S. Herranz-Martín

发表

Current developments in gene therapy for amyotrophic lateral sclerosis

P. Shaw, M. Azzouz, A. Alrafiah, 2015, Expert opinion on biological therapy.

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

A. Higginbottom, P. Shaw, T. Gillingwater, 2017, Disease Models & Mechanisms.

Experimental gene therapies for the NCLs.

Wenfei Liu, R. Ali, Alexander J. Smith, 2020, Biochimica et biophysica acta. Molecular basis of disease.

CLN7 mutation causes aberrant redistribution of protein isoforms and contributes to Batten disease pathobiology

J. Bolaños, T. McKay, A. Rahim, 2022, bioRxiv.

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

C. Lillo, J. Lara, D. Jimeno, 2012, PloS one.

C9orf72 Expansion Disrupts ATM-mediated Chromosomal Break Repair

Evangelia Karyka, A. Higginbottom, C. Liao, 2017, Nature Neuroscience.

Future Prospects of Gene Therapy for Friedreich’s Ataxia

J. Díaz-Nido, S. Herranz-Martín, Gabriel Ocana-Santero, 2021, International journal of molecular sciences.

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

C. Lillo, D. Jimeno, A. Velasco, 2015, Scientific Reports.

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

Amna Z. Shah, R. Ali, Alexander J. Smith, 2019, Human molecular genetics.

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

A. Higginbottom, T. Gillingwater, M. Azzouz, 2017, Disease Models & Mechanisms.