Name
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601	Response of isolated bipolar cells to glycine
602	Response to glutamate in isolated bipolar cells
603	Reversed chloride gradients, demonstrated by cytochemical methods, may be responsible for excitatory GABA effects on selected periglomerular neurons
604	reviewed by
605	Reviewed in
606	reviewed in
607	Reviewed in
608	reviewed in
609	reviewed in
610	Reviewed in
611	Reviewed in
612	Reviewed in
613	reviewed in Haberly 1998).
614	reviewed in Llinas and Walton, 1990).
615	reviewed in McCormick 1998).
616	reviewed in Shepherd 1998). Variable densities of active channels support variable extents of backpropagating impulse in the dendrites
617	Rhodopsin (rods) and red, green and blue opsins (cones), in disc membranes of the distal segment.
618	Rhodopsin (rods) in disc membranes of the distal segment.
619	see also
620	see also
621	see also
622	see also
623	see also Felix and MacLennan, 1971).
624	see also Tseng and Haberly 1989b; reviewed in
625	see Burke 1998 for references). Single-fiber Ia EPSPs have widely varying shapes
626	See SOBiv p140).
627	Selective localization of GABA receptors at symmetric synapses ( and of gluR at asymmetric synapses.)
628	Sensitive to TTX. This generates the impulses that propagate into the axon
629	Sensitive to TTX. This plateau potential underlies impulse bursting
630	Serotonin produced a slowly developing and long-lasting suppression of IM leading to depolarization end excitation
631	Sherman and Koch, 1990).Using electrophysiological recordings and imaging, the density of these channels was found to rapidly decrease with distance from soma and clustered in high density around the base of dendrites
632	showed that the proximal dendrites and somata of hippocampal neurons label for L-type Ca2+ channels and that these channels tend to cluster near the bases of the neural processes. In patch recordings, "HVA-l channels reminiscent of L-type channels were occasionally encountered primarily in the more proximal dendrites" (and in the soma)
633	Silent synapses during development
634	Simultaneous recordings were carried out in visual cortical slices. Assuming open probability of non-NMDA receptor channels to be 0.7, it is suggested that the number of channels available for synaptic transmission between individual pyramidal cells would be 74 (kittens) and 59 (rats)
635	Simultaneous whole-cell recordings, made from the soma and dendrites rat brain slices, showed that AP evoked by either current pulses or synaptic stimulation of parallel or climbing fibers, always occurred first at the soma and decreased in amplitude with increasing distance into the dendrites. Simultaneous somatic and axonal recordings showed that these action potentials were initiated in the axon
636	Simultaneous whole-cell recordings, made from the soma and dendrites rat brain slices, showed that AP evoked by either current pulses or synaptic stimulation of parallel or climbing fibers, always occurred first at the soma and decreased in amplitude with increasing distance into the dendrites. Simultaneous somatic and axonal recordings showed that these action potentials were initiated in the axon. Outside-out patches excised from the soma and dendrites up to about 100um revealed a channel density decreasing with distance from the soma.
637	Single action potential backpropagations show dichotomy of either strong attenuation (26-42%) or weak attenuation (71-87%). The dichotomy seems to be conferred primarily by differences in distribution, density, etc. of voltage dependent sodium and potassium channel (A-type, especially ) along the somatodendritic axis
638	single fiber EPSPs:
639	Single unit extracellular recordings showed a short latency GABAA inhibition that arises from the axon collaterals of pars reticulata projection neurons
640	Single-cell-reverse transcription-polymerase chain reaction analysis of glycine receptor-subunit expression was combined with whole-cell recordings from acutely isolated cholinergic interneurons. Subunits alpha2, beta, alpha3, were found to be associated with receptor properties such as efficacy and desensiutization. Celllular localization of receptors unclear, but presumably on soma (?)