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  • Search Condition : Filter (MeSH = Muscular Atrophy, Spinal / genetics)
Species Resource Title
C.elegans Enhancing GABAergic Transmission Improves Locomotion in a Caenorhabditis elegans Model of Spinal Muscular Atrophy.
DNA material pCAG-HIVgp (RDB04394) , pCMV-VSV-G-RSV-Rev (RDB04393) Unveiling synapse pathology in spinal bulbar muscular atrophy by genome-wide transcriptome analysis of purified motor neurons derived from disease specific iPSCs.
C.elegans tm4255 , tm604 Conserved genes act as modifiers of invertebrate SMN loss of function defects.
C.elegans tm1411 VAPB/ALS8 MSP ligands regulate striated muscle energy metabolism critical for adult survival in caenorhabditis elegans.
C.elegans tm1885 The neuroprotective drug riluzole acts via small conductance Ca2+-activated K+ channels to ameliorate defects in spinal muscular atrophy models.
Yeast pTN-RC5 Genetic Interactions between the Members of the SMN-Gemins Complex in Drosophila.
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.
Mice RBRC00344 Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients.
Mice RBRC00344 , 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.
Drosophila Androgen-dependent neurodegeneration by polyglutamine-expanded human androgen receptor in Drosophila.