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N Gregersen

Showing results (51-60 of 208) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1988
A Scandinavian case of isovaleric acidaemiaA M Gerdes, N Gregersen, P Lúdvigsson, et al.
Nucleic Acids Research|January 25, 1995
One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chiN S Rüdiger, N Gregersen, M C Kielland-Brandt
Acta Paediatrica Scandinavica|July 1, 1986
Riboflavin responsive multiple acyl-CoA dehydrogenation deficiency. Assessment of 3 years of riboflavin treatmentN Gregersen, M F Christensen, E Christensen, et al.
Journal of Inherited Metabolic Disease|January 1, 1978
Glutaric aciduria in two brothersN J Brandt, N Gregersen, E Christensen, et al.
Clinical Chemistry|June 13, 1998
Quantitative analysis of the human epidermal growth factor receptor messenger RNA using reverse transcription-PCR: a methodological study of imprecisionV B Thøgersen, P Bross, N Gregersen, et al.
Scandinavian Journal of Plastic and Reconstructive Surgery|January 1, 1985
Experience with the latissimus dorsi flapI M Nielsen, M Lassen, B N Gregersen, et al.
Biotechniques|September 1, 1994
Detection of a point mutation using short oligonucleotide probes in allele-specific hybridizationA Iitiä, M Mikola, N Gregersen, et al.
Molecular Pathology : MP|September 4, 1999
Detection of clonal B cells in microdissected reactive lymphoproliferations: possible diagnostic pitfalls in PCR analysis of immunoglobulin heavy chain gene rearrangementX G Zhou, K Sandvej, N Gregersen, et al.
Gene|September 16, 1996
Structure of the rat gene encoding the multifunctional acyl-CoA-binding protein: conservation of intron 1 sequences in rodents and man. AddendumJ B Krøll, J Nøhr, N Gregersen, et al.
Molecular Pathology : MP|August 1, 1997
Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children: an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 yearsJ B Lundemose, S Kølvraa, N Gregersen, et al.
Pageof 21

Showing results (51-60 of 208) with videos related to

Sort By:
Pageof 21
Journal of Inherited Metabolic Disease|January 1, 1988
A Scandinavian case of isovaleric acidaemiaA M Gerdes, N Gregersen, P Lúdvigsson, et al.
Nucleic Acids Research|January 25, 1995
One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chiN S Rüdiger, N Gregersen, M C Kielland-Brandt
Acta Paediatrica Scandinavica|July 1, 1986
Riboflavin responsive multiple acyl-CoA dehydrogenation deficiency. Assessment of 3 years of riboflavin treatmentN Gregersen, M F Christensen, E Christensen, et al.
Journal of Inherited Metabolic Disease|January 1, 1978
Glutaric aciduria in two brothersN J Brandt, N Gregersen, E Christensen, et al.
Clinical Chemistry|June 13, 1998
Quantitative analysis of the human epidermal growth factor receptor messenger RNA using reverse transcription-PCR: a methodological study of imprecisionV B Thøgersen, P Bross, N Gregersen, et al.
Scandinavian Journal of Plastic and Reconstructive Surgery|January 1, 1985
Experience with the latissimus dorsi flapI M Nielsen, M Lassen, B N Gregersen, et al.
Biotechniques|September 1, 1994
Detection of a point mutation using short oligonucleotide probes in allele-specific hybridizationA Iitiä, M Mikola, N Gregersen, et al.
Molecular Pathology : MP|September 4, 1999
Detection of clonal B cells in microdissected reactive lymphoproliferations: possible diagnostic pitfalls in PCR analysis of immunoglobulin heavy chain gene rearrangementX G Zhou, K Sandvej, N Gregersen, et al.
Gene|September 16, 1996
Structure of the rat gene encoding the multifunctional acyl-CoA-binding protein: conservation of intron 1 sequences in rodents and man. AddendumJ B Krøll, J Nøhr, N Gregersen, et al.
Molecular Pathology : MP|August 1, 1997
Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children: an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 yearsJ B Lundemose, S Kølvraa, N Gregersen, et al.
Pageof 21