Mass Spectrometric Analysis of <i>N</i>-Glycome of Patatin Proteins from Three Potato Cultivars. [PDF]
Li L, Luo S, Wu Y, Zhou Y, Ma Y, Niu J.
europepmc +1 more source
Role of selenium in the pathophysiology of cardiorenal anaemia syndrome
Abstract Chronic kidney disease (CKD) and cardiovascular disease (CVD) have multiple bidirectional mechanisms, and anaemia is one of the critical factors that are associated with the progression of the two disorders [referred to as cardiorenal anaemia syndrome (CRAS)].
Shigeyuki Arai +2 more
wiley +1 more source
Biomarkers of lung congestion and injury in acute heart failure
Abstract Acute heart failure (AHF) classification and management are primarily based on lung congestion and/or hypoperfusion. The quantification of the vascular and tissue lung damage is not standard practice though biomarkers of lung injury may play a relevant role in this context.
Marco Guazzi +9 more
wiley +1 more source
Distinct O-Linked Glycosylation Systems in Signaling and Immune Regulation. [PDF]
Wang S, Xiao S, Huang Y, Wang X.
europepmc +1 more source
The Expanding Role of Diazirines in Synthetic Methodology
Beyond their established role in photoaffinity labeling, diazirines have emerged as versatile reagents in synthetic chemistry. This review highlights their dual reactivity as carbene and nitrogen‐transfer precursors, showcasing mechanistic insights and diverse applications in cyclopropanations, cycloadditions, skeletal editing, amination, heterocycle ...
Viktor Savic +3 more
wiley +1 more source
Site-Specific Analysis of Bone Morphogenetic Protein Receptor Type 2 <i>N</i>‑Glycosylation Reveals High Heterogeneity at Site Involved in Ligand Binding. [PDF]
Nazaire V +3 more
europepmc +1 more source
Abstract Objective Mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE) is an underrecognized pediatric cortical lesion associated with somatic X‐linked SLC35A2 variants in approximately 50% of individuals. The genetic etiology in individuals without detectable SLC35A2 mutations remains undefined, which limits
Erica Cecchini +13 more
wiley +1 more source
Cross-talk between glycosylation pathways: Mechanistic insights and implications for human diseases. [PDF]
Very N, El Yazidi-Belkoura I.
europepmc +1 more source
Inherited metabolic epilepsies–established diseases, new approaches
Abstract Inherited metabolic epilepsies (IMEs) represent the inherited metabolic disorders (IMDs) in which epilepsy is a prevailing component, often determining other neurodevelopmental outcomes associated with the disorder. The different metabolic pathways affected by individual IMEs are the basis of their rarity and heterogeneity.
Itay Tokatly Latzer, Phillip L. Pearl
wiley +1 more source
Genetic Evolution and Molecular Characterization of PRRSV GP5 in Germany. [PDF]
Pang J +8 more
europepmc +1 more source

