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M Meldal

Showing results (11-20 of 101) with videos related to

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European Journal of Biochemistry|May 15, 1992
Substrate preferences of glutamic-acid-specific endopeptidases assessed by synthetic peptide substrates based on intramolecular fluorescence quenchingK Breddam, M Meldal
Acta Chemica Scandinavica. Series B: Organic Chemistry and Biochemistry|January 1, 1983
Synthesis of disaccharides related to the O-specific polysaccharide of Salmonella typhimuriumK Bock, M Meldal
Glycoconjugate Journal|April 1, 1994
A general approach to the synthesis of O- and N-linked glycopeptidesM Meldal, K Bock
Journal of Combinatorial Chemistry|January 10, 2001
Synthesis of aldehyde building blocks protected as acid labile N-Boc N,O-acetals: toward combinatorial solid phase synthesis of novel peptide isosteresT Groth, M Meldal
Carbohydrate Letters|July 27, 2001
Synthesis of a non-natural T-antigen containing glycosphingolipidL Cipolla, M Meldal
Acta Chemica Scandinavica. Series B: Organic Chemistry and Biochemistry|April 1, 1986
Synthesis of a proposed antigenic hexapeptide from Escherichia coli K88 protein fimbriaeM Meldal, J W Kindtler
Organic & Biomolecular Chemistry|March 1, 2016
C-Terminally modified peptides via cleavage of the HMBA linker by O-, N- or S-nucleophilesJ Hansen, F Diness, M Meldal
Biochemistry|July 7, 1992
Extensive comparison of the substrate preferences of two subtilisins as determined with peptide substrates which are based on the principle of intramolecular quenchingH Grøn, M Meldal, K Breddam
Journal of Combinatorial Chemistry|September 11, 2001
Diffusion of reagents in macrobeadsT Groth, M Grøtli, M Meldal
Carbohydrate Research|December 16, 1991
Controlled reduction of acarbose: conformational analysis of acarbose and the resulting saturated productsK Bock, M Meldal, S Refn
Pageof 11

Showing results (11-20 of 101) with videos related to

Sort By:
Pageof 11
European Journal of Biochemistry|May 15, 1992
Substrate preferences of glutamic-acid-specific endopeptidases assessed by synthetic peptide substrates based on intramolecular fluorescence quenchingK Breddam, M Meldal
Acta Chemica Scandinavica. Series B: Organic Chemistry and Biochemistry|January 1, 1983
Synthesis of disaccharides related to the O-specific polysaccharide of Salmonella typhimuriumK Bock, M Meldal
Glycoconjugate Journal|April 1, 1994
A general approach to the synthesis of O- and N-linked glycopeptidesM Meldal, K Bock
Journal of Combinatorial Chemistry|January 10, 2001
Synthesis of aldehyde building blocks protected as acid labile N-Boc N,O-acetals: toward combinatorial solid phase synthesis of novel peptide isosteresT Groth, M Meldal
Carbohydrate Letters|July 27, 2001
Synthesis of a non-natural T-antigen containing glycosphingolipidL Cipolla, M Meldal
Acta Chemica Scandinavica. Series B: Organic Chemistry and Biochemistry|April 1, 1986
Synthesis of a proposed antigenic hexapeptide from Escherichia coli K88 protein fimbriaeM Meldal, J W Kindtler
Organic & Biomolecular Chemistry|March 1, 2016
C-Terminally modified peptides via cleavage of the HMBA linker by O-, N- or S-nucleophilesJ Hansen, F Diness, M Meldal
Biochemistry|July 7, 1992
Extensive comparison of the substrate preferences of two subtilisins as determined with peptide substrates which are based on the principle of intramolecular quenchingH Grøn, M Meldal, K Breddam
Journal of Combinatorial Chemistry|September 11, 2001
Diffusion of reagents in macrobeadsT Groth, M Grøtli, M Meldal
Carbohydrate Research|December 16, 1991
Controlled reduction of acarbose: conformational analysis of acarbose and the resulting saturated productsK Bock, M Meldal, S Refn
Pageof 11