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Christopher J Squire

Showing results (41-50 of 49) with videos related to

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Bioorganic & Medicinal Chemistry Letters|January 15, 2008
Synthesis and structure-activity relationships of soluble 8-substituted 4-(2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-diones as inhibitors of the Wee1 and Chk1 checkpoint kinasesJeff B Smaill, Ho H Lee, Brian D Palmer, et al.
Bioorganic & Medicinal Chemistry|November 23, 2013
Discovery and characterisation of hydrazines as inhibitors of the immune suppressive enzyme, indoleamine 2,3-dioxygenase 1 (IDO1)Sai-Parng S Fung, Haiyan Wang, Petr Tomek, et al.
Cancer Research|February 12, 2004
In vitro studies with methylproamine: a potent new radioprotectorRoger F Martin, Sam Broadhurst, Monica E Reum, et al.
Protein Science : a Publication of the Protein Society|July 27, 2025
Protease mimicry: Dissecting the ester bond crosslinking mechanics in bacterial adhesin proteinsYuliana Yosaatmadja, Vanessa Ung, Xinlu Liu, et al.
The Journal of Biological Chemistry|January 30, 2003
Trapping HIV-1 reverse transcriptase before and after translocation on DNAStefan G Sarafianos, Arthur D Clark, Steve Tuske, et al.
European Journal of Medicinal Chemistry|May 19, 2017
2-Oxo-3, 4-dihydropyrimido[4, 5-d]pyrimidinyl derivatives as new irreversible pan fibroblast growth factor receptor (FGFR) inhibitorsXueqiang Li, Christopher P Guise, Rana Taghipouran, et al.
Nature Communications|February 12, 2024
Poly-γ-glutamylation of biomoleculesGhader Bashiri, Esther M M Bulloch, William R Bramley, et al.
Oncology and Therapy|June 23, 2021
Validating TDP1 as an Inhibition Target for the Development of Chemosensitizers for Camptothecin-Based Chemotherapy DrugsEuphemia Leung, Jinal Patel, Jennifer A Hollywood, et al.
European Journal of Medicinal Chemistry|September 18, 2007
Synthesis and structure-activity relationships of N-6 substituted analogues of 9-hydroxy-4-phenylpyrrolo[3,4-c]carbazole-1,3(2H,6H)-diones as inhibitors of Wee1 and Chk1 checkpoint kinasesJeff B Smaill, Edward N Baker, R John Booth, et al.
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Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Bioorganic & Medicinal Chemistry Letters|January 15, 2008
Synthesis and structure-activity relationships of soluble 8-substituted 4-(2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-diones as inhibitors of the Wee1 and Chk1 checkpoint kinasesJeff B Smaill, Ho H Lee, Brian D Palmer, et al.
Bioorganic & Medicinal Chemistry|November 23, 2013
Discovery and characterisation of hydrazines as inhibitors of the immune suppressive enzyme, indoleamine 2,3-dioxygenase 1 (IDO1)Sai-Parng S Fung, Haiyan Wang, Petr Tomek, et al.
Cancer Research|February 12, 2004
In vitro studies with methylproamine: a potent new radioprotectorRoger F Martin, Sam Broadhurst, Monica E Reum, et al.
Protein Science : a Publication of the Protein Society|July 27, 2025
Protease mimicry: Dissecting the ester bond crosslinking mechanics in bacterial adhesin proteinsYuliana Yosaatmadja, Vanessa Ung, Xinlu Liu, et al.
The Journal of Biological Chemistry|January 30, 2003
Trapping HIV-1 reverse transcriptase before and after translocation on DNAStefan G Sarafianos, Arthur D Clark, Steve Tuske, et al.
European Journal of Medicinal Chemistry|May 19, 2017
2-Oxo-3, 4-dihydropyrimido[4, 5-d]pyrimidinyl derivatives as new irreversible pan fibroblast growth factor receptor (FGFR) inhibitorsXueqiang Li, Christopher P Guise, Rana Taghipouran, et al.
Nature Communications|February 12, 2024
Poly-γ-glutamylation of biomoleculesGhader Bashiri, Esther M M Bulloch, William R Bramley, et al.
Oncology and Therapy|June 23, 2021
Validating TDP1 as an Inhibition Target for the Development of Chemosensitizers for Camptothecin-Based Chemotherapy DrugsEuphemia Leung, Jinal Patel, Jennifer A Hollywood, et al.
European Journal of Medicinal Chemistry|September 18, 2007
Synthesis and structure-activity relationships of N-6 substituted analogues of 9-hydroxy-4-phenylpyrrolo[3,4-c]carbazole-1,3(2H,6H)-diones as inhibitors of Wee1 and Chk1 checkpoint kinasesJeff B Smaill, Edward N Baker, R John Booth, et al.
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