The mechanism of myotonic dystrophy

[Progressive myoclonic epilepsy in the department of neurology of the University Teaching hospital Point "G"].

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Mifepristone-inducible transgene expression in neural progenitor cells in vitro and in vivo.

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Spinal and bulbar muscular atrophy: pathogenesis and clinical management.

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Dominant GDAP1 mutations cause predominantly mild CMT phenotypes.

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Clinical and genetic analysis of spinocerebellar ataxia in Mali.

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[A transferable "Myasthenogenic" factor in the serum of patients with myasthenia gravis.].

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Challenges in Studying Synapses in Alzheimer's Disease.

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Associations between Pre-Disease Biomarkers of Persistent Organic Pollutants and Amyotrophic Lateral Sclerosis Survival in the Danish Diet, Cancer and Health Study Cohort.

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Cross-Sectional and Longitudinal Diagnostic Performance of Plasma p-tau217 and p-tau217/Aβ42 in Alzheimer's Disease.

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Blood SOD1 Activity in ALS Patients Receiving Tofersen Treatment.

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Outcomes of Intra-Arterial Tenecteplase after Endovascular Reperfusion for Acute Ischemic Stroke Due to Cardioembolism and Non-Cardioembolism: A Secondary Analysis of the POST-TNK Trial.

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A Human Gait Circuit Derived from Brain Lesions and Deep Brain Stimulation.

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Impact of Concomitant Grade I Degenerative Spondylolisthesis on Clinical and Radiographic Outcomes Following Biportal Endoscopic versus Microscopic Laminectomy for Lumbar Spinal Stenosis: A Post Hoc Analysis of a Multicenter Randomized Clinical Trial.

Global spine journal·2026

HMGB1-targeted anti-inflammatory rBox A gene therapy for viral airway infections and systemic inflammatory disease models.

mBio·2026

Mesenchymal Stem Cell Secretome Mitigates Inflammatory Endothelial Dysfunction.

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An Asymmetric Magnetic Hydrogel With Mild Magnetothermal Effect for Safe and Efficient Bone Repair.

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Dual-gene regulation of NGF overexpression and P75NTR knockdown enhances BMSC osteogenesis by suppressing pyroptosis.

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Automated Standardization of the Shear-wave Elastography Effective Region Using DeepLabV3 Improves Malignancy Assessment in Thyroid Nodules: A Single-institution Multicampus Study.

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Related Experiment Videos

The mechanism of myotonic dystrophy

Related Concept Videos

[Progressive myoclonic epilepsy in the department of neurology of the University Teaching hospital Point "G"].

Mifepristone-inducible transgene expression in neural progenitor cells in vitro and in vivo.

Spinal and bulbar muscular atrophy: pathogenesis and clinical management.

Dominant GDAP1 mutations cause predominantly mild CMT phenotypes.

Clinical and genetic analysis of spinocerebellar ataxia in Mali.

[A transferable "Myasthenogenic" factor in the serum of patients with myasthenia gravis.].

Challenges in Studying Synapses in Alzheimer's Disease.

Associations between Pre-Disease Biomarkers of Persistent Organic Pollutants and Amyotrophic Lateral Sclerosis Survival in the Danish Diet, Cancer and Health Study Cohort.

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The mechanism of myotonic dystrophy

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