A spinal muscular atrophy modifier implicates the SMN protein in SNARE complex assembly at neuromuscular synapses

Παρόμοια τεκμήρια

• The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn-/- mice and results in a mouse with spinal muscular atrophy
  από: Umrao R. Monani
  Έκδοση: (2000)
• 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
  από: Park, Gyu-Hwan, κ.ά.
  Έκδοση: (2010)
• Muscle-specific SMN reduction reveals motor neuron–independent disease in spinal muscular atrophy models
  από: Jeong-Ki Kim, κ.ά.
  Έκδοση: (2020)
• Emerging concepts underlying selective neuromuscular dysfunction in infantile-onset spinal muscular atrophy
  από: Gollapalli, Kishore, κ.ά.
  Έκδοση: (2021)
• 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 (<i>SMN2</i>) Gene
  από: Gyu-Hwan Park, κ.ά.
  Έκδοση: (2010)