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Browsing publications by Dr Mojgan Reza.

Newcastle AuthorsTitleYearFull text
Dr Preeti Singh
Maninder Heer
Dr Anastasia Resteu
Dr Aneta Mikulasova
Dr Mojgan Reza
et al.
GATA2 deficiency phenotype associated with tandem duplication of GATA2 and overexpression of GATA2-AS12021
Professor Vasily Grinev
Dr Sirintra Nakjang
Hesta McNeill
Dr Mojgan Reza
Dr Natalia Martinez Soria
et al.
RUNX1/RUNX1T1 mediates alternative splicing and reorganises the transcriptional landscape in leukemia2021
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 Transformation2018
Dr Mojgan Reza
Professor Hanns Lochmuller
Professor Annemieke Aartsma-Rus
Evaluation of serum MMP-9 as predictive biomarker for antisense therapy in Duchenne2017
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 worldwide2017
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 Dystrophy2016
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 experience2016
Dr Mojgan Reza
Dr Steven Laval
Dr Andreas Roos
Professor Hanns Lochmuller
Optimization of Internally Deleted Dystrophin Constructs2016
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 diseases2015
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 hypoplasia2014
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 drisapersen2014
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 deficiency2014
Sally Spendiff
Dr Mojgan Reza
Dr Julie Murphy
Professor Grainne Gorman
Professor Robert Taylor
et al.
Mitochondrial DNA deletions in muscle satellite cells: implications for therapies2013
Dr Mojgan Reza
Dr Steven Laval
Professor Hanns Lochmuller
Optimised dystrophin mini-constructs for gene delivery2013
Dr Mojgan Reza
Daniel Cox
Dr Steven Laval
Dr Amina Chaouch
Dr Rita Barresi
et al.
MRC NMD Centre Biobank: An overview2012
Sally Spendiff
Professor Rita Horvath
Professor Hanns Lochmuller
Dr Mojgan Reza
Dr Julie Murphy
et al.
Mitochondrial DNA mutations in satellite cells2011
Dr Mojgan Reza
Dr Michela Guglieri
Professor Hanns Lochmuller
Two new protocols to enhance the production and isolation of human induced pluripotent stem cell lines2011
Professor Rita Horvath
Dr Julie Murphy
Professor Robert Taylor
Dr Mojgan Reza
Professor Hanns Lochmuller
et al.
Finding the missing gap - mitochondrial DNA deletions in muscle stem cells2010
Dr Mojgan Reza
Dr Rita Barresi
Professor Hanns Lochmuller
MRC NMD Biobank service: an overview2010
Dr Richard Charlton
Dr Debbie Hicks
Dr Mojgan Reza
Professor Volker Straub
Professor Hanns Lochmuller
et al.
Chain-specific antibody testing of collagen VI: An additional pre-screening strategy for the diagnosis of Bethlem myopathy2009