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Stephan Ossowski

Showing results (101-110 of 155) with videos related to

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Science (New York, N.Y.)|July 21, 2007
Common sequence polymorphisms shaping genetic diversity in Arabidopsis thalianaRichard M Clark, Gabriele Schweikert, Christopher Toomajian, et al.
Frontiers in Molecular Neuroscience|May 24, 2021
Environmental Enrichment Induces Epigenomic and Genome Organization Changes Relevant for CognitionSergio Espeso-Gil, Aliaksei Z Holik, Sarah Bonnin, et al.
Elife|December 19, 2013
The genomic landscape of meiotic crossovers and gene conversions in Arabidopsis thalianaErik Wijnker, Geo Velikkakam James, Jia Ding, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|November 10, 2023
Genetic and functional analysis of chymotrypsin-like protease (CTRL) in chronic pancreatitisKatharina Eiseler, Lea Neppl, Andreas W Schmidt, et al.
Scientific Reports|March 11, 2017
A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C SyndromesRoser Urreizti, Anna Maria Cueto-Gonzalez, Héctor Franco-Valls, et al.
Breast (Edinburgh, Scotland)|May 22, 2025
Clinical genome sequencing in patients with hereditary breast and ovarian cancer: Concept, implementation and benefitsDennis Witt, Marc Sturm, Antje Stäbler, et al.
Human Mutation|October 21, 2009
Deep sequencing to reveal new variants in pooled DNA samplesAstrid A Out, Ivonne J H M van Minderhout, Jelle J Goeman, et al.
European Journal of Cancer (Oxford, England : 1990)|December 10, 2022
Germline findings in patients with advanced malignancies screened with paired blood-tumour testing for personalised treatment approachesCristiana Roggia, Sorin Armeanu-Ebinger, Axel Gschwind, et al.
NPJ Genomic Medicine|October 27, 2024
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnosesGerman Demidov, Burcu Yaldiz, José Garcia-Pelaez, et al.
Human Mutation|July 21, 2017
Survival among children with "Lethal" congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN)Jennifer A Wambach, Georg M Stettner, Tobias B Haack, et al.
Pageof 16

Showing results (101-110 of 155) with videos related to

Sort By:
Pageof 16
Science (New York, N.Y.)|July 21, 2007
Common sequence polymorphisms shaping genetic diversity in Arabidopsis thalianaRichard M Clark, Gabriele Schweikert, Christopher Toomajian, et al.
Frontiers in Molecular Neuroscience|May 24, 2021
Environmental Enrichment Induces Epigenomic and Genome Organization Changes Relevant for CognitionSergio Espeso-Gil, Aliaksei Z Holik, Sarah Bonnin, et al.
Elife|December 19, 2013
The genomic landscape of meiotic crossovers and gene conversions in Arabidopsis thalianaErik Wijnker, Geo Velikkakam James, Jia Ding, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|November 10, 2023
Genetic and functional analysis of chymotrypsin-like protease (CTRL) in chronic pancreatitisKatharina Eiseler, Lea Neppl, Andreas W Schmidt, et al.
Scientific Reports|March 11, 2017
A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C SyndromesRoser Urreizti, Anna Maria Cueto-Gonzalez, Héctor Franco-Valls, et al.
Breast (Edinburgh, Scotland)|May 22, 2025
Clinical genome sequencing in patients with hereditary breast and ovarian cancer: Concept, implementation and benefitsDennis Witt, Marc Sturm, Antje Stäbler, et al.
Human Mutation|October 21, 2009
Deep sequencing to reveal new variants in pooled DNA samplesAstrid A Out, Ivonne J H M van Minderhout, Jelle J Goeman, et al.
European Journal of Cancer (Oxford, England : 1990)|December 10, 2022
Germline findings in patients with advanced malignancies screened with paired blood-tumour testing for personalised treatment approachesCristiana Roggia, Sorin Armeanu-Ebinger, Axel Gschwind, et al.
NPJ Genomic Medicine|October 27, 2024
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnosesGerman Demidov, Burcu Yaldiz, José Garcia-Pelaez, et al.
Human Mutation|July 21, 2017
Survival among children with "Lethal" congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN)Jennifer A Wambach, Georg M Stettner, Tobias B Haack, et al.
Pageof 16