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Journal of the American Chemical Society|May 2, 2025
Bilaterally Substituted Terphenyl Molecules Efficiently Inhibit the Interaction between a Protein and a Fully Buried α-Helix in the Malaria Parasite Motor SystemSaurabh Loharch, Cristina Medina-Trillo, Daniel M Sedgwick, et al.Acta Ophthalmologica|April 10, 2016
Functional characterization of eight rare missense CYP1B1 variants involved in congenital glaucoma and their association with null genotypesCristina Medina-Trillo, Jesús-José Ferre-Fernández, José-Daniel Aroca-Aguilar, et al.European Journal of Human Genetics : EJHG|July 30, 2015
Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequencesCristina Medina-Trillo, José-Daniel Aroca-Aguilar, Carmen-Dora Méndez-Hernández, et al.International Journal of Molecular Medicine|January 2, 2026
miR‑205: A dual regulator of angiogenesis in health and disease (Review)Maria Oltra, Miriam Martínez-Santos, Maria Ybarra, et al.Microrna (Shariqah, United Arab Emirates)|March 27, 2015
The Role of hsa-miR-548l Dysregulation as a Putative Modifier Factor for Glaucoma-Associated FOXC1 MutationsCristina Medina-Trillo, José-Daniel Aroca-Aguilar, Jesús-José Ferre-Fernández, et al.Scientific Reports|April 30, 2020
Nucleic acid recognition and antiviral activity of 1,4-substituted terphenyl compounds mimicking all faces of the HIV-1 Rev protein positively-charged α-helixCristina Medina-Trillo, Daniel M Sedgwick, Lidia Herrera, et al.Ophthalmology|December 11, 2012
Null CYP1B1 genotypes in primary congenital and nondominant juvenile glaucomaMaría-Pilar López-Garrido, Cristina Medina-Trillo, Laura Morales-Fernandez, et al.Plos One|January 19, 2019
Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucomaCristina Medina-Trillo, José-Daniel Aroca-Aguilar, Jesús-José Ferre-Fernández, et al.Plos One|March 19, 2015
Hypo- and hypermorphic FOXC1 mutations in dominant glaucoma: transactivation and phenotypic variabilityCristina Medina-Trillo, Francisco Sánchez-Sánchez, José-Daniel Aroca-Aguilar, et al.Scientific Reports|April 12, 2017
Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial DevelopmentJesús-José Ferre-Fernández, José-Daniel Aroca-Aguilar, Cristina Medina-Trillo, et al.Pageof 1