Regulation of phospholipid distribution in the lipid bilayer by flippases and scramblases

T Sakuragi, S Nagata - Nature Reviews Molecular Cell Biology, 2023 - nature.com
Cellular membranes function as permeability barriers that separate cells from the external
environment or partition cells into distinct compartments. These membranes are lipid …

[HTML][HTML] Carleman estimates for semi-discrete parabolic operators and application to the controllability of semi-linear semi-discrete parabolic equations

F Boyer, J Le Rousseau - Annales de l'Institut Henri Poincare (C) Non …, 2014 - Elsevier
In arbitrary dimension, in the discrete setting of finite-differences we prove a Carleman
estimate for a semi-discrete parabolic operator, in which the large parameter is connected to …

P4-ATPases as phospholipid flippases—structure, function, and enigmas

JP Andersen, AL Vestergaard, SA Mikkelsen… - Frontiers in …, 2016 - frontiersin.org
P4-ATPases comprise a family of P-type ATPases that actively transport or flip phospholipids
across cell membranes. This generates and maintains membrane lipid asymmetry, a …

Progressive familial intrahepatic cholestasis

LN Bull, RJ Thompson - Clinics in liver disease, 2018 - liver.theclinics.com
Bile was recognized by the ancient Greeks as 1 of the 4 humors; its importance is still
recognized in twenty-first century medicine, although maybe only by hepatologists. Bile …

Xenobiotic, bile acid, and cholesterol transporters: function and regulation

CD Klaassen, LM Aleksunes - Pharmacological reviews, 2010 - Elsevier
Transporters influence the disposition of chemicals within the body by participating in
absorption, distribution, and elimination. Transporters of the solute carrier family (SLC) …

Progressive familial intrahepatic cholestasis

E Jacquemin - Clinics and research in hepatology and …, 2012 - Elsevier
Progressive familial intrahepatic cholestasis (PFIC) refers to a heterogeneous group of
autosomal-recessive disorders of childhood that disrupt bile formation and present with …

Molecular overview of progressive familial intrahepatic cholestasis

S Amirneni, N Haep, MA Gad… - World journal of …, 2020 - pmc.ncbi.nlm.nih.gov
Cholestasis is a clinical condition resulting from the imapairment of bile flow. This condition
could be caused by defects of the hepatocytes, which are responsible for the complex …

[PDF][PDF] ATP8B1 and ABCB11 analysis in 62 children with normal gamma‐glutamyl transferase progressive familial intrahepatic cholestasis (PFIC): Phenotypic …

A Davit‐Spraul, M Fabre, S Branchereau… - …, 2010 - Wiley Online Library
Progressive familial intrahepatic cholestasis (PFIC) types 1 and 2 are characterized by
normal serum gamma‐glutamyl transferase (GGT) activity and are due to mutations in …

Phospholipid flippases: building asymmetric membranes and transport vesicles

TT Sebastian, RD Baldridge, P Xu… - Biochimica et Biophysica …, 2012 - Elsevier
Phospholipid flippases in the type IV P-type ATPase family (P4-ATPases) are essential
components of the Golgi, plasma membrane and endosomal system that play critical roles in …

Dynamic transbilayer lipid asymmetry

G van Meer - Cold Spring Harbor perspectives in biology, 2011 - cshperspectives.cshlp.org
Cells have thousands of different lipids. In the plasma membrane, and in membranes of the
late secretory and endocytotic pathways, these lipids are not evenly distributed over the two …