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51

Mutation S462P in the PCSK9 gene reduces secretion of mutant PCSK9 without affecting the autocatalytic cleavage

Jamie Cameron, Øystein L. Holla, Jon K. Laerdahl, Mari Ann Kulseth, Knut Erik Berge, Trond P. Leren

Journal:

Atherosclerosis

Year:

2009

Language:

english

File:

PDF, 399 KB

english, 2009

52

Commentary PCSK9 variants: A new database

Sarah E.A. Leigh, Trond P. Leren, Steve E. Humphries

Journal:

Atherosclerosis

Year:

2009

Language:

english

File:

PDF, 103 KB

english, 2009

53

Tangier disease caused by compound heterozygosity for ABCA1 mutations R282X and Y1532C

Jamie Cameron, Trine Ranheim, Bente Halvorsen, Mari Ann Kulseth, Trond P. Leren, Knut Erik Berge

Journal:

Atherosclerosis

Year:

2010

Language:

english

File:

PDF, 425 KB

english, 2010

54

Serum levels of proprotein convertase subtilisin/kexin type 9 in subjects with familial hypercholesterolemia indicate that proprotein convertase subtilisin/kexin type 9 is cleared from plasma by low-density lipoprotein receptor–independent pathways

Jamie Cameron, Martin P. Bogsrud, Kristian Tveten, Thea Bismo StrØm, Kirsten Holven, Knut Erik Berge, Trond P. Leren

Journal:

Translational Research

Year:

2012

Language:

english

File:

PDF, 93 KB

english, 2012

55

MYOCARDIAL STRAIN REVEALS BIVENTRICULAR IMPAIRMENT IN ASYMPTOMATIC ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY MUTATION CARRIERS

Kristina H. Haugaa, Sebastian I. Sarvari, Ole-Gunnar Anfinsen, Trond P. Leren, Otto A. Smiseth, Jan P. Amlie, Thor Edvardsen

Journal:

Journal of the American College of Cardiology

Year:

2010

Language:

english

File:

PDF, 59 KB

english, 2010

56

Effects of lovastatin alone and in combination with cholestyramine on serum lipids and apolipoproteins in heterozygotes for familial hypercholesterolemia

Trond P. Leren, Ingvar Hjermann, Kåre Berg, Paul Leren, Olav P. Foss, Lars Viksmoen

Journal:

Atherosclerosis

Year:

1988

Language:

english

File:

PDF, 663 KB

english, 1988

57

High-Risk Hypertrophic Cardiomyopathy Associated With a Novel Mutation in Cardiac Myosin-Binding Protein C

Pablo García-Pavía, Javier Segovia, Jesús Molano, Roberto Mora, Frederic Kontny, Knut Erik Berge, Trond P. Leren, Luis Alonso-Pulpón

Journal:

Revista Española de Cardiología (English Edition)

Year:

2007

File:

PDF, 167 KB

2007

58

Low density lipoprotein receptors in cultured skin fibroblasts from psoriasis patients

Trond P. Leren, Kjell Maartmann-Moe, Per Thune, Kåre Berg

Journal:

Clinical Genetics

Year:

1984

Language:

english

File:

PDF, 705 KB

english, 1984

59

ATRIOVENTRICULAR CONDUCTION DELAY PREDICTS VENTRICULAR TACHYCARDIA IN LAMIN A/C MUTATION CARRIERS

Hasselberg, Nina E., Edvardsen, Thor, Petri, Helle, Berge, Knut Erik, Leren, Trond, Bundgaard, Henning, Haugaa, Kristina H.

Journal:

Journal of the American College of Cardiology

Year:

2012

Language:

english

File:

PDF, 216 KB

english, 2012

60

Parliamentary Intelligence.

Hasselberg, Nina E., Edvardsen, Thor, Petri, Helle, Berge, Knut Erik, Leren, Trond, Bundgaard, Henning, Haugaa, Kristina H.

Journal:

Year:

1909

Language:

english

File:

PDF, 450 KB

english, 1909

61

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

Berge, Knut Erik, Retterstøl, Kjetil, Romeo, Stefano, Pirazzi, Carlo, Leren, Trond P.

Journal:

Atherosclerosis

Year:

2014

Language:

english

File:

PDF, 523 KB

english, 2014

62

Advertisers’ Index

Berge, Knut Erik, Retterstøl, Kjetil, Romeo, Stefano, Pirazzi, Carlo, Leren, Trond P.

Journal:

Journal of Vascular and Interventional Radiology

Year:

1999

Language:

english

File:

PDF, 90 KB

english, 1999

63

Mutations in the SORT1 gene are unlikely to cause autosomal dominant hypercholesterolemia

Tveten, Kristian, Strøm, Thea Bismo, Cameron, Jamie, Berge, Knut Erik, Leren, Trond P.

Journal:

Atherosclerosis

Year:

2012

Language:

english

File:

PDF, 227 KB

english, 2012

64

Mutation G805R in the transmembrane domain of the LDL receptor gene causes familial hypercholesterolemia by inducing ectodomain cleavage of the LDL receptor in the endoplasmic reticulum

Strøm, Thea Bismo, Tveten, Kristian, Laerdahl, Jon K., Leren, Trond P.

Journal:

Year:

2014

Language:

english

File:

PDF, 2.10 MB

english, 2014

65

Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L inKCNH2

Christiansen, Michael, Hedley, Paula L, Theilade, Juliane, Stoevring, Birgitte, Leren, Trond P, Eschen, Ole, Sørensen, Karina M, Tybjærg-Hansen, Anne, Ousager, Lilian B, Pedersen, Lisbeth N, Frikke-Sc

Journal:

BMC Medical Genetics

Year:

2014

Language:

english

File:

PDF, 278 KB

english, 2014

66

Sorting an LDL receptor with bound PCSK9 to intracellular degradation

Leren, Trond P.

Journal:

Atherosclerosis

Year:

2014

Language:

english

File:

PDF, 448 KB

english, 2014

67

A novel BMPR2 gene mutation associated with exercise-induced pulmonary hypertension in septal defects

Möller, Thomas, Leren, Trond P., Eiklid, Kristin L., Holmstrøm, Henrik, Fredriksen, Per Morten, Thaulow, Erik

Journal:

Scandinavian Cardiovascular Journal

Year:

2010

Language:

english

File:

PDF, 71 KB

english, 2010

68

Causes of hearing impairment in the Norwegian paediatric cochlear implant program

Siem, Geir, Fagerheim, Toril, Jonsrud, Christoffer, Laurent, Claude, Teig, Erik, Harris, Sten, Leren, Trond P., Früh, Andreas, Heimdal, Ketil

Journal:

International Journal of Audiology

Year:

2010

Language:

english

File:

PDF, 210 KB

english, 2010

69

Cell-released substances interfere with low density lipoprotein receptor determination in fibroblasts

Leren, Trond P., Berg, KÅRe

Journal:

Scandinavian Journal of Clinical & Laboratory Investigation

Year:

1985

Language:

english

File:

PDF, 489 KB

english, 1985

70

Functional Analysis of the Synonymous R385R Mutation in the Low-Density Lipoprotein Receptor Gene

Tveten, Kristian, Khoo, Kah-Lin, Berge, Knut Erik, Leren, Trond P., Kulseth, Mari Ann

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2009

Language:

english

File:

PDF, 10.17 MB

english, 2009

71

Low density lipoprotein receptor determination in peripheral blood mononuclear cells: Influence of differences in cell concentration

Leren, Trond P., Blomhoff, Rune, Berg, KaˇRe

Journal:

Scandinavian Journal of Clinical & Laboratory Investigation

Year:

1986

Language:

english

File:

PDF, 872 KB

english, 1986

72

Development of sensitive and specific age- and gender-specific low-density lipoprotein cholesterol cutoffs for diagnosis of first-degree relatives with familial hypercholesterolaemia in cascade testing

Starr, Brian, Hadfield, S. Gaye, Hutten, Barbara A., Lansberg, Peter J., Leren, Trond P., Damgaard, Dorte, Neil, H. Andrew W., Humphries, Steve E.

Journal:

Clinical Chemistry and Laboratory Medicine

Year:

2008

Language:

english

File:

PDF, 517 KB

english, 2008

73

Lecithin:Cholesterol Acyltransferase (LCAT) Deficiency: Renal Lesions with Early Graft Recurrence

Strøm, Erik H., Sund, Ståle, Reier-Nilsen, Morten, Dørje, Christina, Leren, Trond P.

Journal:

Ultrastructural Pathology

Year:

2011

Language:

english

File:

PDF, 1.25 MB

english, 2011

74

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

Strøm, Thea Bismo, Tveten, Kristian, Leren, Trond P.

Journal:

Biochemical Journal

Year:

2014

Language:

english

File:

PDF, 441 KB

english, 2014

75

Familial atrial septal defect in the oval fossa with progressive prolongation of the atrioventricular conduction caused by mutations in the NKX2.5 gene – ERRATUM

Bjørnstad, Per G., Leren, Trond P.

Journal:

Cardiology in the Young

Year:

2009

Language:

english

File:

PDF, 198 KB

english, 2009

76

Diagnosis of Familial Hypercholesterolemia in General Practice Using Clinical Diagnostic Criteria or Genetic Testing as Part of Cascade Genetic Screening

Leren, Trond P., Finborud, Tora Himle, Manshaus, Turid E., Ose, Leiv, Berge, Knut Erik

Journal:

Community Genetics

Year:

2008

Language:

english

File:

PDF, 174 KB

english, 2008

77

Familial atrial septal defect in the oval fossa with progressive prolongation of the atrioventricular conduction caused by mutations in the NKX2.5 gene

Bjørnstad, Per G., Leren, Trond P.

Journal:

Cardiology in the Young

Year:

2009

Language:

english

File:

PDF, 173 KB

english, 2009

78

Nonsense‐mediated decay of human LDL receptor mRNA

Holla, Øystein Lunde, Kulseth, Mari Ann, Berge, Knut Erik, Leren, Trond Paul, Ranheim, Trine

Journal:

Scandinavian Journal of Clinical & Laboratory Investigation

Year:

2009

Language:

english

File:

PDF, 409 KB

english, 2009

79

Mutation p.L799R in the LDLR, which affects the transmembrane domain of the LDLR, prevents membrane insertion and causes secretion of the mutant LDLR

Strøm, Thea Bismo, Laerdahl, Jon K., Leren, Trond P.

Journal:

Human Molecular Genetics

Year:

2015

Language:

english

File:

PDF, 1.35 MB

english, 2015

80

Results of comprehensive diagnostic work-up in ‘idiopathic’ dilated cardiomyopathy

Broch, Kaspar, Andreassen, Arne K, Hopp, Einar, Leren, Trond P, Scott, Helge, Müller, Fredrik, Aakhus, Svend, Gullestad, Lars

Journal:

Year:

2015

Language:

english

File:

PDF, 952 KB

english, 2015

81

Analysis of LDLR mRNA in patients with familial hypercholesterolemia revealed a novel mutation in intron 14, which activates a cryptic splice site

Kulseth, Mari Ann, Berge, Knut Erik, Bogsrud, Martin Prøven, Leren, Trond P

Journal:

Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 362 KB

english, 2010

82

Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia

Pingitore, Piero, Lepore, Saverio Massimo, Pirazzi, Carlo, Mancina, Rosellina Margherita, Motta, Benedetta Maria, Valenti, Luca, Berge, Knut Erik, Retterstøl, Kjetil, Leren, Trond P., Wiklund, Olov, R

Journal:

Journal of Clinical Lipidology

Year:

2016

Language:

english

File:

PDF, 966 KB

english, 2016

83

Jervell and Lange-Nielsen Syndrome in Norwegian Children: Aspects Around Cochlear Implantation, Hearing, and Balance

Siem, Geir, Früh, Andreas, Leren, Trond P., Heimdal, Ketil, Teig, Erik, Harris, Sten

Journal:

Year:

2008

Language:

english

File:

PDF, 335 KB

english, 2008

84

Comparison of clinical and molecular genetic criteria for diagnosing familial hypercholesterolemia

Leren, Trond P, Berge, Knut Erik

Journal:

Clinical Lipidology

Year:

2009

Language:

english

File:

PDF, 359 KB

english, 2009

85

Studies of the autoinhibitory segment comprising residues 31–60 of the prodomain of PCSK9: Possible implications for the mechanism underlying gain-of-function mutations

Wierød, Lene, Cameron, Jamie, Strøm, Thea Bismo, Leren, Trond P.

Journal:

Molecular Genetics and Metabolism Reports

Year:

2016

Language:

english

File:

PDF, 1.32 MB

english, 2016

86

Variable phenotypic expression of nonsense mutation p.Thr5* in the APOE gene

Leren, Trond P., Strøm, Thea Bismo, Berge, Knut Erik

Journal:

Molecular Genetics and Metabolism Reports

Year:

2016

Language:

english

File:

PDF, 339 KB

english, 2016

87

Mutations affecting the transmembrane domain of the LDL receptor: impact of charged residues on the membrane insertion

Strøm, Thea Bismo, Laerdahl, Jon K., Leren, Trond P.

Journal:

Human Molecular Genetics

Year:

2017

Language:

english

File:

PDF, 594 KB

english, 2017

88

Incidence of various types of atherosclerotic disease in patients with genotyped familial hypercholesterolemia

Retterstol, Kjetil, Mundal, Liv, Igland, Jannicke, Seppola Tell, Grethe, Holven, Kirsten, Braglien Veierød, Marit, Leren, Trond Paul

Journal:

Atherosclerosis

Year:

2017

Language:

english

File:

PDF, 52 KB

english, 2017

89

Increased risk of heart failure and atrial fibrillation in heterozygous familial hypercholesterolemia

Hovland, Anders, Mundal, Liv J., Igland, Jannicke, Veierød, Marit B., Holven, Kirsten B., Bogsrud, Martin P., Tell, Grethe S., Leren, Trond P., Retterstøl, Kjetil

Journal:

Atherosclerosis

Year:

2017

Language:

english

File:

PDF, 429 KB

english, 2017

90

Standardized incidence ratio of peripheral arterial disease and aortic stenosis in genotyped familial hypercholesterolemia in Norway during 2001-2009

Mundal, Liv, Igland, Jannicke, Tell, Grethe S., Veierød, Marit, Holven, Kirsten B., Leren, Trond, Retterstol, Kjetil

Journal:

Atherosclerosis

Year:

2017

Language:

english

File:

PDF, 672 KB

english, 2017

91

Long QT syndrome KCNH2 mutation with sequential fetal and maternal sudden death

Tuveng, Jon M., Berling, Britt-Marie, Bunford, Gabor, Vanoye, Carlos G., Welch, Richard C., Leren, Trond P., George, Alfred L., Rognum, Torleiv Ole

Journal:

Forensic Science, Medicine, and Pathology

Year:

2018

Language:

english

File:

PDF, 1.11 MB

english, 2018

92

Subjects with Molecularly Defined Familial Hypercholesterolemia or Familial Defective apoB-100 Are Not Being Adequately Treated

Leren, Trond P., Berge, Knut Erik, Verbeek, Jos

Journal:

Year:

2011

Language:

english

File:

PDF, 110 KB

english, 2011

93

Lifestyle Related Cancer Deaths in Patients with Familial Hypercholesterolemia

Krogh, Henriette W., Mundal, Liv J., Igland, Jannicke, Holven, Kirsten B., Svendsen, Karianne, Bogsrud, Martin P., Leren, Trond P., Retterstøl, Kjetil

Journal:

Atherosclerosis Supplements

Year:

2018

Language:

english

File:

PDF, 211 KB

english, 2018

94

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

Bjune, Katrine, Sundvold, Hilde, Leren, Trond P., Naderi, Soheil

Journal:

Atherosclerosis

Year:

2018

Language:

english

File:

PDF, 1.69 MB

english, 2018

95

A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease

Holst, Anders G., Calloe, Kirstine, Jespersen, Thomas, Cedergreen, Pernille, Winkel, Bo G., Jensen, Henrik Kjaerulf, Leren, Trond P., Haunso, Stig, Svendsen, Jesper Hastrup, Tfelt-Hansen, Jacob

Journal:

Case Reports in Medicine

Year:

2009

Language:

english

File:

PDF, 1.94 MB

english, 2009

96

Characterization of the mechanisms by which missense mutations in the lysosomal acid lipase gene disrupt enzymatic activity

Vinje, Terje, Laerdahl, Jon K, Bjune, Katrine, Leren, Trond P, Strøm, Thea Bismo

Journal:

Human Molecular Genetics

Year:

2019

Language:

english

File:

PDF, 1.47 MB

english, 2019

97

Strategies to prevent cleavage of the linker region between ligand-binding repeats 4 and 5 of the LDL receptor

Strøm, Thea Bismo, Bjune, Katrine, da Costa, Luis Teixeira, Leren, Trond P

Journal:

Human Molecular Genetics

Year:

2019

Language:

english

File:

PDF, 1.10 MB

english, 2019

98

Strategies to prevent cleavage of the linker region between ligand-binding repeats 4 and 5 of the LDL receptor

Strøm, Thea Bismo, Bjune, Katrine, da Costa, Luis Teixeira, Leren, Trond P

Journal:

Human Molecular Genetics

Year:

2019

File:

PDF, 1.10 MB

2019

99

Lysosomal acid lipase does not have a propeptide and should not be considered being a proprotein

Strøm, Thea B., Vinje, Terje, Bjune, Katrine, Costa, Luís T., Laerdahl, Jon K., Leren, Trond P.

Journal:

Proteins: Structure, Function, and Bioinformatics

Year:

2019

Language:

english

File:

PDF, 2.85 MB

english, 2019

100

Association of Low-Density Lipoprotein Cholesterol With Risk of Aortic Valve Stenosis in Familial Hypercholesterolemia

Mundal, Liv J., Hovland, Anders, Igland, Jannicke, Veierød, Marit B., Holven, Kirsten B., Bogsrud, Martin Prøven, Tell, Grethe S., Leren, Trond P., Retterstøl, Kjetil

Journal:

JAMA Cardiology

Year:

2019

File:

PDF, 88 KB

2019

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