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B Auer

Showing results (51-60 of 70) with videos related to

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Journal of Chromatography|June 24, 1988
Clozapine plasma levels determined by high-performance liquid chromatography with ultraviolet detectionC Haring, C Humpel, B Auer, et al.
Molecular & General Genetics : MGG|January 1, 1982
A sensitive radioimmuno assay for thymine dimersH Klocker, B Auer, H J Burtscher, et al.
Molecular and Cellular Biochemistry|September 1, 1994
Transcriptional regulation and autoregulation of the human gene for ADP-ribosyltransferaseS L Oei, H Herzog, M Hirsch-Kauffmann, et al.
European Journal of Biochemistry|June 1, 1987
The Fritz-Lipmann lecture. DNA repair in human cells. Biochemistry of the hereditary diseases Fanconi's anaemia and Cockayne syndromeM Schweiger, B Auer, H J Burtscher, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1989
Human nuclear NAD+ ADP-ribosyltransferase: localization of the gene on chromosome 1q41-q42 and expression of an active human enzyme in Escherichia coliH Herzog, B U Zabel, R Schneider, et al.
Synapse (New York, N.Y.)|January 1, 1990
Effects of haloperidol and clozapine on preprotachykinin-A messenger RNA, tachykinin tissue levels, release and neurokinin-1 receptors in the striato-nigral systemC Humpel, G A Knaus, B Auer, et al.
Journal of Perinatal Medicine|January 1, 1995
Pregnancy-related changes of carnitine and acylcarnitine concentrations of plasma and erythrocytesM Schoderbeck, B Auer, E Legenstein, et al.
Biochimie|January 1, 1995
Regulation of the human poly(ADP-ribosyl) transferase promoter via alternative DNA racket structuresM Schweiger, S L Oei, H Herzog, et al.
Genes & Development|March 1, 1995
Mice lacking ADPRT and poly(ADP-ribosyl)ation develop normally but are susceptible to skin diseaseZ Q Wang, B Auer, L Stingl, et al.
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.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Journal of Chromatography|June 24, 1988
Clozapine plasma levels determined by high-performance liquid chromatography with ultraviolet detectionC Haring, C Humpel, B Auer, et al.
Molecular & General Genetics : MGG|January 1, 1982
A sensitive radioimmuno assay for thymine dimersH Klocker, B Auer, H J Burtscher, et al.
Molecular and Cellular Biochemistry|September 1, 1994
Transcriptional regulation and autoregulation of the human gene for ADP-ribosyltransferaseS L Oei, H Herzog, M Hirsch-Kauffmann, et al.
European Journal of Biochemistry|June 1, 1987
The Fritz-Lipmann lecture. DNA repair in human cells. Biochemistry of the hereditary diseases Fanconi's anaemia and Cockayne syndromeM Schweiger, B Auer, H J Burtscher, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1989
Human nuclear NAD+ ADP-ribosyltransferase: localization of the gene on chromosome 1q41-q42 and expression of an active human enzyme in Escherichia coliH Herzog, B U Zabel, R Schneider, et al.
Synapse (New York, N.Y.)|January 1, 1990
Effects of haloperidol and clozapine on preprotachykinin-A messenger RNA, tachykinin tissue levels, release and neurokinin-1 receptors in the striato-nigral systemC Humpel, G A Knaus, B Auer, et al.
Journal of Perinatal Medicine|January 1, 1995
Pregnancy-related changes of carnitine and acylcarnitine concentrations of plasma and erythrocytesM Schoderbeck, B Auer, E Legenstein, et al.
Biochimie|January 1, 1995
Regulation of the human poly(ADP-ribosyl) transferase promoter via alternative DNA racket structuresM Schweiger, S L Oei, H Herzog, et al.
Genes & Development|March 1, 1995
Mice lacking ADPRT and poly(ADP-ribosyl)ation develop normally but are susceptible to skin diseaseZ Q Wang, B Auer, L Stingl, et al.
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.
Pageof 7