Leren, Trond P.: search on Z-Library

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1

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

Vinje, Terje, Wierød, Lene, Leren, Trond P., Strøm, Thea Bismo

Journal:

Molecular Genetics and Metabolism

Year:

2018

Language:

english

File:

PDF, 604 KB

english, 2018

2

Identification of mutations in the apolipoprotein B-100 gene and in the PCSK9 gene as the cause of hypocholesterolemia

Trond P. Leren, Knut Erik Berge

Journal:

Clinica Chimica Acta

Year:

2008

Language:

english

File:

PDF, 156 KB

english, 2008

3

Effects of intronic mutations in the LDLR gene on pre-mRNA splicing: Comparison of wet-lab and bioinformatics analyses

Øystein L. Holla, Sigve Nakken, Morten Mattingsdal, Trine Ranheim, Knut Erik Berge, Joep C. Defesche, Trond P. Leren

Journal:

Molecular Genetics and Metabolism

Year:

2009

Language:

english

File:

PDF, 596 KB

english, 2009

4

Splice-site mutation c.313+1, G>A in intron 3 of the LDL receptor gene results in transcripts with skipping of exon 3 and inclusion of intron 3

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

Journal:

Clinica Chimica Acta

Year:

2009

Language:

english

File:

PDF, 394 KB

english, 2009

5

Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation

Hasselberg, Nina Eide, Haland, Trine Fink, Saberniak, Jørg, Brekke, Pål Haugar, Berge, Knut Erik, Leren, Trond Paul, Edvardsen, Thor, Haugaa, Kristina Hermann

Journal:

European Heart Journal

Year:

2018

Language:

english

File:

PDF, 453 KB

english, 2018

6

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

7

Identification of deletions and duplications in the low density lipoprotein receptor gene by MLPA

Øystein L. Holla, Christél Teie, Knut Erik Berge, Trond P. Leren

Journal:

Clinica Chimica Acta

Year:

2005

Language:

english

File:

PDF, 155 KB

english, 2005

8

Impact of age on excess risk of coronary heart disease in patients with familial hypercholesterolaemia

Mundal, Liv J, Igland, Jannicke, Veierød, Marit B, Holven, Kirsten Bjørklund, Ose, Leiv, Selmer, Randi Marie, Wisloff, Torbjorn, Kristiansen, Ivar S, Tell, Grethe S, Leren, Trond P, Retterstøl, Kjetil

Journal:

Year:

2018

Language:

english

File:

PDF, 475 KB

english, 2018

9

A common missense mutation (C210G) in the LDL receptor gene among Norwegian familial hypercholesterolemia subjects

Hilde Sundvold, Kari Solberg, Serena Tonstad, Olaug K. Rødningen, Leiv Ose, Kåre Berg, Trond P. Leren

Journal:

Year:

1996

Language:

english

File:

PDF, 166 KB

english, 1996

10

Screening for known mutations in the LDL receptor gene causing familial hypercholesterolemia

Trond P. Leren, Hilde Sundvold, Olaug K. Rødningen, Serena Tonstad, Kari Solberg, Leiv Ose, Kåre Berg

Journal:

Year:

1995

Language:

english

File:

PDF, 637 KB

english, 1995

11

Haplotype analysis at the low density lipoprotein receptor locus in normal and familial hypercholesterolemia Norwegian subjects

Olaug K. Rødningen, Trond P. Leren, Oddveig Røsby, Serena Tonstad, Leiv Ose, Kare Berg

Journal:

Clinical Genetics

Year:

1993

Language:

english

File:

PDF, 699 KB

english, 1993

12

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

13

4-Phenylbutyrate restores the functionality of a misfolded mutant low-density lipoprotein receptor

Kristian Tveten, Øystein L. Holla, Trine Ranheim, Knut E. Berge, Trond P. Leren, Mari A. Kulseth

Journal:

Year:

2007

Language:

english

File:

PDF, 823 KB

english, 2007

14

Mspl RFLP in exon 18 of the LDL receptor gene detectable by PCR

Kari Solberg, Olaug K. Rødningen, Serena Tonstad, Leiv Ose, Kåre Berg, Trond P. Leren

Journal:

Clinical Genetics

Year:

1993

Language:

english

File:

PDF, 98 KB

english, 1993

15

The cytoplasmic domain is not involved in directing Class 5 mutant LDL receptors to lysosomal degradation

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

Journal:

Biochemical and Biophysical Research Communications

Year:

2011

Language:

english

File:

PDF, 495 KB

english, 2011

16

Deletion (1)(p32.2–p32.3) detected by array-CGH in a patient with developmental delay/mental retardation, dysmorphic features and low cholesterol: A new microdeletion syndrome?

Milene Mulatinho, Juan Llerena, Trond P. Leren, P. Nagesh Rao, Fabiola Quintero-Rivera

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 122 KB

english, 2008

17

Further evidence for an association between the Xbal polymorphism at the apolipoprotein B locus and lipoprotein level

Trond P. Leren, Kåre Berg, Ingvar Hjermann, Paul Leren

Journal:

Clinical Genetics

Year:

1988

Language:

english

File:

PDF, 356 KB

english, 1988

18

Disrupted recycling of the low density lipoprotein receptor by PCSK9 is not mediated by residues of the cytoplasmic domain

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

Journal:

Molecular Genetics and Metabolism

Year:

2010

Language:

english

File:

PDF, 705 KB

english, 2010

19

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

20

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

21

Effects of a 9.6-kb deletion of the LDL receptor gene (FH Helsinki) on structure and levels of mRNA

Olaug K. Rødningen, Serena Tonstad, Leiv Ose, Kåre Berg, Trond P. Leren

Journal:

Year:

1998

Language:

english

File:

PDF, 409 KB

english, 1998

22

Doxazosin Increases Low Density Lipoprotein Receptor Activity

Journal:

Basic & Clinical Pharmacology & Toxicology

Year:

1985

Language:

english

File:

PDF, 270 KB

english, 1985

23

New SCN5A mutation in a SUDEP victim with idiopathic epilepsy

Dag Aurlien, Trond P. Leren, Erik Taubøll, Leif Gjerstad

Journal:

Year:

2009

Language:

english

File:

PDF, 206 KB

english, 2009

24

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

25

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

26

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

27

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

28

Genome-wide expression analysis of cells expressing gain of function mutant D374Y-PCSK9

Trine Ranheim, Morten Mattingsdal, Jessica M. Lindvall, Øystein L. Holla, Knut Erik Berge, Mari Ann Kulseth, Trond P. Leren

Journal:

Journal of Cellular Physiology

Year:

2008

Language:

english

File:

PDF, 282 KB

english, 2008

29

Missense mutation W86R in exon 3 of the lipoprotein lipase gene in a boy with chylomicronemia

Daria Pašalić, Zvonko Jurčić, Gordana Stipančić, Goran Ferenčak, Trond P. Leren, Srdjan Djurovic, Ana Stavljenić-Rukavina

Journal:

Clinica Chimica Acta

Year:

2004

Language:

english

File:

PDF, 272 KB

english, 2004

30

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

31

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

32

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

33

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

34

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

35

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

36

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

37

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

38

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

39

Prevalence of genetically verified familial hypercholesterolemia among young (

Bogsrud, Martin P., Ãyri, Linn K.L., Halvorsen, Sigrun, Atar, Dan, Leren, Trond P., Holven, Kirsten B.

Journal:

Journal of Clinical Lipidology

Year:

2020

File:

PDF, 290 KB

2020

40

Screening for point mutations in exon 10 of the low density lipoprotein receptor gene by analysis of single-strand conformation polymorphisms: detection of a nonsense mutation — FH469→Stop

Trond P. Leren, Kari Solberg, Olaug K. Rødningen, Oddveig Røsby, Serena Tonstad, Leiv Ose, Kåre Berg

Journal:

Year:

1993

Language:

english

File:

PDF, 1.42 MB

english, 1993

41

Mutations in APOA-I and ABCA1 in Norwegians with low levels of HDL cholesterol

Knut Erik Berge, Trond P. Leren

Journal:

Clinica Chimica Acta

Year:

2010

Language:

english

File:

PDF, 225 KB

english, 2010

42

Loss-of-function mutation R46L in the PCSK9 gene has little impact on the levels of total serum cholesterol in familial hypercholesterolemia heterozygotes

Thea Bismo Strøm, Øystein L. Holla, Jamie Cameron, Knut Erik Berge, Trond P. Leren

Journal:

Clinica Chimica Acta

Year:

2010

Language:

english

File:

PDF, 312 KB

english, 2010

43

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

44

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

45

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

46

A 9.6 kilobase deletion in the low density lipoprotein receptor gene in Norwegian familial hypercholesterolemia subjects

Olaug K. Rødningen, Oddveig Røshy, Serena Tonstad, Leiv Ose, Kåre Berg, Trond P. Leren

Journal:

Clinical Genetics

Year:

1992

Language:

english

File:

PDF, 960 KB

english, 1992

47

The Prevalence of Mutations in KCNQ1, KCNH2, and SCN5A in an Unselected National Cohort of Young Sudden Unexplained Death Cases

BO GREGERS WINKEL, MAIKEN KUDAHL LARSEN, KNUT ERIK BERGE, TROND PAUL LEREN, PETER HENRIK NISSEN, MORTEN SALLING OLESEN, MADS VILHELM HOLLEGAARD, THOMAS JESPERSEN, LEI YUAN, NIKOLAJ NIELSEN, STIG HAUNS

Journal:

Journal of Cardiovascular Electrophysiology

Year:

2012

Language:

english

File:

PDF, 695 KB

english, 2012

48

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

49

Low density lipoprotein receptor activity in cultured skin fibroblasts from octa- and nonagenarians

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

Journal:

Clinical Genetics

Year:

1985

Language:

english

File:

PDF, 627 KB

english, 1985

50

Berberine decreases PCSK9 expression in HepG2 cells

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

Journal:

Atherosclerosis

Year:

2008

Language:

english

File:

PDF, 468 KB

english, 2008

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