Detalhe da pesquisa
1.
Amniotic membrane conditioned medium (AMCM) reduces inflammatory response on human limbal myofibroblast, and the potential role of lumican.
Mol Vis
; 27: 370-383, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34447239
2.
AS1411 Nucleolin-Specific Binding Aptamers Reduce Pathological Angiogenesis through Inhibition of Nucleolin Phosphorylation.
Int J Mol Sci
; 22(23)2021 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34884955
3.
Corneal neovascularization is inhibited with nucleolin-binding aptamer, AS1411.
Exp Eye Res
; 193: 107977, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32081668
4.
Negative interaction of Staphylococcus aureus on Fusarium falciforme growth ocular isolates in an in vitro mixed biofilm.
Microb Pathog
; 135: 103644, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31351106
5.
Characterization of free fatty acid receptors expression in an obesity rat model with high sucrose diet.
J Recept Signal Transduct Res
; 38(1): 76-82, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29369009
6.
Genome-wide mRNA analysis reveals a TUBD1 isoform profile as a potential biomarker for diabetic retinopathy development.
Exp Eye Res
; 155: 99-106, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28137601
7.
Acro-spondylo-pubic dysostosis associated with cataracts, microcephaly, and normal intelligence.
Am J Med Genet A
; 167A(2): 282-6, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25427842
8.
Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements.
Hum Genet
; 133(3): 331-45, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24154662
9.
Next generation sequencing uncovers a missense mutation in COL4A1 as the cause of familial retinal arteriolar tortuosity.
Graefes Arch Clin Exp Ophthalmol
; 252(11): 1789-94, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25228067
10.
Association study of multiple gene polymorphisms with the risk of adult-onset primary open-angle glaucoma in a Mexican population.
Exp Eye Res
; 107: 59-64, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23206929
11.
Risk Factors for Diabetic Retinopathy in Latin America (Mexico) and the World: A Systematic Review and Meta-Analysis.
J Clin Med
; 12(20)2023 Oct 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37892721
12.
Spontaneous Neutrophil Extracellular Traps Release Are Inflammatory Markers Associated with Hyperglycemia and Renal Failure on Diabetic Retinopathy.
Biomedicines
; 11(7)2023 Jun 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37509431
13.
Seroprevalence of SARS-CoV-2 in Mexican Health Care Workers after Two Years of the Pandemic: The Picture of an Ophthalmic Medical Centre.
Ophthalmic Epidemiol
; 30(4): 400-406, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36184872
14.
Susceptibility to advanced age-related macular degeneration and alleles of complement factor H, complement factor B, complement component 2, complement component 3, and age-related maculopathy susceptibility 2 genes in a Mexican population.
Mol Vis
; 18: 2518-25, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23112567
15.
16S rRNA gene-based identification of bacteria in postoperative endophthalmitis by PCR-Denaturing Gradient Gel Electrophoresis (PCR-DGGE) fingerprinting.
Braz J Microbiol
; 43(1): 283-7, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24031830
16.
SARS-CoV-2 Seroprevalence among the Health Care Staff of an Ophthalmological Reference Centre, a Cross Sectional Study.
Ophthalmic Epidemiol
; 29(5): 483-490, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34530684
17.
Human Amniotic Membrane Mesenchymal Stem Cell-Synthesized PGE2 Exerts an Immunomodulatory Effect on Neutrophil Extracellular Trap in a PAD-4-Dependent Pathway through EP2 and EP4.
Cells
; 11(18)2022 09 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36139406
18.
Homozygosity mapping identifies the Crumbs homologue 1 (Crb1) gene as responsible for a recessive syndrome of retinitis pigmentosa and nanophthalmos.
Am J Med Genet A
; 155A(5): 1001-6, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21484995
19.
Future Perspectives of Therapeutic, Diagnostic and Prognostic Aptamers in Eye Pathological Angiogenesis.
Cells
; 10(6)2021 06 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34200613
20.
Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma.
Mol Vis
; 16: 1162-8, 2010 Jun 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-20664696