Results 31 to 40 of about 33,197 (253)

Induction of Neuronal Morphology in the 661W Cone Photoreceptor Cell Line with Staurosporine. [PDF]

open access: yesPLoS ONE, 2015
PURPOSE:RGC-5 cells undergo differentiation into a neuronal phenotype with low concentrations of staurosporine. Although the RGC-5 cell line was initially thought to be of retinal ganglion cell origin, recent evidence suggests that the RGC-5 line could ...
Alex F Thompson   +3 more
doaj   +1 more source

Necrotic cone photoreceptor cell death in retinitis pigmentosa [PDF]

open access: yesCell Death & Disease, 2015
Retinitis pigmentosa (RP) comprises a group of inherited retinal degenerations, resulting from rod and cone photoreceptor cell death. Genetic studies have identified mutations in more than 50 genes—most of which encode rod-related molecules—that are associated with RP.
Murakami, Y   +6 more
openaire   +2 more sources

Cell-specific DNA methylation patterns of retina-specific genes. [PDF]

open access: yesPLoS ONE, 2012
Many studies have demonstrated that epigenetic mechanisms are important in the regulation of gene expression during embryogenesis, gametogenesis, and other forms of tissue-specific gene regulation.
Shannath L Merbs   +6 more
doaj   +1 more source

AAV9 targets cone photoreceptors in the nonhuman primate retina. [PDF]

open access: yesPLoS ONE, 2013
Transduction of retinal pigment epithelial cells with an adeno-associated viral vector (AAV) based on serotype 2 has partially corrected retinal blindness in Leber congenital amaurosis type 2.
Luk H Vandenberghe   +7 more
doaj   +1 more source

Universality of Form: The Case of Retinal Cone Photoreceptor Mosaics

open access: yesEntropy, 2023
Cone photoreceptor cells are wavelength-sensitive neurons in the retinas of vertebrate eyes and are responsible for color vision. The spatial distribution of these nerve cells is commonly referred to as the cone photoreceptor mosaic.
Alireza Beygi
doaj   +1 more source

Subretinal gene therapy delays vision loss in a Bardet-Biedl Syndrome type 10 mouse model

open access: yesMolecular Therapy: Nucleic Acids, 2023
Blindness in Bardet-Biedl syndrome (BBS) is caused by dysfunction and loss of photoreceptor cells in the retina. BBS10, mutations of which account for approximately 21% of all BBS cases, encodes a chaperonin protein indispensable for the assembly of the ...
Ying Hsu   +12 more
doaj   +1 more source

Investigation of adaptive optics imaging biomarkers for detecting pathological changes of the cone mosaic in patients with type 1 diabetes mellitus [PDF]

open access: yes, 2016
Purpose To investigate a set of adaptive optics (AO) imaging biomarkers for the assessment of changes of the cone mosaic spatial arrangement in patients with type 1 diabetes mellitus (DM1).
Giannini, Daniela   +5 more
core   +6 more sources

Retinal cone and rod photoreceptor cells exhibit differential susceptibility to light‐induced damage [PDF]

open access: yesJournal of Neurochemistry, 2012
J. Neurochem. (2012) 121, 146–156.AbstractAll‐trans‐retinal and its condensation‐products can cause retinal degeneration in a light‐dependent manner and contribute to the pathogenesis of human macular diseases such as Stargardt’s disease and age‐related macular degeneration.
Kiichiro, Okano   +9 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy