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Flavia C Nery

Showing results (1-10 of 14) with videos related to

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Neurology|August 26, 2018
Harnessing the power of the patient perspective for rare disease therapeuticsKathryn J Swoboda, Flavia C Nery
The FEBS Journal|August 2, 2006
Ki-1/57 interacts with PRMT1 and is a substrate for arginine methylationDario O Passos, Gustavo C Bressan, Flavia C Nery, et al.
Neurobiology of Disease|December 8, 2010
Molecular pathways in dystoniaD Cristopher Bragg, Ioanna A Armata, Flavia C Nery, et al.
Plos One|November 8, 2014
4-Phenylbutyrate attenuates the ER stress response and cyclic AMP accumulation in DYT1 dystonia cell modelsJin A Cho, Xuan Zhang, Gregory M Miller, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 13, 2007
Mutant torsinA interferes with protein processing through the secretory pathway in DYT1 dystonia cellsJeffrey W Hewett, Bakhos Tannous, Brian P Niland, et al.
Journal of Neuroscience Methods|June 1, 2014
Microfluidic platform to evaluate migration of cells from patients with DYT1 dystoniaFlavia C Nery, Nadia A Atai, Cintia C da Hora, et al.
Disease Models & Mechanisms|March 13, 2010
Chemical enhancement of torsinA function in cell and animal models of torsion dystoniaSongsong Cao, Jeffrey W Hewett, Fumiaki Yokoi, et al.
Human Molecular Genetics|June 30, 2010
The early-onset torsion dystonia-associated protein, torsinA, is a homeostatic regulator of endoplasmic reticulum stress responsePan Chen, Alexander J Burdette, J Christopher Porter, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
Cardiac defects in spinal muscular atrophy and the role of SMN in cardiomyocyte homeostasisReid Garner, Leillani L Ha, Flavia C Nery, et al.
Annals of Clinical and Translational Neurology|June 20, 2020
Whole-blood dysregulation of actin-cytoskeleton pathway in adult spinal muscular atrophy patientsJennifer J Siranosian, Flavia C Nery, Christiano R R Alves, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Neurology|August 26, 2018
Harnessing the power of the patient perspective for rare disease therapeuticsKathryn J Swoboda, Flavia C Nery
The FEBS Journal|August 2, 2006
Ki-1/57 interacts with PRMT1 and is a substrate for arginine methylationDario O Passos, Gustavo C Bressan, Flavia C Nery, et al.
Neurobiology of Disease|December 8, 2010
Molecular pathways in dystoniaD Cristopher Bragg, Ioanna A Armata, Flavia C Nery, et al.
Plos One|November 8, 2014
4-Phenylbutyrate attenuates the ER stress response and cyclic AMP accumulation in DYT1 dystonia cell modelsJin A Cho, Xuan Zhang, Gregory M Miller, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 13, 2007
Mutant torsinA interferes with protein processing through the secretory pathway in DYT1 dystonia cellsJeffrey W Hewett, Bakhos Tannous, Brian P Niland, et al.
Journal of Neuroscience Methods|June 1, 2014
Microfluidic platform to evaluate migration of cells from patients with DYT1 dystoniaFlavia C Nery, Nadia A Atai, Cintia C da Hora, et al.
Disease Models & Mechanisms|March 13, 2010
Chemical enhancement of torsinA function in cell and animal models of torsion dystoniaSongsong Cao, Jeffrey W Hewett, Fumiaki Yokoi, et al.
Human Molecular Genetics|June 30, 2010
The early-onset torsion dystonia-associated protein, torsinA, is a homeostatic regulator of endoplasmic reticulum stress responsePan Chen, Alexander J Burdette, J Christopher Porter, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
Cardiac defects in spinal muscular atrophy and the role of SMN in cardiomyocyte homeostasisReid Garner, Leillani L Ha, Flavia C Nery, et al.
Annals of Clinical and Translational Neurology|June 20, 2020
Whole-blood dysregulation of actin-cytoskeleton pathway in adult spinal muscular atrophy patientsJennifer J Siranosian, Flavia C Nery, Christiano R R Alves, et al.
Pageof 2