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Recent Advances and Future Perspectives in the Development of Therapeutic Approaches for Neurodegenerative Diseases

Brain sciences, 2020-09, Vol.10 (9), p.633

Bowerman, Melissa

2020

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Spinal muscular atrophy: antisense oligonucleotide therapy opens the door to an integrated therapeutic landscape

Human molecular genetics, 2017-10, Vol.26 (R2), p.R151-R159

2017

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Systemic peptide-mediated oligonucleotide therapy improves long-term survival in spinal muscular atrophy

Proceedings of the National Academy of Sciences - PNAS, 2016-09, Vol.113 (39), p.10962-10967

2016

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Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy

BMC medicine, 2012-03, Vol.10 (1), p.24-24, Article 24

2012

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Therapeutic strategies for spinal muscular atrophy: SMN and beyond

Disease models & mechanisms, 2017-08, Vol.10 (8), p.943-954

2017

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The cross-linguistic categorization of everyday events: A study of cutting and breaking

Cognition, 2008-11, Vol.109 (2), p.235-250

2008

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Can language restructure cognition? The case for space

Trends in cognitive sciences, 2004-03, Vol.8 (3), p.108-114

2004

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Differential effect of Fas activation on spinal muscular atrophy motoneuron death and induction of axonal growth

Cellular and Molecular Biology, 2023-10, Vol.69 (10), p.1-8

2023

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The Relationship between Body Composition, Fatty Acid Metabolism and Diet in Spinal Muscular Atrophy

Brain sciences, 2021-01, Vol.11 (2), p.131

2021

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Abnormal fatty acid metabolism is a core component of spinal muscular atrophy

Annals of clinical and translational neurology, 2019-08, Vol.6 (8), p.1519-1532

2019

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An Induced Pluripotent Stem Cell-Derived Human Blood–Brain Barrier (BBB) Model to Test the Crossing by Adeno-Associated Virus (AAV) Vectors and Antisense Oligonucleotides

Biomedicines, 2023-10, Vol.11 (10), p.2700

2023

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KCC3 loss-of-function contributes to Andermann syndrome by inducing activity-dependent neuromuscular junction defects

Neurobiology of disease, 2017-10, Vol.106, p.35-48

2017

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Targeting the 5′ untranslated region of SMN2 as a therapeutic strategy for spinal muscular atrophy

Molecular therapy. Nucleic acids, 2021-03, Vol.23, p.731-742

2021

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Dysregulation of Tweak and Fn14 in skeletal muscle of spinal muscular atrophy mice

Skeletal muscle, 2022-07, Vol.12 (1), p.1-18, Article 18

2022

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Rho-kinase inactivation prolongs survival of an intermediate SMA mouse model

Human molecular genetics, 2010-04, Vol.19 (8), p.1468-1478

2010

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Funding for spinal muscular atrophy research must continue

Future neurology, 2019-05, Vol.14 (2)

Bowerman, Melissa

2019

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Multi-Study Proteomic and Bioinformatic Identification of Molecular Overlap between Amyotrophic Lateral Sclerosis (ALS) and Spinal Muscular Atrophy (SMA)

Brain sciences, 2018-12, Vol.8 (12), p.212

2018

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Combining multiomics and drug perturbation profiles to identify muscle-specific treatments for spinal muscular atrophy

JCI insight, 2021-07, Vol.6 (13)

2021

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A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathology

Neuromuscular disorders : NMD, 2012-03, Vol.22 (3), p.263-276

2012

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The semantic categories of cutting and breaking events: A crosslinguistic perspective

Cognitive linguistics, 2007-01, Vol.18 (2), p.133-152

2007

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Smn depletion alters profilin II expression and leads to upregulation of the RhoA/ROCK pathway and defects in neuronal integrity

Journal of molecular neuroscience, 2007-05, Vol.32 (2), p.120-131

2007

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A Single Amino Acid Residue Regulates PTEN-Binding and Stability of the Spinal Muscular Atrophy Protein SMN

Cells (Basel, Switzerland), 2020-11, Vol.9 (11), p.2405

2020

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Learning to express motion events in English and Korean: The influence of language-specific lexicalization patterns

Cognition, 1991-12, Vol.41 (1), p.83-121

1991

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SMN, profilin IIa and plastin 3: A link between the deregulation of actin dynamics and SMA pathogenesis

Molecular and cellular neuroscience, 2009-08, Vol.42 (1), p.66-74

2009

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Recent Advances and Future Perspectives in the Development of Therapeutic Approaches for Neurodegenerative Diseases

Spinal muscular atrophy: antisense oligonucleotide therapy opens the door to an integrated therapeutic landscape

Systemic peptide-mediated oligonucleotide therapy improves long-term survival in spinal muscular atrophy

Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy

Therapeutic strategies for spinal muscular atrophy: SMN and beyond

The cross-linguistic categorization of everyday events: A study of cutting and breaking

Can language restructure cognition? The case for space

Differential effect of Fas activation on spinal muscular atrophy motoneuron death and induction of axonal growth

The Relationship between Body Composition, Fatty Acid Metabolism and Diet in Spinal Muscular Atrophy

Abnormal fatty acid metabolism is a core component of spinal muscular atrophy

An Induced Pluripotent Stem Cell-Derived Human Blood–Brain Barrier (BBB) Model to Test the Crossing by Adeno-Associated Virus (AAV) Vectors and Antisense Oligonucleotides

KCC3 loss-of-function contributes to Andermann syndrome by inducing activity-dependent neuromuscular junction defects

Targeting the 5′ untranslated region of SMN2 as a therapeutic strategy for spinal muscular atrophy

Dysregulation of Tweak and Fn14 in skeletal muscle of spinal muscular atrophy mice

Rho-kinase inactivation prolongs survival of an intermediate SMA mouse model

Funding for spinal muscular atrophy research must continue

Interventions Targeting Glucocorticoid-Krüppel-like Factor 15-Branched-Chain Amino Acid Signaling Improve Disease Phenotypes in Spinal Muscular Atrophy Mice

Multi-Study Proteomic and Bioinformatic Identification of Molecular Overlap between Amyotrophic Lateral Sclerosis (ALS) and Spinal Muscular Atrophy (SMA)

Combining multiomics and drug perturbation profiles to identify muscle-specific treatments for spinal muscular atrophy

A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathology

The semantic categories of cutting and breaking events: A crosslinguistic perspective

Smn depletion alters profilin II expression and leads to upregulation of the RhoA/ROCK pathway and defects in neuronal integrity

A Single Amino Acid Residue Regulates PTEN-Binding and Stability of the Spinal Muscular Atrophy Protein SMN

Learning to express motion events in English and Korean: The influence of language-specific lexicalization patterns

SMN, profilin IIa and plastin 3: A link between the deregulation of actin dynamics and SMA pathogenesis

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