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Ute Felbor

Showing results (11-20 of 71) with videos related to

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Healthcare (Basel, Switzerland)|October 27, 2022
Hereditary Breast and Ovarian Cancer Service in Sparsely Populated Western PomeraniaUte Felbor, Robin Bülow, Rita K Schmutzler, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|August 24, 2005
Endostatin phenylalanines 31 and 34 define a receptor binding siteSonja Stahl, Sabine Gaetzner, Thomas D Mueller, et al.
Cancers|April 13, 2023
Quantitative Diffusion-Weighted MRI of NeuroblastomaNiklas Abele, Soenke Langner, Ute Felbor, et al.
Biomedicines|February 25, 2023
Spacer-Supported Thermal Ablation to Prevent Carbonisation and Improve Ablation Size: A Proof of Concept StudyFiona Mankertz, Ole Gemeinhardt, Ute Felbor, et al.
Clinical Case Reports|November 5, 2024
Novel postzygotic <i>RASA1</i> mutation in a patient with Parkes Weber syndrome: A case report and literature reviewRobin A Pilz, Dariush Skowronek, Tamara Ehresmann, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 12, 2020
CRISPR/Cas9-mediated Generation of Human Endothelial Cell Knockout Models of CCM DiseaseKonrad Schwefel, Stefanie Spiegler, Christiane D Much, et al.
Molecular Genetics & Genomic Medicine|May 25, 2019
Precise CCM1 gene correction and inactivation in patient-derived endothelial cells: Modeling Knudson's two-hit hypothesis in vitroStefanie Spiegler, Matthias Rath, Christiane D Much, et al.
Neurogenetics|September 24, 2010
Evidence for anti-angiogenic and pro-survival functions of the cerebral cavernous malformation protein 3Elisa Schleider, Sonja Stahl, Joycelyn Wüstehube, et al.
European Journal of Medical Genetics|March 9, 2013
Birth defects after incestuous mating: calculating the probability of causality and reflecting on the desirability of genetic testingLeo P Ten Kate, Matthias Rath, Ute Felbor, et al.
Journal of Cellular and Molecular Medicine|February 8, 2013
Loss of CCM3 impairs DLL4-Notch signalling: implication in endothelial angiogenesis and in inherited cerebral cavernous malformationsChao You, Ibrahim Erol Sandalcioglu, Philipp Dammann, et al.
Pageof 8

Showing results (11-20 of 71) with videos related to

Sort By:
Pageof 8
Healthcare (Basel, Switzerland)|October 27, 2022
Hereditary Breast and Ovarian Cancer Service in Sparsely Populated Western PomeraniaUte Felbor, Robin Bülow, Rita K Schmutzler, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|August 24, 2005
Endostatin phenylalanines 31 and 34 define a receptor binding siteSonja Stahl, Sabine Gaetzner, Thomas D Mueller, et al.
Cancers|April 13, 2023
Quantitative Diffusion-Weighted MRI of NeuroblastomaNiklas Abele, Soenke Langner, Ute Felbor, et al.
Biomedicines|February 25, 2023
Spacer-Supported Thermal Ablation to Prevent Carbonisation and Improve Ablation Size: A Proof of Concept StudyFiona Mankertz, Ole Gemeinhardt, Ute Felbor, et al.
Clinical Case Reports|November 5, 2024
Novel postzygotic <i>RASA1</i> mutation in a patient with Parkes Weber syndrome: A case report and literature reviewRobin A Pilz, Dariush Skowronek, Tamara Ehresmann, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 12, 2020
CRISPR/Cas9-mediated Generation of Human Endothelial Cell Knockout Models of CCM DiseaseKonrad Schwefel, Stefanie Spiegler, Christiane D Much, et al.
Molecular Genetics & Genomic Medicine|May 25, 2019
Precise CCM1 gene correction and inactivation in patient-derived endothelial cells: Modeling Knudson's two-hit hypothesis in vitroStefanie Spiegler, Matthias Rath, Christiane D Much, et al.
Neurogenetics|September 24, 2010
Evidence for anti-angiogenic and pro-survival functions of the cerebral cavernous malformation protein 3Elisa Schleider, Sonja Stahl, Joycelyn Wüstehube, et al.
European Journal of Medical Genetics|March 9, 2013
Birth defects after incestuous mating: calculating the probability of causality and reflecting on the desirability of genetic testingLeo P Ten Kate, Matthias Rath, Ute Felbor, et al.
Journal of Cellular and Molecular Medicine|February 8, 2013
Loss of CCM3 impairs DLL4-Notch signalling: implication in endothelial angiogenesis and in inherited cerebral cavernous malformationsChao You, Ibrahim Erol Sandalcioglu, Philipp Dammann, et al.
Pageof 8