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projects, collaborate with leading experts, and contribute to the advancement of knowledge in crystal engineering. We have links with The Newcastle upon Tyne Hospital groups and our central goal is to make a
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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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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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