Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ute Felbor

Showing results (51-60 of 71) with videos related to

Pageof 8
Sort By:
Frontiers in Molecular Biosciences|July 26, 2021
Inactivation of Cerebral Cavernous Malformation Genes Results in Accumulation of von Willebrand Factor and Redistribution of Weibel-Palade Bodies in Endothelial CellsChristiane D Much, Barbara S Sendtner, Konrad Schwefel, et al.
Epilepsy & Behavior : E&B|January 28, 2015
Predictive value of EFHC1 variants for the long-term seizure outcome in juvenile myoclonic epilepsyFelix von Podewils, Victoria Kowoll, Winnie Schroeder, et al.
Acta Neuropathologica Communications|April 21, 2026
Tumor-like proliferation of CCM3 knockout endothelial cells: insights from semaxinib treatment and transcriptome profiling of co-culturesValeriia V Saenko, Janne L Feldmann, Dariush Skowronek, et al.
Scientific Reports|April 15, 2020
First interchromosomal insertion in a patient with cerebral and spinal cavernous malformationsRobin A Pilz, Konrad Schwefel, Anja Weise, et al.
Cellular and Molecular Life Sciences : CMLS|June 6, 2022
Contact-dependent signaling triggers tumor-like proliferation of CCM3 knockout endothelial cells in co-culture with wild-type cellsMatthias Rath, Konrad Schwefel, Matteo Malinverno, et al.
European Journal of Medical Genetics|February 24, 2025
Oxford Nanopore long-read sequencing with CRISPR/Cas9-mediated target selection for accurate characterization of copy number variants in the LDLR geneRobin A Pilz, Dariush Skowronek, Loisa D Bonde, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
Prevalence of THAP1 sequence variants in German patients with primary dystoniaAnne S Söhn, Nicola Glöckle, Andrea Duarte Doetzer, et al.
Journal of Neurosurgery|May 7, 2016
Correlation of the venous angioarchitecture of multiple cerebral cavernous malformations with familial or sporadic disease: a susceptibility-weighted imaging study with 7-Tesla MRIPhilipp Dammann, Karsten Wrede, Yuan Zhu, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 10, 2020
Fibronectin rescues aberrant phenotype of endothelial cells lacking either CCM1, CCM2 or CCM3Konrad Schwefel, Stefanie Spiegler, Bettina C Kirchmaier, et al.
Frontiers in Neurology|December 12, 2019
Novel Pathogenic Variants in a Cassette Exon of <i>CCM2</i> in Patients With Cerebral Cavernous MalformationsChristiane D Much, Konrad Schwefel, Dariush Skowronek, et al.
Pageof 8

Showing results (51-60 of 71) with videos related to

Sort By:
Pageof 8
Frontiers in Molecular Biosciences|July 26, 2021
Inactivation of Cerebral Cavernous Malformation Genes Results in Accumulation of von Willebrand Factor and Redistribution of Weibel-Palade Bodies in Endothelial CellsChristiane D Much, Barbara S Sendtner, Konrad Schwefel, et al.
Epilepsy & Behavior : E&B|January 28, 2015
Predictive value of EFHC1 variants for the long-term seizure outcome in juvenile myoclonic epilepsyFelix von Podewils, Victoria Kowoll, Winnie Schroeder, et al.
Acta Neuropathologica Communications|April 21, 2026
Tumor-like proliferation of CCM3 knockout endothelial cells: insights from semaxinib treatment and transcriptome profiling of co-culturesValeriia V Saenko, Janne L Feldmann, Dariush Skowronek, et al.
Scientific Reports|April 15, 2020
First interchromosomal insertion in a patient with cerebral and spinal cavernous malformationsRobin A Pilz, Konrad Schwefel, Anja Weise, et al.
Cellular and Molecular Life Sciences : CMLS|June 6, 2022
Contact-dependent signaling triggers tumor-like proliferation of CCM3 knockout endothelial cells in co-culture with wild-type cellsMatthias Rath, Konrad Schwefel, Matteo Malinverno, et al.
European Journal of Medical Genetics|February 24, 2025
Oxford Nanopore long-read sequencing with CRISPR/Cas9-mediated target selection for accurate characterization of copy number variants in the LDLR geneRobin A Pilz, Dariush Skowronek, Loisa D Bonde, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
Prevalence of THAP1 sequence variants in German patients with primary dystoniaAnne S Söhn, Nicola Glöckle, Andrea Duarte Doetzer, et al.
Journal of Neurosurgery|May 7, 2016
Correlation of the venous angioarchitecture of multiple cerebral cavernous malformations with familial or sporadic disease: a susceptibility-weighted imaging study with 7-Tesla MRIPhilipp Dammann, Karsten Wrede, Yuan Zhu, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 10, 2020
Fibronectin rescues aberrant phenotype of endothelial cells lacking either CCM1, CCM2 or CCM3Konrad Schwefel, Stefanie Spiegler, Bettina C Kirchmaier, et al.
Frontiers in Neurology|December 12, 2019
Novel Pathogenic Variants in a Cassette Exon of <i>CCM2</i> in Patients With Cerebral Cavernous MalformationsChristiane D Much, Konrad Schwefel, Dariush Skowronek, et al.
Pageof 8