Symposia

[1S02m] Cutting-edge optical techniques to visualize the dynamics of various neuronal states

Wed. Jul 29, 2020 9:00 AM - 11:00 AM Room 2

Organizer: Ryohei Yasuda (Max Planck Florida Institute for Neuroscience), Lin Tian (University of California, Davis)

*Videos are available throughout the meeting period.

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[1S02m-Introduction] Introduction

[1S02m-01] Imaging neuronal intracellular signal transduction using multiphoton fluorescence lifetime imaging microscopy

*RYOHEI YASUDA^1,2 (1. Max Planck Florida Institute for Neuroscience, 2. Res Inst. Electronics, Shizuoka Univ)

[1S02m-02] Super-resolution fluorescence assisted diffraction computational tomography reveals the three-dimensional landscape of cellular organelle interactome

*Liangyi Chen¹, Dashan Dong², Xiaoshuai Huang¹, Liuju Li¹, Kebin Shi² (1. State Key Laboratory of Membrane Biology, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking University, 2. State Key Laboratory for Mesoscopic Physics, Collaborative Innovation Center of Quantum Matter, School of Physics, Peking University, Beijing, China)

[1S02m-03] High Resolution Vibrational Imaging of Brain Metabolism

*Lingyan Shi¹ (1. Dept. Bioengineering, University of California San Diego, USA)

[1S02m-04] Fast, wide and contiguous field-of-view two-photon Ca²⁺ imaging

*MASANORI MURAYAMA¹ (1. RIKEN Center for Brain Science)

[1S02m-05] Imaging serotonin dynamics in living behaving animals

*Lin Tian¹, Chunyang Dong¹, Emily Wright¹, Karan Mahe¹ (1. University of California, Davis)

Session information

[1S02m] Cutting-edge optical techniques to visualize the dynamics of various neuronal states

[1S02m-Introduction] Introduction

[1S02m-01] Imaging neuronal intracellular signal transduction using multiphoton fluorescence lifetime imaging microscopy

[1S02m-02] Super-resolution fluorescence assisted diffraction computational tomography reveals the three-dimensional landscape of cellular organelle interactome

[1S02m-03] High Resolution Vibrational Imaging of Brain Metabolism

[1S02m-04] Fast, wide and contiguous field-of-view two-photon Ca²⁺ imaging

[1S02m-05] Imaging serotonin dynamics in living behaving animals

Authentication

Session information

[1S02m] Cutting-edge optical techniques to visualize the dynamics of various neuronal states

[1S02m-Introduction] Introduction

[1S02m-01] Imaging neuronal intracellular signal transduction using multiphoton fluorescence lifetime imaging microscopy

[1S02m-02] Super-resolution fluorescence assisted diffraction computational tomography reveals the three-dimensional landscape of cellular organelle interactome

[1S02m-03] High Resolution Vibrational Imaging of Brain Metabolism

[1S02m-04] Fast, wide and contiguous field-of-view two-photon Ca2+ imaging

[1S02m-05] Imaging serotonin dynamics in living behaving animals

Authentication

[1S02m-04] Fast, wide and contiguous field-of-view two-photon Ca²⁺ imaging