Ectopic synaptogenesis in the mammalian retina caused by rod photoreceptor-specific mutations (Q73088844)

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1 November 2019

title

Ectopic synaptogenesis in the mammalian retina caused by rod photoreceptor-specific mutations (English)

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1 November 2019

author name string

Peng YW

1

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1 November 2019

Hao Y

2

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1 November 2019

Petters RM

3

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1 November 2019

Wong F

4

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1 November 2019

publication date

1 November 2000

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1 November 2019

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1 November 2019

volume

3

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issue

11

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1 November 2019

page(s)

1121-1127

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https://scigraph.springernature.com/pub.10.1038/80639

1 November 2019

exact match

0 references

cites work

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Retinal photoreceptor dystrophies LI. Edward Jackson Memorial Lecture

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Preservation of the Inner Retina in Retinitis Pigmentosa

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Apoptosis: final common pathway of photoreceptor death in rd, rds, and rhodopsin mutant mice

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Dopamine cells and rod bipolar cells contain protein kinase C-like immunoreactivity in some vertebrate retinas

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Rod bipolar cells in the mammalian retina show protein kinase C-like immunoreactivity

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7 January 2021

The rod bipolar cell of the mammalian retina

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Immunocytochemical staining of AII-amacrine cells in the rat retina with antibodies against parvalbumin

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AII amacrine cell population in the rabbit retina: identification by parvalbumin immunoreactivity

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Distributions of two homologous synaptic vesicle proteins, synaptoporin and synaptophysin, in the mammalian retina

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Molecular cloning and characterization of the G protein gamma subunit of cone photoreceptors

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Specific deficit of the ON response in visual transmission by targeted disruption of the mGluR6 gene.

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Diversity of glutamate receptors in the mammalian retina

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Kainic acid induces sprouting of retinal neurons

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Regressive events in neurogenesis.

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A novel signaling pathway from rod photoreceptors to ganglion cells in mammalian retina

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Synaptogenesis in the photoreceptor terminal of the mouse retina

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Rod photoreceptor neurite sprouting in retinitis pigmentosa

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Abnormalities in rod photoreceptors, amacrine cells, and horizontal cells in human retinas with retinitis pigmentosa

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A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

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7 January 2021

Stargardt's ABCR is localized to the disc membrane of retinal rod outer segments

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Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice

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The 220-kDa rim protein of retinal rod outer segments is a member of the ABC transporter superfamily

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Retinal stimulates ATP hydrolysis by purified and reconstituted ABCR, the photoreceptor-specific ATP-binding cassette transporter responsible for Stargardt disease

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Retinal rod photoreceptor-specific gene mutation perturbs cone pathway development.

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Low-frequency damped electroretinographic wavelets in young asymptomatic patients with dominant retinitis pigmentosa: a new electroretinographic finding

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Dominant Retinitis Pigmentosa With Reduced Penetrance

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7 January 2021

Dominant retinitis pigmentosa with reduced penetrance. Further studies of the electroretinogram

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7 January 2021

Identifiers

DOI

10.1038/80639

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11036269%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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