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F Blake

Showing results (91-100 of 141) with videos related to

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Journal of the Academy of Nutrition and Dietetics|January 13, 2022
Beverage Characteristics Perceived as Healthy among Hispanic and African-American Parents of Young ChildrenAllison C Sylvetsky, Son T Hoang, Amanda J Visek, et al.
International Immunology|July 1, 1997
Elevated expression of Bcl-2 and Bcl-x by intestinal intraepithelial lymphocytes: resistance to apoptosis by glucocorticoids and irradiationN Van Houten, S F Blake, E J Li, et al.
Nature|April 14, 1988
The nature and origin of interstellar diamondD F Blake, F Freund, K F Krishnan, et al.
Journal of Medicinal Chemistry|August 19, 1994
Novel benzisoxazole derivatives as potent and selective inhibitors of acetylcholinesteraseA Villalobos, J F Blake, C K Biggers, et al.
Physical Review Letters|April 4, 2015
Linear magnetoresistance caused by mobility fluctuations in n-doped Cd(3)As(2)A Narayanan, M D Watson, S F Blake, et al.
Journal of Comparative Psychology (Washington, D.C. : 1983)|May 15, 2013
Personality structure in brown capuchin monkeys (Sapajus apella): comparisons with chimpanzees (Pan troglodytes), orangutans (Pongo spp.), and rhesus macaques (Macaca mulatta)F Blake Morton, Phyllis C Lee, Hannah M Buchanan-Smith, et al.
Bioorganic & Medicinal Chemistry Letters|March 3, 2007
Tetrazole and ester substituted tetrahydoquinoxalines as potent cholesteryl ester transfer protein inhibitorsC Todd Eary, Zachary S Jones, Robert D Groneberg, et al.
Bioorganic & Medicinal Chemistry Letters|December 17, 2008
3-Hydroxyisoquinolines as inhibitors of HCV NS5b RNA-dependent RNA polymeraseRobert T Hendricks, Stacey R Spencer, James F Blake, et al.
Journal of Medicinal Chemistry|July 6, 2000
Structure-based design and synthesis of a potent matrix metalloproteinase-13 inhibitor based on a pyrrolidinone scaffoldR P Robinson, E R Laird, J F Blake, et al.
Oncology Research|September 23, 2011
Single-agent inhibition of Chk1 is antiproliferative in human cancer cell lines in vitro and inhibits tumor xenograft growth in vivoKurtis D Davies, Michael J Humphries, Francis X Sullivan, et al.
Pageof 15

Showing results (91-100 of 141) with videos related to

Sort By:
Pageof 15
Journal of the Academy of Nutrition and Dietetics|January 13, 2022
Beverage Characteristics Perceived as Healthy among Hispanic and African-American Parents of Young ChildrenAllison C Sylvetsky, Son T Hoang, Amanda J Visek, et al.
International Immunology|July 1, 1997
Elevated expression of Bcl-2 and Bcl-x by intestinal intraepithelial lymphocytes: resistance to apoptosis by glucocorticoids and irradiationN Van Houten, S F Blake, E J Li, et al.
Nature|April 14, 1988
The nature and origin of interstellar diamondD F Blake, F Freund, K F Krishnan, et al.
Journal of Medicinal Chemistry|August 19, 1994
Novel benzisoxazole derivatives as potent and selective inhibitors of acetylcholinesteraseA Villalobos, J F Blake, C K Biggers, et al.
Physical Review Letters|April 4, 2015
Linear magnetoresistance caused by mobility fluctuations in n-doped Cd(3)As(2)A Narayanan, M D Watson, S F Blake, et al.
Journal of Comparative Psychology (Washington, D.C. : 1983)|May 15, 2013
Personality structure in brown capuchin monkeys (Sapajus apella): comparisons with chimpanzees (Pan troglodytes), orangutans (Pongo spp.), and rhesus macaques (Macaca mulatta)F Blake Morton, Phyllis C Lee, Hannah M Buchanan-Smith, et al.
Bioorganic & Medicinal Chemistry Letters|March 3, 2007
Tetrazole and ester substituted tetrahydoquinoxalines as potent cholesteryl ester transfer protein inhibitorsC Todd Eary, Zachary S Jones, Robert D Groneberg, et al.
Bioorganic & Medicinal Chemistry Letters|December 17, 2008
3-Hydroxyisoquinolines as inhibitors of HCV NS5b RNA-dependent RNA polymeraseRobert T Hendricks, Stacey R Spencer, James F Blake, et al.
Journal of Medicinal Chemistry|July 6, 2000
Structure-based design and synthesis of a potent matrix metalloproteinase-13 inhibitor based on a pyrrolidinone scaffoldR P Robinson, E R Laird, J F Blake, et al.
Oncology Research|September 23, 2011
Single-agent inhibition of Chk1 is antiproliferative in human cancer cell lines in vitro and inhibits tumor xenograft growth in vivoKurtis D Davies, Michael J Humphries, Francis X Sullivan, et al.
Pageof 15