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

অনুরূপ উপাদানগুলি

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