Results 71 to 80 of about 19,866 (162)

From Ganglion Cell to Photoreceptor Layer: Timeline of Deterioration in a Rat Ischemia/Reperfusion Model

open access: yesFrontiers in Cellular Neuroscience, 2019
Neuronal damage and impaired vision in different retinal disorders are induced, among other factors, by ischemia/reperfusion (I/R). Since the mechanisms and the progression of ischemic injury are still not completely clarified, a timeline of this retinal
Marina Palmhof   +8 more
doaj   +1 more source

Automated measurements of human cone photoreceptor density in healthy and degenerative retina by region-based segmentation

open access: yesClinical Ophthalmology, 2017
Suguru Miyagawa,1,2 Hisashi Fukuyama,3 Masakazu Hirota,1 Tatsuo Yamaguchi,4 Kazuo Kitamura,4 Takao Endo,3 Hiroyuki Kanda,1 Takeshi Morimoto,1 Takashi Fujikado1 1Department of Applied Visual Science, Osaka University Graduate School of Medicine, Suita ...
Miyagawa S   +8 more
doaj  

Parsimony and complexity: Cell fate assignment in the developing Drosophila eye

open access: yesFly, 2017
The specification of the R7 photoreceptor in the Drosophila eye has become a classic model for understanding how cell fates are assigned in developing systems.
Yannis Emmanuel Mavromatakis   +1 more
doaj   +1 more source

Quantum Dots‐caused Retinal Degeneration in Zebrafish Regulated by Ferroptosis and Mitophagy in Retinal Pigment Epithelial Cells through Inhibiting Spliceosome

open access: yesAdvanced Science
Quantum dots (QDs) are widely used, but their health impact on the visual system is little known. This study aims to elucidate the effects and mechanisms of typical metallic QDs on retinas using zebrafish.
Naying Zheng   +16 more
doaj   +1 more source

Mutant kri1l causes abnormal retinal development via cell cycle arrest and apoptosis induction

open access: yesCell Death Discovery
Damage to the ribosome or an imbalance in protein biosynthesis can lead to some human diseases, such as diabetic retinopathy (DR) and other eye diseases. Here, we reported that the kri1l gene was responsible for retinal development.
Rong Zhang   +13 more
doaj   +1 more source

Mechanisms of cone photoreceptor cell death in models for inherited retinal degeneration

open access: yes, 2012
In hereditary eye diseases of the Retinitis pigmentosa (RP) type, rod photoreceptors degenerate in a mutation-dependent fashion, followed by mutation independent cone cell death. Until today, no adequate treatment is available, but efforts are made to gain more knowledge about the mechanism of photoreceptor degeneration.
openaire   +1 more source

Photoreceptor deletion of pyruvate dehydrogenase E1 subunit α1 induces retinal degeneration and reprograms retinal metabolism. [PDF]

open access: yesMol Metab
Ma H   +11 more
europepmc   +1 more source

Heterochronic transcription factor expression drives cone-dominant retina development in 13-lined ground squirrels. [PDF]

open access: yesElife
Weir K   +11 more
europepmc   +1 more source

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