carnitine transport activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Tyrosine residues are essential for the activity of the human placental taurine transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Mutations in the organic cation/carnitine transporter OCTN2 in primary carnitine deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Membrane localization of the electrogenic cation transporter rOCT1 in rat liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Structure and mechanism of the lactose permease of Escherichia coli

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Structure and mechanism of the glycerol-3-phosphate transporter from Escherichia coli

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Abnormal sodium stimulation of carnitine transport in primary carnitine deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

Functional characterization of the carnitine transporter defective in primary carnitine deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309171200

21 January 2018

Identifiers

DOI

10.1074/JBC.M309171200

1 reference

release_pkcs3tyrfjbpddg524344qohge

5 December 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/pkcs3tyrfjbpddg524344qohge

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference