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  1. Supporting Rare Disease Research with BeHeard 2017

    Type
    Blog Post
    ...muscular atrophy, a disease in which disruption of the smn1 gene results in the degeneration of spinal cord ...19,000 live births (1).  While disruption of the smn1 gene is known to cause spinal muscular atrophy, ...plans on using C. elegans as a model to identify SMN1 interacting partners and perform whole animal screens...molecules that block the neurodegenerative effects of smn1 disruption. As part of his work in C. elegans, Dr...Schiavi will use Addgene plasmids to characterize smn1 interactions with other genes. He will use fluorescent...concrete understanding of the molecular biology behind SMN1 and its interaction partners, Dr. Di Schiavi will...Besta in Milan to test small molecules targeting SMN1 and its partners in mouse cell lines. Dr. Di Schiavi...
  2. Neurodegeneration Plasmid Collection

    Type
    Collection
    ...Parkinson's, FTD Henri Huttunen 71687 pcDNA3.1+ SMN1 myc HIS SMN1 His, Myc CMV Spinal muscular atrophy Gideon...APP GFP T7 Alzheimer's Michael Hecht 72286 pCI SMN1 SMN1 CMV Spinal muscular atrophy Elliot Androphy 72873... Venus CMV Alzheimer's Johanna Ivaska 156022 SMN1-1 SMN1 V5-MCP EF1a Spinal muscular atrophy Eugene Yeo...sensory neuropathy type IE Arthur Riggs 37057 GFP-SMN SMN1 GFP CMV Spinal muscular atrophy Greg Matera 38005...PRNP hU6 Dementia Gerold Schmitt-Ulms 61946 4QQ6 SMN1 His T7 Spinal muscular atrophy Cheryl Arrowsmith...
Showing: 1 - 2 of 2 results