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Kinga Szigeti

Showing results (41-50 of 49) with videos related to

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Neurogenetics|August 25, 2007
Functional, histopathologic and natural history study of neuropathy associated with EGR2 mutationsKinga Szigeti, Wojciech Wiszniewski, Gulam Mustafa Saifi, et al.
Nature|June 19, 2007
Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4JClement Y Chow, Yanling Zhang, James J Dowling, et al.
Plos One|December 24, 2010
A rare myelin protein zero (MPZ) variant alters enhancer activity in vitro and in vivoAnthony Antonellis, Megan Y Dennis, Grzegorz Burzynski, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2026
Binary partitioning of human brain organization due to divergent human cytoskeletal evolutionNicolás Rosas, Ivanna Ihnatovych, Jack A Reeves, et al.
Ebiomedicine|August 21, 2020
CHRFAM7A: A human specific fusion gene, accounts for the translational gap for cholinergic strategies in Alzheimer's diseaseKinga Szigeti, Ivanna Ihnatovych, Barbara Birkaya, et al.
Ebiomedicine|July 30, 2023
Neuronal actin cytoskeleton gain of function in the human brainKinga Szigeti, Ivanna Ihnatovych, Nicolás Rosas, et al.
Ebiomedicine|April 3, 2024
CHRFAM7A diversifies human immune adaption through Ca<sup>2+</sup> signalling and actin cytoskeleton reorganizationKinga Szigeti, Ivanna Ihnatovych, Emily Notari, et al.
American Journal of Human Genetics|October 6, 2010
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathyHeather M McLaughlin, Reiko Sakaguchi, Cuiping Liu, et al.
Brain : a Journal of Neurology|May 23, 2006
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2Kristien Verhoeven, Kristl G Claeys, Stephan Züchner, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Neurogenetics|August 25, 2007
Functional, histopathologic and natural history study of neuropathy associated with EGR2 mutationsKinga Szigeti, Wojciech Wiszniewski, Gulam Mustafa Saifi, et al.
Nature|June 19, 2007
Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4JClement Y Chow, Yanling Zhang, James J Dowling, et al.
Plos One|December 24, 2010
A rare myelin protein zero (MPZ) variant alters enhancer activity in vitro and in vivoAnthony Antonellis, Megan Y Dennis, Grzegorz Burzynski, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2026
Binary partitioning of human brain organization due to divergent human cytoskeletal evolutionNicolás Rosas, Ivanna Ihnatovych, Jack A Reeves, et al.
Ebiomedicine|August 21, 2020
CHRFAM7A: A human specific fusion gene, accounts for the translational gap for cholinergic strategies in Alzheimer's diseaseKinga Szigeti, Ivanna Ihnatovych, Barbara Birkaya, et al.
Ebiomedicine|July 30, 2023
Neuronal actin cytoskeleton gain of function in the human brainKinga Szigeti, Ivanna Ihnatovych, Nicolás Rosas, et al.
Ebiomedicine|April 3, 2024
CHRFAM7A diversifies human immune adaption through Ca<sup>2+</sup> signalling and actin cytoskeleton reorganizationKinga Szigeti, Ivanna Ihnatovych, Emily Notari, et al.
American Journal of Human Genetics|October 6, 2010
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathyHeather M McLaughlin, Reiko Sakaguchi, Cuiping Liu, et al.
Brain : a Journal of Neurology|May 23, 2006
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2Kristien Verhoeven, Kristl G Claeys, Stephan Züchner, et al.
Pageof 5