Results 151 to 160 of about 63,314 (347)

DGAT‐1 deficiency: Congenital diarrhea and dietary treatment

open access: yesJPGN Reports, EarlyView.
Abstract DGAT‐1 (Diacylglycerol Acyltransferase‐1) deficiency is an autosomal recessive disorder which causes severe impairment in lipid absorption. We report a case of an infant suffering from persistent diarrhea starting at the age of four weeks. Further investigations identified DGAT‐1 deficiency as underlying cause.
Clemens Gardemann   +6 more
wiley   +1 more source

The Relationship Between Serum SFRP5, ApoA‐I, HDL3‐C Level and In‐Stent Restenosis After PCI in Acute Myocardial Infarction and the Combined Predictive Value

open access: yesThe Kaohsiung Journal of Medical Sciences, EarlyView.
ABSTRACT This study aims to investigate the relationship between serum secreted frizzled‐related protein 5 (SFRP5), apolipoprotein A‐I (ApoA‐I), high‐density lipoprotein 3‐cholesterol (HDL3‐C) and in‐stent restenosis (ISR) after percutaneous coronary intervention (PCI) in acute myocardial infarction (AMI) and their combined predictive value.
Li‐Qiang Cui, Xue‐Dong Wang
wiley   +1 more source

Monotopic topology is required for lipid droplet targeting of ancient ubiquitous protein 1[S]

open access: yesJournal of Lipid Research, 2013
Ancient ubiquitous protein 1 (AUP1) is a multifunctional protein, which acts on both lipid droplets (LDs) and the endoplasmic reticulum (ER) membrane.
Ana Stevanovic, Christoph Thiele
doaj  

Exploring the dynamic landscape of immunopeptidomics: Unravelling posttranslational modifications and navigating bioinformatics terrain

open access: yesMass Spectrometry Reviews, EarlyView.
Abstract Immunopeptidomics is becoming an increasingly important field of study. The capability to identify immunopeptides with pivotal roles in the human immune system is essential to shift the current curative medicine towards personalized medicine. Throughout the years, the field has matured, giving insight into the current pitfalls. Nowadays, it is
Daniel Flender   +5 more
wiley   +1 more source

Enzymatic activities of the human AGPAT isoform 3 and isoform 5: localization of AGPAT5 to mitochondria[S]

open access: yesJournal of Lipid Research, 2011
The enzyme 1-acylglycerol-3-phosphate-O-acyltransferase (AGPAT) converts lysophosphatidic acid (LPA) to phosphatidic acid (PA). In this study, we show enzymatic properties, tissue distribution, and subcellular localization of human AGPAT3 and AGPAT5.
Sneha S. Prasad   +2 more
doaj  

Home - About - Disclaimer - Privacy