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Nanomaterials (Basel, Switzerland)
|
July 8, 2020
Nanoparticle Recognition on Scanning Probe Microscopy Images Using Computer Vision and Deep Learning
Alexey G Okunev, Mikhail Yu Mashukov, Anna V Nartova, et al.
Current Protocols
|
November 8, 2021
5-Substituted 1,2,4-Triazole-3-Carboxylates and 5-Substituted Ribavirin Analogs Synthesis
Andrey V Matveev, Lyubov E Grebenkina, Alexander N Prutkov, et al.
Microscopy Research and Technique
|
January 8, 2024
DLgram cloud service for deep-learning analysis of microscopy images
Andrey V Matveev, Anna V Nartova, Natalya N Sankova, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
March 12, 2019
Chemical ribosylation of 5-substituted 1,2,4-triazole-3-carboxylates
Alexander N Prutkov, Mikhail V Chudinov, Andrey V Matveev, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
March 5, 2020
5-alkylvinyl-1,2,4-triazole nucleosides: Synthesis and biological evaluation
Alexander N Prutkov, Mikhail V Chudinov, Andrey V Matveev, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 6, 2016
An alternative route to the arylvinyltriazole nucleosides
Mikhail V Chudinov, Alexander N Prutkov, Andrey V Matveev, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 28, 2017
Isosteric ribavirin analogues: Synthesis and antiviral activities
Nikolay I Zhurilo, Mikhail V Chudinov, Andrey V Matveev, et al.
Molecules (Basel, Switzerland)
|
October 26, 2024
Synthesis of Alkyl/Aryloxymethyl Derivatives of 1,2,4-Triazole-3-Carboxamides and Their Biological Activities
Ekaterina A Mikhina, Daria V Stepanycheva, Varvara P Maksimova, et al.
Biomolecules
|
January 25, 2025
Synthesis and Anti-Cancer Activity In Vitro of Synephrine Derivatives
Ekaterina M Zhidkova, Evgeniya S Oleynik, Ekaterina A Mikhina, et al.
International Journal of Molecular Sciences
|
December 11, 2025
Anti-Cancer Outcome of Glucocorticoid Receptor Transrepression by Synephrine Derivatives in Hematological Malignancies
Ekaterina M Zhidkova, Ekaterina D Savina, Daria V Migaleva, et al.
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Search research articles
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
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Nanomaterials (Basel, Switzerland)
|
July 8, 2020
Nanoparticle Recognition on Scanning Probe Microscopy Images Using Computer Vision and Deep Learning
Alexey G Okunev, Mikhail Yu Mashukov, Anna V Nartova, et al.
Current Protocols
|
November 8, 2021
5-Substituted 1,2,4-Triazole-3-Carboxylates and 5-Substituted Ribavirin Analogs Synthesis
Andrey V Matveev, Lyubov E Grebenkina, Alexander N Prutkov, et al.
Microscopy Research and Technique
|
January 8, 2024
DLgram cloud service for deep-learning analysis of microscopy images
Andrey V Matveev, Anna V Nartova, Natalya N Sankova, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
March 12, 2019
Chemical ribosylation of 5-substituted 1,2,4-triazole-3-carboxylates
Alexander N Prutkov, Mikhail V Chudinov, Andrey V Matveev, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
March 5, 2020
5-alkylvinyl-1,2,4-triazole nucleosides: Synthesis and biological evaluation
Alexander N Prutkov, Mikhail V Chudinov, Andrey V Matveev, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 6, 2016
An alternative route to the arylvinyltriazole nucleosides
Mikhail V Chudinov, Alexander N Prutkov, Andrey V Matveev, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 28, 2017
Isosteric ribavirin analogues: Synthesis and antiviral activities
Nikolay I Zhurilo, Mikhail V Chudinov, Andrey V Matveev, et al.
Molecules (Basel, Switzerland)
|
October 26, 2024
Synthesis of Alkyl/Aryloxymethyl Derivatives of 1,2,4-Triazole-3-Carboxamides and Their Biological Activities
Ekaterina A Mikhina, Daria V Stepanycheva, Varvara P Maksimova, et al.
Biomolecules
|
January 25, 2025
Synthesis and Anti-Cancer Activity In Vitro of Synephrine Derivatives
Ekaterina M Zhidkova, Evgeniya S Oleynik, Ekaterina A Mikhina, et al.
International Journal of Molecular Sciences
|
December 11, 2025
Anti-Cancer Outcome of Glucocorticoid Receptor Transrepression by Synephrine Derivatives in Hematological Malignancies
Ekaterina M Zhidkova, Ekaterina D Savina, Daria V Migaleva, et al.
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