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Advances in Experimental Medicine and Biology, ISSN 0065-2598, 2018, Volume 1085, pp. 69 - 77
Journal Article
Orphanet journal of rare diseases, ISSN 1750-1172, 12/2019, Volume 14, Issue 1, pp. 295 - 10
Mutations in the Kelch-like protein 7 (KLHL7) represent a recently described and, to date, poorly characterized etiology of inherited retinal dystrophy.... 
Genetic research | Fluorescence | Development and progression | Genetic aspects | Retinitis pigmentosa | Autosomal dominant | Kelch-like protein 7 | Inherited retinal dystrophy | Kelch
Journal Article
Autophagy, ISSN 1554-8627, 10/2018, Volume 14, Issue 10, pp. 1818 - 1830
Aged and damaged mitochondria can be selectively degraded by specific autophagic elimination, termed mitophagy. Defects in mitophagy have been increasingly... 
Autosomal dominant retinitis pigmentosa | hypoxia | mitophagy | ULK1 | mRNA splicing | PRPF8 | PROTEIN | PARKIN-MEDIATED MITOPHAGY | HIGH-ALTITUDE | MITOCHONDRIA | SELECTIVE AUTOPHAGY | CELL-DEATH | CELL BIOLOGY | SCREEN | MOUSE MODEL | INDUCED RETINAL DEGENERATION | MUTATIONS
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 4/2019, Volume 257, Issue 4, pp. 725 - 731
To evaluate the progression of retinitis pigmentosa (RP) due to mutations in rhodopsin (RHO) by measuring the short-wavelength autofluorescence (SW-AF)... 
Autosomal dominant | RHO | Ophthalmology | Medicine & Public Health | Retinitis pigmentosa | Disease progression | HYPERAUTOFLUORESCENT RING | RETINAL STRUCTURE | RHODOPSIN | OPHTHALMOLOGY | MUTATIONS | Measurement | Glaucoma | Rhodopsin | Stem cells | Fluorescence | Development and progression | Rho protein | Retinitis | Mutation
Journal Article
Journal Article
Journal Article