Heidi R. Fuller
Keele, ENG ST55BG, United Kingdom
Last Updated: 09/26/2026
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Found 42 publications
State of the Art in Sub-Phenotyping Midbrain Dopamine Neurons.
Journal: Biology
Published: August 05, 2024
Gene therapy for spinal muscular atrophy: perspectives on the possibility of optimizing SMN1 delivery to correct all neurological and systemic perturbations.
Journal: Neural regeneration research
Published: May 05, 2024
Proteomic characterization of human LMNA-related congenital muscular dystrophy muscle cells.
Journal: Neuromuscular disorders : NMD
Published: January 19, 2024
Increased NLRP1 mRNA and Protein Expression Suggests Inflammasome Activation in the Dorsolateral Prefrontal and Medial Orbitofrontal Cortex in Schizophrenia.
Journal: Biomolecules
Published: January 15, 2024
Long-range directional growth of neurites induced by magnetic forces.
Journal: Acta biomaterialia
Published: July 23, 2023
AAV9-mediated SMN gene therapy rescues cardiac desmin but not lamin A/C and elastin dysregulation in Smn2B/- spinal muscular atrophy mice.
Journal: Human molecular genetics
Published: June 03, 2023
Plasma and rectal mucosal oxylipin levels during aspirin and eicosapentaenoic acid treatment in the seAFOod polyp prevention trial.
Journal: Prostaglandins, leukotrienes, and essential fatty acids
Published: December 12, 2022
Genotype-Phenotype Correlations in Human Diseases Caused by Mutations of LINC Complex-Associated Genes: A Systematic Review and Meta-Summary.
Journal: Cells
Published: November 11, 2022
The Proteome Signatures of Fibroblasts from Patients with Severe, Intermediate and Mild Spinal Muscular Atrophy Show Limited Overlap.
Journal: Cells
Published: July 29, 2022
Last Updated: 09/26/2026