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Lars Allan Larsen

Showing results (11-20 of 50) with videos related to

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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.
Ugeskrift for Laeger|October 31, 2006
[Screening for fragile X syndrome. International experiences]Jens Vuust, Lars Allan Larsen, Karen Grønskov, et al.
Organogenesis|December 19, 2013
Cilia and coordination of signaling networks during heart developmentKaren Koefoed, Iben Rønn Veland, Lotte Bang Pedersen, et al.
The American Journal of Cardiology|April 1, 2022
Comparison of Outcome in Patients With Familial Versus Spontaneous Atrial Septal DefectAnne Kathrine M Nielsen, Sabrina Gade Ellesøe, Lars Allan Larsen, et al.
Analytical Biochemistry|September 26, 2006
Evaluation of two methods for generating cRNA for microarray experiments from nanogram amounts of total RNAMads Bak, Lene Conley, Jakob Hedegaard, et al.
Cilia|March 28, 2017
Patient-specific three-dimensional explant spheroids derived from human nasal airway epithelium: a simple methodological approach for ex vivo studies of primary ciliary dyskinesiaJune Kehlet Marthin, Elizabeth Munkebjerg Stevens, Lars Allan Larsen, et al.
Genetic Testing|January 27, 2007
Screening of 99 Danish patients with congenital heart disease for GATA4 mutationsLitu Zhang, Zeynep Tümer, Joes Ramsøe Jacobsen, et al.
Genetic Testing|September 4, 2004
GJB2 and GJB6 mutations in 165 Danish patients showing non-syndromic hearing impairmentKaren Grønskov, Lars Allan Larsen, Nanna Dahl Rendtorff, et al.
Cardiovascular Research|February 5, 2003
Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutationsOle Havndrup, Henning Bundgaard, Paal Skytt Andersen, et al.
Congenital Heart Disease|December 19, 2015
Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the LiteratureSabrina Gade Ellesøe, Morten Munk Johansen, Jesper Vandborg Bjerre, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
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.
Ugeskrift for Laeger|October 31, 2006
[Screening for fragile X syndrome. International experiences]Jens Vuust, Lars Allan Larsen, Karen Grønskov, et al.
Organogenesis|December 19, 2013
Cilia and coordination of signaling networks during heart developmentKaren Koefoed, Iben Rønn Veland, Lotte Bang Pedersen, et al.
The American Journal of Cardiology|April 1, 2022
Comparison of Outcome in Patients With Familial Versus Spontaneous Atrial Septal DefectAnne Kathrine M Nielsen, Sabrina Gade Ellesøe, Lars Allan Larsen, et al.
Analytical Biochemistry|September 26, 2006
Evaluation of two methods for generating cRNA for microarray experiments from nanogram amounts of total RNAMads Bak, Lene Conley, Jakob Hedegaard, et al.
Cilia|March 28, 2017
Patient-specific three-dimensional explant spheroids derived from human nasal airway epithelium: a simple methodological approach for ex vivo studies of primary ciliary dyskinesiaJune Kehlet Marthin, Elizabeth Munkebjerg Stevens, Lars Allan Larsen, et al.
Genetic Testing|January 27, 2007
Screening of 99 Danish patients with congenital heart disease for GATA4 mutationsLitu Zhang, Zeynep Tümer, Joes Ramsøe Jacobsen, et al.
Genetic Testing|September 4, 2004
GJB2 and GJB6 mutations in 165 Danish patients showing non-syndromic hearing impairmentKaren Grønskov, Lars Allan Larsen, Nanna Dahl Rendtorff, et al.
Cardiovascular Research|February 5, 2003
Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutationsOle Havndrup, Henning Bundgaard, Paal Skytt Andersen, et al.
Congenital Heart Disease|December 19, 2015
Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the LiteratureSabrina Gade Ellesøe, Morten Munk Johansen, Jesper Vandborg Bjerre, et al.
Pageof 5