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Cathrine Jespersgaard

Showing results (1-10 of 37) with videos related to

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Nature Protocols|June 5, 2007
Single-strand conformation polymorphism analysis using capillary array electrophoresis for large-scale mutation detectionLars Allan Larsen, Cathrine Jespersgaard, Paal Skytt Andersen
Diagnostic Microbiology and Infectious Disease|July 10, 2012
Real-time TaqMan polymerase chain reaction-based genus-identification and pyrosequencing-based species identification of Campylobacter jejuni, C. coli, C. lari, C. upsaliensis, and C. fetus directly on stool samplesSøren Persson, Henrik M Petersen, Cathrine Jespersgaard, et al.
Human Mutation|January 29, 2003
High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the methodPaal Skytt Andersen, Cathrine Jespersgaard, Jens Vuust, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 27, 2004
Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current (ITO,f), are not a frequent cause of long QT syndromeRune Frank-Hansen, Lars Allan Larsen, Paal Andersen, et al.
Anesthesia and Analgesia|May 1, 2012
There is no association between the circadian clock gene HPER3 and cognitive dysfunction after noncardiac surgeryMelissa Voigt Hansen, Lars Simon Rasmussen, Cathrine Jespersgaard, et al.
Human Mutation|April 4, 2003
Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screeningPaal Skytt Andersen, Cathrine Jespersgaard, Jens Vuust, et al.
Diagnostic Microbiology and Infectious Disease|October 5, 2007
Detecting Blastocystis using parasitologic and DNA-based methods: a comparative studyC Rune Stensvold, Maiken C Arendrup, Cathrine Jespersgaard, et al.
American Journal of Medical Genetics. Part A|May 2, 2013
Ring chromosome 9 in a girl with developmental delay and dysmorphic features: case report and review of the literatureElse la Cour Sibbesen, Cathrine Jespersgaard, Daniela Alosi, et al.
Genetic Testing|March 31, 2007
Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systemsKarina Meden Sørensen, Cathrine Jespersgaard, Jens Vuust, et al.
Molecular Cytogenetics|February 9, 2016
Proximal 21q deletion as a result of a de novo unbalanced t(12;21) translocation in a patient with dysmorphic features, hepatomegaly, thick myocardium and delayed psychomotor developmentCathrine Jespersgaard, Ida N Damgaard, Nanna Cornelius, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Nature Protocols|June 5, 2007
Single-strand conformation polymorphism analysis using capillary array electrophoresis for large-scale mutation detectionLars Allan Larsen, Cathrine Jespersgaard, Paal Skytt Andersen
Diagnostic Microbiology and Infectious Disease|July 10, 2012
Real-time TaqMan polymerase chain reaction-based genus-identification and pyrosequencing-based species identification of Campylobacter jejuni, C. coli, C. lari, C. upsaliensis, and C. fetus directly on stool samplesSøren Persson, Henrik M Petersen, Cathrine Jespersgaard, et al.
Human Mutation|January 29, 2003
High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the methodPaal Skytt Andersen, Cathrine Jespersgaard, Jens Vuust, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 27, 2004
Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current (ITO,f), are not a frequent cause of long QT syndromeRune Frank-Hansen, Lars Allan Larsen, Paal Andersen, et al.
Anesthesia and Analgesia|May 1, 2012
There is no association between the circadian clock gene HPER3 and cognitive dysfunction after noncardiac surgeryMelissa Voigt Hansen, Lars Simon Rasmussen, Cathrine Jespersgaard, et al.
Human Mutation|April 4, 2003
Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screeningPaal Skytt Andersen, Cathrine Jespersgaard, Jens Vuust, et al.
Diagnostic Microbiology and Infectious Disease|October 5, 2007
Detecting Blastocystis using parasitologic and DNA-based methods: a comparative studyC Rune Stensvold, Maiken C Arendrup, Cathrine Jespersgaard, et al.
American Journal of Medical Genetics. Part A|May 2, 2013
Ring chromosome 9 in a girl with developmental delay and dysmorphic features: case report and review of the literatureElse la Cour Sibbesen, Cathrine Jespersgaard, Daniela Alosi, et al.
Genetic Testing|March 31, 2007
Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systemsKarina Meden Sørensen, Cathrine Jespersgaard, Jens Vuust, et al.
Molecular Cytogenetics|February 9, 2016
Proximal 21q deletion as a result of a de novo unbalanced t(12;21) translocation in a patient with dysmorphic features, hepatomegaly, thick myocardium and delayed psychomotor developmentCathrine Jespersgaard, Ida N Damgaard, Nanna Cornelius, et al.
Pageof 4