Erratum to "Neocortical area, layers, connections, and gene expression" [Neuroscience Research 55 (2006) 11-27] (DOI:10.1016/j.neures.2006.02.006);Neocortical areas, layers, connections, and gene expression

Neuroscience Research

Volumn 55, Issue 1, 2006, Pages 11-27

  Yamamori, Tetsuo ^a   Rockland, Kathleen S ^b  

^a NATIONAL INSTITUTE FOR BASIC BIOLOGY   (Japan)

^b RIKEN BRAIN SCIENCE INSTITUTE   (Japan)

Author keywords

Area formation; Association cortex; Cortical gradient; Gene expression; Macaque monkey; Postnatal cortical development; Thalamic projection

Indexed keywords

BONE MORPHOGENETIC PROTEIN 12; CALCIUM BINDING PROTEIN; MESSENGER RNA; RETINOL; RETINOL BINDING PROTEIN;

AMYGDALOID NUCLEUS; ARTICLE; AUDITORY CORTEX; BRAIN CORTEX; BRAIN REGION; CAT; DNA MICROARRAY; EPIGENETICS; EYE; FERRET; GENE EXPRESSION; GENETICS; IMMUNOREACTIVITY; LONG TERM POTENTIATION; MACACA; MEMORY; MICROELECTRODE; MOLECULAR BIOLOGY; MONKEY; MOTOR CORTEX; MOUSE STRAIN; NEOCORTEX; NONHUMAN; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; PULVINAR; PYRAMIDAL NERVE CELL; RNA EXTRACTION; RODENT; SYNAPTIC TRANSMISSION; TECHNIQUE; THALAMOCORTICAL TRACT; TWO DIMENSIONAL GEL ELECTROPHORESIS; VISUAL CORTEX;

EID: 33645982900     PISSN: 01680102     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neures.2006.11.001     Document Type: Erratum

References (155)

1. Akil M., and Lewis D.A. Postnatal development of parvalbumin immunoreactivity in axon terminals of basket and chandelier neurons in monkey neocortex. Prog. Neuropsychopharmacol. Biol. Psychiatry 16 (1992) 329-337
2. Alder J., Lee K.J., Jessell T.M., and Hatten M.E. Generation of cerebellar granule neurons in vivo by transplantation of BMP-treated neural progenitor cells. Nat. Neurosci. 2 (1999) 535-540
3. Arimatsu Y., Miyamoto M., Nihonmatsu I., Hirata K., Uratani Y., Hatanaka Y., and Takiguchi-Hayashi K. Early regional specification for a molecular neuronal phenotype in the rat neocortex. Proc. Natl. Acad. Sci. U.S.A. 89 (1992) 8879-8883
4. Arimatsu Y., Ishida M., Sato M., and Kojima M. Corticocortical associative neurons expressing latexin: specific cortical connectivity formed in vivo and in vitro. Cereb. Cortex 9 (1999) 569-576
5. Arimatsu Y., Ishida M., Kaneko T., Ichinose S., and Omori A. Organization and development of corticocortical associative neurons expressing the orphan nuclear receptor Nurr1. J. Comp. Neurol. 466 (2003) 180-196
6. Arlotta P., Molyneaux B.J., Chen J., Inoue J., Kominami R., and Macklis J.D. Neuronal subtype-specific genes that control corticospinal motor neuron development in vivo. Neuron 45 (2005) 207-221
7. Bai W., Ishida M., Okabe M., and Arimatsu Y. Role of the protomap and target-derived signals in the development of intrahemispheric connections. Cereb. Cortex 16 (2006) 124-135
8. Barone P., Dehay C., Berland M., Bullier J., and Kennedy H. Developmental remodeling of primate visual cortical pathways. Cereb. Cortex 5 (1995) 22-38
9. Benson D.L., Huntsman N.M., and Jones E.G. Activity-dependent changes in GAD and preprotachykinin mRNAs in visual cortex of adult monkeys. Cereb. Cortex 4 (1994) 40-51
10. Bear M.F. NMDA-receptor dependent synaptic plasticity in the visual cortex. Prog. Brain Res. 108 (1996) 205-218
11. Berardi N., Pizzorusso T., and Maffei L. Critical periods during sensory development. Curr. Opin. Neurobiol. 10 (2000) 138-145
12. Bolz J., Uziel D., Muhlfriedel S., Gullmar A., Peuckert C., Zarbalis K., Wurst W., Torii M., and Levitt P. Multiple roles of ephrins during the formation of thalamocortical projections: maps and more. J. Neurobiol. 59 (2004) 82-94
13. Boulanger L.M., and Shatz C.J. Immune signalling in neural development, synaptic plasticity and disease. Nat. Rev. Neurosci. 5 (2004) 521-530
14. Bourne J.A., and Rosa M.G. Hierarchical development of the primate visual cortex, as revealed by neurofilament immunoreactivity: Early maturation of the middle temporal area (MT). Cereb. Cortex (2005) (Advance Access published on June 8, 2005)
15. Bourne J.A., Warner C.E., and Rosa M.G. Topographic and laminar maturation of striate cortex in early postnatal marmoset monkeys, as revealed by neurofilament immunohistochemistry. Cereb. Cortex 15 (2005) 740-748
16. Brecht M., Krauss A., Muhammad S., Sinai-Esfahani L., Bellance S., and Margrie T.W. Organization of rat vibrissa motor cortex and adjacent areas according to cytoarchitectonics, microstimulation, and intracellular stimulation of identified cells. J. Comp. Neurol. 479 (2004) 360-373
17. Brown C.E., and Dyck R.H. Rapid, experience-dependent changes in levels of synaptic zinc in primary somatosensory cortex of the adult mouse. J. Neurosci. 22 (2002) 2617-2625
18. Bullier J., Girard P., and Salin P.-A. The role of area 17 in the transfer of information to extrastriate visual cortex. In: Peters A., and Rockland K.S. (Eds). Cerebral Cortex vol. 10 (1994), Plenum Press, New York/London 301-330
19. Burkhalter A. Development of forward and feedback connections between areas V1 and V2 of human visual cortex. Cereb. Cortex 3 (1993) 476-487
20. Butler A.K., Dantzker J.L., Shah R.B., and Callaway E.M. Development of visual cortical axons: layer-specific effects of extrinsic influences and activity blockade. J. Comp. Neurol. 430 (2001) 321-331
21. Callaway E.M. Local circuits in primary visual cortex of the macaque monkey. Annu. Rev. Neurosci. 21 (1998) 47-74
22. Callaway E.M., and Katz L.C. Emergence and refinement of clustered horizontal connections in cat striate cortex. J. Neurosci. 10 (1990) 1134-1153
23. Catania K.C., and Kaas J.H. Areal and callosal connections in the somatosensory cortex of the star-nosed mole. Somatosens. Mot. Res. 18 (2001) 303-311
24. Catalano S.M., Chang C.K., and Shatz C.J. Activity-dependent regulation of NMDAR1 immunoreactivity in the developing visual cortex. J. Neurosci. 17 (1997) 8376-8390
25. Chikaraishi D.M., Deeb S.S., and Sueoka N. Sequence complexity of nuclear RNAs in adult rat tissues. Cell 13 (1978) 111-120
26. Clarke S., and Innocenti G.M. Organization of immature intrahemispheric connections. J. Comp. Neurol. 251 (1986) 1-22
27. Collins C.E., Xu X., Khaytin I., Kaskan P.M., Casagrade V.A., and Kaas J.H. Optical imaging of visually evoked responses in the middle temporal area after deactivation of primary visual cortex in adult primates. Proc. Natl. Acad. Sci. U.S.A. 102 (2005) 5594-5599
28. Condé F., Lund J.S., and Lewis D.A. The hierarchical development of monkey visual cortical regions as revealed by the maturation of parvalbumin-immunoreactive neurons. Brain Res. Dev. Brain Res. 96 (1996) 261-276
29. Coogan T.A., and Van Essen D.C. Development of connections within and between areas V1 and V2 of macaque monkeys. J. Comp. Neurol. 372 (1996) 327-342
30. Crair M.C. Neuronal activity during development: permissive or instructive?. Curr. Opin. Neurobiol. 9 (1999) 88-93
31. Crowley J.C., and Katz L.C. Ocular dominance development revisited. Curr. Opin. Neurobiol. 12 (2002) 104-109
32. DeFelipe J., Gonzalez-Albo M.C., Del Rio M.R., and Elson G.N. Distribution and patterns of connectivity of interneurons containing calbindin, calretinin, and parvalbumin in visual areas of the occipital and temporal lobes of the macaque monkey. J. Comp. Neurol. 412 (1999) 515-526
33. Dong H., Wang Q., Valkova K., Gonchar Y., and Burkhalter A. Experience-dependent development of feedforward and feedback circuits between lower and higher areas of mouse visual cortex. Vision Res. 44 (2004) 3389-3400
34. Donoghue M.J., and Rakic P. Molecular gradients and compartments in the embryonic primate cerebral cortex. Cereb. Cortex 9 (1999) 586-600
35. Douglas R.J., and Martin K.A.C. Neuronal circuits of the neocortex. Annu. Rev. Neurosci. 27 (2004) 419-451
36. Drescher U. The Eph family in the patterning of neural development. Curr. Biol. 7 (1997) R799-R807
37. Dufour A., Seibt J., Passante L., Depaepe V., Ciossek T., Frisen J., Kullander K., Flanagan J.G., Polleux F., and Vanderhaeghen P. Area specificity and topography of thalamocortical projections are controlled by ephrin/Eph genes. Neuron 39 (2003) 453-465
38. Dwyer N.D., and O'Leary D.D. Tbr1 conducts the orchestration of early cortical development. Neuron 29 (2001) 309-311
39. Dyck R.H. Activity-dependent columnar regulation of zinc in the adult primate visual cortex. Invest. Ophthal. Vis. Sci. 35 (1971)
40. Elston G.N. Cortical heterogeneity: implications for visual processing and polysensory integration. J. Neurocytol. 31 (2002) 317-335
41. Evans S.J., Choudary P.V., Vawter M.P., Li J., Meador-Woodruff J.H., Lopez J.F., Burke S.M., Thompson R.C., Myers R.M., Jones E.G., Bunney W.E., Watson S.J., and Akil H. DNA microarray analysis of functionally discrete human brain regions reveals divergent transcriptional profiles. Neurobiol. Dis. 14 (2003) 240-250
42. Felleman D.J., and Van Essen D.C. Distributed hierarchical processing in the primate cerebral cortex. Cereb. Cortex 1 (1991) 1-47
43. Freese J.L., and Amaral D.G. The organization of projections from the amygdala to visual cortical areas TE and V1 in the macaque monkey. J. Comp. Neurol. 486 (2005) 295-317
44. Fox K., and Daw N.W. Do NMDA receptors have a critical function in visual cortical plasticity?. Trends Neurosci. 16 (1993) 116-122
45. Fujita I. The inferior temporal cortex: Architecture, computation, and representation. J. Neurocytol. 31 (2002) 359-371
46. Garel S., Huffman K.J., and Rubenstein J.L. Molecular regionalization of the neocortex is disrupted in Fgf8 hypomorphic mutants. Development 130 (2003) 1903-1914
47. Garel S., and Rubenstein J.L. Intermediate targets in formation of topographic projections: inputs from the thalamocortical system. Trends Neurosci. 27 (2004) 533-539
48. Garey L.J. Brodmann's 'Localisation in the Cerebral Cortex' (1994), Smith-Gordon, London
49. Gilbert S.F. Developmental Biology. 7th ed. (2003), Sinauer Associates, Sunderland, Massachusetts
50. Granger B., Tekaia F., Le Sourd A.M., Rakic P., and Bourgeois J.P. Tempo of neurogenesis and synaptogenesis in the primate cingulate mesocortex: comparison with the neocortex. J. Comp. Neurol. 360 (1995) 363-376
51. Graybiel A.M., and Berson D.M. On the relation between transthalamic and transcortical pathways in the visual system. In: Schmitt F.O., Worden F.G., Adelman G., and Dennis S.G. (Eds). The Organization of the Cerebral Cortex (1981), The MIT Press, Cambridge 285-319
52. Grubb M.S., and Thompson I.D. The influence of early experience on the development of sensory systems. Curr. Opin. Neurobiol. 14 (2004) 503-512
53. Gupta A., Wang Y., and Markram H. Organizing principles for a diversity of GABAergic interneurons and synapses in the neocortex. Science 287 (2000) 273-278
54. Hayashizaki Y., Hirotsune S., Okazaki Y., Hatada I., Shibata H., Kawai J., Hirose K., Watanabe S., Fushiki S., Wada S., et al. Restriction landmark genomic scanning method and its various applications. Electrophoresis 14 (1993) 251-258
55. Hendry S.H., Hockfield S., Jones E.G., and McKay R. Monoclonal antibody that identifies subsets of neurones in the central visual system of monkey and cat. Nature 307 (1984) 267-269
56. Hensch T.K. Critical period plasticity in local cortical circuits. Nat. Rev. Neurosci. 6 (2005) 877-888
57. Hensch T.K., and Stryker M.P. Columnar architecture sculpted by GABA circuits in developing cat visual cortex. Science 303 (2004) 1678-1681
58. Horton J.C., and Hocking D.R. An adult-like pattern of ocular dominance columns in striate cortex of newborn monkeys prior to visual experience. J. Neurosci. 16 (1996) 1791-1807
59. Huang Z.J., Kirkwood A., Pizzorusso T., Porciatti V., Morales B., Bear M.F., Maffei L., and Tonegawa S. BDNF regulates the maturation of inhibition and the critical period of plasticity in mouse visual cortex. Cell 98 (1999) 739-755
60. Huberman A.D., Dehay C., Berland M., Chalupa L.M., and Kennedy H. Early and rapid targeting of eye-specific axonal projections to the dorsal lateral geniculate nucleus in the fetal macaque. J. Neurosci. 25 (2005) 4014-4023
61. Huttenlocher P.R., and Dabholkar A.S. Regional differences in synaptogenesis in human cerebral cortex. J. Comp. Neurol. 387 (1997) 167-178
62. Ichinohe N., and Rockland K.S. Zinc-enriched amygdalo- and hippocampo-cortical connections to the monkey inferotemporal cortices. Neurosci. Res. 53 (2005) 57-68
63. Innocenti G.M. Growth and reshaping of axons in the establishment of visual callosal connections. Science 212 (1981) 824-827
64. Innocenti G.M. Exuberant development of connections, and its possible permissive role in cortical evolution. Trends Neurosci. 18 (1995) 397-402
65. Jones E.G. The role of afferent activity in the maintenance of primate neocortical function. J. Exp. Biol. 153 (1990) 155-176
66. Jones E.G., Dell'anna M.E., Molinari M., Rausell E., and Hashikawa T. Subdivisions of macaque monkey auditory cortex revealed by calcium-binding protein immunoreactivity. J. Comp. Neurol. 362 (1995) 153-170
67. Jones E.G., and Rubenstein J.L. Expression of regulatory genes during differentiation of thalamic nuclei in mouse and monkey. J. Comp. Neurol. 477 (2004) 55-80
68. Kaas J.H. The future of mapping sensory cortex in primates: three of many remaining issues. Philos. Trans. R. Soc. Lond. B Biol. Sci. 360 (2005) 653-664
69. Katz L.C. Specificity in the Development of Vertical Connections in Cat Striate Cortex. Eur. J. Neurosci. 3 (1991) 1-9
70. Katz L.C., and Crowley J.C. Development of cortical circuits: lessons from ocular dominance columns. Nat. Rev. Neurosci. 3 (2002) 34-42
71. Kennedy H., and Bullier J. A double-labeling investigation of the afferent connectivity to cortical areas V1 and V2 of the macaque monkey. J. Neurosci. 5 (1985) 2815-2830
72. Komatsu Y., Watakabe A., Hashikawa T., Tochitani S., and Yamamori T. Retinol-binding protein gene is highly expressed in higher-order association areas of the primate neocortex. Cereb. Cortex 15 (2005) 96-108
73. Kondo H., Hashikawa T., Tanaka K., and Jones E.G. Neurochemical gradient along the monkey occipito-temporal cortical pathway. Neuroreport 5 (1994) 613-616
74. Kostovic I., and Rakic P. Development of prestriate visual projections in the monkey and human fetal cerebrum revealed by transient cholinesterase staining. J. Neurosci. 4 (1984) 25-42
75. Kozloski J., Hamzei-Sichani F., and Yuste R. Stereotyped position of local synaptic targets in neocortex. Science 293 (2001) 868-872
76. Krubitzer L., and Huffman K.J. Arealization of the neocortex in mammals: genetic and epigenetic contributions to the phenotype. Brain Behav. Evol. 55 (2000) 322-335
77. Kuljis R.O., and Rakic P. Hypercolumns in primate visual cortex can develop in the absence of cues from photoreceptors. Proc. Natl. Acad. Sci. 87 (1990) 5303-5306
78. LaMantia A.S., and Rakic P. Axon overproduction and elimination in the corpus collosum of the developing rhesus monkey. J. Neurosci. 10 (1990) 2156-2175
79. Land P.W., and Shamalla-Hannah L. Experience-dependent plasticity of zinc-containing cortical circuits during a critical period of postnatal development. J. Comp. Neurol. 447 (2002) 43-56
80. Lee J.L.C., Everitt B.J., and Thomas K.L. Independent cellular processes for hippocampal memory consolidation and reconsolidation. Science 304 (2004) 839-843
81. Lee K.J., Mendelsohn M., and Jessell T.M. Neuronal patterning by BMPs: a requirement for GDF7 in the generation of a discrete class of commissural interneurons in the mouse spinal cord. Genes Dev. 12 (1998) 3394-3407
82. Levitt J.B., Yoshioka T., and Lund J.S. Connections between the pulvinar complex and cytochrome oxidase-defined compartments in visual area V2 of macaque monkey. Exp. Brain Res. 104 (1995) 419-430
83. Levitt P. A monoclonal antibody to limbic system neurons. Science 223 (1984) 299-301
84. Levitt P. Structural and functional maturation of the developing primate brain. J. Pediatr. 143 (2003) S35-S45
85. Lewis D.A. Development of the prefrontal cortex during adolescence: insights into vulnerable neural circuits in schizophrenia. Neuropsychopharmacology 16 (1997) 385-398
86. Lewis D.A., Hashimoto T., and Volk D.W. Cortical inhibitory neurons and schizophrenia. Nat. Rev. Neurosci. 6 (2005) 312-324
87. Liu Z., Richmond B.J., Murray E.A., Saunders R.C., Steenrod S., Stubblefield B.K., Montague D.M., and Ginns E.I. DNA targeting of rhinal cortex D2 receptor protein reversibly blocks learning of cues that predict reward. Proc. Natl. Acad. Sci. U.S.A. 101 (2004) 12336-12341
88. Lopez-Bendito G., and Molnar Z. Thalamocortical development: how are we going to get there?. Nat. Rev. Neurosci. 4 (2003) 276-289
89. Lujan R., Shigemoto R., and Lopez-Bendito G. Glutamate and GABA receptor signalling in the developing brain. Neuroscience 130 (2005) 567-580
90. Markram H., Toledo-Rodriguez M., Wang Y., Gupta A., Silberberg G., and Wu C. Interneurons of the neocortical inhibitory system. Nat. Rev. Neurosci. 5 (2004) 793-807
91. Maquet P. The role of sleep in learning and memory. Science 294 (2001) 1048-1052
92. McConnell S.K., Ghosh A., and Shatz C.J. Subplate neurons pioneer the first axon pathway from the cerebral cortex. Science 245 (1989) 978-982
93. Meissirel C., Dehay C., Berland M., and Kennedy H. Segregation of callosal and association pathways during development in the visual cortex of the primate. J. Neurosci. 11 (1991) 3297-3316
94. Meroni P.L., Raschi E., Testoni C., and Borghi M.O. Endothelial cell activation by antiphospholipid antibodies. Clin. Immunol. 112 (2004) 169-174
95. Miro-Bernie, N., Ichinohe, N., Perez-Clausell, J., Rockland, K.S., in press. Zinc-rich transient vertical modules in the rat retrosplenial cortex during postnatal development. Neuroscience.
96. Mitchell B.D., and Macklis J.D. Large-scale maintenance of dual projections by callosal and frontal cortical projection neurons in adult mice. J. Comp. Neurol. 482 (2005) 17-32
97. Miyashita Y. Cognitive memory: cellular and network machines and their top-down control. Science 306 (2004) 435-440
98. Molnar Z., and Blakemore C. How do thalamic axons find their way to the cortex?. Trends Neurosci. 18 (1995) 389-397
99. Murayama Y., Fujita I., and Kato M. Contrasting forms of synaptic plasticity in monkey inferotemporal and primary visual cortices. NeuroReport 8 (1997) 1503-1508
100. Newsome W.T., and Allman J.M. Interhemispheric connections of visual cortex in the owl monkey, Aotus trivirgatus, and the bushbaby, Galago senegalensis. J. Comp. Neurol. 194 (1980) 209-233
101. Northcutt R.G., and Kaas J.H. The emergence and evolution of mammalian neocortex. Trends Neurosci. 18 (1995) 373-379
102. O'Leary D.D. Do cortical areas emerge from a protocortex?. Trends Neurosci. 12 (1989) 400-406
103. O'Leary D.D., and Nakagawa Y. Patterning centers, regulatory genes and extrinsic mechanisms controlling arealization of the neocortex. Curr. Opin. Neurobiol. 12 (2002) 14-25
104. Oldham M.C., and Geschwind D.H. Evolutionary genetics: the human brain - adaptation at many levels. Eur. J. Hum. Genet. 13 (2005) 520-522
105. Pallas S.L. Intrinsic and extrinsic factors that shape neocortical specification. Trends Neurosci. 24 (2001) 417-423
106. Price S.R., De Marco Garcia N.V., Ranscht B., and Jessell T.M. Regulation of motor neuron pool sorting by differential expression of type II Cadherins. Cell 109 (2002) 205-216
107. Rakic P. Specification of cerebral cortical areas. Science 241 (1988) 170-176
108. Rakic P., Bourgeois J.P., Eckenhoff M.F., Zecevic N., and Goldman-Rakic P.S. Concurrent overproduction of synapses in diverse regions of the primate cerebral cortex. Science 232 (1986) 232-235
109. Rescher U., and Gerke V. Annexins-unique membrane binding proteins with diverse functions. J. Cell. Sci. 117 (2004) 2631-2639
110. Rockland K.S. Elements of cortical architecture hierarchy revisited. In: Rockland K.S., Kaas J., and Peters A. (Eds). Cerebral Cortex vol. 12 (1997), Plenum Press, New York/London 243-293
111. Rockland K.S. Complex microstructures of sensory cortical connections. Curr. Opin. Neurobiol. 8 (1998) 545-551
112. Rockland K.S., and Pandya D.N. Laminar origins and terminations of cortical connections of the occipital lobe in the rhesus monkey. Brain Res. 179 (1979) 3-20
113. Rockland K.S., Andresen J., Cowie R.J., and Robinson D.L. Single axon analysis of pulvinocortical connections to several visual areas in the macaque. J. Comp. Neurol. 406 (1999) 221-250
114. Roland P.E., and Zilles K. Structural divisions and functional fields in the human cerebral cortex. Brain Res. Rev. 26 (1998) 87-105
115. Rosa M.G., and Tweedale R. Brain maps, great and small: lessons from comparative studies of primate visual cortical organization. Philos. Trans. R. Soc. Lond. B Biol. Sci. 360 (2005) 665-691
116. Rubenstein J.L., Anderson S., Shi L., Miyashita-Lin E., Bulfone A., and Hevner R. Genetic control of cortical regionalization and connectivity. Cereb. Cortex 9 (1999) 524-532
117. Salin P.A., Girard P., and Bullier J. Visuotopic organization of corticocortical connections in the visual system. Prog. Brain Res. 95 (1993) 169-178
118. Seibt J., Schuurmans C., Gradwhol G., Dehay C., Vanderhaeghen P., Guillemot F., and Polleux F. Neurogenin2 specifies the connectivity of thalamic neurons by controlling axon responsiveness to intermediate target cues. Neuron 39 (2003) 439-452
119. Selemon L.D., and Goldman-Rakic P.S. Common cortical and subcortical targets of the dorsolateral prefrontal and posterior parietal cortices in the rhesus monkey: Evidence for a distributed neural network subserving spatially guided behavior. J. Neurosci. 8 (1988) 4049-4068
120. Seltzer B., Cola M.G., Gutierrez C., Massee M., Weldon C., and Cusick C. Overlapping and nonoverlapping cortical projections to cortex of the superior temporal sulcus in the rhesus monkey: double anterograde tracer studies. J. Comp. Neurol. 370 (1996) 173-190
121. Sharma J., Angelucci A., and Sur M. Induction of visual orientation modules in auditory cortex. Nature 404 (2000) 841-847
122. Shipp S., and Zeki S. The functional organization of area V2. I. specialization across stripes and layers. Vis. Neurosci. 19 (2002) 187-210
123. Schlaggar B.L., and O'Leary D.D. Potential of visual cortex to develop an array of functional units unique to somatosensory cortex. Science 252 (1991) 1556-1560
124. Su A.I., Cooke M.P., Ching K.A., Hakak Y., Walker J.R., Wiltshire T., Orth A.P., Vega R.G., Sapinoso L.M., Moqrich A., Patapoutian A., Hampton G.M., Schultz P.G., and Hogenesch J.B. Large-scale analysis of the human and mouse transcriptomes. Proc. Natl. Acad. Sci. U.S.A. 99 (2002) 4465-4470
125. Sugino K., Hempel C.M., Miller M.N., Hattox A.M., Shapiro P., Wu C., Huang Z.J., and Nelson S.B. Molecular taxonomy of major neuronal classes in the adult mouse forebrain. Nat. Neurosci. 9 (2006) 99-107
126. Sur M., Garraghty P.E., and Roe A.W. Experimentally induced visual projections into auditory thalamus and cortex. Science 242 (1988) 1437-1441
127. Sur M., and Leamey C.A. Development and plasticity of cortical areas and networks. Nat. Rev. Neurosci. 2 (2001) 251-262
128. Suzuki S.C., Inoue T., Kimura Y., Tanaka T., and Takeichi M. Neuronal circuits are subdivided by differential expression of type-II classic cadherins in postnatal mouse brains. Mol. Cell. Neurosci. 9 (1997) 433-447
129. Suzuki H., Yaoi T., Kawai J., Hara A., Kuwajima G., and Wantanabe S. Restriction landmark cDNA scanning (RLCS): a novel cDNA display system using two-dimensional gel electrophoresis. Nucl. Acids. Res. 24 (1996) 289-294
130. Takahata, T, Komatsu, Y, Watakabe A Hashikawa, T, Tochitani, S, Yamamori, T., 2005. Activity-dependent expression of occ1 in excitatory neurons is a characteristic feature of the primate visual cortex. Cereb. Cortex Sep 8 [Epub ahead of print].
131. Tanaka K. Inferotemporal cortex and object vision. Annu. Rev. Neurosci. 19 (1996) 109-139
132. Tanaka K. Columns for complex visual object features in the inferotemporal cortex: clustering of cells with similar but slightly different stimulus selectivities. Cereb. Cortex 13 (2003) 90-99
133. Tighilet B., Hashikawa T., and Jones E.G. Cell- and lamina-specific expression and activity-dependent regulation of type II calcium/calmodulin-dependent protein kinase isoforms in monkey visual cortex. J. Neurosci. 18 (1998) 2129-2146
134. Tochitani S., Liang F., Watakabe A., Hashikawa T., and Yamamori T. The occ1 gene is preferentially expressed in the primary visual cortex in an activity-dependent manner: a pattern of gene expression related to the cytoarchitectonic area in adult macaque neocortex. Eur. J. Neurosci. 13 (2001) 297-307
135. Tochitani S., Hashikawa T., and Yamamori T. Expression of occ1 mRNA in the visual cortex during postnatal development in macaques. Neurosci. Lett. 337 (2003) 114-116
136. Tokuyama W., Okuno H., Hashimoto T., Xin Li Y., and Miyashita Y. BDNF upregulation during declarative memory formation in monkey inferior temporal cortex. Nat. Neurosci. 11 (2000) 1134-1142
137. Toledo-Rodriguez M., Blumenfeld B., Wu C., Luo J., Attali B., Goodman P., and Markram H. Correlation maps allow neuronal electrical properties to be predicted from single-cell gene expression profiles in rat neocortex. Cereb. Cortex 14 (2004) 1310-1327
138. Vanduffel W., Payne B.R., Lomber S.G., and Orban G.A. Functional impact of cerebral connections. Proc. Natl. Acad. Sci. U.S.A. 94 (1997) 7617-7620
139. Van Essen D.C., Newsome W.T., and Maunsell J.H. The visual field representation in striate cortex of the macaque monkey: asymmetries, anisotropies, and individual variability. Vision Res. 24 (1984) 429-448
140. Van Essen D.C., Lewis J.W., Drury H.A., Hadjikhani N., Tootell R.B., Bakircioglu M., and Miller M.I. Mapping visual cortex in monkeys and humans using surface-based atlases. Vision Res. 41 (2001) 1359-1378
141. Wagner E., Luo T., and Drager U.C. Retinoic acid synthesis in the postnatal mouse brain marks distinct developmental stages and functional systems. Cereb. Cortex 12 (2002) 1244-1253
142. Wallace M.T., Ramachandran R., and Stein B.E. A revised view of sensory cortical parcellation. Proc. Natl. Acad. Sci. U.S.A. 101 (2004) 2167-2172
143. Watakabe A., Sugai T., Nakaya N., Wakabayashi K., Takahashi H., Yamamori T., and Nawa H. Similarity and variation in gene expression among human cerebral cortical subregions revealed by DNA macroarrays: technical consideration of RNA expression profiling from postmortem samples. Brain Res. Mol. Brain Res. 88 (2001) 74-82
144. Wiesel T.N., and Hubel D.H. Single-cell responses in striate cortex of kittens deprived of vision in one eye. J. Neurophysiol. 26 (1963) 1003-1017
145. Wiesel T.N., and Hubel D.H. Comparison of the effects of unilateral and bilateral eye closure on cortical unit responses in kittens. J. Neurophysiol. 28 (1965) 1029-1040
146. Wiesel T.N., and Hubel D.H. Extent of recovery from the effects of visual deprivation in kittens. J. Neurophysiol. 28 (1965) 1060-1072
147. Windrem M.S., and Finlay B.L. Thalamic ablations and neocortical development: alterations of cortical cytoarchitecture and cell number. Cereb. Cortex 1 (1991) 230-240
148. Wolberg A.S., and Roubey R.A. Annexin A2: better left alone. Blood 105 (2005) 1845-1846
149. Wong-Riley M.T., and Jacobs P. AMPA glutamate receptor subunit 2 in normal and visually deprived macaque visual cortex. Vis. Neurosci. 19 (2002) 563-573
150. Xu L., Tanigawa H., and Fujita I. Distribution of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate-type glutamate receptor subunits (GluR2/3) along the ventral visual pathway in the monkey. J. Comp. Neurol. 456 (2003) 396-407
151. Yanez I.B., Munoz A., Contreras J., Gonzales J., Rodriguesz-Veiga E., and DeFelipe J. Double bouquet cell in the human cerebral cortex and a comparison with other mammals. J. Comp. Neurol. 486 (2005) 344-360
152. Zangenehpour S., and Chaudhuri A. Patchy organization and asymmetric distribution of the neural correlates of face processing in monkey inferotemporal cortex. Curr. Biol. 15 (2005) 993-1005
153. Zapala M.A., Hovatta I., Ellison J.A., Wodicka L., Del Rio J.A., Tennant R., Tynan W., Broide R.S., Helton R., Stoveken B.S., Winrow C., Lockhart D.J., Reilly J.F., Young W.G., Bloom F.E., Lockhart D.J., and Barlow C. Adult mouse brain gene expression patterns bear an embryologic imprint. Proc. Natl. Acad. Sci. U.S.A. 102 (2005) 10357-10362
154. Zhang J., and McCrae K.R. Annexin A2 mediates endothelial cell activation by antiphospholipid/anti-2 glycoprotein. Blood 105 (2005) 1964-1969
155. Zilles K., Palomero-Gallagher N., and Schleicher A. Transmitter receptors and functional anatomy of the cerebral cortex. J. Anat. 205 (2004) 417-432