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Publikováno v:
International Ophthalmology. 41:1917-1927
Color vision deficiencies are a group of vision disorders, characterized by abnormal color discrimination. They include red-green color blindness, yellow-blue color blindness and achromatopsia, among others. The deficiencies are caused by mutations i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::458deee33544aea27c80081b1234cf70
https://doi.org/10.1007/s10792-021-01717-0
https://doi.org/10.1007/s10792-021-01717-0
Autor:
Jay Neitz, Maureen Neitz
Publikováno v:
Genes, Vol 12, Iss 1180, p 1180 (2021)
Light absorption by photopigment molecules expressed in the photoreceptors in the retina is the first step in seeing. Two types of photoreceptors in the human retina are responsible for image formation: rods, and cones. Except at very low light level
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::999bf113c7fb1c3b17bbbf09b2101b37
https://www.mdpi.com/2073-4425/12/8/1180
https://www.mdpi.com/2073-4425/12/8/1180
Autor:
Stefanie Fenske, Jörn Walter, Elvir Becirovic, Johanna Wagner, Lisa Maria Riedmayr, Victoria Splith, Klara Sonnie Hinrichsmeyer, Karl Nordström, Gilles Gasparoni, Martin Biel, Christian Wahl-Schott, Sybille Böhm, Stylianos Michalakis, René D. Rötzer
Publikováno v:
Science Advances
Inherited blindness can be treated with a safe gene therapy approach using activation of functionally equivalent genes.
Catalytically inactive dCas9 fused to transcriptional activators (dCas9-VPR) enables activation of silent genes. Many disease
Catalytically inactive dCas9 fused to transcriptional activators (dCas9-VPR) enables activation of silent genes. Many disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88831a6fd6b2646d33201b7f9814f456
https://doi.org/10.1126/sciadv.aba5614
https://doi.org/10.1126/sciadv.aba5614
In catarrhine primates, trichromatic color vision is associated with the presence of three opsin genes that absorb light at three different wavelengths. The OPN1LW and OPN1MW genes are found on the X chromosome. Their proximity and similarity suggest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95482ebc120e54408691906b13314078
Autor:
Angelos Kalitzeos, Emily J Patterson, Jessica C. Gardner, Maureen Neitz, Jay Neitz, Melissa Kasilian, Alison J. Hardcastle, Michel Michaelides, Joseph Carroll
Publikováno v:
Investigative Ophthalmology & Visual Science
Purpose To assess residual cone structure in subjects with mutations in exon 2, 3, and 4 of the OPN1LW or OPN1MW opsin. Methods Thirteen males had their OPN1LW/OPN1MW opsin genes characterized. The cone mosaic was imaged using both confocal and nonco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a10bc1275ac624fd545c2512251967a7
http://europepmc.org/articles/PMC6103386
http://europepmc.org/articles/PMC6103386
Publikováno v:
Experimental Eye Research. 209:108669
M-opsin, encoded by opn1mw gene, is involved in green-light perception of mice. The role of M-opsin in emmetropization of mice remains uncertain. To answer the above question, 4-week-old wild-type (WT) mice were exposed to white light or green light
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a112705651c4f9d8e9c48812a1340bba
https://doi.org/10.1016/j.exer.2021.108669
https://doi.org/10.1016/j.exer.2021.108669
Autor:
Comar, William D., Ph.D.
G protein-coupled receptors (GPCRs) make up the largest family of cell surface protein receptors and are involved in a number of diverse biological processes. The association of GPCRs, whether they be monomeric, dimeric, or oligomeric, is hypothesize
Autor:
Michel Michaelides, Thiran Jayasundera, Mark E. Pennesi, Kari Branham, Sarwar Zahid, Dana Schlegel, John R. Heckenlively
Publikováno v:
Retinal Dystrophy Gene Atlas ISBN: 9783319108667
OPN1LW and OPN1MW lie side by side on the X-chromosome and encode the long-wavelength (red) and middle-wavelength (green) cone opsins, respectively. Mutations in these genes cause a wide array of X-linked conditions ranging from red-green dyschromato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03398a79c074818a6fca995b50117430
https://doi.org/10.1007/978-3-319-10867-4_53
https://doi.org/10.1007/978-3-319-10867-4_53
Publikováno v:
Vision Research. 116:13-24
Chromatic contrast sensitivity may be a more sensitive measure of an individual's visual function than achromatic contrast sensitivity. Here, the first aim was to quantify individual- and age-related variations in chromatic contrast sensitivity to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b76c29a3fbc7f13331d34bac2e26115f
https://doi.org/10.1016/j.visres.2015.08.015
https://doi.org/10.1016/j.visres.2015.08.015