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Christine R Kaneski

Showing results (1-10 of 21) with videos related to

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Molecular Genetics and Metabolism Reports|September 12, 2022
Generation of GLA-knockout human embryonic stem cell lines to model peripheral neuropathy in Fabry diseaseChristine R Kaneski, John A Hanover, Ulrike H Schueler Hoffman
Journal of the Neurological Sciences|March 17, 2007
The cerebral vasculopathy of Fabry diseaseDavid F Moore, Christine R Kaneski, Hasan Askari, et al.
Molecular Genetics and Metabolism Reports|July 5, 2022
Generation of an <i>in vitro</i> model for peripheral neuropathy in Fabry disease using CRISPR-Cas9 in the nociceptive dorsal root ganglion cell line 50B11Christine R Kaneski, John A Hanover, Ulrike H Schueler Hoffman
Annals of Neurology|February 6, 2009
Translational read-through of a nonsense mutation in ATP7A impacts treatment outcome in Menkes diseaseStephen G Kaler, Jingrong Tang, Anthony Donsante, et al.
Journal of Lipid Research|June 8, 2010
Use of lissamine rhodamine ceramide trihexoside as a functional assay for alpha-galactosidase A in intact cellsChristine R Kaneski, Raphael Schiffmann, Roscoe O Brady, et al.
Molecular Genetics and Metabolism|July 30, 2016
Development of a model system for neuronal dysfunction in Fabry diseaseChristine R Kaneski, Roscoe O Brady, John A Hanover, et al.
Molecular Genetics and Metabolism|July 24, 2007
Establishment and characterization of Fabry disease endothelial cells with an extended lifespanJin-Song Shen, Xing-Li Meng, Raphael Schiffmann, et al.
Investigative Ophthalmology & Visual Science|March 11, 2008
Isolated ocular disease is associated with decreased mucolipin-1 channel conductanceEhud Goldin, Rafael C Caruso, William Benko, et al.
Biochemical and Biophysical Research Communications|October 15, 2005
Improved intracellular delivery of glucocerebrosidase mediated by the HIV-1 TAT protein transduction domainKyun Oh Lee, Nga Luu, Christine R Kaneski, et al.
Human Genetics|July 26, 2005
Heightened stress response in primary fibroblasts expressing mutant eIF2B genes from CACH/VWM leukodystrophy patientsLiraz Kantor, Heather P Harding, David Ron, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Molecular Genetics and Metabolism Reports|September 12, 2022
Generation of GLA-knockout human embryonic stem cell lines to model peripheral neuropathy in Fabry diseaseChristine R Kaneski, John A Hanover, Ulrike H Schueler Hoffman
Journal of the Neurological Sciences|March 17, 2007
The cerebral vasculopathy of Fabry diseaseDavid F Moore, Christine R Kaneski, Hasan Askari, et al.
Molecular Genetics and Metabolism Reports|July 5, 2022
Generation of an <i>in vitro</i> model for peripheral neuropathy in Fabry disease using CRISPR-Cas9 in the nociceptive dorsal root ganglion cell line 50B11Christine R Kaneski, John A Hanover, Ulrike H Schueler Hoffman
Annals of Neurology|February 6, 2009
Translational read-through of a nonsense mutation in ATP7A impacts treatment outcome in Menkes diseaseStephen G Kaler, Jingrong Tang, Anthony Donsante, et al.
Journal of Lipid Research|June 8, 2010
Use of lissamine rhodamine ceramide trihexoside as a functional assay for alpha-galactosidase A in intact cellsChristine R Kaneski, Raphael Schiffmann, Roscoe O Brady, et al.
Molecular Genetics and Metabolism|July 30, 2016
Development of a model system for neuronal dysfunction in Fabry diseaseChristine R Kaneski, Roscoe O Brady, John A Hanover, et al.
Molecular Genetics and Metabolism|July 24, 2007
Establishment and characterization of Fabry disease endothelial cells with an extended lifespanJin-Song Shen, Xing-Li Meng, Raphael Schiffmann, et al.
Investigative Ophthalmology & Visual Science|March 11, 2008
Isolated ocular disease is associated with decreased mucolipin-1 channel conductanceEhud Goldin, Rafael C Caruso, William Benko, et al.
Biochemical and Biophysical Research Communications|October 15, 2005
Improved intracellular delivery of glucocerebrosidase mediated by the HIV-1 TAT protein transduction domainKyun Oh Lee, Nga Luu, Christine R Kaneski, et al.
Human Genetics|July 26, 2005
Heightened stress response in primary fibroblasts expressing mutant eIF2B genes from CACH/VWM leukodystrophy patientsLiraz Kantor, Heather P Harding, David Ron, et al.
Pageof 3