Adam C Miller

Summary

Affiliation: Fred Hutchinson Cancer Research Center
Country: USA

Publications

  1. pmc Neurobeachin is required postsynaptically for electrical and chemical synapse formation
    Adam C Miller
    Division of Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue N, Seattle, WA 98109, USA Electronic address
    Curr Biol 25:16-28. 2015
  2. pmc RNA-seq-based mapping and candidate identification of mutations from forward genetic screens
    Adam C Miller
    Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA
    Genome Res 23:679-86. 2013
  3. pmc Rapid reverse genetic screening using CRISPR in zebrafish
    Arish N Shah
    Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA
    Nat Methods 12:535-40. 2015

Collaborators

Detail Information

Publications3

  1. pmc Neurobeachin is required postsynaptically for electrical and chemical synapse formation
    Adam C Miller
    Division of Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue N, Seattle, WA 98109, USA Electronic address
    Curr Biol 25:16-28. 2015
    ..The molecular pathways required for electrical synaptogenesis are not well understood, and whether they share mechanisms of formation with chemical synapses is not clear...
  2. pmc RNA-seq-based mapping and candidate identification of mutations from forward genetic screens
    Adam C Miller
    Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA
    Genome Res 23:679-86. 2013
    ..Overall, we show that RNA-seq is a fast, reliable, and cost-effective method to map and identify mutations that will greatly facilitate the power of forward genetics in vertebrate models...
  3. pmc Rapid reverse genetic screening using CRISPR in zebrafish
    Arish N Shah
    Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA
    Nat Methods 12:535-40. 2015
    ..By deep sequencing target loci, we found that 90% of the genes were effectively screened. We conclude that CRISPR can be used as a powerful reverse genetic screening strategy in vivo in a vertebrate system. ..