Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia - sprookjes - yvandenbroek - TriplyDB

Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia

Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia

http://www.wikidata.org/entity/Q24294711

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Abetalipoproteinemia: two case reports and literature review Multiple functions of microsomal triglyceride transfer protein Taurine reduces the secretion of apolipoprotein B100 and lipids in HepG2 cells Proteomic analysis of the enterocyte brush border Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia Lysophosphatidylcholine acyltransferase 3 knockdown-mediated liver lysophosphatidylcholine accumulation promotes very low density lipoprotein production by enhancing microsomal triglyceride transfer protein expression Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein Function Molecular characterization of Tunisian families with abetalipoproteinemia and identification of a novel mutation in MTTP gene Molecular processes that handle -- and mishandle -- dietary lipids Mutations of the microsomal triglyceride-transfer-protein gene in abetalipoproteinemia Mechanisms of lipid malabsorption in Cystic Fibrosis: the impact of essential fatty acids deficiency New drugs for treating dyslipidemia: beyond statins Familial hypercholesterolemia: present and future management New Era of Lipid-Lowering Drugs Familial hypobetalipoproteinemia: a review Nascent lipidated apolipoprotein B is transported to the Golgi as an incompletely folded intermediate as probed by its association with network of endoplasmic reticulum molecular chaperones, GRP94, ERp72, BiP, calreticulin, and cyclophilin B A novel abetalipoproteinemia genotype. Identification of a missense mutation in the 97-kDa subunit of the microsomal triglyceride transfer protein that prevents complex formation with protein disulfide isomerase Monogenic dyslipidemias: window on determinants of plasma lipoprotein metabolism apo B gene knockout in mice results in embryonic lethality in homozygotes and neural tube defects, male infertility, and reduced HDL cholesterol ester and apo A-I transport rates in heterozygotes Identification of a novel isoform of microsomal triglyceride transfer protein A deficiency of microsomal triglyceride transfer protein reduces apolipoprotein B secretion In vivo biochemical and gene expression analyses of the antioxidant activities and hypocholesterolaemic properties of Tamarindus indica fruit pulp extract ARP-1/COUP-TF II determines hepatoma phenotype by acting as both a transcriptional repressor of microsomal triglyceride transfer protein and an inducer of CYP7A1 Demonstration of a physical interaction between microsomal triglyceride transfer protein and apolipoprotein B during the assembly of ApoB-containing lipoproteins Interfacial properties of apolipoprotein B292-593 (B6.4-13) and B611-782 (B13-17). Insights into the structure of the lipovitellin homology region in apolipoprotein B.Autosomal recessive cerebellar ataxias.Expression of microsomal triglyceride transfer protein in lipoprotein-synthesizing tissues of the developing chicken embryo Inhibition of hepatic microsomal triglyceride transfer protein - a novel therapeutic option for treatment of homozygous familial hypercholesterolemia Apolipoprotein B-containing lipoproteins in retinal aging and age-related macular degeneration.Analysis of the role of microsomal triglyceride transfer protein in the liver of tissue-specific knockout mice.Recent progress in understanding protein and lipid factors affecting hepatic VLDL assembly and secretion.Apolipoprotein B-containing lipoprotein assembly in microsomal triglyceride transfer protein-deficient McA-RH7777 cells.Lipid antigens in immunity.A powerful test of parent-of-origin effects for quantitative traits using haplotypes A severe form of abetalipoproteinemia caused by new splicing mutations of microsomal triglyceride transfer protein (MTTP).Guidelines for the diagnosis and management of chylomicron retention disease based on a review of the literature and the experience of two centers.The significance of genetic polymorphisms in modulating the response to lipid-lowering drugs.Therapeutic considerations for postprandial dyslipidaemia.Jejunal wall triglyceride concentration of morbidly obese persons is lower in those with type 2 diabetes mellitus.The polymorphism at codon 54 of the FABP2 gene increases fat absorption in human intestinal explants.

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P2860

Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia

http://www.wikidata.org/entity/Q24294711

description

1992 nî lūn-bûn

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1992 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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1992 թվականի նոյեմբերին հրատարակված գիտական հոդված

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1992年の論文

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1992年論文

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1992年論文

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1992年論文

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1992年論文

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1992年论文

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name

Absence of microsomal triglyce ...... uals with abetalipoproteinemia

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Absence of microsomal triglyce ...... uals with abetalipoproteinemia

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Absence of microsomal triglyce ...... uals with abetalipoproteinemia

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Absence of microsomal triglyce ...... uals with abetalipoproteinemia

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Absence of microsomal triglyce ...... uals with abetalipoproteinemia

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Absence of microsomal triglyce ...... uals with abetalipoproteinemia

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Absence of microsomal triglyce ...... uals with abetalipoproteinemia

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Absence of microsomal triglyce ...... uals with abetalipoproteinemia

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Absence of microsomal triglyce ...... uals with abetalipoproteinemia

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Absence of microsomal triglyce ...... uals with abetalipoproteinemia

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Absence of microsomal triglyce ...... uals with abetalipoproteinemia

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Absence of microsomal triglyce ...... uals with abetalipoproteinemia

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Absence of microsomal triglyce ...... uals with abetalipoproteinemia

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Microsomal triglyceride transfer protein

lipid metabolism

abetalipoproteinemia