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- Calabresi, Laura2
- Olivecrona, Gunilla2
- Aasa, Ulrika1
- Ackerman, Jacobo Miranda1
- Ahmarani, Lena1
- Ahn, in Sook1
- Alabi, Adekunle1
- Aligabi, Zahra1
- Alvarez-Jarreta, Jorge1
- Anto, Liya1
- Arnemo, Jon M1
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- Auclair, Nickolas1
- Balamir, Melek1
- Ballentine, Samuel J1
- Bansal, Aruna T1
- Beaulieu, Jean-François1
- Bentley, Kirsten1
- Bhatt, Deepak L1
- Bjorkhem, Ingemar1
- Blencowe, Montgomery1
- Blesso, Christopher N1
- Blomberg, Niek1
- Boucher, Jeremie1
- Brosch, Mario1
Regular Research Articles
30 Results
- Research ArticleOpen Access
Amodiaquine promotes testosterone production and de novo synthesis of cholesterol and triglycerides in Leydig cells
Journal of Lipid ResearchVol. 62100152Published online: November 18, 2021- Yujeong Choi
- Eun Goo Lee
- Gibbeum Lee
- Mi Gyeong Jeong
- Hyo Kyeong Kim
- Ji-Hyun Oh
- and others
Cited in Scopus: 0Testosterone is a hormone essential for male reproductive function. It is produced primarily by Leydig cells in the testicle through activation of steroidogenic acute regulatory protein and a series of steroidogenic enzymes, including a cytochrome P450 side-chain cleavage enzyme (cytochome P450 family 11 subfamily A member 1), 17α-hydroxylase (cytochrome P450 family 17 subfamily A member 1), and 3β-hydroxysteroid dehydrogenase. These steroidogenic enzymes are mainly regulated at the transcriptional level, and their expression is increased by the nuclear receptor 4A1. - Research ArticleOpen Access
Gene networks and pathways for plasma lipid traits via multitissue multiomics systems analysis
Journal of Lipid ResearchVol. 62100019Published online: January 5, 2021- Montgomery Blencowe
- In Sook Ahn
- Zara Saleem
- Helen Luk
- Ingrid Cely
- Ville-Petteri Mäkinen
- and others
Cited in Scopus: 0Genome-wide association studies (GWASs) have implicated ∼380 genetic loci for plasma lipid regulation. However, these loci only explain 17–27% of the trait variance, and a comprehensive understanding of the molecular mechanisms has not been achieved. In this study, we utilized an integrative genomics approach leveraging diverse genomic data from human populations to investigate whether genetic variants associated with various plasma lipid traits, namely, total cholesterol, high and low density lipoprotein cholesterol (HDL and LDL), and triglycerides, from GWASs were concentrated on specific parts of tissue-specific gene regulatory networks. - Research ArticleOpen Access
Hepatic deletion of Mboat7 (LPIAT1) causes activation of SREBP-1c and fatty liver
Journal of Lipid ResearchVol. 62100031Published online: February 5, 2021- Mingfeng Xia
- Preethi Chandrasekaran
- Shunxing Rong
- Xiaorong Fu
- Matthew A. Mitsche
Cited in Scopus: 0Genetic variants that increase the risk of fatty liver disease and cirrhosis have recently been identified in the proximity of membrane-bound O-acyltransferase domain-containing 7 (MBOAT7). To elucidate the link between these variants and fatty liver disease, we characterized Mboat7 liver-specific KO mice (Mboat7 LSKO). Chow-fed Mboat7 LSKO mice developed fatty livers and associated liver injury. Lipidomic analysis of liver using MS revealed a pronounced reduction in 20-carbon PUFA content in phosphatidylinositols (PIs) but not in other phospholipids. - Research ArticleOpen Access
Lipid signature of advanced human carotid atherosclerosis assessed by mass spectrometry imaging
Journal of Lipid ResearchVol. 62100020Published online: January 5, 2021- Astrid M. Moerman
- Mirjam Visscher
- Nuria Slijkhuis
- Kim Van Gaalen
- Bram Heijs
- Theo Klein
- and others
Cited in Scopus: 0Carotid atherosclerosis is a risk factor for ischemic stroke, one of the main causes of mortality and disability worldwide. The disease is characterized by plaques, heterogeneous deposits of lipids, and necrotic debris in the vascular wall, which grow gradually and may remain asymptomatic for decades. However, at some point a plaque can evolve to a high-risk plaque phenotype, which may trigger a cerebrovascular event. Lipids play a key role in the development and progression of atherosclerosis, but the nature of their involvement is not fully understood. - Research ArticleOpen Access
Distinct patterns of apolipoprotein C-I, C-II, and C-III isoforms are associated with markers of Alzheimer’s disease
Journal of Lipid ResearchVol. 62100014Published online: December 17, 2020- Yueming Hu
- Cristiana Meuret
- Ashley Martinez
- Hussein N. Yassine
- Dobrin Nedelkov
Cited in Scopus: 0Apolipoproteins C-I, C-II, and C-III interact with ApoE to regulate lipoprotein metabolism and contribute to Alzheimer's disease pathophysiology. In plasma, apoC-I and C-II exist as truncated isoforms, while apoC-III exhibits multiple glycoforms. This study aimed to 1) delineate apoC-I, C-II, and C-III isoform profiles in cerebrospinal fluid (CSF) and plasma in a cohort of nondemented older individuals (n = 61), and 2) examine the effect of APOE4 on these isoforms and their correlation with CSF Aβ42, a surrogate of brain amyloid accumulation.