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Journal of Molecular Recognition : JMR
|
March 13, 2012
Characterization of a high-affinity human antibody with a disulfide bridge in the third complementarity-determining region of the heavy chain
Juan Carlos Almagro, Gopalan Raghunathan, Eric Beil, et al.
Structure (London, England : 1993)
|
December 7, 2002
Structures of the cancer-related Aurora-A, FAK, and EphA2 protein kinases from nanovolume crystallography
Jacek Nowakowski, Ciarán N Cronin, Duncan E McRee, et al.
Journal of Medicinal Chemistry
|
September 11, 2024
Discovery of TYRA-300: First Oral Selective FGFR3 Inhibitor for the Treatment of Urothelial Cancers and Achondroplasia
Robert L Hudkins, Eric Allen, Alexandra Balcer, et al.
Journal of Medicinal Chemistry
|
March 31, 2026
Structure-Based Design of a Novel Covalent 4-(1-Methylindol-3-yl)pyrimidin-2-amine Series Targeting FGFR2 Resistance Mutations
Robert L Hudkins, Eric Allen, Samhita Iyer, et al.
Molecular Cancer Therapeutics
|
October 14, 2025
Dabogratinib (TYRA-300), an FGFR3 isoform-selective inhibitor: preclinical and initial clinical evidence of anti-tumor activity
Jacqueline H Starrett, Eric L Allen, Melissa Neal, et al.
Journal of Molecular Biology
|
March 16, 2010
Human framework adaptation of a mouse anti-human IL-13 antibody
Johan Fransson, Alexey Teplyakov, Gopalan Raghunathan, et al.
JCI Insight
|
April 3, 2025
TYRA-300, an FGFR3-selective inhibitor, promotes bone growth in two FGFR3-driven models of chondrodysplasia
Jacqueline H Starrett, Clara Lemoine, Matthias Guillo, et al.
The Journal of Biological Chemistry
|
June 19, 2014
Targeting the ion channel Kv1.3 with scorpion venom peptides engineered for potency, selectivity, and half-life
Wilson Edwards, Wai-Ping Fung-Leung, Chichi Huang, et al.
Cell Metabolism
|
February 19, 2019
A Long-Acting PYY<sub>3-36</sub> Analog Mediates Robust Anorectic Efficacy with Minimal Emesis in Nonhuman Primates
Shamina M Rangwala, Katharine D'Aquino, Yue-Mei Zhang, et al.
Structure (London, England : 1993)
|
July 10, 2004
Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases
John R Somoza, Robert J Skene, Bradley A Katz, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Journal of Molecular Recognition : JMR
|
March 13, 2012
Characterization of a high-affinity human antibody with a disulfide bridge in the third complementarity-determining region of the heavy chain
Juan Carlos Almagro, Gopalan Raghunathan, Eric Beil, et al.
Structure (London, England : 1993)
|
December 7, 2002
Structures of the cancer-related Aurora-A, FAK, and EphA2 protein kinases from nanovolume crystallography
Jacek Nowakowski, Ciarán N Cronin, Duncan E McRee, et al.
Journal of Medicinal Chemistry
|
September 11, 2024
Discovery of TYRA-300: First Oral Selective FGFR3 Inhibitor for the Treatment of Urothelial Cancers and Achondroplasia
Robert L Hudkins, Eric Allen, Alexandra Balcer, et al.
Journal of Medicinal Chemistry
|
March 31, 2026
Structure-Based Design of a Novel Covalent 4-(1-Methylindol-3-yl)pyrimidin-2-amine Series Targeting FGFR2 Resistance Mutations
Robert L Hudkins, Eric Allen, Samhita Iyer, et al.
Molecular Cancer Therapeutics
|
October 14, 2025
Dabogratinib (TYRA-300), an FGFR3 isoform-selective inhibitor: preclinical and initial clinical evidence of anti-tumor activity
Jacqueline H Starrett, Eric L Allen, Melissa Neal, et al.
Journal of Molecular Biology
|
March 16, 2010
Human framework adaptation of a mouse anti-human IL-13 antibody
Johan Fransson, Alexey Teplyakov, Gopalan Raghunathan, et al.
JCI Insight
|
April 3, 2025
TYRA-300, an FGFR3-selective inhibitor, promotes bone growth in two FGFR3-driven models of chondrodysplasia
Jacqueline H Starrett, Clara Lemoine, Matthias Guillo, et al.
The Journal of Biological Chemistry
|
June 19, 2014
Targeting the ion channel Kv1.3 with scorpion venom peptides engineered for potency, selectivity, and half-life
Wilson Edwards, Wai-Ping Fung-Leung, Chichi Huang, et al.
Cell Metabolism
|
February 19, 2019
A Long-Acting PYY<sub>3-36</sub> Analog Mediates Robust Anorectic Efficacy with Minimal Emesis in Nonhuman Primates
Shamina M Rangwala, Katharine D'Aquino, Yue-Mei Zhang, et al.
Structure (London, England : 1993)
|
July 10, 2004
Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases
John R Somoza, Robert J Skene, Bradley A Katz, et al.
Page
of 3