F. Vieira

发表

Design, power, and interpretation of studies in the standard murine model of ALS

J. E. Kranz, J. Heywood, A. Bostrom, 2008, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Hypothesis and Theory: Roles of Arginine Methylation in C9orf72-Mediated ALS and FTD

F. Vieira, Anna L. Gill, A. Premasiri, 2021, Frontiers in Cellular Neuroscience.

CuATSM efficacy is independently replicated in a SOD1 mouse model of ALS while unmetallated ATSM therapy fails to reveal benefits

S. Perrin, K. Thompson, F. Vieira, 2017, IBRO reports.

ALSUntangled 38: L-serine

Gary L. Pattee, R. Conwit, J. Licht, 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.

ALSUntangled No. 36: Accilion

R. Conwit, J. Licht, P. Andersen, 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Type I PRMT Inhibition Protects Against C9ORF72 Arginine-Rich Dipeptide Repeat Toxicity

F. Vieira, Anna L. Gill, A. Premasiri, 2020, bioRxiv.

SOD1-positive aggregate accumulation in the CNS predicts slower disease progression and increased longevity in a mutant SOD1 mouse model of ALS

J. Grimm, K. Thompson, F. Vieira, 2019, Scientific Reports.

Phase IIa trial of fingolimod for amyotrophic lateral sclerosis demonstrates acceptable acute safety and tolerability

S. Paganoni, S. Perrin, J. Berry, 2017, Muscle & nerve.

Dexpramipexole Is Ineffective in Two Models of ALS Related Neurodegeneration

S. Finkbeiner, S. Perrin, K. Thompson, 2014, PloS one.

A human-derived antibody targets misfolded SOD1 and ameliorates motor symptoms in mouse models of amyotrophic lateral sclerosis

S. Perrin, R. Nitsch, C. Hock, 2018, Science Translational Medicine.

A Quick Phenotypic Neurological Scoring System for Evaluating Disease Progression in the SOD1-G93A Mouse Model of ALS.

K. Thompson, F. Vieira, T. Hatzipetros, 2015, Journal of visualized experiments : JoVE.

Guidelines for preclinical animal research in ALS/MND: A consensus meeting

Albert C. Ludolph, Linda Greensmith, Heiko G. Niessen, 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Proteomic Analysis Reveals Differentially Regulated Protein Acetylation in Human Amyotrophic Lateral Sclerosis Spinal Cord

Han-Pil Choi, Z. Fei, N. Kowall, 2013, PloS one.

Degeneration of proprioceptive sensory nerve endings in mice harboring amyotrophic lateral sclerosis–causing mutations

F. Vieira, Gregorio Valdez, T. Hatzipetros, 2015, The Journal of comparative neurology.

From transcriptome analysis to therapeutic anti-CD40L treatment in the SOD1 model of amyotrophic lateral sclerosis

S. Perrin, J. Lincecum, K. Thompson, 2010, Nature Genetics.

C57BL/6J congenic Prp-TDP43A315T mice develop progressive neurodegeneration in the myenteric plexus of the colon without exhibiting key features of ALS

Crystal Davis, Cathleen Lutz, S. Perrin, 2014, Brain Research.

Consumer-grade wearables and machine learning sensitively capture disease progression in amyotrophic lateral sclerosis

F. Vieira, A. Premasiri, A. S. Gupta, 2023, medRxiv.

No Benefit from Chronic Lithium Dosing in a Sibling-Matched, Gender Balanced, Investigator-Blinded Trial Using a Standard Mouse Model of Familial ALS

S. Perrin, K. Thompson, F. Vieira, 2009, PloS one.

The ALS-inducing factors, TDP43A315T and SOD1G93A, directly affect and sensitize sensory neurons to stress

F. Vieira, Gregorio Valdez, T. Hatzipetros, 2018, Scientific Reports.

Primary Neurons and Differentiated NSC-34 Cells Are More Susceptible to Arginine-Rich ALS Dipeptide Repeat Protein-Associated Toxicity than Non-Differentiated NSC-34 and CHO Cells

F. Vieira, Beth Levine, Monica Z. Wang, 2019, International journal of molecular sciences.

Guanabenz Treatment Accelerates Disease in a Mutant SOD1 Mouse Model of ALS

S. Perrin, B. Jiang, J. Lincecum, 2015, PloS one.

A machine-learning based objective measure for ALS disease severity

Michael P. Brenner, A. Jansen, Kevin McCloskey, 2022, npj Digital Medicine.

Reduced C9orf72 expression exacerbates polyGR toxicity in patient iPSC-derived motor neurons and a Type I protein arginine methyltransferase inhibitor reduces that toxicity

F. Vieira, Anna L. Gill, Kyle R. Denton, 2023, Frontiers in Cellular Neuroscience.

ALSUntangled No. 34: GM604.

Gary L. Pattee, R. Conwit, J. Licht, 2016, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Degeneration of proprioceptive sensory nerve endings in mice harboring amyotrophic lateral sclerosis–causing mutations

F. Vieira, Gregorio Valdez, T. Hatzipetros, 2015, The Journal of comparative neurology.

Design, power, and interpretation of studies in the standard murine model of ALS

J. E. Kranz, J. Heywood, A. Bostrom, 2008, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

PERK modulation, with GSK2606414, Sephin1 or salubrinal, failed to produce therapeutic benefits in the SOD1G93A mouse model of ALS

K. Thompson, F. Vieira, Valerie R. Tassinari, 2023, bioRxiv.

ALSUntangled No. 36: Accilion

Gary L. Pattee, R. Conwit, J. Licht, 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.

At-home wearables and machine learning sensitively capture disease progression in amyotrophic lateral sclerosis

Anoopum S. Gupta, F. Vieira, A. Premasiri, 2023, Nature communications.