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B Wermuth

Showing results (61-70 of 87) with videos related to

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Human Genetics|February 1, 1995
Ornithine transcarbamylase deficiency: new sites with increased probability of mutationE O Oppliger Leibundgut, S Liechti-Gallati, J P Colombo, et al.
Human Mutation|January 1, 1996
Ornithine transcarbamylase deficiency: characterization of gene mutations and polymorphismsE O Oppliger Leibundgut, B Wermuth, J P Colombo, et al.
Enzyme|January 1, 1991
Direct and indirect mutation analyses in patients with ornithine transcarbamylase deficiencyS Liechti-Gallati, C Dionisi, C Bachmann, et al.
FEBS Letters|February 15, 1988
Genotyping of human class I alcohol dehydrogenase. Analysis of enzymatically amplified DNA with allele-specific oligonucleotidesK Gennari, B Wermuth, D Muellener, et al.
Archives of Biochemistry and Biophysics|August 1, 1974
8-(6-Aminohexyl)-amino-adenine nucleotide derivatives for affinity chromatographyC Y Lee, D A Lappi, B Wermuth, et al.
The Journal of Biological Chemistry|November 5, 1988
Human carbonyl reductase. Nucleotide sequence analysis of a cDNA and amino acid sequence of the encoded proteinB Wermuth, K M Bohren, G Heinemann, et al.
Schweizerische Medizinische Wochenschrift|December 14, 1991
[Determination of alcohol dehydrogenase genotype: no correlation between isoenzyme pattern and liver cirrhosis]B Wermuth, E Ernst, J P von Wartburg, et al.
Blood|October 1, 1993
Fibrinogen Bern I: substitution gamma 337 Asn-->Lys is responsible for defective fibrin monomer polymerizationC Steinmann, P Reber, M Jungo, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 30, 2005
Misleading diagnosis of partial N-acetylglutamate synthase deficiency based on enzyme measurement corrected by mutation analysisM Heckmann, B Wermuth, J Häberle, et al.
Human Mutation|March 26, 2003
Gene structure of human carbamylphosphate synthetase 1 and novel mutations in patients with neonatal onsetJ Häberle, E Schmidt, S Pauli, et al.
Pageof 9

Showing results (61-70 of 87) with videos related to

Sort By:
Pageof 9
Human Genetics|February 1, 1995
Ornithine transcarbamylase deficiency: new sites with increased probability of mutationE O Oppliger Leibundgut, S Liechti-Gallati, J P Colombo, et al.
Human Mutation|January 1, 1996
Ornithine transcarbamylase deficiency: characterization of gene mutations and polymorphismsE O Oppliger Leibundgut, B Wermuth, J P Colombo, et al.
Enzyme|January 1, 1991
Direct and indirect mutation analyses in patients with ornithine transcarbamylase deficiencyS Liechti-Gallati, C Dionisi, C Bachmann, et al.
FEBS Letters|February 15, 1988
Genotyping of human class I alcohol dehydrogenase. Analysis of enzymatically amplified DNA with allele-specific oligonucleotidesK Gennari, B Wermuth, D Muellener, et al.
Archives of Biochemistry and Biophysics|August 1, 1974
8-(6-Aminohexyl)-amino-adenine nucleotide derivatives for affinity chromatographyC Y Lee, D A Lappi, B Wermuth, et al.
The Journal of Biological Chemistry|November 5, 1988
Human carbonyl reductase. Nucleotide sequence analysis of a cDNA and amino acid sequence of the encoded proteinB Wermuth, K M Bohren, G Heinemann, et al.
Schweizerische Medizinische Wochenschrift|December 14, 1991
[Determination of alcohol dehydrogenase genotype: no correlation between isoenzyme pattern and liver cirrhosis]B Wermuth, E Ernst, J P von Wartburg, et al.
Blood|October 1, 1993
Fibrinogen Bern I: substitution gamma 337 Asn-->Lys is responsible for defective fibrin monomer polymerizationC Steinmann, P Reber, M Jungo, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 30, 2005
Misleading diagnosis of partial N-acetylglutamate synthase deficiency based on enzyme measurement corrected by mutation analysisM Heckmann, B Wermuth, J Häberle, et al.
Human Mutation|March 26, 2003
Gene structure of human carbamylphosphate synthetase 1 and novel mutations in patients with neonatal onsetJ Häberle, E Schmidt, S Pauli, et al.
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