Publicacions
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Gavaldà-Navarro A, Mirra S, Manso Y, Sánchez-Infantes D, Giralt M, Soriano E and Villarroya-Gombau F.
The armadillo-repeat containing X-linked protein 3, ARMCX3, is a negative regulator of the browning of adipose tissue associated with obesity.
INTERNATIONAL JOURNAL OF OBESITY . 46(9): 1652-1661. Nº de cites: 1
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Toulis V, Casaroli-Marano R, Camós-Carreras A, Figueras-Roca M, Sánchez-Dalmau B, Muñoz E, Ashraf NS, Ferreira AF, Khan N, Marfany G and do Carmo Costa M.
Altered retinal structure and function in Spinocerebellar ataxia type 3
NEUROBIOLOGY OF DISEASE . 170: 105774-105774. Nº de cites: 5
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Luque J, Mendes I, Gómez B, Morte B, de Heredia ML, Herreras E, Corrochano V, Bueren J, Gallano P, Artuch-Iriberri R, Fillat C, Pérez-Jurado LA, Montoliu L, Carracedo Á, Millán JM, Webb SM, Palau F, CIBERER Network and Lapunzina P.
CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative
CLINICAL GENETICS . 101(5-6): 481-493. Nº de cites: 8
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García-Arroyo R, Gavaldà-Navarro A, Villarroya-Gombau F, Marfany G and Mirra S.
Overexpression of CERKL Protects Retinal Pigment Epithelium Mitochondria from Oxidative Stress Effects.
ANTIOXIDANTS . 10(12): 2018. Nº de cites: 7
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Mirra S, Arroyo RG, Domènech EB, Gavaldà-Navarro A, Herrera-Úbeda C, Oliva C, Garcia-Fernàndez J, Artuch-Iriberri R, Villarroya-Gombau F and Marfany G.
CERKL, a retinal dystrophy gene, regulates mitochondrial function and dynamics in the mammalian retina
NEUROBIOLOGY OF DISEASE . 156: 105405-105405. Nº de cites: 15
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Sánchez-Bellver L, Toulis V and Marfany G.
On the Wrong Track: Alterations of Ciliary Transport in Inherited Retinal Dystrophies.
Frontiers in Cell and Developmental Biology . 9: 623734-623734. Nº de cites: 12
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Aísa-Marín I, García-Arroyo R, Mirra S and Marfany G.
The Alter Retina: Alternative Splicing of Retinal Genes in Health and Disease.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 22(4): 1855. Nº de cites: 18
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Aísa-Marín I, Lopez MJ and Marfany G.
Data on the generation of two Nr2e3 mouse models by CRISPR / Cas9D10A nickase.
Data in brief . 33: 106447-106447. Nº de cites: 2
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Aísa-Marín I, Lopez MJ, Milla S, Lillo J, Navarro G, de la Villa P and Marfany G.
Nr2e3 functional domain ablation by CRISPR-Cas9D10A identifies a new isoform and generates retinitis pigmentosa and enhanced S-cone syndrome models.
NEUROBIOLOGY OF DISEASE . 146: 105122-105122. Nº de cites: 9
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Toulis V, García-Monclús S, de la Peña-Ramírez C, Arenas-Galnares R, Abril JF, Todi SV, Khan N, Garanto A, Costa MDC and Marfany G.
The Deubiquitinating Enzyme Ataxin-3 Regulates Ciliogenesis and Phagocytosis in the Retina.
CELL REPORTS . 33(6): 108360-108360. Nº de cites: 21