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Plos One|December 18, 2018
Identification of myocilin as a blood plasma protein and analysis of its role in leukocyte adhesion to endothelial cell monolayersJosé-Daniel Aroca-Aguilar, Ana Fernández-Navarro, Jesús Ontañón, et al.
Molecular Vision|November 22, 2008
Heterozygous expression of myocilin glaucoma mutants increases secretion of the mutant forms and reduces extracellular processed myocilinJosé-Daniel Aroca-Aguilar, Francisco Sánchez-Sánchez, Francisco Martínez-Redondo, et al.
Investigative Ophthalmology & Visual Science|August 22, 2009
Functional role of proteolytic processing of recombinant myocilin in self-aggregationJosé-Daniel Aroca-Aguilar, Francisco Martínez-Redondo, Francisco Sánchez-Sánchez, et al.
International Journal of Molecular Sciences|July 2, 2021
Null cyp1b1 Activity in Zebrafish Leads to Variable Craniofacial Defects Associated with Altered Expression of Extracellular Matrix and Lipid Metabolism GenesSusana Alexandre-Moreno, Juan-Manuel Bonet-Fernández, Raquel Atienzar-Aroca, et al.
Plos One|January 24, 2013
Bicarbonate-dependent secretion and proteolytic processing of recombinant myocilinJosé-Daniel Aroca-Aguilar, Francisco Martínez-Redondo, Alba Martín-Gil, et al.
Investigative Ophthalmology & Visual Science|October 8, 2010
Interaction of recombinant myocilin with the matricellular protein SPARC: functional implicationsJosé-Daniel Aroca-Aguilar, Francisco Sánchez-Sánchez, Sikha Ghosh, 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.
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.
Molecular Vision|July 25, 2006
Heterozygous CYP1B1 gene mutations in Spanish patients with primary open-angle glaucomaMaría-Pilar López-Garrido, Francisco Sánchez-Sánchez, Francisco López-Martínez, et al.
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