Примери за използване на Nucleotide analogues на Английски и техните преводи на Български
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Patients with previous exposure to nucleoside/nucleotide analogues.
Nucleoside and nucleotide analogues have been demonstrated in vitro and in vivo to cause a variable degree of mitochondrial damage.
The active substance in Vistide, cidofovir,is an antiviral medicine that belongs to the class‘nucleotide analogues'.
Nucleoside and nucleotide analogues have been demonstrated in vitro and in vivo to cause a variable degree of mitochondrial damage.
Occurrence of lactic acidosis(in the absence of hypoxaemia) sometimes fatal, and usually associated with severe hepatomegaly with steatosis have been reported with the use of nucleoside/ nucleotide analogues. .
Nucleoside and nucleotide analogues have been demonstrated in vitro and in vivo to cause a variable degree of mitochondrial damage.
These findings should be considered for any child exposed in utero to nucleotide and nucleotide analogues, who presents with severe clinical findings of unknown etiology, particularly neurologic findings.
Nucleoside and nucleotide analogues have been demonstrated in vitro and in vivo to cause a variable degree of mitochondrial damage.
Nucleoside and nucleotide reverse transcriptase inhibitors(NRTIs) 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.
Nucleoside and nucleotide analogues have been demonstrated in vitro and in vivo to cause a variable degree of mitochondrial damage.
Mitochondrial dysfunction: nucleoside and nucleotide analogues have been demonstrated in vitro and in vivo to cause a variable degree of mitochondrial damage.
Nucleoside and nucleotide analogues may impact mitochondrial function to a variable degree, which is most pronounced with stavudine, didanosine and zidovudine.
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.
While nucleoside/nucleotide analogues like tenofovir suppress HBV replication during treatment, they usually do not lead to a cure and long-term therapy is generally required.
In children whose mother took nucleoside and nucleotide analogues during pregnancy, the benefit from the reduced chance of being infected with HIV is greater than the risk of suffering from side effects.
In children whose mothers took nucleoside and nucleotide analogues during pregnancy, the benefit from the reduced chance of being infected with HIV is greater than the risk of suffering from side effects.
Any child exposed in utero to nucleoside and nucleotide analogues, should have clinical and laboratory follow-up and should be fully investigated for possible mitochondrial dysfunction in cases which have relevant signs or symptoms.
Any child exposed in utero to nucleoside and nucleotide analogues, even HIV-negative children, should have clinical and laboratory follow-up and should be fully investigated for possible mitochondrial dysfunction in case of relevant signs or symptoms.
Any child exposed in utero to nucleoside and nucleotide analogues, even HIV-negative children, should have clinical and laboratory follow-up and should be fully investigated for possible mitochondrial dysfunction in case of relevant signs or symptoms.
Any child exposed in utero to nucleoside and nucleotide analogues, even HIV negative children, should have clinical and laboratory follow-up and should be fully investigated for possible mitochondrial dysfunction in case of relevant signs or symptoms.
Sofosbuvir- direct acting nucleotide analogue inhibitor, NS5B polymerase inhibitor.
Entaliv, a nucleotide analogue these agents used to fight against the infection of HBV, HCV, herpes simplex and HIV.
X vir, a nucleotide analogue these agents used to fight against the infection of HBV, HCV, herpes simplex and HIV.
Tenofovir disoproxil is converted in vivo to tenofovir, a nucleoside monophosphate(nucleotide) analogue of adenosine monophosphate.
Tenofovir disoproxil fumarate is converted in vivo to tenofovir,a nucleoside monophosphate(nucleotide) analogue of adenosine monophosphate.
Cronvir a nucleotide analogue these agents used for treatment of infection affected by HBV, HCV, herpes simplex and HIV.
Tenofovir disoproxil is absorbed and converted to the active substance tenofovir,which is a nucleoside monophosphate(nucleotide) analogue.
The principal mode of action of 3TC-TP is inhibition of RT via DNA chain termination after incorporation of the nucleotide analogue.
In combination studies of emtricitabine with protease inhibitors(PIs),nucleoside, nucleotide and non-nucleoside analogue inhibitors of HIV reverse transcriptase, additive to synergistic effects were observed.
Intracellular hydrolytic prodrug cleavage catalysed by enzymes including carboxylesterase 1 andsequential phosphorylation steps catalysed by nucleotide kinases result in formation of the pharmacologically active uridine nucleoside analogue triphosphate.