Results 251 to 260 of about 299,739 (289)

Progress in Molecular Imprinting—From Inhibition of Enzymatic Activity to Regulation of Cellular Pathways

open access: yesMedicinal Research Reviews, EarlyView.
ABSTRACT Molecular imprinting is a very powerful tool in life science. The research areas benefiting from a wide range of capabilities of molecularly imprinted polymeric nanoparticles (nanoMIPs) include sample preparation, extraction, sensing/detection, diagnostics, and drug delivery.
Milada Vodova   +2 more
wiley   +1 more source

Current Analytical Strategies for mRNA-Based Therapeutics. [PDF]

open access: yesMolecules
Camperi J   +5 more
europepmc   +1 more source

Navigating Uncertainties in RT-qPCR and Infectivity Assessment of Norovirus. [PDF]

open access: yesFood Environ Virol
Mirmahdi RS   +3 more
europepmc   +1 more source

Comprehensive nucleoside analysis of archaeal RNA modification profiles reveals an m<sup>7</sup>G in the conserved P loop of 23S rRNA. [PDF]

open access: yesCell Rep
Tsai YL   +10 more
europepmc   +1 more source

pH-Reversible Cationic RNase A Conjugates for Enhanced Cellular Delivery and Tumor Cell Killing

open access: closedBiomacromolecules, 2015
Intracellularly-acting therapeutic proteins are considered promising alternatives for the treatment of various diseases. Major limitations of their application are low efficiency of intracellular delivery and possible reduction of protein activity during derivatization.
Xiaowen Liu   +7 more
openalex   +3 more sources

RNase PH catalyzes a synthetic reaction, the addition of nucleotides to the 3′ end of RNA

open access: closedBiochimie, 1990
Escherichia coli RNase PH is a phosphate-dependent exoribonuclease that has been implicated in the 3' processing of tRNA precursors. It degrades RNA chains in a phosphorolytic manner releasing nucleoside diphosphates as products. Here we show that RNase PH also catalyzes a synthetic reaction, the addition of nucleotides to the 3' termini of RNA ...
K A Ost, Murray P. Deutscher
openalex   +4 more sources

[68] Preparation of bacterial DNA by the phenol-pH 9-RNases method

open access: closed, 1967
Publisher Summary This chapter describes the method for the extraction of DNA from bacterial cells using phenol. Phenol treatment is considered one of the most effective methods for deproteinization. Whereas a neutral or acidic buffer (pH 5-7) extracts RNA into aqueous phase, rather than DNA from bacterial cells, in phenol treatment slightly alkaline
Kin‐ichiro Miura
openalex   +3 more sources

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