Detalhe da pesquisa
1.
Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in Ubiquitination.
Am J Hum Genet
; 99(2): 470-80, 2016 Aug 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27486781
2.
Age-related macular degeneration associated polymorphism rs10490924 in ARMS2 results in deficiency of a complement activator.
J Neuroinflammation
; 14(1): 4, 2017 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28086806
3.
Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degeneration.
Hum Mol Genet
; 23(19): 5197-210, 2014 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24833722
4.
Acid sphingomyelinase (aSMase) deficiency leads to abnormal microglia behavior and disturbed retinal function.
Biochem Biophys Res Commun
; 464(2): 434-40, 2015 Aug 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-26129774
5.
CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis.
J Clin Invest
; 133(8)2023 04 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36862503
6.
Testing for Known Retinal Degeneration Mutants in Mouse Strains.
Methods Mol Biol
; 1834: 45-58, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30324435
7.
Microglia Analysis in Retinal Degeneration Mouse Models.
Methods Mol Biol
; 1753: 159-166, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29564787
8.
Immunomodulation with minocycline rescues retinal degeneration in juvenile neuronal ceroid lipofuscinosis mice highly susceptible to light damage.
Dis Model Mech
; 11(9)2018 09 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30042155
9.
Cystoid edema, neovascularization and inflammatory processes in the murine Norrin-deficient retina.
Sci Rep
; 8(1): 5970, 2018 04 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-29654250
10.
Crocin, a plant-derived carotenoid, modulates microglial reactivity.
Biochem Biophys Rep
; 12: 245-250, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29214225
11.
Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7.
Sci Rep
; 6: 21307, 2016 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-26887858