Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Elena V. Olshevskaya"'
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 17 (2024)
Retinal membrane guanylyl cyclase (RetGC), regulated by guanylyl cyclase activating proteins (GCAPs) via negative calcium-feedback, is one of the most critically important enzymes in vertebrate rod and cone physiology, enabling their sensitivity to l
Externí odkaz:
https://doaj.org/article/402a69cc8a804204891b27ece2fd3e17
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 5 (2012)
Guanylyl cyclase activating proteins (GCAP)1 are calcium/magnesium binding proteins within neuronal calcium sensor proteins group (NCS) of the EF-hand proteins superfamily. GCAPs activate retinal guanylyl cyclase (RetGC) in vertebrate photoreceptors
Externí odkaz:
https://doaj.org/article/403994875e3345669362809e02f6986d
Publikováno v:
The Journal of Biological Chemistry
Mutations in the GUCY2D gene coding for the dimeric human retinal membrane guanylyl cyclase (RetGC) isozyme RetGC1 cause various forms of blindness, ranging from rod dysfunction to rod and cone degeneration. We tested how the mutations causing recess
Publikováno v:
The Journal of Biological Chemistry
Different forms of photoreceptor degeneration cause blindness. Retinal degeneration-3 protein (RD3) deficiency in photoreceptors leads to recessive congenital blindness. We proposed that aberrant activation of the retinal membrane guanylyl cyclase (R
Publikováno v:
Journal of Biological Chemistry. 294:13729-13739
Deficiency of RD3 (retinal degeneration 3) protein causes recessive blindness and photoreceptor degeneration in humans and in the rd3 mouse strain, but the disease mechanism is unclear. Here, we present evidence that RD3 protects photoreceptors from
Publikováno v:
The Journal of Biological Chemistry
Retinal degeneration-3 protein (RD3) deficiency causes photoreceptor dysfunction and rapid degeneration in the rd3 mouse strain and in human Leber's congenital amaurosis, a congenital retinal dystrophy that results in early vision loss. However, the
Autor:
Shinya Sato, Elena V. Olshevskaya, Alexander M. Dizhoor, Vladimir J. Kefalov, Igor V. Peshenko
Publikováno v:
The Journal of Neuroscience. 38:2990-3000
The Arg838Ser mutation in retinal membrane guanylyl cyclase 1 (RetGC1) has been linked to autosomal dominant cone–rod dystrophy type 6 (CORD6). It is believed that photoreceptor degeneration is caused by the altered sensitivity of RetGC1 to calcium
Autor:
Samuel G. Jacobson, Seher Abbas, Alexander M. Dizhoor, Elena V. Olshevskaya, Artur V. Cideciyan, Alexander Scholten, Alexander Sumaroka, Igor V. Peshenko, Karl-Wilhelm Koch
The guanylyl cyclase-activating protein, GCAP1, activates photoreceptor membrane guanylyl cyclase (RetGC) in the light, when free Ca(2+) concentrations decline, and decelerates the cyclase in the dark, when Ca(2+) concentrations rise. Here, we report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98bbb5106754ebf588b800018040ecdd
https://europepmc.org/articles/PMC6416442/
https://europepmc.org/articles/PMC6416442/
Publikováno v:
Journal of Biological Chemistry. 291:19713-19723
Retinal degeneration 3 (RD3) protein, essential for normal expression of retinal membrane guanylyl cyclase (RetGC) in photoreceptor cells, blocks RetGC catalytic activity and stimulation by guanylyl cyclase-activating proteins (GCAPs). In a mouse ret
Autor:
Qing Ruan, K. Tyler McCullough, Elena V. Olshevskaya, Seok Hong Min, Shreyasi Choudhury, William W. Hauswirth, Jim Peterson, Xi-Qin Ding, Shannon E. Boye, Igor V. Peshenko, Zhonghong Zhang, Sanford L. Boye, Alexander M. Dizhoor
Publikováno v:
Human Gene Therapy. 26:575-592
Mutations in GUCY2D are the cause of Leber congenital amaurosis type 1 (LCA1). GUCY2D encodes retinal guanylate cyclase-1 (retGC1), a protein expressed exclusively in outer segments of photoreceptors and essential for timely recovery from photoexcita