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Biophysical Basis of the in vivo Electroretinogram of the Mouse: Current Source Density Analysis of Genetically and Pharmacologically Isolated Rod photoreceptor-driven Currents

https://doi.org/10.1101/2025.02.05.636690

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cne.901880204openalex-snapshot

Rods and cones in the mouse retina. I. Structural analysis using light and electron microscopy

inferredcites →https://doi.org/10.1016/0005-2728(93)90038-hopenalex-snapshot

Amplification and kinetics of the activation steps in phototransduction

inferredcites →https://doi.org/10.1016/0014-4835(90)90086-aopenalex-snapshot

Na+,K+-ATPase of the photoreceptor: Selective expression of α3 and β2 isoforms

inferredcites →https://doi.org/10.1016/0278-4327(85)90004-5openalex-snapshot

Chapter 2 Retinal pigment epithelial cell contributions to the electroretinogram and electrooculogram

inferredcites →https://doi.org/10.1016/0896-6273(89)90267-5openalex-snapshot

Characterization of a voltage-gated K+ channel that accelerates the rod response to dim light

inferredcites →https://doi.org/10.1016/j.bpj.2009.06.037openalex-snapshot

RGS9 Concentration Matters in Rod Phototransduction

inferredcites →https://doi.org/10.1016/j.bpj.2012.10.023openalex-snapshot

Cytoplasm Resistivity of Mammalian Atrial Myocardium Determined by Dielectrophoresis and Impedance Methods

inferredcites →https://doi.org/10.1016/j.bpj.2015.09.015openalex-snapshot

Importance of the Voltage Dependence of Cardiac Na/K ATPase Isozymes

inferredcites →https://doi.org/10.1016/j.exer.2018.02.024openalex-snapshot

Loss of cone function without degeneration in a novel Gnat2 knock-out mouse

inferredcites →https://doi.org/10.1016/j.neuron.2012.07.029openalex-snapshot

Calcium Feedback to cGMP Synthesis Strongly Attenuates Single-Photon Responses Driven by Long Rhodopsin Lifetimes

inferredcites →https://doi.org/10.1016/j.preteyeres.2013.12.003openalex-snapshot

The rod-driven a-wave of the dark-adapted mammalian electroretinogram

inferredcites →https://doi.org/10.1016/j.visres.2004.09.002openalex-snapshot

In vivo studies of signaling in rod pathways of the mouse using the electroretinogram

inferredcites →https://doi.org/10.1016/s0006-3495(70)86308-1openalex-snapshot

Dark Current and Photocurrent in Retinal Rods

inferredcites →https://doi.org/10.1016/s0006-3495(72)86145-9openalex-snapshot

Kinetics of the Photocurrent of Retinal Rods

inferredcites →https://doi.org/10.1016/s0006-3495(83)84368-9openalex-snapshot

Effect of tortuous extracellular pathways on resistance measurements

inferredcites →https://doi.org/10.1038/ncomms1540openalex-snapshot

Modulation of rod photoreceptor output by HCN1 channels is essential for regular mesopic cone vision

inferredcites →https://doi.org/10.1073/pnas.1606428113openalex-snapshot

In vivo optical imaging of physiological responses to photostimulation in human photoreceptors

inferredcites →https://doi.org/10.1073/pnas.1620572114openalex-snapshot

In vivo optophysiology reveals that G-protein activation triggers osmotic swelling and increased light scattering of rod photoreceptors

inferredcites →https://doi.org/10.1073/pnas.2202485119openalex-snapshot

Human cone elongation responses can be explained by photoactivated cone opsin and membrane swelling and osmotic response to phosphate produced by RGS9-catalyzed GTPase

inferredcites →https://doi.org/10.1085/jgp.201611692openalex-snapshot

Bright flash response recovery of mammalian rods in vivo is rate limited by RGS9

inferredcites →https://doi.org/10.1085/jgp.202012687openalex-snapshot

Loss of the K+ channel Kv2.1 greatly reduces outward dark current and causes ionic dysregulation and degeneration in rod photoreceptors

inferredcites →https://doi.org/10.1101/2025.01.28.635195openalex-snapshot

Biophysical Basis of the in vivo Electroretinogram of the Mouse: 4-Shell Current Source Density Model

inferredcites →https://doi.org/10.1111/j.1460-9568.1990.tb00409.xopenalex-snapshot

Complex Expression Patterns for Na+,K+ ‐ATPase Isoforms in Retina and Optic Nerve

inferredcites →https://doi.org/10.1111/j.1469-7793.1999.0479p.xopenalex-snapshot

Light adaptation and dark adaptation of human rod photoreceptors measured from the a‐wave of the electroretinogram

inferredcites →https://doi.org/10.1111/j.1469-7793.1999.813ab.xopenalex-snapshot

Properties and functional roles of hyperpolarization‐gated currents in guinea‐pig retinal rods

inferredcites →https://doi.org/10.1113/jphysiol.1992.sp019111openalex-snapshot

A quantitative account of the activation steps involved in phototransduction in amphibian photoreceptors.

inferredcites →https://doi.org/10.1113/jphysiol.2002.017640openalex-snapshot

Functional characterisation and subcellular localisation of HCN1 channels in rabbit retinal rod photoreceptors

inferredcites →https://doi.org/10.1113/jphysiol.2005.088468openalex-snapshot

Extremely rapid recovery of human cone circulating current at the extinction of bleaching exposures

inferredcites →https://doi.org/10.1113/jphysiol.2014.272518openalex-snapshot

Rhodopsin in the rod surface membrane regenerates more rapidly than bulk rhodopsin in the disc membranes in vivo

inferredcites →https://doi.org/10.1126/sciadv.abc1124openalex-snapshot

The optoretinogram reveals the primary steps of phototransduction in the living human eye

inferredcites →https://doi.org/10.1152/jn.1980.44.5.897openalex-snapshot

Light-evoked changes in [K+]0 in retina of intact cat eye

inferredcites →https://doi.org/10.1152/jn.1985.54.6.1607openalex-snapshot

Laminar profile of resistivity in frog retina

inferredcites →https://doi.org/10.1152/jn.1994.72.1.84openalex-snapshot

Current source density (CSD) analysis of retinal field potentials. I. Methodological considerations and depth profiles

inferredcites →https://doi.org/10.1152/physrev.00027.2007openalex-snapshot

Diffusion in Brain Extracellular Space

inferredcites →https://doi.org/10.1167/iovs.08-2659openalex-snapshot

Selective Hcn1 Channels Inhibition by Ivabradine in Mouse Rod Photoreceptors

inferredcites →https://doi.org/10.1167/iovs.17-22248openalex-snapshot

Transretinal ERG in Studying Mouse Rod Phototransduction: Comparison With Local ERG Across the Rod Outer Segments

inferredcites →https://doi.org/10.1364/oe.409193openalex-snapshot

Optoretinography of individual human cone photoreceptors

inferredcites →https://doi.org/10.1364/ol.398868openalex-snapshot

Optoretinogram: optical measurement of human cone and rod photoreceptor responses to light

inferredcites →https://doi.org/10.1371/journal.pone.0150024openalex-snapshot

Morphological Diversity of the Rod Spherule: A Study of Serially Reconstructed Electron Micrographs

inferredcites →https://doi.org/10.1523/jneurosci.19-22-09878.1999openalex-snapshot

Cellular and Subcellular Specification of Na,K-ATPase α and β Isoforms in the Postnatal Development of Mouse Retina

inferredcites →https://doi.org/10.1523/jneurosci.5391-09.2010openalex-snapshot

Control of Rhodopsin's Active Lifetime by Arrestin-1 Expression in Mammalian Rods

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1101/2025.11.09.687427openalex-snapshot

Biophysical Basis of the in vivo ERG of the Mouse: Rod, RPE and Müller glial Cell Contributions To Dark and to Light-driven Changes in Sub-Retinal Space [K + ] o

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