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of 4
pro vyhledávání: '"Nilsson, Simon RO"'
Autor:
Hvoslef-Eide, Martha, Nilsson, Simon Ro, Hailwood, Jonathan M, Robbins, Trevor W, Saksida, Lisa M, Mar, Adam C, Bussey, Timothy J
Important tools in the study of prefrontal cortical-dependent executive functions are cross-species behavioural tasks with translational validity. A widely used test of executive function and attention in humans is the continuous performance task (CP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0a8ca22842084dae0a88b03ef6f2688
Autor:
Kim, Chi Hun, Hvoslef-Eide, Martha, Nilsson, Simon RO, Johnson, Mark R, Herbert, Bronwen R, Robbins, Trevor W, Saksida, Lisa M, Bussey, Timothy J, Mar, Adam C
Publikováno v:
Brain and Mind Institute Researchers' Publications
RATIONALE: Continuous performance tests (CPTs) are widely used to assess attentional processes in a variety of disorders including Alzheimer's disease and schizophrenia. Common human CPTs require discrimination of sequentially presented, visually pat
Autor:
Alsiö, Johan, Phillips, Benjamin U, Sala-Bayo, Júlia, Nilsson, Simon RO, Calafat-Pla, Teresa C, Rizwand, Arazo, Plumbridge, Jessica M, López-Cruz, Laura, Dalley, Jeffrey W, Cardinal, Rudolf N, Mar, Adam C, Robbins, Trevor W
RATIONALE: Dopamine D2-like receptors (D2R) are important drug targets in schizophrenia and Parkinson's disease, but D2R ligands also cause cognitive inflexibility such as poor reversal learning. The specific role of D2R in reversal learning remains
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa087c04c2754f8aa71051bd93f79e2a
Autor:
Nilsson, Simon Ro, Fejgin, Kim, Gastambide, Francois, Vogt, Miriam A, Kent, Brianne A, Nielsen, Vibeke, Nielsen, Jacob, Gass, Peter, Robbins, Trevor W, Saksida, Lisa M, Stensbøl, Tine B, Tricklebank, Mark D, Didriksen, Michael, Bussey, Timothy J
A chromosomal microdeletion at the 22q11.2 locus is associated with extensive cognitive impairments, schizophrenia and other psychopathology in humans. Previous reports indicate that mouse models of the 22q11.2 microdeletion syndrome (22q11.2DS) may
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::651128ccb80cea1650b4dad7eeef436a