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Lars Allan Larsen

Showing results (1-10 of 50) with videos related to

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Ugeskrift for Laeger|January 19, 2011
[Chromosomal changes in congenital heart disease]Lars Allan Larsen
Progress in Molecular and Subcellular Biology|December 13, 2006
The hedgehog signaling pathway in cancerJanni Vestergaard, Mads Bak, Lars Allan Larsen
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
Pharmacogenomics|July 2, 2003
The Hedgehog signaling pathway--implications for drug targets in cancer and neurodegenerative disordersMads Bak, Claus Hansen, Niels Tommerup, et al.
Current Protocols in Human Genetics|April 23, 2008
Single-strand conformation polymorphism analysis using capillary electrophoresisLars Allan Larsen, Michael Christiansen, Jens Vuust, et al.
Cellular and Molecular Life Sciences : CMLS|August 13, 2013
Of mice and men: molecular genetics of congenital heart diseaseTroels Askhøj Andersen, Karin de Linde Lind Troelsen, Lars Allan Larsen
Genetic Testing|February 3, 2005
Identification of a novel EYA1 splice-site mutation in a Danish branchio-oto-renal syndrome familyAnn Marie Henriksen, Zeynep Tümer, Niels Tommerup, 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.
European Journal of Medical Genetics|February 9, 2024
TBX5 variants and cardiac phenotype: A systematic review of the literature and a novel variantAnne Kathrine Møller Nielsen, Anna Maria Dehn, Vibeke Hjortdal, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Ugeskrift for Laeger|January 19, 2011
[Chromosomal changes in congenital heart disease]Lars Allan Larsen
Progress in Molecular and Subcellular Biology|December 13, 2006
The hedgehog signaling pathway in cancerJanni Vestergaard, Mads Bak, Lars Allan Larsen
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
Pharmacogenomics|July 2, 2003
The Hedgehog signaling pathway--implications for drug targets in cancer and neurodegenerative disordersMads Bak, Claus Hansen, Niels Tommerup, et al.
Current Protocols in Human Genetics|April 23, 2008
Single-strand conformation polymorphism analysis using capillary electrophoresisLars Allan Larsen, Michael Christiansen, Jens Vuust, et al.
Cellular and Molecular Life Sciences : CMLS|August 13, 2013
Of mice and men: molecular genetics of congenital heart diseaseTroels Askhøj Andersen, Karin de Linde Lind Troelsen, Lars Allan Larsen
Genetic Testing|February 3, 2005
Identification of a novel EYA1 splice-site mutation in a Danish branchio-oto-renal syndrome familyAnn Marie Henriksen, Zeynep Tümer, Niels Tommerup, 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.
European Journal of Medical Genetics|February 9, 2024
TBX5 variants and cardiac phenotype: A systematic review of the literature and a novel variantAnne Kathrine Møller Nielsen, Anna Maria Dehn, Vibeke Hjortdal, et al.
Pageof 5