Risk prediction of ventricular arrhythmias and myocardial function in Lamin A/C mutation positive subjects von Hasselberg, Nina E, Edvardsen, Thor, Petri, Helle, Berge, Knut E, Leren, Trond P, Bundgaard, Henning, Haugaa, Kristina H

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Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation von Hasselberg, Nina Eide, Haland, Trine Fink, Saberniak, Jørg, Brekke, Pål Haugar, Berge, Knut Erik, Leren, Trond Paul, Edvardsen, Thor, Haugaa, Kristina Hermann

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Effect of mutations in the PCSK9 gene on the cell surface LDL receptors von Cameron, Jamie, Holla, Øystein L., Ranheim, Trine, Kulseth, Mari Ann, Berge, Knut Erik, Leren, Trond P.

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Subjects with low plasma HDL cholesterol levels are characterized by an inflammatory and oxidative phenotype von Holven, Kirsten B, Retterstøl, Kjetil, Ueland, Thor, Ulven, Stine M, Nenseter, Marit S, Sandvik, Marit, Narverud, Ingunn, Berge, Knut E, Ose, Leiv, Aukrust, Pål, Halvorsen, Bente

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Overexpression of ABCG5 and ABCG8 promotes biliary cholesterol secretion and reduces fractional absorption of dietary cholesterol von Yu, Liqing, Li-Hawkins, Jia, Hammer, Robert E, Berge, Knut E, Horton, Jay D, Cohen, Jonathan C, Hobbs, Helen H

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Accumulation of Dietary Cholesterol in Sitosterolemia Caused by Mutations in Adjacent ABC Transporters von Berge, Knut E., Tian, Hui, Graf, Gregory A., Yu, Liqing, Grishin, Nick V., Schultz, Joshua, Kwiterovich, Peter, Shan, Bei, Barnes, Robert, Hobbs, Helen H.

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Subjects with molecularly defined familial hypercholesterolemia or familial defective apoB-100 are not being adequately treated von Leren, Trond P, Berge, Knut Erik

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Description of a Large Family with Autosomal Dominant Hypercholesterolemia Associated with the APOE p.Leu167del Mutation von Marduel, Marie, Ouguerram, Khadija, Serre, Valérie, Bonnefont-Rousselot, Dominique, Marques-Pinheiro, Alice, Erik Berge, Knut, Devillers, Martine, Luc, Gérald, Lecerf, Jean-Michel, Tosolini, Laurent, Erlich, Danièle, Peloso, Gina M., Stitziel, Nathan, Nitchké, Patrick, Jaïs, Jean-Philippe, Abifadel, Marianne, Kathiresan, Sekar, Leren, Trond Paul, Rabès, Jean-Pierre, Boileau, Catherine, Varret, Mathilde

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Rapid molecular diagnostics of severe primary immunodeficiency determined by using targeted next-generation sequencing von Yu, Hui, PhD, Zhang, Victor Wei, MD, PhD, Stray-Pedersen, Asbjørg, MD, PhD, Hanson, Imelda Celine, MD, Forbes, Lisa R., MD, de la Morena, M. Teresa, MD, Chinn, Ivan K., MD, Gorman, Elizabeth, PhD, Mendelsohn, Nancy J., MD, Pozos, Tamara, MD, PhD, Wiszniewski, Wojciech, MD, PhD, Nicholas, Sarah K., MD, Yates, Anne B., MD, Moore, Lindsey E., DO, Berge, Knut Erik, MD, PhD, Sorte, Hanne, MS, Bayer, Diana K., DO, ALZahrani, Daifulah, MD, Geha, Raif S., MD, Feng, Yanming, PhD, Wang, Guoli, PhD, Orange, Jordan S., MD, PhD, Lupski, James R., MD, PhD, DSc (hon), Wang, Jing, MD, Wong, Lee-Jun, PhD

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Regulation of ATP-binding Cassette Sterol Transporters ABCG5 and ABCG8 by the Liver X Receptors α and β von Repa, Joyce J., Berge, Knut E., Pomajzl, Chris, Richardson, James A., Hobbs, Helen, Mangelsdorf, David J.

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Severe hypertriglyceridemia in Norway: prevalence, clinical and genetic characteristics von Retterstøl, Kjetil, Narverud, Ingunn, Selmer, Randi, Berge, Knut E, Osnes, Ingvild V, Ulven, Stine M, Halvorsen, Bente, Aukrust, Pål, Holven, Kirsten B, Iversen, Per O

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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 acid... von TVETEN, Kristian, HOLLA, Øystein L, CAMERON, Jamie, BISMO STRØM, Thea, ERIK BERGE, Knut, LAERDAHL, Jon K, LEREN, Trond P

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Mutations in the SORT1 gene are unlikely to cause autosomal dominant hypercholesterolemia von Tveten, Kristian, Strøm, Thea Bismo, Cameron, Jamie, Berge, Knut Erik, Leren, Trond P

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Heritability of plasma noncholesterol sterols and relationship to DNA sequence polymorphism in ABCG5 and ABCG8 von Berge, Knut E, von Bergmann, Klaus, Lutjohann, Dieter, Guerra, Rudy, Grundy, Scott M, Hobbs, Helen H, Cohen, Jonathan C

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Mutations in ATP-cassette binding proteins G5 (ABCG5) and G8 (ABCG8) causing sitosterolemia von Hubacek, Jaroslav A., Berge, Knut E., Cohen, Jonathan C., Hobbs, Helen H.

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Affinity and kinetics of proprotein convertase subtilisin/kexin type 9 binding to low-density lipoprotein receptors on HepG2 cells von Mousavi, Seyed A, Berge, Knut E, Berg, Trond, Leren, Trond P

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4‐Phenylbutyrate restores the functionality of a misfolded mutant low‐density lipoprotein receptor von Tveten, Kristian, Holla, Øystein L., Ranheim, Trine, Berge, Knut E., Leren, Trond P., Kulseth, Mari A.

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PCSK9-mediated degradation of the LDL receptor generates a 17 kDa C-terminal LDL receptor fragment von Tveten, Kristian, Str⊘m, Thea Bismo, Berge, Knut Erik, Leren, Trond P.

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Role of the C-terminal domain of PCSK9 in degradation of the LDL receptors von Holla, Øystein L., Cameron, Jamie, Tveten, Kristian, Str⊘m, Thea Bismo, Berge, Knut Erik, Laerdahl, Jon K., Leren, Trond P.

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ABCB4 sequence variations in young adults with cholesterol gallstone disease von Nakken, Karl Esten, Labori, Knut Jørgen, Rødningen, Olaug K., Nakken, Sigve, Berge, Knut E., Eiklid, Kristin, Ræder, Morten G.

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