Results 141 to 150 of about 3,095,271 (376)
Mechanism and therapy of hereditary angioedema typ III and role of the contact system in inflammatory diseases [PDF]
Combinations of proinflammatory and procoagulant reactions are associated with a variety of disorders affecting the cardiovascular system. Vascular leakage contributes to the pathology of conditions such as, sepsis, allergy and anaphylactic reactions ...
Björkqvist, Jenny
core +1 more source
This work offers unique Ginger‐based 3D‐printable resins that can print customizable high‐resolution complex designs. The customizable printing backbone of Zingerol prints also mimics various human bones' strength. Acquisition of in‐vivo biocompatibility in rat model with no severe inflammatory response, along with in‐vitro antioxidant and ex‐vivo anti‐
Simran Jindal +9 more
wiley +1 more source
Herediter anjioödemde kısa dönem danazol profilaksisi ile implant tedavisi: Vaka raporu
Herediter anjio ödem (HAÖ), C1 esteraz inhibitör proteininin konjenital eksikliğine bağlı olarak meydana gelen, nadir gözlenen, otozomal dominant bir hastalıktır. HAÖ atakları, spontan veya bir travmaya bağlı olarak, ekstremitelerde, yüzde, göğüste, hava
Zeynep Burçin Gönen +4 more
doaj +1 more source
Transition metal oxy/carbo‐nitrides show great promise as catalysts for sustainable processes. A Mn‐Mo mixed‐metal oxynitride attains remarkable performance for the direct synthesis of acetonitrile, an important commodity chemical, via sequential C─N and C─C coupling from syngas (C1) and ammonia (N1) feedstocks.
M. Elena Martínez‐Monje +7 more
wiley +1 more source
Background Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare autosomal dominant disease characterized by episodes of acute subcutaneous swelling, and/or recurrent severe abdominal pain.
Anna Valerieva +3 more
doaj +1 more source
Molecular Genetics of C1 Inhibitor
More than 100 different C1 inhibitor gene mutations have been described in hereditary angioedema (HAE) patients. Sixty-nine mutations have been reported in patients with the quantitative C1 inhibitor defect (type 1 HAE) in two recent large-scale studies. These changes were found distributed over all exons and exon/intron boundaries.
openaire +2 more sources
The serpin C1 inhibitor (C1-INH) is the only regulator of classical complement activation as well as the major regulator of the contact system. Its importance is demonstrated by hereditary angioedema (HAE), a severe disease with potentially life ...
A. Schoenfeld, Eric Lahrsen, S. Alban
semanticscholar +1 more source
A C1-inhibitor-complex assay (INCA): a method to detect C1 activation in vitro and in vivo. [PDF]
C.E. Hack +4 more
openalex +1 more source
This review presents a focused and integrated perspective on copper‐based catalysts for the selective electrochemical reduction of CO2 to methanol. It elucidates active site dynamics, mechanistic pathways, and structure–activity relationships, while connecting fundamental insights with catalyst design, reactor engineering, and techno‐economic ...
Debabrata Bagchi +7 more
wiley +1 more source
Role for the third constant domain of the IgG H chain in activation of complement in the presence of C1 inhibitor. [PDF]
Mariko Okada, S Utsumi
openalex +1 more source

