Pah(enu2) mice, created by chemically induced genetic mutation, are characterized by biochemical phenotypes closely resembling untreated human phenylketonuria (PKU). However, studies conducted in adult Pah(enu2) mice have shown no indices of the severe mental retardation that characterizes untreated PKU. The present experiments explored recognition of novel spatial and nonspatial information in Pah(enu2) mice by two nonassociative tests that do not use explicit reinforcement and avoid lengthy training. Moreover, we evaluated emotional reactivity by the Elevated Plus Maze. Finally, the performance of affected mutants was compared with that of their unaffected and heterozygous littermates and also with that of mice of the C57BL/6 (C57) inbred...
Abstract Background Disrupted-in-Schizophrenia 1 (DISC1) is considered to be a candidate susceptibil...
One of the characteristic manifestations of several neurodegenerative diseases is the progressive de...
Cognitive impairment is a prominent feature in a range of different movement disorders. Children wit...
Phenylketonuria (PKU) is one of the most common human inborn errors of metabolism, caused by phenyla...
Phenylketonuria (PKU) is one of the most common human inborn errors of metabolism, caused by phenyla...
Phenylalanine hydroxylase (Pah)-deficient “PKU mice ” have a mutation in the Pah gene that causes ph...
To unravel the role of gene mutations in the healthy and the diseased state, countless studies have ...
3 SUMMARY Hereditary cerebellar ataxias represent a heterogeneous group of neurodegenerative disorde...
We report on a battery of behavioral screening tests that successfully identified several neurobehav...
Cognitive decline is apparent in the early stages of Huntington's disease and progressively worsens ...
linical data suggest that brain catecholamines and serotonin are deficient in phenylketonuria (PKU),...
We report on a battery of behavioral screening tests that successfully identified several neurobehav...
Hyperphenylalaninemia (HPA) refers to all clinical conditions characterized by increased amounts of ...
Apolipoprotein E-knockout (apoEKO) mice were characterized behaviorally to evaluate the impact of ap...
Abstract Background Disrupted-in-Schizophrenia 1 (DISC1) is considered to be a candidate susceptibil...
One of the characteristic manifestations of several neurodegenerative diseases is the progressive de...
Cognitive impairment is a prominent feature in a range of different movement disorders. Children wit...
Phenylketonuria (PKU) is one of the most common human inborn errors of metabolism, caused by phenyla...
Phenylketonuria (PKU) is one of the most common human inborn errors of metabolism, caused by phenyla...
Phenylalanine hydroxylase (Pah)-deficient “PKU mice ” have a mutation in the Pah gene that causes ph...
To unravel the role of gene mutations in the healthy and the diseased state, countless studies have ...
3 SUMMARY Hereditary cerebellar ataxias represent a heterogeneous group of neurodegenerative disorde...
We report on a battery of behavioral screening tests that successfully identified several neurobehav...
Cognitive decline is apparent in the early stages of Huntington's disease and progressively worsens ...
linical data suggest that brain catecholamines and serotonin are deficient in phenylketonuria (PKU),...
We report on a battery of behavioral screening tests that successfully identified several neurobehav...
Hyperphenylalaninemia (HPA) refers to all clinical conditions characterized by increased amounts of ...
Apolipoprotein E-knockout (apoEKO) mice were characterized behaviorally to evaluate the impact of ap...
Abstract Background Disrupted-in-Schizophrenia 1 (DISC1) is considered to be a candidate susceptibil...
One of the characteristic manifestations of several neurodegenerative diseases is the progressive de...
Cognitive impairment is a prominent feature in a range of different movement disorders. Children wit...