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Organic Letters
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August 31, 2002
Total synthesis of luminacin D
J Brad Shotwell, Evan S Krygowski, John Hines, et al.
Angewandte Chemie (International Ed. in English)
|
October 16, 2012
Small-molecule inhibitors of the interaction between the E3 ligase VHL and HIF1α
Dennis L Buckley, Jeffrey L Gustafson, Inge Van Molle, et al.
Nature Cell Biology
|
April 30, 2026
The atypical E3 ligase HOIL-1 safeguards the ribosome during cellular stress
Todd Douglas, Pengju Nie, Jiasheng Zhang, et al.
Nature Chemical Biology
|
July 5, 2011
Small-molecule hydrophobic tagging-induced degradation of HaloTag fusion proteins
Taavi K Neklesa, Hyun Seop Tae, Ashley R Schneekloth, et al.
Cell Chemical Biology
|
November 14, 2017
Lessons in PROTAC Design from Selective Degradation with a Promiscuous Warhead
Daniel P Bondeson, Blake E Smith, George M Burslem, et al.
Chemistry & Biology
|
September 21, 2006
A chemical and genetic approach to the mode of action of fumagillin
Yi Zhang, Jing Ruey Yeh, Andrew Mara, et al.
Communications Biology
|
October 2, 2018
Androgen receptor degradation by the proteolysis-targeting chimera ARCC-4 outperforms enzalutamide in cellular models of prostate cancer drug resistance
Jemilat Salami, Shanique Alabi, Ryan R Willard, et al.
ACS Chemical Biology
|
August 28, 2013
A bidirectional system for the dynamic small molecule control of intracellular fusion proteins
Taavi K Neklesa, Devin J Noblin, Alexander P Kuzin, et al.
Biochemistry
|
June 1, 2018
Targeting the C481S Ibrutinib-Resistance Mutation in Bruton's Tyrosine Kinase Using PROTAC-Mediated Degradation
Alexandru D Buhimschi, Haley A Armstrong, Momar Toure, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 22, 2015
Development of small molecules targeting the pseudokinase Her3
Sang Min Lim, Ting Xie, Kenneth D Westover, et al.
Page
of 16
Search research articles
Search
Showing results (131-140 of 155) with videos related to
Sort By:
Page
of 16
Organic Letters
|
August 31, 2002
Total synthesis of luminacin D
J Brad Shotwell, Evan S Krygowski, John Hines, et al.
Angewandte Chemie (International Ed. in English)
|
October 16, 2012
Small-molecule inhibitors of the interaction between the E3 ligase VHL and HIF1α
Dennis L Buckley, Jeffrey L Gustafson, Inge Van Molle, et al.
Nature Cell Biology
|
April 30, 2026
The atypical E3 ligase HOIL-1 safeguards the ribosome during cellular stress
Todd Douglas, Pengju Nie, Jiasheng Zhang, et al.
Nature Chemical Biology
|
July 5, 2011
Small-molecule hydrophobic tagging-induced degradation of HaloTag fusion proteins
Taavi K Neklesa, Hyun Seop Tae, Ashley R Schneekloth, et al.
Cell Chemical Biology
|
November 14, 2017
Lessons in PROTAC Design from Selective Degradation with a Promiscuous Warhead
Daniel P Bondeson, Blake E Smith, George M Burslem, et al.
Chemistry & Biology
|
September 21, 2006
A chemical and genetic approach to the mode of action of fumagillin
Yi Zhang, Jing Ruey Yeh, Andrew Mara, et al.
Communications Biology
|
October 2, 2018
Androgen receptor degradation by the proteolysis-targeting chimera ARCC-4 outperforms enzalutamide in cellular models of prostate cancer drug resistance
Jemilat Salami, Shanique Alabi, Ryan R Willard, et al.
ACS Chemical Biology
|
August 28, 2013
A bidirectional system for the dynamic small molecule control of intracellular fusion proteins
Taavi K Neklesa, Devin J Noblin, Alexander P Kuzin, et al.
Biochemistry
|
June 1, 2018
Targeting the C481S Ibrutinib-Resistance Mutation in Bruton's Tyrosine Kinase Using PROTAC-Mediated Degradation
Alexandru D Buhimschi, Haley A Armstrong, Momar Toure, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 22, 2015
Development of small molecules targeting the pseudokinase Her3
Sang Min Lim, Ting Xie, Kenneth D Westover, et al.
Page
of 16