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Bioconjugate Chemistry
|
November 8, 2019
Three-Component Bioorthogonal Reactions on Cellular DNA and RNA
Masayuki Tera, Nathan W Luedtke
Methods in Enzymology
|
July 28, 2020
Cross-linking cellular nucleic acids via a target-directing double click reagent
Masayuki Tera, Nathan W Luedtke
Angewandte Chemie (International Ed. in English)
|
September 22, 2018
Intercalation-enhanced "Click" Crosslinking of DNA
Masayuki Tera, Zahra Harati Taji, Nathan W Luedtke
Nucleic Acids Symposium Series (2004)
|
September 15, 2009
G-quadruplex recognition by macrocyclic hexaoxazole (6OTD) dimer
Keisuke Iida, Masayuki Tera, Kazuo Shin-Ya, et al.
Chembiochem : a European Journal of Chemical Biology
|
June 29, 2018
In Vivo Incorporation of Azide Groups into DNA by Using Membrane-Permeable Nucleotide Triesters
Masayuki Tera, Stella M K Glasauer, Nathan W Luedtke
Nucleic Acids Symposium Series (2004)
|
September 15, 2009
Synthesis of potent G-quadruplex binders of macrocyclic heptaoxazole and evaluation of their activities
Masayuki Tera, Keisuke Iida, Kazuo Shin-ya, et al.
Chemical Communications (Cambridge, England)
|
October 21, 2009
G-quadruplex recognition by macrocyclic hexaoxazole (6OTD) dimer: greater selectivity than monomer
Keisuke Iida, Masayuki Tera, Takatsugu Hirokawa, et al.
Journal of Nucleic Acids
|
August 12, 2010
Synthesis of Macrocyclic Hexaoxazole (6OTD) Dimers, Containing Guanidine and Amine Functionalized Side Chains, and an Evaluation of Their Telomeric G4 Stabilizing Properties
Keisuke Iida, Masayuki Tera, Takatsugu Hirokawa, et al.
Chemical Communications (Cambridge, England)
|
July 15, 2021
Stabilization of telomeric G-quadruplex by ligand binding increases susceptibility to S1 nuclease
Ryo Ishikawa, Mizuho Yasuda, Shogo Sasaki, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
August 15, 2015
Design and synthesis of a berberine dimer: a fluorescent ligand with high affinity towards G-quadruplexes
Masayuki Tera, Takatsugu Hirokawa, Sachiko Okabe, et al.
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of 5
Search research articles
Search
Showing results (1-10 of 44) with videos related to
Sort By:
Page
of 5
Bioconjugate Chemistry
|
November 8, 2019
Three-Component Bioorthogonal Reactions on Cellular DNA and RNA
Masayuki Tera, Nathan W Luedtke
Methods in Enzymology
|
July 28, 2020
Cross-linking cellular nucleic acids via a target-directing double click reagent
Masayuki Tera, Nathan W Luedtke
Angewandte Chemie (International Ed. in English)
|
September 22, 2018
Intercalation-enhanced "Click" Crosslinking of DNA
Masayuki Tera, Zahra Harati Taji, Nathan W Luedtke
Nucleic Acids Symposium Series (2004)
|
September 15, 2009
G-quadruplex recognition by macrocyclic hexaoxazole (6OTD) dimer
Keisuke Iida, Masayuki Tera, Kazuo Shin-Ya, et al.
Chembiochem : a European Journal of Chemical Biology
|
June 29, 2018
In Vivo Incorporation of Azide Groups into DNA by Using Membrane-Permeable Nucleotide Triesters
Masayuki Tera, Stella M K Glasauer, Nathan W Luedtke
Nucleic Acids Symposium Series (2004)
|
September 15, 2009
Synthesis of potent G-quadruplex binders of macrocyclic heptaoxazole and evaluation of their activities
Masayuki Tera, Keisuke Iida, Kazuo Shin-ya, et al.
Chemical Communications (Cambridge, England)
|
October 21, 2009
G-quadruplex recognition by macrocyclic hexaoxazole (6OTD) dimer: greater selectivity than monomer
Keisuke Iida, Masayuki Tera, Takatsugu Hirokawa, et al.
Journal of Nucleic Acids
|
August 12, 2010
Synthesis of Macrocyclic Hexaoxazole (6OTD) Dimers, Containing Guanidine and Amine Functionalized Side Chains, and an Evaluation of Their Telomeric G4 Stabilizing Properties
Keisuke Iida, Masayuki Tera, Takatsugu Hirokawa, et al.
Chemical Communications (Cambridge, England)
|
July 15, 2021
Stabilization of telomeric G-quadruplex by ligand binding increases susceptibility to S1 nuclease
Ryo Ishikawa, Mizuho Yasuda, Shogo Sasaki, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
August 15, 2015
Design and synthesis of a berberine dimer: a fluorescent ligand with high affinity towards G-quadruplexes
Masayuki Tera, Takatsugu Hirokawa, Sachiko Okabe, et al.
Page
of 5