Cristina Medina-Trillo

发表

Null CYP1B1 genotypes in primary congenital and nondominant juvenile glaucoma.

J. García-Feijóo, J. Escribano, J. Martinez-de-la-Casa, 2013, Ophthalmology.

Functional characterization of eight rare missense CYP1B1 variants involved in congenital glaucoma and their association with null genotypes

J. Escribano, J. Aroca-Aguilar, Juan-Manuel Bonet-Fernández, 2016, Acta ophthalmologica.

Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development

M. Gut, M. Cortón, J. García-Feijóo, 2017, Scientific Reports.

Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma

J. García-Feijóo, J. Escribano, C. Mendez-Hernandez, 2019, PloS one.

Nucleic acid recognition and antiviral activity of 1,4-substituted terphenyl compounds mimicking all faces of the HIV-1 Rev protein positively-charged α-helix

L. Bedoya, J. Alcamí, S. Fustero, 2020, Scientific Reports.

Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences

J. García-Feijóo, J. Escribano, C. Mendez-Hernandez, 2015, European Journal of Human Genetics.

Hypo- and Hypermorphic FOXC1 Mutations in Dominant Glaucoma: Transactivation and Phenotypic Variability

J. García-Feijóo, C. Ayuso, F. Blanco-Kelly, 2015, PLoS ONE.

Null CYP1B1 genotypes in primary congenital and nondominant juvenile glaucoma.

J. García-Feijóo, María-Pilar López-Garrido, Cristina Medina-Trillo, 2013, Ophthalmology.

Nucleic acid recognition and antiviral activity of 1,4-substituted terphenyl compounds mimicking all faces of the HIV-1 Rev protein positively-charged α-helix

L. Bedoya, J. Alcamí, S. Fustero, 2020, Scientific Reports.