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Browsing publications by Professor Andrew Cant

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
Professor Andrew Cant
Dr Andrew Gennery
Dr Mary Slatter
Combined liver and hematopoietic stem cell transplantation in patients with X-linked hyper-IgM syndrome2019
Dr Zohreh Nademi
Dr Mary Slatter
Dr Mario Abinun
Dr Terence Flood
Professor Sophie Hambleton
et al.		Hematopoietic stem cell transplantation for cytidine triphosphate synthase 1 (CTPS1) deficiency2019
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
Professor Andrew Cant
RNAseq Supports the Molecular Genetic Diagnosis of Late-Onset ADA Deficiency2019
Dr Terence Flood
Professor Sophie Hambleton
Dr Mario Abinun
Dr Stephen Owens
Professor Andrew Cant
et al.		Two decades of excellent transplant survival for chronic granulomatous disease: A supraregional immunology transplant center report2019
Dr Katherine Sturgess
Dr Rachel Dickinson
Dr Andrew Gennery
Professor Andrew Cant
Professor Graham Jackson
et al.		In vivo T-depleted reduced intensity transplantation for GATA2-related immune dysfunction.2018
Dr Venetia Bigley
Dr Urszula Cytlak-Chaudhuri
Dr Laura Jardine
Dr Kile Green
Dr Merry Gunawan
et al.		Biallelic interferon regulatory factor 8 mutation: A complex immunodeficiency syndrome with dendritic cell deficiency, monocytopenia, and immune dysregulation2018
Professor Andrew Cant
Disease evolution and response to rapamycin in activated phosphoinositide 3-kinase δ syndrome: The European society for immunodeficiencies-activated phosphoinositide 3-kinase δ syndrome registry2018
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
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