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Virginia Mattis
Virginia Mattis
Fujifilm Cellular Dynamics
Verified email at cshs.org
Title
Cited by
Cited by
Year
Induced pluripotent stem cells from a spinal muscular atrophy patient
AD Ebert, J Yu, FF Rose Jr, VB Mattis, CL Lorson, JA Thomson, ...
Nature 457 (7227), 277-280, 2009
19302009
Induced pluripotent stem cells from patients with Huntington's disease show CAG-repeat-expansion-associated phenotypes
Hd iPsc Consortium
Cell stem cell 11 (2), 264-278, 2012
4822012
Developmental alterations in Huntington's disease neural cells and pharmacological rescue in cells and mice
Nature neuroscience 20 (5), 648-660, 2017
1832017
A non-sequence-specific requirement for SMN protein activity: the role of aminoglycosides in inducing elevated SMN protein levels
EC Wolstencroft, V Mattis, AA Bajer, PJ Young, CL Lorson
Human Molecular Genetics 14 (9), 1199-1210, 2005
1632005
Delivery of recombinant follistatin lessens disease severity in a mouse model of spinal muscular atrophy
FF Rose Jr, VB Mattis, H Rindt, CL Lorson
Human molecular genetics 18 (6), 997-1005, 2009
1372009
Induced pluripotent stem cells: a new revolution for clinical neurology?
VB Mattis, CN Svendsen
The Lancet Neurology 10 (4), 383-394, 2011
1312011
Targeting ATM ameliorates mutant Huntingtin toxicity in cell and animal models of Huntington’s disease
XH Lu, VB Mattis, N Wang, I Al-Ramahi, N van den Berg, SA Fratantoni, ...
Science translational medicine 6 (268), 268ra178-268ra178, 2014
1272014
EZ spheres: a stable and expandable culture system for the generation of pre-rosette multipotent stem cells from human ESCs and iPSCs
AD Ebert, BC Shelley, AM Hurley, M Onorati, V Castiglioni, TN Patitucci, ...
Stem cell research 10 (3), 417-427, 2013
1232013
Novel aminoglycosides increase SMN levels in spinal muscular atrophy fibroblasts
VB Mattis, R Rai, J Wang, CWT Chang, T Coady, CL Lorson
Human genetics 120, 589-601, 2006
1202006
HD iPSC-derived neural progenitors accumulate in culture and are susceptible to BDNF withdrawal due to glutamate toxicity
VB Mattis, C Tom, S Akimov, J Saeedian, ME Østergaard, AL Southwell, ...
Human molecular genetics 24 (11), 3257-3271, 2015
1192015
Delivery of a read-through inducing compound, TC007, lessens the severity of a spinal muscular atrophy animal model
VB Mattis, AD Ebert, MY Fosso, CW Chang, CL Lorson
Human molecular genetics 18 (20), 3906-3913, 2009
1132009
Human Huntington’s disease iPSC-derived cortical neurons display altered transcriptomics, morphology, and maturation
SR Mehta, CM Tom, Y Wang, C Bresee, D Rushton, PP Mathkar, J Tang, ...
Cell reports 25 (4), 1081-1096. e6, 2018
952018
Huntington’s disease patient-derived astrocytes display electrophysiological impairments and reduced neuronal support
VJ Garcia, DJ Rushton, CM Tom, ND Allen, PJ Kemp, CN Svendsen, ...
Frontiers in neuroscience 13, 669, 2019
562019
A SMNΔ7 read-through product confers functionality to the SMNΔ7 protein
VB Mattis, M Bowerman, R Kothary, CL Lorson
Neuroscience letters 442 (1), 54-58, 2008
502008
Modeling Huntington׳ s disease with patient-derived neurons
VB Mattis, CN Svendsen
Brain Research 1656, 76-87, 2017
472017
Bioenergetic deficits in Huntington’s disease iPSC-derived neural cells and rescue with glycolytic metabolites
Human molecular genetics 29 (11), 1757-1771, 2020
402020
A patient-derived cellular model for Huntington’s disease reveals phenotypes at clinically relevant CAG lengths
CLK Hung, T Maiuri, LE Bowie, R Gotesman, S Son, M Falcone, ...
Molecular Biology of the Cell 29 (23), 2809-2820, 2018
372018
Neonatal immune-tolerance in mice does not prevent xenograft rejection
VB Mattis, DR Wakeman, C Tom, HB Dodiya, SY Yeung, AH Tran, ...
Experimental neurology 254, 90-98, 2014
372014
Subcutaneous administration of TC007 reduces disease severity in an animal model of SMA
VB Mattis, MY Fosso, CW Chang, CL Lorson
BMC neuroscience 10, 1-6, 2009
352009
Optimizing maturity and dose of iPSC-derived dopamine progenitor cell therapy for Parkinson’s disease
BM Hiller, DJ Marmion, CA Thompson, NA Elliott, H Federoff, P Brundin, ...
NPJ Regenerative medicine 7 (1), 24, 2022
342022
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