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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 EcoRI
H 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 mutants
T 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 3
U 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 endonucleases
A 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 proteins
S 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 mutants
R Geiger, T Rüter, J Alves, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 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 EcoRI
H 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 mutants
T 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 3
U 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 endonucleases
A 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 proteins
S 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 mutants
R Geiger, T Rüter, J Alves, et al.
Page
of 2