Skip to Main Content
ADVERTISEMENT
SCROLL TO CONTINUE WITH CONTENT



Property Value
Status
Version
Ad File
Disable Ads Flag
Environment
Moat Init
Moat Ready
Contextual Ready
Contextual URL
Contextual Initial Segments
Contextual Used Segments
AdUnit
SubAdUnit
Custom Targeting
Ad Events
Invalid Ad Sizes
Advertisement
Journal of Lipid Research
Open access logo
Close
  • Home
  • Articles & Volumes
    • Back
    • Papers in Press
    • Current Volume
    • List of Volumes
  • For Authors
    • Back
    • Information for Authors
    • Permission to Reuse Published Material
    • Submit Manuscript 
  • Journal Info
    • Back
    • 2023 Media Kit 
    • About Open Access 
    • About the Journal
    • Contact Information
    • Editorial Board 
    • New Content Alerts
  • Special collections
  • Images in Lipid Research
  • Virtual Issues
  • Thematic Reviews
  • Methods Papers
  • Commentaries
  • Patient Oriented
  • Regular Research Articles
  • Other ASBMB Publications
    • Back
    • Journal of Biological Chemistry
    • Molecular & Cellular Proteomics
    • ASBMB Today 
Advanced searchSave search

Please enter a term before submitting your search.

Ok
  • Submit
  • Log in
  • Register
  • Log in
    • Submit
    • Log in
Skip menu
    x

    Filter:

    Filters applied

    • Regular Research Articles
    • lipoproteinsRemove lipoproteins filter
    • phospholipidRemove phospholipid filter
    Clear all

    Article Type

    • Research Article3

    Publication Date

    • Last Year1
    • Last 2 Years2
    • Last 5 Years3
    Please choose a date range between 2021 and 2022.

    Author

    • Calabresi, Laura2
    • Parini, Paolo2
    • Pavanello, Chiara2
    • Aasa, Ulrika1
    • Arnemo, Jon M1
    • Bjorkhem, Ingemar1
    • Camejo, Gérman1
    • Fröbert, Ole1
    • Hurt-Camejo, Eva1
    • Kindberg, Jonas1
    • Lhomme, Marie1
    • Mihna, Daniel1
    • Morton, Richard E1
    • Ossoli, Alice1
    • Pedrelli, Matteo1
    • Risè, Patrizia1
    • Strazzella, Arianna1
    • Turri, Marta1
    • Veglia, Fabrizio1
    • Walentinsson, Anna1
    • Westerståhl, Maria1
    • Öörni, Katariina1

    Journal

    • Journal of Lipid Research3

    Keyword

    • CE3
    • cholesteryl ester3
    • PL3
    • TG3
    • triglyceride3
    • CETP2
    • cholesteryl ester transfer protein2
    • TC2
    • total cholesterol2
    • UC2
    • 1,6-diphenyl-1,3,5 hexatriene1
    • 1-(4-trimethylammoniumphenyl)-1,3,5-hexatriene1
    • AD1
    • ApoB1
    • ApoF1
    • CEC1
    • CEFA1
    • CM1
    • DPH1
    • FC1
    • FLD1
    • FPLC1
    • HyperTC1

    Access Filter

    • Open Access

    Regular Research Articles

    3 Results
    Subscribe to collection
    • Export
      • PDF
      • Citation

    Please select at least one article in order to proceed.

    Ok
    FilterHide Filter
    • Research Article
      Open Access

      Plasma FA composition in familial LCAT deficiency indicates SOAT2-derived cholesteryl ester formation in humans

      Journal of Lipid Research
      Vol. 63Issue 7100232Published online: May 18, 2022
      • Chiara Pavanello
      • Alice Ossoli
      • Arianna Strazzella
      • Patrizia Risè
      • Fabrizio Veglia
      • Marie Lhomme
      • and others
      Cited in Scopus: 0
      • Preview Hide Preview
      • Download PDF
      • Export Citation
        Mutations in the LCAT gene cause familial LCAT deficiency (Online Mendelian Inheritance in Man ID: #245900), a very rare metabolic disorder. LCAT is the only enzyme able to esterify cholesterol in plasma, whereas sterol O-acyltransferases 1 and 2 are the enzymes esterifying cellular cholesterol in cells. Despite the complete lack of LCAT activity, patients with familial LCAT deficiency exhibit circulating cholesteryl esters (CEs) in apoB-containing lipoproteins. To analyze the origin of these CEs, we investigated 24 carriers of LCAT deficiency in this observational study.
        Plasma FA composition in familial LCAT deficiency indicates SOAT2-derived cholesteryl ester formation in humans
      • Research Article
        Open Access

        Apolipoprotein F concentration, activity, and the properties of LDL controlling ApoF activation in hyperlipidemic plasma

        Journal of Lipid Research
        Vol. 63Issue 2100166Published online: January 7, 2022
        • Richard E. Morton
        • Daniel Mihna
        Cited in Scopus: 0
        • Preview Hide Preview
        • Download PDF
        • Export Citation
          Apolipoprotein F (ApoF) modulates lipoprotein metabolism by selectively inhibiting cholesteryl ester transfer protein activity on LDL. This ApoF activity requires that it is bound to LDL. How hyperlipidemia alters total plasma ApoF and its binding to LDL are poorly understood. In this study, total plasma ApoF and LDL-bound ApoF were quantified by ELISA (n = 200). Plasma ApoF was increased 31% in hypercholesterolemic plasma but decreased 20% in hypertriglyceridemia. However, in donors with combined hypercholesterolemia and hypertriglyceridemia, the elevated triglyceride ameliorated the rise in ApoF caused by hypercholesterolemia alone.
          Apolipoprotein F concentration, activity, and the properties of LDL controlling ApoF activation in hyperlipidemic plasma
        • Research Article
          Open Access

          Vasculoprotective properties of plasma lipoproteins from brown bears (Ursus arctos)

          Journal of Lipid Research
          Vol. 62100065Published online: March 10, 2021
          • Matteo Pedrelli
          • Paolo Parini
          • Jonas Kindberg
          • Jon M. Arnemo
          • Ingemar Bjorkhem
          • Ulrika Aasa
          • and others
          Cited in Scopus: 0
          • Preview Hide Preview
          • Download PDF
          • Export Citation
            Plasma cholesterol and triglyceride (TG) levels are twice as high in hibernating brown bears (Ursus arctos) than healthy humans. Yet, bears display no signs of early stage atherosclerosis development when adult. To explore this apparent paradox, we analyzed plasma lipoproteins from the same 10 bears in winter (hibernation) and summer using size exclusion chromatography, ultracentrifugation, and electrophoresis. LDL binding to arterial proteoglycans (PGs) and plasma cholesterol efflux capacity (CEC) were also evaluated.
            Vasculoprotective properties of plasma lipoproteins from brown bears (Ursus arctos)
          Page 1 of 1

          Login to your account

          Show
          Forgot password?
          Don’t have an account?
          Create a Free Account

          If you don't remember your password, you can reset it by entering your email address and clicking the Reset Password button. You will then receive an email that contains a secure link for resetting your password

          If the address matches a valid account an email will be sent to __email__ with instructions for resetting your password

          Cancel
          • Home
          • Articles & Volumes
          • Papers in Press
          • Current Volume
          • List of Volumes
          • For Authors
          • Information for Authors
          • Permissions
          • Submit Manuscript
          • Contact Us
          • Contact Information
          • Journal Info
          • 2023 Media Kit
          • Open Access
          • About the Journal
          • Editorial Board
          • New Content Alerts
          • Special collections
          • Images in Lipid Research
          • Virtual Issues
          • Thematic Reviews
          • Methods Papers
          • Commentaries
          • Patient Oriented
          • Regular Research Articles
          • Other ASBMB Publications
          • Journal of Biological Chemistry
          • Molecular & Cellular Proteomics
          • ASBMB Today

          ASBMB  ASBMB  ASBMB  ASBMB

          ISSN 0022-2275
          We use cookies to help provide and enhance our service and tailor content. To update your cookie settings, please visit the for this site.
          Copyright © 2022 Elsevier Inc. except certain content provided by third parties. The content on this site is intended for healthcare professionals.

          • Privacy Policy  
          • Terms and Conditions  
          • Accessibility  
          • Elsevier Help & Contact

          RELX