Serine racemase deletion disrupts memory for order and alters cortical dendritic morphology.
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Gliotransmitter Release from Astrocytes: Functional, Developmental, and Pathological Implications in the BrainDendritic spine pathology in schizophreniaDeveloping treatments for cognitive deficits in schizophrenia: the challenge of translation.Pathogenic disruption of DISC1-serine racemase binding elicits schizophrenia-like behavior via D-serine depletion.Astrocyte-induced synaptogenesis is mediated by transforming growth factor β signaling through modulation of D-serine levels in cerebral cortex neuronsDevelopment of antipsychotic medications with novel mechanisms of action based on computational modeling of hippocampal neuropathology.Cell-type specific mechanisms of D-serine uptake and release in the brainA Synaptic Function Approach to Investigating Complex Psychiatric Diseases.D-serine deficiency attenuates the behavioral and cellular effects induced by the hallucinogenic 5-HT(2A) receptor agonist DOIThe NMDA Receptor and Schizophrenia: From Pathophysiology to Treatment.The postnatal development of D-serine in the retinas of two mouse strains, including a mutant mouse with a deficiency in D-amino acid oxidase and a serine racemase knockout mouseThe NMDA receptor as a target for cognitive enhancementMultiple risk pathways for schizophrenia converge in serine racemase knockout mice, a mouse model of NMDA receptor hypofunctionNeuroplasticity signaling pathways linked to the pathophysiology of schizophrenia.The NMDA receptor 'glycine modulatory site' in schizophrenia: D-serine, glycine, and beyond.The glutamate hypothesis of schizophrenia: evidence from human brain tissue studies.Cognitive abilities on transitive inference using a novel touchscreen technology for mice.Glutamate receptor composition of the post-synaptic density is altered in genetic mouse models of NMDA receptor hypo- and hyperfunction.The NMDA receptor co-agonists, D-serine and glycine, regulate neuronal dendritic architecture in the somatosensory cortex.Translating glutamate: from pathophysiology to treatment.MicroRNA-132 dysregulation in schizophrenia has implications for both neurodevelopment and adult brain function.Neuronal D-serine regulates dendritic architecture in the somatosensory cortexAltered acquisition and extinction of amphetamine-paired context conditioning in genetic mouse models of altered NMDA receptor function.D-Serine and Serine Racemase Are Associated with PSD-95 and Glutamatergic Synapse Stability.D-serine as a gliotransmitter and its roles in brain development and disease.D-serine in the midbrain periaqueductal gray contributes to morphine tolerance in rats.D-serine increases adult hippocampal neurogenesis.Spontaneous object recognition and its relevance to schizophrenia: a review of findings from pharmacological, genetic, lesion and developmental rodent models.Glutamatergic transmission in schizophrenia: from basic research to clinical practiceMicroRNAs: a light into the "black box" of neuropediatric diseases?Serine racemase: an unconventional enzyme for an unconventional transmitter.D-serine and schizophrenia: an update.Translating advances in the molecular basis of schizophrenia into novel cognitive treatment strategies.Memory for the order of events in specific sequences: contributions of the hippocampus and medial prefrontal cortex.Chronic D-serine reverses arc expression and partially rescues dendritic abnormalities in a mouse model of NMDA receptor hypofunctionFailure of NMDA receptor hypofunction to induce a pathological reduction in PV-positive GABAergic cell markers.Enhanced astrocytic d-serine underlies synaptic damage after traumatic brain injury.An mGlu5-Positive Allosteric Modulator Rescues the Neuroplasticity Deficits in a Genetic Model of NMDA Receptor Hypofunction in Schizophrenia.Subchronic pharmacological and chronic genetic NMDA receptor hypofunction differentially regulate the Akt signaling pathway and Arc expression in juvenile and adult mice.Altered CREB Binding to Activity-Dependent Genes in Serine Racemase Deficient Mice, a Mouse Model of Schizophrenia.
P2860
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P2860
Serine racemase deletion disrupts memory for order and alters cortical dendritic morphology.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Serine racemase deletion disru ...... cortical dendritic morphology.
@en
type
label
Serine racemase deletion disru ...... cortical dendritic morphology.
@en
prefLabel
Serine racemase deletion disru ...... cortical dendritic morphology.
@en
P2093
P2860
P1476
Serine racemase deletion disru ...... cortical dendritic morphology.
@en
P2093
B R Kanter
H Eichenbaum
L M DeVito
P2860
P304
P356
10.1111/J.1601-183X.2010.00656.X
P407
P577
2010-11-02T00:00:00Z