Detalhe da pesquisa
1.
A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma.
Cell
; 187(2): 464-480.e10, 2024 01 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38242088
2.
Stress resilience-enhancing drugs preserve tissue structure and function in degenerating retina via phosphodiesterase inhibition.
Proc Natl Acad Sci U S A
; 120(19): e2221045120, 2023 05 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37126699
3.
Photoreceptor deficits appear at eye opening in Rs1 mutant mouse models of X-linked retinoschisis.
Exp Eye Res
; 242: 109872, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38514024
4.
Norrin, frizzled-4, and Lrp5 signaling in endothelial cells controls a genetic program for retinal vascularization.
Cell
; 139(2): 285-98, 2009 Oct 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-19837032
5.
Retinoschisin deficiency induces persistent aberrant waves of activity affecting neuroglial signaling in the retina.
J Neurosci
; 2022 Jul 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35906066
6.
Glucose uptake by GLUT1 in photoreceptors is essential for outer segment renewal and rod photoreceptor survival.
FASEB J
; 36(8): e22428, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35766190
7.
Glaucoma Genetic Risk Scores in the Million Veteran Program.
Ophthalmology
; 129(11): 1263-1274, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35718050
8.
A Splicing Mutation in Slc4a5 Results in Retinal Detachment and Retinal Pigment Epithelium Dysfunction.
Int J Mol Sci
; 23(4)2022 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35216333
9.
Mouse models of X-linked juvenile retinoschisis have an early onset phenotype, the severity of which varies with genotype.
Hum Mol Genet
; 28(18): 3072-3090, 2019 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31174210
10.
Role of monocarboxylate transporters in regulating metabolic homeostasis in the outer retina: Insight gained from cell-specific Bsg deletion.
FASEB J
; 34(4): 5401-5419, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32112484
11.
The circadian clock gene Bmal1 is required to control the timing of retinal neurogenesis and lamination of Müller glia in the mouse retina.
FASEB J
; 33(8): 8745-8758, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31002540
12.
Conditional deletion of Des1 in the mouse retina does not impair the visual cycle in cones.
FASEB J
; 33(4): 5782-5792, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30645148
13.
Microglial activation in an amyotrophic lateral sclerosis-like model caused by Ranbp2 loss and nucleocytoplasmic transport impairment in retinal ganglion neurons.
Cell Mol Life Sci
; 76(17): 3407-3432, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-30944974
14.
Modulating GLUT1 expression in retinal pigment epithelium decreases glucose levels in the retina: impact on photoreceptors and Müller glial cells.
Am J Physiol Cell Physiol
; 316(1): C121-C133, 2019 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30462537
15.
Reduced expression of the nob8 gene does not normalize the distribution or function of mGluR6 in the mouse retina.
Mol Vis
; 25: 890-901, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-32025181
16.
Deletion of GLUT1 in mouse lens epithelium leads to cataract formation.
Exp Eye Res
; 172: 45-53, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29604281
17.
Impact of MCT1 Haploinsufficiency on the Mouse Retina.
Adv Exp Med Biol
; 1074: 375-380, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29721966
18.
A missense mutation in Grm6 reduces but does not eliminate mGluR6 expression or rod depolarizing bipolar cell function.
J Neurophysiol
; 118(2): 845-854, 2017 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28490646
19.
Glycosylation of rhodopsin is necessary for its stability and incorporation into photoreceptor outer segment discs.
Hum Mol Genet
; 24(10): 2709-23, 2015 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25637522
20.
Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation.
Hum Mol Genet
; 24(24): 6958-74, 2015 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26405179