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L Bolund

Showing results (81-90 of 146) with videos related to

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Cytometry|December 21, 2000
A strategy combining flow sorting and comparative genomic hybridization for studying genetic aberrations at different stages of colorectal tumorigenesis in ulcerative colitisO P Clausen, S N Andersen, H Strøomkjaer, et al.
FEBS Letters|November 7, 1988
Assignment of the human aminopeptidase N (peptidase E) gene to chromosome 15q13-qterT A Kruse, L Bolund, K H Grzeschik, et al.
Experimental Cell Research|December 1, 1993
Correction of steroid sulfatase deficiency by gene transfer into basal cells of tissue-cultured epidermis from patients with recessive X-linked ichthyosisT G Jensen, U B Jensen, P K Jensen, et al.
Prenatal Diagnosis|July 25, 2013
Methylation-specific multiplex ligation-dependent probe amplification: utility for prenatal diagnosis of parental origin in human triploidyM W Joergensen, A A Rasmussen, I Niemann, et al.
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1995
Molecular diagnosis and characterization of medium-chain acyl-CoA dehydrogenase deficiencyB S Andresen, P Bross, T G Jensen, et al.
Cancer Genetics and Cytogenetics|February 1, 1989
Genetically different cell subpopulations in hydatidiform moles. A study of three cases by RFLP, flow cytometric, cytogenetic, HLA, and morphologic analysesL Sunde, L O Vejerslev, J K Larsen, et al.
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.
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.
Pageof 15

Showing results (81-90 of 146) with videos related to

Sort By:
Pageof 15
Cytometry|December 21, 2000
A strategy combining flow sorting and comparative genomic hybridization for studying genetic aberrations at different stages of colorectal tumorigenesis in ulcerative colitisO P Clausen, S N Andersen, H Strøomkjaer, et al.
FEBS Letters|November 7, 1988
Assignment of the human aminopeptidase N (peptidase E) gene to chromosome 15q13-qterT A Kruse, L Bolund, K H Grzeschik, et al.
Experimental Cell Research|December 1, 1993
Correction of steroid sulfatase deficiency by gene transfer into basal cells of tissue-cultured epidermis from patients with recessive X-linked ichthyosisT G Jensen, U B Jensen, P K Jensen, et al.
Prenatal Diagnosis|July 25, 2013
Methylation-specific multiplex ligation-dependent probe amplification: utility for prenatal diagnosis of parental origin in human triploidyM W Joergensen, A A Rasmussen, I Niemann, et al.
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1995
Molecular diagnosis and characterization of medium-chain acyl-CoA dehydrogenase deficiencyB S Andresen, P Bross, T G Jensen, et al.
Cancer Genetics and Cytogenetics|February 1, 1989
Genetically different cell subpopulations in hydatidiform moles. A study of three cases by RFLP, flow cytometric, cytogenetic, HLA, and morphologic analysesL Sunde, L O Vejerslev, J K Larsen, et al.
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.
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.
Pageof 15