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L Bolund

Showing results (61-70 of 146) with videos related to

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Clinical Genetics|April 1, 1993
Identification of a supernumerary der(18) chromosome by a rational strategy for the cytogenetic typing of small marker chromosomes with chromosome-specific DNA probesJ Koch, H Fischer, H Askholm, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Fast one-step procedure for the detection of nucleic acids in situ by primer-induced sequence-specific labeling with fluorescein-12-dUTPJ Koch, J Mogensen, S Pedersen, et al.
Nucleic Acids Research|January 11, 1988
Detection of alpha 1-antitrypsin genotypes by analysis of amplified DNA sequencesK B Petersen, S Kølvraa, L Bolund, et al.
Reproduction, Fertility, and Development|August 12, 2004
Production of transgenic porcine blastocysts by hand-made cloningP M Kragh, G Vajta, T J Corydon, et al.
European Journal of Biochemistry|May 23, 1991
Repetitive sequences involved in the recombination leading to deletion of exon 5 of the low-density-lipoprotein receptor gene in a patient with familial hypercholesterolemiaN S Rüdiger, P S Hansen, M Jørgensen, et al.
Scandinavian Journal of Immunology|June 10, 2000
Strain-specific variations in the development of dendritic cells in murine bone-marrow culturesM S Petersen, H E Toldbod, S Holtz, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|January 1, 1995
Simultaneous detection of centromere-specific probes and chromosome painting libraries by a combination of primed in situ labelling and chromosome painting (PRINS-painting)J Hindkjaer, C A Brandt, J Koch, et al.
Differentiation; Research in Biological Diversity|May 1, 1991
Morphological differentiation and changes in polypeptide synthesis pattern during regeneration of human epidermal tissue developed in vitroP K Jensen, S J Fey, P M Larsen, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency due to heterozygosity for the common mutation and an allele resulting in low levels of MCAD mRNAB S Andresen, P Bross, I Knudsen, et al.
Human Mutation|September 8, 1999
Protein misfolding and degradation in genetic diseasesP Bross, T J Corydon, B S Andresen, et al.
Pageof 15

Showing results (61-70 of 146) with videos related to

Sort By:
Pageof 15
Clinical Genetics|April 1, 1993
Identification of a supernumerary der(18) chromosome by a rational strategy for the cytogenetic typing of small marker chromosomes with chromosome-specific DNA probesJ Koch, H Fischer, H Askholm, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Fast one-step procedure for the detection of nucleic acids in situ by primer-induced sequence-specific labeling with fluorescein-12-dUTPJ Koch, J Mogensen, S Pedersen, et al.
Nucleic Acids Research|January 11, 1988
Detection of alpha 1-antitrypsin genotypes by analysis of amplified DNA sequencesK B Petersen, S Kølvraa, L Bolund, et al.
Reproduction, Fertility, and Development|August 12, 2004
Production of transgenic porcine blastocysts by hand-made cloningP M Kragh, G Vajta, T J Corydon, et al.
European Journal of Biochemistry|May 23, 1991
Repetitive sequences involved in the recombination leading to deletion of exon 5 of the low-density-lipoprotein receptor gene in a patient with familial hypercholesterolemiaN S Rüdiger, P S Hansen, M Jørgensen, et al.
Scandinavian Journal of Immunology|June 10, 2000
Strain-specific variations in the development of dendritic cells in murine bone-marrow culturesM S Petersen, H E Toldbod, S Holtz, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|January 1, 1995
Simultaneous detection of centromere-specific probes and chromosome painting libraries by a combination of primed in situ labelling and chromosome painting (PRINS-painting)J Hindkjaer, C A Brandt, J Koch, et al.
Differentiation; Research in Biological Diversity|May 1, 1991
Morphological differentiation and changes in polypeptide synthesis pattern during regeneration of human epidermal tissue developed in vitroP K Jensen, S J Fey, P M Larsen, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency due to heterozygosity for the common mutation and an allele resulting in low levels of MCAD mRNAB S Andresen, P Bross, I Knudsen, et al.
Human Mutation|September 8, 1999
Protein misfolding and degradation in genetic diseasesP Bross, T J Corydon, B S Andresen, et al.
Pageof 15