| P2093 | author name string | Ping Chen | |
| | Yili Yang | |
| | Digavalli V Sivarao | |
| | Michael K Ahlijanian | |
| | Rick Pieschl | |
| | Yu-Wen Li | |
| P2860 | cites work | Inhibition of cerebral type 1 cannabinoid receptors is associated with impaired auditory mismatch negativity generation in the ketamine model of schizophrenia | Q48262695 |
| | Anesthesia suppresses nonsynchronous responses to repetitive broadband stimuli | Q48317516 |
| | Neural mechanisms of involuntary attention to acoustic novelty and change | Q48358719 |
| | Correlating stimulus-specific adaptation of cortical neurons and local field potentials in the awake rat. | Q48416930 |
| | Mismatch negativity results from bilateral asymmetric dipole sources in the frontal and temporal lobes | Q48473261 |
| | CP-101,606, a potent neuroprotectant selective for forebrain neurons | Q48656217 |
| | Activation of glutamatergic neurotransmission by ketamine: a novel step in the pathway from NMDA receptor blockade to dopaminergic and cognitive disruptions associated with the prefrontal cortex | Q48728126 |
| | Is there pre-attentive memory-based comparison of pitch? | Q48813112 |
| | Frontal and temporal sources of mismatch negativity in healthy controls, patients at onset of schizophrenia in adolescence and others at 15 years after onset | Q48875405 |
| | Ro 25-6981, a highly potent and selective blocker of N-methyl-D-aspartate receptors containing the NR2B subunit. Characterization in vitro | Q48946347 |
| | The effects of a sub-anaesthetic dose of ketamine on human selective attention. | Q50497639 |
| | Ketamine-induced deficits in auditory and visual context-dependent processing in healthy volunteers: implications for models of cognitive deficits in schizophrenia. | Q51370914 |
| | Modulation of [3H]MK-801 binding to NMDA receptors in vivo and in vitro. | Q51396890 |
| | Ketamine increases the amplitude of the 40-Hz auditory steady-state response in humans. | Q51543070 |
| | The effect of ketamine on human somatosensory evoked potentials and its modification by nitrous oxide. | Q51742100 |
| | Stimulus-specific adaptation beyond pure tones. | Q51808674 |
| | Midlatency auditory event-related potentials in mice: comparison to midlatency auditory ERPs in humans. | Q51998622 |
| | Discrimination of speech-like contrasts in the auditory thalamus and cortex. | Q52213063 |
| | Differential Contribution of Frontal and Temporal Cortices to Auditory Change Detection: fMRI and ERP Results | Q58808126 |
| | Cerebral mechanisms underlying orienting of attention towards auditory frequency changes | Q61715804 |
| | Lesions of frontal cortex diminish the auditory mismatch negativity | Q61716048 |
| | Acoustic features and acoustic changes are represented by different central pathways | Q71742656 |
| | Multiple generators in the auditory automatic discrimination process in humans | Q78104365 |
| | A source analysis of the late human auditory evoked potentials | Q87302198 |
| | Human posterior auditory cortex gates novel sounds to consciousness | Q24564674 |
| | Circuit-based framework for understanding neurotransmitter and risk gene interactions in schizophrenia | Q24646206 |
| | Antinociceptive activity of CP-101,606, an NMDA receptor NR2B subunit antagonist | Q24672789 |
| | Mismatch negativity: translating the potential | Q26830827 |
| | Novel NMDA receptor modulators: an update | Q26849614 |
| | A distributed cortical network for auditory sensory memory in humans | Q28288707 |
| | Cerebral generators of mismatch negativity (MMN) and its magnetic counterpart (MMNm) elicited by sound changes | Q28302740 |
| | When doors of perception close: bottom-up models of disrupted cognition in schizophrenia | Q30406872 |
| | Cortical mapping of mismatch negativity with deviance detection property in rat. | Q30445701 |
| | Nonhuman primate model of schizophrenia using a noninvasive EEG method | Q30448209 |
| | Mismatch responses in the awake rat: evidence from epidural recordings of auditory cortical fields | Q30454875 |
| | Comparison of the effects of acute and chronic administration of ketamine on hippocampal oscillations: relevance for the NMDA receptor hypofunction model of schizophrenia | Q30455798 |
| | Mismatch negativity encoding of prediction errors predicts S-ketamine-induced cognitive impairments | Q30457813 |
| | Auditory cortical and hippocampal-system mismatch responses to duration deviants in urethane-anesthetized rats | Q30458893 |
| | Stimulus-specific adaptation and deviance detection in the inferior colliculus | Q30459025 |
| | Nicotine, Auditory Sensory Memory, and sustained Attention in a Human Ketamine Model of Schizophrenia: Moderating Influence of a Hallucinatory Trait | Q30462575 |
| | Epidural Auditory Event-Related Potentials in the Rat to Frequency and duration Deviants: Evidence of Mismatch Negativity? | Q30472071 |
| | Mismatch brain response to speech sound changes in rats | Q30473201 |
| | Memory-based mismatch response to frequency changes in rats | Q30474157 |
| | Reductions in the N1 and P2 auditory event-related potentials in first-hospitalized and chronic schizophrenia | Q30474411 |
| | Neurophysiological biomarkers for drug development in schizophrenia | Q30486447 |
| | The mismatch negativity: a review of underlying mechanisms. | Q30490060 |
| | Mismatch negativity generation in the human 5HT2A agonist and NMDA antagonist model of psychosis. | Q30490102 |
| | Glutamatergic modulation of auditory information processing in the human brain | Q30506046 |
| | GluN2B in corticostriatal circuits governs choice learning and choice shifting. | Q30541844 |
| | Mechanisms of human attention: event-related potentials and oscillations | Q30662212 |
| | Auditory processing that leads to conscious perception: a unique window to central auditory processing opened by the mismatch negativity and related responses | Q33705970 |
| | Expression of the NR2B-NMDA receptor trafficking complex in prefrontal cortex from a group of elderly patients with schizophrenia. | Q33846961 |
| | Forebrain NR2B overexpression facilitating the prefrontal cortex long-term potentiation and enhancing working memory function in mice. | Q33927303 |
| | Mouse behavioral endophenotypes for schizophrenia | Q34113125 |
| | "Primitive intelligence" in the auditory cortex | Q34224650 |
| | LORETA current source density for duration mismatch negativity and neuropsychological assessment in early schizophrenia | Q34664140 |
| | Early sensory contributions to contextual encoding deficits in schizophrenia | Q35136571 |
| | NMDA receptor function: subunit composition versus spatial distribution | Q36544668 |
| | NR2A- and NR2B-containing NMDA receptors in the prelimbic medial prefrontal cortex differentially mediate trace, delay, and contextual fear conditioning | Q36914507 |
| | A specialized NMDA receptor function in layer 5 recurrent microcircuitry of the adult rat prefrontal cortex | Q36954984 |
| | Speech evoked potentials: from the laboratory to the clinic | Q37153522 |
| | Mismatch negativity is a breakthrough biomarker for understanding and treating psychotic disorders | Q37191789 |
| | Role of cortical N-methyl-D-aspartate receptors in auditory sensory memory and mismatch negativity generation: implications for schizophrenia | Q37277143 |
| | Effects of nicotine on the neurophysiological and behavioral effects of ketamine in humans | Q37511387 |
| | Allosteric modulators of NR2B-containing NMDA receptors: molecular mechanisms and therapeutic potential | Q37548763 |
| | Mismatch negativity (MMN), the deviance-elicited auditory deflection, explained. | Q37581117 |
| | Neurophysiologic effect of GWAS derived schizophrenia and bipolar risk variants | Q37698539 |
| | Prefrontal cortical network connections: key site of vulnerability in stress and schizophrenia | Q37846278 |
| | The mismatch negativity: an index of cognitive decline in neuropsychiatric and neurological diseases and in ageing | Q37882222 |
| | Auditory deviance detection revisited: evidence for a hierarchical novelty system | Q37888862 |
| | The mismatch negativity (MMN)--a unique window to disturbed central auditory processing in ageing and different clinical conditions. | Q37968372 |
| | Treating working memory deficits in schizophrenia: a review of the neurobiology | Q38134983 |
| | Deviance detection based on regularity encoding along the auditory hierarchy: electrophysiological evidence in humans | Q38161840 |
| | An overview of stimulus-specific adaptation in the auditory thalamus. | Q38171697 |
| | The auditory novelty system: an attempt to integrate human and animal research | Q38178363 |
| | Nonprimary auditory thalamic representation of acoustic change | Q38572450 |
| | Stability of mismatch negativity deficits and their relationship to functional impairments in chronic schizophrenia | Q40392506 |
| | Cellular and synaptic localization of NMDA and non-NMDA receptor subunits in neocortex: organizational features related to cortical circuitry, function and disease | Q40397861 |
| | Generators of electrical and magnetic mismatch responses in humans | Q40424097 |
| | Modulation of early auditory processing during selective listening to rapidly presented tones | Q41139673 |
| | Brain-stem auditory evoked potentials in squirrel monkey (Saimiri sciureus). | Q41258115 |
| | NMDA receptors subserve persistent neuronal firing during working memory in dorsolateral prefrontal cortex | Q43238242 |
| | Effect of ketamine on the neuromagnetic mismatch field in healthy humans. | Q43698776 |
| | Mismatch negativity predicts psychotic experiences induced by NMDA receptor antagonist in healthy volunteers | Q43842059 |
| | The neural circuitry of pre-attentive auditory change-detection: an fMRI study of pitch and duration mismatch negativity generators | Q43935189 |
| | Prefrontal cortex involvement in preattentive auditory deviance detection: neuroimaging and electrophysiological evidence | Q45216546 |
| | Blockade of NMDA GluN2B receptors selectively impairs behavioral flexibility but not initial discrimination learning. | Q45348307 |
| | Ketamine modulates theta and gamma oscillations. | Q45937104 |
| | Comparison of the ex vivo receptor occupancy profile of ketamine to several NMDA receptor antagonists in mouse hippocampus. | Q46005157 |
| | Multiple brain systems generating the rat auditory evoked potential. I. Characterization of the auditory cortex response | Q46119703 |
| | Multiple brain systems generating the rat auditory evoked potential. II. Dissociation of auditory cortex and non-lemniscal generator systems | Q46270064 |
| | Spectral interactions, but no mismatch negativity, in auditory cortex of anesthetized rat. | Q46448365 |
| | Mismatch negativity deficits are associated with poor functioning in schizophrenia patients | Q46596814 |
| | Effects of an NMDA-receptor antagonist MK-801 on an MMN-like response recorded in anesthetized rats | Q46714792 |
| | Ketamine produces lasting disruptions in encoding of sensory stimuli | Q46726606 |
| | Deviance-elicited changes in event-related potentials are attenuated by ketamine in mice | Q46730772 |
| | Diminished responsiveness of ERPs in schizophrenic subjects to changes in auditory stimulation parameters: implications for theories of cortical dysfunction | Q48221375 |
| P304 | page(s) | 96 | |
| P577 | publication date | 2014-08-05 | |
| P1433 | published in | Frontiers in Psychiatry | Q27723495 |
| P1476 | title | NR2B Antagonist CP-101,606 Abolishes Pitch-Mediated Deviance Detection in Awake Rats | |
| P478 | volume | 5 | |