Issues

Cover picture: A rapid increase in Ca²⁺ concentration in the apical region of mouse vomeronasal sensory neurons obtained by flash photolysis of caged Ca²⁺ (top left) activates an inward current at the holding potential of – 50 mV (top center), with a fast mono-exponential rising phase (top right). Immunocytochemistry shows that the Ca²⁺ -activated Cl⁻ channels TMEM16A/anoctamin1 and TMEM16B/anoctamin2 coexpress in the microvilli of the same vomeronasal sensory neuron from an OMP-GFP mouse (see article by Dibattista et al., 3–15).