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Thomas R Webb

Showing results (51-60 of 78) with videos related to

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RNA (New York, N.Y.)|May 31, 2018
Inhibition of SF3B1 by molecules targeting the spliceosome results in massive aberrant exon skippingGang Wu, Liying Fan, Michael N Edmonson, et al.
The Journal of Biological Chemistry|February 4, 2017
USP39 Deubiquitinase Is Essential for <i>KRAS</i> Oncogene-driven CancerJulia M Fraile, Eusebio Manchado, Amaia Lujambio, et al.
Nucleic Acids Research|March 14, 2014
Sudemycin E influences alternative splicing and changes chromatin modificationsPaolo Convertini, Manli Shen, Philip M Potter, et al.
Journal of the American Heart Association|June 23, 2026
Multiomic Reference Map of Endothelial Mechanosensitive Pathways Under Athero- and Erosion-Prone FlowGiulio Vidotto, Sara Luzzi, Jonathan D Humphries, et al.
Oncotarget|June 13, 2015
The splicing modulator sudemycin induces a specific antitumor response and cooperates with ibrutinib in chronic lymphocytic leukemiaSílvia Xargay-Torrent, Mónica López-Guerra, Laia Rosich, et al.
Blood Advances|May 13, 2024
Deep PIM kinase substrate profiling reveals new rational cotherapeutic strategies for acute myeloid leukemiaTejashree Joglekar, Alexander Chin, Alin Voskanian-Kordi, et al.
Journal of Medicinal Chemistry|February 3, 2006
Design and synthesis of 5-aryl-pyridone-carboxamides as inhibitors of anaplastic lymphoma kinaseRongshi Li, Liquan Xue, Tong Zhu, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2016
Identification and characterization of influenza variants resistant to a viral endonuclease inhibitorMin-Suk Song, Gyanendra Kumar, William R Shadrick, et al.
Nature Communications|December 7, 2017
The anthelmintic praziquantel is a human serotoninergic G-protein-coupled receptor ligandJohn D Chan, Pauline M Cupit, Gihan S Gunaratne, et al.
Journal of Medicinal Chemistry|September 3, 2004
Design of 2,5-dimethyl-3-(6-dimethyl-4-methylpyridin-3-yl)-7-dipropylaminopyrazolo[1,5-a]pyrimidine (NBI 30775/R121919) and structure--activity relationships of a series of potent and orally active corticotropin-releasing factor receptor antagonistsChen Chen, Keith M Wilcoxen, Charles Q Huang, et al.
Pageof 8

Showing results (51-60 of 78) with videos related to

Sort By:
Pageof 8
RNA (New York, N.Y.)|May 31, 2018
Inhibition of SF3B1 by molecules targeting the spliceosome results in massive aberrant exon skippingGang Wu, Liying Fan, Michael N Edmonson, et al.
The Journal of Biological Chemistry|February 4, 2017
USP39 Deubiquitinase Is Essential for <i>KRAS</i> Oncogene-driven CancerJulia M Fraile, Eusebio Manchado, Amaia Lujambio, et al.
Nucleic Acids Research|March 14, 2014
Sudemycin E influences alternative splicing and changes chromatin modificationsPaolo Convertini, Manli Shen, Philip M Potter, et al.
Journal of the American Heart Association|June 23, 2026
Multiomic Reference Map of Endothelial Mechanosensitive Pathways Under Athero- and Erosion-Prone FlowGiulio Vidotto, Sara Luzzi, Jonathan D Humphries, et al.
Oncotarget|June 13, 2015
The splicing modulator sudemycin induces a specific antitumor response and cooperates with ibrutinib in chronic lymphocytic leukemiaSílvia Xargay-Torrent, Mónica López-Guerra, Laia Rosich, et al.
Blood Advances|May 13, 2024
Deep PIM kinase substrate profiling reveals new rational cotherapeutic strategies for acute myeloid leukemiaTejashree Joglekar, Alexander Chin, Alin Voskanian-Kordi, et al.
Journal of Medicinal Chemistry|February 3, 2006
Design and synthesis of 5-aryl-pyridone-carboxamides as inhibitors of anaplastic lymphoma kinaseRongshi Li, Liquan Xue, Tong Zhu, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2016
Identification and characterization of influenza variants resistant to a viral endonuclease inhibitorMin-Suk Song, Gyanendra Kumar, William R Shadrick, et al.
Nature Communications|December 7, 2017
The anthelmintic praziquantel is a human serotoninergic G-protein-coupled receptor ligandJohn D Chan, Pauline M Cupit, Gihan S Gunaratne, et al.
Journal of Medicinal Chemistry|September 3, 2004
Design of 2,5-dimethyl-3-(6-dimethyl-4-methylpyridin-3-yl)-7-dipropylaminopyrazolo[1,5-a]pyrimidine (NBI 30775/R121919) and structure--activity relationships of a series of potent and orally active corticotropin-releasing factor receptor antagonistsChen Chen, Keith M Wilcoxen, Charles Q Huang, et al.
Pageof 8