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Michael Sendtner

Showing results (151-160 of 176) with videos related to

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The Journal of Experimental Medicine|January 13, 2019
Heterozygous <i>Tbk1</i> loss has opposing effects in early and late stages of ALS in miceDavid Brenner, Kirsten Sieverding, Clara Bruno, et al.
Diabetes|November 30, 2011
Na(+)-D-glucose cotransporter SGLT1 is pivotal for intestinal glucose absorption and glucose-dependent incretin secretionValentin Gorboulev, Annette Schürmann, Volker Vallon, et al.
Nature Communications|November 1, 2017
Plekhg5-regulated autophagy of synaptic vesicles reveals a pathogenic mechanism in motoneuron diseasePatrick Lüningschrör, Beyenech Binotti, Benjamin Dombert, et al.
Cell Stem Cell|March 11, 2022
A cholinergic neuroskeletal interface promotes bone formation during postnatal growth and exerciseStephen Gadomski, Claire Fielding, Andrés García-García, et al.
Journal of the American Heart Association|November 26, 2025
Vascular and Neural Transcriptomics Reveal Stage-Dependent Pathways to Inflammation and Cognitive Dysfunction in a Rat Model of HypertensionPhilipp Arndt, Lorena Morton, Michael Briese, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|June 25, 2025
Neuropathic Pain and Distinct CASPR2 Autoantibody IgG Subclasses Drive Neuronal HyperexcitabilityMargarita Habib, Anna-Lena Wiessler, Patrik Fischer, et al.
Cell|September 22, 2009
Synaptic PRG-1 modulates excitatory transmission via lipid phosphate-mediated signalingThorsten Trimbuch, Prateep Beed, Johannes Vogt, et al.
Scientific Reports|April 13, 2019
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosisAnnelot M Dekker, Frank P Diekstra, Sara L Pulit, et al.
Brain : a Journal of Neurology|October 9, 2010
Loss of striatal type 1 cannabinoid receptors is a key pathogenic factor in Huntington's diseaseCristina Blázquez, Anna Chiarlone, Onintza Sagredo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 14, 2018
Comprehensive analysis of the mutation spectrum in 301 German ALS familiesKathrin Müller, David Brenner, Patrick Weydt, et al.
Pageof 18

Showing results (151-160 of 176) with videos related to

Sort By:
Pageof 18
The Journal of Experimental Medicine|January 13, 2019
Heterozygous <i>Tbk1</i> loss has opposing effects in early and late stages of ALS in miceDavid Brenner, Kirsten Sieverding, Clara Bruno, et al.
Diabetes|November 30, 2011
Na(+)-D-glucose cotransporter SGLT1 is pivotal for intestinal glucose absorption and glucose-dependent incretin secretionValentin Gorboulev, Annette Schürmann, Volker Vallon, et al.
Nature Communications|November 1, 2017
Plekhg5-regulated autophagy of synaptic vesicles reveals a pathogenic mechanism in motoneuron diseasePatrick Lüningschrör, Beyenech Binotti, Benjamin Dombert, et al.
Cell Stem Cell|March 11, 2022
A cholinergic neuroskeletal interface promotes bone formation during postnatal growth and exerciseStephen Gadomski, Claire Fielding, Andrés García-García, et al.
Journal of the American Heart Association|November 26, 2025
Vascular and Neural Transcriptomics Reveal Stage-Dependent Pathways to Inflammation and Cognitive Dysfunction in a Rat Model of HypertensionPhilipp Arndt, Lorena Morton, Michael Briese, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|June 25, 2025
Neuropathic Pain and Distinct CASPR2 Autoantibody IgG Subclasses Drive Neuronal HyperexcitabilityMargarita Habib, Anna-Lena Wiessler, Patrik Fischer, et al.
Cell|September 22, 2009
Synaptic PRG-1 modulates excitatory transmission via lipid phosphate-mediated signalingThorsten Trimbuch, Prateep Beed, Johannes Vogt, et al.
Scientific Reports|April 13, 2019
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosisAnnelot M Dekker, Frank P Diekstra, Sara L Pulit, et al.
Brain : a Journal of Neurology|October 9, 2010
Loss of striatal type 1 cannabinoid receptors is a key pathogenic factor in Huntington's diseaseCristina Blázquez, Anna Chiarlone, Onintza Sagredo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 14, 2018
Comprehensive analysis of the mutation spectrum in 301 German ALS familiesKathrin Müller, David Brenner, Patrick Weydt, et al.
Pageof 18