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N Gregersen

Showing results (61-70 of 208) with videos related to

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Clinical Genetics|January 1, 1978
Glutaric aciduria in progressive choreo-athetosisN J Brandt, S Brandt, E Christensen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 16, 1987
Improved methods for the detection of unique sequences in Southern blots of mammalian DNA by non-radioactive biotinylated DNA hybridization probesN Gregersen, J Koch, S Kølvraa, et al.
Advances in Experimental Medicine and Biology|March 10, 2000
Biochemical characterisation of mutations of human medium-chain acyl-CoA dehydrogenaseS Udvari, P Bross, B S Andresen, et al.
The Journal of Pediatrics|April 1, 1979
Treatment of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria). Experience with diet, riboflavin, and GABA analogueN J Brandt, N Gregersen, E Christensen, et al.
Journal of Lipid Research|July 1, 1991
Detection of the apoB-3500 mutation (glutamine for arginine) by gene amplification and cleavage with MspIP S Hansen, N Rüdiger, A Tybjaerg-Hansen, et al.
Clinical Chemistry|October 1, 1992
Two novel nonradioactive polymerase chain reaction-based assays of dried blood spots, genomic DNA, or whole cells for fast, reliable detection of Z and S mutations in the alpha 1-antitrypsin geneB S Andresen, I Knudsen, P K Jensen, et al.
Clinical Genetics|December 1, 1989
Prenatal diagnosis of alpha-1-antitrypsin deficiency using polymerase chain reaction (PCR). Comparison of conventional RFLP methods with PCR used in combination with allele specific oligonucleotides or RFLP analysisM Schwartz, K B Petersen, N Gregersen, et al.
Chromosoma|October 1, 1989
Oligonucleotide-priming methods for the chromosome-specific labelling of alpha satellite DNA in situJ E Koch, S Kølvraa, K B Petersen, et al.
Biochemical Society Transactions|July 26, 2000
Mutations of human medium-chian acyl-CoA dehydrogenaseS Udvari, P Bross, B S Andresen, et al.
Clinical Genetics|June 18, 1998
A novel missense mutation (402C-->T) in exon 1 in the EDA gene in a family with X-linked hypohidrotic ectodermal dysplasiaJ M Hertz, K Nørgaard Hansen, I Juncker, et al.
Pageof 21

Showing results (61-70 of 208) with videos related to

Sort By:
Pageof 21
Clinical Genetics|January 1, 1978
Glutaric aciduria in progressive choreo-athetosisN J Brandt, S Brandt, E Christensen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 16, 1987
Improved methods for the detection of unique sequences in Southern blots of mammalian DNA by non-radioactive biotinylated DNA hybridization probesN Gregersen, J Koch, S Kølvraa, et al.
Advances in Experimental Medicine and Biology|March 10, 2000
Biochemical characterisation of mutations of human medium-chain acyl-CoA dehydrogenaseS Udvari, P Bross, B S Andresen, et al.
The Journal of Pediatrics|April 1, 1979
Treatment of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria). Experience with diet, riboflavin, and GABA analogueN J Brandt, N Gregersen, E Christensen, et al.
Journal of Lipid Research|July 1, 1991
Detection of the apoB-3500 mutation (glutamine for arginine) by gene amplification and cleavage with MspIP S Hansen, N Rüdiger, A Tybjaerg-Hansen, et al.
Clinical Chemistry|October 1, 1992
Two novel nonradioactive polymerase chain reaction-based assays of dried blood spots, genomic DNA, or whole cells for fast, reliable detection of Z and S mutations in the alpha 1-antitrypsin geneB S Andresen, I Knudsen, P K Jensen, et al.
Clinical Genetics|December 1, 1989
Prenatal diagnosis of alpha-1-antitrypsin deficiency using polymerase chain reaction (PCR). Comparison of conventional RFLP methods with PCR used in combination with allele specific oligonucleotides or RFLP analysisM Schwartz, K B Petersen, N Gregersen, et al.
Chromosoma|October 1, 1989
Oligonucleotide-priming methods for the chromosome-specific labelling of alpha satellite DNA in situJ E Koch, S Kølvraa, K B Petersen, et al.
Biochemical Society Transactions|July 26, 2000
Mutations of human medium-chian acyl-CoA dehydrogenaseS Udvari, P Bross, B S Andresen, et al.
Clinical Genetics|June 18, 1998
A novel missense mutation (402C-->T) in exon 1 in the EDA gene in a family with X-linked hypohidrotic ectodermal dysplasiaJ M Hertz, K Nørgaard Hansen, I Juncker, et al.
Pageof 21