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Browsing publications by Dr Karin Engelhardt

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 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 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
Dr Rui Chen
Dr Florian Gothe
Victoria Shuttleworth
Dr Vicky Brocklebank
et al.		Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT22019
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
ZNF341 controls STAT3 expression and thereby immunocompetence2018
Dr Karin Engelhardt
Professor Sophie Hambleton
14 Years after Discovery: Clinical Follow-up on 15 Patients with Inducible Co-Stimulator Deficiency2017
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 Tarana Singh Dang
Dr Joe Willet
Helen Griffin
Dr Graeme O'Boyle
Dr Mario Abinun
et al.		Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency2016
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