Studying lipoprotein trafficking in zebrafish, the case of chylomicron retention disease

Metabolic insights from zebrafish genetics, physiology, and chemical biology

(2015) Amnon Schlegel et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Animal model of Sar1b deficiency presents lipid absorption deficits similar to Anderson disease

(2015) Daniel S. Levic et al.   JOURNAL OF MOLECULAR MEDICINE-JMM

Making designer mutants in model organisms

(2014) Y. Peng et al.   DEVELOPMENT

Lxr-driven enterocyte lipid droplet formation delays transport of ingested lipids

(2014) Lourdes Cruz-Garcia et al.   JOURNAL OF LIPID RESEARCH

A Regulator of Secretory Vesicle Size, Kelch-Like Protein 12, Facilitates the Secretion of Apolipoprotein B100 and Very-Low-Density Lipoproteins—Brief Report

(2013) Chutikarn Butkinaree et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

The Endoplasmic Reticulum Coat Protein II Transport Machinery Coordinates Cellular Lipid Secretion and Cholesterol Biosynthesis

(2013) Lee G. D. Fryer et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Vesicle-mediated ER export of proteins and lipids

(2012) Amanda D. Gillon et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS

RETRACTED: Visualization of lipid metabolism in the zebrafish intestine reveals a relationship between NPC1L1-mediated cholesterol uptake and dietary fatty acid

(2012) James W. Walters et al.   CHEMISTRY & BIOLOGY

Ubiquitin-dependent regulation of COPII coat size and function

(2012) Lingyan Jin et al.   NATURE

ApoB-containing lipoproteins regulate angiogenesis by modulating expression of VEGF receptor 1

(2012) Inbal Avraham-Davidi et al.   NATURE MEDICINE

Molecular analysis and intestinal expression of SAR1 genes and proteins in Anderson's disease (Chylomicron retention disease)

(2011) Amandine Georges et al.   Orphanet Journal of Rare Diseases

Guidelines for the diagnosis and management of chylomicron retention disease based on a review of the literature and the experience of two centers

(2010) Noel Peretti et al.   Orphanet Journal of Rare Diseases