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Browsing publications by
Dr Mojgan Reza
Newcastle Authors
Title
Year
Full text
Dr Lynsey McKenzie
Hasan Issa
Sandeep Potluri
Dr Helen Blair
Asmida Isa
et al.
The Oncogenic Transcription Factor RUNX1/ETO Corrupts Cell Cycle Regulation to Drive Leukemic Transformation
2018
Dr Mojgan Reza
Professor Hanns Lochmuller
Professor Annemieke Aartsma-Rus
Evaluation of serum MMP-9 as predictive biomarker for antisense therapy in Duchenne
2017
Dr Mojgan Reza
Daniel Cox
Lauren Phillips
Michael Grieves
Rebecca Crow
et al.
MRC Centre Neuromuscular Biobank (Newcastle and London): Supporting and facilitating rare and neuromuscular disease research worldwide
2017
Dr Mojgan Reza
Dr Steven Laval
Professor Hanns Lochmuller
Autologous skeletal muscle derived cells expressing a novel functional dystrophin provide a potential therapy for Duchenne Muscular Dystrophy
2016
Dr Andreas Roos
Daniel Cox
Dr Mojgan Reza
Dr Michela Guglieri
Professor Volker Straub
et al.
MRC biobank Newcastle - A five-year review of the John Walton Muscular Dystrophy Research Centre experience
2016
Dr Mojgan Reza
Dr Steven Laval
Dr Andreas Roos
Professor Hanns Lochmuller
Optimization of Internally Deleted Dystrophin Constructs
2016
Dr Stephen Lynn
Dr Monica Ensini
Dr Mojgan Reza
Professor Hanns Lochmuller
The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases
2015
Dr Veronika Boczonadi
Dr Juliane Mueller
Dr Angela Pyle
Dr Jennifer Munkley
Michele Giunta
et al.
EXOSC8
mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia
2014
Dr Mojgan Reza
Dr Mattia Calissano
Professor Hanns Lochmuller
Professor Annemieke Aartsma-Rus
MMP-9 serum levels increase over time in Duchenne muscular dystrophy patients and decrease upon treatment with drisapersen
2014
Abdulraheem Almalki
Dr Charlotte Alston
Dr Mojgan Reza
Professor Robert Lightowlers
Professor Bobby McFarland
et al.
Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency
2014
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