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Michael Sendtner

Showing results (131-140 of 176) with videos related to

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Circulation|March 22, 2015
Vascular signal transducer and activator of transcription-3 promotes angiogenesis and neuroplasticity long-term after strokeChristian J Hoffmann, Ulrike Harms, Andre Rex, et al.
Nucleic Acids Research|December 1, 2021
Loss of full-length hnRNP R isoform impairs DNA damage response in motoneurons by inhibiting Yb1 recruitment to chromatinHanaa Ghanawi, Luisa Hennlein, Abdolhossein Zare, et al.
Acta Neuropathologica|March 30, 2016
Neurofilament depletion improves microtubule dynamics via modulation of Stat3/stathmin signalingPreeti Yadav, Bhuvaneish T Selvaraj, Florian L P Bender, et al.
Plos One|October 19, 2012
Leukemia inhibitory factor protects axons in experimental autoimmune encephalomyelitis via an oligodendrocyte-independent mechanismMelissa M Gresle, Estella Alexandrou, Qizhu Wu, et al.
European Journal of Immunology|January 29, 2015
Thymocyte-derived BDNF influences T-cell maturation at the DN3/DN4 transition stageRalf A Linker, De-Hyung Lee, Anne-Christine Flach, et al.
Nature Neuroscience|November 8, 2016
C9ORF72 interaction with cofilin modulates actin dynamics in motor neuronsRajeeve Sivadasan, Daniel Hornburg, Carsten Drepper, et al.
The Journal of Cell Biology|January 8, 2003
A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophyUmrao R Monani, Matthew T Pastore, Tatiana O Gavrilina, et al.
The Journal of Cell Biology|January 6, 2023
Plastin 3 rescues cell surface translocation and activation of TrkB in spinal muscular atrophyLuisa Hennlein, Hanaa Ghanawi, Florian Gerstner, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|March 14, 2012
Analysis of European case-control studies suggests that common inherited variation in mitochondrial DNA is not involved in susceptibility to amyotrophic lateral sclerosisCatherine J E Ingram, Michael E Weale, Christopher A Plaster, et al.
Human Molecular Genetics|February 8, 2017
Pathogenic inflammation in the CNS of mice carrying human PLP1 mutationsJanos Groh, Hana C Friedman, Nadiya Orel, et al.
Pageof 18

Showing results (131-140 of 176) with videos related to

Sort By:
Pageof 18
Circulation|March 22, 2015
Vascular signal transducer and activator of transcription-3 promotes angiogenesis and neuroplasticity long-term after strokeChristian J Hoffmann, Ulrike Harms, Andre Rex, et al.
Nucleic Acids Research|December 1, 2021
Loss of full-length hnRNP R isoform impairs DNA damage response in motoneurons by inhibiting Yb1 recruitment to chromatinHanaa Ghanawi, Luisa Hennlein, Abdolhossein Zare, et al.
Acta Neuropathologica|March 30, 2016
Neurofilament depletion improves microtubule dynamics via modulation of Stat3/stathmin signalingPreeti Yadav, Bhuvaneish T Selvaraj, Florian L P Bender, et al.
Plos One|October 19, 2012
Leukemia inhibitory factor protects axons in experimental autoimmune encephalomyelitis via an oligodendrocyte-independent mechanismMelissa M Gresle, Estella Alexandrou, Qizhu Wu, et al.
European Journal of Immunology|January 29, 2015
Thymocyte-derived BDNF influences T-cell maturation at the DN3/DN4 transition stageRalf A Linker, De-Hyung Lee, Anne-Christine Flach, et al.
Nature Neuroscience|November 8, 2016
C9ORF72 interaction with cofilin modulates actin dynamics in motor neuronsRajeeve Sivadasan, Daniel Hornburg, Carsten Drepper, et al.
The Journal of Cell Biology|January 8, 2003
A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophyUmrao R Monani, Matthew T Pastore, Tatiana O Gavrilina, et al.
The Journal of Cell Biology|January 6, 2023
Plastin 3 rescues cell surface translocation and activation of TrkB in spinal muscular atrophyLuisa Hennlein, Hanaa Ghanawi, Florian Gerstner, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|March 14, 2012
Analysis of European case-control studies suggests that common inherited variation in mitochondrial DNA is not involved in susceptibility to amyotrophic lateral sclerosisCatherine J E Ingram, Michael E Weale, Christopher A Plaster, et al.
Human Molecular Genetics|February 8, 2017
Pathogenic inflammation in the CNS of mice carrying human PLP1 mutationsJanos Groh, Hana C Friedman, Nadiya Orel, et al.
Pageof 18