Abstract
Fluorescence background and light scattering impede all-optical mapping of neural function in intact tissue. Hadamard microscopy enabled simultaneous optogenetic stimulation and fluorescence recording of Ca2+ responses in six thousand neurons in acute brain slices.
© 2018 The Author(s)
PDF ArticleMore Like This
Kevin T. Takasaki, Matthew T. Valley, Emily Turschak, Rui Liu, and Jack Waters
JTu3A.60 Clinical and Translational Biophotonics (Translational) 2018
Chunyu Fang, Xuechun Wang, Lanxin Zhu, Tingting Chu, Yusha Li, Dan Zhu, and Peng Fei
Tu3K.4 Conference on Lasers and Electro-Optics/Pacific Rim (CLEO/PR) 2018
Michael L. Castanares and Vincent R. Daria
JTh5A.3 Clinical and Translational Biophotonics (Translational) 2018