When you enter multiple keywords separated by space, your search will contain results that match any of the keywords (OR search).
  • 8 Hits
  • Search Condition : Filter (MeSH = Muscular Atrophy, Spinal / genetics)
Species Resource
Drosophila Androgen-dependent neurodegeneration by polyglutamine-expanded human androgen receptor in Drosophila.
Yeast pTN-RC5 Genetic Interactions between the Members of the SMN-Gemins Complex in Drosophila.
C.elegans tm1885 The neuroprotective drug riluzole acts via small conductance Ca2+-activated K+ channels to ameliorate defects in spinal muscular atrophy models.
C.elegans tm1411 VAPB/ALS8 MSP ligands regulate striated muscle energy metabolism critical for adult survival in caenorhabditis elegans.
C.elegans tm4255 , tm604 Conserved genes act as modifiers of invertebrate SMN loss of function defects.
Mice B6D2-Tg(CAG-AR*97Q)7-8Sobu(RBRC00344) , B6SJL-TgN(hAndR/CAGn)/1(RBRC00373) Heat shock protein 70 chaperone overexpression ameliorates phenotypes of the spinal and bulbar muscular atrophy transgenic mouse model by reducing nuclear-localized mutant androgen receptor protein.
Mice B6D2-Tg(CAG-AR*97Q)7-8Sobu(RBRC00344) Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients.
DNA material S. pombe YFP-FLAG-His SpYFH19G10 (SPW087754) Specific splicing defects in S. pombe carrying a degron allele of the Survival of Motor Neuron gene.