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Saskia Biskup

Showing results (161-170 of 226) with videos related to

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International Journal of Molecular Sciences|April 3, 2021
Refining Genotypes and Phenotypes in <i>KCNA2</i>-Related Neurological DisordersJan H Döring, Julian Schröter, Jerome Jüngling, et al.
Nature Communications|February 12, 2024
The molecular interaction pattern of lenvatinib enables inhibition of wild-type or kinase-mutated FGFR2-driven cholangiocarcinomaStephan Spahn, Fabian Kleinhenz, Ekaterina Shevchenko, et al.
Orphanet Journal of Rare Diseases|March 19, 2013
Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrumMatthis Synofzik, Anne S Soehn, Janina Gburek-Augustat, et al.
The Journal of Biological Chemistry|November 27, 2013
A direct interaction between leucine-rich repeat kinase 2 and specific β-tubulin isoforms regulates tubulin acetylationBernard M H Law, Victoria A Spain, Veronica H L Leinster, et al.
Orphanet Journal of Rare Diseases|April 18, 2015
Phenotypic and molecular insights into CASK-related disorders in malesUte Moog, Tatjana Bierhals, Kristina Brand, et al.
NPJ Precision Oncology|September 4, 2021
Targeting extracellular and juxtamembrane FGFR2 mutations in chemotherapy-refractory cholangiocarcinomaMichael Bitzer, Stephan Spahn, Sepideh Babaei, et al.
Annals of Neurology|November 23, 2006
Localization of LRRK2 to membranous and vesicular structures in mammalian brainSaskia Biskup, Darren J Moore, Fulvio Celsi, et al.
Annals of Neurology|November 26, 2013
GRIN2B mutations in West syndrome and intellectual disability with focal epilepsyJohannes R Lemke, Rik Hendrickx, Kirsten Geider, et al.
British Journal of Cancer|May 27, 2020
Cancer incidence and spectrum among children with genetically confirmed Beckwith-Wiedemann spectrum in Germany: a retrospective cohort studySümeyye Cöktü, Claudia Spix, Melanie Kaiser, et al.
Ear and Hearing|July 13, 2023
Variability in Cochlear Implantation Outcomes in a Large German Cohort With a Genetic Etiology of Hearing LossAnke Tropitzsch, Thore Schade-Mann, Philipp Gamerdinger, et al.
Pageof 23

Showing results (161-170 of 226) with videos related to

Sort By:
Pageof 23
International Journal of Molecular Sciences|April 3, 2021
Refining Genotypes and Phenotypes in <i>KCNA2</i>-Related Neurological DisordersJan H Döring, Julian Schröter, Jerome Jüngling, et al.
Nature Communications|February 12, 2024
The molecular interaction pattern of lenvatinib enables inhibition of wild-type or kinase-mutated FGFR2-driven cholangiocarcinomaStephan Spahn, Fabian Kleinhenz, Ekaterina Shevchenko, et al.
Orphanet Journal of Rare Diseases|March 19, 2013
Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrumMatthis Synofzik, Anne S Soehn, Janina Gburek-Augustat, et al.
The Journal of Biological Chemistry|November 27, 2013
A direct interaction between leucine-rich repeat kinase 2 and specific β-tubulin isoforms regulates tubulin acetylationBernard M H Law, Victoria A Spain, Veronica H L Leinster, et al.
Orphanet Journal of Rare Diseases|April 18, 2015
Phenotypic and molecular insights into CASK-related disorders in malesUte Moog, Tatjana Bierhals, Kristina Brand, et al.
NPJ Precision Oncology|September 4, 2021
Targeting extracellular and juxtamembrane FGFR2 mutations in chemotherapy-refractory cholangiocarcinomaMichael Bitzer, Stephan Spahn, Sepideh Babaei, et al.
Annals of Neurology|November 23, 2006
Localization of LRRK2 to membranous and vesicular structures in mammalian brainSaskia Biskup, Darren J Moore, Fulvio Celsi, et al.
Annals of Neurology|November 26, 2013
GRIN2B mutations in West syndrome and intellectual disability with focal epilepsyJohannes R Lemke, Rik Hendrickx, Kirsten Geider, et al.
British Journal of Cancer|May 27, 2020
Cancer incidence and spectrum among children with genetically confirmed Beckwith-Wiedemann spectrum in Germany: a retrospective cohort studySümeyye Cöktü, Claudia Spix, Melanie Kaiser, et al.
Ear and Hearing|July 13, 2023
Variability in Cochlear Implantation Outcomes in a Large German Cohort With a Genetic Etiology of Hearing LossAnke Tropitzsch, Thore Schade-Mann, Philipp Gamerdinger, et al.
Pageof 23