2017 - Fellow of the American Association for the Advancement of Science (AAAS)
His main research concerns Retinal, Genetics, Retina, Retinitis pigmentosa and Retinal degeneration. His Retinal study integrates concerns from other disciplines, such as Genetic enhancement and Cell biology. His Retina research integrates issues from Immunocytochemistry, Pathology and Anatomy, Optic nerve.
His Retinitis pigmentosa research incorporates elements of Mutation and Rhodopsin. As a part of the same scientific study, he usually deals with the Retinal degeneration, concentrating on Electroretinography and frequently concerns with Point mutation. His Progressive retinal atrophy research includes elements of Locus and Exon.
Gustavo D. Aguirre mainly focuses on Genetics, Retinal, Retina, Retinal degeneration and Molecular biology. His Genetics and Gene, Progressive retinal atrophy, Locus, Genetic linkage and Candidate gene investigations all form part of his Genetics research activities. His Retinal study combines topics in areas such as Genetic enhancement and Pathology.
His study looks at the relationship between Retina and topics such as Cell biology, which overlap with Mutant. His research in Retinal degeneration intersects with topics in Retinitis pigmentosa and Outer nuclear layer. His Molecular biology study incorporates themes from Complementary DNA, Gene expression and Transducin.
Gustavo D. Aguirre mainly investigates Retinal, Retina, Cell biology, Retinal degeneration and Genetics. The Retinal study combines topics in areas such as Genetic enhancement and Bioinformatics. His Genetic enhancement research incorporates themes from Molecular biology, Cancer research, Recombinant DNA and Virology.
His Retina research is multidisciplinary, incorporating perspectives in In vivo and Pathology. His Cell biology research focuses on Mutant and how it relates to Achromatopsia and Erg. His study on Retinal degeneration also encompasses disciplines like
Gustavo D. Aguirre mostly deals with Retinal, Retina, Retinal degeneration, Retinitis pigmentosa and Genetics. His Retinal research is multidisciplinary, incorporating elements of Genetic enhancement and Cell biology. His research integrates issues of Vector and Molecular biology in his study of Genetic enhancement.
His biological study spans a wide range of topics, including Ophthalmology, Anatomy, Bioinformatics and Pathology. Gustavo D. Aguirre interconnects Degeneration, Cancer research, Light damage and Outer nuclear layer in the investigation of issues within Retinal degeneration. His study on Progressive retinal atrophy is often connected to Blindness as part of broader study in Retinitis pigmentosa.
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Gene therapy restores vision in a canine model of childhood blindness.
Gregory M. Acland;Gustavo D. Aguirre;Jharna Ray;Qi Zhang.
Nature Genetics (2001)
Long-Term Restoration of Rod and Cone Vision by Single Dose rAAV-Mediated Gene Transfer to the Retina in a Canine Model of Childhood Blindness
Gregory M. Acland;Gustavo D. Aguirre;Jean Bennett;Tomas S. Aleman.
Molecular Therapy (2005)
Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement
Artur V. Cideciyan;Samuel G. Jacobson;William A. Beltran;Alexander Sumaroka.
Proceedings of the National Academy of Sciences of the United States of America (2013)
Encapsulated cell-based delivery of CNTF reduces photoreceptor degeneration in animal models of retinitis pigmentosa.
Weng Tao;Rong Wen;Moses B Goddard;Sandy D Sherman.
Investigative Ophthalmology & Visual Science (2002)
Unique topographic separation of two spectral classes of cones in the mouse retina
A Szél;P Röhlich;A R Caffé;B Juliusson.
The Journal of Comparative Neurology (1992)
Gene therapy rescues cone function in congenital achromatopsia
András M. Komáromy;John J. Alexander;John J. Alexander;Jessica S. Rowlan;Monique M. Garcia;Monique M. Garcia.
Human Molecular Genetics (2010)
A Linkage Map of the Canine Genome
Cathryn S. Mellersh;Amelia A. Langston;Gregory M. Acland;Melissa A. Fleming.
Genomics (1997)
Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect
Gustavo D Aguirre;Victoria Baldwin;Sue Pearce-Kelling;Kristina Narfström.
Molecular Vision (1998)
Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa
William A. Beltran;Artur V. Cideciyan;Alfred S. Lewin;Simone Iwabe.
Proceedings of the National Academy of Sciences of the United States of America (2012)
A second-generation genetic linkage map of the domestic dog, Canis familiaris.
Mark W. Neff;Karl W. Broman;Cathryn S. Mellersh;Kunal Ray.
Genetics (1999)
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