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Schematic Diagram of Solid Ground Curing Process. Solid ground curing utilizes the general process of hardening of photopolymers by a complete lighting and hardening of the entire surface, using specially prepared masks. [6] In SGC process, each layer of the prototype is cured by exposing to an ultra violet (UV) lamp instead of by laser scanning.
Server-Gated Cryptography (SGC), also known as International Step-Up by Netscape, is a defunct mechanism that was used to step up from 40-bit or 56-bit to 128-bit cipher suites with SSL. It was created in response to United States federal legislation on the export of strong cryptography in the 1990s. [ 1 ]
An alternative hypothesis states that a second, non-heme binding site accounts for the second NO dependent activation process to give the fully active enzyme. [2] Under conditions of oxidative stress, Fe(II)sGC can be oxidized and lose its heme. Heme-free (apo-sGC) no longer responds to NO, but does respond to so-called sGC activator compounds.
Soluble guanylate cyclase (sGC) stimulators are a class of drugs developed to treat heart failure, pulmonary hypertension, and other diseases. The first-in-class medication was riociguat , approved in 2013 for pulmonary hypertension.
Guanylate cyclase (EC 4.6.1.2, also known as guanyl cyclase, guanylyl cyclase, or GC; systematic name GTP diphosphate-lyase (cyclizing; 3′,5′-cyclic-GMP-forming)) is a lyase enzyme that converts guanosine triphosphate (GTP) to cyclic guanosine monophosphate (cGMP) and pyrophosphate: [1]
The Haeco-CSG process was designed to make stereophonic vinyl LP records compatible with mono playback equipment. These recordings were intended to make the two-channel stereo mix automatically "fold-down" properly to a single mono channel.
AOL upholds a rigorous editorial process to ensure what we publish is fair, accurate and trustworthy. The best hiking shoes of 2025, according to hiking experts Jennifer Beaudry
Vericiguat is a direct stimulator of soluble guanylate cyclase, an important enzyme in vascular smooth muscle cells. Specifically, vericiguat binds to the beta-subunit of the target site on the soluble guanylate cyclase enzyme. [11]