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Kyle V Butler

Showing results (11-20 of 19) with videos related to

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Journal of Medicinal Chemistry|November 3, 2016
Discovery of G Protein-Biased D2 Dopamine Receptor Partial AgonistsXin Chen, John D McCorvy, Matthew G Fischer, et al.
Journal of Chemical Information and Modeling|February 3, 2009
Novel inhibitors of human histone deacetylase (HDAC) identified by QSAR modeling of known inhibitors, virtual screening, and experimental validationHao Tang, Xiang S Wang, Xi-Ping Huang, et al.
Nature Biotechnology|November 13, 2019
Dose-dependent activation of gene expression is achieved using CRISPR and small molecules that recruit endogenous chromatin machineryAnna M Chiarella, Kyle V Butler, Berkley E Gryder, et al.
SLAS Discovery : Advancing Life Sciences R & D|May 31, 2019
Pathway-Based High-Throughput Chemical Screen Identifies Compounds That Decouple Heterochromatin TransformationsIan A MacDonald, Kyle V Butler, Laura E Herring, et al.
Nature Chemical Biology|December 12, 2017
Structure-inspired design of β-arrestin-biased ligands for aminergic GPCRsJohn D McCorvy, Kyle V Butler, Brendan Kelly, et al.
Journal of Medicinal Chemistry|November 3, 2016
Structure-Based Design of a Covalent Inhibitor of the SET Domain-Containing Protein 8 (SETD8) Lysine MethyltransferaseKyle V Butler, Anqi Ma, Wenyu Yu, et al.
Journal of Medicinal Chemistry|July 18, 2014
Discovery of a selective, substrate-competitive inhibitor of the lysine methyltransferase SETD8Anqi Ma, Wenyu Yu, Fengling Li, et al.
Frontiers in Oncology|February 16, 2023
MS0621, a novel small-molecule modulator of Ewing sarcoma chromatin accessibility, interacts with an RNA-associated macromolecular complex and influences RNA splicingTamara Vital, Aminah Wali, Kyle V Butler, et al.
ACS Chemical Biology|November 25, 2015
A Potent, Selective, and Cell-Active Inhibitor of Human Type I Protein Arginine MethyltransferasesMohammad S Eram, Yudao Shen, Magdalena Szewczyk, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Journal of Medicinal Chemistry|November 3, 2016
Discovery of G Protein-Biased D2 Dopamine Receptor Partial AgonistsXin Chen, John D McCorvy, Matthew G Fischer, et al.
Journal of Chemical Information and Modeling|February 3, 2009
Novel inhibitors of human histone deacetylase (HDAC) identified by QSAR modeling of known inhibitors, virtual screening, and experimental validationHao Tang, Xiang S Wang, Xi-Ping Huang, et al.
Nature Biotechnology|November 13, 2019
Dose-dependent activation of gene expression is achieved using CRISPR and small molecules that recruit endogenous chromatin machineryAnna M Chiarella, Kyle V Butler, Berkley E Gryder, et al.
SLAS Discovery : Advancing Life Sciences R & D|May 31, 2019
Pathway-Based High-Throughput Chemical Screen Identifies Compounds That Decouple Heterochromatin TransformationsIan A MacDonald, Kyle V Butler, Laura E Herring, et al.
Nature Chemical Biology|December 12, 2017
Structure-inspired design of β-arrestin-biased ligands for aminergic GPCRsJohn D McCorvy, Kyle V Butler, Brendan Kelly, et al.
Journal of Medicinal Chemistry|November 3, 2016
Structure-Based Design of a Covalent Inhibitor of the SET Domain-Containing Protein 8 (SETD8) Lysine MethyltransferaseKyle V Butler, Anqi Ma, Wenyu Yu, et al.
Journal of Medicinal Chemistry|July 18, 2014
Discovery of a selective, substrate-competitive inhibitor of the lysine methyltransferase SETD8Anqi Ma, Wenyu Yu, Fengling Li, et al.
Frontiers in Oncology|February 16, 2023
MS0621, a novel small-molecule modulator of Ewing sarcoma chromatin accessibility, interacts with an RNA-associated macromolecular complex and influences RNA splicingTamara Vital, Aminah Wali, Kyle V Butler, et al.
ACS Chemical Biology|November 25, 2015
A Potent, Selective, and Cell-Active Inhibitor of Human Type I Protein Arginine MethyltransferasesMohammad S Eram, Yudao Shen, Magdalena Szewczyk, et al.
Pageof 2