Heightened susceptibility to interference in an animal model of amnesia: Impairment in encoding, storage, retrieval – or all three?
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[1] E. Warrington,et al. Amnesic Syndrome: Consolidation or Retrieval? , 1970, Nature.
[2] D Marr,et al. Simple memory: a theory for archicortex. , 1971, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[3] E. Warrington,et al. Further analysis of the prior learning effect in amnesic patients , 1978, Neuropsychologia.
[4] Leslie G. Ungerleider. Two cortical visual systems , 1982 .
[5] R. Mansfield,et al. Analysis of visual behavior , 1982 .
[6] G. Paxinos,et al. The Rat Brain in Stereotaxic Coordinates , 1983 .
[7] L. Nadel,et al. The medial temporal region and memory consolidation: A new hypothesis , 2014 .
[8] A P Shimamura,et al. Priming Effects in Amnesia: Evidence for a Dissociable Memory Function , 1986, The Quarterly journal of experimental psychology. A, Human experimental psychology.
[9] Hans J. Markowitsch,et al. Primate learning tasks reveal strong impairments in patients with presenile or senile dementia of the Alzheimer type , 1987, Brain and Cognition.
[10] J. Delacour,et al. A new one-trial test for neurobiological studies of memory in rats. 1: Behavioral data , 1988, Behavioural Brain Research.
[11] D. Amaral,et al. Lesions of perirhinal and parahippocampal cortex that spare the amygdala and hippocampal formation produce severe memory impairment , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[12] L. Squire,et al. The medial temporal lobe memory system , 1991, Science.
[13] E T Rolls,et al. Neurophysiological mechanisms underlying face processing within and beyond the temporal cortical visual areas. , 1992, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[14] A. Ennaceur,et al. A new one-trial test for neurobiological studies of memory in rats. III. Spatial vs. non-spatial working memory , 1992, Behavioural Brain Research.
[15] M. Mishkin,et al. Effects on visual recognition of combined and separate ablations of the entorhinal and perirhinal cortex in rhesus monkeys , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[16] Dave G. Mumby,et al. Rhinal cortex lesions and object recognition in rats , 1994 .
[17] E. Murray,et al. Preserved Recognition Memory for Small Sets, and Impaired Stimulus Identification for Large Sets, Following Rhinal Cortex Ablations in Monkeys , 1994, The European journal of neuroscience.
[18] D. Mumby,et al. Rhinal cortex lesions and object recognition in rats. , 1994, Behavioral neuroscience.
[19] D. Bilkey,et al. Lesions of rat perirhinal cortex exacerbate the memory deficit observed following damage to the fimbria-fornix. , 1995, Behavioral neuroscience.
[20] D. Amaral,et al. Perirhinal and postrhinal cortices of the rat: A review of the neuroanatomical literature and comparison with findings from the monkey brain , 1995, Hippocampus.
[21] J. Aggleton,et al. Neurotoxic lesions of the perirhinal cortex do not mimic the behavioural effects of fornix transection in the rat , 1996, Behavioural Brain Research.
[22] M W Brown,et al. Mapping visual recognition memory through expression of the immediate early gene c-fos. , 1996, Neuroreport.
[23] L R Squire,et al. Memory, memory impairment, and the medial temporal lobe. , 1996, Cold Spring Harbor symposia on quantitative biology.
[24] L R Squire,et al. Impaired recognition memory in patients with lesions limited to the hippocampal formation. , 1997, Behavioral neuroscience.
[25] L. Squire,et al. The human perirhinal cortex and recognition memory , 1998, Hippocampus.
[26] M. Mishkin,et al. Object Recognition and Location Memory in Monkeys with Excitotoxic Lesions of the Amygdala and Hippocampus , 1998, The Journal of Neuroscience.
[27] D. Amaral,et al. Perirhinal and postrhinal cortices of the rat: Interconnectivity and connections with the entorhinal cortex , 1998, The Journal of comparative neurology.
[28] L R Squire,et al. Impaired recognition memory on the doors and people test after damage limited to the hippocampal region , 1999, Hippocampus.
[29] Malcolm W. Brown,et al. Different Contributions of the Hippocampus and Perirhinal Cortex to Recognition Memory , 1999, The Journal of Neuroscience.
[30] S. J. Martin,et al. Reversible neural inactivation reveals hippocampal participation in several memory processes , 1999, Nature Neuroscience.
[31] T. Bussey,et al. Functionally Dissociating Aspects of Event Memory: the Effects of Combined Perirhinal and Postrhinal Cortex Lesions on Object and Place Memory in the Rat , 1999, The Journal of Neuroscience.
[32] Sophie L. Dix,et al. Extending the spontaneous preference test of recognition: evidence of object-location and object-context recognition , 1999, Behavioural Brain Research.
[33] T. Poggio,et al. Hierarchical models of object recognition in cortex , 1999, Nature Neuroscience.
[34] Seth J. Ramus,et al. Dissociation between the effects of damage to perirhinal cortex and area TE. , 1999, Learning & memory.
[35] T. Bussey,et al. Distinct patterns of behavioural impairments resulting from fornix transection or neurotoxic lesions of the perirhinal and postrhinal cortices in the rat , 2000, Behavioural Brain Research.
[36] L. Squire,et al. The visual paired-comparison task as a measure of declarative memory. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[37] M. Mishkin,et al. Neurotoxic lesions of perirhinal cortex impair visual recognition memory in rhesus monkeys , 2001, Neuroreport.
[38] R. Burwell. Borders and cytoarchitecture of the perirhinal and postrhinal cortices in the rat , 2001, The Journal of comparative neurology.
[39] L. Saksida,et al. Perirhinal cortex resolves feature ambiguity in complex visual discriminations , 2002, The European journal of neuroscience.
[40] M. Freedman,et al. Changes to the object recognition system in patients with dementia of the Alzheimer's type. , 2002, Brain and cognition.
[41] David Gaffan,et al. Against memory systems. , 2002, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[42] L. Saksida,et al. The organization of visual object representations: a connectionist model of effects of lesions in perirhinal cortex , 2002, The European journal of neuroscience.
[43] Paul E. Gilbert,et al. Recognition memory for complex visual discriminations is influenced by stimulus interference in rodents with perirhinal cortex damage. , 2003, Learning & memory.
[44] L. Saksida,et al. Impairments in visual discrimination after perirhinal cortex lesions: testing ‘declarative’ vs. ‘perceptual‐mnemonic’ views of perirhinal cortex function , 2003, The European journal of neuroscience.
[45] Andy C. H. Lee,et al. Associative and recognition memory for novel objects in dementia: implications for diagnosis , 2003, The European journal of neuroscience.
[46] A. Revonsuo,et al. Visual object recognition in early Alzheimer's disease: deficits in semantic processing , 2003, Acta neurologica Scandinavica.
[47] R. O’Reilly,et al. Modeling hippocampal and neocortical contributions to recognition memory: a complementary-learning-systems approach. , 2003, Psychological review.
[48] Nelson Cowan,et al. Verbal recall in amnesiacs under conditions of diminished retroactive interference. , 2004, Brain : a journal of neurology.
[49] R. Clark,et al. The medial temporal lobe. , 2004, Annual review of neuroscience.
[50] Ranjan Duara,et al. Semantic interference deficits and the detection of mild Alzheimer's disease and mild cognitive impairment without dementia , 2004, Journal of the International Neuropsychological Society.
[51] M. Eacott,et al. Impaired object recognition with increasing levels of feature ambiguity in rats with perirhinal cortex lesions , 2004, Behavioural Brain Research.
[52] J. Wixted. The psychology and neuroscience of forgetting. , 2004, Annual review of psychology.
[53] Rosemary A. Cowell,et al. Double Dissociation between the Effects of Peri-Postrhinal Cortex and Hippocampal Lesions on Tests of Object Recognition and Spatial Memory: Heterogeneity of Function within the Temporal Lobe , 2004, The Journal of Neuroscience.
[54] D. Gaffan,et al. Dissociated effects of perirhinal cortex ablation, fornix transection and amygdalectomy: evidence for multiple memory systems in the primate temporal lobe , 2004, Experimental Brain Research.
[55] J. Rodd,et al. Processing Objects at Different Levels of Specificity , 2004, Journal of Cognitive Neuroscience.
[56] Nelson Cowan,et al. Just lying there, remembering: Improving recall of prose in amnesic patients with mild cognitive impairment by minimising interference , 2005, Memory.
[57] T. Bussey,et al. Glutamate Receptors in Perirhinal Cortex Mediate Encoding, Retrieval, and Consolidation of Object Recognition Memory , 2005, The Journal of Neuroscience.
[58] J. Holdstock,et al. The Quarterly Journal of Experimental Psychology , 2005 .
[59] L. Saksida,et al. Object memory and perception in the medial temporal lobe: an alternative approach , 2005, Current Opinion in Neurobiology.
[60] Andy C. H. Lee,et al. Behavioral / Systems / Cognitive Functional Specialization in the Human Medial Temporal Lobe , 2005 .
[61] Andy C. H. Lee,et al. Specialization in the medial temporal lobe for processing of objects and scenes , 2005, Hippocampus.
[62] Malcolm W. Brown,et al. Contrasting Hippocampal and Perirhinalcortex Function using Immediate Early Gene Imaging , 2005, The Quarterly journal of experimental psychology. B, Comparative and physiological psychology.
[63] T. Bussey,et al. Transient Inactivation of Perirhinal Cortex Disrupts Encoding, Retrieval, and Consolidation of Object Recognition Memory , 2005, The Journal of Neuroscience.
[64] T. Bussey,et al. Removal of cholinergic input to perirhinal cortex disrupts object recognition but not spatial working memory in the rat , 2005, The European journal of neuroscience.
[65] Rosemary A. Cowell,et al. Why Does Brain Damage Impair Memory? A Connectionist Model of Object Recognition Memory in Perirhinal Cortex , 2006, The Journal of Neuroscience.
[66] L. Saksida,et al. Memory, perception, and the ventral visual‐perirhinal‐hippocampal stream: Thinking outside of the boxes , 2007, Hippocampus.
[67] Rosemary A. Cowell,et al. Perirhinal cortex resolves feature ambiguity in configural object recognition and perceptual oddity tasks. , 2007, Learning & memory.
[68] C. Price,et al. Perirhinal Contributions to Human Visual Perception , 2007, Current Biology.
[69] L. Saksida,et al. Scopolamine infused into perirhinal cortex improves object recognition memory by blocking the acquisition of interfering object information. , 2007, Learning & memory.
[70] D. Done,et al. Evidence for a dissociation of structural and semantic knowledge in dementia of the Alzheimer type (DAT) , 2007, Neuropsychologia.
[71] Andy C. H. Lee,et al. Differing profiles of face and scene discrimination deficits in semantic dementia and Alzheimer's disease , 2007, Neuropsychologia.
[72] Rosemary A. Cowell,et al. Perceptual Functions of Perirhinal Cortex in Rats: Zero-Delay Object Recognition and Simultaneous Oddity Discriminations , 2007, The Journal of Neuroscience.
[73] Andy C. H. Lee,et al. Activating the medial temporal lobe during oddity judgment for faces and scenes. , 2008, Cerebral cortex.
[74] Richard G M Morris,et al. Faster forgetting contributes to impaired spatial memory in the PDAPP mouse: deficit in memory retrieval associated with increased sensitivity to interference? , 2008, Learning & memory.
[75] Boyer D. Winters,et al. Object recognition memory: Neurobiological mechanisms of encoding, consolidation and retrieval , 2008, Neuroscience & Biobehavioral Reviews.
[76] Michaela Dewar,et al. Delaying interference enhances memory consolidation in amnesic patients. , 2009, Neuropsychology.