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Vincent Timmerman

Showing results (51-60 of 152) with videos related to

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Journal of Neuroinflammation|July 24, 2012
Acute injury in the peripheral nervous system triggers an alternative macrophage responseElke Ydens, Anje Cauwels, Bob Asselbergh, et al.
Autophagy|December 19, 2024
Autophagy induction by piplartine ameliorates axonal degeneration caused by mutant HSPB1 and HSPB8 in Charcot-Marie-Tooth type 2 neuropathiesAngela Sisto, Tamira van Wermeskerken, Michael Pancher, et al.
Muscle & Nerve|March 31, 2004
Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophyGert Hünermund, Anja Schirmacher, Bernd Ringelstein, et al.
Journal of Neurology|February 22, 2011
Reduced penetrance in hereditary motor neuropathy caused by TRPV4 Arg269Cys mutationJosé Berciano, Jonathan Baets, Elena Gallardo, et al.
Neuromuscular Disorders : NMD|May 19, 2012
Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patientsJoy Irobi, Anne Holmgren, Vicky De Winter, et al.
Molecular and Cellular Neurosciences|March 31, 2005
Experimental Charcot-Marie-Tooth type 1A: a cDNA microarrays analysisTiziana Vigo, Lucilla Nobbio, Paul Van Hummelen, et al.
Journal of Neuromuscular Diseases|November 18, 2016
Characterization of New Transgenic Mouse Models for Two Charcot-Marie-Tooth-Causing HspB1 Mutations using the Rosa26 LocusDelphine Bouhy, Thomas Geuens, Vicky De Winter, et al.
Acta Neuropathologica Communications|January 13, 2017
Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative diseaseThomas Geuens, Vicky De Winter, Nicholas Rajan, et al.
Metabolites|May 24, 2024
The Metabolic and Lipidomic Fingerprint of Torin1 Exposure in Mouse Embryonic Fibroblasts Using Untargeted MetabolomicsRani Robeyns, Angela Sisto, Elias Iturrospe, et al.
Brain : a Journal of Neurology|December 13, 2022
Downregulation of PMP22 ameliorates myelin defects in iPSC-derived human organoid cultures of CMT1AJonas Van Lent, Leen Vendredy, Elias Adriaenssens, et al.
Pageof 16

Showing results (51-60 of 152) with videos related to

Sort By:
Pageof 16
Journal of Neuroinflammation|July 24, 2012
Acute injury in the peripheral nervous system triggers an alternative macrophage responseElke Ydens, Anje Cauwels, Bob Asselbergh, et al.
Autophagy|December 19, 2024
Autophagy induction by piplartine ameliorates axonal degeneration caused by mutant HSPB1 and HSPB8 in Charcot-Marie-Tooth type 2 neuropathiesAngela Sisto, Tamira van Wermeskerken, Michael Pancher, et al.
Muscle & Nerve|March 31, 2004
Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophyGert Hünermund, Anja Schirmacher, Bernd Ringelstein, et al.
Journal of Neurology|February 22, 2011
Reduced penetrance in hereditary motor neuropathy caused by TRPV4 Arg269Cys mutationJosé Berciano, Jonathan Baets, Elena Gallardo, et al.
Neuromuscular Disorders : NMD|May 19, 2012
Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patientsJoy Irobi, Anne Holmgren, Vicky De Winter, et al.
Molecular and Cellular Neurosciences|March 31, 2005
Experimental Charcot-Marie-Tooth type 1A: a cDNA microarrays analysisTiziana Vigo, Lucilla Nobbio, Paul Van Hummelen, et al.
Journal of Neuromuscular Diseases|November 18, 2016
Characterization of New Transgenic Mouse Models for Two Charcot-Marie-Tooth-Causing HspB1 Mutations using the Rosa26 LocusDelphine Bouhy, Thomas Geuens, Vicky De Winter, et al.
Acta Neuropathologica Communications|January 13, 2017
Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative diseaseThomas Geuens, Vicky De Winter, Nicholas Rajan, et al.
Metabolites|May 24, 2024
The Metabolic and Lipidomic Fingerprint of Torin1 Exposure in Mouse Embryonic Fibroblasts Using Untargeted MetabolomicsRani Robeyns, Angela Sisto, Elias Iturrospe, et al.
Brain : a Journal of Neurology|December 13, 2022
Downregulation of PMP22 ameliorates myelin defects in iPSC-derived human organoid cultures of CMT1AJonas Van Lent, Leen Vendredy, Elias Adriaenssens, et al.
Pageof 16