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.
Differential interference contrast microscopy with adjustable plastic Sanderson prisms.
Appl Opt
; 59(11): 3404-3410, 2020 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32400452
3.
Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.
Hum Genet
; 136(8): 941-949, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28620713
4.
Therapeutic targeting of the complement system in ocular disease.
Drug Discov Today
; 28(11): 103757, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37657753
5.
IL-22 receptor signaling in Paneth cells is critical for their maturation, microbiota colonization, Th17-related immune responses, and anti-Salmonella immunity.
Mucosal Immunol
; 14(2): 389-401, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33060802
6.
Dual SMAD inhibition and Wnt inhibition enable efficient and reproducible differentiations of induced pluripotent stem cells into retinal ganglion cells.
Sci Rep
; 10(1): 11828, 2020 07 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-32678240
7.
Molecular Genetics and Functional Analysis Implicate CDKN2BAS1-CDKN2B Involvement in POAG Pathogenesis.
Cells
; 9(9)2020 08 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32825664
8.
SNP located in an AluJb repeat downstream of TMCO1, rs4657473, is protective for POAG in African Americans.
Br J Ophthalmol
; 103(10): 1530-1536, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30862618
9.
Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and TNXB genes.
Clin Epigenetics
; 11(1): 6, 2019 01 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30642396
10.
Variations in TIMP3 are associated with age-related macular degeneration.
Proc Natl Acad Sci U S A
; 107(28): E112-3, 2010 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-20615939
11.
Mutation spectrum of NDP, FZD4 and TSPAN12 genes in Indian patients with retinopathy of prematurity.
Br J Ophthalmol
; 102(2): 276-281, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28982955
12.
Abnormal Complement Activation and Inflammation in the Pathogenesis of Retinopathy of Prematurity.
Front Immunol
; 8: 1868, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29312345