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Nature Communications
|
November 14, 2020
A computational method for detection of ligand-binding proteins from dose range thermal proteome profiles
Nils Kurzawa, Isabelle Becher, Sindhuja Sridharan, et al.
Journal of Proteome Research
|
January 22, 2025
PeptideForest: Semisupervised Machine Learning Integrating Multiple Search Engines for Peptide Identification
Tristan Ranff, Matthew Dennison, Jeroen Bédorf, et al.
ACS Chemical Biology
|
July 8, 2016
A Modular Probe Strategy for Drug Localization, Target Identification and Target Occupancy Measurement on Single Cell Level
Anna Rutkowska, Douglas W Thomson, Johanna Vappiani, et al.
ACS Chemical Biology
|
August 23, 2012
Chemical proteomic analysis reveals the drugability of the kinome of Trypanosoma brucei
Michael D Urbaniak, Toby Mathieson, Marcus Bantscheff, et al.
Nature Chemical Biology
|
July 21, 2022
Systematic discovery of biomolecular condensate-specific protein phosphorylation
Sindhuja Sridharan, Alberto Hernandez-Armendariz, Nils Kurzawa, et al.
Cell Surface (Amsterdam, Netherlands)
|
December 10, 2021
The multi-target aspect of an MmpL3 inhibitor: The BM212 series of compounds bind EthR2, a transcriptional regulator of ethionamide activation
Alice R Moorey, Alejandro Cabanillas, Sarah M Batt, et al.
Molecular and Cellular Biology
|
January 13, 2016
Mutational Analysis of Glycogen Synthase Kinase 3β Protein Kinase Together with Kinome-Wide Binding and Stability Studies Suggests Context-Dependent Recognition of Kinases by the Chaperone Heat Shock Protein 90
Jing Jin, Ruijun Tian, Adrian Pasculescu, et al.
Scientific Reports
|
October 4, 2019
Chemical proteomics reveals target selectivity of clinical Jak inhibitors in human primary cells
H Christian Eberl, Thilo Werner, Friedrich B Reinhard, et al.
Nature Methods
|
November 3, 2015
Thermal proteome profiling monitors ligand interactions with cellular membrane proteins
Friedrich B M Reinhard, Dirk Eberhard, Thilo Werner, et al.
ACS Chemical Biology
|
February 19, 2014
The commonly used PI3-kinase probe LY294002 is an inhibitor of BET bromodomains
Antje Dittmann, Thilo Werner, Chun-Wa Chung, et al.
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of 12
Search research articles
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Showing results (51-60 of 120) with videos related to
Sort By:
Page
of 12
Nature Communications
|
November 14, 2020
A computational method for detection of ligand-binding proteins from dose range thermal proteome profiles
Nils Kurzawa, Isabelle Becher, Sindhuja Sridharan, et al.
Journal of Proteome Research
|
January 22, 2025
PeptideForest: Semisupervised Machine Learning Integrating Multiple Search Engines for Peptide Identification
Tristan Ranff, Matthew Dennison, Jeroen Bédorf, et al.
ACS Chemical Biology
|
July 8, 2016
A Modular Probe Strategy for Drug Localization, Target Identification and Target Occupancy Measurement on Single Cell Level
Anna Rutkowska, Douglas W Thomson, Johanna Vappiani, et al.
ACS Chemical Biology
|
August 23, 2012
Chemical proteomic analysis reveals the drugability of the kinome of Trypanosoma brucei
Michael D Urbaniak, Toby Mathieson, Marcus Bantscheff, et al.
Nature Chemical Biology
|
July 21, 2022
Systematic discovery of biomolecular condensate-specific protein phosphorylation
Sindhuja Sridharan, Alberto Hernandez-Armendariz, Nils Kurzawa, et al.
Cell Surface (Amsterdam, Netherlands)
|
December 10, 2021
The multi-target aspect of an MmpL3 inhibitor: The BM212 series of compounds bind EthR2, a transcriptional regulator of ethionamide activation
Alice R Moorey, Alejandro Cabanillas, Sarah M Batt, et al.
Molecular and Cellular Biology
|
January 13, 2016
Mutational Analysis of Glycogen Synthase Kinase 3β Protein Kinase Together with Kinome-Wide Binding and Stability Studies Suggests Context-Dependent Recognition of Kinases by the Chaperone Heat Shock Protein 90
Jing Jin, Ruijun Tian, Adrian Pasculescu, et al.
Scientific Reports
|
October 4, 2019
Chemical proteomics reveals target selectivity of clinical Jak inhibitors in human primary cells
H Christian Eberl, Thilo Werner, Friedrich B Reinhard, et al.
Nature Methods
|
November 3, 2015
Thermal proteome profiling monitors ligand interactions with cellular membrane proteins
Friedrich B M Reinhard, Dirk Eberhard, Thilo Werner, et al.
ACS Chemical Biology
|
February 19, 2014
The commonly used PI3-kinase probe LY294002 is an inhibitor of BET bromodomains
Antje Dittmann, Thilo Werner, Chun-Wa Chung, et al.
Page
of 12