Search Results - "Roder, John"
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Behavioral Phenotypes of Disc1 Missense Mutations in Mice
Published in Neuron (Cambridge, Mass.) (03-05-2007)“…To support the role of DISC1 in human psychiatric disorders, we identified and analyzed two independently derived ENU-induced mutations in Exon 2 of mouse…”
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The involvement of the NMDA receptor d-serine/glycine site in the pathophysiology and treatment of schizophrenia
Published in Neuroscience and biobehavioral reviews (01-02-2010)“…Hypofunction of the N-methyl- d-aspartate receptor (NMDAR) has been implicated in the pathophysiology of schizophrenia. The NMDAR contains a d-serine/glycine…”
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A Dopamine D2 Receptor-DISC1 Protein Complex may Contribute to Antipsychotic-Like Effects
Published in Neuron (Cambridge, Mass.) (17-12-2014)“…Current antipsychotic drugs primarily target dopamine D2 receptors (D2Rs), in conjunction with other receptors such as those for serotonin. However, these…”
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Mice with reduced NMDA receptor glycine affinity model some of the negative and cognitive symptoms of schizophrenia
Published in Psychopharmacologia (01-10-2008)“…Rationale Schizophrenic patients demonstrate prominent negative and cognitive symptoms that are poorly responsive to antipsychotic treatment. Abnormal…”
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Disrupted-In-Schizophrenia-1 (DISC1) interactome and mental disorders: Impact of mouse models
Published in Neuroscience and biobehavioral reviews (01-09-2014)“…Disrupted-In-Schizophrenia-1 (DISC1) has captured much attention because it predisposes individuals to a wide range of mental illnesses. Notably, a number of…”
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D-Serine Augments NMDA-NR2B Receptor-Dependent Hippocampal Long-Term Depression and Spatial Reversal Learning
Published in Neuropsychopharmacology (New York, N.Y.) (01-04-2008)“…The contributions of hippocampal long-term depression (LTD) to explicit learning and memory are poorly understood. Electrophysiological and behavioral studies…”
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Maternal immune activation during gestation interacts with Disc1 point mutation to exacerbate schizophrenia-related behaviors in mice
Published in The Journal of neuroscience (01-05-2013)“…Schizophrenia is thought to result from interactions between susceptible genotypes and environmental risk factors. DISC1 is an important gene for schizophrenia…”
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Synergistic interactions between PDE4B and GSK-3: DISC1 mutant mice
Published in Neuropharmacology (01-03-2012)“…Disrupted-In-Schizophrenia-1 (DISC1) is a strong genetic risk factor associated with psychiatric disorders. Two distinct mutations in the second exon of the…”
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Contributions of the d-serine pathway to schizophrenia
Published in Neuropharmacology (01-03-2012)“…The glutamate neurotransmitter system is one of the major candidate pathways for the pathophysiology of schizophrenia, and increased understanding of the…”
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Neto1 is a novel CUB-domain NMDA receptor-interacting protein required for synaptic plasticity and learning
Published in PLoS biology (01-02-2009)“…The N-methyl-D-aspartate receptor (NMDAR), a major excitatory ligand-gated ion channel in the central nervous system (CNS), is a principal mediator of synaptic…”
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NCS-1 in the Dentate Gyrus Promotes Exploration, Synaptic Plasticity, and Rapid Acquisition of Spatial Memory
Published in Neuron (Cambridge, Mass.) (10-09-2009)“…The molecular underpinnings of exploration and its link to learning and memory remain poorly understood. Here we show that inducible, modest overexpression of…”
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Mania-like behavior induced by genetic dysfunction of the neuron-specific Na+,K+-ATPase α3 sodium pump
Published in Proceedings of the National Academy of Sciences - PNAS (01-11-2011)“…Bipolar disorder is a debilitating psychopathology with unknown etiology. Accumulating evidence suggests the possible involvement of Na+,K+-ATPase dysfunction…”
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13
A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions
Published in Human molecular genetics (15-07-2010)“…Down syndrome (DS) is caused by the presence of an extra copy of human chromosome 21 (Hsa21) and is the most common genetic cause for developmental cognitive…”
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Dual inhibitor of PDE7 and GSK-3 – VP1.15 acts as antipsychotic and cognitive enhancer in C57BL/6J mice
Published in Neuropharmacology (01-01-2013)“…Cognitive deficit is a core of schizophrenia and it is not effectively treated by the available antipsychotic drugs, hence new and more effective therapy is…”
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Specific Inhibition of Phosphodiesterase-4B Results in Anxiolysis and Facilitates Memory Acquisition
Published in Neuropsychopharmacology (New York, N.Y.) (01-03-2016)“…Cognitive dysfunction is a core feature of dementia and a prominent feature in psychiatric disease. As non-redundant regulators of intracellular cAMP…”
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Cognitive Deficits in Calsyntenin-2-deficient Mice Associated with Reduced GABAergic Transmission
Published in Neuropsychopharmacology (New York, N.Y.) (01-02-2016)“…Calsyntenin-2 has an evolutionarily conserved role in cognition. In a human genome-wide screen, the CLSTN2 locus was associated with verbal episodic memory,…”
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Mice lacking neuronal calcium sensor-1 show social and cognitive deficits
Published in Behavioural brain research (02-03-2020)“…•Neuronal Calcium Sensor-1 (NCS-1) is implicated in brain disorders.•Ncs1 knockout mice have a mild deficit in social approach.•Ncs1 knockout mice have…”
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Mania-like behavior induced by genetic dysfunction of the neuron-specific Na+,K+-ATPase alpha 3 sodium pump
Published in Proceedings of the National Academy of Sciences - PNAS (01-11-2011)“…Bipolar disorder is a debilitating psychopathology with unknown etiology. Accumulating evidence suggests the possible involvement of Na+,K+-ATPase dysfunction…”
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19
A Far-Red Emitting Probe for Unambiguous Detection of Mobile Zinc in Acidic Vesicles and Deep Tissue
Published in Chemical science (Cambridge) (01-01-2015)“…Imaging mobile zinc in acidic environments remains challenging because most small-molecule optical probes display pH-dependent fluorescence. Here we report a…”
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Characterization of Cognitive Deficits in Mice With an Alternating Hemiplegia-Linked Mutation
Published in Behavioral neuroscience (01-12-2015)“…Cognitive impairment is a prominent feature in a range of different movement disorders. Children with Alternating Hemiplegia of Childhood are prone to…”
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