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Browsing publications by Angela Grainger

Newcastle AuthorsTitleYearFull text
Dr Ina Schim van der Loeff
Dr Mario Abinun
Angela Grainger
Dr Karin Engelhardt
Professor Sophie Hambleton
et al.		Defective neutrophil development and specific granule deficiency caused by a homozygous splice-site mutation in SMARCD22021
Dr Florian Gothe
Catherine Hatton
Angela Grainger
Dr Venetia Bigley
Dr Joanna Perthen
et al.		A novel case of homozygous IFNAR1 deficiency with haemophagocytic lymphohistiocytosis2020
Dr Florian Gothe
Emeritus Professor Drew Rowan
Angela Grainger
Professor Andrew Cant
Dr Mary Slatter
et al.		Novel Gain-of-Function Mutation in Stat1 Sumoylation Site Leads to CMC/CID Phenotype Responsive to Ruxolitinib2019
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 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
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 Emily Mavin
Angela Grainger
Dr Xiao Wang
Professor Andrew Gennery
Regulatory T cell subsets, T cell receptor repertoire, and autoantibodies in RAG1-deficient Omenn syndrome2012
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
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