Results 1 to 10 of about 11,506,565 (250)

Insights into the structure and activity of prototype foamy virus RNase H

open access: yesRetrovirology, 2012
Background RNase H is an endonuclease that hydrolyzes the RNA strand in RNA/DNA hybrids. Retroviral reverse transcriptases harbor a C-terminal RNase H domain whose activity is essential for viral replication.
Leo Berit   +4 more
doaj   +2 more sources

Structure-Based Design of Novel Thiazolone[3,2-a]pyrimidine Derivatives as Potent RNase H Inhibitors for HIV Therapy [PDF]

open access: yesMolecules
Ribonuclease H (RNase H) was identified as an important target for HIV therapy. Currently, no RNase H inhibitors have reached clinical status. Herein, a series of novel thiazolone[3,2-a]pyrimidine-containing RNase H inhibitors were developed, based on ...
Xuan-De Zhu   +8 more
doaj   +2 more sources

Design, Synthesis and Biological Evaluation of 3-Hydrazonoindolin-2-one Derivatives as Novel HIV-1 RNase H Inhibitors [PDF]

open access: yesMolecules
Targeting ribonuclease H (RNase H) has emerged as a highly promising strategy for treating HIV-1. In this study, a series of novel 3-hydrazonoindolin-2-one derivatives were designed and synthesized as potential inhibitors of HIV-1 RNase H.
Yiying Zhang   +10 more
doaj   +2 more sources

Ultrasensitive RNase H activity detection using the transcription-based hybrid probe and CRISPR/cas12a signal amplifier [PDF]

open access: yesFrontiers in Pharmacology
Ribonuclease H (RNase H), a critical functional protein in replication and genome stability, is emerging as a crucial therapeutic target for various diseases, including immune disorders.
Sheng Ding   +6 more
doaj   +2 more sources

N-Hydroxypiridinedione: A Privileged Heterocycle for Targeting the HBV RNase H [PDF]

open access: yesMolecules
Hepatitis B virus (HBV) remains a global health threat. Ribonuclease H (RNase H), part of the virus polymerase protein, cleaves the pgRNA template during viral genome replication.
Dimitrios Moianos   +8 more
doaj   +2 more sources

Synthesis, biophysical properties, and RNase H activity of 6’-difluoro[4.3.0]bicyclo-DNA [PDF]

open access: yesBeilstein J Org Chem, 2019
Here we present the synthesis, the biophysical properties, and the RNase H profile of 6’-difluorinated [4.3.0]bicyclo-DNA (6’-diF-bc4,3-DNA). The difluorinated thymidine phosphoramidite building block was synthesized starting from an already known gem ...
Sibylle Frei   +5 more
core   +3 more sources

Targeting HIV-1 RNase H: N’-(2-Hydroxy-benzylidene)-3,4,5-Trihydroxybenzoylhydrazone as Selective Inhibitor Active against NNRTIs-Resistant Variants [PDF]

open access: yesViruses, 2020
HIV-1 infection requires life-long treatment and with 2.1 million new infections/year, faces the challenge of an increased rate of transmitted drug-resistant mutations.
Angela Corona   +12 more
doaj   +2 more sources

Cycling Probe Technology with RNase H Attached to an Oligonucleotide

open access: yesBioTechniques, 1996
A streptavidin-RNase H gene fusion was constructed by cloning the Thermus thermophilus RNase H coding sequence in the streptavidin expression vector pTSA18F.
F. Bekkaoui   +4 more
doaj   +2 more sources

An RNase H‐Like gene complements resistance to Bean common mosaic necrosis virus in Phaseolus vulgaris [PDF]

open access: yesThe Plant Genome
Bean common mosaic virus and Bean common mosaic necrosis virus (BCMNV) are related positive‐sense RNA potyviruses that limit the production of common bean (Phaseolus vulgaris L.) worldwide.
Alvaro Soler‐Garzón   +1 more
doaj   +2 more sources

Accurately modeling RNase H-mediated antisense oligonucleotide efficacy [PDF]

open access: yesMolecular Therapy: Nucleic Acids
Antisense oligonucleotides (ASOs) are a powerful class of drugs with the potential to treat a wide range of human diseases. However, the prediction of ASO efficacy remains challenging, as large-scale and costly experimental screens are typically required
Barney Hill   +8 more
doaj   +2 more sources

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