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Molecular & Cellular Proteomics : MCP
|
December 6, 2006
An antiproliferative genetic screening identifies a peptide aptamer that targets calcineurin and up-regulates its activity
Benoît de Chassey, Ivan Mikaelian, Anne-Laure Mathieu, et al.
Antiviral Research
|
August 14, 2012
A small molecule screen in yeast identifies inhibitors targeting protein-protein interactions within the vaccinia virus replication complex
Olivier Flusin, Laurent Saccucci, Céline Contesto-Richefeu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 13, 2013
CDK10/cyclin M is a protein kinase that controls ETS2 degradation and is deficient in STAR syndrome
Vincent J Guen, Carly Gamble, Marc Flajolet, et al.
Chemistry & Biology
|
April 14, 2015
Tamoxifen inhibits CDK5 kinase activity by interacting with p35/p25 and modulates the pattern of tau phosphorylation
Caroline Corbel, Bing Zhang, Annabelle Le Parc, et al.
Marine Drugs
|
October 12, 2019
Kinase-Based Screening of Marine Natural Extracts Leads to the Identification of a Cytotoxic High Molecular Weight Metabolite from the Mediterranean Sponge <i>Crambe tailliezi</i>
Thi-Ngoc-Dung Nguyen, Omid Feizbakhsh, Estelle Sfecci, et al.
ACS Chemical Biology
|
July 14, 2016
From Peptide Aptamers to Inhibitors of FUR, Bacterial Transcriptional Regulator of Iron Homeostasis and Virulence
Sophie Mathieu, Cheickna Cissé, Sylvia Vitale, et al.
Biotechnology Journal
|
June 18, 2011
First BRET-based screening assay performed in budding yeast leads to the discovery of CDK5/p25 interaction inhibitors
Caroline Corbel, Qian Wang, Hadjira Bousserouel, et al.
Journal of Medicinal Chemistry
|
January 9, 2009
Pyrazolo[1,5-a]-1,3,5-triazine as a purine bioisostere: access to potent cyclin-dependent kinase inhibitor (R)-roscovitine analogue
Florence Popowycz, Guy Fournet, Cédric Schneider, et al.
European Journal of Medicinal Chemistry
|
May 14, 2020
Identification of a new series of flavopiridol-like structures as kinase inhibitors with high cytotoxic potency
Nada Ibrahim, Pascal Bonnet, Jean-Daniel Brion, et al.
Chembiochem : a European Journal of Chemical Biology
|
January 27, 2015
Tampering with cell division by using small-molecule inhibitors of CDK-CKS protein interactions
Amel Hamdi, Aurélien Lesnard, Peggy Suzanne, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 35) with videos related to
Sort By:
Page
of 4
Molecular & Cellular Proteomics : MCP
|
December 6, 2006
An antiproliferative genetic screening identifies a peptide aptamer that targets calcineurin and up-regulates its activity
Benoît de Chassey, Ivan Mikaelian, Anne-Laure Mathieu, et al.
Antiviral Research
|
August 14, 2012
A small molecule screen in yeast identifies inhibitors targeting protein-protein interactions within the vaccinia virus replication complex
Olivier Flusin, Laurent Saccucci, Céline Contesto-Richefeu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 13, 2013
CDK10/cyclin M is a protein kinase that controls ETS2 degradation and is deficient in STAR syndrome
Vincent J Guen, Carly Gamble, Marc Flajolet, et al.
Chemistry & Biology
|
April 14, 2015
Tamoxifen inhibits CDK5 kinase activity by interacting with p35/p25 and modulates the pattern of tau phosphorylation
Caroline Corbel, Bing Zhang, Annabelle Le Parc, et al.
Marine Drugs
|
October 12, 2019
Kinase-Based Screening of Marine Natural Extracts Leads to the Identification of a Cytotoxic High Molecular Weight Metabolite from the Mediterranean Sponge <i>Crambe tailliezi</i>
Thi-Ngoc-Dung Nguyen, Omid Feizbakhsh, Estelle Sfecci, et al.
ACS Chemical Biology
|
July 14, 2016
From Peptide Aptamers to Inhibitors of FUR, Bacterial Transcriptional Regulator of Iron Homeostasis and Virulence
Sophie Mathieu, Cheickna Cissé, Sylvia Vitale, et al.
Biotechnology Journal
|
June 18, 2011
First BRET-based screening assay performed in budding yeast leads to the discovery of CDK5/p25 interaction inhibitors
Caroline Corbel, Qian Wang, Hadjira Bousserouel, et al.
Journal of Medicinal Chemistry
|
January 9, 2009
Pyrazolo[1,5-a]-1,3,5-triazine as a purine bioisostere: access to potent cyclin-dependent kinase inhibitor (R)-roscovitine analogue
Florence Popowycz, Guy Fournet, Cédric Schneider, et al.
European Journal of Medicinal Chemistry
|
May 14, 2020
Identification of a new series of flavopiridol-like structures as kinase inhibitors with high cytotoxic potency
Nada Ibrahim, Pascal Bonnet, Jean-Daniel Brion, et al.
Chembiochem : a European Journal of Chemical Biology
|
January 27, 2015
Tampering with cell division by using small-molecule inhibitors of CDK-CKS protein interactions
Amel Hamdi, Aurélien Lesnard, Peggy Suzanne, et al.
Page
of 4