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Flavonoids regulate LDLR through different mechanisms tied to their specific structures

Journal of lipid research, 2024-05, Vol.65 (5), p.100539-100539, Article 100539

2024

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Variants in the CETP gene affect levels of HDL cholesterol by reducing the amount, and not the specific lipid transfer activity, of secreted CETP

PloS one, 2023-12, Vol.18 (12), p.e0294764-e0294764

2023

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Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia

Clinical genetics, 2004-05, Vol.65 (5), p.419-422

Leren, TP

2004

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Functional characterization of missense variants affecting the extracellular domains of ABCA1 using a fluorescence-based assay

Journal of lipid research, 2024-01, Vol.65 (1), p.100482-100482, Article 100482

2024

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MK-2206, an allosteric inhibitor of AKT, stimulates LDLR expression and LDL uptake: A potential hypocholesterolemic agent

Atherosclerosis, 2018-09, Vol.276, p.28-38

2018

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Right ventricular mechanical dispersion is related to malignant arrhythmias: a study of patients with arrhythmogenic right ventricular cardiomyopathy and subclinical right ventricular dysfunction

European heart journal, 2011-05, Vol.32 (9), p.1089-1096

2011

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Effect of mutations in the PCSK9 gene on the cell surface LDL receptors

Human molecular genetics, 2006-05, Vol.15 (9), p.1551-1558

2006

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PCSK9 acts as a chaperone for the LDL receptor in the endoplasmic reticulum

Biochemical journal, 2014-01, Vol.457 (1), p.99-105

2014

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Sex-specific relevance of diabetes to occlusive vascular and other mortality: a collaborative meta-analysis of individual data from 980 793 adults from 68 prospective studies

The lancet. Diabetes & endocrinology, 2018-07, Vol.6 (7), p.538-546

2018

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Missense mutation Q384K in the APOB gene affecting the large lipid transfer module of apoB reduces the secretion of apoB-100 in the liver without reducing the secretion of apoB-48 in the intestine

Journal of clinical lipidology, 2023-11, Vol.17 (6), p.800-807

2023

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Sorting an LDL receptor with bound PCSK9 to intracellular degradation

Atherosclerosis, 2014-11, Vol.237 (1), p.76-81

Leren, Trond P

2014

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Risk prediction of ventricular arrhythmias and myocardial function in Lamin A/C mutation positive subjects

Europace (London, England), 2014-04, Vol.16 (4), p.563-571

2014

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The risk of various types of cardiovascular diseases in mutation positive familial hypercholesterolemia; a review

Frontiers in genetics, 2022-12, Vol.13, p.1072108-1072108

2022

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The unique role of proprotein convertase subtilisin/kexin 9 in cholesterol homeostasis

Journal of internal medicine, 2009-12, Vol.266 (6), p.507-519

2009

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Subjects with molecularly defined familial hypercholesterolemia or familial defective apoB-100 are not being adequately treated

PloS one, 2011-02, Vol.6 (2), p.e16721-e16721

2011

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Missense mutations in the PCSK9 gene are associated with hypocholesterolemia and possibly increased response to statin therapy

Arteriosclerosis, thrombosis, and vascular biology, 2006-05, Vol.26 (5), p.1094

2006

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Left ventricular mechanical dispersion by tissue Doppler imaging: a novel approach for identifying high-risk individuals with long QT syndrome

European heart journal, 2009-02, Vol.30 (3), p.330-337

2009

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High prevalence of exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia mutation-positive family members diagnosed by cascade genetic screening

Europace (London, England), 2010-03, Vol.12 (3), p.417-423

2010

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PCSK9-mediated degradation of the LDL receptor generates a 17 kDa C-terminal LDL receptor fragment

Journal of lipid research, 2013-06, Vol.54 (6), p.1560-1566

2013

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Role of the C-terminal domain of PCSK9 in degradation of the LDL receptors

Journal of lipid research, 2011-10, Vol.52 (10), p.1787-1794

2011

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Interaction between the ligand-binding domain of the LDL receptor and the C-terminal domain of PCSK9 is required for PCSK9 to remain bound to the LDL receptor during endosomal acidification

Human molecular genetics, 2012-03, Vol.21 (6), p.1402-1409

2012

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Genetics of hypertrophic cardiomyopathy in Norway

Clinical genetics, 2014-10, Vol.86 (4), p.355-360

2014

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Prevalence of cholesteryl ester storage disease among hypercholesterolemic subjects and functional characterization of mutations in the lysosomal acid lipase gene

Molecular genetics and metabolism, 2018-02, Vol.123 (2), p.169-176

2018

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Type 1 hyperlipoproteinemia due to a novel deletion of exons 3 and 4 in the GPIHBP1 gene

Atherosclerosis, 2014-05, Vol.234 (1), p.30-33

2014

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Flavonoids regulate LDLR through different mechanisms tied to their specific structures

Variants in the CETP gene affect levels of HDL cholesterol by reducing the amount, and not the specific lipid transfer activity, of secreted CETP

Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia

Functional characterization of missense variants affecting the extracellular domains of ABCA1 using a fluorescence-based assay

MK-2206, an allosteric inhibitor of AKT, stimulates LDLR expression and LDL uptake: A potential hypocholesterolemic agent

Right ventricular mechanical dispersion is related to malignant arrhythmias: a study of patients with arrhythmogenic right ventricular cardiomyopathy and subclinical right ventricular dysfunction

Effect of mutations in the PCSK9 gene on the cell surface LDL receptors

PCSK9 acts as a chaperone for the LDL receptor in the endoplasmic reticulum

Sex-specific relevance of diabetes to occlusive vascular and other mortality: a collaborative meta-analysis of individual data from 980 793 adults from 68 prospective studies

Missense mutation Q384K in the APOB gene affecting the large lipid transfer module of apoB reduces the secretion of apoB-100 in the liver without reducing the secretion of apoB-48 in the intestine

Sorting an LDL receptor with bound PCSK9 to intracellular degradation

Risk prediction of ventricular arrhythmias and myocardial function in Lamin A/C mutation positive subjects

Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds

The risk of various types of cardiovascular diseases in mutation positive familial hypercholesterolemia; a review

The unique role of proprotein convertase subtilisin/kexin 9 in cholesterol homeostasis

Subjects with molecularly defined familial hypercholesterolemia or familial defective apoB-100 are not being adequately treated

Missense mutations in the PCSK9 gene are associated with hypocholesterolemia and possibly increased response to statin therapy

Left ventricular mechanical dispersion by tissue Doppler imaging: a novel approach for identifying high-risk individuals with long QT syndrome

High prevalence of exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia mutation-positive family members diagnosed by cascade genetic screening

PCSK9-mediated degradation of the LDL receptor generates a 17 kDa C-terminal LDL receptor fragment

Role of the C-terminal domain of PCSK9 in degradation of the LDL receptors

Interaction between the ligand-binding domain of the LDL receptor and the C-terminal domain of PCSK9 is required for PCSK9 to remain bound to the LDL receptor during endosomal acidification

Genetics of hypertrophic cardiomyopathy in Norway

Prevalence of cholesteryl ester storage disease among hypercholesterolemic subjects and functional characterization of mutations in the lysosomal acid lipase gene

Type 1 hyperlipoproteinemia due to a novel deletion of exons 3 and 4 in the GPIHBP1 gene

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