日期:
2020 年 — 2026 年
2020
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影响因子:

Corrigendum to: Functional characterization of missense variants affecting the extracellular domains of ABCA1 using a fluorescence-based assay [Journal of Lipid Research 65/1 (2024) 100482]

更正:利用基于荧光的检测方法对影响 ABCA1 胞外结构域的错义变异进行功能表征 [脂质研究杂志 65/1 (2024) 100482]

Teigen, Marianne; Ølnes, Åsa Schawlann; Bjune, Katrine; Leren, Trond P; Bogsrud, Martin Prøven; Strøm, Thea Bismo

Flavonoids regulate LDLR through different mechanisms tied to their specific structures

黄酮类化合物通过与其特定结构相关的不同机制来调节 LDLR

Katrine Bjune, Pia Skovholt Halvorsen, Helle Wangensteen, Trond P Leren, Martin Prøven Bogsrud, Thea Bismo Strøm

Functional characterization of missense variants affecting the extracellular domains of ABCA1 using a fluorescence-based assay

使用荧光检测法对影响 ABCA1 胞外域的错义变异进行功能表征

Marianne Teigen, Åsa Schawlann Ølnes, Katrine Bjune, Trond P Leren, Martin Prøven Bogsrud, Thea Bismo Strøm

Variants in the CETP gene affect levels of HDL cholesterol by reducing the amount, and not the specific lipid transfer activity, of secreted CETP

CETP基因的变异通过减少分泌的CETP的数量(而非其特定的脂质转移活性)来影响HDL胆固醇水平。

Åsa Schawlann Ølnes ,Marianne Teigen ,Jon K Laerdahl ,Trond P Leren ,Thea Bismo Strøm ,Katrine Bjune

Association of Familial Hypercholesterolemia and Statin Use With Risk of Dementia in Norway

挪威家族性高胆固醇血症和使用他汀类药物与痴呆风险的关联

Mundal, Liv J; Igland, Jannicke; Svendsen, Karianne; Holven, Kirsten B; Leren, Trond P; Retterstøl, Kjetil

The risk of various types of cardiovascular diseases in mutation positive familial hypercholesterolemia; a review

突变阳性家族性高胆固醇血症患者罹患各种心血管疾病的风险:一项综述

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

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

低密度脂蛋白胆固醇与家族性高胆固醇血症患者主动脉瓣狭窄风险的相关性

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

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

APOE基因中无义突变p.Thr5*的表型表达具有多样性

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

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

对 PCSK9 前结构域 31-60 位残基组成的自抑制片段的研究:对获得功能突变机制的可能影响

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

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

LDL受体基因跨膜结构域中的G805R突变通过诱导内质网中LDL受体的胞外结构域切割,导致家族性高胆固醇血症。

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