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V Harris

Showing results (291-300 of 309) with videos related to

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Bioorganic & Medicinal Chemistry Letters|April 8, 2014
From virtual to clinical: The discovery of PGN-1531, a novel antagonist of the prostanoid EP4 receptorJon Sutton, David E Clark, Christopher Higgs, et al.
Journal of Medicinal Chemistry|July 21, 1998
Selective endothelin A receptor antagonists. 3. Discovery and structure-activity relationships of a series of 4-phenoxybutanoic acid derivativesP C Astles, C Brealey, T J Brown, et al.
Journal of Medicinal Chemistry|July 21, 1998
Selective endothelin A receptor antagonists. 4. Discovery and structure-activity relationships of stilbene acid and alcohol derivativesP C Astles, T J Brown, F Halley, et al.
Biochemistry|March 17, 2010
Stimulation of lignocellulosic biomass hydrolysis by proteins of glycoside hydrolase family 61: structure and function of a large, enigmatic familyPaul V Harris, Ditte Welner, K C McFarland, et al.
Plos One|February 13, 2025
Passive acoustic monitoring of baleen whale seasonal presence across the New York BightBobbi J Estabrook, Lisa A Bonacci-Sullivan, Danielle V Harris, et al.
Chemical Reviews|April 9, 2015
The ONIOM Method and Its ApplicationsLung Wa Chung, W M C Sameera, Romain Ramozzi, et al.
Medicine|March 23, 2017
Oral microbiome in HIV-associated periodontitisMarc Noguera-Julian, Yolanda Guillén, Jessica Peterson, et al.
Journal of Medicinal Chemistry|March 15, 2000
Selective ET(A) antagonists. 5. Discovery and structure-activity relationships of phenoxyphenylacetic acid derivativesP C Astles, T J Brown, F Halley, et al.
Bioorganic & Medicinal Chemistry Letters|November 11, 2006
Identification and optimisation of a series of substituted 5-(1H-pyrazol-3-yl)-thiophene-2-hydroxamic acids as potent histone deacetylase (HDAC) inhibitorsSteve Price, Walter Bordogna, Richard J Bull, et al.
Bioorganic & Medicinal Chemistry Letters|November 17, 2006
Identification and optimisation of a series of substituted 5-pyridin-2-yl-thiophene-2-hydroxamic acids as potent histone deacetylase (HDAC) inhibitorsSteve Price, Walter Bordogna, Ruth Braganza, et al.
Pageof 31

Showing results (291-300 of 309) with videos related to

Sort By:
Pageof 31
Bioorganic & Medicinal Chemistry Letters|April 8, 2014
From virtual to clinical: The discovery of PGN-1531, a novel antagonist of the prostanoid EP4 receptorJon Sutton, David E Clark, Christopher Higgs, et al.
Journal of Medicinal Chemistry|July 21, 1998
Selective endothelin A receptor antagonists. 3. Discovery and structure-activity relationships of a series of 4-phenoxybutanoic acid derivativesP C Astles, C Brealey, T J Brown, et al.
Journal of Medicinal Chemistry|July 21, 1998
Selective endothelin A receptor antagonists. 4. Discovery and structure-activity relationships of stilbene acid and alcohol derivativesP C Astles, T J Brown, F Halley, et al.
Biochemistry|March 17, 2010
Stimulation of lignocellulosic biomass hydrolysis by proteins of glycoside hydrolase family 61: structure and function of a large, enigmatic familyPaul V Harris, Ditte Welner, K C McFarland, et al.
Plos One|February 13, 2025
Passive acoustic monitoring of baleen whale seasonal presence across the New York BightBobbi J Estabrook, Lisa A Bonacci-Sullivan, Danielle V Harris, et al.
Chemical Reviews|April 9, 2015
The ONIOM Method and Its ApplicationsLung Wa Chung, W M C Sameera, Romain Ramozzi, et al.
Medicine|March 23, 2017
Oral microbiome in HIV-associated periodontitisMarc Noguera-Julian, Yolanda Guillén, Jessica Peterson, et al.
Journal of Medicinal Chemistry|March 15, 2000
Selective ET(A) antagonists. 5. Discovery and structure-activity relationships of phenoxyphenylacetic acid derivativesP C Astles, T J Brown, F Halley, et al.
Bioorganic & Medicinal Chemistry Letters|November 11, 2006
Identification and optimisation of a series of substituted 5-(1H-pyrazol-3-yl)-thiophene-2-hydroxamic acids as potent histone deacetylase (HDAC) inhibitorsSteve Price, Walter Bordogna, Richard J Bull, et al.
Bioorganic & Medicinal Chemistry Letters|November 17, 2006
Identification and optimisation of a series of substituted 5-pyridin-2-yl-thiophene-2-hydroxamic acids as potent histone deacetylase (HDAC) inhibitorsSteve Price, Walter Bordogna, Ruth Braganza, et al.
Pageof 31