Results 231 to 240 of about 33,197 (253)

Restoration of Cone Photoreceptor Function in Retinitis Pigmentosa (RP): Retinal Cell-Based Therapy

2019
The major cause of hereditary blindness in North America is retinitis pigmentosa (RP), which is a group of inherited retinal diseases characterized by the onset of night blindness, early loss of peripheral vision, and late loss of central vision.
Henry J. Kaplan, Wei Wang, Douglas C. Dean   +2 more
openaire   +1 more source

Early detection of cone photoreceptor cell loss in retinitis pigmentosa using adaptive optics scanning laser ophthalmoscopy

Graefe's Archive for Clinical and Experimental Ophthalmology, 2019
The purpose of the study was to investigate the characteristics of the parafoveal cone density changes in patients with retinitis pigmentosa (RP) using adaptive optics scanning laser ophthalmoscopy (AO-SLO).A total of 14 eyes of RP patients and 10 eyes of control subjects were examined.
Shunji, Nakatake, Yusuke, Murakami, Jun, Funatsu, Yoshito, Koyanagi, Masato, Akiyama, Yukihide, Momozawa, Tatsuro, Ishibashi, Koh-Hei, Sonoda, Yasuhiro, Ikeda   +8 more
openaire   +2 more sources

Low-error, high-speed, and large-scale hardware implementation of retinal photoreceptor cells: Cone and rod cells

AEU - International Journal of Electronics and Communications
Gilda Ghanbarpour, Milad Ghanbarpour
exaly   +2 more sources

Diffusible factors produced by cultured neural retinal cells enhance in vitro differentiation of pineal cone photoreceptors of developing quail embryos

Developmental Brain Research, 1997
The avian pineal is a photoreceptive organ and is believed to function as a circadian clock. Avian pineal cells are secretory rudimentary photoreceptors, and previous studies have demonstrated that there are two types of photoreceptors in developing quail pineals, one of which is rhodopsin-like immunoreactive and the other iodopsin-like immunoreactive.
openaire   +2 more sources

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

2013
In den angeborenen Augenerkrankungen des Retinitis Pigmentosa (RP) Typs, degenerieren Mutationsabhängig zuerst die Stäbchen, während die nachfolgende Zapfendegeneration Mutationsunabhängig abläuft. Bis heute gibt es keine zufriedenstellende RP Therapie.
openaire   +1 more source

Retinal cone photoreceptors from pluripotent stem cells for macular regeneration

2023
Ning Zhao, Zi-Bing Jin
openaire   +1 more source

Sigma 1 Receptor Co-Localizes with NRF2 in Retinal Photoreceptor Cells

Antioxidants, 2021
Jing Wang, Brendan Marshall, Sylvia B Smith   +2 more
exaly  

Evaluation of the role of Sigma 1 receptor and Cullin3 in retinal photoreceptor cells

Free Radical Biology and Medicine, 2023
Sylvia B Smith
exaly  

Cloning and localization of RPE65 mRNA in salamander cone photoreceptor cells

Biochimica Et Biophysica Acta Gene Regulatory Mechanisms, 1998
T Michael Redmond, Rosalie K Crouch
exaly  

Generation of three-dimensional retinal organoids expressing rhodopsin and S- and M-cone opsins from mouse stem cells

Biochemical and Biophysical Research Communications, 2018
Kaori Ueda, Akishi Onishi, Makoto Nakamura   +2 more
exaly