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Elisavet Preza

Showing results (1-10 of 18) with videos related to

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Molecular and Cellular Neurosciences|September 21, 2020
Modelling frontotemporal dementia using patient-derived induced pluripotent stem cellsGeorgie Lines, Jackie M Casey, Elisavet Preza, et al.
Molecular Neurobiology|May 21, 2018
Correction to: Impaired Bioenergetics in Mutant Mitochondrial DNA Determines Cell Fate during Seizure-Like ActivityStjepana Kovac, Elisavet Preza, Henry Houlden, et al.
Molecular Neurobiology|April 29, 2018
Impaired Bioenergetics in Mutant Mitochondrial DNA Determines Cell Fate During Seizure-Like ActivityStjepana Kovac, Elisavet Preza, Henry Houlden, et al.
Cells|February 12, 2026
From Dish to Trial: Building Translational Models of ALSIlias Salamotas, Sotiria Stavropoulou De Lorenzo, Aggeliki Stachtiari, et al.
The Journal of Biological Chemistry|April 1, 2017
Mutations in valosin-containing protein (VCP) decrease ADP/ATP translocation across the mitochondrial membrane and impair energy metabolism in human neuronsMarthe H R Ludtmann, Charles Arber, Fernando Bartolome, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 13, 2013
Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisationYo-Tsen Liu, Joshua Hersheson, Vincent Plagnol, et al.
Plos One|September 2, 2017
iPSC-derived neuronal models of PANK2-associated neurodegeneration reveal mitochondrial dysfunction contributing to early diseaseCharles Arber, Plamena R Angelova, Sarah Wiethoff, et al.
American Journal of Human Genetics|December 4, 2012
Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesisGavin Charlesworth, Vincent Plagnol, Kira M Holmström, et al.
Aging Cell|January 13, 2022
Disruption of ER-mitochondria tethering and signalling in C9orf72-associated amyotrophic lateral sclerosis and frontotemporal dementiaPatricia Gomez-Suaga, Gábor M Mórotz, Andrea Markovinovic, et al.
Neuron|March 19, 2013
Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levelsFernando Bartolome, Hsiu-Chuan Wu, Victoria S Burchell, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Molecular and Cellular Neurosciences|September 21, 2020
Modelling frontotemporal dementia using patient-derived induced pluripotent stem cellsGeorgie Lines, Jackie M Casey, Elisavet Preza, et al.
Molecular Neurobiology|May 21, 2018
Correction to: Impaired Bioenergetics in Mutant Mitochondrial DNA Determines Cell Fate during Seizure-Like ActivityStjepana Kovac, Elisavet Preza, Henry Houlden, et al.
Molecular Neurobiology|April 29, 2018
Impaired Bioenergetics in Mutant Mitochondrial DNA Determines Cell Fate During Seizure-Like ActivityStjepana Kovac, Elisavet Preza, Henry Houlden, et al.
Cells|February 12, 2026
From Dish to Trial: Building Translational Models of ALSIlias Salamotas, Sotiria Stavropoulou De Lorenzo, Aggeliki Stachtiari, et al.
The Journal of Biological Chemistry|April 1, 2017
Mutations in valosin-containing protein (VCP) decrease ADP/ATP translocation across the mitochondrial membrane and impair energy metabolism in human neuronsMarthe H R Ludtmann, Charles Arber, Fernando Bartolome, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 13, 2013
Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisationYo-Tsen Liu, Joshua Hersheson, Vincent Plagnol, et al.
Plos One|September 2, 2017
iPSC-derived neuronal models of PANK2-associated neurodegeneration reveal mitochondrial dysfunction contributing to early diseaseCharles Arber, Plamena R Angelova, Sarah Wiethoff, et al.
American Journal of Human Genetics|December 4, 2012
Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesisGavin Charlesworth, Vincent Plagnol, Kira M Holmström, et al.
Aging Cell|January 13, 2022
Disruption of ER-mitochondria tethering and signalling in C9orf72-associated amyotrophic lateral sclerosis and frontotemporal dementiaPatricia Gomez-Suaga, Gábor M Mórotz, Andrea Markovinovic, et al.
Neuron|March 19, 2013
Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levelsFernando Bartolome, Hsiu-Chuan Wu, Victoria S Burchell, et al.
Pageof 2