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Journal of Lipid Research
|
January 11, 2019
A large scale high-throughput screen identifies chemical inhibitors of phosphatidylinositol 4-kinase type II alpha
Nivedita Sengupta, Marko Jović, Elena Barnaeva, et al.
Bioorganic & Medicinal Chemistry
|
December 2, 2014
Norbornane-based nucleoside and nucleotide analogues locked in North conformation
Milan Dejmek, Michal Šála, Hubert Hřebabecký, et al.
Structure (London, England : 1993)
|
June 11, 2022
Discovery of isonucleotidic CDNs as potent STING agonists with immunomodulatory potential
Milan Dejmek, Michal Šála, Andrea Brazdova, et al.
Autophagy
|
May 15, 2023
Identifying a selective inhibitor of autophagy that targets ATG12-ATG3 protein-protein interaction
Gal Chaim Nuta, Yuval Gilad, Nadav Goldberg, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
March 8, 2026
Pregnane X receptor antagonist MI-891 reduces hepatic triglycerides in PXR-CAR-CYP3A4/3A7-humanized mice
Klára Dohnalová, Rajamanikkam Kamaraj, Martin Ambrož, et al.
Journal of Medicinal Chemistry
|
April 22, 2015
Highly Selective Phosphatidylinositol 4-Kinase IIIβ Inhibitors and Structural Insight into Their Mode of Action
Ivana Mejdrová, Dominika Chalupská, Martin Kögler, et al.
Nucleic Acids Research
|
November 22, 2023
Reactivation of the G1 enhancer landscape underlies core circuitry addiction to SWI/SNF
Katerina Cermakova, Ling Tao, Milan Dejmek, et al.
Journal of Medicinal Chemistry
|
July 12, 2025
Discovery of PXR Antagonist MI891 and PXR Degrader MI1013 and Their Roles in Hepatic Gene Regulation
Rajamanikkam Kamaraj, Ivana Mejdrová, Maria Krutakova, et al.
RSC Medicinal Chemistry
|
September 2, 2024
Discovery of highly potent SARS-CoV-2 nsp14 methyltransferase inhibitors based on adenosine 5'-carboxamides
Hugo Kocek, Dominika Chalupská, Milan Dejmek, et al.
ACS Omega
|
August 7, 2023
Rational Design of Highly Potent SARS-CoV-2 nsp14 Methyltransferase Inhibitors
Milan Štefek, Dominika Chalupská, Karel Chalupský, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 93) with videos related to
Sort By:
Page
of 10
Journal of Lipid Research
|
January 11, 2019
A large scale high-throughput screen identifies chemical inhibitors of phosphatidylinositol 4-kinase type II alpha
Nivedita Sengupta, Marko Jović, Elena Barnaeva, et al.
Bioorganic & Medicinal Chemistry
|
December 2, 2014
Norbornane-based nucleoside and nucleotide analogues locked in North conformation
Milan Dejmek, Michal Šála, Hubert Hřebabecký, et al.
Structure (London, England : 1993)
|
June 11, 2022
Discovery of isonucleotidic CDNs as potent STING agonists with immunomodulatory potential
Milan Dejmek, Michal Šála, Andrea Brazdova, et al.
Autophagy
|
May 15, 2023
Identifying a selective inhibitor of autophagy that targets ATG12-ATG3 protein-protein interaction
Gal Chaim Nuta, Yuval Gilad, Nadav Goldberg, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
March 8, 2026
Pregnane X receptor antagonist MI-891 reduces hepatic triglycerides in PXR-CAR-CYP3A4/3A7-humanized mice
Klára Dohnalová, Rajamanikkam Kamaraj, Martin Ambrož, et al.
Journal of Medicinal Chemistry
|
April 22, 2015
Highly Selective Phosphatidylinositol 4-Kinase IIIβ Inhibitors and Structural Insight into Their Mode of Action
Ivana Mejdrová, Dominika Chalupská, Martin Kögler, et al.
Nucleic Acids Research
|
November 22, 2023
Reactivation of the G1 enhancer landscape underlies core circuitry addiction to SWI/SNF
Katerina Cermakova, Ling Tao, Milan Dejmek, et al.
Journal of Medicinal Chemistry
|
July 12, 2025
Discovery of PXR Antagonist MI891 and PXR Degrader MI1013 and Their Roles in Hepatic Gene Regulation
Rajamanikkam Kamaraj, Ivana Mejdrová, Maria Krutakova, et al.
RSC Medicinal Chemistry
|
September 2, 2024
Discovery of highly potent SARS-CoV-2 nsp14 methyltransferase inhibitors based on adenosine 5'-carboxamides
Hugo Kocek, Dominika Chalupská, Milan Dejmek, et al.
ACS Omega
|
August 7, 2023
Rational Design of Highly Potent SARS-CoV-2 nsp14 Methyltransferase Inhibitors
Milan Štefek, Dominika Chalupská, Karel Chalupský, et al.
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of 10