Publications by authors named "Heidi Fuller"

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Characterising PMP22-Proximal Partners in a Schwann Cell Model of Charcot-Marie-Tooth Disease Type1A.
Ian Holt, Nicholas Emery, Monte A Gates, Sharon J Brown, Sally L Shirran, Heidi R Fuller

Biology (Basel)· November 2025

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Gene therapy for spinal muscular atrophy: perspectives on the possibility of optimizing SMN1 delivery to correct all neurological and systemic perturbations.
Sharon J Brown, Rafael J Yáñez-Muñoz, Heidi R Fuller

Neural Regen Res· July 2025

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Long-range directional growth of neurites induced by magnetic forces.
Tasmin Nahar, Monte Gates, Emilie Secret, Jean-Michel Siaugue, Jérôme Fresnais, Heidi R Fuller

Acta Biomater· January 2025

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State of the Art in Sub-Phenotyping Midbrain Dopamine Neurons.
Valentina Basso, Máté D Döbrössy, Lachlan H Thompson, Deniz Kirik, Heidi R Fuller

Biology (Basel)· September 2024

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Proteomic characterization of human LMNA-related congenital muscular dystrophy muscle cells.
Emily C Storey, Ian Holt, Sharon Brown, Silvia Synowsky, Sally Shirran, Heidi R Fuller

Neuromuscul Disord· May 2024

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Increased NLRP1 mRNA and Protein Expression Suggests Inflammasome Activation in the Dorsolateral Prefrontal and Medial Orbitofrontal Cortex in Schizophrenia.
Ena Španić Popovački, Dora Vogrinc, Heidi R Fuller, Lea Langer Horvat, Davor Mayer

Biomolecules· March 2024

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Enhanced expression of the human Survival motor neuron 1 gene from a codon-optimised cDNA transgene in vitro and in vivo.
Neda A M Nafchi, Ellie M Chilcott, Sharon Brown, Heidi R Fuller, Melissa Bowerman

Gene Ther· December 2023

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AAV9-mediated SMN gene therapy rescues cardiac desmin but not lamin A/C and elastin dysregulation in Smn2B/- spinal muscular atrophy mice.
Sharon J Brown, Darija Šoltić, Silvia A Synowsky, Sally L Shirran, Ellie Chilcott, Heidi R Fuller

Hum Mol Genet· October 2023

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Genotype-Phenotype Correlations in Human Diseases Caused by Mutations of LINC Complex-Associated Genes: A Systematic Review and Meta-Summary.
Emily C Storey, Heidi R Fuller

Cells· December 2022

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A meta-summary and bioinformatic analysis identified interleukin 6 as a master regulator of COVID-19 severity biomarkers.
Mohannad Ghanem, Sharon J Brown, Aysha Eat Mohamed, Heidi R Fuller

Cytokine· November 2022

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The Proteome Signatures of Fibroblasts from Patients with Severe, Intermediate and Mild Spinal Muscular Atrophy Show Limited Overlap.
Sharon J Brown, Rachel A Kline, Silvia A Synowsky, Sally L Shirran, Ian Holt, Heidi R Fuller

Cells· August 2022

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Investigation of the blood proteome in response to spinal cord injury in rodent models.
Charlotte H Hulme, Heidi R Fuller, John Riddell, Sally L Shirran, Catherine H Botting

Spinal Cord· April 2022

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An interaction of heart disease-associated proteins POPDC1/2 with XIRP1 in transverse tubules and intercalated discs.
Ian Holt, Heidi R Fuller, Roland F R Schindler, Sally L Shirran, Thomas Brand

BMC Mol Cell Biol· December 2020

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Quantitative proteomic profiling of the rat substantia nigra places glial fibrillary acidic protein at the hub of proteins dysregulated during aging: Implications for idiopathic Parkinson's disease.
Yolanda Gómez-Gálvez, Heidi R Fuller, Silvia Synowsky, Sally L Shirran, Monte A Gates

J Neurosci Res· July 2020

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Muscle cell differentiation and development pathway defects in Emery-Dreifuss muscular dystrophy.
Emily C Storey, Ian Holt, Glenn E Morris, Heidi R Fuller

Neuromuscul Disord· June 2020

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Molecular Crosstalk Between Non-SMN-Related and SMN-Related Spinal Muscular Atrophy.
Darija Šoltić, Heidi R Fuller

Neurosci Insights· March 2020

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Lamin A/C dysregulation contributes to cardiac pathology in a mouse model of severe spinal muscular atrophy.
Darija Šoltić, Hannah K Shorrock, Hazel Allardyce, Emma L Wilson, Ian Holt, Heidi R Fuller

Hum Mol Genet· November 2019

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Nesprin-1-alpha2 associates with kinesin at myotube outer nuclear membranes, but is restricted to neuromuscular junction nuclei in adult muscle.
Ian Holt, Heidi R Fuller, Le Thanh Lam, Caroline A Sewry, Sally L Shirran

Sci Rep· October 2019

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Two Cases of Spinal Muscular Atrophy Type II with Eosinophilic Oesophagitis.
Heidi R Fuller, Hannah K Shorrock, Thomas H Gillingwater, Anna Pigott, Victoria Smith

J Neuromuscul Dis· July 2019

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A Systematic Review and Meta-Analysis of the Effectiveness of Surgical Decompression in Treating Patients with Malignant Middle Cerebral Artery Infarction.
Wisha Gul, Heidi R Fuller, Helen Wright, Jon Sen

World Neurosurg· December 2018

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Multi-Study Proteomic and Bioinformatic Identification of Molecular Overlap between Amyotrophic Lateral Sclerosis (ALS) and Spinal Muscular Atrophy (SMA).
Darija Šoltić, Melissa Bowerman, Joanne Stock, Hannah K Shorrock, Thomas H Gillingwater, Heidi R Fuller

Brain Sci· December 2018

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Proteomic analysis of age-related changes in ovine cerebrospinal fluid.
Carl P C Chen, Jane E Preston, Shaobo Zhou, Heidi R Fuller, David G A Morgan

Exp Gerontol· July 2018

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Two independent proteomic approaches provide a comprehensive analysis of the synovial fluid proteome response to Autologous Chondrocyte Implantation.
Charlotte H Hulme, Emma L Wilson, Heidi R Fuller, Sally Roberts, James B Richardson

Arthritis Res Ther· May 2018

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Proteomic mapping of differentially vulnerable pre-synaptic populations identifies regulators of neuronal stability in vivo.
Maica Llavero Hurtado, Heidi R Fuller, Andrew M S Wong, Samantha L Eaton, Thomas H Gillingwater

Sci Rep· September 2017

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Gene expression profiling of the dorsolateral and medial orbitofrontal cortex in schizophrenia.
Mihovil Mladinov, Goran Sedmak, Heidi R Fuller, Mirjana Babić Leko, Davor Mayer

Transl Neurosci· November 2016

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