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K Brayton

Showing results (1-10 of 8) with videos related to

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Brain Research|October 19, 1979
Computer simulation of a dendrodendritic synaptic circuit for self- and lateral-inhibition in the olfactory bulbG M Shepherd, R K Brayton
Neuroscience|April 1, 1987
Logic operations are properties of computer-simulated interactions between excitable dendritic spinesG M Shepherd, R K Brayton
Experientia|July 15, 1987
Precursors to regulatory peptides: their proteolytic processingP C Andrews, K Brayton, J E Dixon
Nature|May 3, 1987
An amino-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2A G DiLella, J Marvit, K Brayton, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1985
Signal enhancement in distal cortical dendrites by means of interactions between active dendritic spinesG M Shepherd, R K Brayton, J P Miller, et al.
Nucleic Acids Research|July 24, 1987
GT to AT transition at a splice donor site causes skipping of the preceding exon in phenylketonuriaJ Marvit, A G DiLella, K Brayton, et al.
Biochemistry|April 19, 1988
Phenylalanine hydroxylase deficiency caused by a single base substitution in an exon of the human phenylalanine hydroxylase geneU Lichter-Konecki, D S Konecki, A G DiLella, et al.
American Heart Journal|May 14, 2020
Are cost advantages from a modern Indian hospital transferable to the United States?F Erhun, R S Kaplan, V G Narayanan, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Brain Research|October 19, 1979
Computer simulation of a dendrodendritic synaptic circuit for self- and lateral-inhibition in the olfactory bulbG M Shepherd, R K Brayton
Neuroscience|April 1, 1987
Logic operations are properties of computer-simulated interactions between excitable dendritic spinesG M Shepherd, R K Brayton
Experientia|July 15, 1987
Precursors to regulatory peptides: their proteolytic processingP C Andrews, K Brayton, J E Dixon
Nature|May 3, 1987
An amino-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2A G DiLella, J Marvit, K Brayton, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1985
Signal enhancement in distal cortical dendrites by means of interactions between active dendritic spinesG M Shepherd, R K Brayton, J P Miller, et al.
Nucleic Acids Research|July 24, 1987
GT to AT transition at a splice donor site causes skipping of the preceding exon in phenylketonuriaJ Marvit, A G DiLella, K Brayton, et al.
Biochemistry|April 19, 1988
Phenylalanine hydroxylase deficiency caused by a single base substitution in an exon of the human phenylalanine hydroxylase geneU Lichter-Konecki, D S Konecki, A G DiLella, et al.
American Heart Journal|May 14, 2020
Are cost advantages from a modern Indian hospital transferable to the United States?F Erhun, R S Kaplan, V G Narayanan, et al.
Pageof 1