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M Lancelin

Showing results (21-30 of 33) with videos related to

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Biochemistry|July 16, 1991
Tertiary structure of conotoxin GIIIA in aqueous solutionJ M Lancelin, D Kohda, S Tate, et al.
The Journal of Biological Chemistry|October 20, 1995
Kalicludines and kaliseptine. Two different classes of sea anemone toxins for voltage sensitive K+ channelsH Schweitz, T Bruhn, E Guillemare, et al.
FEBS Letters|May 2, 1994
NMR structures of ferredoxin chloroplastic transit peptide from Chlamydomonas reinhardtii promoted by trifluoroethanol in aqueous solutionJ M Lancelin, I Bally, G J Arlaud, et al.
Biochemistry|December 22, 1992
Structure-activity relationships of mu-conotoxin GIIIA: structure determination of active and inactive sodium channel blocker peptides by NMR and simulated annealing calculationsK Wakamatsu, D Kohda, H Hatanaka, et al.
Biochimica Et Biophysica Acta|February 12, 2000
Primary structure determinants of the pH- and temperature-dependent aggregation of thioredoxinS D Lemaire, J M Richardson, A Goyer, et al.
Canadian Journal of Microbiology|January 22, 2004
Screening of nonpolyenic antifungal metabolites produced by clinical isolates of actinomycetesS Lemriss, F Laurent, A Couble, et al.
European Journal of Biochemistry|August 6, 1998
The single mutation Trp35-->Ala in the 35-40 redox site of Chlamydomonas reinhardtii thioredoxin h affects its biochemical activity and the pH dependence of C36-C39 1H-13C NMRI Krimm, S Lemaire, E Ruelland, et al.
The Journal of Biological Chemistry|September 15, 1991
Active site of mu-conotoxin GIIIA, a peptide blocker of muscle sodium channelsK Sato, Y Ishida, K Wakamatsu, et al.
Plant Molecular Biology|June 1, 1995
Chlamydomonas reinhardtii thioredoxins: structure of the genes coding for the chloroplastic m and cytosolic h isoforms; expression in Escherichia coli of the recombinant proteins, purification and biochemical propertiesM Stein, J P Jacquot, E Jeannette, et al.
Biochimica Et Biophysica Acta|May 13, 1993
A comparative study of the solution structures of tachyplesin I and a novel anti-HIV synthetic peptide, T22 ([Tyr5,12, Lys7]-polyphemusin II), determined by nuclear magnetic resonanceH Tamamura, M Kuroda, M Masuda, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Biochemistry|July 16, 1991
Tertiary structure of conotoxin GIIIA in aqueous solutionJ M Lancelin, D Kohda, S Tate, et al.
The Journal of Biological Chemistry|October 20, 1995
Kalicludines and kaliseptine. Two different classes of sea anemone toxins for voltage sensitive K+ channelsH Schweitz, T Bruhn, E Guillemare, et al.
FEBS Letters|May 2, 1994
NMR structures of ferredoxin chloroplastic transit peptide from Chlamydomonas reinhardtii promoted by trifluoroethanol in aqueous solutionJ M Lancelin, I Bally, G J Arlaud, et al.
Biochemistry|December 22, 1992
Structure-activity relationships of mu-conotoxin GIIIA: structure determination of active and inactive sodium channel blocker peptides by NMR and simulated annealing calculationsK Wakamatsu, D Kohda, H Hatanaka, et al.
Biochimica Et Biophysica Acta|February 12, 2000
Primary structure determinants of the pH- and temperature-dependent aggregation of thioredoxinS D Lemaire, J M Richardson, A Goyer, et al.
Canadian Journal of Microbiology|January 22, 2004
Screening of nonpolyenic antifungal metabolites produced by clinical isolates of actinomycetesS Lemriss, F Laurent, A Couble, et al.
European Journal of Biochemistry|August 6, 1998
The single mutation Trp35-->Ala in the 35-40 redox site of Chlamydomonas reinhardtii thioredoxin h affects its biochemical activity and the pH dependence of C36-C39 1H-13C NMRI Krimm, S Lemaire, E Ruelland, et al.
The Journal of Biological Chemistry|September 15, 1991
Active site of mu-conotoxin GIIIA, a peptide blocker of muscle sodium channelsK Sato, Y Ishida, K Wakamatsu, et al.
Plant Molecular Biology|June 1, 1995
Chlamydomonas reinhardtii thioredoxins: structure of the genes coding for the chloroplastic m and cytosolic h isoforms; expression in Escherichia coli of the recombinant proteins, purification and biochemical propertiesM Stein, J P Jacquot, E Jeannette, et al.
Biochimica Et Biophysica Acta|May 13, 1993
A comparative study of the solution structures of tachyplesin I and a novel anti-HIV synthetic peptide, T22 ([Tyr5,12, Lys7]-polyphemusin II), determined by nuclear magnetic resonanceH Tamamura, M Kuroda, M Masuda, et al.
Pageof 4