Примери за използване на Polymerases на Английски и техните преводи на Български
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There are many different RNA polymerases.
It is also only a weak inhibitor of mammalian DNA polymerases alpha and beta.
While enzymes like polymerases had been used to operate on this information.
Rilpivirine does not inhibit the human cellular DNA polymerases α, β and γ.
HIV-2 reverse transcriptase andeukaryotic DNA polymerases(such as human DNA polymerases α, β, γ, or δ) are not inhibited by nevirapine.
Tenofovir diphosphate is a weak inhibitor of cellular polymerases α, β, and γ.
He suggested that mutations are due to the fact that polymerases in some cases incorporate non-complementary nucleotides into the sequence.
Coconut water is very refreshing and contains simple sugars, electrolytes, minerals, acid phosphatise, catalase, dehydrogenise,peroxidise and polymerases.
Entecavir-TP is a weak inhibitor of cellular DNA polymerases α, β, and δ with Ki values of 18 to 40 µM.
As a part of RNA and DNA polymerases it is also crucial for the reproduction of RNA and DNA molecules and consequently for cell partition and protein synthesis.
Doravirine does not inhibit the human cellular DNA polymerases α, ß, and mitochondrial DNA polymerase γ.
Efavirenz non-competitively inhibits HIV-1 reverse transcriptase(RT) and does not significantly inhibit human immunodeficiency virus-2(HIV-2) RT orcellular deoxyribonucleic acid(DNA) polymerases(α, β, γ, and δ).
GS-461203 is neither an inhibitor of human DNA and RNA polymerases nor an inhibitor of mitochondrial RNA polymerase. .
Nevirapine is a non-competitive inhibitor of the HIV-1 reverse transcriptase, but it does not havea biologically significant inhibitory effect on the HIV-2 reverse transcriptase or on eukaryotic DNA polymerases α, β, γ, or δ.
Reported that higher fidelity thermostable DNA polymerases such as Vent account for as much as 30% of DNA polymerase sales.
Doxorubicin may exert its antitumour and toxic effects by a number of mechanisms including inhibition of topoisomerase II,intercalation with DNA and RNA polymerases, free radical formation and membrane binding.
Entavir is a poor inhibitor of cellular DNA polymerases α, β and in which mitochondrial DNA polymerase gamma with ki values ranging from 18 to>160µM.
During interphase, the chromatin is structurally loose to allow access to RNA and DNA polymerases that transcribe and replicate the DNA.
Cidofovir diphosphate inhibits these viral polymerases at concentrations that are 8- to 600-fold lower than those needed to inhibit human cellular DNA polymerases alpha, beta, and gamma.
GS-461203(the active metabolite of sofosbuvir)is not an inhibitor of human DNA and RNA polymerases nor an inhibitor of mitochondrial RNA polymerase. .
Adefovir diphosphate selectively inhibits HBV DNA polymerases at concentrations 12-, 700-, and10-fold lower than those needed to inhibit human DNA polymerases α, β, and γ, respectively.
Both emtricitabine triphosphate and tenofovir diphosphate are weak inhibitors of mammalian DNA polymerases and there was no evidence of toxicity to mitochondria in vitro and in vivo.
Scientists have long assumed that the DNA polymerases on the leading and lagging strands somehow coordinate with each other throughout the replication process, so that one does not get ahead of the other during the unraveling process and cause mutations.
The active substance in Rubraca, rucaparib,blocks the activity of a family of proteins called poly(ADPribose) polymerases(PARPs) that help to repair damaged DNA in cells(both normal and cancer cells).
Scientists have long assumed that the DNA polymerases on the leading and lagging strands somehow coordinate with each other throughout the replication process, so that one does not get ahead of the other during the unravelling process and cause mutations.
Dasabuvir had reduced activity in biochemical assays against NS5B polymerases from HCV genotypes 2a, 2b, 3a and 4a(IC50 values ranging from 900 nM to> 20 μM).
Tenofovir diphosphate is a weak inhibitor of mammalian DNA polymerases that include mitochondrial DNA polymerase γ and there is no evidence of mitochondrial toxicity in vitro based on several assays including mitochondrial DNA analyses.
Biochemical data support selective inhibition of HSV-1, HSV-2 and HCMV DNA polymerases by cidofovir diphosphate, the active intracellular metabolite of cidofovir.
The cytoplasm of any cell is swimming with ribosomes,RNA polymerases, tRNA and mRNA molecules and enzymes, all carrying out their reactions independently of each other.