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interferonopathies [PMID: 34671122]. Our group previously identified a type I interferonopathy associated with homozygous mutation of STAT2 [PMID: 31836668]. We have generated a mouse model of this disorder, in which
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real difference for patients living with this condition. With a focus on high-impact publications and grant applications, the post-doc will have the opportunity to shape their own research agenda while
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advanced patient-derived tumour models and use them to test promising therapeutic targets that exploit vulnerabilities caused by loss of the SMARCB1 gene. This role offers an excellent opportunity to further
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