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By Meyer, Hurst, Gray, Lewis

The 5th variation keeps its completeness, updates the insurance of bipolar applied sciences, and complements the dialogue of bicmos. It presents a extra unified therapy of electronic and analog circuit layout whereas strengthening the insurance of cmos. The bankruptcy on non-linear analog circuits has been got rid of and bankruptcy eleven has been up-to-date to incorporate an operational amplifier instance. versions for integrated-circuit energetic units bipolar, mos, and bicmos integrated-circuit know-how single-transistor and multiple-transistor amplifiers present mirrors, energetic lots, and references output phases operational amplifiers with single-ended outputs frequency reaction of built-in circuits suggestions frequency reaction and balance of suggestions amplifiers nonlinear analog circuits noise in built-in circuits totally differential operational amplifiers

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J Neurosci 19(10):3827–3835. 29 30 Handbook of Brain Microcircuits Rinaldi T, Silberberg G, Markram H (2007a) Hyperconnectivity of Local Neocortical Microcircuitry Induced by Prenatal Exposure to Valproic Acid. Cereb Cortex. Rinaldi T, Kulangara K, Antoniello K, Markram H (2007b) Elevated NMDA receptor levels and enhanced postsynaptic long-term potentiation induced by prenatal exposure to valproic acid. Proceedings of the National Academy of Sciences 104:13501–13506. Silberberg G, Gupta A, Markram H (2002) Stereotypy in neocortical microcircuits.

The presence of these calcium-binding proteins correlates with the morphology of the different types of inhibitory cells and their specific connections with the spiny cells, which form 85% of their synaptic targets. The parvalbumin-containing cells, like chandelier and basket cells, which target the soma, proximal dendrites, and axon initial segment, seem well-positioned to control the output of the cell. The calbindin- or calretinincontaining cells, such as the double bouquet cells or Martinotti cells, form synapses with the more distal dendrites and thus are probably concerned with controlling the input to pyramidal cells, which are their major targets.

Cereb Cortex 9(9):1953–1956. Jones EG, Burton H (1976) Areal differences in the laminar distribution of thalamic afferents in cortical fields of the insular, parietal and temporal regions of primates. J Comp Neurol 168:197–247. Keller A (1995) Synaptic organization of the barrel cortex. In: Jones EG and Diamond IT, eds. Cerebral Cortex, Vol. 11. The Barrel Cortex of Rodents, pp. 221–262. New York: Plenum Press. Lewis DA, Lund JS (1990) Heterogeneity of chandelier neurons in monkey neocortex: corticotropin-releasing factor- and parvalbumin-immunoreactive populations.

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