Jamie S. Mitchell
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 14 publications
Macular Pigment and Retinal Reflectance in a Feasibility Study of Multiple Sclerosis: Toward Novel Biomarkers of Hidden Disease Processes.
Journal: Investigative ophthalmology & visual science
Published: August 12, 2026
Central and Peripheral Alterations of Retinal and Choroidal Vasculature in Multiple Sclerosis: Insights from Multimodal Imaging.
Journal: Ophthalmology science
Published: November 13, 2025
Investigating the eye in Down syndrome as a window to Alzheimer's disease: the REVEAL protocol - a clinical cross-sectional study.
Journal: BMJ open
Published: July 05, 2025
Choroidal and retinal vascular changes in adults with Down syndrome: Insights into the Alzheimer's disease continuum.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: November 20, 2024
Integrated transcriptome landscape of ALS identifies genome instability linked to TDP-43 pathology.
Journal: Nature communications
Published: September 09, 2022
A Non-Toxic Concentration of Telomerase Inhibitor BIBR1532 Fails to Reduce TERT Expression in a Feeder-Free Induced Pluripotent Stem Cell Model of Human Motor Neurogenesis.
Journal: International journal of molecular sciences
Published: March 16, 2021
Distinct responses of neurons and astrocytes to TDP-43 proteinopathy in amyotrophic lateral sclerosis.
Journal: Brain : a journal of neurology
Published: September 16, 2019
Delineating Astrocytic Cytokine Responses in a Human Stem Cell Model of Neural Trauma.
Journal: Journal of neurotrauma
Published: August 28, 2019
Widespread FUS mislocalization is a molecular hallmark of amyotrophic lateral sclerosis.
Journal: Brain : a journal of neurology
Published: April 09, 2019
G-quadruplex-binding small molecules ameliorate C9orf72 FTD/ALS pathology in vitro and in vivo.
Journal: EMBO molecular medicine
Published: November 09, 2017
Sense and antisense RNA are not toxic in Drosophila models of C9orf72-associated ALS/FTD.
Journal: Acta neuropathologica
Published: September 24, 2017
Intron retention and nuclear loss of SFPQ are molecular hallmarks of ALS.
Journal: Nature communications
Published: September 07, 2017
Last Updated: 09/26/2026