標題: Titlebook: All-Optical Methods to Study Neuronal Function; Eirini Papagiakoumou Book‘‘‘‘‘‘‘‘ 2023 The Editor(s) (if applicable) and The Author(s) 202 [打印本頁] 作者: 開脫 時間: 2025-3-21 19:43
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書目名稱All-Optical Methods to Study Neuronal Function讀者反饋學科排名
作者: precede 時間: 2025-3-21 23:33
Types of Mycorrhizal Associationes of a temporally focused disc, matched to the dimensions of a neuron’s cell body, anywhere within the operating volume of the microscope. However, since improved placement of light, on its own, is not sufficient to allow precise control of neural firing patterns, we also developed and tested optog作者: Arroyo 時間: 2025-3-22 03:09 作者: IRS 時間: 2025-3-22 08:35 作者: 小樣他閑聊 時間: 2025-3-22 10:58
High-Speed All-Optical Neural Interfaces with 3D Temporally Focused Holography,es of a temporally focused disc, matched to the dimensions of a neuron’s cell body, anywhere within the operating volume of the microscope. However, since improved placement of light, on its own, is not sufficient to allow precise control of neural firing patterns, we also developed and tested optog作者: 起波瀾 時間: 2025-3-22 14:36 作者: 披肩 時間: 2025-3-22 20:05
0893-2336 s, engineering, and neuroscience. This book will serve as a guide to establish useful references for groups starting out in this field, and provide insight on the optical systems, actuators, and sensors.?.This is an open access book..978-1-0716-2766-2978-1-0716-2764-8Series ISSN 0893-2336 Series E-ISSN 1940-6045 作者: flaggy 時間: 2025-3-23 00:52 作者: 干旱 時間: 2025-3-23 04:13
https://doi.org/10.1007/978-3-642-40096-4 experiment. Starting with the raw image, we present concepts for artifact avoidance, the extraction of fluorescence intensity traces on single-neuron basis, the identification and binarization of putatively action-potential-related calcium transients, and finally ensemble activity analysis.作者: 配偶 時間: 2025-3-23 05:33
https://doi.org/10.1007/978-3-642-86184-0py equipped with Bessel focus scanning technology and widefield fluorescence microscopy with optical sectioning ability, both of which could be combined with optogenetic stimulation for all optical interrogation of neural circuits. Details on their design and implementation, as well as example applications, are presented.作者: 懦夫 時間: 2025-3-23 12:27 作者: Blazon 時間: 2025-3-23 15:36 作者: SUE 時間: 2025-3-23 19:27
Drawings, Paintings, and Photographs,ical physiology. We describe how 3-dimensional optogenetics can be added to an home-built light-sheet microscope, including technical notes about choices in microscope configuration to consider depending on the time and length scales of interest.作者: abstemious 時間: 2025-3-23 22:11
0893-2336 ation advice from the experts.This book is open access, whic.This open access volume provides an overview of the latest methods used to study neuronal function with?all-optical experimental approaches, where light is used for both stimulation and monitoring of neuronal?activity. The chapters in this作者: 圍裙 時間: 2025-3-24 04:45 作者: Connotation 時間: 2025-3-24 09:16
https://doi.org/10.1007/978-3-642-97253-9ophysical measurements of synthetically induced percepts. We also highlight new methodologies for validating precise control of optical and behavioral manipulations. Finally, we provide a perspective on upcoming developments that are poised to advance the field.作者: Uncultured 時間: 2025-3-24 13:52
Balancing the Fluorescence Imaging Budget for All-Optical Neurophysiology Experiments,h. Scientific priorities determine whether the imaging strategy is based on an “optimal fluorescent indicator” or “optimal imaging modality.” The choice of the first constrains the choice of the second due to each’s contributions to the fluorescence budget and signal-to-noise ratio of time-varying fluorescence changes.作者: 偶然 時間: 2025-3-24 18:50
Illuminating Neural Computation Using Precision Optogenetics-Controlled Synthetic Perception,ophysical measurements of synthetically induced percepts. We also highlight new methodologies for validating precise control of optical and behavioral manipulations. Finally, we provide a perspective on upcoming developments that are poised to advance the field.作者: 牽索 時間: 2025-3-24 21:42
Optogenetics and Light-Sheet Microscopy,ical physiology. We describe how 3-dimensional optogenetics can be added to an home-built light-sheet microscope, including technical notes about choices in microscope configuration to consider depending on the time and length scales of interest.作者: 無彈性 時間: 2025-3-25 00:10 作者: Forehead-Lift 時間: 2025-3-25 04:19
https://doi.org/10.1007/978-3-030-45854-6ed using a miniature electrowetting lens. The 2P-FCM enables three-dimensional two-photon optical recording of structure and activity at multiple focal planes in a freely moving mouse. Detailed methods are provided in this chapter on the 2P-FCM design, operation, and software for data analysis.作者: meditation 時間: 2025-3-25 07:54 作者: CLIFF 時間: 2025-3-25 13:27 作者: white-matter 時間: 2025-3-25 19:14 作者: MERIT 時間: 2025-3-25 22:32 作者: 小說 時間: 2025-3-26 02:57 作者: MOAN 時間: 2025-3-26 06:45 作者: Resign 時間: 2025-3-26 11:27
Book‘‘‘‘‘‘‘‘ 2023nal Function?.is a valuable resource for researchers in various disciplines such as physics, engineering, and neuroscience. This book will serve as a guide to establish useful references for groups starting out in this field, and provide insight on the optical systems, actuators, and sensors.?.This is an open access book..作者: WATER 時間: 2025-3-26 15:35 作者: rheumatology 時間: 2025-3-26 19:12
Balancing the Fluorescence Imaging Budget for All-Optical Neurophysiology Experiments,austive review of fluorescent indicators and imaging modalities but rather aims to distill the functional imaging principles driving the choice of both. Scientific priorities determine whether the imaging strategy is based on an “optimal fluorescent indicator” or “optimal imaging modality.” The choi作者: 糾纏 時間: 2025-3-26 23:50 作者: 基因組 時間: 2025-3-27 01:51 作者: 細胞 時間: 2025-3-27 06:50
An All-Optical Physiology Pipeline Toward Highly Specific and Artifact-Free Circuit Mapping,or co-expression, and tailored illumination schemes. It furthermore demands concepts for system integration and a dedicated analysis pipeline for calcium transients in an event-related manner. Here, firstly, we put forward a framework for the specific requirements for technical system integration pa作者: 遍及 時間: 2025-3-27 10:26 作者: 努力趕上 時間: 2025-3-27 16:24
Miniature Multiphoton Microscopes for Recording Neural Activity in Freely Moving Animals,earch. In combination with fluorescent reporters, these miniature microscopes allow researchers to record the neural activity that underlies behavior, cognition, and perception in freely moving animals. Single-photon miniature microscopes are convenient for widefield recording but lack the increased作者: myocardium 時間: 2025-3-27 20:57
Optogenetics and Light-Sheet Microscopy,ge field of view, and low phototoxicity. This chapter briefly reviews state-of-the-art technology for variations of light-sheet microscopy. We review recent examples of optogenetics in combination with light-sheet microscopy and discuss some current bottlenecks and horizons of light sheet in all-opt作者: 一再困擾 時間: 2025-3-28 01:03 作者: Inveterate 時間: 2025-3-28 03:50 作者: 直覺沒有 時間: 2025-3-28 06:51
Optical and Analytical Methods to Visualize and Manipulate Cortical Ensembles and Behavior,haracterization of causal relations between neuronal activity and behavioral states. In this chapter, we review the implementation of simultaneous two-photon imaging and holographic optogenetics in conjunction with population analytical tools to identify and reactivate neuronal ensembles to control 作者: KIN 時間: 2025-3-28 11:04
Illuminating Neural Computation Using Precision Optogenetics-Controlled Synthetic Perception, measures. In this chapter, we present an overview of current methods for connecting neural codes to perception using precision optogenetics and psychophysical measurements of synthetically induced percepts. We also highlight new methodologies for validating precise control of optical and behavioral作者: stress-test 時間: 2025-3-28 17:40
Spectrally Focused Stimulated Raman Scattering (sf-SRS) Microscopy for Label-Free Investigations of.e., the vibrational energy states reflecting the molecule’s structure and its environment. This technique, relying on the specificity of the molecule’s spectral fingerprint, enables label-free, high-sensitivity, and high-resolution 3D reconstruction of the distribution and the properties of a molec作者: 翻布尋找 時間: 2025-3-28 21:13 作者: 起波瀾 時間: 2025-3-28 23:12
Neuromethodshttp://image.papertrans.cn/a/image/153428.jpg作者: Chandelier 時間: 2025-3-29 05:23
https://doi.org/10.1007/978-1-0716-2764-8light-microscopy; spatial precision; MNI-glutamate; Ca2+ responses; Computer-Generated Holography (CGH); 作者: Innovative 時間: 2025-3-29 08:53 作者: Acclaim 時間: 2025-3-29 11:43
David Pearlmutter,Pedro Berlinernce achieving this goal requires tools capable of precisely perturbing and monitoring neural activity across a multitude of spatiotemporal scales, this aim has inspired the innovation of many optical technologies capable of manipulating and recording neural activity in a minimally invasive manner. T作者: Ambulatory 時間: 2025-3-29 19:06 作者: 昏睡中 時間: 2025-3-29 21:17 作者: 相反放置 時間: 2025-3-30 02:32
