Publicacions
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Navas-Pérez E, Vicente-García C, Mirra S, Burguera D, Fernandez-Castillo N, Ferrán JL, López-Mayorga M, Alaiz-Noya M, Suárez-Pereira I, Antón-Galindo E, Ulloa F, Herrera-Úbeda C, Cuscó P, Falcón-Moya R, Rodríguez-Moreno A, D'Aniello S, Cormand B, Marfany G, Soriano E, Carrión ÁM, Carvajal JJ and Garcia-Fernàndez J.
Characterization of an eutherian gene cluster generated after transposon domestication identifies Bex3 as relevant for advanced neurological functions.
Genome Biology . 21(1): 267-267. Nº de cites: 12
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Domènech EB, Andres R, Lopez MJ, Mirra S, García-Arroyo R, Milla S, Sava F, Andilla J, Loza-Álvarez P, de la Villa P, Gonzalez R and Marfany G.
A New Cerkl Mouse Model Generated by CRISPR-Cas9 Shows Progressive Retinal Degeneration and Altered Morphological and Electrophysiological Phenotype.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE . 61(8): 14-14. Nº de cites: 15
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Mirra S, Marfany G and Garcia-Fernàndez J.
Under pressure: Cerebrospinal fluid contribution to the physiological homeostasis of the eye.
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY . 102: 40-47. Nº de cites: 3
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B Domènech E and Marfany G.
The Relevance of Oxidative Stress in the Pathogenesis and Therapy of Retinal Dystrophies.
ANTIOXIDANTS . 9(4): . Nº de cites: 118
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Toulis V, Cortés-González V, Castro-Miró M, Sallum JF, Català-Mora J, Villanueva-Mendoza C, Ciccioli M, Gonzalez R, Valero R and Marfany G.
Increasing the Genetic Diagnosis Yield in Inherited Retinal Dystrophies: Assigning Pathogenicity to Novel Non-canonical Splice Site Variants
GENES . 11(4): 378-378. Nº de cites: 13
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Toulis V and Marfany G.
By the Tips of Your Cilia: Ciliogenesis in the Retina and the Ubiquitin-Proteasome System.
Advances in Experimental Medicine and Biology . 1233: 303-310. Nº de cites: 5
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Esquerdo-Barragán M, Brooks MJ, Toulis V, Swaroop A and Marfany G.
Expression of deubiquitinating enzyme genes in the developing mammal retina.
MOLECULAR VISION . 25: 800-813. Nº de cites: 8
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Valero R, De-Castro M, Jiménez-Ochoa S, Rodríguez-Ezcurra JJ, Marfany G and Gonzalez R.
Aberrant Splicing Events Associated to CDH23 Noncanonical Splice Site Mutations in a Proband with Atypical Usher Syndrome 1
GENES . 10(10): . Nº de cites: 15
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Bolinches-Amorós A, León M, Del Buey Furió V, Marfany G, Gonzalez R, Erceg S and Lukovic D.
Generation of an iPSC line from a retinitis pigmentosa patient carrying a homozygous mutation in CERKL and a healthy sibling.
STEM CELL RESEARCH . 38: 101455-101455. Nº de cites: 6
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Trigueros S, Domènech EB, Toulis V and Marfany G.
In Vitro Gene Delivery in Retinal Pigment Epithelium Cells by Plasmid DNA-Wrapped Gold Nanoparticles.
GENES . 10(4): . Nº de cites: 35