All Stories

  1. Suppression of toxicity of the mutant huntingtin protein by its interacting compound, desonide
  2. HIPK3 modulates autophagy and HTT protein levels in neuronal and mouse models of Huntington disease
  3. NUB1 suppression of Huntington toxicity: mechanistic insights
  4. Gpr52 is a potential target for Huntington's disease and contributes to selective degeneration
  5. TR-FRET Assays of Huntingtin Protein Fragments Reveal Temperature and PolyQ Length-Dependent Conformational Changes
  6. Drugging unconventional targets: insights from Huntington's disease
  7. High-throughput High-content Detection of Genetic Modifiers of Neurodegeneration in Human Stem Cell Derived Neurons
  8. Identification of NUB1 as a suppressor of mutant Huntingtin toxicity via enhanced protein clearance
  9. A novel human embryonic stem cell‐derived Huntington's disease neuronal model exhibits mutant huntingtin (mHTT) aggregates and soluble mHTT‐dependent neurodegeneration
  10. Extracellular Calcium Controls Background Current and Neuronal Excitability via an UNC79-UNC80-NALCN Cation Channel Complex
  11. Regulation of the NALCN Sodium Leak Channel by Neuropeptides
  12. Peptide neurotransmitters activate a cation channel complex of NALCN and UNC-80
  13. The Neuronal Channel NALCN Contributes Resting Sodium Permeability and Is Required for Normal Respiratory Rhythm
  14. Inhibition of Na+ channel currents in rat myoblasts by 4-aminopyridine
  15. Boundary Events: Contact-Dependent and Contact-Facilitated Signaling between Platelets