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N Gregersen

Showing results (131-140 of 208) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|November 9, 1991
Specific diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in dried blood spots by a polymerase chain reaction (PCR) assay detecting a point-mutation (G985) in the MCAD geneN Gregersen, A I Blakemore, V Winter, et al.
The European Respiratory Journal|May 1, 1992
Alpha 1-antitrypsin alleles in patients with pulmonary emphysema, detected by DNA amplification (PCR) and oligonucleotide probesK Bruun-Petersen, G Bruun-Petersen, R Dahl, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 30, 1989
Detection of point mutations in amplified single copy genes by biotin-labelled oligonucleotides: diagnosis of variants of alpha-1-antitrypsinN Gregersen, V Winter, K B Petersen, et al.
Clinical Genetics|April 1, 1996
Two novel mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in a Spanish populationA Cenarro, H K Jensen, F Civeira, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 11, 1981
Urinary excretion of succinylacetone and delta-aminolevulinic acid in patients with hereditary tyrosinemiaE Christensen, B B Jacobsen, N Gregersen, et al.
Human Mutation|August 29, 2001
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationshipN Gregersen, B S Andresen, M J Corydon, et al.
Archives of Disease in Childhood|December 22, 2000
A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiencyE H Touma, M S Rashed, C Vianey-Saban, et al.
Nature Nanotechnology|March 25, 2014
Random nanolasing in the Anderson localized regimeJ Liu, P D Garcia, S Ek, et al.
Clinical Genetics|March 1, 1990
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridizationJ Koch, S Kølvraa, N Hobolt, et al.
Biochimica Et Biophysica Acta|October 13, 1992
Expression of wild-type and mutant medium-chain acyl-CoA dehydrogenase (MCAD) cDNA in eucaryotic cellsT G Jensen, B S Andresen, P Bross, et al.
Pageof 21

Showing results (131-140 of 208) with videos related to

Sort By:
Pageof 21
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 9, 1991
Specific diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in dried blood spots by a polymerase chain reaction (PCR) assay detecting a point-mutation (G985) in the MCAD geneN Gregersen, A I Blakemore, V Winter, et al.
The European Respiratory Journal|May 1, 1992
Alpha 1-antitrypsin alleles in patients with pulmonary emphysema, detected by DNA amplification (PCR) and oligonucleotide probesK Bruun-Petersen, G Bruun-Petersen, R Dahl, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 30, 1989
Detection of point mutations in amplified single copy genes by biotin-labelled oligonucleotides: diagnosis of variants of alpha-1-antitrypsinN Gregersen, V Winter, K B Petersen, et al.
Clinical Genetics|April 1, 1996
Two novel mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in a Spanish populationA Cenarro, H K Jensen, F Civeira, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 11, 1981
Urinary excretion of succinylacetone and delta-aminolevulinic acid in patients with hereditary tyrosinemiaE Christensen, B B Jacobsen, N Gregersen, et al.
Human Mutation|August 29, 2001
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationshipN Gregersen, B S Andresen, M J Corydon, et al.
Archives of Disease in Childhood|December 22, 2000
A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiencyE H Touma, M S Rashed, C Vianey-Saban, et al.
Nature Nanotechnology|March 25, 2014
Random nanolasing in the Anderson localized regimeJ Liu, P D Garcia, S Ek, et al.
Clinical Genetics|March 1, 1990
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridizationJ Koch, S Kølvraa, N Hobolt, et al.
Biochimica Et Biophysica Acta|October 13, 1992
Expression of wild-type and mutant medium-chain acyl-CoA dehydrogenase (MCAD) cDNA in eucaryotic cellsT G Jensen, B S Andresen, P Bross, et al.
Pageof 21