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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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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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Cascade genetic screening for familial hypercholesterolemia

Clinical genetics, 2004-12, Vol.66 (6), p.483-487

Leren, TP

2004

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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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Characterization of novel mutations in the catalytic domain of the PCSK9 gene

Journal of internal medicine, 2008-04, Vol.263 (4), p.420-431

2008

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Molecular autopsy in young sudden cardiac death victims with suspected cardiomyopathy

Forensic science international, 2012-06, Vol.219 (1), p.33-38

2012

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Postmortem genetic testing of the ryanodine receptor 2 (RYR2) gene in a cohort of sudden unexplained death cases

International journal of legal medicine, 2013-01, Vol.127 (1), p.139-144

2013

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Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers

Scandinavian journal of clinical and laboratory investigation, 2008, Vol.68 (5), p.362-368

2008

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Risk factors related to carotid intima-media thickness and plaque in children with familial hypercholesterolemia and control subjects

Arteriosclerosis, thrombosis, and vascular biology, 1996-08, Vol.16 (8), p.984-991

1996

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Molecular analysis of three known and one novel LPL variants in patients with type I hyperlipoproteinemia

Nutrition, metabolism, and cardiovascular diseases, 2018-02, Vol.28 (2), p.158-164

2018

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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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A functional polymorphism in the promoter region of the microsomal triglyceride transfer protein (MTP -493G/T) influences lipoprotein phenotype in familial hypercholesterolemia

Arteriosclerosis, thrombosis, and vascular biology, 2000-07, Vol.20 (7), p.1784-1788

2000

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Molecular genetics of familial hypercholesterolaemia in Norway

Journal of internal medicine, 1997-03, Vol.241 (3), p.185-193

1997

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Is responsiveness to lovastatin in familial hypercholesterolaemia heterozygotes influenced by the specific mutation in the low-density lipoprotein receptor gene?

European journal of clinical investigation, 1995-12, Vol.25 (12), p.967-973

1995

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Carotid intima-media thickness and plaque in patients with familial hypercholesterolaemia mutations and control subjects

European journal of clinical investigation, 1998-12, Vol.28 (12), p.971-979

1998

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Does maternal or paternal heredity affect carotid atherosclerosis in children with familial hypercholesterolaemia?

Acta Paediatrica, 2000-12, Vol.89 (12), p.1490-1492

2000

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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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Screening for mutations of the apolipoprotein B gene causing hypocholesterolemia

Human genetics, 1998-01, Vol.102 (1), p.44-49

1998

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Characterization of a human apolipoprotein E gene enhancer element and its associated protein factors

The Journal of biological chemistry, 1990-06, Vol.265 (16), p.9496-9504

1990

Volltextzugriff (PDF)

P818Incidence of coronary heart disease in patients with familiar hypercholesterolemia compared to age- and sex- matched controls

European heart journal, 2019-10, Vol.40 (Supplement_1)

2019

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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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The genetic algorithm applied to haplotype data at the LDL receptor locus

Computer methods and programs in biomedicine, 2000, Vol.61 (1), p.1-9

2000

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Application of long polymerase chain reaction in the study of the LDL receptor gene

Scandinavian journal of clinical and laboratory investigation, 1996-02, Vol.56 (1), p.93-96

1996

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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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Identification of the apo B-3500 mutation in the Norwegian population

Scandinavian journal of clinical and laboratory investigation, 1995, Vol.55 (3), p.217-221

1995

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

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

Cascade genetic screening for familial hypercholesterolemia

Genetics of hypertrophic cardiomyopathy in Norway

Characterization of novel mutations in the catalytic domain of the PCSK9 gene

Molecular autopsy in young sudden cardiac death victims with suspected cardiomyopathy

Postmortem genetic testing of the ryanodine receptor 2 (RYR2) gene in a cohort of sudden unexplained death cases

Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers

Risk factors related to carotid intima-media thickness and plaque in children with familial hypercholesterolemia and control subjects

Molecular analysis of three known and one novel LPL variants in patients with type I hyperlipoproteinemia

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

A functional polymorphism in the promoter region of the microsomal triglyceride transfer protein (MTP -493G/T) influences lipoprotein phenotype in familial hypercholesterolemia

Molecular genetics of familial hypercholesterolaemia in Norway

Is responsiveness to lovastatin in familial hypercholesterolaemia heterozygotes influenced by the specific mutation in the low-density lipoprotein receptor gene?

Carotid intima-media thickness and plaque in patients with familial hypercholesterolaemia mutations and control subjects

Does maternal or paternal heredity affect carotid atherosclerosis in children with familial hypercholesterolaemia?

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

Screening for mutations of the apolipoprotein B gene causing hypocholesterolemia

Characterization of a human apolipoprotein E gene enhancer element and its associated protein factors

P818Incidence of coronary heart disease in patients with familiar hypercholesterolemia compared to age- and sex- matched controls

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

The genetic algorithm applied to haplotype data at the LDL receptor locus

Application of long polymerase chain reaction in the study of the LDL receptor gene

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

Identification of the apo B-3500 mutation in the Norwegian population

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