Human genetic studies have demonstrated that the neuregulin 1 gene (NRG1) is involved in the development of schizophrenia. Alternative splicing of NRG1 results in at least 15 distinct isoforms and all contain an extracellular epidermal growth factor (EGF)-like domain, which is sufficient for Nrg1's biological activity. Here, we characterize a heterozygous mutant model for mouse EGF-like domain neuregulin 1 (Nrg1) regarding schizophrenia-related behavioral domains. A comprehensive, multitiered phenotyping strategy was used to investigate locomotion, exploration, anxiety-related behaviors, and sensorimotor gating. Nrg1 mutant mice exhibited a hyper-locomotive phenotype and an improved ability to habituate to a new environment. Extensive analy...
Elevated levels of the type III (III) isoforms of neuregulin 1 (NRG1) have been observed in the brai...
Background: The Neuregulin 1 transmembrane domain heterozygous mutant (Nrg1 TM HET) mouse is used to...
Schizophrenia is a chronic, disabling neuropsychiatric disorder with complex genetic origins. The de...
Human genetic studies have shown that neuregulin 1 (NRG1) is a potential susceptibility gene for sch...
Neuregulins (Nrg) are a gene family that binds to tyrosine kinase receptors of the ErbB family. The ...
Neuregulin 1 (NRG1), which has been implicated in the development of schizophrenia, is expressed wid...
Neuregulin-1 (NRG1) is one of the susceptibility genes for schizophrenia and implicated in the neuro...
Clinical genetic studies have implicated neuregulin-1 [NRG1] as a leading susceptibility gene for sc...
Neuregulin 1 (NRG1) is a schizophrenia candidate gene whose protein product is involved in neuronal ...
Neuregulin 1 (Nrg1) has been widely recognized as a candidate gene for schizophrenia. This study the...
Neuregulin 1 (NRG1) is a schizophrenia candidate gene whose protein product is involved in neuronal ...
The Neuregulin 1 transmembrane domain heterozygous mutant (Nrg1 TM HET) mouse is used to investigate...
Neuregulin-1 (NRG1) has been identified as a candidate susceptibility gene for schizophrenia. In the...
BACKGROUND: The Neuregulin 1 transmembrane domain heterozygous mutant (Nrg1 TM HET) mouse is used to...
Neuregulin 1 (Nrg1) has been implicated in the development of schizophrenia and influences key neuro...
Elevated levels of the type III (III) isoforms of neuregulin 1 (NRG1) have been observed in the brai...
Background: The Neuregulin 1 transmembrane domain heterozygous mutant (Nrg1 TM HET) mouse is used to...
Schizophrenia is a chronic, disabling neuropsychiatric disorder with complex genetic origins. The de...
Human genetic studies have shown that neuregulin 1 (NRG1) is a potential susceptibility gene for sch...
Neuregulins (Nrg) are a gene family that binds to tyrosine kinase receptors of the ErbB family. The ...
Neuregulin 1 (NRG1), which has been implicated in the development of schizophrenia, is expressed wid...
Neuregulin-1 (NRG1) is one of the susceptibility genes for schizophrenia and implicated in the neuro...
Clinical genetic studies have implicated neuregulin-1 [NRG1] as a leading susceptibility gene for sc...
Neuregulin 1 (NRG1) is a schizophrenia candidate gene whose protein product is involved in neuronal ...
Neuregulin 1 (Nrg1) has been widely recognized as a candidate gene for schizophrenia. This study the...
Neuregulin 1 (NRG1) is a schizophrenia candidate gene whose protein product is involved in neuronal ...
The Neuregulin 1 transmembrane domain heterozygous mutant (Nrg1 TM HET) mouse is used to investigate...
Neuregulin-1 (NRG1) has been identified as a candidate susceptibility gene for schizophrenia. In the...
BACKGROUND: The Neuregulin 1 transmembrane domain heterozygous mutant (Nrg1 TM HET) mouse is used to...
Neuregulin 1 (Nrg1) has been implicated in the development of schizophrenia and influences key neuro...
Elevated levels of the type III (III) isoforms of neuregulin 1 (NRG1) have been observed in the brai...
Background: The Neuregulin 1 transmembrane domain heterozygous mutant (Nrg1 TM HET) mouse is used to...
Schizophrenia is a chronic, disabling neuropsychiatric disorder with complex genetic origins. The de...