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J C Culberson

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Evolutionary Computation|February 18, 1999
On the futility of blind search: an algorithmic view of "no free lunch"J C Culberson
Journal of Chemical Information and Computer Sciences|June 21, 2001
Comparison of knowledge-based and distance geometry approaches for generation of molecular conformationsB P Feuston, M D Miller, J C Culberson, et al.
Journal of Neurophysiology|April 18, 1998
Dorsal horn spatial representation of simple cutaneous stimuliP B Brown, R Millecchia, J J Lawson, et al.
Nucleic Acids Research|April 25, 1994
Effect of template secondary structure on the inhibition of HIV-1 reverse transcriptase by a pyridinone non-nucleoside inhibitorD B Olsen, S S Carroll, J C Culberson, et al.
Organic Letters|March 27, 2001
3,8-Diazabicyclo[3.2.1]octan-2-one peptide mimetics: synthesis of a conformationally restricted inhibitor of farnesyltransferaseC J Dinsmore, J M Bergman, M J Bogusky, et al.
The Journal of Peptide Research : Official Journal of the American Peptide Society|August 17, 1999
Conformation of a novel tetrapeptide inhibitor NH2-D-Trp-D-Met-Phe(pCl)-Gla-NH2 bound to farnesyl-protein transferaseM J Bogusky, J C Culberson, S M Pitzenberger, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 1, 1991
Somatotopic organization of single primary afferent axon projections to cat spinal cord dorsal hornP B Brown, W E Gladfelter, J C Culberson, et al.
Journal of Medicinal Chemistry|May 15, 1992
Carboxylic acid replacement structure-activity relationships in suosan type sweeteners. A sweet taste antagonist. 1G W Muller, J C Culberson, G Roy, et al.
Protein Science : a Publication of the Protein Society|April 1, 1995
NMR studies of novel inhibitors bound to farnesyl-protein transferaseK S Koblan, J C Culberson, S J Desolms, et al.
Biochemistry|March 1, 1994
Human immunodeficiency virus type 1 protease inhibitors: evaluation of resistance engendered by amino acid substitutions in the enzyme's substrate binding siteV V Sardana, A J Schlabach, P Graham, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Evolutionary Computation|February 18, 1999
On the futility of blind search: an algorithmic view of "no free lunch"J C Culberson
Journal of Chemical Information and Computer Sciences|June 21, 2001
Comparison of knowledge-based and distance geometry approaches for generation of molecular conformationsB P Feuston, M D Miller, J C Culberson, et al.
Journal of Neurophysiology|April 18, 1998
Dorsal horn spatial representation of simple cutaneous stimuliP B Brown, R Millecchia, J J Lawson, et al.
Nucleic Acids Research|April 25, 1994
Effect of template secondary structure on the inhibition of HIV-1 reverse transcriptase by a pyridinone non-nucleoside inhibitorD B Olsen, S S Carroll, J C Culberson, et al.
Organic Letters|March 27, 2001
3,8-Diazabicyclo[3.2.1]octan-2-one peptide mimetics: synthesis of a conformationally restricted inhibitor of farnesyltransferaseC J Dinsmore, J M Bergman, M J Bogusky, et al.
The Journal of Peptide Research : Official Journal of the American Peptide Society|August 17, 1999
Conformation of a novel tetrapeptide inhibitor NH2-D-Trp-D-Met-Phe(pCl)-Gla-NH2 bound to farnesyl-protein transferaseM J Bogusky, J C Culberson, S M Pitzenberger, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 1, 1991
Somatotopic organization of single primary afferent axon projections to cat spinal cord dorsal hornP B Brown, W E Gladfelter, J C Culberson, et al.
Journal of Medicinal Chemistry|May 15, 1992
Carboxylic acid replacement structure-activity relationships in suosan type sweeteners. A sweet taste antagonist. 1G W Muller, J C Culberson, G Roy, et al.
Protein Science : a Publication of the Protein Society|April 1, 1995
NMR studies of novel inhibitors bound to farnesyl-protein transferaseK S Koblan, J C Culberson, S J Desolms, et al.
Biochemistry|March 1, 1994
Human immunodeficiency virus type 1 protease inhibitors: evaluation of resistance engendered by amino acid substitutions in the enzyme's substrate binding siteV V Sardana, A J Schlabach, P Graham, et al.
Pageof 2