Chemical modification and design of anti-miRNA oligonucleotides
KA Lennox, MA Behlke - Gene therapy, 2011 - nature.com
Antisense techniques have been employed for over 30 years to suppress expression of
target RNAs. Recently, microRNAs (miRNAs) have emerged as a new class of small, non …
target RNAs. Recently, microRNAs (miRNAs) have emerged as a new class of small, non …
Strategies to modulate microRNA functions for the treatment of cancer or organ injury
Cancer and organ injury—such as that occurring in the perioperative period, including acute
lung injury, myocardial infarction, and acute gut injury—are among the leading causes of …
lung injury, myocardial infarction, and acute gut injury—are among the leading causes of …
Cellular localization of long non-coding RNAs affects silencing by RNAi more than by antisense oligonucleotides
KA Lennox, MA Behlke - Nucleic acids research, 2016 - academic.oup.com
Thousands of long non-coding RNAs (lncRNAs) have been identified in mammalian cells.
Some have important functions and their dysregulation can contribute to a variety of disease …
Some have important functions and their dysregulation can contribute to a variety of disease …
Computing in mammalian cells with nucleic acid strand exchange
DNA strand displacement has been widely used for the design of molecular circuits, motors,
and sensors in cell-free settings. Recently, it has been shown that this technology can also …
and sensors in cell-free settings. Recently, it has been shown that this technology can also …
Nano-flares for mRNA regulation and detection
AE Prigodich, DS Seferos, MD Massich, DA Giljohann… - ACS …, 2009 - ACS Publications
We build off the previously described concept of a nanoflare to develop an oligonucleotide
gold nanoparticle conjugate that is capable of both detecting and regulating intracellular …
gold nanoparticle conjugate that is capable of both detecting and regulating intracellular …
Short locked nucleic acid antisense oligonucleotides potently reduce apolipoprotein B mRNA and serum cholesterol in mice and non-human primates
EM Straarup, N Fisker, M Hedtjärn… - Nucleic acids …, 2010 - academic.oup.com
The potency and specificity of locked nucleic acid (LNA) antisense oligonucleotides was
investigated as a function of length and affinity. The oligonucleotides were designed to …
investigated as a function of length and affinity. The oligonucleotides were designed to …
Impact of guanidine-containing backbone linkages on stereopure antisense oligonucleotides in the CNS
P Kandasamy, Y Liu, V Aduda, S Akare… - Nucleic acids …, 2022 - academic.oup.com
Attaining sufficient tissue exposure at the site of action to achieve the desired
pharmacodynamic effect on a target is an important determinant for any drug discovery …
pharmacodynamic effect on a target is an important determinant for any drug discovery …
A direct comparison of anti-microRNA oligonucleotide potency
KA Lennox, MA Behlke - Pharmaceutical research, 2010 - Springer
Purpose Cataloguing endogenous miRNA targets by inhibiting miRNA function is
fundamental to understanding the biological importance of each miRNA in gene regulatory …
fundamental to understanding the biological importance of each miRNA in gene regulatory …
Improved performance of anti-miRNA oligonucleotides using a novel non-nucleotide modifier
KA Lennox, R Owczarzy, DM Thomas… - … Therapy-Nucleic Acids, 2013 - cell.com
Anti-microRNA oligonucleotides (AMOs) are steric blocking antisense reagents that inhibit
microRNA (miRNA) function by hybridizing and repressing the activity of a mature miRNA …
microRNA (miRNA) function by hybridizing and repressing the activity of a mature miRNA …
Mesyl phosphoramidate antisense oligonucleotides as an alternative to phosphorothioates with improved biochemical and biological properties
SK Miroshnichenko, OA Patutina… - Proceedings of the …, 2019 - National Acad Sciences
Here we describe a DNA analog in which the mesyl (methanesulfonyl) phosphoramidate
group is substituted for the natural phosphodiester group at each internucleotidic position …
group is substituted for the natural phosphodiester group at each internucleotidic position …