Mental retardation in individuals with Down syndrome (DS) is thought to result from anomalous development and function of the brain; however, the underlying neuropathological processes have yet to be determined. Early implementation of special care programs result in limited, and temporary, cognitive improvements in DS individuals. In the present study, we investigated the possible neural correlates of these limited improvements. More specifically, we studied cortical pyramidal cells in the frontal cortex of Ts65Dn mice, a partial trisomy of murine chromosome 16 (MMU16) model characterized by cognitive deficits, hyperactivity, behavioral disruption and reduced attention levels similar to those observed in DS, and their control littermates. ...
Ts65Dn mouse is the most widely accepted model for Down syndrome. We previously showed that environm...
Down syndrome (DS) is the most common genetic disorder associated with mental retardation. It has be...
Down syndrome (DS), a genetic condition due to triplication of Chromosome 21, is characterized by nu...
Down syndrome (DS) is the most common genetic disorder associated with mental retardation, affecting...
Down syndrome (DS), which is due to triplication of chromosome 21, is constantly associated with int...
Since the discovery in the 1970s that dendritic abnormalities in cortical pyramidal neurons are the ...
Down syndrome (DS) results in various degrees of cognitive deficits. In DS mouse models, recovery of...
Down syndrome (DS), a genetic condition caused by triplication of chromosome 21, is characterized by...
Down Syndrome (DS) is a highly prevalent developmental disorder, affecting 1/700 births. Intellectua...
Since the discovery in the 1970s that dendritic abnormalities in cortical pyramidal neurons are the ...
Down syndrome (DS) is the most common chromosomal aneuploidy. Although trisomy on chromosome 21 can ...
Down syndrome (DS), the most prevalent cause of intellectual disability, stems from a chromosomal an...
Down syndrome (DS), the most frequent genetic cause of intellectual disability and developmental del...
Down Syndrome (DS) is a highly prevalent developmental disorder, affecting 1/700 births. Intellectua...
Ts65Dn mice are partially trisomic for the distal region of MMU16, which is homologous with the obli...
Ts65Dn mouse is the most widely accepted model for Down syndrome. We previously showed that environm...
Down syndrome (DS) is the most common genetic disorder associated with mental retardation. It has be...
Down syndrome (DS), a genetic condition due to triplication of Chromosome 21, is characterized by nu...
Down syndrome (DS) is the most common genetic disorder associated with mental retardation, affecting...
Down syndrome (DS), which is due to triplication of chromosome 21, is constantly associated with int...
Since the discovery in the 1970s that dendritic abnormalities in cortical pyramidal neurons are the ...
Down syndrome (DS) results in various degrees of cognitive deficits. In DS mouse models, recovery of...
Down syndrome (DS), a genetic condition caused by triplication of chromosome 21, is characterized by...
Down Syndrome (DS) is a highly prevalent developmental disorder, affecting 1/700 births. Intellectua...
Since the discovery in the 1970s that dendritic abnormalities in cortical pyramidal neurons are the ...
Down syndrome (DS) is the most common chromosomal aneuploidy. Although trisomy on chromosome 21 can ...
Down syndrome (DS), the most prevalent cause of intellectual disability, stems from a chromosomal an...
Down syndrome (DS), the most frequent genetic cause of intellectual disability and developmental del...
Down Syndrome (DS) is a highly prevalent developmental disorder, affecting 1/700 births. Intellectua...
Ts65Dn mice are partially trisomic for the distal region of MMU16, which is homologous with the obli...
Ts65Dn mouse is the most widely accepted model for Down syndrome. We previously showed that environm...
Down syndrome (DS) is the most common genetic disorder associated with mental retardation. It has be...
Down syndrome (DS), a genetic condition due to triplication of Chromosome 21, is characterized by nu...