Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia
about
Abetalipoproteinemia: two case reports and literature reviewMultiple functions of microsomal triglyceride transfer proteinTaurine reduces the secretion of apolipoprotein B100 and lipids in HepG2 cellsProteomic analysis of the enterocyte brush borderMolecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemiaLysophosphatidylcholine acyltransferase 3 knockdown-mediated liver lysophosphatidylcholine accumulation promotes very low density lipoprotein production by enhancing microsomal triglyceride transfer protein expressionNovel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein FunctionMolecular characterization of Tunisian families with abetalipoproteinemia and identification of a novel mutation in MTTP geneMolecular processes that handle -- and mishandle -- dietary lipidsMutations of the microsomal triglyceride-transfer-protein gene in abetalipoproteinemiaMechanisms of lipid malabsorption in Cystic Fibrosis: the impact of essential fatty acids deficiencyNew drugs for treating dyslipidemia: beyond statinsFamilial hypercholesterolemia: present and future managementNew Era of Lipid-Lowering DrugsFamilial hypobetalipoproteinemia: a reviewNascent 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 BA 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 isomeraseMonogenic dyslipidemias: window on determinants of plasma lipoprotein metabolismapo 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 heterozygotesIdentification of a novel isoform of microsomal triglyceride transfer proteinA deficiency of microsomal triglyceride transfer protein reduces apolipoprotein B secretionIn vivo biochemical and gene expression analyses of the antioxidant activities and hypocholesterolaemic properties of Tamarindus indica fruit pulp extractARP-1/COUP-TF II determines hepatoma phenotype by acting as both a transcriptional repressor of microsomal triglyceride transfer protein and an inducer of CYP7A1Demonstration of a physical interaction between microsomal triglyceride transfer protein and apolipoprotein B during the assembly of ApoB-containing lipoproteinsInterfacial 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 embryoInhibition of hepatic microsomal triglyceride transfer protein - a novel therapeutic option for treatment of homozygous familial hypercholesterolemiaApolipoprotein 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 haplotypesA 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.
P2860
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P2860
Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia
description
1992 nî lūn-bûn
@nan
1992 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Absence of microsomal triglyce ...... uals with abetalipoproteinemia
@ast
Absence of microsomal triglyce ...... uals with abetalipoproteinemia
@en
Absence of microsomal triglyce ...... uals with abetalipoproteinemia
@en-gb
Absence of microsomal triglyce ...... uals with abetalipoproteinemia
@nl
type
label
Absence of microsomal triglyce ...... uals with abetalipoproteinemia
@ast
Absence of microsomal triglyce ...... uals with abetalipoproteinemia
@en
Absence of microsomal triglyce ...... uals with abetalipoproteinemia
@en-gb
Absence of microsomal triglyce ...... uals with abetalipoproteinemia
@nl
prefLabel
Absence of microsomal triglyce ...... uals with abetalipoproteinemia
@ast
Absence of microsomal triglyce ...... uals with abetalipoproteinemia
@en
Absence of microsomal triglyce ...... uals with abetalipoproteinemia
@en-gb
Absence of microsomal triglyce ...... uals with abetalipoproteinemia
@nl
P2093
P921
P3181
P356
P1433
P1476
Absence of microsomal triglyce ...... uals with abetalipoproteinemia
@en
P2093
C Eisenberg
J R Wetterau
L P Aggerbeck
P304
P3181
P356
10.1126/SCIENCE.1439810
P407
P577
1992-11-06T00:00:00Z