Complete protein sequence and identification of structural domains of human apolipoprotein B
about
Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100LDL receptor/lipoprotein recognition: endosomal weakening of ApoB and ApoE binding to the convex face of the LR5 repeatInduction of RNA editing at heterologous sites by sequences in apolipoprotein B mRNATranslational control mechanisms in metabolic regulation: critical role of RNA binding proteins, microRNAs, and cytoplasmic RNA granulesSecondary structure for the apolipoprotein B mRNA editing site. Au-binding proteins interact with a stem loopMultiple functions encoded by the N-terminal PAT domain of adipophilinapo 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 and characterization of a 315-base pair enhancer, located more than 55 kilobases 5' of the apolipoprotein B gene, that confers expression in the intestineA worldwide population study of the Ag-system haplotypes, a genetic polymorphism of human low-density lipoproteinTopological mapping of complement component C9 by recombinant DNA techniques suggests a novel mechanism for its insertion into target membranes.Familial defective apolipoprotein B-100: enhanced binding of monoclonal antibody MB47 to abnormal low density lipoproteins.Isolation and characterization of sulfhydryl and disulfide peptides of human apolipoprotein B-100.Specific postendocytic proteolysis of apolipoprotein B in oocytes does not abolish receptor recognition.Truncated apo B-70.5-containing lipoproteins bind to megalin but not the LDL receptorApolipoprotein B-containing lipoprotein assembly in microsomal triglyceride transfer protein-deficient McA-RH7777 cells.Resonance energy transfer from a cylindrical distribution of donors to a plane of acceptors. Location of apo-B100 protein on the human low-density lipoprotein particle.Cryoelectron microscopy of low density lipoprotein in vitreous iceAnderson's disease: genetic exclusion of the apolipoprotein-B gene in two familiesMolecular and metabolic basis for the metabolic disorder normotriglyceridemic abetalipoproteinemiaFamilial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the fCatabolic rate of low density lipoprotein is influenced by variation in the apolipoprotein B geneInference of a molecular defect of apolipoprotein B in hypobetalipoproteinemia by linkage analysis in a large kindredApolipoprotein B metabolism: tracer kinetics, models, and metabolic studies.Murine mammary-derived cells secrete the N-terminal 41% of human apolipoprotein B on high density lipoprotein-sized lipoproteins containing a triacylglycerol-rich core.Negatively cooperative binding of high-density lipoprotein to the HDL receptor SR-BIExpression of human apolipoprotein B and assembly of lipoprotein(a) in transgenic mice.Identification of individuals by analysis of biallelic DNA markers, using PCR and solid-phase minisequencingThree-dimensional structure of low density lipoproteins by electron cryomicroscopyFamilial ligand-defective apolipoprotein B. Identification of a new mutation that decreases LDL receptor binding affinity.Structural relationship of human apolipoprotein B48 to apolipoprotein B100.Recent advances in lipoprotein and atherosclerosis research at Baylor College of Medicine. Apolipoprotein B, lipoprotein[a], and transplantation arteriopathyIncreased catabolic rate of low density lipoproteins in humans with cholesteryl ester transfer protein deficiencyConformation and stability properties of B17: I. Analytical investigations using circular dichroism.Liver, lipoproteins and disease: I. Biochemistry of lipoprotein metabolism.Truncated variants of apolipoprotein B cause hypobetalipoproteinaemiaThe small leucine-rich repeat proteoglycans in tissue repair and atherosclerosisIdentification of two regions in apolipoprotein B100 that are exposed on the cytosolic side of the endoplasmic reticulum membraneMonogenic hypocholesterolaemic lipid disorders and apolipoprotein B metabolism.Specificity and promiscuity among naturally processed peptides bound to HLA-DR alleles.Autosomal dominant hypercholesterolemia: needs for early diagnosis and cascade screening in the tunisian population.
P2860
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P2860
Complete protein sequence and identification of structural domains of human apolipoprotein B
description
1986 nî lūn-bûn
@nan
1986 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1986 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
name
Complete protein sequence and ...... ains of human apolipoprotein B
@ast
Complete protein sequence and ...... ains of human apolipoprotein B
@en
Complete protein sequence and ...... ains of human apolipoprotein B
@nl
type
label
Complete protein sequence and ...... ains of human apolipoprotein B
@ast
Complete protein sequence and ...... ains of human apolipoprotein B
@en
Complete protein sequence and ...... ains of human apolipoprotein B
@nl
prefLabel
Complete protein sequence and ...... ains of human apolipoprotein B
@ast
Complete protein sequence and ...... ains of human apolipoprotein B
@en
Complete protein sequence and ...... ains of human apolipoprotein B
@nl
P2093
P356
P1433
P1476
Complete protein sequence and ...... ains of human apolipoprotein B
@en
P2093
B Blackhart
L M Powell
S C Wallis
T L Innerarity
W H Taylor
P2888
P356
10.1038/323734A0
P407
P577
1986-10-01T00:00:00Z
P6179
1025706495