Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome.
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Medical treatment of aortic aneurysms in Marfan syndrome and other heritable conditionsHuman genetic variation influences vitamin C homeostasis by altering vitamin C transport and antioxidant enzyme functionDysregulated hepatic expression of glucose transporters in chronic disease: contribution of semicarbazide-sensitive amine oxidase to hepatic glucose uptakeUnderstanding pyrroline-5-carboxylate synthetase deficiency: clinical, molecular, functional, and expression studies, structure-based analysis, and novel therapy with argininePostnatal exposure to chromium through mother's milk accelerates follicular atresia in F1 offspring through increased oxidative stress and depletion of antioxidant enzymesCutis laxa: intersection of elastic fiber biogenesis, TGFβ signaling, the secretory pathway and metabolismThe Concise Guide to PHARMACOLOGY 2013/14: transporters.The SLC2 (GLUT) family of membrane transporters.The pathobiology of vascular malformations: insights from human and model organism genetics.Arterial Tortuosity Syndrome: homozygosity for two novel and one recurrent SLC2A10 missense mutations in three families with severe cardiopulmonary complications in infancy and a literature review.GLUT10 is required for the development of the cardiovascular system and the notochord and connects mitochondrial function to TGFβ signalingGLUT10 deficiency leads to oxidative stress and non-canonical αvβ3 integrin-mediated TGFβ signalling associated with extracellular matrix disarray in arterial tortuosity syndrome skin fibroblastsA mitochondria-targeted derivative of ascorbate: MitoC.Expression of conventional and novel glucose transporters, GLUT1, -9, -10, and -12, in vascular smooth muscle cellsHepatic expression and cellular distribution of the glucose transporter family.Ascorbic acid repletion: A possible therapy for diabetic macular edema?U937 cell apoptosis induced by arsenite is prevented by low concentrations of mitochondrial ascorbic acid with hardly any effect mediated by the cytosolic fraction of the vitamin.Fructose transport-deficient Staphylococcus aureus reveals important role of epithelial glucose transporters in limiting sugar-driven bacterial growth in airway surface liquidMitochondrial ascorbic acid is responsible for enhanced susceptibility of U937 cells to the toxic effects of peroxynitrite.Mitochondrial uncoupler carbonyl cyanide M-chlorophenylhydrazone induces the multimer assembly and activity of repair enzyme protein L-isoaspartyl methyltransferase.The complexity of elastic fibre biogenesis in the skin--a perspective to the clinical heterogeneity of cutis laxa.Thymosin β₄ knockdown disrupts mitochondrial functions of SW480 human colon cancer cells.Distribution of glucose transporters in renal diseases.GLUT10-Lacking in Arterial Tortuosity Syndrome-Is Localized to the Endoplasmic Reticulum of Human Fibroblasts.A computer model simulating human glucose absorption and metabolism in health and metabolic disease states.GLUT10 Maintains the Integrity of Major Arteries through Regulation of Redox Homeostasis and Mitochondrial Function.Effect of heat stress on protein utilization and nutrient transporters in meat-type chickens.Arterial tortuosity syndrome: 40 new families and literature review.GLUT4 Is Not Necessary for Overload-Induced Glucose Uptake or Hypertrophic Growth in Mouse Skeletal Muscle.Affinity resins as new tools for identifying target proteins of ascorbic acid.Glucose transporter type 10-lacking in arterial tortuosity syndrome-facilitates dehydroascorbic acid transport.Defect in proline synthesis: pyrroline-5-carboxylate reductase 1 deficiency leads to a complex clinical phenotype with collagen and elastin abnormalities.Multifaced Roles of the αvβ3 Integrin in Ehlers-Danlos and Arterial Tortuosity Syndromes' Dermal Fibroblasts.Melatonin transport into mitochondria.Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity.Adult presentation of arterial tortuosity syndrome in a 51-year-old woman with a novel homozygous c.1411+1G>A mutation in the SLC2A10 gene
P2860
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P2860
Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
name
Mitochondrial GLUT10 facilitat ...... arterial tortuosity syndrome.
@ast
Mitochondrial GLUT10 facilitat ...... arterial tortuosity syndrome.
@en
Mitochondrial GLUT10 facilitat ...... arterial tortuosity syndrome.
@nl
type
label
Mitochondrial GLUT10 facilitat ...... arterial tortuosity syndrome.
@ast
Mitochondrial GLUT10 facilitat ...... arterial tortuosity syndrome.
@en
Mitochondrial GLUT10 facilitat ...... arterial tortuosity syndrome.
@nl
prefLabel
Mitochondrial GLUT10 facilitat ...... arterial tortuosity syndrome.
@ast
Mitochondrial GLUT10 facilitat ...... arterial tortuosity syndrome.
@en
Mitochondrial GLUT10 facilitat ...... arterial tortuosity syndrome.
@nl
P2093
P2860
P356
P1476
Mitochondrial GLUT10 facilitat ...... arterial tortuosity syndrome.
@en
P2093
Chao-Hung Cheng
Chia-Jung Chang
Hsun-Yi Huang
Yi-Ching Lee
P2860
P304
P356
10.1093/HMG/DDQ286
P577
2010-07-16T00:00:00Z