Results 131 to 140 of about 60,943 (273)

Aggregation of the Constitutively Active K296E Rhodopsin Mutant Contributes to Retinal Degeneration

open access: yesThe FASEB Journal, Volume 39, Issue 14, 31 July 2025.
The K296E rhodopsin mutation causes autosomal dominant retinitis pigmentosa. The pathogenic effect of the mutation has typically been attributed to effects related to the constitutive activity detected in the mutant in some studies. We demonstrate here that the K296E rhodopsin mutant aggregates.
Sreelakshmi Vasudevan   +2 more
wiley   +1 more source

Chronic non-communicable diseases in patients and families with retinitis pigmentosa

open access: yesMedisur, 2023
Background: retinitis pigmentosa, an ocular disease of genetic origin and low prevalence, slowly progresses over years towards severe visual impairment and affects social performance. In the Ophthalmology Service of the Dr.
Raisa Hernández Baguer   +5 more
doaj  

Copper metabolism in retinitis pigmentosa. [PDF]

open access: bronze, 1976
DK Gahlot   +4 more
openalex   +1 more source

Adaptive optics fundus images of cone photoreceptors in the macula of patients with retinitis pigmentosa

open access: yesClinical Ophthalmology, 2013
Naoki Tojo, Tomoko Nakamura, Chiharu Fuchizawa, Toshihiko Oiwake, Atsushi HayashiDepartment of Ophthalmology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, JapanBackground: The purpose of this study was to examine
Tojo N   +4 more
doaj  

Fuchs uveitis,heterochromia,and uveitis as a coincidental finding in a case

open access: yesمجله دانشگاه علوم پزشکی بیرجند, 2013
The classical clinical triad of retinitis pigmentosa is arteriolar attenuation , retinal bone-spicule pigmentation and waxy disc pallor.   A 33 year old female patient is introduced here.
Gholamhossein Yaghoobi   +1 more
doaj  

Altered cellular immunity and suppressor cell activity in patients with primary retinitis pigmentosa. [PDF]

open access: bronze, 1981
C. D. Heredia   +4 more
openalex   +1 more source

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