Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Sharon T. Cload"'
Autor:
Anthony D. Keefe, Sharon T. Cload
Publikováno v:
Current Opinion in Chemical Biology. 12:448-456
Aptamers, a promising new class of therapeutics, are single-stranded oligonucleotides generated via an in vitro selection process that bind to and inhibit the activity of target proteins in a manner similar to therapeutic antibodies. In order to enha
Autor:
Jeffrey Kurz, Sara Chesworth Keene, John L. Diener, Ryan M. Boomer, Jayaram Srinivasan, Charles Wilson, David Epstein, Markus Kurz, Jill Blanchard, Nobuko Hamaguchi, Sharon T. Cload
Publikováno v:
Chemistry & Biology. 11(4):499-508
Two molecular sensors that specifically recognize ADP in a background of over 100-fold molar excess of ATP are described. These sensors are nucleic-acid based and comprise a general method for monitoring protein kinase activity. The ADP-aptamer scint
Autor:
John L. Diener, Sharon T. Cload, Markus Kurz, Anthony D. Keefe, Sara Chesworth Keene, Ryan M. Boomer, Charles Wilson, Alicia Ferguson
Publikováno v:
Nucleic Acids Research. 32:1756-1766
We have utilized in vitro selection technology to develop allosteric ribozyme sensors that are specific for the small molecule analytes caffeine or aspartame. Caffeine- or aspartame-responsive ribozymes were converted into fluorescence-based RiboRepo
Autor:
Alanna Schepartz, Sharon T. Cload
Publikováno v:
Journal of the American Chemical Society. 116:437-442
We devised a single-step selection method to identify short sequences within the folded Rev response element (RRE) of the human immunodeficiency virus (HIV) RNA genome that are proximal and able to bind short oligonucleotides. The method employed a l
Publikováno v:
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. 34(1)
Small molecule drugs are relatively effective in working on 'drugable' targets such as GPCRs, ion channels, kinases, proteases, etc but ineffective at blocking protein-protein interactions that represent an emerging class of 'nondrugable' central ner
Publikováno v:
ChemInform. 39
Aptamers are non-naturally occurring structured oligonucleotides that may bind to small molecules, peptides, and proteins. Typically, aptamers are generated by an in vitro selection process referred to as SELEX (systematic evolution of ligands by exp
Publikováno v:
Accounts of chemical research. 41(1)
Aptamers are non-naturally occurring structured oligonucleotides that may bind to small molecules, peptides, and proteins. Typically, aptamers are generated by an in vitro selection process referred to as SELEX (systematic evolution of ligands by exp
Autor:
Paula Burmeister, Charles Wilson, Chunhua Wang, Scott D. Lewis, Thomas Green Mccauley, Markus Kurz, Anthony D. Keefe, P. Shannon Pendergrast, Jason R. Killough, Alicia Ferguson, Sharon T. Cload, Lillian R. Horwitz, Kristin Thompson, John L. Diener
Publikováno v:
Oligonucleotides. 16(4)
Aptamers are short oligonucleotides that fold into well-defined three-dimensional architectures thereby enabling specific binding to molecular targets such as proteins. To be successful as a novel therapeutic modality, it is important for aptamers to
Publikováno v:
The Aptamer Handbook: Functional Oligonucleotides and Their Applications
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e23e7c0974876e18807e9d327563a51c
https://doi.org/10.1002/3527608192.ch17
https://doi.org/10.1002/3527608192.ch17