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F Schuber

Showing results (71-80 of 90) with videos related to

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Chemical Immunology|June 14, 2000
CD38 in T- and B-cell functionsP Deterre, V Berthelier, B Bauvois, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 1995
Targeted gene transfer into hepatoma cells with lipopolyamine-condensed DNA particles presenting galactose ligands: a stage toward artificial virusesJ S Remy, A Kichler, V Mordvinov, et al.
Biochemical Pharmacology|May 15, 1988
Potent inhibition of cholesterol biosynthesis in 3T3 fibroblasts by N-[(1,5,9)-trimethyldecyl]-4 alpha,10-dimethyl-8-aza-trans-decal-3 beta-ol, a new 2,3-oxidosqualene cyclase inhibitorN Gerst, A Duriatti, F Schuber, et al.
The Biochemical Journal|May 23, 1998
Human CD38 is an authentic NAD(P)+ glycohydrolaseV Berthelier, J M Tixier, H Muller-Steffner, et al.
British Journal of Cancer|April 7, 2005
Induction of effective and antigen-specific antitumour immunity by a liposomal ErbB2/HER2 peptide-based vaccination constructA Roth, F Rohrbach, R Weth, et al.
The Journal of Biological Chemistry|May 15, 1992
Slow-binding inhibition of NAD+ glycohydrolase by arabino analogues of beta-NADH M Muller-Steffner, O Malver, L Hosie, et al.
European Journal of Immunology|January 1, 1991
Parameters affecting the immunogenicity of a liposome-associated synthetic hexapeptide antigenB Frisch, S Muller, J P Briand, et al.
Molecular Immunology|April 1, 1993
Induction of immune response against a short synthetic peptide antigen coupled to small neutral liposomes containing monophosphoryl lipid AM Friede, S Muller, J P Briand, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1976
Alpha-methyl ornithine, a potent competitive inhibitor of ornithine decarboxylase, blocks proliferation of rat hepatoma cells in cultureP S Mamont, P Böhlen, P P McCann, et al.
Pharmaceutical Research|October 12, 2000
Lectin-mediated drug targeting: selection of valency, sugar type (Gal/Lac), and spacer length for cluster glycosides as parameters to distinguish ligand binding to C-type asialoglycoprotein receptors and galectinsS André, B Frisch, H Kaltner, et al.
Pageof 9

Showing results (71-80 of 90) with videos related to

Sort By:
Pageof 9
Chemical Immunology|June 14, 2000
CD38 in T- and B-cell functionsP Deterre, V Berthelier, B Bauvois, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 1995
Targeted gene transfer into hepatoma cells with lipopolyamine-condensed DNA particles presenting galactose ligands: a stage toward artificial virusesJ S Remy, A Kichler, V Mordvinov, et al.
Biochemical Pharmacology|May 15, 1988
Potent inhibition of cholesterol biosynthesis in 3T3 fibroblasts by N-[(1,5,9)-trimethyldecyl]-4 alpha,10-dimethyl-8-aza-trans-decal-3 beta-ol, a new 2,3-oxidosqualene cyclase inhibitorN Gerst, A Duriatti, F Schuber, et al.
The Biochemical Journal|May 23, 1998
Human CD38 is an authentic NAD(P)+ glycohydrolaseV Berthelier, J M Tixier, H Muller-Steffner, et al.
British Journal of Cancer|April 7, 2005
Induction of effective and antigen-specific antitumour immunity by a liposomal ErbB2/HER2 peptide-based vaccination constructA Roth, F Rohrbach, R Weth, et al.
The Journal of Biological Chemistry|May 15, 1992
Slow-binding inhibition of NAD+ glycohydrolase by arabino analogues of beta-NADH M Muller-Steffner, O Malver, L Hosie, et al.
European Journal of Immunology|January 1, 1991
Parameters affecting the immunogenicity of a liposome-associated synthetic hexapeptide antigenB Frisch, S Muller, J P Briand, et al.
Molecular Immunology|April 1, 1993
Induction of immune response against a short synthetic peptide antigen coupled to small neutral liposomes containing monophosphoryl lipid AM Friede, S Muller, J P Briand, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1976
Alpha-methyl ornithine, a potent competitive inhibitor of ornithine decarboxylase, blocks proliferation of rat hepatoma cells in cultureP S Mamont, P Böhlen, P P McCann, et al.
Pharmaceutical Research|October 12, 2000
Lectin-mediated drug targeting: selection of valency, sugar type (Gal/Lac), and spacer length for cluster glycosides as parameters to distinguish ligand binding to C-type asialoglycoprotein receptors and galectinsS André, B Frisch, H Kaltner, et al.
Pageof 9