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Hippocampus
|
March 8, 2000
Hippocampal mossy fibers and swimming navigation learning in two vole species occupying different habitats
M G Pleskacheva, D P Wolfer, I F Kupriyanova, et al.
Experientia
|
September 15, 1989
Using genetically-defined rodent strains for the identification of hippocampal traits relevant for two-way avoidance behavior: a non-invasive approach
H P Lipp, H Schwegler, W E Crusio, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
June 17, 2005
mPer1 and mPer2 mutant mice show regular spatial and contextual learning in standardized tests for hippocampus-dependent learning
M Zueger, A Urani, S Chourbaji, et al.
Annals of the New York Academy of Sciences
|
January 17, 1996
Mice homozygous for a modified beta-amyloid precursor protein (beta APP) gene show impaired behavior and high incidence of agenesis of the corpus callosum
U Müller, N Cristina, Z W Li, et al.
Cell
|
December 2, 1994
Behavioral and anatomical deficits in mice homozygous for a modified beta-amyloid precursor protein gene
U Müller, N Cristina, Z W Li, et al.
Human Molecular Genetics
|
August 1, 2000
Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome
R Chrast, H S Scott, R Madani, et al.
EMBO Reports
|
March 22, 2001
Genetic disruption of mineralocorticoid receptor leads to impaired neurogenesis and granule cell degeneration in the hippocampus of adult mice
P Gass, O Kretz, D P Wolfer, et al.
The EMBO Journal
|
October 3, 1999
Deletion of the ryanodine receptor type 3 (RyR3) impairs forms of synaptic plasticity and spatial learning
D Balschun, D P Wolfer, F Bertocchini, et al.
Translational Psychiatry
|
March 11, 2015
Lack of parvalbumin in mice leads to behavioral deficits relevant to all human autism core symptoms and related neural morphofunctional abnormalities
M Wöhr, D Orduz, P Gregory, et al.
Behavior Genetics
|
October 13, 2006
Deletion of the Coffin-Lowry syndrome gene Rsk2 in mice is associated with impaired spatial learning and reduced control of exploratory behavior
R Poirier, S Jacquot, C Vaillend, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 59) with videos related to
Sort By:
Page
of 6
Hippocampus
|
March 8, 2000
Hippocampal mossy fibers and swimming navigation learning in two vole species occupying different habitats
M G Pleskacheva, D P Wolfer, I F Kupriyanova, et al.
Experientia
|
September 15, 1989
Using genetically-defined rodent strains for the identification of hippocampal traits relevant for two-way avoidance behavior: a non-invasive approach
H P Lipp, H Schwegler, W E Crusio, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
June 17, 2005
mPer1 and mPer2 mutant mice show regular spatial and contextual learning in standardized tests for hippocampus-dependent learning
M Zueger, A Urani, S Chourbaji, et al.
Annals of the New York Academy of Sciences
|
January 17, 1996
Mice homozygous for a modified beta-amyloid precursor protein (beta APP) gene show impaired behavior and high incidence of agenesis of the corpus callosum
U Müller, N Cristina, Z W Li, et al.
Cell
|
December 2, 1994
Behavioral and anatomical deficits in mice homozygous for a modified beta-amyloid precursor protein gene
U Müller, N Cristina, Z W Li, et al.
Human Molecular Genetics
|
August 1, 2000
Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome
R Chrast, H S Scott, R Madani, et al.
EMBO Reports
|
March 22, 2001
Genetic disruption of mineralocorticoid receptor leads to impaired neurogenesis and granule cell degeneration in the hippocampus of adult mice
P Gass, O Kretz, D P Wolfer, et al.
The EMBO Journal
|
October 3, 1999
Deletion of the ryanodine receptor type 3 (RyR3) impairs forms of synaptic plasticity and spatial learning
D Balschun, D P Wolfer, F Bertocchini, et al.
Translational Psychiatry
|
March 11, 2015
Lack of parvalbumin in mice leads to behavioral deficits relevant to all human autism core symptoms and related neural morphofunctional abnormalities
M Wöhr, D Orduz, P Gregory, et al.
Behavior Genetics
|
October 13, 2006
Deletion of the Coffin-Lowry syndrome gene Rsk2 in mice is associated with impaired spatial learning and reduced control of exploratory behavior
R Poirier, S Jacquot, C Vaillend, et al.
Page
of 6