Publicaciones (9) Publicaciones de SAÚL HERRANZ MARTÍN

2021

  1. Future prospects of gene therapy for Friedreich’s ataxia

    International Journal of Molecular Sciences, Vol. 22, Núm. 4, pp. 1-18

2020

  1. Experimental gene therapies for the NCLs

    Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1866, Núm. 9

2019

  1. Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten disease

    Human Molecular Genetics, Vol. 28, Núm. 23, pp. 3867-3879

2017

  1. C9orf72 expansion disrupts ATM-mediated chromosomal break repair

    Nature Neuroscience, Vol. 20, Núm. 9, pp. 1225-1235

  2. Viral delivery of C9orf72 hexanucleotide repeat expansions in mice leads to repeat-length-dependent neuropathology and behavioural deficits

    DMM Disease Models and Mechanisms, Vol. 10, Núm. 7, pp. 859-868

2015

  1. CRB2 completes a fully expressed Crumbs complex in the Retinal Pigment Epithelium

    Scientific Reports, Vol. 5

  2. Current developments in gene therapy for amyotrophic lateral sclerosis

    Expert Opinion on Biological Therapy, Vol. 15, Núm. 7, pp. 935-947

2014

  1. Gene therapy: A promising approach to treating spinal muscular atrophy

    Human Gene Therapy, Vol. 25, Núm. 7, pp. 575-586

2012

  1. Immunocytochemical Evidence of the Localization of the Crumbs Homologue 3 Protein (CRB3) in the Developing and Mature Mouse Retina

    PLoS ONE, Vol. 7, Núm. 11