Results 21 to 30 of about 2,139,065 (244)

Severe dengue in children associates with dysregulation of lipid homeostasis, complement cascade and retinol transport [PDF]

open access: yesClinical and Translational Medicine, 2023
Aleksha Panwar   +11 more
doaj   +2 more sources

RBP4 in Ageing [PDF]

open access: yesBiomedicines
Background: The protein that binds to retinol 4 (RBP4), is a lipocalin-family protein, secreted primarily by the adipose tissue and the liver, and has also been reported to be produced by other tissues, including the kidney.
María Paz Nieto-Bona   +2 more
doaj   +2 more sources

Biological Functions of RBP4 and Its Relevance for Human Diseases

open access: yesFrontiers in Physiology, 2021
Retinol binding protein 4 (RBP4) is a member of the lipocalin family and the major transport protein of the hydrophobic molecule retinol, also known as vitamin A, in the circulation.
Julia S. Steinhoff   +3 more
doaj   +1 more source

The transport of retinol in human plasma [PDF]

open access: yesFEBS Letters, 1969
Evidence in support of the view that tryptophanrich prealbumin [l] may serve as the specific transport protein for retinol in human plasma has previously been reported by Alvsaker, Haugli and Laland [2]. Since thyroxine is transported partly by this protein [3] , thyroxine and retinol would then share the same transport protein. In order to investigate
Johannessen, S.   +2 more
openaire   +2 more sources

An in vitro model for vitamin A transport across the human blood–brain barrier

open access: yeseLife, 2023
Vitamin A, supplied by the diet, is critical for brain health, but little is known about its delivery across the blood–brain barrier (BBB). Brain microvascular endothelial-like cells (BMECs) differentiated from human-derived induced pluripotent stem ...
Chandler B Est, Regina M Murphy
doaj   +1 more source

Identification of Transthyretin Tetramer Kinetic Stabilizers That Are Capable of Inhibiting the Retinol-Dependent Retinol Binding Protein 4-Transthyretin Interaction [PDF]

open access: yes, 2021
Dissociation of transthyretin (TTR) tetramers may lead to misfolding and aggregation of pro-amyloidogenic monomers, which underlies TTR amyloidosis (ATTR) pathophysiology.
Arun, Raja   +7 more
core   +1 more source

Liver Retinol Transporter and Receptor for Serum Retinol-binding Protein (RBP4) [PDF]

open access: yesJournal of Biological Chemistry, 2013
Vitamin A (retinol) is absorbed in the small intestine, stored in liver, and secreted into circulation bound to serum retinol-binding protein (RBP4). Circulating retinol may be taken up by extrahepatic tissues or recycled back to liver multiple times before it is finally metabolized or degraded.
Philomena, Alapatt   +9 more
openaire   +2 more sources

Intact vitamin A transport is critical for cold-mediated adipose tissue browning and thermogenesis

open access: yesMolecular Metabolism, 2020
Objective: Transformation of white into brown fat (“browning”) reduces obesity in many preclinical models and holds great promise as a therapeutic concept in metabolic disease. Vitamin A metabolites (retinoids) have been linked to thermogenic programming
Anna Fenzl   +11 more
doaj   +1 more source

TNF receptor–related factor 3 inactivation promotes the development of intrahepatic cholangiocarcinoma through NF‐κB‐inducing kinase–mediated hepatocyte transdifferentiation

open access: yesHepatology, EarlyView., 2022
Abstract Background and Aims Intrahepatic cholangiocarcinoma (ICC) is a deadly but poorly understood disease, and its treatment options are very limited. The aim of this study was to identify the molecular drivers of ICC and search for therapeutic targets.
Yuto Shiode   +16 more
wiley   +1 more source

Genetic predisposition to porto‐sinusoidal vascular disorder: A functional genomic‐based, multigenerational family study

open access: yesHepatology, EarlyView., 2022
A deleterious variant of FCHSD1 results in mTOR pathway overactivation and may cause porto‐sinusoidal vascular disorder (PSVD). The pedigree of the family demonstrated an autosomal dominant disease with variable expressivity. Whole‐genome sequencing and Sanger sequencing both validated the existence of the FCHSD1 variant and the heterozygosity of c ...
Jingxuan Shan   +19 more
wiley   +1 more source

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