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 von Medina-Trillo, Cristina, Sedgwick, Daniel M., Herrera, Lidia, Beltrán, Manuela, Moreno, Ángela, Barrio, Pablo, Bedoya, Luis. M., Alcamí, José, Fustero, Santos, Gallego, José

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Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma von Medina-Trillo, Cristina, Aroca-Aguilar, José-Daniel, Ferre-Fernández, Jesús-José, Alexandre-Moreno, Susana, Morales, Laura, Méndez-Hernández, Carmen-Dora, García-Feijoo, Julián, Escribano, Julio

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Null CYP1B1 Genotypes in Primary Congenital and Nondominant Juvenile Glaucoma von López-Garrido, María-Pilar, PhD, Medina-Trillo, Cristina, MS, Morales-Fernandez, Laura, MD, Garcia-Feijoo, Julián, MD, PhD, Martínez-de-la-Casa, José-María, MD, PhD, García-Antón, Maite, MS, Escribano, Julio, PhD

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Hypo- and hypermorphic FOXC1 mutations in dominant glaucoma: transactivation and phenotypic variability von Medina-Trillo, Cristina, Sánchez-Sánchez, Francisco, Aroca-Aguilar, José-Daniel, Ferre-Fernández, Jesús-José, Morales, Laura, Méndez-Hernández, Carmen-Dora, Blanco-Kelly, Fiona, Ayuso, Carmen, García-Feijoo, Julián, Escribano, Julio

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Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development von Ferre-Fernández, Jesús-José, Aroca-Aguilar, José-Daniel, Medina-Trillo, Cristina, Bonet-Fernández, Juan-Manuel, Méndez-Hernández, Carmen-Dora, Morales-Fernández, Laura, Corton, Marta, Cabañero-Valera, María-José, Gut, Marta, Tonda, Raul, Ayuso, Carmen, Coca-Prados, Miguel, García-Feijoo, Julián, Escribano, Julio

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Functional characterization of eight rare missense CYP1B1 variants involved in congenital glaucoma and their association with null genotypes von Medina‐Trillo, Cristina, Ferre‐Fernández, Jesús‐José, Aroca‐Aguilar, José‐Daniel, Bonet‐Fernández, Juan‐Manuel, Escribano, Julio

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Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences von Medina-Trillo, Cristina, Aroca-Aguilar, José-Daniel, Méndez-Hernández, Carmen-Dora, Morales, Laura, García-Antón, Maite, García-Feijoo, Julián, Escribano, Julio

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Functional characterization of eight rare missense CYP 1B1 variants involved in congenital glaucoma and their association with null genotypes von Medina‐Trillo, Cristina, Ferre‐Fernández, Jesús‐José, Aroca‐Aguilar, José‐Daniel, Bonet‐Fernández, Juan‐Manuel, Escribano, Julio

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Whole-exome sequencing of congenital glaucoma patients reveals hypermorphic variants in GPATCH3, a new gene involved in ocular and craniofacial development von Ferré Fernández, Jesús José, Aroca Aguilar, José Daniel, Medina Trillo, Cristina, Bonet Fernández, Juan Manuel, Méndez Hernández, Carmen Dora, Morales Fernández, Laura, Cortón, Marta, Cabañero Valera, María José, Gut, Marta, Tonda, Raúl, Ayuso, Carmen, Coca Prados, Miguel, García Feijóo, Julián, Escribano, Julio

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