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

https://doi.org/10.1371/journal.pone.0150024
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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.21188openalex-snapshot
Rod bipolar cells and horizontal cells form displaced synaptic contacts with rods in the outer nuclear layer of the nob2 retina
inferredcites →https://doi.org/10.1002/cne.21612openalex-snapshot
Type 4 OFF cone bipolar cells of the mouse retina express calsenilin and contact cones as well as rods
inferredcites →https://doi.org/10.1002/cne.23452openalex-snapshot
Structural organization and function of mouse photoreceptor ribbon synapses involve the immunoglobulin protein synaptic cell adhesion molecule 1
inferredcites →https://doi.org/10.1002/cne.23552openalex-snapshot
DSCAM localization and function at the mouse cone synapse
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/10.1002/cne.902400410openalex-snapshot
Chemical and electrical synapses between photoreceptors in the retina of the turtle, Chelydra serpentina
inferredcites →https://doi.org/10.1007/bf00406626openalex-snapshot
Elektronenmikroskopische Untersuchungen �ber die Photoreceptoren und Receptorensynapsen bei reinen St�bchen- und Zapfennetzh�uten
inferredcites →https://doi.org/10.1007/s00018-012-1230-zopenalex-snapshot
Characterization of neurite outgrowth and ectopic synaptogenesis in response to photoreceptor dysfunction
inferredcites →https://doi.org/10.1016/j.tins.2014.07.009openalex-snapshot
Neuronal remodeling in retinal circuit assembly, disassembly, and reassembly
inferredcites →https://doi.org/10.1016/s0022-5320(58)90050-9openalex-snapshot
Ultrastructure of retinal rod synapses of the guinea pig eye as revealed by three-dimensional reconstructions from serial sections
inferredcites →https://doi.org/10.1016/s0896-6273(00)80560-7openalex-snapshot
A Novel Signaling Pathway from Rod Photoreceptors to Ganglion Cells in Mammalian Retina
inferredcites →https://doi.org/10.1016/s0896-6273(03)00086-2openalex-snapshot
The Presynaptic Active Zone Protein Bassoon Is Essential for Photoreceptor Ribbon Synapse Formation in the Retina
inferredcites →https://doi.org/10.1017/s095252380623102xopenalex-snapshot
Thenob2mouse, a null mutation inCacna1f: Anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses
inferredcites →https://doi.org/10.1038/ng774openalex-snapshot
Nrl is required for rod photoreceptor development
inferredcites →https://doi.org/10.1038/nmeth.2072openalex-snapshot
Elastic volume reconstruction from series of ultra-thin microscopy sections
inferredcites →https://doi.org/10.1038/nn.3772openalex-snapshot
LKB1 and AMPK regulate synaptic remodeling in old age
inferredcites →https://doi.org/10.1038/nn1320openalex-snapshot
Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function
inferredcites →https://doi.org/10.1073/pnas.0605211103openalex-snapshot
Dendrites of rod bipolar cells sprout in normal aging retina
inferredcites →https://doi.org/10.1073/pnas.0705465104openalex-snapshot
A typology of photoreceptor gene expression patterns in the mouse
inferredcites →https://doi.org/10.1073/pnas.92.23.10658openalex-snapshot
An alternative pathway for signal flow from rod photoreceptors to ganglion cells in mammalian retina.
inferredcites →https://doi.org/10.1073/pnas.96.2.736openalex-snapshot
Morphological, physiological, and biochemical changes in rhodopsin knockout mice
inferredcites →https://doi.org/10.1073/pnas.96.24.14130openalex-snapshot
An alternative pathway for rod signals in the rodent retina: Rod photoreceptors, cone bipolar cells, and the localization of glutamate receptors
inferredcites →https://doi.org/10.1083/jcb.2.3.307openalex-snapshot
ELECTRON MICROSCOPE OBSERVATIONS ON SYNAPTIC VESICLES IN SYNAPSES OF THE RETINAL RODS AND CONES
inferredcites →https://doi.org/10.1083/jcb.4.4.459openalex-snapshot
The Fine Structure of the Rod-Bipolar Cell Synapse in the Retina of the Albino Rat
inferredcites →https://doi.org/10.1093/hmg/ddi336openalex-snapshot
Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina
inferredcites →https://doi.org/10.1098/rstb.1970.0036openalex-snapshot
Organization of the outer plexiform layer of the primate retina: Electron microscopy of Golgi-impregnated Cells
inferredcites →https://doi.org/10.1111/j.1460-9568.2007.05886.xopenalex-snapshot
Structural and functional remodeling in the retina of a mouse with a photoreceptor synaptopathy: plasticity in the rod and degeneration in the cone system
inferredcites →https://doi.org/10.1167/iovs.03-0741openalex-snapshot
Morphological Characterization of the Retina of the CNGA3 −/− Rho −/− Mutant Mouse Lacking Functional Cones and Rods
inferredcites →https://doi.org/10.1186/1756-0500-3-25openalex-snapshot
Characterization of the retinal proteome during rod photoreceptor genesis
inferredcites →https://doi.org/10.1371/journal.pone.0038011openalex-snapshot
TrakEM2 Software for Neural Circuit Reconstruction
inferredcites →https://doi.org/10.1523/jneurosci.0267-12.2012openalex-snapshot
Guidance-Cue Control of Horizontal Cell Morphology, Lamination, and Synapse Formation in the Mammalian Outer Retina
inferredcites →https://doi.org/10.1523/jneurosci.0442-12.2012openalex-snapshot
Ablation of Retinal Horizontal Cells from Adult Mice Leads to Rod Degeneration and Remodeling in the Outer Retina
inferredcites →https://doi.org/10.1523/jneurosci.1373-13.2013openalex-snapshot
Development and Plasticity of Outer Retinal Circuitry Following Genetic Removal of Horizontal Cells
inferredcites →https://doi.org/10.1523/jneurosci.2202-14.2015openalex-snapshot
DSCAM Promotes Refinement in the Mouse Retina through Cell Death and Restriction of Exploring Dendrites
inferredcites →https://doi.org/10.1523/jneurosci.3580-11.2011openalex-snapshot
Age-Related Alterations in Neurons of the Mouse Retina
inferredcites →https://doi.org/10.1523/jneurosci.3764-04.2005openalex-snapshot
Impaired Channel Targeting and Retinal Degeneration in Mice Lacking the Cyclic Nucleotide-Gated Channel Subunit CNGB1
inferredcites →https://doi.org/10.1523/jneurosci.4749-11.2012openalex-snapshot
Photoreceptor Coupling Mediated by Connexin36 in the Primate Retina
inferredcites →https://doi.org/10.3389/fnana.2014.00105openalex-snapshot
Some OFF bipolar cell types make contact with both rods and cones in macaque and mouse retinas

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.3985168openalex-extracted
inferred← citeshttps://doi.org/10.1007/978-3-319-59575-7_22openalex-snapshot
Computer Assisted Segmentation Tool: A Machine Learning Based Image Segmenting Tool for TrakEM2
inferred← citeshttps://doi.org/10.1007/s00424-021-02548-9openalex-snapshot
Transmission at rod and cone ribbon synapses in the retina
inferred← citeshttps://doi.org/10.1016/j.crmeth.2022.100253openalex-snapshot
Rapid 3D-STORM Imaging of Diverse Molecular Targets in Tissue
inferred← citeshttps://doi.org/10.1016/j.isci.2020.101830openalex-snapshot
Disturbed Presynaptic Ca2+ Signaling in Photoreceptors in the EAE Mouse Model of Multiple Sclerosis
inferred← citeshttps://doi.org/10.1016/j.xops.2023.100321openalex-snapshot
From Soma to Synapse: Imaging Age-Related Rod Photoreceptor Changes in the Mouse with Visible Light OCT
inferred← citeshttps://doi.org/10.1016/j.ydbio.2021.04.001openalex-snapshot
Development and maintenance of vision’s first synapse
inferred← citeshttps://doi.org/10.1101/2024.10.18.619115openalex-snapshot
P23H rhodopsin aggregation in the ER causes synaptic protein imbalance in rod photoreceptors
inferred← citeshttps://doi.org/10.1101/2025.02.05.636690openalex-snapshot
Biophysical Basis of the in vivo Electroretinogram of the Mouse: Current Source Density Analysis of Genetically and Pharmacologically Isolated Rod photoreceptor-driven Currents
inferred← citeshttps://doi.org/10.1101/753012openalex-snapshot
NRL- and CRX-guided gene network modulates photoreceptor presynapse size and positioning during retinal development
inferred← citeshttps://doi.org/10.1111/ahe.12865openalex-snapshot
Student remote and distance research in neuroanatomy: Mapping Dscaml1 expression with a LacZ gene trap in mouse brain
inferred← citeshttps://doi.org/10.1152/physrev.00026.2018openalex-snapshot
Sensory Processing at Ribbon Synapses in the Retina and the Cochlea
inferred← citeshttps://doi.org/10.1167/iovs.61.3.11openalex-snapshot
Critical Decrease in the Level of Axon Guidance Receptor ROBO1 in Rod Synaptic Terminals Is Followed by Axon Retraction
inferred← citeshttps://doi.org/10.1242/dmm.052256openalex-snapshot
P23H rhodopsin accumulation causes transient disruptions to synaptic protein levels in rod photoreceptors in a model of retinitis pigmentosa
inferred← citeshttps://doi.org/10.1371/journal.pone.0290257openalex-snapshot
The rod synapse in aging wildtype and Dscaml1 mutant mice
inferred← citeshttps://doi.org/10.1523/jneurosci.2267-22.2023openalex-snapshot
Three-Dimensional Ultrastructure of the Normal Rod Photoreceptor Synapse and Degenerative Changes Induced by Retinal Detachment
inferred← citeshttps://doi.org/10.3390/cells14030206openalex-snapshot
Early Synapse-Specific Alterations of Photoreceptor Mitochondria in the EAE Mouse Model of Multiple Sclerosis
inferred← citeshttps://doi.org/10.3390/ijms27062579openalex-snapshot
Early Reduction in Mitochondrial Membrane Potential in Synaptic Mitochondria Contribute to Synaptic Pathology in the EAE Mouse Model of Multiple Sclerosis
inferred← citeshttps://doi.org/10.7554/elife.63844openalex-snapshot
The mammalian rod synaptic ribbon is essential for Cav channel facilitation and ultrafast synaptic vesicle fusion
inferred← citeshttps://doi.org/10.7554/elife.73039openalex-snapshot
Analysis of rod/cone gap junctions from the reconstruction of mouse photoreceptor terminals
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