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N Gregersen

Showing results (71-80 of 208) with videos related to

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Human Molecular Genetics|September 1, 1994
Amino acid polymorphism (Gly209Ser) in the ACADS geneM J Kristensen, S Kmoch, P Bross, et al.
Human Genetics|March 1, 1991
Localisation of RFLPs of the medium chain acyl-CoA dehydrogenase geneA I Blakemore, S Kolvraa, N Gregersen, et al.
FEBS Letters|December 18, 1995
Human ClpP protease: cDNA sequence, tissue-specific expression and chromosomal assignment of the geneP Bross, B S Andresen, I Knudsen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 28, 1980
Non-ketotic C6-C10-dicarboxylic aciduria: biochemical investigations of two casesN Gregersen, F Rosleff, S Kølvraa, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Riboflavin-responsive epilepsy in a patient with SER209 variant form of short-chain acyl-CoA dehydrogenaseS Kmoch, J Zeman, M Hrebícek, et al.
The Journal of Pediatrics|May 1, 1977
Glutaric aciduria: clinical and laboratory findings in two brothersN Gregersen, N J Brandt, E Christensen, et al.
European Journal of Pediatrics|November 1, 1995
Medium-chain acyl-CoA dehydrogenase deficiency presenting in the neonatal period: the first Italian caseA B Burlina, M J Bennett, N Gregersen, et al.
Molecular Genetics and Metabolism|April 8, 2010
Misfolding of short-chain acyl-CoA dehydrogenase leads to mitochondrial fission and oxidative stressS P Schmidt, T J Corydon, C B Pedersen, et al.
Ugeskrift for Laeger|October 23, 1989
[Isovaleric acidemia]A M Gerdes, N Gregersen, F Güttler, et al.
Journal of Inherited Metabolic Disease|August 18, 2000
Defective folding and rapid degradation of mutant proteins is a common disease mechanism in genetic disordersN Gregersen, P Bross, M M Jørgensen, et al.
Pageof 21

Showing results (71-80 of 208) with videos related to

Sort By:
Pageof 21
Human Molecular Genetics|September 1, 1994
Amino acid polymorphism (Gly209Ser) in the ACADS geneM J Kristensen, S Kmoch, P Bross, et al.
Human Genetics|March 1, 1991
Localisation of RFLPs of the medium chain acyl-CoA dehydrogenase geneA I Blakemore, S Kolvraa, N Gregersen, et al.
FEBS Letters|December 18, 1995
Human ClpP protease: cDNA sequence, tissue-specific expression and chromosomal assignment of the geneP Bross, B S Andresen, I Knudsen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 28, 1980
Non-ketotic C6-C10-dicarboxylic aciduria: biochemical investigations of two casesN Gregersen, F Rosleff, S Kølvraa, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Riboflavin-responsive epilepsy in a patient with SER209 variant form of short-chain acyl-CoA dehydrogenaseS Kmoch, J Zeman, M Hrebícek, et al.
The Journal of Pediatrics|May 1, 1977
Glutaric aciduria: clinical and laboratory findings in two brothersN Gregersen, N J Brandt, E Christensen, et al.
European Journal of Pediatrics|November 1, 1995
Medium-chain acyl-CoA dehydrogenase deficiency presenting in the neonatal period: the first Italian caseA B Burlina, M J Bennett, N Gregersen, et al.
Molecular Genetics and Metabolism|April 8, 2010
Misfolding of short-chain acyl-CoA dehydrogenase leads to mitochondrial fission and oxidative stressS P Schmidt, T J Corydon, C B Pedersen, et al.
Ugeskrift for Laeger|October 23, 1989
[Isovaleric acidemia]A M Gerdes, N Gregersen, F Güttler, et al.
Journal of Inherited Metabolic Disease|August 18, 2000
Defective folding and rapid degradation of mutant proteins is a common disease mechanism in genetic disordersN Gregersen, P Bross, M M Jørgensen, et al.
Pageof 21