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M Hirsch-Kauffmann

Showing results (51-60 of 63) with videos related to

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Human Mutation|January 1, 1997
Human APRT deficiency: indication for multiple origins of the most common Caucasian mutation and detection of a novel type of mutation involving intrastrand-templated repairC Menardi, R Schneider, F Neuschmid-Kaspar, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1975
In vivo and in vitro phosphorylation of DNA-dependent RNA polymerase of Escherichia coli by bacteriophage-T7-induced protein kinaseW Zillig, H Fujiki, W Blum, et al.
European Journal of Biochemistry|April 1, 1975
Transcriptional units for ribosomal proteins of Escherichia coliM Hirsch-Kauffmann, M Schweiger, P Herrlich, et al.
Protoplasma|January 1, 1975
Protein kinase of AcetabulariaH S Pai, P Dehm, M Schweiger, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|October 1, 1974
Proceedings: Transcriptional units for ribosomal proteinsM Hirsch-Kauffmann, M Schweiger, P Herrlich, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Werner syndrome: characterization of mutations in the WRN gene in an affected familyC Meisslitzer, W Ruppitsch, H Weirich-Schwaiger, et al.
European Journal of Cell Biology|October 1, 1987
Isolation of a cDNA clone for human NAD+: protein ADP-ribosyltransferaseR Schneider, B Auer, C Kühne, et al.
FEBS Letters|March 15, 2001
Characterization of recombinant human nicotinamide mononucleotide adenylyl transferase (NMNAT), a nuclear enzyme essential for NAD synthesisM Schweiger, K Hennig, F Lerner, et al.
Mechanisms of Ageing and Development|July 5, 1996
Werner syndrome: studies in an affected family reveal a cellular phenotype of unaffected siblingsH G Weirich, H Weirich-Schwaiger, H Kofler, et al.
European Journal of Biochemistry|November 1, 1975
The sex-factor-dependent exclusion of coli virus T7H Ponta, C L Pon, P Herrlich, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Human Mutation|January 1, 1997
Human APRT deficiency: indication for multiple origins of the most common Caucasian mutation and detection of a novel type of mutation involving intrastrand-templated repairC Menardi, R Schneider, F Neuschmid-Kaspar, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1975
In vivo and in vitro phosphorylation of DNA-dependent RNA polymerase of Escherichia coli by bacteriophage-T7-induced protein kinaseW Zillig, H Fujiki, W Blum, et al.
European Journal of Biochemistry|April 1, 1975
Transcriptional units for ribosomal proteins of Escherichia coliM Hirsch-Kauffmann, M Schweiger, P Herrlich, et al.
Protoplasma|January 1, 1975
Protein kinase of AcetabulariaH S Pai, P Dehm, M Schweiger, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|October 1, 1974
Proceedings: Transcriptional units for ribosomal proteinsM Hirsch-Kauffmann, M Schweiger, P Herrlich, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Werner syndrome: characterization of mutations in the WRN gene in an affected familyC Meisslitzer, W Ruppitsch, H Weirich-Schwaiger, et al.
European Journal of Cell Biology|October 1, 1987
Isolation of a cDNA clone for human NAD+: protein ADP-ribosyltransferaseR Schneider, B Auer, C Kühne, et al.
FEBS Letters|March 15, 2001
Characterization of recombinant human nicotinamide mononucleotide adenylyl transferase (NMNAT), a nuclear enzyme essential for NAD synthesisM Schweiger, K Hennig, F Lerner, et al.
Mechanisms of Ageing and Development|July 5, 1996
Werner syndrome: studies in an affected family reveal a cellular phenotype of unaffected siblingsH G Weirich, H Weirich-Schwaiger, H Kofler, et al.
European Journal of Biochemistry|November 1, 1975
The sex-factor-dependent exclusion of coli virus T7H Ponta, C L Pon, P Herrlich, et al.
Pageof 7