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10.1038/srep14613

http://scihub22266oqcxt.onion/10.1038/srep14613
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suck abstract from ncbi


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pmid26423861
      Sci+Rep 2015 ; 5 (ä): 14613
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  • Bridging the translational divide: identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous gene #MMPMID26423861
  • Nithianantharajah J ; McKechanie AG ; Stewart TJ ; Johnstone M ; Blackwood DH ; St Clair D ; Grant SG ; Bussey TJ ; Saksida LM
  • Sci Rep 2015[Oct]; 5 (ä): 14613 PMID26423861 show ga
  • Development of effective therapies for brain disorders has been hampered by a lack of translational cognitive testing methods. We present the first example of using the identical touchscreen-based cognitive test to assess mice and humans carrying disease-related genetic mutations. This new paradigm has significant implications for improving how we measure and model cognitive dysfunction in human disorders in animals, thus bridging the gap towards effective translation to the clinic.
  • |Adult [MESH]
  • |Animals [MESH]
  • |Case-Control Studies [MESH]
  • |Cognition Disorders/*diagnosis/genetics [MESH]
  • |DNA Copy Number Variations [MESH]
  • |Diagnosis, Computer-Assisted [MESH]
  • |Female [MESH]
  • |Guanylate Kinases/*genetics [MESH]
  • |Humans [MESH]
  • |Male [MESH]
  • |Mice, Inbred C57BL [MESH]
  • |Mice, Knockout [MESH]
  • |Middle Aged [MESH]
  • |Mutation [MESH]
  • |Photic Stimulation [MESH]
  • |Protein Biosynthesis [MESH]
  • |Schizophrenia/diagnosis/genetics [MESH]
  • |Sequence Homology, Amino Acid [MESH]
  • |Spatial Learning [MESH]
  • |Tumor Suppressor Proteins/*genetics [MESH]
  • |User-Computer Interface [MESH]


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