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M Crest

Showing results (21-30 of 37) with videos related to

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The Journal of Biological Chemistry|January 25, 1992
Kaliotoxin, a novel peptidyl inhibitor of neuronal BK-type Ca(2+)-activated K+ channels characterized from Androctonus mauretanicus mauretanicus venomM Crest, G Jacquet, M Gola, et al.
Waste Management (New York, N.Y.)|September 28, 2007
Multiple-scale dynamic leaching of a municipal solid waste incineration ashD Guyonnet, F Bodénan, G Brons-Laot, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 24, 1999
Distribution in rat brain of binding sites of kaliotoxin, a blocker of Kv1.1 and Kv1.3 alpha-subunitsC Mourre, M N Chernova, M F Martin-Eauclaire, et al.
Nephron|January 1, 1982
A study of the cardiotoxicity of uremic middle molecules on embryonic chick heartsP Bernard, M Crest, J B Rinaudo, et al.
International Journal of Peptide and Protein Research|May 1, 1994
Leiurotoxin I, a scorpion toxin specific for Ca(2+)-activated K+ channels. Structure-activity analysis using synthetic analogsJ M Sabatier, V Fremont, K Mabrouk, et al.
FEBS Letters|April 14, 1997
Maurotoxin, a four disulfide bridge toxin from Scorpio maurus venom: purification, structure and action on potassium channelsR Kharrat, P Mansuelle, F Sampieri, et al.
The Journal of Biological Chemistry|December 15, 1993
Synthesis and characterization of kaliotoxin. Is the 26-32 sequence essential for potassium channel recognition?R Romi, M Crest, M Gola, et al.
The Journal of Peptide Research : Official Journal of the American Peptide Society|March 22, 2000
Maurotoxin and the Kv1.1 channel: voltage-dependent binding upon enantiomerization of the scorpion toxin disulfide bridge Cys31-Cys34C Lecomte, R Ben Khalifa, M F Martin-Eauclaire, et al.
European Journal of Biochemistry|February 15, 1997
A potassium-channel toxin from the sea anemone Bunodosoma granulifera, an inhibitor for Kv1 channels. Revision of the amino acid sequence, disulfide-bridge assignment, chemical synthesis, and biological activityJ Cotton, M Crest, F Bouet, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 6, 2001
Selective blocking of voltage-gated K+ channels improves experimental autoimmune encephalomyelitis and inhibits T cell activationC Beeton, J Barbaria, P Giraud, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
The Journal of Biological Chemistry|January 25, 1992
Kaliotoxin, a novel peptidyl inhibitor of neuronal BK-type Ca(2+)-activated K+ channels characterized from Androctonus mauretanicus mauretanicus venomM Crest, G Jacquet, M Gola, et al.
Waste Management (New York, N.Y.)|September 28, 2007
Multiple-scale dynamic leaching of a municipal solid waste incineration ashD Guyonnet, F Bodénan, G Brons-Laot, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 24, 1999
Distribution in rat brain of binding sites of kaliotoxin, a blocker of Kv1.1 and Kv1.3 alpha-subunitsC Mourre, M N Chernova, M F Martin-Eauclaire, et al.
Nephron|January 1, 1982
A study of the cardiotoxicity of uremic middle molecules on embryonic chick heartsP Bernard, M Crest, J B Rinaudo, et al.
International Journal of Peptide and Protein Research|May 1, 1994
Leiurotoxin I, a scorpion toxin specific for Ca(2+)-activated K+ channels. Structure-activity analysis using synthetic analogsJ M Sabatier, V Fremont, K Mabrouk, et al.
FEBS Letters|April 14, 1997
Maurotoxin, a four disulfide bridge toxin from Scorpio maurus venom: purification, structure and action on potassium channelsR Kharrat, P Mansuelle, F Sampieri, et al.
The Journal of Biological Chemistry|December 15, 1993
Synthesis and characterization of kaliotoxin. Is the 26-32 sequence essential for potassium channel recognition?R Romi, M Crest, M Gola, et al.
The Journal of Peptide Research : Official Journal of the American Peptide Society|March 22, 2000
Maurotoxin and the Kv1.1 channel: voltage-dependent binding upon enantiomerization of the scorpion toxin disulfide bridge Cys31-Cys34C Lecomte, R Ben Khalifa, M F Martin-Eauclaire, et al.
European Journal of Biochemistry|February 15, 1997
A potassium-channel toxin from the sea anemone Bunodosoma granulifera, an inhibitor for Kv1 channels. Revision of the amino acid sequence, disulfide-bridge assignment, chemical synthesis, and biological activityJ Cotton, M Crest, F Bouet, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 6, 2001
Selective blocking of voltage-gated K+ channels improves experimental autoimmune encephalomyelitis and inhibits T cell activationC Beeton, J Barbaria, P Giraud, et al.
Pageof 4