Sort by
Refine Your Search
-
scientist to study the human-specific genetic mechanisms of development and function of cortical neurons. Join us to undertake a highly interdisciplinary project focusing on a long-standing and fascinating
-
that mimick human striatal function and we are using these systems to study the mechanisms of Parkinson’s disease. The system, that involves a high density multielectrode array enables us to measure single
-
can easily use the setups. The researcher will use the set-ups to analyze the LCE precursor flow, also comparing with results from simulations and theory, and continuously revise and improve
-
, Reliability and Trust (SnT) at the University of Luxembourg is a leading international research and innovation centre in secure, reliable and trustworthy ICT systems and services. We play an instrumental role
-
apply: Strong interest in Social Justice, Criminal Procedure, Legal Theory and Human Rights preferably with a specialisation on the use of Artificial Intelligence in Governance and Justice Proven ability
-
electrophysiology to translational models, including animal studies and analyses of human tissue samples. This full-stack methodology enables us to directly link molecular channel function with disease phenotypes
-
, Reliability and Trust (SnT) at the University of Luxembourg is a leading international research and innovation centre in secure, reliable and trustworthy ICT systems and services. We play an instrumental role
-
, Reliability and Trust (SnT) at the University of Luxembourg is a leading international research and innovation centre in secure, reliable and trustworthy ICT systems and services. We play an instrumental role
-
will reflect in its strategic focus the European political agenda of a dual (digital and green) transition and topics related to European sovereignty. Your role We are looking for 2 PostDocs who will
-
functional screens and read out mutation identities via barcode sequencing. By providing a direct link between sequence and function MAGESTIC enables massively scaled screens of precise mutations, with