Examples of using Nucleoside in English and their translations into German
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Belongs to: antimetabolite, nucleoside.
Nucleoside and nucleotide reverse transcriptase inhibitors, ATC code.
Pharmacotherapeutic group: nucleoside and nucleotide reverse transcriptase inhibitors.
Another notable modified base is hypoxanthine,a deaminated adenine base whose nucleoside is called inosine I.
Naïve patients also received nucleoside reverse transcriptase inhibitors.
People also translate
Of nucleoside should triphosphate mangosteen for anthraquinones with confirmed heterogeneous acidosis.
Where the phosphate group proximal to the nucleoside the site of the phosphate-ester bond.
Cangrelor is deactivated rapidly in theplasma by dephosphorylation to form its primary metabolite, a nucleoside.
Pharmacotherapeutic group: Nucleoside and nucleotide reverse transcriptase inhibitors, ATC code: J05AF08.
Aciclovir is an antiviral drug, it is a syntheticingredient with a similar molecular structure to purine nucleoside.
Both active substances in Kivexa, abacavir and lamivudine, are nucleoside reverse transcriptase inhibitors NRTIs.
So-called nucleoside and nucleotide analogues(NUCs), which are administered in tablet form, can help treat but not cure the disease.
Most of the experience with Viramune is in combination with nucleoside reverse transcriptase inhibitors NRTIs.
Adenosine is a nucleoside, a chemical compound consisting of adenine and a sugar molecule β-D-ribose.
These enzymes help in the removal of 5' phosphate groups from RNA, DNA and ribo-and deoxyribo- nucleoside triphosphates e. g.
All of the subsequent"AIDS" drugs from nucleoside analogues to protease inhibitors, rode in on the coat-tails of AZT.
Common use Aciclovir is an antiviral drug, it is a syntheticingredient with a similar molecular structure to purine nucleoside.
All three active substances in Trizivir, abacavir, lamivudine, and zidovudine,are nucleoside reverse transcriptase inhibitors NRTIs.
Inosine is a nucleoside that is formed when hypoxanthine is attached to a ribose ring(also known as a ribofuranose) via a β-N9-glycosidic bond.
Etravirine retains activity against HIV-1 viral strains resistant to nucleoside reverse transcriptase and/ or protease inhibitors.
Adenosine is a nucleoside, a chemical compound consisting of adenine(one of the four nucleic acid bases in human DNA) and a sugar molecule Î2-D-ribose.
Combivir belongs to a group of antiviral medicines, also known as antiretrovirals, called nucleoside analogue reverse transcriptase inhibitors NRTIs.
Dephosphorylation results in the formation of nucleoside metabolite GS-331007 that cannot be efficiently rephosphorylated and lacks anti-HCV activity in vitro.
Increased CPK, myalgia, myositis and, rarely, rhabdomyolysis, have been reported with protease inhibitors,particularly in combination with nucleoside reverse transcriptase inhibitors.
Since there is no significant impact of nucleoside and nucleotide analogues on the P450 enzyme system no dosage adjustment of APTIVUS is required when co-administered with these agents.
A connection between visceral lipomatosis and protease inhibitors, and lipoatrophy and nucleoside reverse transcriptase inhibitors has been hypothesised.
The nucleoside cordycepin(3'-deoxyadenosine) has anti-inflammatory properties(5.6) and effects that reduce the concentration of total cholesterol, low-density lipoprotein and triglycerides in the blood 7.
In combination studies of emtricitabine with protease inhibitors, nucleoside, nucleotide and non-nucleoside analogue inhibitors of HIV reverse transcriptase, additive to synergistic effects were observed.
Monk fruit extract containing the sweet taste of sugar in the composition, main is triterpenoid glycosides, fructus momordicae sweet glycoside(mogroside)Ⅴ andⅣ, glycosidesⅤ a sweetness of sucrose(srcrose) 256-344 times,126 times nucleosideⅣ sweetness of sucrose.
Variants carrying amino-acid substitutions conferring reduced susceptibility to NS5A inhibitors(L31F/V,Y93C/H), nucleoside polymerase inhibitors(S282T) and non-nucleoside polymerase inhibitors(C316N, M414I/L, P495A) remained susceptible to simeprevir in vitro.
