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pro vyhledávání: '"Lindsey S. MacLeod"'
Autor:
Isabelle Boutet, Charles A. Collin, Lindsey S. MacLeod, Claude Messier, Matthew R. Holahan, Elizabeth Berry-Kravis, Reno M. Gandhi, Cary S. Kogan
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 11 (2018)
To generate meaningful information, translational research must employ paradigms that allow extrapolation from animal models to humans. However, few studies have evaluated translational paradigms on the basis of defined validation criteria. We outlin
Externí odkaz:
https://doaj.org/article/7cf6800844ef4d399e59424c5ce0c331
Autor:
Cary S. Kogan, Isabelle Boutet, Réno M. Gandhi, Claude Messier, Matthew R. Holahan, Elizabeth Berry-Kravis, Lindsey S. MacLeod, Charles A. Collin
Publikováno v:
Frontiers in Molecular Neuroscience
Frontiers in Molecular Neuroscience, Vol 11 (2018)
Frontiers in Molecular Neuroscience, Vol 11 (2018)
To generate meaningful information, translational research must employ paradigms that allow extrapolation from animal models to humans. However, few studies have evaluated translational paradigms on the basis of defined validation criteria. We outlin
Publikováno v:
Behavioural Pharmacology. 23:89-97
Neurotransmission at dopamine (DA) and glutamate synapses has been implicated in conditioning place preference (CPP) in rats, but different receptor subtypes may be differentially involved in acquisition and expression. A balanced CPP was used to stu
Publikováno v:
Neuroreport
Fragile X syndrome is the most common cause of inherited intellectual disability and is caused by the lack of fragile X mental retardation protein (FMRP) expression. In-vitro findings in mice and post-mortem autopsies in humans are characterized by d
Autor:
Cary S. Kogan, Réno M. Gandhi, Lindsey S. MacLeod, Elizabeth Berry-Kravis, Claude Messier, Charles A. Collin
Publikováno v:
Genes, brain, and behavior. 9(1)
Fragile X syndrome (FXS) is the most prevalent form of heritable mental retardation. It arises from a mutation in the FMR1 gene on the X chromosome that interferes with expression of fragile X mental retardation protein (FMRP) and leads to a wide ran