Mutations in the SLC2A10 gene cause arterial abnormalities in mice (Q46231602)

20 December 2017

title

Mutations in the SLC2A10 gene cause arterial abnormalities in mice (English)

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20 December 2017

8

Yuan-Tsong Chen

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20 December 2017

Yi-Ching Lee

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author name string

Chao-Hung Cheng

1

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20 December 2017

Tateki Kikuchi

2

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20 December 2017

Yen-Hui Chen

3

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20 December 2017

Nagham George Abd-Al-Ahad Sabbagha

4

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20 December 2017

Yi-Ching Lee

5

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20 December 2017

Huei-Ju Pan

6

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20 December 2017

Chen Chang

7

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20 December 2017

publication date

21 November 2008

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20 December 2017

published in

Cardiovascular Research

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20 December 2017

volume

81

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20 December 2017

issue

2

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20 December 2017

page(s)

381-388

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20 December 2017

The extended GLUT-family of sugar/polyol transport facilitators: nomenclature, sequence characteristics, and potential function of its novel members (review)

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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

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

21 January 2018

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GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood-brain barrier hexose carrier

21 January 2018

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Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome.

21 January 2018

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Glucose transporter-1-deficient mice exhibit impaired development and deformities that are similar to diabetic embryopathy.

21 January 2018

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

21 January 2018

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

21 January 2018

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Aneurysm syndromes caused by mutations in the TGF-beta receptor

21 January 2018

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A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

21 January 2018

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Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan syndrome-related disorders.

21 January 2018

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Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

21 January 2018

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Comprehensive molecular screening of the FBN1 gene favors locus homogeneity of classical Marfan syndrome

21 January 2018

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Mutations in transforming growth factor-beta receptor type II cause familial thoracic aortic aneurysms and dissections

21 January 2018

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Abnormal angiogenesis but intact hematopoietic potential in TGF-beta type I receptor-deficient mice

21 January 2018

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Perinatal lethality and endothelial cell abnormalities in several vessel compartments of fibulin-1-deficient mice

21 January 2018

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Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1

21 January 2018

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Perturbations of vascular homeostasis and aortic valve abnormalities in fibulin-4 deficient mice.

21 January 2018

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Mutation of mouse Mayp/Pstpip2 causes a macrophage autoinflammatory disease.

21 January 2018

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A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy.

21 January 2018

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21 January 2018

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Efficient and fast targeted production of murine models based on ENU mutagenesis

21 January 2018

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Four sibs with arterial tortuosity: description and review of the literature

21 January 2018

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New insights into elastin and vascular disease.

21 January 2018

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Connective tissue growth factor mediates high glucose effects on matrix degradation through tissue inhibitor of matrix metalloproteinase type 1: implications for diabetic nephropathy

21 January 2018

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Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes

21 January 2018

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Analysis of the accuracy and implications of simple methods for predicting the secondary structure of globular proteins

21 January 2018

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21 January 2018

Identifiers

DOI

10.1093/CVR/CVN319

1 reference

20 December 2017

PubMed ID

19028722

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20 December 2017