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Diversity of Lipid Function in Atherogenesis: A Focus on Endothelial Mechanobiology

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Localization of Atherosclerosis

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Hemodynamic Shear Stress and Its Role in Atherosclerosis

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Prevalence of Systemic Atherosclerosis Burdens and Overlapping Stroke Etiologies and Their Associations With Long-term Vascular Prognosis in Stroke With Intracranial Atherosclerotic Disease

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The circulatory system of Amphioxus (Branchiostoma floridae) I. Morphology of the major vessels of the pharyngeal area

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Handbook of Disease Burdens and Quality of Life Measures

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Regulation of eNOS in Caveolae

inferredcites →https://doi.org/10.1007/978-1-4684-7508-1openalex-snapshot

Dynamics of Arterial Flow

inferredcites →https://doi.org/10.1007/978-1-4684-7508-1_2openalex-snapshot

Fluid Mechanics of Arterial Flow

inferredcites →https://doi.org/10.1007/bf00307456openalex-snapshot

The circulatory system of amphioxus (Branchiostoma floridae)

inferredcites →https://doi.org/10.1007/bf01870794openalex-snapshot

Lateral motion of membrane proteins and biological function

inferredcites →https://doi.org/10.1007/bf02066350openalex-snapshot

Cytoplasmic microfilaments in endothelial cells of flow loaded canine carotid arteries

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Mechanisms of endothelial cell migration

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Cell Surface Area Regulation and Membrane Tension

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Cell motility: the integrating role of the plasma membrane

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Caveolae and transcytosis in endothelial cells: role in atherosclerosis

inferredcites →https://doi.org/10.1007/s00441-008-0710-9openalex-snapshot

Endothelial microparticles in diseases

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SMAD6 transduces endothelial cell flow responses required for blood vessel homeostasis

inferredcites →https://doi.org/10.1007/s11745-999-0481-6openalex-snapshot

Effects of eicosapentaenoic acid and docosahexaenoic acid on plasma membrane fluidity of aortic endothelial cells

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High Cholesterol/Low Cholesterol: Effects in Biological Membranes: A Review

inferredcites →https://doi.org/10.1007/s12195-010-0136-9openalex-snapshot

Endothelial Cell Membrane Sensitivity to Shear Stress is Lipid Domain Dependent

inferredcites →https://doi.org/10.1016/0014-4800(80)90061-1openalex-snapshot

The effect of local blood flow patterns on endothelial cell morphology

inferredcites →https://doi.org/10.1016/0021-9150(76)90054-xopenalex-snapshot

Scanning electron microscopy in the evaluation of endothelial integrity of the fatty lesion in atherosclerosis

inferredcites →https://doi.org/10.1016/0021-9150(77)90061-2openalex-snapshot

Aortic endothelial cell morphology observed in situ by scanning electron microscopy during atherogenesis in the rabbit

inferredcites →https://doi.org/10.1016/0021-9290(92)90287-bopenalex-snapshot

Changes in the microstructure of cultured porcine aortic endothelial cells in the early stage after applying a fluid-imposed shear stress

inferredcites →https://doi.org/10.1016/0026-2862(84)90031-1openalex-snapshot

Response of cultured endothelial cells to steady flow

inferredcites →https://doi.org/10.1016/0040-8166(79)90050-8openalex-snapshot

Octopus microvasculature: Permeability to ferritin and carbon

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Cytokines as communication signals between leukocytes and endothelial cells

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Mechanisms of endothelial stiffening in dyslipidemia and aging: Oxidized lipids and shear stress

inferredcites →https://doi.org/10.1016/bs.mcb.2015.11.008openalex-snapshot

Localization and signaling of GPCRs in lipid rafts

inferredcites →https://doi.org/10.1016/j.ancard.2008.02.016openalex-snapshot

Microparticules endothéliales circulantes : un nouveau marqueur du dysfonctionnement vasculaire

inferredcites →https://doi.org/10.1016/j.atherosclerosis.2017.01.013openalex-snapshot

ATP binding cassette A1 (ABCA1) mediates microparticle formation during high-density lipoprotein (HDL) biogenesis

inferredcites →https://doi.org/10.1016/j.atherosclerosis.2019.08.014openalex-snapshot

2019 ESC/EAS guidelines for the management of dyslipidaemias: Lipid modification to reduce cardiovascular risk

inferredcites →https://doi.org/10.1016/j.atherosclerosis.2020.09.020openalex-snapshot

Transendothelial transport of lipoproteins

inferredcites →https://doi.org/10.1016/j.bbacli.2014.11.006openalex-snapshot

The predictive role of circulating microparticles in patients with chronic heart failure

inferredcites →https://doi.org/10.1016/j.bbalip.2014.08.016openalex-snapshot

Localization of VE-cadherin in plasmalemmal cholesterol rich microdomains and the effects of cholesterol depletion on VE-cadherin mediated cell–cell adhesion

inferredcites →https://doi.org/10.1016/j.bbamem.2009.08.016openalex-snapshot

Sphingolipid/cholesterol regulation of neurotransmitter receptor conformation and function

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Ceramide: From lateral segregation to mechanical stress

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How polyunsaturated fatty acids modify molecular organization in membranes: Insight from NMR studies of model systems

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The influence of cholesterol on membrane protein structure, function, and dynamics studied by molecular dynamics simulations

inferredcites →https://doi.org/10.1016/j.bbamem.2016.10.002openalex-snapshot

Eicosapentaenoic acid reduces membrane fluidity, inhibits cholesterol domain formation, and normalizes bilayer width in atherosclerotic-like model membranes

inferredcites →https://doi.org/10.1016/j.bbamem.2019.183139openalex-snapshot

OxLDL alterations in endothelial cell membrane dynamics leads to changes in vesicle trafficking and increases cell susceptibility to injury

inferredcites →https://doi.org/10.1016/j.bbrc.2005.05.019openalex-snapshot

Cellular localization and interaction of ABCA1 and caveolin-1 in aortic endothelial cells after HDL incubation

inferredcites →https://doi.org/10.1016/j.bbrc.2013.03.134openalex-snapshot

Early VEGFR2 activation in response to flow is VEGF-dependent and mediated by MMP activity

inferredcites →https://doi.org/10.1016/j.biochi.2006.10.009openalex-snapshot

Eicosapentaenoic acid modifies lipid composition in caveolae and induces translocation of endothelial nitric oxide synthase

inferredcites →https://doi.org/10.1016/j.biochi.2010.03.022openalex-snapshot

Cavin proteins: New players in the caveolae field

inferredcites →https://doi.org/10.1016/j.bpj.2013.11.4502openalex-snapshot

Microvascular Endothelial Cells Migrate Upstream and Align Against the Shear Stress Field Created by Impinging Flow

inferredcites →https://doi.org/10.1016/j.bpj.2016.05.034openalex-snapshot

Shear-Induced Nitric Oxide Production by Endothelial Cells

inferredcites →https://doi.org/10.1016/j.bpj.2018.11.3127openalex-snapshot

Interplay between Membrane Curvature and Cholesterol: Role of Palmitoylated Caveolin-1

inferredcites →https://doi.org/10.1016/j.bpj.2019.03.016openalex-snapshot

Cholesterol Depletion by MβCD Enhances Cell Membrane Tension and Its Variations-Reducing Integrity

inferredcites →https://doi.org/10.1016/j.cardiores.2005.05.004openalex-snapshot

Decreased caveolin-1 in atheroma: Loss of antiproliferative control of vascular smooth muscle cells in atherosclerosis

inferredcites →https://doi.org/10.1016/j.cardiores.2005.07.003openalex-snapshot

Oxidized LDL downregulates ATP-binding cassette transporter-1 in human vascular endothelial cells via inhibiting liver X receptor (LXR)

inferredcites →https://doi.org/10.1016/j.cardiores.2007.02.014openalex-snapshot

Laminar shear stress up-regulates the expression of stearoyl-CoA desaturase-1 in vascular endothelial cells

inferredcites →https://doi.org/10.1016/j.cardiores.2007.03.023openalex-snapshot

Life history of eNOS: Partners and pathways

inferredcites →https://doi.org/10.1016/j.cardiores.2007.04.012openalex-snapshot

Molecular interaction between caveolin-1 and ABCA1 on high-density lipoprotein-mediated cholesterol efflux in aortic endothelial cells

inferredcites →https://doi.org/10.1016/j.carpath.2012.06.006openalex-snapshot

Vascular endothelium, hemodynamics, and the pathobiology of atherosclerosis

inferredcites →https://doi.org/10.1016/j.cell.2005.02.022openalex-snapshot

Nuclear Movement Regulated by Cdc42, MRCK, Myosin, and Actin Flow Establishes MTOC Polarization in Migrating Cells

inferredcites →https://doi.org/10.1016/j.cell.2007.11.042openalex-snapshot

PTRF-Cavin, a Conserved Cytoplasmic Protein Required for Caveola Formation and Function

inferredcites →https://doi.org/10.1016/j.cell.2010.12.031openalex-snapshot

Cells Respond to Mechanical Stress by Rapid Disassembly of Caveolae

inferredcites →https://doi.org/10.1016/j.cell.2013.02.031openalex-snapshot

Nuclear Positioning

inferredcites →https://doi.org/10.1016/j.chemphyslip.2016.04.001openalex-snapshot

Cholesterol's location in lipid bilayers

inferredcites →https://doi.org/10.1016/j.clinbiochem.2015.02.003openalex-snapshot

Predictive role of circulating endothelial-derived microparticles in cardiovascular diseases

inferredcites →https://doi.org/10.1016/j.cmet.2008.07.008openalex-snapshot

Deletion of Cavin/PTRF Causes Global Loss of Caveolae, Dyslipidemia, and Glucose Intolerance

inferredcites →https://doi.org/10.1016/j.cmet.2009.06.003openalex-snapshot

Genetic Evidence Supporting a Critical Role of Endothelial Caveolin-1 during the Progression of Atherosclerosis

inferredcites →https://doi.org/10.1016/j.crhy.2013.05.003openalex-snapshot

Blood flow and arterial endothelial dysfunction: Mechanisms and implications

inferredcites →https://doi.org/10.1016/j.devcel.2018.12.005openalex-snapshot

Membrane Curvature and Tension Control the Formation and Collapse of Caveolar Superstructures

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2018.05.068openalex-snapshot

Cholesterol crystals increase vascular permeability by inactivating SHP2 and disrupting adherens junctions

inferredcites →https://doi.org/10.1016/j.immuni.2014.10.008openalex-snapshot

Leukocyte Migration into Inflamed Tissues

inferredcites →https://doi.org/10.1016/j.jbiomech.2004.09.030openalex-snapshot

Molecular basis of the effects of shear stress on vascular endothelial cells

inferredcites →https://doi.org/10.1016/j.lfs.2005.05.040openalex-snapshot

Lipids, lipid rafts and caveolae: Their importance for GPCR signaling and their centrality to the endocannabinoid system

inferredcites →https://doi.org/10.1016/j.tcb.2015.10.010openalex-snapshot

Caveolae: One Function or Many?

inferredcites →https://doi.org/10.1016/j.tcm.2008.11.004openalex-snapshot

Monocyte-Endothelial Cell Interactions in the Development of Atherosclerosis

inferredcites →https://doi.org/10.1016/j.tem.2011.04.001openalex-snapshot

Fat caves: caveolae, lipid trafficking and lipid metabolism in adipocytes

inferredcites →https://doi.org/10.1016/j.tibs.2004.07.002openalex-snapshot

Ancestral lipid biosynthesis and early membrane evolution

inferredcites →https://doi.org/10.1016/j.yexcr.2004.11.001openalex-snapshot

Differential effects of shear stress and cyclic stretch on focal adhesion remodeling, site-specific FAK phosphorylation, and small GTPases in human lung endothelial cells

inferredcites →https://doi.org/10.1016/j.yjmcc.2016.12.005openalex-snapshot

Intercellular transfer of miR-126-3p by endothelial microparticles reduces vascular smooth muscle cell proliferation and limits neointima formation by inhibiting LRP6

inferredcites →https://doi.org/10.1016/s0002-9440(10)63209-9openalex-snapshot

Assembly and Reorientation of Stress Fibers Drives Morphological Changes to Endothelial Cells Exposed to Shear Stress

inferredcites →https://doi.org/10.1016/s0006-3495(00)76382-xopenalex-snapshot

Quantitative Morphodynamics of Endothelial Cells within Confluent Cultures in Response to Fluid Shear Stress

inferredcites →https://doi.org/10.1016/s0006-3495(03)74981-9openalex-snapshot

Cascades of Transient Pores in Giant Vesicles: Line Tension and Transport

inferredcites →https://doi.org/10.1016/s0006-3495(90)82444-9openalex-snapshot

Elastic deformation and failure of lipid bilayer membranes containing cholesterol

inferredcites →https://doi.org/10.1016/s0008-6363(03)00367-5openalex-snapshot

Microparticles in cardiovascular diseases

inferredcites →https://doi.org/10.1016/s0014-5793(02)03070-3openalex-snapshot

E‐selectin and ICAM‐1 are incorporated into detergent‐insoluble membrane domains following clustering in endothelial cells

inferredcites →https://doi.org/10.1016/s0022-2275(20)38178-5openalex-snapshot

Identification of multiple subclasses of plasma low density lipoproteins in normal humans.

inferredcites →https://doi.org/10.1016/s0968-0004(99)01408-5openalex-snapshot

Ceramide and apoptosis

inferredcites →https://doi.org/10.1016/s1097-2765(01)00164-2openalex-snapshot

A PPARγ-LXR-ABCA1 Pathway in Macrophages Is Involved in Cholesterol Efflux and Atherogenesis

inferredcites →https://doi.org/10.1016/s2214-109x(20)30117-0openalex-snapshot

Global and regional prevalence, burden, and risk factors for carotid atherosclerosis: a systematic review, meta-analysis, and modelling study

inferredcites →https://doi.org/10.1021/acs.chemrev.8b00451openalex-snapshot

Emerging Diversity in Lipid–Protein Interactions

inferredcites →https://doi.org/10.1021/bi00011a039openalex-snapshot

Doubly-lipid-modified protein sequence motifs exhibit long-lived anchorage to lipid bilayer membranes

inferredcites →https://doi.org/10.1021/bi00038a029openalex-snapshot

Biosynthesis and Palmitoylation of Endothelial Nitric Oxide Synthase: Mutagenesis of Palmitoylation Sites, Cysteines-15 and/or -26, Argues against Depalmitoylation-Induced Translocation of the Enzyme

inferredcites →https://doi.org/10.1021/bi00099a013openalex-snapshot

Effect of alkyl chain unsaturation and cholesterol intercalation on oxygen transport in membranes: a pulse ESR spin labeling study

inferredcites →https://doi.org/10.1021/bi00486a023openalex-snapshot

Microimmiscibility and three-dimensional dynamic structures of phosphatidylcholine-cholesterol membranes: translational diffusion of a copper complex in the membrane

inferredcites →https://doi.org/10.1021/bi961720eopenalex-snapshot

Palmitoylation of Endothelial Nitric Oxide Synthase Is Necessary for Optimal Stimulated Release of Nitric Oxide: Implications for Caveolae Localization

inferredcites →https://doi.org/10.1021/j100300a003openalex-snapshot

Physical properties of surfactant bilayer membranes: thermal transitions, elasticity, rigidity, cohesion and colloidal interactions

inferredcites →https://doi.org/10.1038/307648a0openalex-snapshot

Induction of human vascular endothelial stress fibres by fluid shear stress

inferredcites →https://doi.org/10.1038/35080071openalex-snapshot

How proteins move lipids and lipids move proteins

inferredcites →https://doi.org/10.1038/72869openalex-snapshot

Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient mice

inferredcites →https://doi.org/10.1038/82176openalex-snapshot

In vivo delivery of the caveolin-1 scaffolding domain inhibits nitric oxide synthesis and reduces inflammation

inferredcites →https://doi.org/10.1038/aps.2010.87openalex-snapshot

Caveolae and caveolin-1 mediate endocytosis and transcytosis of oxidized low density lipoprotein in endothelial cells

inferredcites →https://doi.org/10.1038/cr.2011.56openalex-snapshot

Regulation of cellular senescence by the essential caveolar component PTRF/Cavin-1

inferredcites →https://doi.org/10.1038/ijir.2009.59openalex-snapshot

The endothelial cell in health and disease: its function, dysfunction, measurement and therapy

inferredcites →https://doi.org/10.1038/jhh.2008.138openalex-snapshot

Endothelial microparticles: a universal marker of vascular health?

inferredcites →https://doi.org/10.1038/nature03952openalex-snapshot

A mechanosensory complex that mediates the endothelial cell response to fluid shear stress

inferredcites →https://doi.org/10.1038/nature08147openalex-snapshot

Emerging roles for lipids in shaping membrane-protein function

inferredcites →https://doi.org/10.1038/ncomms11805openalex-snapshot

In vivo modulation of endothelial polarization by Apelin receptor signalling

inferredcites →https://doi.org/10.1038/ncomms13516openalex-snapshot

Genome-wide RNAi screen reveals ALK1 mediates LDL uptake and transcytosis in endothelial cells

inferredcites →https://doi.org/10.1038/ncomms8292openalex-snapshot

Physical principles of membrane remodelling during cell mechanoadaptation

inferredcites →https://doi.org/10.1038/ncpcardio1397openalex-snapshot

Hemodynamic shear stress and the endothelium in cardiovascular pathophysiology

inferredcites →https://doi.org/10.1038/nm1238openalex-snapshot

Ceramide upregulation causes pulmonary cell apoptosis and emphysema-like disease in mice

inferredcites →https://doi.org/10.1038/nm977openalex-snapshot

PAF-mediated pulmonary edema: a new role for acid sphingomyelinase and ceramide

inferredcites →https://doi.org/10.1038/nrm.2017.36openalex-snapshot

Vascular heterogeneity and specialization in development and disease

inferredcites →https://doi.org/10.1038/nrm2596openalex-snapshot

Mechanotransduction in vascular physiology and atherogenesis

inferredcites →https://doi.org/10.1038/nrmicro2815openalex-snapshot

The early evolution of lipid membranes and the three domains of life

inferredcites →https://doi.org/10.1038/s41467-017-01186-zopenalex-snapshot

Hyperlipidemia-induced cholesterol crystal production by endothelial cells promotes atherogenesis

inferredcites →https://doi.org/10.1038/s41467-019-13782-2openalex-snapshot

An Abl-FBP17 mechanosensing system couples local plasma membrane curvature and stress fiber remodeling during mechanoadaptation

inferredcites →https://doi.org/10.1038/s41586-019-1140-4openalex-snapshot

SR-B1 drives endothelial cell LDL transcytosis via DOCK4 to promote atherosclerosis

inferredcites →https://doi.org/10.1038/s41598-020-72309-8openalex-snapshot

Physiologic blood flow is turbulent

inferredcites →https://doi.org/10.1038/s41598-021-85476-zopenalex-snapshot

High intraluminal pressure promotes vascular inflammation via caveolin-1

inferredcites →https://doi.org/10.1038/s42003-021-02285-wopenalex-snapshot

Integration of substrate- and flow-derived stresses in endothelial cell mechanobiology

inferredcites →https://doi.org/10.1038/sj.bjp.0706173openalex-snapshot

Ceramide alters endothelial cell permeability by a nonapoptotic mechanism

inferredcites →https://doi.org/10.1038/sj.emboj.7601204openalex-snapshot

Dynamics in the plasma membrane: how to combine fluidity and order

inferredcites →https://doi.org/10.1038/srep31596openalex-snapshot

Structural and functional characterization of endothelial microparticles released by cigarette smoke

inferredcites →https://doi.org/10.1038/srep37127openalex-snapshot

Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma

inferredcites →https://doi.org/10.1039/c2sm25263eopenalex-snapshot

Effects of cholesterol on nano-mechanical properties of the living cell plasma membrane

inferredcites →https://doi.org/10.1042/bsr20182144openalex-snapshot

Inhibition of acid sphingomyelinase activity ameliorates endothelial dysfunction in db/db mice

inferredcites →https://doi.org/10.1056/nejm199901143400207openalex-snapshot

Atherosclerosis — An Inflammatory Disease

inferredcites →https://doi.org/10.1063/1.5129812openalex-snapshot

Good advice for endothelial cells: Get in line, relax tension, and go with the flow

inferredcites →https://doi.org/10.1063/1.5133645openalex-snapshot

Mechanobiology of dynamic enzyme systems

inferredcites →https://doi.org/10.1073/pnas.1018572108openalex-snapshot

Shear rheology of lipid monolayers and insights on membrane fluidity

inferredcites →https://doi.org/10.1073/pnas.170282597openalex-snapshot

Molecular mechanism of endothelial growth arrest by laminar shear stress

inferredcites →https://doi.org/10.1073/pnas.2014029117openalex-snapshot

Shear stress activates mitochondrial oxidative phosphorylation by reducing plasma membrane cholesterol in vascular endothelial cells

inferredcites →https://doi.org/10.1073/pnas.82.10.3272openalex-snapshot

Preferential orientation of centrioles toward the heart in endothelial cells of major blood vessels is reestablished after reversal of a segment.

inferredcites →https://doi.org/10.1073/pnas.83.7.2114openalex-snapshot

Turbulent fluid shear stress induces vascular endothelial cell turnover in vitro.

inferredcites →https://doi.org/10.1073/pnas.85.6.1841openalex-snapshot

Hydrodynamic hyperpolarization of endothelial cells.

inferredcites →https://doi.org/10.1073/pnas.93.13.6448openalex-snapshot

Targeting of nitric oxide synthase to endothelial cell caveolae via palmitoylation: implications for nitric oxide signaling.

inferredcites →https://doi.org/10.1073/pnas.96.6.3154openalex-snapshot

Spatial and temporal regulation of gap junction connexin43 in vascular endothelial cells exposed to controlled disturbed flows in vitro

inferredcites →https://doi.org/10.1074/jbc.271.32.19251openalex-snapshot

The Sphingomyelin-Ceramide Signaling Pathway Is Involved in Oxidized Low Density Lipoprotein-induced Cell Proliferation

inferredcites →https://doi.org/10.1074/jbc.272.41.25437openalex-snapshot

Dissecting the Interaction between Nitric Oxide Synthase (NOS) and Caveolin

inferredcites →https://doi.org/10.1074/jbc.273.10.5419openalex-snapshot

Caveolins, a Family of Scaffolding Proteins for Organizing “Preassembled Signaling Complexes” at the Plasma Membrane

inferredcites →https://doi.org/10.1074/jbc.273.16.9681openalex-snapshot

Oxidized Low Density Lipoprotein Induces Apoptosis in Cultured Human Umbilical Vein Endothelial Cells by Common and Unique Mechanisms

inferredcites →https://doi.org/10.1074/jbc.273.42.27389openalex-snapshot

Apoptosis and Activation of the Sphingomyelin-Ceramide Pathway Induced by Oxidized Low Density Lipoproteins Are Not Causally Related in ECV-304 Endothelial Cells

inferredcites →https://doi.org/10.1074/jbc.274.43.30361openalex-snapshot

Mildly Oxidized Low Density Lipoprotein Induces Contraction of Human Endothelial Cells through Activation of Rho/Rho Kinase and Inhibition of Myosin Light Chain Phosphatase

inferredcites →https://doi.org/10.1074/jbc.274.45.32512openalex-snapshot

Oxidized Low Density Lipoprotein Displaces Endothelial Nitric-oxide Synthase (eNOS) from Plasmalemmal Caveolae and Impairs eNOS Activation

inferredcites →https://doi.org/10.1074/jbc.274.46.33148openalex-snapshot

Depalmitoylation of Endothelial Nitric-oxide Synthase by Acyl-protein Thioesterase 1 Is Potentiated by Ca2+-Calmodulin

inferredcites →https://doi.org/10.1074/jbc.275.15.11278openalex-snapshot

High Density Lipoprotein Prevents Oxidized Low Density Lipoprotein-induced Inhibition of Endothelial Nitric-oxide Synthase Localization and Activation in Caveolae

inferredcites →https://doi.org/10.1074/jbc.m105408200openalex-snapshot

Caveolin-1 Null Mice Are Viable but Show Evidence of Hyperproliferative and Vascular Abnormalities

inferredcites →https://doi.org/10.1074/jbc.m202465200openalex-snapshot

Hypercholesterolemia Promotes a CD36-dependent and Endothelial Nitric-oxide Synthase-mediated Vascular Dysfunction

inferredcites →https://doi.org/10.1074/jbc.m210375200openalex-snapshot

Transient Mechanoactivation of Neutral Sphingomyelinase in Caveolae to Generate Ceramide

inferredcites →https://doi.org/10.1074/jbc.m301179200openalex-snapshot

Localized Cdc42 Activation, Detected Using a Novel Assay, Mediates Microtubule Organizing Center Positioning in Endothelial Cells in Response to Fluid Shear Stress

inferredcites →https://doi.org/10.1080/09687680802620351openalex-snapshot

The fat controller: roles of palmitoylation in intracellular protein trafficking and targeting to membrane microdomains (Review)

inferredcites →https://doi.org/10.1083/jcb.103.1.63openalex-snapshot

Expression and intracellular distribution of stress fibers in aortic endothelium.

inferredcites →https://doi.org/10.1083/jcb.200210135openalex-snapshot

Shear stress–induced endothelial cell polarization is mediated by Rho and Rac but not Cdc42 or PI 3-kinases

inferredcites →https://doi.org/10.1083/jcb.201003086openalex-snapshot

Caveolin-1 is ubiquitinated and targeted to intralumenal vesicles in endolysosomes for degradation

inferredcites →https://doi.org/10.1083/jcb.201504042openalex-snapshot

Caveolae protect endothelial cells from membrane rupture during increased cardiac output

inferredcites →https://doi.org/10.1083/jcb.79.1.27openalex-snapshot

Open junctions in the endothelium of the postcapillary venules of the diaphragm.

inferredcites →https://doi.org/10.1083/jcb.96.6.1677openalex-snapshot

Visualization of the binding, endocytosis, and transcytosis of low-density lipoprotein in the arterial endothelium in situ.

inferredcites →https://doi.org/10.1089/ars.2010.3361openalex-snapshot

Effects of Shear Stress and Stretch on Endothelial Function

inferredcites →https://doi.org/10.1089/ars.2010.3619openalex-snapshot

Lipid Raft Redox Signaling: Molecular Mechanisms in Health and Disease

inferredcites →https://doi.org/10.1089/ars.2010.3679openalex-snapshot

Flow Shear Stress and Atherosclerosis: A Matter of Site Specificity

inferredcites →https://doi.org/10.1089/ars.2013.5624openalex-snapshot

Mechanotransduction in the Endothelium: Role of Membrane Proteins and Reactive Oxygen Species in Sensing, Transduction, and Transmission of the Signal with Altered Blood Flow

inferredcites →https://doi.org/10.1089/hum.2018.120openalex-snapshot

ABCA1 Overexpression in Endothelial Cells In Vitro Enhances ApoAI-Mediated Cholesterol Efflux and Decreases Inflammation

inferredcites →https://doi.org/10.1091/mbc.e02-11-0761openalex-snapshot

Differential Caveolin-1 Polarization in Endothelial Cells during Migration in Two and Three Dimensions

inferredcites →https://doi.org/10.1091/mbc.e11-04-0287openalex-snapshot

Nesprin-3 regulates endothelial cell morphology, perinuclear cytoskeletal architecture, and flow-induced polarization

inferredcites →https://doi.org/10.1093/ajcn/71.1.213sopenalex-snapshot

Fatty acid modulation of endothelial activation

inferredcites →https://doi.org/10.1093/bja/aeh163openalex-snapshot

Physiology of the endothelium

inferredcites →https://doi.org/10.1093/cvr/cvt044openalex-snapshot

Does low and oscillatory wall shear stress correlate spatially with early atherosclerosis? A systematic review

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A novel assay uncovers an unexpected role for SR-BI in LDL transcytosis

inferredcites →https://doi.org/10.1093/cvr/cvx226openalex-snapshot

Endothelial permeability, LDL deposition, and cardiovascular risk factors—a review

inferredcites →https://doi.org/10.1093/ehjqcco/qcaa060openalex-snapshot

The burden of atherosclerosis in Portugal

inferredcites →https://doi.org/10.1093/eurheartj/ehab484openalex-snapshot

2021 ESC Guidelines on cardiovascular disease prevention in clinical practice

inferredcites →https://doi.org/10.1093/eurheartj/ehr304openalex-snapshot

Nitric oxide synthases: regulation and function

inferredcites →https://doi.org/10.1093/eurheartj/ehz455openalex-snapshot

2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk

inferredcites →https://doi.org/10.1093/eurheartj/ehz962openalex-snapshot

Low-density lipoproteins cause atherosclerotic cardiovascular disease: pathophysiological, genetic, and therapeutic insights: a consensus statement from the European Atherosclerosis Society Consensus Panel

inferredcites →https://doi.org/10.1093/jn/126.suppl_4.1053sopenalex-snapshot

The Role of Oxidized Low Density Lipoprotein in Atherogenesis

inferredcites →https://doi.org/10.1093/ndt/gfu275openalex-snapshot

The evolution of blood pressure and the rise of mankind

inferredcites →https://doi.org/10.1096/fj.01-0434fjeopenalex-snapshot

Rate sensitivity of shear‐induced changes in the lateral diffusion of endothelial cell membrane lipids: a role for membrane perturbation in shear‐induced MAPK activation

inferredcites →https://doi.org/10.1096/fj.11-183350openalex-snapshot

Caveolin‐1 deficiency decreases atherosclerosis by hampering leukocyte influx into the arterial wall and generating a regulatory T‐cell response

inferredcites →https://doi.org/10.1096/fj.201601244rropenalex-snapshot

Endothelial microparticles prevent lipid‐induced endothelial damage via Akt/eNOS signaling and reduced oxidative stress

inferredcites →https://doi.org/10.1096/fj.202002144ropenalex-snapshot

Functional lipidomics of vascular endothelial cells in response to laminar shear stress

inferredcites →https://doi.org/10.1097/00000539-200009000-00007openalex-snapshot

Hematocrit, Volume Expander, Temperature, and Shear Rate Effects on Blood Viscosity

inferredcites →https://doi.org/10.1097/00041433-200410000-00005openalex-snapshot

Caveolin-1 and caveolae in atherosclerosis: differential roles in fatty streak formation and neointimal hyperplasia

inferredcites →https://doi.org/10.1098/rstb.2007.2128openalex-snapshot

The shear stress of it all: the cell membrane and mechanochemical transduction

inferredcites →https://doi.org/10.1098/rstb.2018.0221openalex-snapshot

The plasma membrane as a mechanochemical transducer

inferredcites →https://doi.org/10.1101/cshperspect.a006528openalex-snapshot

Endothelial Cell-to-Cell Junctions: Adhesion and Signaling in Physiology and Pathology

inferredcites →https://doi.org/10.1111/febs.12263openalex-snapshot

What does S ‐palmitoylation do to membrane proteins?

inferredcites →https://doi.org/10.1111/febs.15781openalex-snapshot

Protein S‐Palmitoylation: advances and challenges in studying a therapeutically important lipid modification

inferredcites →https://doi.org/10.1111/j.1523-1755.2005.00256.xopenalex-snapshot

Endothelial cell dysfunction: The syndrome in making

inferredcites →https://doi.org/10.1111/j.1525-142x.2005.05040.xopenalex-snapshot

The origin of the endothelial cells: an evo‐devo approach for the invertebrate/vertebrate transition of the circulatory system

inferredcites →https://doi.org/10.1111/j.1538-7836.2005.01780.xopenalex-snapshot

Elevation of circulating endothelial microparticles in patients with chronic renal failure

inferredcites →https://doi.org/10.1111/j.1582-4934.2008.00639.xopenalex-snapshot

Circulating endothelial cells, microparticles and progenitors: key players towards the definition of vascular competence

inferredcites →https://doi.org/10.1111/j.1600-0854.2009.01023.xopenalex-snapshot

Biogenesis of Caveolae: Stepwise Assembly of Large Caveolin and Cavin Complexes

inferredcites →https://doi.org/10.1111/j.1939-165x.2009.00152.xopenalex-snapshot

Immunomagnetic isolation of canine circulating endothelial and endothelial progenitor cells

inferredcites →https://doi.org/10.1111/jcmm.12607openalex-snapshot

Endothelial microparticles reduce ICAM ‐1 expression in a micro RNA ‐222‐dependent mechanism

inferredcites →https://doi.org/10.1111/jth.12253openalex-snapshot

Evolutionary origins of the blood vascular system and endothelium

inferredcites →https://doi.org/10.1111/tra.12533openalex-snapshot

Transcellular vesicular transport in epithelial and endothelial cells: Challenges and opportunities

inferredcites →https://doi.org/10.1111/tra.12586openalex-snapshot

Transverse distribution of plasma membrane bilayer cholesterol: Picking sides

inferredcites →https://doi.org/10.1113/jp276245openalex-snapshot

Novel mechanisms regulating endothelial barrier function in the pulmonary microcirculation

inferredcites →https://doi.org/10.1113/jphysiol.2002.031534openalex-snapshot

Endothelial nitric oxide synthase, caveolae and the development of atherosclerosis

inferredcites →https://doi.org/10.1115/1.2891384openalex-snapshot

Vascular Fluid Mechanics, the Arterial Wall, and Atherosclerosis

inferredcites →https://doi.org/10.1115/1.3120861openalex-snapshot

Response of Arteries to Near-Wall Fluid Dynamic Behavior

inferredcites →https://doi.org/10.1115/1.3138275openalex-snapshot

Vascular Endothelial Morphology as an Indicator of the Pattern of Blood Flow

inferredcites →https://doi.org/10.1115/1.3138276openalex-snapshot

The Dynamic Response of Vascular Endothelial Cells to Fluid Shear Stress

showing the first 200 of 361

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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GPR91 mediates low shear stress-induced endothelial ferroptosis via EGR1-dependent GPX4 repression

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New opportunities for identifying the risk of cardiovascular events in young people: the role of familial hypercholesterolemia

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Qing-Xue-Xiao-Zhi Formula Attenuates Trimethylamine N-Oxide-Induced Atherosclerosis Via Myd88 S-Palmitoylation-Mediated Pparα/Nf-Κb Crosstalk in Endothelial Inflammation

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Distinct Features of Vascular Diseases in COVID-19

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Identification of Important Genes Associated with the Development of Atherosclerosis

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Role of Hyperlipidemia in the Development of Endothelial Dysfunction

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Clinical significance of polyunsaturated fatty acids in the prevention of cardiovascular diseases

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Comparative analysis of lipid components in fresh Crassostrea Hongkongensis (raw) and its dried products by using high-performance liquid chromatography/quadrupole time-of-flight mass spectrometry (HPLC/Q-TOF-MS)

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Effects of Atherogenic Factors on Endothelial Cells: Bioinformatics Analysis of Differentially Expressed Genes and Signaling Pathways

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Effects of Incretin-Based Treatment on the Diastolic (Dys)Function in Patients with Uncontrolled Type 2 Diabetes Mellitus: A Prospective Study with 1-Year Follow-Up

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Genetic and Epigenetic Regulation of Lipoxygenase Pathways and Reverse Cholesterol Transport in Atherogenesis

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Self-Similar Functional Circuit Models of Arteries and Deterministic Fractal Operators: Theoretical Revelation for Biomimetic Materials

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Involvement of the Innate Immune System in the Pathogenesis of Chronic Obstructive Pulmonary Disease

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Involvement of Fatty Acids and Their Metabolites in the Development of Inflammation in Atherosclerosis

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Molecular Pharmacology of Inflammation Resolution in Atherosclerosis

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The Importance of the Plasma Membrane in Atherogenesis

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Participation of Krüppel-like Factors in Atherogenesis

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Impact of a Precision Intervention for Vascular Health in Middle-Aged and Older Postmenopausal Women Using Polar Heart Rate Sensors: A 24-Week RCT Study Based on the New Compilation of Tai Chi (Bafa Wubu)

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Realce de la placa de aterosclerosis intracraneal como marcador de su riesgo clínico y actividad inflamatoria

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The Past, Present, and Future of Dyslipidemia: A Narrative Review

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