Memory retrieval under the control of the prefrontal cortex

References

• Squire LR. Mechanisms of memory. Science 1986; 232: 1612–9
   PubMed Web of Science ®Google Scholar
• Scoville WB, Milner B. Loss of recent memory after bilateral hippocampal lesions. JNeurol Neurosurg Psychiatry 1957; 20: 11–21
   PubMed Web of Science ®Google Scholar
• Teng E, Squire LR. Memory for places learned long ago is intact after hippocampal damage. Nature 1999; 400: 675–7
   PubMed Web of Science ®Google Scholar
• Kapur N, Ellison D, Smith MP, McLellan DL, Burrows EH. Focal retrograde amnesia following bilateral temporal lobe pathology. A neuropsychological and magnetic resonance study. Brain 1992; 115: 73–85
   PubMed Web of Science ®Google Scholar
• Kapur N, Ellison D, Parkin AJ, Hunkin NM, Burrows E, Sampson SA. Bilateral temporal lobe pathology with sparing of medial temporal lobe structures: lesion profile and pattern of memory disorder. Neuropsychologia 1994; 32: 23–38
   PubMed Web of Science ®Google Scholar
• Zola-Morgan SM, Squire LR. The primate hippocampal formation: evidence for a time-limited role in memory storage. Science 1990; 250: 288–90
   PubMed Web of Science ®Google Scholar
• Bontempi B, Laurent-Demir C, Destrade C, Jaffard R. Time-dependent reorganization of brain circuitry underlying long-term memory storage. Nature 1999; 400: 671–5
   PubMed Web of Science ®Google Scholar
• Mishkin M. A memory system in the monkey. Philos Trans R Soc Lond B Biol Sci 1982; 298: 83–95
   PubMed Web of Science ®Google Scholar
• Miyashita Y. Inferior temporal cortex: where visual perception meets memory. Annu Rev Neurosci 1993; 16: 245–63
   PubMed Web of Science ®Google Scholar
• Penfield W, Perot P. The brain's record of auditory and visual experience. Brain 1963; 86: 595–696
   PubMed Web of Science ®Google Scholar
• Fuster JM. The Prefrontal Cortex: Anatomy, Physiology, and Neuropsychology of the Frontal Lobe. 3rd edn. Lippincott-Raven, Philadelphia, PA 1997
   Google Scholar
• Petrides M. Frontal lobes and memory. Handbook of Neuropsychology, F Boller, J Grafman. Elsevier, Amsterdam 1989; Vol 3: 75–90
   Google Scholar
• Stuss DT, Benson DF. The Frontal Lobes. Raven Press, New York, NY 1986
   Google Scholar
• Janowsky JS, Shimamura AP, Kritchevsky M, Squire LR. Cognitive impairment following frontal lobe damage and its relevance to human amnesia. Behav Neurosci 1989; 103: 548–60
   PubMed Web of Science ®Google Scholar
• Goldman-Rakic PS. Circuitry of primate prefrontal cortex and regulation of behavior by representational memory. Handbook of Physiology. Neurophysiology, F Plum. American Physiological Society, Bethesda, MD 1987; Vol V: 373–417, Section 1
   Google Scholar
• Felleman DJ, Van Essen DC. Distributed hierarchical processing in the primate cerebral cortex. Cereb Cortex 1991; 1: 1–47
   PubMed Web of Science ®Google Scholar
• Tootell RB, Dale AM, Sereno MI, Malach R. New images from human visual cortex. Trends Neurosci 1996; 19: 481–9
   PubMed Web of Science ®Google Scholar
• Ungerleider LG. Functional brain imaging studies of cortical mechanisms for memory. Science 1995; 270: 769–75
   PubMed Web of Science ®Google Scholar
• Sakai K, Miyashita Y. Neural organization for the long-term memory of paired associates. Nature 1991; 354: 152–5
   PubMed Web of Science ®Google Scholar
• Miyashita Y. Neuronal correlate of visual associative long-term memory in the primate temporal cortex. Nature 1988; 335: 817–20
   PubMed Web of Science ®Google Scholar
• Higuchi S, Miyashita Y. Formation of mnemonic neuronal responses to visual paired associates in inferotemporal cortex is impaired by perirhinal and entorhinal lesions. Proc Natl Acad Sci USA 1996; 93: 739–43
   PubMed Web of Science ®Google Scholar
• Naya Y, Sakai K, Miyashita Y. Activity of primate inferotemporal neurons related to a sought target in pair-association task. Proc Natl Acad Sci USA 1996; 93: 2664–9
   PubMed Web of Science ®Google Scholar
• Nyberg I, Cabeza R, Tulving E. Asymmetric frontal activation during episodic memory: what kind of specificity. Trends Cognit Sci 1998; 2: 419–20
   PubMed Web of Science ®Google Scholar
• Fletcher PC, Frith CD, Rugg MD. The functional neuroanatomy of episodic memory. Trends Neurosci 1997; 20: 213–8
   PubMed Web of Science ®Google Scholar
• Gabrieli JD. Cognitive neuroscience of human memory. Annu Rev Psychol 1998; 49: 87–115
   PubMed Web of Science ®Google Scholar
• Schacter DL, Buckner RL, Koutstaal W. Memory, consciousness and neuroimaging. Philos Trans R Soc Lond B Biol Sci 1998; 353: 1861–78
   PubMed Web of Science ®Google Scholar
• Andreasen NC, O'Leary DS, Arndt S, Cizadlo T, Rezai K, Watkins GL. I. PET studies of memory: novel and practiced free recall of complex narratives. Neuroimage 1995; 2: 284–95
   PubMed Web of Science ®Google Scholar
• Andreasen NC, O'Leary DS, Cizadlo T, Arndt S, Rezai K, Watkins GL. II. PET studies of memory: novel versus practiced free recall of word lists. Neuroimage 1995; 2: 296–305
   PubMed Web of Science ®Google Scholar
• Buckner RL, Koutstaal W, Schacter DL, Wagner AD, Rosen BR. Functional-anatomic study of episodic retrieval using fMRI. I. Retrieval effort versus retrieval success. Neuroimage 1998; 7: 151–62
   PubMed Web of Science ®Google Scholar
• Fletcher PC, Shallice T, Frith CD, Frackowiak RSJ, Dolan RJ. The functional roles of prefrontal cortex in episodic memory. II. Retrieval. Brain 1998; 121: 1249–56
   PubMed Web of Science ®Google Scholar
• Henson RN, Rugg MD, Shallice T, Josephs O, Dolan RJ. Recollection and familiarity in recognition memory: an event-related functional magnetic resonance imaging study. JNeurosci 1999; 19: 3962–72
   PubMed Web of Science ®Google Scholar
• Kopelman MD, Stevens TG, Foli S, Grasby P. PET activation of the medial temporal lobe in learning. Brain 1998; 121: 875–87
   PubMed Web of Science ®Google Scholar
• Nyberg L, Tulving E, Habib R, Nilsson LG, Kapur S, Houle S. Functional brain maps of retrieval mode and recovery of episodic information. Neuroreport 1995; 7: 249–52
   PubMed Web of Science ®Google Scholar
• Nyberg L, McIntosh AR, Houle S, Nilsson LG, Tulving E. Activation of medial temporal structures during episodic memory retrieval. Nature 1996; 380: 715–7
   PubMed Web of Science ®Google Scholar
• Rugg MD, Fletcher PC, Frith CD, Frackowiak RSJ, Dolan RJ. Differential activation of the prefrontal cortex in successful and unsuccessful memory retrieval. Brain 1996; 119: 2073–83
   PubMed Web of Science ®Google Scholar
• Rugg MD, Fletcher PC, Frith CD, Frackowiak RSJ, Dolan RJ. Brain regions supporting intentional and incidental memory: a PET study. Neuroreport 1997; 8: 1283–7
   PubMed Web of Science ®Google Scholar
• Rugg MD, Fletcher PC, Allan K, Frith CD, Frackowiak RSJ, Dolan RJ. Neural correlates of memory retrieval during recognition memory and cued recall. Neuroimage 1998; 8: 262–73
   PubMed Web of Science ®Google Scholar
• Schacter DL, Alpert NM, Savage CR, Rauch SL, Albert MS. Conscious recollection and the human hippocampal formation: evidence from positron emission tomography. Proc Natl Acad Sci USA 1996; 93: 321–5
   PubMed Web of Science ®Google Scholar
• Schacter DL, Reiman E, Curran T, Yun LS, Bandy D, McDermott KB. Neuroanatomical correlates of veridical and illusory recognition memory: evidence from positron emission tomography. Neuron 1996; 17: 267–74
   PubMed Web of Science ®Google Scholar
• Konishi S, Nakajima K, Uchida I, Kameyama M, Nakahara K, Sekihara K. Transient activation of inferior prefrontal cortex during cognitive set shifting. Nature Neurosci 1998; 1: 80–4
   PubMed Web of Science ®Google Scholar
• Talairach J, Tournoux P. Co-planar Stereotaxic Atlas of the Human Brain: a 3-dimensional Proportional System, an Approach to Cerebral Imaging. G. Thieme, StuttgartGermany 1988
   Google Scholar
• Kapur S, Craik FI, Jones C, Brown GM, Houle S, Tulving E. Functional role of the prefrontal cortex in retrieval of memories: a PET study. Neuroreport 1995; 6: 1880–4
   PubMed Web of Science ®Google Scholar
• Wagner AD, Desmond JE, Glover GH, Gabrieli JD. Prefrontal cortex and recognition memory. Functional-MRI evidence for context-dependent retrieval processes. Brain 1998; 121: 1985–2002
   PubMed Web of Science ®Google Scholar
• Shallice T. From Neuropsychology to Mental Structure. Cambridge University Press, Camgridge 1988
   Google Scholar
• Buckner RL, Koutstaal W, Schacter DL, Dale AM, Rotte M, Rosen BR. Functional-anatomic study of episodic retrieval. II. Selective averaging of event-related fMRI trials to test the retrieval success hypothesis. Neuroimage 1998; 7: 163–75
   PubMed Web of Science ®Google Scholar
• MacLeod AK, Buckner RL, Miezin FM, Petersen SE, Raichle ME. Right anterior prefrontal cortex activation during semantic monitoring and working memory. Neuroimage 1998; 7: 41–8
   PubMed Web of Science ®Google Scholar
• Janowsky JS, Shimamura AP, Squire LR. Source memory impairment in patients with frontal lobe lesions. Neuropsychologia 1989; 27: 1043–56
   PubMed Web of Science ®Google Scholar
• Shimamura AP, Janowsky JS, Squire LR. Memory for the temporal order of events in patients with frontal lobe lesions and amnesic patients. Neuropsychologia 1990; 28: 803–13
   PubMed Web of Science ®Google Scholar
• Della Sala S, Laiacona M, Spinnler H, Trivelli C. Autobiographical recollection and frontal damage. Neuropsychologia 1993; 31: 823–39
   PubMed Web of Science ®Google Scholar
• Gershberg FB, Shimamura AP. Impaired use of organizational strategies in free recall following frontal lobe damage. Neuropsychologia 1995; 33: 1305–33
   PubMed Web of Science ®Google Scholar
• Incisa della Rocchetta A, Milner B. Strategic search and retrieval inhibition: the role of the frontal lobes. Neuropsychologia 1993; 31: 503–24
   PubMed Web of Science ®Google Scholar
• Moscovitch M, Melo B. Strategic retrieval and the frontal lobes: evidence from confabulation and amnesia. Neuropsychologia 1997; 35: 1017–34
   PubMed Web of Science ®Google Scholar
• Swick D, Knight RT. Is prefrontal cortex involved in cued recall? A neuropsychological test of PET findings. Neuropsychologia 1996; 34: 1019–28
   PubMed Web of Science ®Google Scholar
• Thompson-Schill SL, Swick D, Farah MJ, D'Esposito M, Kan IP, Knight RT. Verb generation in patients with focal frontal lesions: a neuropsychological test of neuroimaging findings. Proc Natl Acad Sci USA 1998; 95: 15855–60
   PubMed Web of Science ®Google Scholar
• Eacott MJ, Gaffan D. Inferotemporal-frontal disconnection: the uncinate fascicle and visual associative learning in monkeys. Eur J Neurosci 1992; 4: 1320–32
   PubMed Web of Science ®Google Scholar
• Hasegawa I, Fukushima T, Ihara T, Miyashita Y. Callosal window between prefrontal cortices: cognitive interaction to retrieve long-term memory. Science 1998; 281: 814–8
   PubMed Web of Science ®Google Scholar
• Parker A, Gaffan D. Interaction of frontal and perirhinal cortices in visual object recognition memory in monkeys. Eur J Neurosci 1998; 10: 3044–57
   PubMed Web of Science ®Google Scholar
• Gaffan D, Eacott MJ. Uncinate fascicle section leaves delayed matching-to-sample intact, with both large and small stimulus sets. Exp Brain Res 1995; 105: 175–80
   PubMed Web of Science ®Google Scholar
• Gutnikov SA, Ma YY, Gaffan D. Temporo-frontal disconnection impairs visual-visual paired association learning but not configural learning in Macaca monkeys. Eur J Neurosci 1997; 9: 1524–9
   PubMed Web of Science ®Google Scholar
• Parker A, Gaffan D. Memory after frontal/temporal disconnection in monkeys: conditional and non-conditional tasks, unilateral and bilateral frontal lesions. Neuropsychologia 1998; 36: 259–71
   PubMed Web of Science ®Google Scholar
• Kroll NE, Markowitsch HJ, Knight RT, von Cramon DY. Retrieval of old memories: the temporofrontal hypothesis. Brain 1997; 120: 1377–99
   PubMed Web of Science ®Google Scholar
• Gazzaniga MS. Principles of human brain organization derived from split-brain studies. Neuron 1995; 14: 217–28
   PubMed Web of Science ®Google Scholar
• Black P, Myers RE. Visual functions of the forebrain commissures in chimpanzee. Science 1964; 146: 799–800
   PubMed Web of Science ®Google Scholar
• Gross CG, Bender DB, Mishkin M. Contributions of the corpus callosum and the anterior commissure to visual activation of inferior temporal neurons. JNeurophysiol 1977; 131: 227–39
   Google Scholar
• Gazzaniga MS. Cross-cuing mechanisms and ipsilateral eye-hand control in split-brain monkeys. Exp Neurol 1969; 23: 11–7
   PubMed Web of Science ®Google Scholar
• Hamilton CR, Vermeire BA. Localization of visual functions with partially split-brain monkeys. Two Hemispheres - One Brain: Functions of the Corpus Callosum, F Leopre, M Ptito, HH Jasper. Alan R Liss, New York, NY 1986; 315–33
   Google Scholar
• Pandya DN, Seltzer B. The topography of commissural fibers. Two Hemispheres - One Brain: Functions of the Corpus Callosum, F Leopre, M Ptito, HH Jasper. Alan R Liss, New York, NY 1986; 47–73
   Google Scholar
• Tomita H, Obayashi M, Nakahara K, Hasegawa I, Miyashita Y. Top-down signal from the prefrontal cortex in executive control of memory retrieval. Nature 1999; 401: 699–703
   PubMed Web of Science ®Google Scholar
• Sidtis JJ, Volpe BT, Holtzman JD, Wilson DH, Gazzaniga MS. Cognitive interaction after staged callosal section: evidence for transfer of semantic activation. Science 1981; 212: 344–6
   PubMed Web of Science ®Google Scholar