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A Fliess

Showing results (11-20 of 17) with videos related to

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Nucleic Acids Research|November 25, 1986
Site directed mutagenesis experiments suggest that Glu 111, Glu 144 and Arg 145 are essential for endonucleolytic activity of EcoRIH Wolfes, J Alves, A Fliess, et al.
Gene|April 30, 1990
Probing the function of individual amino acid residues in the DNA binding site of the EcoRI restriction endonuclease by analysing the toxicity of genetically engineered mutantsT Oelgeschläger, R Geiger, T Rüter, et al.
Biochemistry|March 21, 1989
Changing the hydrogen-bonding potential in the DNA binding site of EcoRI by site-directed mutagenesis drastically reduces the enzymatic activity, not, however, the preference of this restriction endonuclease for cleavage within the site-GAATTC-J Alves, T Rüter, R Geiger, et al.
Biochimica Et Biophysica Acta|October 23, 1990
Genetic engineering, isolation and characterization of a truncated Escherichia coli elongation factor Tu comprising domains 2 and 3U Pieper, H J Ehbrecht, A Fliess, et al.
Nucleic Acids Research|April 25, 1986
Role of thymidine residues in DNA recognition by the EcoRI and EcoRV restriction endonucleasesA Fliess, H Wolfes, A Rosenthal, et al.
Bioscience, Biotechnology, and Biochemistry|December 4, 1998
Computational analysis of the amino acid residue sequences of amaranth and some other proteinsS Gorinstein, M Zemser, A Fliess, et al.
Biochemistry|March 21, 1989
Genetic engineering of EcoRI mutants with altered amino acid residues in the DNA binding site: physicochemical investigations give evidence for an altered monomer/dimer equilibrium for the Gln144Lys145 and Gln144Lys145Lys200 mutantsR Geiger, T Rüter, J Alves, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Nucleic Acids Research|November 25, 1986
Site directed mutagenesis experiments suggest that Glu 111, Glu 144 and Arg 145 are essential for endonucleolytic activity of EcoRIH Wolfes, J Alves, A Fliess, et al.
Gene|April 30, 1990
Probing the function of individual amino acid residues in the DNA binding site of the EcoRI restriction endonuclease by analysing the toxicity of genetically engineered mutantsT Oelgeschläger, R Geiger, T Rüter, et al.
Biochemistry|March 21, 1989
Changing the hydrogen-bonding potential in the DNA binding site of EcoRI by site-directed mutagenesis drastically reduces the enzymatic activity, not, however, the preference of this restriction endonuclease for cleavage within the site-GAATTC-J Alves, T Rüter, R Geiger, et al.
Biochimica Et Biophysica Acta|October 23, 1990
Genetic engineering, isolation and characterization of a truncated Escherichia coli elongation factor Tu comprising domains 2 and 3U Pieper, H J Ehbrecht, A Fliess, et al.
Nucleic Acids Research|April 25, 1986
Role of thymidine residues in DNA recognition by the EcoRI and EcoRV restriction endonucleasesA Fliess, H Wolfes, A Rosenthal, et al.
Bioscience, Biotechnology, and Biochemistry|December 4, 1998
Computational analysis of the amino acid residue sequences of amaranth and some other proteinsS Gorinstein, M Zemser, A Fliess, et al.
Biochemistry|March 21, 1989
Genetic engineering of EcoRI mutants with altered amino acid residues in the DNA binding site: physicochemical investigations give evidence for an altered monomer/dimer equilibrium for the Gln144Lys145 and Gln144Lys145Lys200 mutantsR Geiger, T Rüter, J Alves, et al.
Pageof 2