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Matthieu Schapira

Showing results (81-90 of 148) with videos related to

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Nature Communications|August 12, 2021
Structure, mechanism and crystallographic fragment screening of the SARS-CoV-2 NSP13 helicaseJoseph A Newman, Alice Douangamath, Setayesh Yadzani, et al.
Bioorganic & Medicinal Chemistry|February 26, 2013
Bromo-deaza-SAH: a potent and selective DOT1L inhibitorWenyu Yu, David Smil, Fengling Li, et al.
The Journal of Biological Chemistry|March 18, 2014
Trimethylation of histone H3 lysine 36 by human methyltransferase PRDM9 proteinMohammad S Eram, Susan P Bustos, Evelyne Lima-Fernandes, et al.
Journal of Medicinal Chemistry|February 20, 2026
Development of a Dual Chemical Probe for the USP16 and HDAC6 Zinc-Finger Ubiquitin-Binding DomainMadhushika Silva, Mandeep Mann, Bijan Mirabi, et al.
Journal of Medicinal Chemistry|October 12, 2017
Small Molecule Antagonists of the Interaction between the Histone Deacetylase 6 Zinc-Finger Domain and UbiquitinRachel J Harding, Renato Ferreira de Freitas, Patrick Collins, et al.
ACS Infectious Diseases|July 6, 2016
Identification of small molecule inhibitors that block the <i>Toxoplasma gondii</i> rhoptry kinase ROP18Catherine Simpson, Nathaniel G Jones, Emily A Hull-Ryde, et al.
The Biochemical Journal|August 26, 2009
A survey of proteins encoded by non-synonymous single nucleotide polymorphisms reveals a significant fraction with altered stability and activityAbdellah Allali-Hassani, Gregory A Wasney, Irene Chau, et al.
Molecular & Cellular Proteomics : MCP|September 6, 2007
A comparative analysis of perturbations caused by a gene knock-out, a dominant negative allele, and a set of peptide aptamersNadia Abed, Marc Bickle, Bernard Mari, et al.
Journal of Medicinal Chemistry|March 1, 2013
Exploiting an allosteric binding site of PRMT3 yields potent and selective inhibitorsFeng Liu, Fengling Li, Anqi Ma, et al.
Journal of Medicinal Chemistry|December 27, 2021
Correction to "Structure-Activity Relationship of USP5 Inhibitors"Mandeep K Mann, Carlos A Zepeda-Velázquez, Héctor González-Álvarez, et al.
Pageof 15

Showing results (81-90 of 148) with videos related to

Sort By:
Pageof 15
Nature Communications|August 12, 2021
Structure, mechanism and crystallographic fragment screening of the SARS-CoV-2 NSP13 helicaseJoseph A Newman, Alice Douangamath, Setayesh Yadzani, et al.
Bioorganic & Medicinal Chemistry|February 26, 2013
Bromo-deaza-SAH: a potent and selective DOT1L inhibitorWenyu Yu, David Smil, Fengling Li, et al.
The Journal of Biological Chemistry|March 18, 2014
Trimethylation of histone H3 lysine 36 by human methyltransferase PRDM9 proteinMohammad S Eram, Susan P Bustos, Evelyne Lima-Fernandes, et al.
Journal of Medicinal Chemistry|February 20, 2026
Development of a Dual Chemical Probe for the USP16 and HDAC6 Zinc-Finger Ubiquitin-Binding DomainMadhushika Silva, Mandeep Mann, Bijan Mirabi, et al.
Journal of Medicinal Chemistry|October 12, 2017
Small Molecule Antagonists of the Interaction between the Histone Deacetylase 6 Zinc-Finger Domain and UbiquitinRachel J Harding, Renato Ferreira de Freitas, Patrick Collins, et al.
ACS Infectious Diseases|July 6, 2016
Identification of small molecule inhibitors that block the <i>Toxoplasma gondii</i> rhoptry kinase ROP18Catherine Simpson, Nathaniel G Jones, Emily A Hull-Ryde, et al.
The Biochemical Journal|August 26, 2009
A survey of proteins encoded by non-synonymous single nucleotide polymorphisms reveals a significant fraction with altered stability and activityAbdellah Allali-Hassani, Gregory A Wasney, Irene Chau, et al.
Molecular & Cellular Proteomics : MCP|September 6, 2007
A comparative analysis of perturbations caused by a gene knock-out, a dominant negative allele, and a set of peptide aptamersNadia Abed, Marc Bickle, Bernard Mari, et al.
Journal of Medicinal Chemistry|March 1, 2013
Exploiting an allosteric binding site of PRMT3 yields potent and selective inhibitorsFeng Liu, Fengling Li, Anqi Ma, et al.
Journal of Medicinal Chemistry|December 27, 2021
Correction to "Structure-Activity Relationship of USP5 Inhibitors"Mandeep K Mann, Carlos A Zepeda-Velázquez, Héctor González-Álvarez, et al.
Pageof 15