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Browsing publications by Dr David McDonald.

Newcastle AuthorsTitleYearFull text
Dr Chun Chen
Emily Mossman
Dr David McDonald
Dr Alasdair Blain
Laura Bone
et al.
Astrocytic Changes in Mitochondrial Oxidative Phosphorylation Protein Levels in Parkinson's Disease2022
Dr Jack Leslie
Erik Ramon Gil
Kathryn Gilroy
Dr Saimir Luli
Maja Laszczewska
et al.
CXCR2 inhibition enables NASH-HCC immunotherapy2022
Dan Hipps
Dr Philip Dobson
Charlotte Warren
Dr David McDonald
Andrew Fuller
et al.
Detecting respiratory chain defects in osteoblasts from osteoarthritic patients using imaging mass cytometry2022
Dr Laura Jardine
Dr Simone Webb
Issac Goh
Dr Gary Reynolds
Dr Michael Mather
et al.
Blood and immune development in human fetal bone marrow and Down syndrome2021
Dr Gary Reynolds
Dr Peter Vegh
Dr James Fletcher
Dr Beth Poyner
Emily Stephenson
et al.
Developmental cell programs are co-opted in inflammatory skin disease2021
Dr Chun Chen
Dr David McDonald
Dr Alasdair Blain
Dr Ashwin Sachdeva
Laura Bone
et al.
Imaging mass cytometry reveals generalised deficiency in OXPHOS complexes in Parkinson’s disease2021
Charlotte Warren
Dr David McDonald
Professor David Deehan
Professor Robert Taylor
Dr Andrew Filby
et al.
Decoding mitochondrial heterogeneity in single muscle fibres by imaging mass cytometry2020
Dr Dorin-Mirel Popescu
Dr Rachel Botting
Emily Stephenson
Dr Kile Green
Dr Simone Webb
et al.
Decoding human fetal liver haematopoiesis2019
Dr Florian Gothe
Dr David McDonald
Dr Meghan Acres
Dr Karin Engelhardt
Professor Sophie Hambleton
et al.
Human interleukin-2 receptor β mutations associated with defects in immunity and peripheral tolerance2019
Dr Laura Jardine
Dr Sarah Wiscombe
Dr Gary Reynolds
Dr David McDonald
Andrew Fuller
et al.
Lipopolysaccharide inhalation recruits monocytes and dendritic cell subsets to the alveolar airspace.2019
Dr David McDonald
Dr Lindsay Nicholson
Professor Anne Dickinson
Dr Andrew Filby
Dr Xiao Wang
et al.
Global phenotypic characterisation of human platelet lysate expanded MSCs by high-throughput flow cytometry2018
Dr Gary Reynolds
James Fletcher
Dr Laura Jardine
David Dixon
Emily Stephenson
et al.
Single-cell RNA-seq reveals new types of human blood dendritic cells, monocytes, and progenitors2017
Dr David McDonald
Dr Bernadette Carroll
Nicholas Robertson
Dr Helen Griffin
Professor Jeremy Lakey
et al.
Dual Proteolytic Pathways Govern Glycolysis and Immune Competence2014
Professor Sophie Hambleton
Dr David McDonald
Dr Helen Griffin
Angela Grainger
Dr Louise Reynard
et al.
Autosomal recessive combines immunodeficiency due to loss of function mutation in Tripeptidyl Peptidase II2012
Dr Helen Griffin
Dr David McDonald
Dr Rachel Dickinson
Angela Grainger
Dr Louise Reynard
et al.
Whole exome sequencing as a diagnostic tool in primary immunodeficiency2012
Dr Rachel Dickinson
Dr Helen Griffin
Dr Venetia Bigley
Dr Louise Reynard
Raf Hussain
et al.
Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency2011
Dr David McDonald
Dr Helen Griffin
Angela Grainger
Dr Louise Reynard
Professor John Loughlin
et al.
Whole-exome deep sequencing identifies a novel causative mutation in primary immunodeficiency2011
Professor Sophie Hambleton
Professor Andrew Cant
Professor Andrew Gennery
Dr David McDonald
A novel human immunodeficiency disorder associated with a mutation in the T cell receptor a subunit constant gene (TRAC)2010
Dr David McDonald
Professor Heather Cordell
Dr Peter Donaldson
Professor Simon Pearce
The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22 gene) predisposes to autoimmune Addison's disease2009
Dr David McDonald
Professor Simon Pearce
Thyroid peroxidase forms thionamide-sensitive homodimers: relevance for immunomodulation of thyroid autoimmunity2009
Professor Simon Pearce
Dr David McDonald
Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency2008