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Browsing publications by Dr David Swan

Newcastle AuthorsTitleYearFull text
Dr David Swan
Dr Karin Engelhardt
Dr Rui Chen
Dr Rolando Berlinguer Palmini
Dr Tarana Singh Dang
et al.
An essential role for the Zn2+ transporter ZIP7 in B cell development2019
Dr David Swan
Dr Chris Lamb
Savitri Pandey
Dr Karin Engelhardt
Dr Rui Chen
et al.
Immunodeficiency, autoimmune thrombocytopenia and enterocolitis caused by autosomal recessive deficiency of PIK3CD-encoded phosphoinositide 3-kinase δ2019
Dr Christopher Duncan
Angela Grainger
Andrew Skelton
Raf Hussain
Dr Joe Willet
et al.
Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20)2018
Dr Meghan Acres
Dr Florian Gothe
Angela Grainger
Andrew Skelton
Dr David Swan
et al.
STAT5B deficiency due to a novel missense mutation in the coiled-coil domain2018
Dr Karin Engelhardt
Dr Yaobo Xu
Angela Grainger
Dr David Swan
Dr Joe Willet
et al.
Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome Sequencing2017
Dr Amy Anderson
Dr David Swan
Oliver Eltherington
Dr Arthur Pratt
Dr Gary Reynolds
et al.
Tolerogenic dendritic cells generated with dexamethasone and vitamin D3 regulate rheumatoid arthritis CD4+ T-cells partly via TGF-β12017
Dr Kenneth Taylor
Dr David Swan
Dr Arthur Affleck
Professor Nick Reynolds
Treatment of moderate-to-severe atopic eczema in adults within the UK: Results of a national survey of dermatologists2017
Professor Sophie Hambleton
Professor Andrew Cant
Dr Karin Engelhardt
Dr David Swan
Dr Joe Willet
et al.
Autoimmunity In STAT3 Gain Of Function Mutations; Broadening The Phenotype2015
Dr Karin Engelhardt
Dr David Swan
Dr Yaobo Xu
Dr Mauro Santibanez Koref
Professor Andrew Cant
et al.
Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations2015
Dr Karin Engelhardt
Yaobo Xu
Angela Grainger
Dr David Swan
Dr Joe Willet
et al.
Identification Of Heterozygous Single- And Multi-exon Deletions In IL7R By Whole Exome Sequencing2015
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