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NMDA receptors are upregulated and trafficked to the plasma membrane after sigma-1 receptor activation in the rat hippocampus

The Journal of neuroscience, 2014-08, Vol.34 (34), p.11325-11338

2014

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Differential effects of N -acetyl-aspartyl-glutamate on synaptic and extrasynaptic NMDA receptors are subunit- and pH-dependent in the CA1 region of the mouse hippocampus

Neurobiology of disease, 2015-10, Vol.82, p.580-592

2015

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PRMT inhibitor promotes SMN2 exon 7 inclusion and synergizes with nusinersen to rescue SMA mice

EMBO molecular medicine, 2023-11, Vol.15 (11), p.e17683-e17683

2023

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Aberrant Subcellular Dynamics of Sigma-1 Receptor Mutants Underlying Neuromuscular Diseases

Molecular pharmacology, 2016-09, Vol.90 (3), p.238-253

2016

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Muscle overexpression of Klf15 via an AAV8-Spc5-12 construct does not provide benefits in spinal muscular atrophy mice

Gene therapy, 2019-11, Vol.27 (10-11), p.505-515

2019

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Non-uniform dystrophin re-expression after CRISPR-mediated exon excision in the dystrophin/utrophin double-knockout mouse model of DMD

Molecular therapy. Nucleic acids, 2022-12, Vol.30, p.379-397

2022

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Antibody-oligonucleotide conjugate achieves CNS delivery in animal models for spinal muscular atrophy

JCI insight, 2022-12, Vol.7 (24)

2022

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Glycine-induced NMDA receptor internalization provides neuroprotection and preserves vasculature following ischemic stroke

iScience, 2022-01, Vol.25 (1), p.103539-103539, Article 103539

2022

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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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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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Plasminogen is a critical regulator of cutaneous wound healing

Thrombosis and haemostasis, 2016, Vol.115 (5), p.1001-1009

2016

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Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1G93A amyotrophic lateral sclerosis

Skeletal muscle, 2024-10, Vol.14 (1)

2024

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Light modulation ameliorates expression of circadian genes and disease progression in spinal muscular atrophy mice

Human molecular genetics, 2018-10, Vol.27 (20), p.3582-3597

2018

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Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1G93A amyotrophic lateral sclerosis (ALS) mouse model

Skeletal muscle, 2024-10, Vol.14 (1), p.23, Article 23

2024

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Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1 G93A amyotrophic lateral sclerosis (ALS) mouse model

Skeletal muscle, 2024-10, Vol.14 (1), p.23

2024

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Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1 G93A amyotrophic lateral sclerosis (ALS) mouse model

Skeletal muscle, 2024-10, Vol.14 (1), p.1-24

2024

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Exon skipping induces uniform dystrophin rescue with dose-dependent restoration of serum miRNA biomarkers and muscle biophysical properties

Molecular therapy. Nucleic acids, 2022-09, Vol.29, p.955-968

2022

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Expression and Localization of the Serine Proteases High-Temperature Requirement Factor A1, Serine Protease 23, and Serine Protease 35 in the Mouse Ovary

Endocrinology (Philadelphia), 2008-10, Vol.149 (10), p.5070-5077

2008

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Multivalent sialic acid conjugates inhibit adenovirus type 37 from binding to and infecting human corneal epithelial cells

Antiviral research, 2007-02, Vol.73 (2), p.92-100

2007

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Expression and Localization of the Serine Proteases High-Temperature Requirement Factor Al, Serine Protease 23, and Serine Protease 35 in the Mouse Ovary

Endocrinology (Philadelphia), 2008, Vol.149 (10), p.5070-5077

2008

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En komparativ förståelse av ämnesdidaktiska prepositioner

Nordidactica, 2019 (2019:3), p.45

2019

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Inspiring self-reflective dialogues through aesthetic learning processes: Learning by drawing

Developing a Didactic Framework Across and Beyond School Subjects, 2024, p.131-143

1, 2024

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Genomic organization and promoter analysis of the human heat shock factor 2 gene

Cell stress & chaperones, 2001-10, Vol.6 (4), p.377-385

2001

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NMDA receptors are upregulated and trafficked to the plasma membrane after sigma-1 receptor activation in the rat hippocampus

Differential effects of N -acetyl-aspartyl-glutamate on synaptic and extrasynaptic NMDA receptors are subunit- and pH-dependent in the CA1 region of the mouse hippocampus

PRMT inhibitor promotes SMN2 exon 7 inclusion and synergizes with nusinersen to rescue SMA mice

Aberrant Subcellular Dynamics of Sigma-1 Receptor Mutants Underlying Neuromuscular Diseases

Muscle overexpression of Klf15 via an AAV8-Spc5-12 construct does not provide benefits in spinal muscular atrophy mice

Non-uniform dystrophin re-expression after CRISPR-mediated exon excision in the dystrophin/utrophin double-knockout mouse model of DMD

Antibody-oligonucleotide conjugate achieves CNS delivery in animal models for spinal muscular atrophy

Glycine-induced NMDA receptor internalization provides neuroprotection and preserves vasculature following ischemic stroke

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

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

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

Plasminogen is a critical regulator of cutaneous wound healing

Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1G93A amyotrophic lateral sclerosis

Light modulation ameliorates expression of circadian genes and disease progression in spinal muscular atrophy mice

Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1G93A amyotrophic lateral sclerosis (ALS) mouse model

Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1 G93A amyotrophic lateral sclerosis (ALS) mouse model

Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1 G93A amyotrophic lateral sclerosis (ALS) mouse model

Exon skipping induces uniform dystrophin rescue with dose-dependent restoration of serum miRNA biomarkers and muscle biophysical properties

Expression and Localization of the Serine Proteases High-Temperature Requirement Factor A1, Serine Protease 23, and Serine Protease 35 in the Mouse Ovary

Multivalent sialic acid conjugates inhibit adenovirus type 37 from binding to and infecting human corneal epithelial cells

Expression and Localization of the Serine Proteases High-Temperature Requirement Factor Al, Serine Protease 23, and Serine Protease 35 in the Mouse Ovary

En komparativ förståelse av ämnesdidaktiska prepositioner

Inspiring self-reflective dialogues through aesthetic learning processes: Learning by drawing

Genomic organization and promoter analysis of the human heat shock factor 2 gene

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