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Julia Vogt

Showing results (31-40 of 51) with videos related to

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Human Mutation|November 5, 2013
Analysis of crossover breakpoints yields new insights into the nature of the gene conversion events associated with large NF1 deletions mediated by nonallelic homologous recombinationKathrin Bengesser, Julia Vogt, Tanja Mussotter, et al.
Plos One|May 20, 2025
Does pre-emptive dexamethasone provide prophylaxis against sugammadex-induced bradycardia? A retrospective studyJonathan S Jahr, Pamela A Chia, Tristan Grogan, et al.
Pain|March 14, 2012
Nonpain goal pursuit inhibits attentional bias to painMartien G S Schrooten, Stefaan Van Damme, Geert Crombez, et al.
Human Mutation|April 28, 2017
panelcn.MOPS: Copy-number detection in targeted NGS panel data for clinical diagnosticsGundula Povysil, Antigoni Tzika, Julia Vogt, et al.
International Journal of Molecular Sciences|April 13, 2023
Co-Culture of Mesenchymal Stem Cells and Ligamentocytes on Triphasic Embroidered Poly(L-lactide-co-ε-caprolactone) and Polylactic Acid Scaffolds for Anterior Cruciate Ligament Enthesis Tissue EngineeringClemens Gögele, Julia Vogt, Judith Hahn, et al.
Plos One|November 28, 2012
Detailing radio frequency heating induced by coronary stents: a 7.0 Tesla magnetic resonance studyDavide Santoro, Lukas Winter, Alexander Müller, et al.
Genes, Chromosomes & Cancer|February 2, 2012
Internal tumor burden in neurofibromatosis Type I patients with large NF1 deletionsLan Kluwe, Rosa Nguyen, Julia Vogt, et al.
Journal of Medical Case Reports|December 14, 2011
Delineation of the clinical phenotype associated with non-mosaic type-2 NF1 deletions: two case reportsJulia Vogt, Rosa Nguyen, Lan Kluwe, et al.
Human Mutation|February 1, 2011
Mosaic type-1 NF1 microdeletions as a cause of both generalized and segmental neurofibromatosis type-1 (NF1)Ludwine Messiaen, Julia Vogt, Kathrin Bengesser, et al.
Molecular Metabolism|December 30, 2023
Endothelin receptor B-deficient mice are protected from high-fat diet-induced metabolic syndromeMartina Feger, Leonie Meier, Jörg Strotmann, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Human Mutation|November 5, 2013
Analysis of crossover breakpoints yields new insights into the nature of the gene conversion events associated with large NF1 deletions mediated by nonallelic homologous recombinationKathrin Bengesser, Julia Vogt, Tanja Mussotter, et al.
Plos One|May 20, 2025
Does pre-emptive dexamethasone provide prophylaxis against sugammadex-induced bradycardia? A retrospective studyJonathan S Jahr, Pamela A Chia, Tristan Grogan, et al.
Pain|March 14, 2012
Nonpain goal pursuit inhibits attentional bias to painMartien G S Schrooten, Stefaan Van Damme, Geert Crombez, et al.
Human Mutation|April 28, 2017
panelcn.MOPS: Copy-number detection in targeted NGS panel data for clinical diagnosticsGundula Povysil, Antigoni Tzika, Julia Vogt, et al.
International Journal of Molecular Sciences|April 13, 2023
Co-Culture of Mesenchymal Stem Cells and Ligamentocytes on Triphasic Embroidered Poly(L-lactide-co-ε-caprolactone) and Polylactic Acid Scaffolds for Anterior Cruciate Ligament Enthesis Tissue EngineeringClemens Gögele, Julia Vogt, Judith Hahn, et al.
Plos One|November 28, 2012
Detailing radio frequency heating induced by coronary stents: a 7.0 Tesla magnetic resonance studyDavide Santoro, Lukas Winter, Alexander Müller, et al.
Genes, Chromosomes & Cancer|February 2, 2012
Internal tumor burden in neurofibromatosis Type I patients with large NF1 deletionsLan Kluwe, Rosa Nguyen, Julia Vogt, et al.
Journal of Medical Case Reports|December 14, 2011
Delineation of the clinical phenotype associated with non-mosaic type-2 NF1 deletions: two case reportsJulia Vogt, Rosa Nguyen, Lan Kluwe, et al.
Human Mutation|February 1, 2011
Mosaic type-1 NF1 microdeletions as a cause of both generalized and segmental neurofibromatosis type-1 (NF1)Ludwine Messiaen, Julia Vogt, Kathrin Bengesser, et al.
Molecular Metabolism|December 30, 2023
Endothelin receptor B-deficient mice are protected from high-fat diet-induced metabolic syndromeMartina Feger, Leonie Meier, Jörg Strotmann, et al.
Pageof 6