Toggle Main Menu Toggle Search

Open Access padlockePrints

Browsing publications by Daniel Cox

Newcastle AuthorsTitleYearFull text
Heather Hilsden
Daniel Cox
Professor Volker Straub
High-Density Lipoprotein-Associated Cholesterol Abnormalities in a Clinical Outcomes Study of Dysferlin-Deficient Limb-Girdle Muscular Dystrophy Type R22025
Izzy Matthews
Dr Pratima Mehra
Daniel Cox
Vellia Justian
Zoe Laidler
et al.		Strategy for drug repurposing in fibroadipogenic replacement during muscle wasting: application to duchenne muscular dystrophy2025
Dr Ana Topf
Daniel Cox
Dr Valeria Di Leo
Professor Chiara Marini Bettolo
Professor Jordi Diaz Manera
et al.		Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy2024
Esther Fernández-Simón
Rasya Gokul Nath
Adrienne Unsworth
Dr Marianela Schiava
Professor Giorgio Tasca
et al.		Single cell RNA sequencing of human FAPs reveals different functional stages in Duchenne muscular dystrophy2024
Dr Ursula Moore
Esther Fernández-Simón
Dr Marianela Schiava
Daniel Cox
Meredith James
et al.		Myostatin and follistatin as monitoring and prognostic biomarkers in dysferlinopathy2023
Andrew Galloway
Daniel Cox
Dr Ana Topf
Heather Hilsden
Professor Michela Guglieri
et al.		The John Walton Muscular Dystrophy Research Centre Biobank2023
Daniel Cox
Professor Volker Straub
Limb-girdle muscular dystrophy type 2B causes HDL-C abnormalities in patients and statin-resistant muscle wasting in dysferlin-deficient mice2022
Dr Ana Topf
Daniel Cox
Dr Lizzie Harris
STIM1 and ORAI1 mutations leading to tubular aggregate myopathies are sensitive to the Store-operated Ca2+-entry modulators CIC-37 and CIC-392022
Daniel Cox
Professor Volker Straub
Elevation of fast but not slow troponin I in the circulation of patients with Becker and Duchenne muscular dystrophy2021
Daniel Cox
Professor Giorgio Tasca
Dr Richard Charlton
INPP5K and SIL1 associated pathologies with overlapping clinical phenotypes converge through dysregulation of PHGDH2021
Daniel Cox
Professor Volker Straub
High prevalence of plasma lipid abnormalities in human and canine Duchenne and Becker muscular dystrophies depicts a new type of primary genetic dyslipidemia2020
Daniel Cox
Mitochondrial fragmentation enables localized signaling required for cell repair2020
Daniel Cox
Matt Henderson
Professor Volker Straub
Dr Rita Barresi
A simple and rapid immunoassay predicts dysferlinopathies in peripheral blood film2019
Daniel Cox
Silvia Cipriani
Dr Sally Spendiff
Emily O'Connor
Professor Rita Horvath
et al.		SIL1 deficiency causes degenerative changes of peripheral nerves and neuromuscular junctions in fish, mice and human2019
Emily O'Connor
Dr Ana Topf
Dr Sally Spendiff
Daniel Cox
Dr Andreas Roos
et al.		Clinical and research strategies for limb-girdle congenital myasthenic syndromes2018
12