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Titlebook: Cardiovascular Disease; Molecular and Cellul Linda L. Gallo Book 1987 Springer Science+Business Media New York 1987 Lipid.atherosclerosis.c

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https://doi.org/10.1007/978-0-387-48894-3versus C. but ΔHDL.-C correlated with loss of body fat in E only. Relative to C., HLA was reduced from base line (7.7 ± 0.3 mU/ml per min) in both D (-0.97 ± 0.31, . < 0.01) and E (-0.70 ± 0.30. . < 0.05). whereas increases in LPLA were not significant for D(. < 0.21) or E (.= 0.13) Both ΔHLA and ΔL
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https://doi.org/10.1007/978-3-642-58643-9owing that basic amino acids (lysine and arginine) of the ligands (apo E and apo B) mediate receptor binding. The receptor-binding domain of apo E has been localized to basic amino acids in the vicinity of residues 140 to 160. Naturally occurring variants of apo E with single amino acid substitution
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Pain from Metastatic Bone Tumorsa 58-amino-acid region that contains up to 18 carbohydrate chains linked to serine or threonine, and a 22-amino-acid membrane-spanning region..Mutations in the LDL receptor gene are responsible for familial hypercholesterolemia (FH), an autosomal dominant disease that affects one out of every 500 pe
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Lymphoscintigraphy in Malignant Diseasezygous E. or E. phenotype. The decreased LDL concentration in the E. subjects was secondary to both a decreased synthesis rate and an increased fractional catabolic rate (FCR) of LDL. When the FCR of the LDL from both types of subjects were compared in the same subject, the LDL from the E. subject w
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Pain from Metastatic Bone Tumorsntracellular cholesterol content. Uptake of A-LDL did not appear to occur via the scavenger receptor on MPM since (1) pretreatment of cells with trypsin resulted in less inhibition of cholesterol esterification by A-LDL than by acetyl-LDL, and (2) cross-competition studies with radiolabeled ligands
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Novel Radiopharmaceuticals for TherapyAfter oxidation by exposure to 5 μM CuSO4 for 24 hr, the radioactivity bound to protein was significantly greater than that in nonoxidized control LDL or in oxidized LDL labeled with 2-[l-.C]palmitoylphosphatidylcholine. Ultrafiltration revealed that 20-30% of the total label from arachi-donate was
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Analysis of the , Translation Product of mRNA Coding for Chick Intestine Apolipoprotein A-Ipolymerase. This . transcribed RNA was then translated in a cell-free system in the presence of [.S]methionine. The primary translation product was immunoprecipitated with anti-apo A-I antiserum and subjected to two-dimensional gel electrophoresis. The isoform pattern of this translation product was
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