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Aleksandar Rakovic

Showing results (11-20 of 46) with videos related to

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Human Molecular Genetics|May 29, 2010
Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patientsAleksandar Rakovic, Anne Grünewald, Philip Seibler, et al.
Neurobiology of Aging|February 3, 2012
ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndromeAnne Grünewald, Björn Arns, Philip Seibler, et al.
Frontiers in Cellular Neuroscience|April 11, 2022
Electrophysiological Properties of Induced Pluripotent Stem Cell-Derived Midbrain Dopaminergic Neurons Correlate With Expression of Tyrosine HydroxylaseAleksandar Rakovic, Dorothea Voß, Franca Vulinovic, et al.
Parkinsonism & Related Disorders|February 5, 2020
Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency?Julien F Bally, David P Breen, Susen Schaake, et al.
Cell Death and Differentiation|October 31, 2018
PINK1-dependent mitophagy is driven by the UPS and can occur independently of LC3 conversionAleksandar Rakovic, Jonathan Ziegler, Christoph U Mårtensson, et al.
Cell Death & Disease|June 5, 2026
Selective vulnerability of dopaminergic neurons in Parkinson's disease connects PRKN and differential expression of CHCHD2 and GPNMBFranca Vulinovic, Arian Hach, Zied Landoulsi, et al.
EMBO Molecular Medicine|September 26, 2018
USP14 inhibition corrects an <i>in vivo</i> model of impaired mitophagyJoy Chakraborty, Sophia von Stockum, Elena Marchesan, et al.
International Journal of Molecular Sciences|September 9, 2022
Mutant WDR45 Leads to Altered Ferritinophagy and Ferroptosis in β-Propeller Protein-Associated NeurodegenerationSokhna Haissatou Diaw, Christos Ganos, Simone Zittel, et al.
Brain : a Journal of Neurology|September 1, 2018
Iron overload is accompanied by mitochondrial and lysosomal dysfunction in WDR45 mutant cellsPhilip Seibler, Lena F Burbulla, Marija Dulovic, et al.
Science Advances|March 11, 2022
H-ABC- and dystonia-causing <i>TUBB4A</i> mutations show distinct pathogenic effectsVictor Krajka, Franca Vulinovic, Mariya Genova, et al.
Pageof 5

Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|May 29, 2010
Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patientsAleksandar Rakovic, Anne Grünewald, Philip Seibler, et al.
Neurobiology of Aging|February 3, 2012
ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndromeAnne Grünewald, Björn Arns, Philip Seibler, et al.
Frontiers in Cellular Neuroscience|April 11, 2022
Electrophysiological Properties of Induced Pluripotent Stem Cell-Derived Midbrain Dopaminergic Neurons Correlate With Expression of Tyrosine HydroxylaseAleksandar Rakovic, Dorothea Voß, Franca Vulinovic, et al.
Parkinsonism & Related Disorders|February 5, 2020
Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency?Julien F Bally, David P Breen, Susen Schaake, et al.
Cell Death and Differentiation|October 31, 2018
PINK1-dependent mitophagy is driven by the UPS and can occur independently of LC3 conversionAleksandar Rakovic, Jonathan Ziegler, Christoph U Mårtensson, et al.
Cell Death & Disease|June 5, 2026
Selective vulnerability of dopaminergic neurons in Parkinson's disease connects PRKN and differential expression of CHCHD2 and GPNMBFranca Vulinovic, Arian Hach, Zied Landoulsi, et al.
EMBO Molecular Medicine|September 26, 2018
USP14 inhibition corrects an <i>in vivo</i> model of impaired mitophagyJoy Chakraborty, Sophia von Stockum, Elena Marchesan, et al.
International Journal of Molecular Sciences|September 9, 2022
Mutant WDR45 Leads to Altered Ferritinophagy and Ferroptosis in β-Propeller Protein-Associated NeurodegenerationSokhna Haissatou Diaw, Christos Ganos, Simone Zittel, et al.
Brain : a Journal of Neurology|September 1, 2018
Iron overload is accompanied by mitochondrial and lysosomal dysfunction in WDR45 mutant cellsPhilip Seibler, Lena F Burbulla, Marija Dulovic, et al.
Science Advances|March 11, 2022
H-ABC- and dystonia-causing <i>TUBB4A</i> mutations show distinct pathogenic effectsVictor Krajka, Franca Vulinovic, Mariya Genova, et al.
Pageof 5