Results 281 to 290 of about 476,060 (306)
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Nanoscale, 2020
A signal amplification strategy based on an RNase H-powered DNA walking machine for RNase H activity detection.
Yafang Wang+9 more
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A signal amplification strategy based on an RNase H-powered DNA walking machine for RNase H activity detection.
Yafang Wang+9 more
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RNases H: Structure and mechanism
DNA Repair, 2019RNases H are a family of endonucleases that hydrolyze RNA residues in various nucleic acids. These enzymes are present in all branches of life, and their counterpart domains are also found in reverse transcriptases (RTs) from retroviruses and retroelements.
Marcin Nowotny+2 more
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Function of RNase H in DNA replication revealed by RNase H defective mutants of Escherichia coli
Molecular and General Genetics MGG, 1984Escherichia coli rnh mutants were isolated using localized mutagenesis and selective measurements of RNase H activity in mutagenized cell extracts with [3H]poly(rC) X poly(dG) as substrate. RNase H activity in extracts of one mutant, ON152 (rnh-91), was undetectable (less than 0.05% of that of wild-type cells).
Tuneko Okazaki, Tohru Ogawa
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Stereochemical Course of Escherichia coli RNase H.
ChemInform, 2002A new enzymatic method has allowed the assignment of the stereochemistry of E. coli RNase-H-assisted hydrolysis of RNA labelled within the scissile bond with (R(p))-phosphorothioate. This method is based on a stereospecific, two-step enzymatic conversion of cytidine 5'-[(18)O]phosphorothioate into the corresponding 5'-alpha-[(18)O]thiotriphosphate ...
Alina Owczarek+3 more
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RNase H Activation by Stereoregular Boranophosphate Oligonucleotide
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Dmitri S. Sergueev+3 more
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Pyridopyrimidinone inhibitors of HIV-1 RNase H
European Journal of Medicinal Chemistry, 2014Using a structure based pharmacophore design, a weak inhibitor of RNase H, identified from a small library of two metal binding HIV-1 integrase inhibitors, was optimized for potency and physicochemical properties. This manuscript describes the SAR and in vivo DMPK for the pyridopyrimidinone class of inhibitors.
Emile J. Velthuisen+11 more
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2007
Antisense oligonucleotides (ASOs) are designed to modulate the information transfer from gene to protein-in essence to alter mRNA intermediary metabolism. mRNA intermediary metabolism is extremely complex beginning with transcription and concluding with degradation usually after translation.
Hongjiang Wu+2 more
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Antisense oligonucleotides (ASOs) are designed to modulate the information transfer from gene to protein-in essence to alter mRNA intermediary metabolism. mRNA intermediary metabolism is extremely complex beginning with transcription and concluding with degradation usually after translation.
Hongjiang Wu+2 more
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The Analyst, 2021
Radar-like monitor for RNase H detection in vitro and for intercellular imaging.
Yalei Hu+6 more
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Radar-like monitor for RNase H detection in vitro and for intercellular imaging.
Yalei Hu+6 more
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Discrimination between mammalian RNases H-1 and H-2
Analytical Biochemistry, 1991The two principal RNases H in mammalian cells, H-1 and H-2, differ in their responses to sale, divalent metal, and sulfhydryl inhibition. Specific reaction conditions that provide unambiguous discrimination between RNases H-1 and H-2 with only two assays are described. The assays were used for identification in a new purification procedure for RNases H-
Cheryl J. Heard, Mehran Goulian
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Boranophosphates Support the RNase H Cleavage of Polyribonucleotides
Antisense and Nucleic Acid Drug Development, 1999Modification of the phosphodiester linkages in DNA by replacing one of the nonbridging oxygens with borane, BH3, produces an isoelectronic mimic of DNA called boranophosphates. Nonstereoregular oligodeoxyribonucleoside all-boranophosphates are shown here for the first time to elicit the RNase H hydrolysis of polyribonucleotides. We compared the ability
Vladimir Rait, Barbara Ramsay Shaw
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