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Virginia B Mattis

Showing results (21-30 of 30) with videos related to

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NPJ Regenerative Medicine|April 22, 2022
Optimizing maturity and dose of iPSC-derived dopamine progenitor cell therapy for Parkinson's diseaseBenjamin M Hiller, David J Marmion, Cayla A Thompson, et al.
Cell Transplantation|July 11, 2015
In Vivo Tracking of Human Neural Progenitor Cells in the Rat Brain Using Magnetic Resonance Imaging Is Not Enhanced by Ferritin ExpressionKsenija Bernau, Christina M Lewis, Anna M Petelinsek, et al.
Frontiers in Aging Neuroscience|November 16, 2020
The Interaction of Aging and Cellular Stress Contributes to Pathogenesis in Mouse and Human Huntington Disease NeuronsEmily Machiela, Ritika Jeloka, Nicholas S Caron, et al.
Experimental Neurology|January 21, 2014
Neonatal immune-tolerance in mice does not prevent xenograft rejectionVirginia B Mattis, Dustin R Wakeman, Colton Tom, et al.
Scientific Reports|March 26, 2021
The difficulty to model Huntington's disease in vitro using striatal medium spiny neurons differentiated from human induced pluripotent stem cellsKim Le Cann, Alec Foerster, Corinna Rösseler, et al.
Stem Cell Reports|May 1, 2018
Inducible Expression of GDNF in Transplanted iPSC-Derived Neural Progenitor CellsAslam Abbasi Akhtar, Genevieve Gowing, Naomi Kobritz, et al.
Stem Cell Research|March 12, 2013
EZ spheres: a stable and expandable culture system for the generation of pre-rosette multipotent stem cells from human ESCs and iPSCsAllison D Ebert, Brandon C Shelley, Amanda M Hurley, et al.
Human Molecular Genetics|March 6, 2015
HD iPSC-derived neural progenitors accumulate in culture and are susceptible to BDNF withdrawal due to glutamate toxicityVirginia B Mattis, Colton Tom, Sergey Akimov, et al.
Molecular Therapy. Nucleic Acids|July 8, 2024
<i>CircHTT(2,3,4,5,6)</i> <i>-</i> co-evolving with the <i>HTT</i> CAG-repeat tract - modulates Huntington's disease phenotypesJasmin Morandell, Alan Monziani, Martina Lazioli, et al.
Science Translational Medicine|December 26, 2014
Targeting ATM ameliorates mutant Huntingtin toxicity in cell and animal models of Huntington's diseaseXiao-Hong Lu, Virginia B Mattis, Nan Wang, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
NPJ Regenerative Medicine|April 22, 2022
Optimizing maturity and dose of iPSC-derived dopamine progenitor cell therapy for Parkinson's diseaseBenjamin M Hiller, David J Marmion, Cayla A Thompson, et al.
Cell Transplantation|July 11, 2015
In Vivo Tracking of Human Neural Progenitor Cells in the Rat Brain Using Magnetic Resonance Imaging Is Not Enhanced by Ferritin ExpressionKsenija Bernau, Christina M Lewis, Anna M Petelinsek, et al.
Frontiers in Aging Neuroscience|November 16, 2020
The Interaction of Aging and Cellular Stress Contributes to Pathogenesis in Mouse and Human Huntington Disease NeuronsEmily Machiela, Ritika Jeloka, Nicholas S Caron, et al.
Experimental Neurology|January 21, 2014
Neonatal immune-tolerance in mice does not prevent xenograft rejectionVirginia B Mattis, Dustin R Wakeman, Colton Tom, et al.
Scientific Reports|March 26, 2021
The difficulty to model Huntington's disease in vitro using striatal medium spiny neurons differentiated from human induced pluripotent stem cellsKim Le Cann, Alec Foerster, Corinna Rösseler, et al.
Stem Cell Reports|May 1, 2018
Inducible Expression of GDNF in Transplanted iPSC-Derived Neural Progenitor CellsAslam Abbasi Akhtar, Genevieve Gowing, Naomi Kobritz, et al.
Stem Cell Research|March 12, 2013
EZ spheres: a stable and expandable culture system for the generation of pre-rosette multipotent stem cells from human ESCs and iPSCsAllison D Ebert, Brandon C Shelley, Amanda M Hurley, et al.
Human Molecular Genetics|March 6, 2015
HD iPSC-derived neural progenitors accumulate in culture and are susceptible to BDNF withdrawal due to glutamate toxicityVirginia B Mattis, Colton Tom, Sergey Akimov, et al.
Molecular Therapy. Nucleic Acids|July 8, 2024
<i>CircHTT(2,3,4,5,6)</i> <i>-</i> co-evolving with the <i>HTT</i> CAG-repeat tract - modulates Huntington's disease phenotypesJasmin Morandell, Alan Monziani, Martina Lazioli, et al.
Science Translational Medicine|December 26, 2014
Targeting ATM ameliorates mutant Huntingtin toxicity in cell and animal models of Huntington's diseaseXiao-Hong Lu, Virginia B Mattis, Nan Wang, et al.
Pageof 3