Macular Week: Recent advances in pharmacotherapy for Stargardt disease

by DBGen Ocular Genomics

Macular Week is all about sensitizing and informing patients, associations, professionals and society of latest achievements on macular degenerative pathologies. In this publication, we will focus on ...

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DBGen and the UB-CIBERER U-718 group present their current research in genetic diagnosis and animal models of inherited retinal dystrophies in ARVO 2019

by DBGen Ocular Genomics

Dr. Gemma Marfany (co-founder and scientific board member of DBGen) presented an oral communication in ARVO 2019 (held in Vancouver, 2-6 May) to show the most prominent results of the research that hi...

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RPGeNet v2.0 allows visualizing interactions of more than 270 causative genes of inherited retinal dystrophies

by DBGen Ocular Genomics

RPGeNet is a network dedicated to provide a graphical platform that links retinal dystrophies causative genes with their molecular interactors. The aim of this network is granting researchers a tool t...

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First patient treated in ProQR STELLAR phase 1/2 gene therapy clinical trial for Usher Syndrome Type II

by DBGen Ocular Genomics

Usher syndrome is a genetic disorder that presents recessive inheritance and is characterized by hearing loss and retinitis pigmentosa, traits that may be total or partial.

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Interview with Marcela Ciccioli on progress of LHON patients treated with gene therapy in China

by DBGen Ocular Genomics

We firmly believe that the achievements of women in the field of hereditary eye diseases have to be made visible and acknowledged worldwide. For this reason, and to celebrate the International Women

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First CRISPR gene editing therapy for inherited visual disorders

by DBGen Ocular Genomics

On the 30th November EDIT-101, developed by Editas Medicine, received the approval from the Food and Drug Administration (FDA) to be the first in vivo CRISPR medicine administered to people anywhere i...

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Advances in gene therapies for Leber congenital amaurosis

by DBGen Ocular Genomics

A different gene therapy (QR-110, developed by the Dutch biotech company ProQR) is being evaluated for the treatment of people with another form of LCA caused by a specific mutation in the CEP290 gene...

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CERKL a Retinitis Pigmentosa gene and a suggestive therapy target

by DBGen Ocular Genomics

Our group has long been interested in identifying genes responsible for retinal dystrophy, and was the first to identify CERKL, a retinitis pigmentosa and cone-rod dystrophy causative gene. The precis...

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Congreso RD2018 presenta avances y próximas terapias para tratar las Distrofias de Retina

by DBGen Ocular Genomics

En el mes septiembre de 2018 se celebraron en Irlanda dos congresos muy relevantes para las enfermedades oculares, el Simposio Internacional sobre Degeneración de la Retina RD2018 y la Conferencia IS...

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Revolución en el diagnóstico genético, nuestro aporte para la revista Barraquer

by DBGen Ocular Genomics

Las fundadoras y directoras de la empresa DBGen Ocular Genomics, la Dra. Roser Gonzàlez y la Dra. Gemma Marfany, fueron invitadas a participar en el mes de junio como columnistas del número 32 de la...

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Córneas para trasplante generadas por impresoras 3D

by DBGen Ocular Genomics

Recientemente (finales de mayo de 2018), investigadores de la University of Newcastle publicaron un artículo en que demuestran que la fabricación de córneas en el laboratorio mediante impresoras 3D...

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Small chaperones to treat retinitis pigmentosa

by DBGen Ocular Genomics

Rhodopsin is the main photopigment in rods. Many mutations in the rhodopsin gene translate into a misfolded nonfunctional protein that is toxic, thus causing photoreceptor death and premature retiniti...

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