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Claus-Eric Ott

Showing results (31-40 of 42) with videos related to

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The Oncologist|April 22, 2026
Liquid biopsy-based detection of acquired MET resistance enables sequential targeted therapy in MET fusion-positive NSCLCStanislav Rosnev, Katharina Klein, Lukas Heukamp, et al.
American Journal of Human Genetics|January 20, 2007
Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndromeEva Klopocki, Harald Schulze, Gabriele Strauss, et al.
The Oncologist|June 17, 2024
A diagnostic challenge of KIT p.V559D and BRAF p.G469A mutations in a paragastric massStefan Habringer, Jana Ihlow, Karsten Kleo, et al.
Genome Biology|October 16, 2014
Deletions of chromosomal regulatory boundaries are associated with congenital diseaseJonas Ibn-Salem, Sebastian Köhler, Michael I Love, et al.
American Journal of Human Genetics|February 7, 2008
Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disordersAnne Michalk, Sigmar Stricker, Jutta Becker, et al.
Plos Genetics|March 22, 2018
Impaired proteoglycan glycosylation, elevated TGF-β signaling, and abnormal osteoblast differentiation as the basis for bone fragility in a mouse model for gerodermia osteodysplasticaWing Lee Chan, Magdalena Steiner, Tomasz Witkos, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2019
PEDIA: prioritization of exome data by image analysisTzung-Chien Hsieh, Martin A Mensah, Jean T Pantel, et al.
Cancers|July 27, 2022
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European AncestryMartine Dumont, Nana Weber-Lassalle, Charles Joly-Beauparlant, et al.
Communications Biology|October 6, 2022
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriersChristopher Hakkaart, John F Pearson, Louise Marquart, et al.
Nature Genetics|July 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
The Oncologist|April 22, 2026
Liquid biopsy-based detection of acquired MET resistance enables sequential targeted therapy in MET fusion-positive NSCLCStanislav Rosnev, Katharina Klein, Lukas Heukamp, et al.
American Journal of Human Genetics|January 20, 2007
Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndromeEva Klopocki, Harald Schulze, Gabriele Strauss, et al.
The Oncologist|June 17, 2024
A diagnostic challenge of KIT p.V559D and BRAF p.G469A mutations in a paragastric massStefan Habringer, Jana Ihlow, Karsten Kleo, et al.
Genome Biology|October 16, 2014
Deletions of chromosomal regulatory boundaries are associated with congenital diseaseJonas Ibn-Salem, Sebastian Köhler, Michael I Love, et al.
American Journal of Human Genetics|February 7, 2008
Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disordersAnne Michalk, Sigmar Stricker, Jutta Becker, et al.
Plos Genetics|March 22, 2018
Impaired proteoglycan glycosylation, elevated TGF-β signaling, and abnormal osteoblast differentiation as the basis for bone fragility in a mouse model for gerodermia osteodysplasticaWing Lee Chan, Magdalena Steiner, Tomasz Witkos, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2019
PEDIA: prioritization of exome data by image analysisTzung-Chien Hsieh, Martin A Mensah, Jean T Pantel, et al.
Cancers|July 27, 2022
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European AncestryMartine Dumont, Nana Weber-Lassalle, Charles Joly-Beauparlant, et al.
Communications Biology|October 6, 2022
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriersChristopher Hakkaart, John F Pearson, Louise Marquart, et al.
Nature Genetics|July 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
Pageof 5