Publications by Dr Florian Gothe - ePrints

Browsing publications by Dr Florian Gothe.

Newcastle Authors	Title	Year
Dr Florian Gothe Qian Zhang Dr Christopher Duncan Professor Sophie Hambleton	Human inherited complete STAT2 deficiency underlies inflammatory viral diseases	2023
Dr Florian Gothe Catherine Hatton Angela Grainger Dr Venetia Bigley Dr Joanna Perthen et al.	A Novel Case of Homozygous Interferon Alpha/Beta Receptor Alpha Chain (IFNAR1) Deficiency With Hemophagocytic Lymphohistiocytosis	2022
Dr Florian Gothe Catherine Hatton Dr Helen Griffin Dr Christopher Duncan Professor Sophie Hambleton et al.	Aberrant inflammatory responses to type I interferon in STAT2 or IRF9 deficiency	2022
Dr Florian Gothe Professor Sophie Hambleton	STAT5B restrains human B-cell differentiation to maintain humoral immune homeostasis	2022
Dr Aidan Hanrath Catherine Hatton Dr Florian Gothe Connie Browne Dr Simon Cockell et al.	Type I Interferon receptor (IFNAR2) deficiency reveals Zika virus cytopathicity in human macrophages and microglia	2022
Catherine Hatton Dr Rachel Botting Dr Maria Duenas Fadic Dr Iram Haq Dr Bernard Verdon et al.	Delayed induction of type I and III interferons mediates nasal epithelial cell permissiveness to SARS-CoV-2	2021
Dr Florian Gothe Sophie Howarth Dr Christopher Duncan Professor Sophie Hambleton	Monogenic susceptibility to live viral vaccines	2021
Dr Florian Gothe Professor Sophie Hambleton	The expansion of human T-bet^highCD21^low B cells is T cell dependent	2021
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 tolerance	2019
Dr Florian Gothe Emeritus Professor Drew Rowan Angela Grainger Professor Andrew Cant Professor Mary Slatter et al.	Novel Gain-of-Function Mutation in Stat1 Sumoylation Site Leads to CMC/CID Phenotype Responsive to Ruxolitinib	2019
Dr Christopher Duncan Dr Benjamin Thompson Dr Rui Chen Dr Florian Gothe Victoria Shuttleworth et al.	Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2	2019
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 domain	2018