Functional analysis of disulfide linkages clustered within the amino terminus of human apolipoprotein B.
about
Multiple molecular chaperones interact with apolipoprotein B during its maturation. The network of endoplasmic reticulum-resident chaperones (ERp72, GRP94, calreticulin, and BiP) interacts with apolipoprotein b regardless of its lipidation stateMicrosomal triglyceride transfer protein and its role in apoB-lipoprotein assemblyInterfacial 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.Nonsynonymous mutations within APOB in human familial hypobetalipoproteinemia: evidence for feedback inhibition of lipogenesis and postendoplasmic reticulum degradation of apolipoprotein BRecent progress in understanding protein and lipid factors affecting hepatic VLDL assembly and secretion.Apolipoprotein B metabolism: tracer kinetics, models, and metabolic studies.Identification of protein disulfide isomerase 1 as a key isomerase for disulfide bond formation in apolipoprotein B100.Protein disulfide isomerases contribute differentially to the endoplasmic reticulum-associated degradation of apolipoprotein B and other substratesMTP inhibition as a treatment for dyslipidaemias: time to deliver or empty promises?Defining lipid-interacting domains in the N-terminal region of apolipoprotein B.Reconstituting initial events during the assembly of apolipoprotein B-containing lipoproteins in a cell-free system.Apolipoprotein B100 biogenesis: a complex array of intracellular mechanisms regulating folding, stability, and lipoprotein assembly.A novel nontruncating APOB gene mutation, R463W, causes familial hypobetalipoproteinemia.Assembly and secretion of very low density lipoproteins containing apolipoprotein B48 in transfected McA-RH7777 cells. Lack of evidence that palmitoylation of apolipoprotein B48 is required for lipoprotein secretion.Identification of the proteoglycan binding site in apolipoprotein B48.Disruption of disulfide bonds is responsible for impaired secretion in human complement factor H deficiency.Identification of domains in apolipoprotein B100 that confer a high requirement for the microsomal triglyceride transfer protein.The N-linked oligosaccharides at the amino terminus of human apoB are important for the assembly and secretion of VLDL.A malfunction in triglyceride transfer from the intracellular lipid pool to apoB in enterocytes of SOD1-deficient mice.Interfacial properties of amphipathic beta strand consensus peptides of apolipoprotein B at oil/water interfaces.Can modulators of apolipoproteinB biogenesis serve as an alternate target for cholesterol-lowering drugs?Mutual interaction between oxidative stress and endoplasmic reticulum stress in the pathogenesis of diseases specifically focusing on non-alcoholic fatty liver disease
P2860
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P2860
Functional analysis of disulfide linkages clustered within the amino terminus of human apolipoprotein B.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh-hant
name
Functional analysis of disulfi ...... nus of human apolipoprotein B.
@en
Functional analysis of disulfi ...... nus of human apolipoprotein B.
@nl
type
label
Functional analysis of disulfi ...... nus of human apolipoprotein B.
@en
Functional analysis of disulfi ...... nus of human apolipoprotein B.
@nl
prefLabel
Functional analysis of disulfi ...... nus of human apolipoprotein B.
@en
Functional analysis of disulfi ...... nus of human apolipoprotein B.
@nl
P2093
P2860
P356
P1476
Functional analysis of disulfi ...... nus of human apolipoprotein B.
@en
P2093
Avramoglu RK
P2860
P304
P356
10.1074/JBC.273.13.7244
P407
P577
1998-03-01T00:00:00Z