Stuart R. Cobb
Edinburgh, SCT EH89XD, United Kingdom
Last Updated: 09/26/2026
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Found 37 publications
FMR1 gene therapy restores activity-driven inhibition and prevents audiogenic seizures in Fmr1 -/y mice.
Journal: bioRxiv : the preprint server for biology
Published: June 29, 2026
AAV9-Mediated PTEN Gene Therapy Rescues Hepatic Pathology and Neuroanatomical Abnormalities in a Murine Model of PTEN Hamartoma Tumour Syndrome.
Journal: Pharmaceutics
Published: June 03, 2026
Neonatal expression of human FMRP isoform corrects cortical deficits and improves behavior in a mouse model of fragile X syndrome.
Journal: Molecular therapy. Nucleic acids
Published: April 01, 2026
Self-regulating gene therapy ameliorates phenotypes and overcomes gene dosage sensitivity in a mouse model of Rett syndrome.
Journal: Science translational medicine
Published: April 02, 2025
Publisher Correction: Rett syndrome.
Journal: Nature reviews. Disease primers
Published: March 25, 2025
Engineering Toxoplasma gondii secretion systems for intracellular delivery of multiple large therapeutic proteins to neurons.
Journal: Nature microbiology
Published: December 02, 2023
Long-term muscle-specific overexpression of DOK7 in mice using AAV9-tMCK-DOK7.
Journal: Molecular therapy. Nucleic acids
Published: April 04, 2023
Novel MECP2 gene therapy is effective in a multicenter study using two mouse models of Rett syndrome and is safe in non-human primates.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: October 08, 2022
Disrupted inhibition may give clues in understanding neurodevelopmental disorders.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: January 25, 2020
Neurophysiological Signatures of Motor Impairment in Patients with Rett Syndrome.
Journal: Annals of neurology
Published: November 17, 2019
Last Updated: 09/26/2026