IJMS | Free Full-Text | Genomic Variability in the Survival Motor Neuron Genes (SMN1 and SMN2): Implications for Spinal Muscular Atrophy Phenotype and Therapeutics Development
Reduced Survival of Motor Neuron (SMN) Protein in Motor Neuronal Progenitors Functions Cell Autonomously to Cause Spinal Muscular Atrophy in Model Mice Expressing the Human Centromeric (SMN2) Gene | Journal of Neuroscience
SMA Awareness Month 1: What is SMA? – Bilkent UNAM iGEM Team
Copy Number Variations in the Survival Motor Neuron Genes: Implications for Spinal Muscular Atrophy and Other Neurodegenerative Diseases | Semantic Scholar
The Function of Survival Motor Neuron Complex and Its Role in Spinal Muscular Atrophy Pathogenesis - ScienceDirect
The many faces of SMN: deciphering the function critical to spinal muscular atrophy pathogenesis | Future Neurology
SMN1 and SMN2 contribute to spinal muscular atrophy (SMA). In healthy... | Download Scientific Diagram
Frontiers | The Need for SMN-Independent Treatments of Spinal Muscular Atrophy (SMA) to Complement SMN-Enhancing Drugs
Survival of motor neuron - Wikipedia
Survival Motor Neuron Protein 1 - an overview | ScienceDirect Topics
Spinal Muscular Atrophy as a Treatable Disease: Disease-Modifying Therapies Improving Clinical Outcomes and Quality of Life - Neurology Advisor
Spinal muscular atrophy | Nature Reviews Disease Primers
The survival of motor neuron gene (SMN) consists of 9 exons, with the... | Download Scientific Diagram
JCM | Free Full-Text | New Treatments in Spinal Muscular Atrophy: Positive Results and New Challenges
Spinal Muscular Atrophy Pathophysiology - Rare Disease Advisor
Converging Mechanisms of p53 Activation Drive Motor Neuron Degeneration in Spinal Muscular Atrophy - ScienceDirect
Discovery of Risdiplam, a Selective Survival of Motor Neuron-2 (SMN2) Gene Splicing Modifier for the Treatment of Spinal Muscular Atrophy (SMA) | Journal of Medicinal Chemistry
Spinal-Muscular-Atrophy – OrthoPaedia
Is Good Housekeeping the Key to Motor Neuron Survival?: Cell
Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick? | Nature Reviews Neuroscience
![PDF] Genomic Variability in the Survival Motor Neuron Genes (SMN1 and SMN2): Implications for Spinal Muscular Atrophy Phenotype and Therapeutics Development | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/e390febd3fb064f09c54d6166c7a143bbb17953b/5-Figure2-1.png "PDF] Genomic Variability in the Survival Motor Neuron Genes (SMN1 and SMN2): Implications for Spinal Muscular Atrophy Phenotype and Therapeutics Development | Semantic Scholar")
PDF] Genomic Variability in the Survival Motor Neuron Genes (SMN1 and SMN2): Implications for Spinal Muscular Atrophy Phenotype and Therapeutics Development | Semantic Scholar
Decreased function of survival motor neuron protein impairs endocytic pathways | PNAS
IJMS | Free Full-Text | Regulation of Survival Motor Neuron Gene Expression by Calcium Signaling
Spinal Muscular Atrophy: Causes, Symptoms Of This Genetic Disorder With World's Most Expensive Drug
Cell type diversity of requirement for survival motor neuron | Download Scientific Diagram
Biogen on X: "#SMA is caused by a mutation in the survival motor neuron 1 (SMN1) gene, which maintains the health and normal function of motor neurons. https://t.co/uUdVjujm9P" / X
