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Nature Chemical Biology
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October 18, 2018
Structural insights into binding specificity, efficacy and bias of a β<sub>2</sub>AR partial agonist
Matthieu Masureel, Yaozhong Zou, Louis-Philippe Picard, et al.
Nature Chemical Biology
|
December 4, 2018
Publisher Correction: Structural insights into binding specificity, efficacy and bias of a β<sub>2</sub>AR partial agonist
Matthieu Masureel, Yaozhong Zou, Louis-Philippe Picard, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 2, 2017
Atomic structure of a toxic, oligomeric segment of SOD1 linked to amyotrophic lateral sclerosis (ALS)
Smriti Sangwan, Anni Zhao, Katrina L Adams, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 24, 2012
Preconfiguration of the antigen-binding site during affinity maturation of a broadly neutralizing influenza virus antibody
Aaron G Schmidt, Huafeng Xu, Amir R Khan, et al.
Nature
|
January 14, 2011
Structure and function of an irreversible agonist-β(2) adrenoceptor complex
Daniel M Rosenbaum, Cheng Zhang, Joseph A Lyons, et al.
Nature Communications
|
November 1, 2016
EGFR oligomerization organizes kinase-active dimers into competent signalling platforms
Sarah R Needham, Selene K Roberts, Anton Arkhipov, et al.
Nature Communications
|
October 20, 2018
The architecture of EGFR's basal complexes reveals autoinhibition mechanisms in dimers and oligomers
Laura C Zanetti-Domingues, Dimitrios Korovesis, Sarah R Needham, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 2024
Discovery of lirafugratinib (RLY-4008), a highly selective irreversible small-molecule inhibitor of FGFR2
Heike Schönherr, Pelin Ayaz, Alexander M Taylor, et al.
Cancer Discovery
|
June 4, 2023
RLY-4008, the First Highly Selective FGFR2 Inhibitor with Activity across FGFR2 Alterations and Resistance Mutations
Vivek Subbiah, Vaibhav Sahai, Dejan Maglic, et al.
Journal of Medicinal Chemistry
|
September 29, 2023
Identification of GDC-1971 (RLY-1971), a SHP2 Inhibitor Designed for the Treatment of Solid Tumors
Alexander M Taylor, Bret R Williams, Fabrizio Giordanetto, et al.
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of 15
Search research articles
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Showing results (131-140 of 142) with videos related to
Sort By:
Page
of 15
Nature Chemical Biology
|
October 18, 2018
Structural insights into binding specificity, efficacy and bias of a β<sub>2</sub>AR partial agonist
Matthieu Masureel, Yaozhong Zou, Louis-Philippe Picard, et al.
Nature Chemical Biology
|
December 4, 2018
Publisher Correction: Structural insights into binding specificity, efficacy and bias of a β<sub>2</sub>AR partial agonist
Matthieu Masureel, Yaozhong Zou, Louis-Philippe Picard, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 2, 2017
Atomic structure of a toxic, oligomeric segment of SOD1 linked to amyotrophic lateral sclerosis (ALS)
Smriti Sangwan, Anni Zhao, Katrina L Adams, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 24, 2012
Preconfiguration of the antigen-binding site during affinity maturation of a broadly neutralizing influenza virus antibody
Aaron G Schmidt, Huafeng Xu, Amir R Khan, et al.
Nature
|
January 14, 2011
Structure and function of an irreversible agonist-β(2) adrenoceptor complex
Daniel M Rosenbaum, Cheng Zhang, Joseph A Lyons, et al.
Nature Communications
|
November 1, 2016
EGFR oligomerization organizes kinase-active dimers into competent signalling platforms
Sarah R Needham, Selene K Roberts, Anton Arkhipov, et al.
Nature Communications
|
October 20, 2018
The architecture of EGFR's basal complexes reveals autoinhibition mechanisms in dimers and oligomers
Laura C Zanetti-Domingues, Dimitrios Korovesis, Sarah R Needham, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 2024
Discovery of lirafugratinib (RLY-4008), a highly selective irreversible small-molecule inhibitor of FGFR2
Heike Schönherr, Pelin Ayaz, Alexander M Taylor, et al.
Cancer Discovery
|
June 4, 2023
RLY-4008, the First Highly Selective FGFR2 Inhibitor with Activity across FGFR2 Alterations and Resistance Mutations
Vivek Subbiah, Vaibhav Sahai, Dejan Maglic, et al.
Journal of Medicinal Chemistry
|
September 29, 2023
Identification of GDC-1971 (RLY-1971), a SHP2 Inhibitor Designed for the Treatment of Solid Tumors
Alexander M Taylor, Bret R Williams, Fabrizio Giordanetto, et al.
Page
of 15