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Nature Chemical Biology
|
January 20, 2017
Target engagement: Shining a light
Kilian V M Huber
ACS Medicinal Chemistry Letters
|
April 16, 2020
Importance of Quantifying Drug-Target Engagement in Cells
Jakub Stefaniak, Kilian V M Huber
Methods in Molecular Biology (Clifton, N.J.)
|
December 25, 2015
Profiling of Small Molecules by Chemical Proteomics
Kilian V M Huber, Giulio Superti-Furga
Methods in Molecular Biology (Clifton, N.J.)
|
August 9, 2023
Global Assessment of Drug Target Engagement and Selectivity of Covalent Cysteine-Reactive Inhibitors Using Alkyne-Functionalized Probes
Elisabeth M Rothweiler, Kilian V M Huber
Biological Chemistry
|
February 22, 2022
Covalent fragment-based ligand screening approaches for identification of novel ubiquitin proteasome system modulators
Elisabeth M Rothweiler, Paul E Brennan, Kilian V M Huber
Expert Opinion on Drug Discovery
|
April 17, 2023
Open resources for chemical probes and their implications for future drug discovery
Esra Balıkçı, Anne-Sophie M C Marques, Jesper S Hansen, et al.
Expert Opinion on Drug Discovery
|
March 3, 2025
Drug repurposing in amyotrophic lateral sclerosis (ALS)
Emily Carroll, Jakub Scaber, Kilian V M Huber, et al.
International Immunopharmacology
|
October 12, 2020
Discovery of novel immunopharmacological ligands targeting the IL-17 inflammatory pathway
Elia Álvarez-Coiradas, Cristian R Munteanu, Laura Díaz-Sáez, et al.
ACS Chemical Biology
|
May 9, 2014
Evaluating the promiscuous nature of tyrosine kinase inhibitors assessed in A431 epidermoid carcinoma cells by both chemical- and phosphoproteomics
Piero Giansanti, Christian Preisinger, Kilian V M Huber, et al.
Cell Reports
|
October 26, 2022
DNA double-strand break-derived RNA drives TIRR/53BP1 complex dissociation
Ruth F Ketley, Federica Battistini, Adele Alagia, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 59) with videos related to
Sort By:
Page
of 6
Nature Chemical Biology
|
January 20, 2017
Target engagement: Shining a light
Kilian V M Huber
ACS Medicinal Chemistry Letters
|
April 16, 2020
Importance of Quantifying Drug-Target Engagement in Cells
Jakub Stefaniak, Kilian V M Huber
Methods in Molecular Biology (Clifton, N.J.)
|
December 25, 2015
Profiling of Small Molecules by Chemical Proteomics
Kilian V M Huber, Giulio Superti-Furga
Methods in Molecular Biology (Clifton, N.J.)
|
August 9, 2023
Global Assessment of Drug Target Engagement and Selectivity of Covalent Cysteine-Reactive Inhibitors Using Alkyne-Functionalized Probes
Elisabeth M Rothweiler, Kilian V M Huber
Biological Chemistry
|
February 22, 2022
Covalent fragment-based ligand screening approaches for identification of novel ubiquitin proteasome system modulators
Elisabeth M Rothweiler, Paul E Brennan, Kilian V M Huber
Expert Opinion on Drug Discovery
|
April 17, 2023
Open resources for chemical probes and their implications for future drug discovery
Esra Balıkçı, Anne-Sophie M C Marques, Jesper S Hansen, et al.
Expert Opinion on Drug Discovery
|
March 3, 2025
Drug repurposing in amyotrophic lateral sclerosis (ALS)
Emily Carroll, Jakub Scaber, Kilian V M Huber, et al.
International Immunopharmacology
|
October 12, 2020
Discovery of novel immunopharmacological ligands targeting the IL-17 inflammatory pathway
Elia Álvarez-Coiradas, Cristian R Munteanu, Laura Díaz-Sáez, et al.
ACS Chemical Biology
|
May 9, 2014
Evaluating the promiscuous nature of tyrosine kinase inhibitors assessed in A431 epidermoid carcinoma cells by both chemical- and phosphoproteomics
Piero Giansanti, Christian Preisinger, Kilian V M Huber, et al.
Cell Reports
|
October 26, 2022
DNA double-strand break-derived RNA drives TIRR/53BP1 complex dissociation
Ruth F Ketley, Federica Battistini, Adele Alagia, et al.
Page
of 6