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1 recurrent negative feedback collaterals onto somatodendritic 5-HT(1A) and 5-HT(1D) autoreceptors thus
2                               An increase in somatodendritic 5-HT(1A) autoreceptor density in the dor
3 fect postulated to result from activation of somatodendritic 5-HT(1A) autoreceptors in the DRN.
4 minopeptidase-like protein subunits comprise somatodendritic A-type channels in mammalian neurons.
5  the unitary conductance (gamma) of neuronal somatodendritic A-type K(+) channels composed of Kv4 por
6 hat Kv4.2 subunits are major constituents of somatodendritic A-type K(+) channels in these four types
7 nisms of inactivation gating of the neuronal somatodendritic A-type K(+) current and the cardiac I(to
8 s mediate most of the subthreshold-operating somatodendritic A-type K+ current in CNS neurons.
9                      Subthreshold-activating somatodendritic A-type potassium channels have fundament
10 wly than responses mediated by postsynaptic (somatodendritic) A1Rs in cultured neurons.
11 equired excitation of DA neurons mediated by somatodendritic alpha4beta2 nAChRs, as well as enhanceme
12  to KYNA (>/=100 nm) inhibited activation of somatodendritic alpha7 nAChRs; the IC(50) for KYNA was a
13 rthermore, the MT network was reduced in the somatodendritic and AIS compartments, and both the heavy
14  binding protein calretinin (CR) in both the somatodendritic and axonal compartment.
15 ll as in membrane protein trafficking in the somatodendritic and axonal compartments of differentiate
16                      Plasma membranes of the somatodendritic and axonal domains of neurons are known
17 vesicular organelles that are present in the somatodendritic and axonal domains of neurons.
18  a physiological and physical bridge between somatodendritic and axonal domains.
19 s are highly polarized cells having distinct somatodendritic and axonal domains.
20 npolarized distribution of ATP7B between the somatodendritic and axonal domains.
21 hysiological and physical bridge between the somatodendritic and axonal domains.
22 d Kv3.1b, are differentially targeted to the somatodendritic and axonal membrane, respectively, the l
23        Although initially inserted into both somatodendritic and axonal membranes, VGSCs are concentr
24 aneous transmission was due to activation of somatodendritic and axonal receptors while the depressio
25 ed to soma and dendrites and postulated that somatodendritic and axonal/presynaptic isoforms of N-typ
26 tion by forming at least two steps involving somatodendritic and ciliary sorting decisions.
27       This inhibition targeted both proximal somatodendritic and distal apical dendritic domains of g
28 eling was detected in many axonal as well as somatodendritic and glial profiles.
29 of elevated extracellular DA levels, altered somatodendritic and presynaptic D2 DA receptor (D2R) fun
30 erway to examine the sensitivity of both the somatodendritic and terminal 5-HT autoreceptors in malno
31 tion was observed in male mouse dopaminergic somatodendritic and terminal regions.
32 e like calcium channels localize to both the somatodendritic and the axonal compartment of larval cra
33 stic frequency in the theta range across the somatodendritic arbor and specific STA measurements were
34 along with limited DAT endocytic activity in somatodendritic areas.
35      All of these subunits were localized to somatodendritic as well as axonal cell compartments.
36 and VGLUT2 in its subcellular location, with somatodendritic as well as axonal expression.
37  and in the sensory cortex, and are found at somatodendritic as well as nerve terminal sites in the r
38 PAT-labeled 5-HT(1a) binding in pre-synaptic somatodendritic autoreceptors on dorsal raphe nucleus re
39 -layer pyramidal neurons across their entire somatodendritic axis for several months.
40 to a reconfiguration of inhibition along the somatodendritic axis of pyramidal cells, and enhances th
41 ion of T-type Ca2+ channels along the entire somatodendritic axis of sensory thalamocortical (TC) neu
42 e quantitative changes in boosting along the somatodendritic axis suggest that inputs from different
43 angential current flow (perpendicular to the somatodendritic axis) modulates synaptic efficacy acutel
44     (2) Radial current flow (parallel to the somatodendritic axis) modulates synaptic efficacy consis
45  the degree of boosting may differ along the somatodendritic axis.
46 nterneurons, this plasticity was observed at somatodendritic basket cell synapses, but not at distal
47 lar matrix, and NF-186 overexpression caused somatodendritic brevican clustering.
48                                     Finally, somatodendritic but not axonal application of GABA evoke
49 2-LO regulates LTP by enhancing postsynaptic somatodendritic Ca(2+) influx through L-type channels du
50 y combined in situ patch clamp recordings of somatodendritic calcium currents in an identified adult
51 a(v)2 homolog, Dmca1A, underlies HVA and LVA somatodendritic calcium currents in the same neuron.
52 ition, we show that Dmca1A underlies the HVA somatodendritic calcium currents in vivo.
53 nt somatic APs, it must scale with the local somatodendritic capacitance.
54 s, the AIS location is finely tuned with the somatodendritic capacitive load, serving as a homeostati
55 nd flattened (dendrites limited to lamina I) somatodendritic categories.
56  normally localized to highly phosphorylated somatodendritic clusters in neurons.
57 d Kv2.2 heteromultimers did not aggregate in somatodendritic clusters observed with expression of Kv2
58 ly phosphorylated, localized in high-density somatodendritic clusters, and has a relatively depolariz
59 umption that mislocalization of tau into the somatodendritic compartment (6) and accumulation of fibr
60 rs that immunocytochemically highlight their somatodendritic compartment and brush, respectively.
61           SLITRK1 is further enriched in the somatodendritic compartment and cytoplasmic vesicles of
62 n growth) became selectively targeted to the somatodendritic compartment and excluded from axons by p
63 nsistent with an adaptation occurring in the somatodendritic compartment and independent of a circuit
64  neurons, PMCA2b was abundant throughout the somatodendritic compartment and often extended into the
65 trast, CaV3.1 channels were localized to the somatodendritic compartment and proximal axon, but were
66  products traverse different pathways in the somatodendritic compartment before axonal entry.
67  of both sexes is distributed throughout the somatodendritic compartment but is particularly enriched
68  client, was rerouted from the axonal to the somatodendritic compartment by dominant-negative SEC24D.
69 n together, our results demonstrate that the somatodendritic compartment directly inhibits myelinatio
70 tion of mouse tau, its redistribution to the somatodendritic compartment in cortical and hippocampal
71 py revealed abundant ErbB4 expression in the somatodendritic compartment in which it accumulates at,
72           Shal is predominantly found in the somatodendritic compartment in which it influences oscil
73 ressed with the pore-forming subunits in the somatodendritic compartment of CNS neurons.
74                     Our study shows that the somatodendritic compartment of DA neurons matures before
75 at MAP1B light chain (LC) accumulates in the somatodendritic compartment of hippocampal neurons, wher
76 geted Channelrhodopsin-2 specifically to the somatodendritic compartment of neurons in mice in vivo.
77 nking results in aberrant myelination of the somatodendritic compartment of neurons.
78 xons of L4-L2/3 synapses, rather than on the somatodendritic compartment of presynaptic L4 neurons.
79 emonstrate the mislocalization of tau in the somatodendritic compartment of RGCs subjected to high in
80 cure, but shows a restricted invasion of the somatodendritic compartment of the cell.
81  be activated by glutamate released from the somatodendritic compartment of the postsynaptic pyramida
82 icroscopic analyses, which revealed that the somatodendritic compartment was the principal target of
83 tial segment (AIS) electrically connects the somatodendritic compartment with the axon and converts t
84 , axons and dendrites (or more properly, the somatodendritic compartment) are radically different.
85 ly, misfolded Tau can be internalized at the somatodendritic compartment, or the axon terminals and i
86            atRA increased translation in the somatodendritic compartment, similar to brain-derived ne
87 l plate neurons, localizing primarily to the somatodendritic compartment.
88 throcyte membrane skeleton structure, in the somatodendritic compartment.
89  levels, and electronic propagation from the somatodendritic compartment.
90 not induce autophagy in either the axonal or somatodendritic compartment.
91 he microtubule-associated protein 2-positive somatodendritic compartment.
92 mposed on the proximal end of the AIS by the somatodendritic compartment.
93  subcellular distribution for ZNF804A within somatodendritic compartments and a nanoscopic organizati
94 n occur in the absence of pyramidal neuronal somatodendritic compartments and are temporally correlat
95      Endogenous ZNF804A protein localized to somatodendritic compartments and colocalized with the pu
96 as restricted to C1 neurons and filled their somatodendritic compartments and efferent axons 7-28 day
97 by formation in axons by days 4-7, spread to somatodendritic compartments by days 7-10 and neuron dea
98 he co-existence of MOR and CB1r-ir in common somatodendritic compartments of catecholaminergic neuron
99 ors located on the presynaptic terminals and somatodendritic compartments of cortical GABAergic inter
100                     We find that GSK3beta in somatodendritic compartments of hippocampal neurons beco
101 an exacerbated NMDAR-DeltaCa(2+) response in somatodendritic compartments of MNCs of RVH rats, and (2
102 4.2) mRNAs and regulates their expression in somatodendritic compartments of neurons.
103 might differentially influence inhibition in somatodendritic compartments of pyramidal neurons and af
104 tentials propagated reliably into axonal and somatodendritic compartments with conduction velocities
105 , with alpha7 targeted preferentially to the somatodendritic compartments, whereas alpha4beta2 was lo
106  cells with functionally distinct axonal and somatodendritic compartments.
107 itiation and the boundary between axonal and somatodendritic compartments.
108 caused HCN1 to be mistargeted throughout CA1 somatodendritic compartments.
109 t to depend on inward current originating in somatodendritic compartments.
110 nhibitory interneurons, thus bypassing their somatodendritic compartments.
111 e mutant protein specifically accumulates in somatodendritic compartments.
112 elated neural rhythms, but the importance of somatodendritic conductances in rhythm generation is sti
113            We hypothesize that an inhibitory somatodendritic cue is necessary to prevent non-axonal m
114 hannel KCNB1 (Kv2.1), which conducts a major somatodendritic current in cortex and hippocampus, is kn
115 ed the magnitude of D2R-dependent inhibitory somatodendritic currents and blunted the impact of D2R a
116 neurons display prominent, non-desensitizing somatodendritic D2-autoreceptor responses that show pron
117 anism was suggested by the observations that somatodendritic D2R activation produces hyperpolarizatio
118 nd RyR-dependent ER Ca(2+) stores facilitate somatodendritic DA release in the SNc.
119 ), suggesting a mechanism for maintenance of somatodendritic DA release with limited Ca(2+) entry.
120 which couple to IP(3) production), increased somatodendritic DA release, whereas CPCCOEt, an mGluR1 a
121 ng a functional role for ER Ca(2+) stores in somatodendritic DA release.
122 ocalization and function of Kv2.1, the major somatodendritic delayed rectifier voltage-dependent K+ c
123 t glutamate triggers GABA release only after somatodendritic depolarization and action potential gene
124 regions and a shift from a nuclear to a more somatodendritic distribution by approximately P13.
125 ribution in the first 2 postnatal weeks to a somatodendritic distribution in adult brain.
126 n filaments had no significant effect on the somatodendritic distribution of BC1 RNA.
127      This likely relates to the differential somatodendritic distribution of mGluRs and mAChRs and ma
128         More generally, we conclude that the somatodendritic distribution of Na(V) channels is a majo
129 fen protein displays a microtubule-dependent somatodendritic distribution pattern that overlaps with
130 R appeared as punctate structures within the somatodendritic domain and by electron microscopy was sh
131  of EAAT3 in neurons, its restriction to the somatodendritic domain and its clustering near postsynap
132        As expected, FMRP is expressed in the somatodendritic domain in virtually all neurons.
133  initial segment (AIS) along with the entire somatodendritic domain of adult male mouse dopaminergic
134 solateral domain of epithelial cells and the somatodendritic domain of neurons is mediated by recogni
135 brane of polarized epithelial cells, and the somatodendritic domain of neurons through interactions w
136 ter ATP7B and the vesicle-SNARE VAMP4 to the somatodendritic domain of rat hippocampal neurons is med
137 istribution in pyramidal neurons, across the somatodendritic domain, depends on ongoing cyclic adenos
138 the soma, autophagosomes are confined to the somatodendritic domain, facilitating cargo degradation a
139  of the AIS, but not its position within the somatodendritic domain, is the major causal determinant
140 logs FXR1P and FXR2P are well studied in the somatodendritic domain, recent evidence suggests that th
141 nter the soma and remain confined within the somatodendritic domain.
142 rity is established, how distinct axonal and somatodendritic domains are maintained, and how integral
143 ent of membrane molecules between axonal and somatodendritic domains is unclear.
144 teractions is supported by colocalization in somatodendritic domains of cortical neurons in culture a
145 rs formed alpha1/beta-containing clusters on somatodendritic domains of MNTB principal neurons, coloc
146  regulators that are selectively targeted to somatodendritic domains of neurons.
147 thesized in, and released from, postsynaptic somatodendritic domains that are readily accessible to w
148 d proteins, which are normally restricted to somatodendritic domains, redistribute into the former ax
149 ctrin is found in neurons in both axonal and somatodendritic domains, using proteomics, biochemistry,
150 RNA, proteins, and lipids into the axonal or somatodendritic domains.
151 ion barrier is formed between the axonal and somatodendritic domains.
152 ctional differences between their axonal and somatodendritic domains.
153                                              Somatodendritic dopamine (DA) release in the substantia
154 his study examined the mechanisms underlying somatodendritic dopamine and noradrenaline transmission
155 re the time course and calcium dependence of somatodendritic dopamine release in the ventral tegmenta
156 he mechanisms and functional consequences of somatodendritic dopamine transmission in the VTA vary am
157 ratios and decreased extracellular levels of somatodendritic dopamine, consistent with a decrease in
158 us implicating endosomal trafficking through somatodendritic early endosomes in L1-mediated axon grow
159                Our data demonstrate that key somatodendritic electrical conduction properties are hig
160  preferential axonal targeting and selective somatodendritic endocytosis.
161 lation of L1/NgCAM occurs via nondegradative somatodendritic endosomes and subsequent anterograde axo
162 Early Endosomal Protein 21 kDa) localizes to somatodendritic endosomes, and downregulation of NEEP21
163 dependent pathway (transcytosis), traversing somatodendritic endosomes.
164 21 kD) as a regulator of L1/NgCAM sorting in somatodendritic endosomes.
165 -rectifier Kv2.1 potassium channels regulate somatodendritic excitability during periods of repetitiv
166 but how these circuits interact to shape the somatodendritic excitability of Purkinje cells during mo
167 likely to play a major role as modulators of somatodendritic excitability.
168  expression continues through P35, with peak somatodendritic expression at P21.
169  of NMDARs on axons, indicating an exclusive somatodendritic expression of functional NMDARs.
170                                              Somatodendritic expression of Kv7.2 or Kv7.3 subunits wa
171 omous activity, while synaptic activation of somatodendritic GABA(A) receptors regulates the axonal i
172 -G (480-kDa ankyrin-G) promotes stability of somatodendritic GABAergic synapses in vitro and in vivo.
173                                              Somatodendritic Girk currents evoked by the GABA(B) rece
174       The acute cocaine-induced weakening of somatodendritic Girk signaling complements the previousl
175  with a similar morphology but reversed I(h) somatodendritic gradient to that previously observed in
176 cede the appearance of SWDs and that altered somatodendritic HVA currents are not required for abnorm
177                                          The somatodendritic IA (A-type) K(+) current underlies neuro
178 ofoundly shape the trafficking and gating of somatodendritic iGluRs, is unknown.
179 ortical inhibition is recruited by classical somatodendritic integration rather than direct activatio
180 roperties and may be a critical component of somatodendritic ISA channels in the brain.
181         Kv4 channels are responsible for the somatodendritic ISA s.
182         Kv4 channels are responsible for the somatodendritic ISA s.
183 and computational modeling showed that while somatodendritic K(v)7 channels are strongly activated by
184                                              Somatodendritic L-type Ca2+ channels have long been view
185 n Alzheimer's disease (AD), we asked whether somatodendritic levels of human BC200 RNA are deregulate
186      On the basis of these findings plus the somatodendritic localization of RACK1, we hypothesize th
187 f SNc neurons, suggesting that activation of somatodendritic M5 increases the intrinsic excitability
188                       Although activation of somatodendritic M5 receptors on SNc neurons leads to inc
189 ique to provide qualitative and quantitative somatodendritic measures of gigantopyramidal neurons acr
190 density innervation of 5-HT terminals on the somatodendritic membrane and a complete absence on the A
191 the function of alpha7 nAChRs located on the somatodendritic membrane of hippocampal interneurons.
192 cipal contributors to A-type channels in the somatodendritic membrane of mammalian brain neurons.
193 cells of SCA1 mice and indicate that altered somatodendritic membrane trafficking and loss of protein
194                                          The somatodendritic membrane was immunopositive for mGluR1al
195 plasmic vacuoles contained proteins from the somatodendritic membrane, including mGluR1, GluRDelta1/D
196  the distal axon is estimated as <1% that of somatodendritic membrane.
197 g the ICAMs, because it is only expressed in somatodendritic membranes of telencephalic neurons.
198 ude that in addition to previously described somatodendritic MOR-li, a substantial amount of MOR-li i
199 long been thought to be homogeneous in their somatodendritic morphology and physiology.
200                              We analyzed the somatodendritic morphology and ultrastructure of these t
201 ouse cortex undergoes significant changes in somatodendritic morphology during the critical period fo
202 nomic groups could be discriminated based on somatodendritic morphology for both superficial and giga
203 esent study characterized and quantified the somatodendritic morphology of neocortical neurons in pre
204 e evaluated potassium channel expression and somatodendritic morphology of projection neurons and the
205  we studied the developmental changes of the somatodendritic morphology of subplate neurons with spec
206 it robust projection-specific differences in somatodendritic morphology, cellular excitability, and l
207 elevated neuronal rigidity, and reshaping of somatodendritic morphology.
208               Altogether, the data show that somatodendritic MORs in POMC neurons inhibit neuronal ac
209 dhesion molecule 2 (JAM2) as an inhibitor of somatodendritic myelination in spinal cord neurons, ther
210 stribution of membrane proteins to axonal or somatodendritic neuronal compartments is fundamental to
211 , serum ICAM-5 may be a potential marker for somatodendritic neuronal damage.
212 ge results from a compromise between AIS and somatodendritic oscillators.
213 s respond with transient Ca(2+) increase and somatodendritic oxytocin release following neuropeptide
214 CNQ2 and KCNQ3 proteins are colocalized in a somatodendritic pattern on pyramidal and polymorphic neu
215 M interneuron models that incorporated I(M), somatodendritic placement of Kv7 channels best reproduce
216        Polarized neurons maintain axonal and somatodendritic plasma membrane domains without an obvio
217 d a uniform distribution of receptors in the somatodendritic plasma membrane when imaged over a 1 min
218 gly expressed and distributed throughout the somatodendritic plasma membrane.
219 te for delivering signaling receptors to the somatodendritic plasma membrane.
220 events mediating receptor insertion into the somatodendritic plasma membrane.
221 erved a transient appearance of NgCAM on the somatodendritic plasma membrane.
222 ic micron-scale domains within extrasynaptic somatodendritic plasma membranes of pyramidal neurons.
223 esicles, caused loss of TGN localization and somatodendritic polarity of ATP7B.
224 ab5 in rat hippocampal neurons abrogates the somatodendritic polarity of the transferrin receptor and
225                M5R was located mainly to VTA somatodendritic profiles (71%; n = 627), at least one-th
226 beling during P5-P10 was mainly localized in somatodendritic profiles but also was readily seen in ax
227 localized to endomembranes in DAT-containing somatodendritic profiles but showed a more prominent, si
228 mmunogold labeling was predominately seen in somatodendritic profiles throughout the PPT/LTD complex.
229               CB1r immunoreactivity (-ir) in somatodendritic profiles was more often localized to the
230 densities of NK3Rs in PVN AVP- or OC-labeled somatodendritic profiles were measured by quantitative i
231                                              Somatodendritic profiles with CB1r-ir typically received
232 the CB1r-immunoreactive structures, 66% were somatodendritic profiles, 22% were axon terminals, and t
233                                           In somatodendritic profiles, 5-HT1A gold particles were mai
234 HT1A immunoreactivity was mainly observed in somatodendritic profiles, but it was also present in sma
235 he cytoplasm and near asymmetric synapses on somatodendritic profiles.
236 s population, striatal MSNs have dichotomous somatodendritic properties that mirror differences in th
237 n, functions in the neuronal soma to exclude somatodendritic proteins from axonal transport carriers.
238 ion of axonal retrograde carriers containing somatodendritic proteins toward the soma.
239 rom the brain and colocalizes with Cav1.2 in somatodendritic puncta of cortical neurons in culture.
240 and whether it plays a role in axonal versus somatodendritic receptor localization.
241 shy cells of the cochlear nucleus, expressed somatodendritic receptors (alpha1/beta heteromers) and s
242  retrieval for the polarized distribution of somatodendritic receptors at steady state.
243 e that small endosomal carriers derived from somatodendritic recycling endosomes can serve to redistr
244 phin, which is known to be secreted from the somatodendritic region and has been shown previously to
245 xon guidance; localization of Kalirin to the somatodendritic region of adult neurons provides the bas
246 nterneurons and GluR6-containing KARs in the somatodendritic region of both interneurons and pyramida
247  Shh signal transduction originates from the somatodendritic region of the neurons and occurs in neur
248 ity and form strong synapses on the proximal somatodendritic region.
249 w fluorescent protein-SERT from axons to the somatodendritic region.
250 related to calmodulin (CaM) and localized in somatodendritic regions of principal neurons throughout
251 targeted mitochondria are accumulated in the somatodendritic regions where mature lysosomes are predo
252 th approaches demonstrated that, in midbrain somatodendritic regions, HA-DAT was present in the plasm
253 dritic with scattered puncta in neuropil and somatodendritic regions.
254 in translocation predominantly occurs in the somatodendritic regions; such distribution is associated
255         Here, we provide the first report of somatodendritic release of CCK in the brain in male Spra
256 lts in enhancement of inhibition through the somatodendritic release of CCK.
257                                              Somatodendritic release of dopamine (DA) in midbrain rep
258        This activity is regulated in part by somatodendritic release of dopamine and subsequent feedb
259 mediated synaptic current that resulted from somatodendritic release of dopamine in brain slices take
260                                          The somatodendritic release of dopamine within the ventral t
261 vesicles that mediate the activity-dependent somatodendritic release of multiple retrograde signals i
262        Despite early convincing evidence for somatodendritic release of neurohypophysial peptides in
263 entricular (i.c.v.) NPS evoked a significant somatodendritic release of OXT within the PVN as assesse
264      Here, we provide the first evidence for somatodendritic release of the satiety peptide cholecyst
265                                Surprisingly, somatodendritic release was maximal in 1.5 mm Ca(2+), wi
266 ) and oxytocin (OT) undergo Ca(2+)-dependent somatodendritic release within the supraoptic and parave
267       Coupled with limited uptake, prolonged somatodendritic release would facilitate DA-mediated vol
268 hers ATP7A at the trans-Golgi network in the somatodendritic segments of motor neurons and that alter
269 up the Kv4.2 potassium channels (involved in somatodendritic signal integration and attenuation of de
270                      Significance statement: Somatodendritic signaling using endocannabinoids or nitr
271 uggest that the M3 subtype is present on the somatodendritic site of glycinergic neurones and is main
272 -HT(1A) receptor; Rh-CT(5-HT1A) localizes to somatodendritic sites and is efficiently trafficked to d
273  from both terminals in projection areas and somatodendritic sites within the ventral midbrain.
274 the primary recognition event that underlies somatodendritic sorting and contribute to the evolving v
275                          Herein we show that somatodendritic sorting of various transmembrane recepto
276  is distributed in a gradient throughout the somatodendritic space.
277 keleton, exclusion of both axon-specific and somatodendritic-specific cell surface proteins, and accu
278  that these properties underpin a whole-cell somatodendritic spike generation mechanism that makes th
279 'shadow') and identified on the basis of its somatodendritic structure.
280 s of the voltage-gated K+ channel underlying somatodendritic subthreshold A-type currents (I(SA)) in
281     Kv4.2 is a major pore-forming subunit in somatodendritic subthreshold A-type potassium current (I
282             Kv4 channels mediate most of the somatodendritic subthreshold operating A-type current (I
283 EEP21 leads to missorting of L1/NgCAM to the somatodendritic surface as well as to lysosomes.
284  VGSCs in hippocampal neurons to limit their somatodendritic surface expression, although exerting li
285 MPA-type glutamate receptors (AMPARs) to the somatodendritic surface of rat hippocampal pyramidal neu
286 phas (alpha) 1, 2, 3 subunits was located on somatodendritic surfaces of neurochemically distinct mye
287 urons with a unique mechanism for regulating somatodendritic synthesis of nitric oxide.
288 fects occurred without altering AIS Na(+) or somatodendritic T-type channel activity and could be med
289 can direct apical targeting in epithelia and somatodendritic targeting in neurons.
290 as been suggested that this is equivalent to somatodendritic targeting in neurons.
291 d tau hyperphosphorylation in the absence of somatodendritic tau inclusions.
292  levels in the brain and a greater extent of somatodendritic tau redistribution by three months of ag
293 RN) were examined with whole-cell recording, somatodendritic three-dimensional reconstructions and mo
294 v) channel alpha subunit responsible for the somatodendritic transient or A-type current I(SA) that a
295                               Differences in somatodendritic transmission would be expected in vivo t
296  two corresponding timescales throughout the somatodendritic tree.
297              Syt10 colocalized with IGF-1 in somatodendritic vesicles of olfactory bulb neurons, and
298 t that there is a decrease in the content of somatodendritic vesicular dopamine in the Lep(ob/ob) mic
299          Rapidly activating and inactivating somatodendritic voltage-gated K(+) (Kv) currents, I(A),
300 ining pattern for PICK1-immunoreactivity was somatodendritic with scattered puncta in neuropil and so

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