Results 251 to 260 of about 38,660 (297)
Status quo and future developments in the diagnosis and treatment of hereditary angioedema
Summary Hereditary angioedema (HAE) is a rare hereditary disease characterized by edema, which can be life‐threatening in case of swelling in the larynx. The most common form of HAE is caused by a mutation of the SERPING1 gene and is characterized by a deficiency (type I) or loss of function (type II) of the C1 inhibitor (C1‐INH), leading to excessive ...
Andreas Recke
wiley +1 more source
Glycan Signatures on Neutrophils in an Equine Model for Autoimmune Uveitis. [PDF]
Sprenzel CJ +3 more
europepmc +1 more source
Abstract Objective Dravet syndrome (DS) is a severe neurodevelopmental disorder caused by pathogenic variants in the SCN1A gene, which encodes the voltage‐gated sodium channel Nav1.1 α subunit. Experiments in animal models of DS—including the haploinsufficient Scn1a+/− mouse—have identified impaired excitability of interneurons in the hippocampus and ...
Limei Zhu +5 more
wiley +1 more source
Blood group O expression in normal tissues and tumors
The H antigen (O blood group), the precursor to A and B blood groups, is expressed on human erythrocytes. Two novel monoclonal antibodies generated using sea lamprey immunization, Tn4‐31L and OmcFL3‐02, specifically detect the H antigen on glycan microarrays, glycoproteins, and human cells.
Ea Kristine Clarisse Tulin +11 more
wiley +1 more source
Identification of SARS-CoV-2-binding lectins on a commercial lectin array. [PDF]
Neetu +5 more
europepmc +1 more source
Agglutinin chip screening of B cell surface biomarkers in Hashimoto's thyroiditis for therapeutic targeting. [PDF]
Ren JL, Wang XM.
europepmc +1 more source
Amniotic fluid glycoproteins as potential ligands for macrophage galactose-type C-type lectin and their possible implications for immunoregulation during pregnancy. [PDF]
Szczykutowicz J +2 more
europepmc +1 more source

