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Yinghong Gao

Showing results (1-10 of 27) with videos related to

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Journal of Chemical Information and Modeling|June 23, 2009
Elucidating molecular overlays from pairwise alignments using a genetic algorithmGareth Jones, Yinghong Gao, Carleton R Sage
Journal of Chemical Information and Modeling|January 24, 2006
The use of consensus scoring in ligand-based virtual screeningJ Christian Baber, William A Shirley, Yinghong Gao, et al.
Environmental Science and Pollution Research International|February 7, 2020
Magnetic-activated carbon composites derived from iron sludge and biological sludge for sulfonamide antibiotic removalJunli Wan, Jian Ding, Wanchun Tan, et al.
Bioorganic & Medicinal Chemistry|October 9, 2007
The use of ligand-based de novo design for scaffold hopping and sidechain optimization: two case studiesMiklos Feher, Yinghong Gao, J Christian Baber, et al.
Molecular Endocrinology (Baltimore, Md.)|June 2, 2005
A point mutation in the human melanin concentrating hormone receptor 1 reveals an important domain for cellular traffickingJun Fan, Stephen J Perry, Yinghong Gao, et al.
The Biochemical Journal|February 13, 2013
A broad activity screen in support of a chemogenomic map for kinase signalling research and drug discoveryYinghong Gao, Stephen P Davies, Martin Augustin, et al.
Bioorganic & Medicinal Chemistry Letters|June 14, 2008
Discovery of a potent, selective, and less flexible selective norepinephrine reuptake inhibitor (sNRI)Dongpei Wu, Joseph Pontillo, Brett Ching, et al.
Journal of Medicinal Chemistry|October 13, 2006
Determination of the binding mode of thienopyrimidinedione antagonists to the human gonadotropin releasing hormone receptor using structure-activity relationships, site-directed mutagenesis, and homology modelingStephen F Betz, Francisco M Lio, Yinghong Gao, et al.
Biochemistry|December 21, 2006
Allosteric and orthosteric binding modes of two nonpeptide human gonadotropin-releasing hormone receptor antagonistsSusan K Sullivan, Michael S Brown, Yinghong Gao, et al.
Journal of Medicinal Chemistry|December 24, 2004
4-{(2R)-[3-Aminopropionylamido]-3-(2,4-dichlorophenyl)propionyl}-1-{2-[(2-thienyl)ethylaminomethyl]phenyl}piperazine as a potent and selective melanocortin-4 receptor antagonist--design, synthesis, and characterizationChen Chen, Joseph Pontillo, Beth A Fleck, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Journal of Chemical Information and Modeling|June 23, 2009
Elucidating molecular overlays from pairwise alignments using a genetic algorithmGareth Jones, Yinghong Gao, Carleton R Sage
Journal of Chemical Information and Modeling|January 24, 2006
The use of consensus scoring in ligand-based virtual screeningJ Christian Baber, William A Shirley, Yinghong Gao, et al.
Environmental Science and Pollution Research International|February 7, 2020
Magnetic-activated carbon composites derived from iron sludge and biological sludge for sulfonamide antibiotic removalJunli Wan, Jian Ding, Wanchun Tan, et al.
Bioorganic & Medicinal Chemistry|October 9, 2007
The use of ligand-based de novo design for scaffold hopping and sidechain optimization: two case studiesMiklos Feher, Yinghong Gao, J Christian Baber, et al.
Molecular Endocrinology (Baltimore, Md.)|June 2, 2005
A point mutation in the human melanin concentrating hormone receptor 1 reveals an important domain for cellular traffickingJun Fan, Stephen J Perry, Yinghong Gao, et al.
The Biochemical Journal|February 13, 2013
A broad activity screen in support of a chemogenomic map for kinase signalling research and drug discoveryYinghong Gao, Stephen P Davies, Martin Augustin, et al.
Bioorganic & Medicinal Chemistry Letters|June 14, 2008
Discovery of a potent, selective, and less flexible selective norepinephrine reuptake inhibitor (sNRI)Dongpei Wu, Joseph Pontillo, Brett Ching, et al.
Journal of Medicinal Chemistry|October 13, 2006
Determination of the binding mode of thienopyrimidinedione antagonists to the human gonadotropin releasing hormone receptor using structure-activity relationships, site-directed mutagenesis, and homology modelingStephen F Betz, Francisco M Lio, Yinghong Gao, et al.
Biochemistry|December 21, 2006
Allosteric and orthosteric binding modes of two nonpeptide human gonadotropin-releasing hormone receptor antagonistsSusan K Sullivan, Michael S Brown, Yinghong Gao, et al.
Journal of Medicinal Chemistry|December 24, 2004
4-{(2R)-[3-Aminopropionylamido]-3-(2,4-dichlorophenyl)propionyl}-1-{2-[(2-thienyl)ethylaminomethyl]phenyl}piperazine as a potent and selective melanocortin-4 receptor antagonist--design, synthesis, and characterizationChen Chen, Joseph Pontillo, Beth A Fleck, et al.
Pageof 3