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Stephan Ossowski

Showing results (61-70 of 155) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|June 30, 2016
Chromosome-level assembly of Arabidopsis thaliana Ler reveals the extent of translocation and inversion polymorphismsLuis Zapata, Jia Ding, Eva-Maria Willing, et al.
European Journal of Human Genetics : EJHG|August 15, 2013
Accurate molecular diagnosis of phenylketonuria and tetrahydrobiopterin-deficient hyperphenylalaninemias using high-throughput targeted sequencingDaniel Trujillano, Belén Perez, Justo González, et al.
Frontiers in Immunology|June 24, 2021
Absence of Non-Canonical, Inhibitory <i>MYD88</i> Splice Variants in B Cell Lymphomas Correlates With Sustained NF-κB SignalingYamel Cardona Gloria, Stephan H Bernhart, Sven Fillinger, et al.
Genome Research|October 23, 2012
Complementation contributes to transcriptome complexity in maize (Zea mays L.) hybrids relative to their inbred parentsAnja Paschold, Yi Jia, Caroline Marcon, et al.
Molecular Genetics & Genomic Medicine|February 10, 2023
Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndromeDennis Witt, Ulrike Faust, Gertrud Strobl-Wildemann, et al.
International Journal of Molecular Sciences|June 13, 2025
Long-Read Sequencing Identifies Mosaic Sequence Variations in Friedreich's Ataxia-GAA RepeatsJoohyun Park, Claudia Dufke, Zofia Fleszar, et al.
Cancers|August 23, 2020
Distinct Mutation Patterns Reveal Melanoma Subtypes and Influence Immunotherapy Response in Advanced Melanoma PatientsFranz J Hilke, Tobias Sinnberg, Axel Gschwind, et al.
Frontiers in Immunology|March 25, 2026
Dysregulated NK-cell gene expression defines the enduring symptoms of long COVID-19Urvi Ray, Antje Schulze Selting, Roshan Priyarangana Perera, et al.
Frontiers in Immunology|November 3, 2018
LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental IsodisomyPere Soler-Palacín, Marina Garcia-Prat, Andrea Martín-Nalda, et al.
Frontiers in Oncology|April 22, 2025
Case Report: FGFR2 inhibitor resistance via <i>PIK3CA</i> and <i>CDKN2A/B</i> in an intrahepatic cholangiocarcinoma patient with <i>FGFR2-SH3GLB1</i> fusionNadja Ballin, Alexander Ott, Olga Seibel-Kelemen, et al.
Pageof 16

Showing results (61-70 of 155) with videos related to

Sort By:
Pageof 16
Proceedings of the National Academy of Sciences of the United States of America|June 30, 2016
Chromosome-level assembly of Arabidopsis thaliana Ler reveals the extent of translocation and inversion polymorphismsLuis Zapata, Jia Ding, Eva-Maria Willing, et al.
European Journal of Human Genetics : EJHG|August 15, 2013
Accurate molecular diagnosis of phenylketonuria and tetrahydrobiopterin-deficient hyperphenylalaninemias using high-throughput targeted sequencingDaniel Trujillano, Belén Perez, Justo González, et al.
Frontiers in Immunology|June 24, 2021
Absence of Non-Canonical, Inhibitory <i>MYD88</i> Splice Variants in B Cell Lymphomas Correlates With Sustained NF-κB SignalingYamel Cardona Gloria, Stephan H Bernhart, Sven Fillinger, et al.
Genome Research|October 23, 2012
Complementation contributes to transcriptome complexity in maize (Zea mays L.) hybrids relative to their inbred parentsAnja Paschold, Yi Jia, Caroline Marcon, et al.
Molecular Genetics & Genomic Medicine|February 10, 2023
Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndromeDennis Witt, Ulrike Faust, Gertrud Strobl-Wildemann, et al.
International Journal of Molecular Sciences|June 13, 2025
Long-Read Sequencing Identifies Mosaic Sequence Variations in Friedreich's Ataxia-GAA RepeatsJoohyun Park, Claudia Dufke, Zofia Fleszar, et al.
Cancers|August 23, 2020
Distinct Mutation Patterns Reveal Melanoma Subtypes and Influence Immunotherapy Response in Advanced Melanoma PatientsFranz J Hilke, Tobias Sinnberg, Axel Gschwind, et al.
Frontiers in Immunology|March 25, 2026
Dysregulated NK-cell gene expression defines the enduring symptoms of long COVID-19Urvi Ray, Antje Schulze Selting, Roshan Priyarangana Perera, et al.
Frontiers in Immunology|November 3, 2018
LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental IsodisomyPere Soler-Palacín, Marina Garcia-Prat, Andrea Martín-Nalda, et al.
Frontiers in Oncology|April 22, 2025
Case Report: FGFR2 inhibitor resistance via <i>PIK3CA</i> and <i>CDKN2A/B</i> in an intrahepatic cholangiocarcinoma patient with <i>FGFR2-SH3GLB1</i> fusionNadja Ballin, Alexander Ott, Olga Seibel-Kelemen, et al.
Pageof 16