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Mouse Retinal Phenotyping

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Cover of 'Mouse Retinal Phenotyping'

Table of Contents

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    Book Overview
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    Chapter 1 Morphological Survey from Neurons to Circuits of the Mouse Retina
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    Chapter 2 Measuring Retinal Function in the Mouse
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    Chapter 3 Modeling Retinal Diseases Using Genetic Approaches in Mice
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    Chapter 4 Cell Culture Analysis of the Phagocytosis of Photoreceptor Outer Segments by Primary Mouse RPE Cells
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    Chapter 5 Two-Photon Microscopy (TPM) and Fluorescence Lifetime Imaging Microscopy (FLIM) of Retinal Pigment Epithelium (RPE) of Mice In Vivo
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    Chapter 6 RPE Visual Cycle and Biochemical Phenotypes of Mutant Mouse Models
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    Chapter 7 Use of Direct Current Electroretinography for Analysis of Retinal Pigment Epithelium Function in Mouse Models
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    Chapter 8 Disruption of Rhodopsin Dimerization in Mouse Rod Photoreceptors by Synthetic Peptides Targeting Dimer Interface
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    Chapter 9 Experimental Approaches for Defining the Role of the Ca2+-Modulated ROS-GC System in Retinal Rods of Mouse
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    Chapter 10 Microglia Analysis in Retinal Degeneration Mouse Models
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    Chapter 11 Determination of Mitochondrial Oxygen Consumption in the Retina Ex Vivo: Applications for Retinal Disease
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    Chapter 12 Analysis of Feedback Signaling from Horizontal Cells to Photoreceptors in Mice
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    Chapter 13 Assessment of the Absolute Excitatory Level of the Retina by Flicker ERG
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    Chapter 14 Ex Vivo Functional Evaluation of Synaptic Transmission from Rods to Rod Bipolar Cells in Mice
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    Chapter 15 Functional and Morphological Analysis of OFF Bipolar Cells
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    Chapter 16 Immunohistochemical Phenotyping of Mouse Amacrine Cell Subtypes
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    Chapter 17 Phenotyping of Gap-Junctional Coupling in the Mouse Retina
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    Chapter 18 Ganglion Cell Assessment in Rodents with Retinal Degeneration
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    Chapter 19 Morphological Identification of Melanopsin-Expressing Retinal Ganglion Cell Subtypes in Mice
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    Chapter 20 Functional Assessment of Melanopsin-Driven Light Responses in the Mouse: Multielectrode Array Recordings
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    Chapter 21 In Vitro Assays for Mouse Müller Cell Phenotyping Through microRNA Profiling in the Damaged Retina
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    Chapter 22 Analysis of Retinal Vascular Plexuses and Interplexus Connections
Attention for Chapter 13: Assessment of the Absolute Excitatory Level of the Retina by Flicker ERG
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Chapter title
Assessment of the Absolute Excitatory Level of the Retina by Flicker ERG
Chapter number 13
Book title
Mouse Retinal Phenotyping
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7720-8_13
Pubmed ID
Book ISBNs
978-1-4939-7719-2, 978-1-4939-7720-8
Authors

Naoyuki Tanimoto, Mathias W. Seeliger

Abstract

Electroretinography (ERG) is important for functional diagnostics of the retina. Types of information about retinal function obtainable by ERG differ depending on recording conditions, e.g., a combination of light stimulus and adaptation. In terms of stimulation, single-flash and flicker stimuli are frequently used because response properties have been well investigated, allowing an assessment of fundamental retinal functionality; for example, how photoreceptors and bipolar cells, including signal transmission between them, are affected under pathological conditions. Usually, ERGs are recorded with a nonzero lower cutoff frequency of amplifiers to avoid certain artifacts, and additionally, responses are averaged over time so that non-event-related signals are cancelled out. However, the improved signal quality is associated with a loss of information. Especially in steady-state flicker ERG, information about the absolute baseline of recordings is missing because the prestimulus baseline is not included on the recording trace as well as because a zero response is obtained in all cases in which the signal baseline stays constant for a sufficient amount of time. In other words, it is impossible to tell from the conventional flicker ERG whether a zero signal is obtained under conditions of maximal or no excitation of the visual system. In this chapter, we describe a direct current ERG protocol (featuring a lower cutoff frequency of zero) with repetitive single flashes mimicking conventional flicker that contains a defined onset. Using this recording protocol, it is possible to assess not only the absolute excitatory level of the retina but also the development of steady-state responses from the single flash response.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 4 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 4 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 25%
Researcher 1 25%
Student > Master 1 25%
Unknown 1 25%
Readers by discipline Count As %
Medicine and Dentistry 2 50%
Agricultural and Biological Sciences 1 25%
Unknown 1 25%