Glucose transporter 10 and arterial tortuosity syndrome: the vitamin C connection (Q37765032)

22 August 2017

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title

Glucose transporter 10 and arterial tortuosity syndrome: the vitamin C connection (English)

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arterial tortuosity syndrome

22 August 2017

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Fernando Segade

1

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PubMed ID

20547159

22 August 2017

language of work or name

English

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publication date

12 June 2010

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22 August 2017

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22 August 2017

584

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22 August 2017

14

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22 August 2017

2990-2994

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Biophysical mechanisms of stroke

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Ischemic stroke in an adolescent with arterial tortuosity syndrome

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Tortuosity, kinking, and coiling of the carotid artery: expression of atherosclerosis or aging?

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Three new families with arterial tortuosity syndrome.

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families.

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari families

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Glucose transporters in the 21st Century

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Sequence and functional analysis of GLUT10: a glucose transporter in the Type 2 diabetes-linked region of chromosome 20q12-13.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Molecular cloning of a novel member of the GLUT family of transporters, SLC2a10 (GLUT10), localized on chromosome 20q13.1: a candidate gene for NIDDM susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Expression of Class III facilitative glucose transporter genes (GLUT-10 and GLUT-12) in mouse and human adipose tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Genetic analysis of the GLUT10 glucose transporter (SLC2A10) polymorphisms in Caucasian American type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Isozymes of mammalian hexokinase: structure, subcellular localization and metabolic function

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Live imaging of glucose homeostasis in nuclei of COS-7 cells

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Diffusion across the nuclear envelope inhibited by depletion of the nuclear Ca2+ store.

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

ChREBP, a transcriptional regulator of glucose and lipid metabolism

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

O-GlcNAc modification of transcription factors, glucose sensing and glucotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Cysteine-scanning mutagenesis of transmembrane segment 7 of the GLUT1 glucose transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Collagens, modifying enzymes and their mutations in humans, flies and worms

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Elastic fibres in health and disease

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Vitamin C. Biosynthesis, recycling and degradation in mammals

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

The biochemical functions of ascorbic acid

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Vitamin C transport systems of mammalian cells

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Protein-disulfide isomerase- and protein thiol-dependent dehydroascorbate reduction and ascorbate accumulation in the lumen of the endoplasmic reticulum

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Cardiovascular malformations in infants of diabetic mothers

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Disturbed morphogenesis of cardiac outflow tract and increased rate of aortic arch anomalies in the offspring of diabetic rats

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Vitamin C supplementation of the maternal diet reduces the rate of malformation in the offspring of diabetic rats.

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Aortic wall damage in mice unable to synthesize ascorbic acid

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Fibulin-5/DANCE is essential for elastogenesis in vivo

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Making sense of latent TGFbeta activation

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Dysregulation of TGF-beta activation contributes to pathogenesis in Marfan syndrome

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Elastin is an essential determinant of arterial morphogenesis

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Mutations in the SLC2A10 gene cause arterial abnormalities in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

Absence of arterial phenotype in mice with homozygous slc2A10 missense substitutions

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.06.011

10.1016/J.FEBSLET.2010.06.011

21 January 2018

Identifiers

DOI

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22 August 2017

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PubMed ID

20547159