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UnknownLong-Term Intraocular Pressure-Lowering Effects and Adverse Events of Ripasudil in Patients with Glaucoma or Ocular Hypertension over 24 Months.
Not available
S-EPMC8989847 | biostudies-literature
UnknownCrossover Randomized Study of Pharmacologic Effects of Ripasudil-Brimonidine Fixed-Dose Combination Versus Ripasudil or Brimonidine.
Not available
S-EPMC10329961 | biostudies-literature
UnknownData on early postoperative changes in aqueous monocyte chemoattractant protein-1 levels after phacoemulsification.
Not available
S-EPMC5114530 | biostudies-literature
UnknownEffects of the timing of electroporation during in vitro maturation on triple gene editing in porcine embryos using CRISPR/Cas9 system.
Not available
S-EPMC8899406 | biostudies-literature
UnknownMultiple gene editing in porcine embryos using a combination of microinjection, electroporation, and transfection methods.
Not available
S-EPMC9631378 | biostudies-literature
TranscriptomicsTranscription profiling of human retinal pigment epithelium (RPE) cell line (ARPE-19) in response to combination treatment of TGF and TNF
The purpose of this study is to determine the changes in gene expression by a human retinal pigment epithelium (RPE) cell line (ARPE-19) in response to combination treatment of TGF and TNF, which induces phenotypic changes in vitro that mimic the EMT (Epithelial-to-Mesenchymal Transition). For this ...
ORGANISM(S): Homo sapiens 
2009-09-15 | E-GEOD-12548 | biostudies-arrayexpress
UnknownThe angiogenic effects of exosomes secreted from retinal pigment epithelial cells on endothelial cells.
Not available
S-EPMC7218265 | biostudies-literature
UnknownSuberoylanilide hydroxamic acid (SAHA) inhibits transforming growth factor-beta 2-induced increases in aqueous humor outflow resistance.
Not available
S-EPMC8406002 | biostudies-literature
UnknownEffect of laser suture lysis on filtration openings: a prospective three-dimensional anterior segment optical coherence tomography study.
Not available
S-EPMC4565948 | biostudies-literature
UnknownPhenotype of cytochrome P4501B1 gene (CYP1B1) mutations in Japanese patients with primary congenital glaucoma.
Not available
S-EPMC1771574 | biostudies-literature
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