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Journal of Internal Medicine|November 26, 2009
The unique role of proprotein convertase subtilisin/kexin 9 in cholesterol homeostasisS A Mousavi, K E Berge, T P Leren
Clinical Genetics|August 1, 1997
Analyses of mutations in the human renal kallikrein (hKLK1) gene and their possible relevance to blood pressure regulation and risk of myocardial infarctionK E Berge, A Bakken, M Bøhn, et al.
Clinical Genetics|December 1, 1993
Insertion/deletion (I/D) polymorphism at the locus for angiotensin I-converting enzyme and parental history of myocardial infarctionM Bøhn, K E Berge, A Bakken, et al.
Clinical Genetics|December 1, 1993
Insertion/deletion (I/D) polymorphism at the locus for angiotensin I-converting enzyme and myocardial infarctionM Bøhn, K E Berge, A Bakken, et al.
Clinical Genetics|August 1, 1997
A DNA polymorphism at the angiotensin II type 1 receptor (AT1R) locus and myocardial infarctionK E Berge, A Bakken, M Bøhn, et al.
Human Mutation|October 23, 2001
Mutations in ATP-cassette binding proteins G5 (ABCG5) and G8 (ABCG8) causing sitosterolemiaJ A Hubacek, K E Berge, J C Cohen, et al.
Clinical Genetics|March 31, 1998
Studies on effects of Lp(a) lipoprotein on gene expression in endothelial cells in vitroK E Berge, S Djurovic, H J Muller, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|June 17, 2006
Low-density lipoprotein receptor activity in Epstein-Barr virus-transformed lymphocytes from heterozygotes for the D374Y mutation in the PCSK9 geneØ L Holla, J Cameron, K E Berge, et al.
Physiological Research|August 18, 2004
Polymorphisms in ABCG5 and ABCG8 transporters and plasma cholesterol levelsJ A Hubácek, K E Berge, J Stefková, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|April 12, 2001
Detection of mRNA for the terminal complement components C5, C6, C8 and C9 in human umbilical vein endothelial cells in vitroH Langeggen, K E Berge, P Macor, et al.
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