Loss of Pde6a Induces Rod Outer Segment Shrinkage and Visual Alterations in pde6aQ70X Mutant Zebrafish, a Relevant Model of Retinal Dystrophy
Retinitis pigmentosa (RP) is one of the most common forms of inherited retinal degeneration with 1/4,000 people being affected. The vision alteration primarily begins with rod photoreceptor degeneration, then the degenerative process continues with cone photoreceptor death. Variants in 71 genes have...
Main Authors: | Lucie Crouzier, Camille Diez, Elodie M. Richard, Nicolas Cubedo, Clément Barbereau, Mireille Rossel, Thomas Delaunay, Tangui Maurice, Benjamin Delprat |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2021-05-01
|
Series: | Frontiers in Cell and Developmental Biology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fcell.2021.675517/full |
Similar Items
-
Implications of dimeric activation of PDE6 for rod phototransduction
by: Trevor D. Lamb, et al.
Published: (2018-08-01) -
A quantitative account of mammalian rod phototransduction with PDE6 dimeric activation: responses to bright flashes
by: Trevor D. Lamb, et al.
Published: (2020-01-01) -
Novel variants in PDE6A and PDE6B genes and its phenotypes in patients with retinitis pigmentosa in Chinese families
by: Yuyu Li, et al.
Published: (2022-01-01) -
Novel PDE6A mutation in an Emirati patient with retinitis pigmentosa
by: Pratibha Nair, et al.
Published: (2017-01-01) -
RPGR, a prenylated retinal ciliopathy protein, is targeted to cilia in a prenylation- and PDE6D-dependent manner
by: Nirmal Dutta, et al.
Published: (2016-09-01)