Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Andrzej Grajkowski

Showing results (11-20 of 34) with videos related to

Pageof 4
Sort By:
Current Protocols|January 11, 2023
An Alternate Process for the Solid-Phase Synthesis and Solid-Phase Purification of Synthetic Nucleic Acid SequencesBrian M Cawrse, Mayumi Takahashi, Andrzej Grajkowski, et al.
The Journal of Organic Chemistry|March 12, 2021
Innovative 2'-<i>O</i>-Imino-2-propanoate-Protecting Group for Effective Solid-Phase Synthesis and 2'-<i>O</i>-Deprotection of RNA SequencesMayumi Takahashi, Andrzej Grajkowski, Brian M Cawrse, et al.
Current Protocols|May 4, 2021
An Improved PEG-Linked Solid Support for Minimizing Process-Related Impurities During Solid-Phase Synthesis of DNA and RNA SequencesAndrzej Grajkowski, Mayumi Takahashi, Brian M Cawrse, et al.
Current Protocols|January 14, 2022
Use of Arabinonucleosides for Development and Implementation of a Novel 2'-O-Protecting Group for Efficient Solid-Phase Synthesis and 2'-O-Deprotection of RNA SequencesMayumi Takahashi, Brian M Cawrse, Andrzej Grajkowski, et al.
Bioorganic & Medicinal Chemistry|October 2, 2020
An expedient process for reducing the formation of process-related impurities during solid-phase synthesis of potential nucleic acid-based drugsAndrzej Grajkowski, Mayumi Takahashi, Brian M Cawrse, et al.
Bioconjugate Chemistry|October 15, 2010
Convenient synthesis of a propargylated cyclic (3'-5') diguanylic acid and its "click" conjugation to a biotinylated azideAndrzej Grajkowski, Jacek Cieślak, Alexei Gapeev, et al.
Current Protocols in Nucleic Acid Chemistry|December 15, 2010
Time-dependent thermocontrol of the hydrophilic and lipophilic properties of DNA oligonucleotide prodrugsCristina Ausín, Andrzej Grajkowski, Jacek Cieślak, et al.
Annals of the New York Academy of Sciences|January 6, 2006
Design and development of thermolytic DNA oligonucleotide prodrugsAndrzej Grajkowski, Joao Pedras-Vasconcelos, Cristina Ausín, et al.
Nucleic Acids Research|November 10, 2011
Permanent or reversible conjugation of 2'-O- or 5'-O-aminooxymethylated nucleosides with functional groups as a convenient and efficient approach to the modification of RNA and DNA sequencesJacek Cieslak, Andrzej Grajkowski, Cristina Ausín, et al.
Current Protocols in Nucleic Acid Chemistry|April 11, 2019
An Improved Strategy for the Chemical Synthesis of 3',5'-Cyclic Diguanylic AcidAndrzej Grajkowski, Mayumi Takahashi, Tomasz Kaczyński, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Current Protocols|January 11, 2023
An Alternate Process for the Solid-Phase Synthesis and Solid-Phase Purification of Synthetic Nucleic Acid SequencesBrian M Cawrse, Mayumi Takahashi, Andrzej Grajkowski, et al.
The Journal of Organic Chemistry|March 12, 2021
Innovative 2'-<i>O</i>-Imino-2-propanoate-Protecting Group for Effective Solid-Phase Synthesis and 2'-<i>O</i>-Deprotection of RNA SequencesMayumi Takahashi, Andrzej Grajkowski, Brian M Cawrse, et al.
Current Protocols|May 4, 2021
An Improved PEG-Linked Solid Support for Minimizing Process-Related Impurities During Solid-Phase Synthesis of DNA and RNA SequencesAndrzej Grajkowski, Mayumi Takahashi, Brian M Cawrse, et al.
Current Protocols|January 14, 2022
Use of Arabinonucleosides for Development and Implementation of a Novel 2'-O-Protecting Group for Efficient Solid-Phase Synthesis and 2'-O-Deprotection of RNA SequencesMayumi Takahashi, Brian M Cawrse, Andrzej Grajkowski, et al.
Bioorganic & Medicinal Chemistry|October 2, 2020
An expedient process for reducing the formation of process-related impurities during solid-phase synthesis of potential nucleic acid-based drugsAndrzej Grajkowski, Mayumi Takahashi, Brian M Cawrse, et al.
Bioconjugate Chemistry|October 15, 2010
Convenient synthesis of a propargylated cyclic (3'-5') diguanylic acid and its "click" conjugation to a biotinylated azideAndrzej Grajkowski, Jacek Cieślak, Alexei Gapeev, et al.
Current Protocols in Nucleic Acid Chemistry|December 15, 2010
Time-dependent thermocontrol of the hydrophilic and lipophilic properties of DNA oligonucleotide prodrugsCristina Ausín, Andrzej Grajkowski, Jacek Cieślak, et al.
Annals of the New York Academy of Sciences|January 6, 2006
Design and development of thermolytic DNA oligonucleotide prodrugsAndrzej Grajkowski, Joao Pedras-Vasconcelos, Cristina Ausín, et al.
Nucleic Acids Research|November 10, 2011
Permanent or reversible conjugation of 2'-O- or 5'-O-aminooxymethylated nucleosides with functional groups as a convenient and efficient approach to the modification of RNA and DNA sequencesJacek Cieslak, Andrzej Grajkowski, Cristina Ausín, et al.
Current Protocols in Nucleic Acid Chemistry|April 11, 2019
An Improved Strategy for the Chemical Synthesis of 3',5'-Cyclic Diguanylic AcidAndrzej Grajkowski, Mayumi Takahashi, Tomasz Kaczyński, et al.
Pageof 4