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B Wermuth

Showing results (71-80 of 87) with videos related to

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Journal of Molecular Biology|December 16, 1994
Expression, crystallization and preliminary crystallographic analysis of human carbonyl reductaseK M Bohren, B Wermuth, D Harrison, et al.
European Journal of Pediatrics|June 5, 2001
Genetic analysis of carbamoylphosphate synthetase I and ornithine transcarbamylase deficiency using fibroblastsB Rapp, J Häberle, M Linnebank, et al.
Pediatric Research|December 16, 1998
Effect of increasing dietary threonine intakes on amino acid metabolism of the central nervous system and peripheral tissues in growing ratsG Boehm, H Cervantes, G Georgi, et al.
European Journal of Pediatrics|May 1, 1994
Medium-chain acyl-CoA dehydrogenase deficiency does not correlate with apparent life-threatening events and the sudden infant death syndrome: results from phenylpropionate loading tests and DNA analysisJ M Penzien, G Molz, U N Wiesmann, et al.
Journal of Inherited Metabolic Disease|August 1, 1997
Mutation of ornithine transcarbamylase (H136R) in a girl with severe intermittent orotic aciduria but normal enzyme activityS Vella, F Steiner, V Schlumbom, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Partial N-acetylglutamate synthetase deficiency: a new case with uncontrollable movement disordersA B Burlina, C Bachmann, B Wermuth, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 8, 2000
Partial N-acetyl-glutamate synthetase deficiency masquerading as a valproic acid-induced Reye-like syndromeP P Forget, M van Oosterhout, J A Bakker, et al.
Biochemical and Biophysical Research Communications|March 29, 1991
Human carbonyl and aldose reductases: new catalytic functions in tetrahydrobiopterin biosynthesisY S Park, C W Heizmann, B Wermuth, et al.
Blood|September 15, 1994
A new substitution, gamma 358 Ser-->Cys, in fibrinogen Milano VII causes defective fibrin polymerizationC Steinmann, C Bögli, M Jungo, et al.
Enzyme & Protein|January 1, 1996
Combined 3-methylglutaconic and 3-hydroxy-3-methylglutaric aciduria with endocardial fibroelastosis and dilatative cardiomyopathy in male and female siblings with partial deficiency of complex II/III in fibroblastsS Ruesch, S Krähenbühl, S Kleinle, et al.
Pageof 9

Showing results (71-80 of 87) with videos related to

Sort By:
Pageof 9
Journal of Molecular Biology|December 16, 1994
Expression, crystallization and preliminary crystallographic analysis of human carbonyl reductaseK M Bohren, B Wermuth, D Harrison, et al.
European Journal of Pediatrics|June 5, 2001
Genetic analysis of carbamoylphosphate synthetase I and ornithine transcarbamylase deficiency using fibroblastsB Rapp, J Häberle, M Linnebank, et al.
Pediatric Research|December 16, 1998
Effect of increasing dietary threonine intakes on amino acid metabolism of the central nervous system and peripheral tissues in growing ratsG Boehm, H Cervantes, G Georgi, et al.
European Journal of Pediatrics|May 1, 1994
Medium-chain acyl-CoA dehydrogenase deficiency does not correlate with apparent life-threatening events and the sudden infant death syndrome: results from phenylpropionate loading tests and DNA analysisJ M Penzien, G Molz, U N Wiesmann, et al.
Journal of Inherited Metabolic Disease|August 1, 1997
Mutation of ornithine transcarbamylase (H136R) in a girl with severe intermittent orotic aciduria but normal enzyme activityS Vella, F Steiner, V Schlumbom, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Partial N-acetylglutamate synthetase deficiency: a new case with uncontrollable movement disordersA B Burlina, C Bachmann, B Wermuth, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 8, 2000
Partial N-acetyl-glutamate synthetase deficiency masquerading as a valproic acid-induced Reye-like syndromeP P Forget, M van Oosterhout, J A Bakker, et al.
Biochemical and Biophysical Research Communications|March 29, 1991
Human carbonyl and aldose reductases: new catalytic functions in tetrahydrobiopterin biosynthesisY S Park, C W Heizmann, B Wermuth, et al.
Blood|September 15, 1994
A new substitution, gamma 358 Ser-->Cys, in fibrinogen Milano VII causes defective fibrin polymerizationC Steinmann, C Bögli, M Jungo, et al.
Enzyme & Protein|January 1, 1996
Combined 3-methylglutaconic and 3-hydroxy-3-methylglutaric aciduria with endocardial fibroelastosis and dilatative cardiomyopathy in male and female siblings with partial deficiency of complex II/III in fibroblastsS Ruesch, S Krähenbühl, S Kleinle, et al.
Pageof 9