The alpha-tocopherol transfer protein (Q28236418)

https://doi.org/10.1016%2FS0083-6729%2807%2976003-X

26 March 2017

author name string

D Manor

1

0 references

S Morley

2

0 references

D. Manor

1

1 reference

https://doi.org/10.1016%2FS0083-6729%2807%2976003-X

26 March 2017

S. Morley

2

1 reference

https://doi.org/10.1016%2FS0083-6729%2807%2976003-X

26 March 2017

language of work or name

English

0 references

publication date

2007

1 reference

https://doi.org/10.1016%2FS0083-6729%2807%2976003-X

26 March 2017

published in

Vitamins and Hormones

1 reference

https://doi.org/10.1016%2FS0083-6729%2807%2976003-X

26 March 2017

volume

76

0 references

page(s)

45-65

1 reference

https://doi.org/10.1016%2FS0083-6729%2807%2976003-X

Familial isolated vitamin E deficiency. Extensive study of a large family with a 5-year therapeutic follow-up.

26 March 2017

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Myoclonic dystonia as unique presentation of isolated vitamin E deficiency in a young patient

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Ataxia with isolated vitamin E deficiency: case report and review of the literature

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Human alpha-tocopherol transfer protein: cDNA cloning, expression and chromosomal localization

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Fluorescent tocopherols as probes of inter-vesicular transfer catalyzed by the alpha-tocopherol transfer protein

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An essential role for a phospholipid transfer protein in yeast Golgi function

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Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families.

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Secretion of alpha-tocopherol from cultured rat hepatocytes.

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Vitamin E kinetics and the function of tocopherol regulatory proteins

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Neuromyopathy and vitamin E deficiency in man

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Vitamin E: molecular and biological function

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An α-tocopherol binding protein in rat liver cytoplasm

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Rat liver alpha-tocopherol binding protein

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Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families

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A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia

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Chiral discrimination in the exchange of alpha-tocopherol stereoisomers between plasma and red blood cells

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Plasma clearance and net uptake of alpha-tocopherol and low-density lipoprotein by tissues in WHHL and control rabbits

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Localization of alpha-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disorders.

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Multiple sequence alignment with hierarchical clustering

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ON THE EXISTENCE OF A HITHERTO UNRECOGNIZED DIETARY FACTOR ESSENTIAL FOR REPRODUCTION.

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High-density lipoprotein (HDL3)-associated alpha-tocopherol is taken up by HepG2 cells via the selective uptake pathway and resecreted with endogenously synthesized apo-lipoprotein B-rich lipoprotein particles

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7 January 2021

Adult-onset spinocerebellar dysfunction caused by a mutation in the gene for the alpha-tocopherol-transfer protein

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7 January 2021

Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiency

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7 January 2021

pH‐dependent translocation of α‐tocopherol transfer protein (α‐TTP) between hepatic cytosol and late endosomes

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7 January 2021

Ataxia with isolated vitamin E deficiency: a Japanese family carrying a novel mutation in the alpha-tocopherol transfer protein gene

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Affinity for alpha-tocopherol transfer protein as a determinant of the biological activities of vitamin E analogs

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Localization of alpha-tocopherol transfer protein in rat brain.

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Biokinetics of and discrimination between dietary RRR- and SRR-alpha-tocopherols in the male rat

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Alpha-tocopherol transfer protein is important for the normal development of placental labyrinthine trophoblasts in mice

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7 January 2021

Vitamin E is essential for mouse placentation but not for embryonic development itself

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7 January 2021

Alpha-tocopherol transfer protein is specifically localized at the implantation site of pregnant mouse uterus

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7 January 2021

Human placental trophoblast cells express alpha-tocopherol transfer protein

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7 January 2021

Tocopherol-binding proteins of hepatic cytosol

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7 January 2021

Inter- and intra-individual vitamin E uptake in healthy subjects is highly repeatable across a wide supplementation dose range

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7 January 2021

Isolated deficiency of vitamin E with progressive neurologic deterioration

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7 January 2021

Identification, purification, and immunochemical characterization of a tocopherol-binding protein in rat liver cytosol

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7 January 2021

Effects of long-term vitamin E supplementation on cardiovascular events and cancer: a randomized controlled trial

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Is tocopherol associated protein a misnomer?

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Alpha-tocopherol metabolism is abnormal in scavenger receptor class B type I (SR-BI)-deficient mice.

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Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families

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Supplemental therapy in isolated vitamin E deficiency improves the peripheral neuropathy and prevents the progression of ataxia

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7 January 2021

Kinetics of transfer of alpha-tocopherol between model and native plasma lipoproteins.

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The cytotoxicity of vitamin E is both vitamer- and cell-specific and involves a selectable trait

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Vitamin E deficiency in dogs with retinal pigment epithelial dystrophy

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The molecular basis of vitamin E retention: structure of human alpha-tocopherol transfer protein

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Crystal structure of human alpha-tocopherol transfer protein bound to its ligand: implications for ataxia with vitamin E deficiency

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Absence of VLDL secretion does not affect alpha-tocopherol content in peripheral tissues

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Molecular determinants of heritable vitamin E deficiency

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Utility of a fluorescent vitamin E analogue as a probe for tocopherol transfer protein activity

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7 January 2021

Transfer of steroids and alpha-tocopherol between liposomal membranes

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7 January 2021

Preparation of fluorescent tocopherols for use in protein binding and localization with the alpha-tocopherol transfer protein

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7 January 2021

ATP-binding cassette transporter A1 mediates cellular secretion of alpha-tocopherol

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7 January 2021

Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein

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7 January 2021

Ligand specificity in the CRAL-TRIO protein family

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7 January 2021

Clinicopathological report of retinitis pigmentosa with vitamin E deficiency caused by mutation of the alpha-tocopherol transfer protein gene

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7 January 2021

Distribution of alpha- and gamma-tocopherols in Atlantic salmon (Salmo salar) tissues.

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7 January 2021

Selective accumulation of alpha-tocopherol in Drosophila is associated with cytochrome P450 tocopherol-omega-hydroxylase activity but not alpha-tocopherol transfer protein

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Vitamin E suppresses isoprostane generation in vivo and reduces atherosclerosis in ApoE-deficient mice

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Supplementation with low doses of vitamin E protects LDL from lipid peroxidation in men and women.

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Intracellular trafficking of vitamin E in hepatocytes: the role of tocopherol transfer protein

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Biochemical consequences of heritable mutations in the alpha-tocopherol transfer protein

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Ataxia with vitamin E deficiency and severe dystonia: report of a case

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Inter- and intra-individual variation in plasma and red blood cell vitamin E after supplementation.

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Glycolipid transfer protein and intracellular traffic of glucosylceramide

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Purification and characterization of the alpha-tocopherol transfer protein from rat liver

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Enhanced inflammatory responses in alpha-tocopherol transfer protein null mice.

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Treatment of ataxia in isolated vitamin E deficiency caused by alpha-tocopherol transfer protein deficiency

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Vitamin E deficiency and neurologic disease

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Randomised controlled trial of vitamin E in patients with coronary disease: Cambridge Heart Antioxidant Study (CHAOS)

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Supernatant protein factor in complex with RRR-alpha-tocopherylquinone: a link between oxidized Vitamin E and cholesterol biosynthesis

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Friedreich's disease: V. Variant form with vitamin E deficiency and normal fat absorption

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Antioxidant systems of the avian embryo: tissue-specific accumulation and distribution of vitamin E in the turkey embryo during development

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alpha-Tocopherol transfer protein gene: exon skipping of all transcripts causes ataxia

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Increased atherosclerosis in hyperlipidemic mice deficient in alpha -tocopherol transfer protein and vitamin E

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Vitamin E in humans: demand and delivery

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Ataxia caused by mutations in the alpha-tocopherol transfer protein gene

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Influence of dietary vitamin E on the intermembrane transfer of alpha-tocopherol as mediated by an alpha-tocopherol binding protein

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Retinitis pigmentosa and ataxia caused by a mutation in the gene for the alpha-tocopherol-transfer protein

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7 January 2021

Friedreich-like ataxia with retinitis pigmentosa caused by the His101Gln mutation of the alpha-tocopherol transfer protein gene

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7 January 2021

Postmortem study of ataxia with retinitis pigmentosa by mutation of the alpha-tocopherol transfer protein gene

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7 January 2021

Delayed-onset ataxia in mice lacking alpha -tocopherol transfer protein: model for neuronal degeneration caused by chronic oxidative stress

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7 January 2021

Vitamin E supplementation and cardiovascular events in high-risk patients

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7 January 2021

Vitamin E and vascular homeostasis: implications for atherosclerosis

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7 January 2021

Enhancement of the Transfer of α‐Tocopherol between Liposomes and Mitochondria by Rat‐Liver Protein(s)

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7 January 2021