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1 proportion of dopaminergic and GABAergic VTA projections to 10 target nuclei: anterior cingulate, pre
2                                  Mapping the projections to 11 areas of 3,579 neurons in mouse audito
3                                              Projections to 2030 indicate an increase in the number o
4            Our vulnerability assessment uses projections (to 2039) from three downscaled climate mode
5                                              Projections to 2060 indicate loss of an additional 286 k
6 timates are similar to recent sea-level rise projections to 2100 at some locations.
7  historical hindcasts (1850-2005) and future projections to 2100 following representative concentrati
8 tion of tectal neurons with a defined axonal projection to a second-order visual area: id2b:gal4-posi
9           Neurons in the CeA send long-range projections to a number of extra-amygdala targets, but t
10  computation to compare disturbance-impacted projections to a population's normal range of variation,
11 ch comprise melanopsin-expressing types with projections to a small subset of central targets, select
12 w that a specific subset of superficial mPFC projections to a subfield of nucleus accumbens (NAc) neu
13 ecause RTN, unlike C1, has direct excitatory projections to abdominal premotor neurons.
14                     However, WHO's 2017 cost projections to achieve health-related Sustainable Develo
15 otyped topographical pattern, send divergent projections to amygdala subnuclei, and differ in their p
16     The broadly-distributed, non-topographic projections to and from the olfactory cortex may suggest
17 , an abnormal sensitivity of thalamocortical projections to antipsychotics, and an abnormal acoustic-
18                     Terminations of pulvinar projections to area 17 was largely in superficial cortic
19                                              Projections to area 2 were restricted and were predomina
20 were counted so that the relative density of projections to areas 2 and 5 from other cortical fields
21 found that the claustral territories sending projections to areas PE and PEc partially overlapped zon
22         In addition, we investigated the IPS projections to areas V4, TEO, PO, and MT using retrograd
23 l pathways, and sends a prominent descending projection to ascending and premotor, subpallial stages
24 orm surges with probabilistic sea-level rise projections to assess future coastal inundation in New Y
25                    We use these transmission projections to assess the change in burden in 2050 and 2
26 , dmPFC, vmPFC projections to NAcS, or vmPFC projections to basolateral amygdala, to punished EtOH-SA
27 ns, have caused the resulting variability in projections to be viewed as the irreducible uncertainty
28 ived cortical neurons send widespread axonal projections to both hemispheres of rats with ischemic le
29           KEY POINTS: There are serotonergic projections to both the main (MOB) and the accessory olf
30 avior, which is mediated by their collateral projections to both the motor-related layers of the supe
31                               Because of its projections to brain regions regulating reward and anxie
32  to the basal ganglia and through descending projections to brainstem motor circuits.SIGNIFICANCE STA
33 n to the caudal medulla primarily and axonal projections to brainstem motor nuclei most prominently,
34  respiratory group, but RTN has very limited projections to brainstem regions that regulate arousal (
35 at of the RTN, however, consistent with C1's projections to brainstem wake-promoting structures.
36    The presubiculum sends a dense, bilateral projection to caudal parts of the entorhinal cortex.
37 es within the parabrachial complex, and lack projections to caudal ventral respiratory group.
38 hese findings support the hypothesis that LC projections to CeA are critical for the expression of de
39 ce for cross-species conservation of sensory projections to central emotion-processing brain regions.
40  although the contribution of these indirect projections to circadian photoreception is currently poo
41  interface and performs a gene-subset linear projection to cluster heterogeneous samples by Gene Onto
42 f dendritic spines, new patterns of cortical projections to contralateral pre-motor cortex, and upreg
43 ially inhomogeneous structure of cholinergic projections to cortex.
44     It is still widely thought that cortical projections to distant brain areas derive by and large f
45  GRP neurons revealed ascending polysynaptic projections to distinct areas and nuclei in the brainste
46 t physiological roles, consistent with their projections to distinct areas within the brain.
47 tes, V1 layers (L)2/3 and 4B send segregated projections to distinct cytochrome oxidase (CO) stripes
48 tions of pyramidal neurons (PNs) send axonal projections to distinct targets, suggesting multiple cel
49  is sensitive to reward and sends excitatory projection to dopaminergic nuclei.
50 tic manipulations of either the avBST or its projections to downstream regions, and 48 h later were t
51  injured cord may reconstruct the descending projections to enhance cardiovascular performance.
52 n medium spiny striatal neurons and in their projections to entopeduncular nucleus/substantia nigra a
53 GMP catabolism, is downregulated in striatal projections to entopeduncular nucleus/substantia nigra,
54      We combined these effects with economic projections to estimate net changes in nutrient availabi
55 ility, and costs were combined with lifetime projections to evaluate lifetime cost-effectiveness of t
56 s increases, states must have individualized projections to evaluate the unique challenges they will
57 iated inactivation of OFC-->BLA or BLA-->OFC projections to evaluate their respective contributions t
58 also found at least sparse cerebrocerebellar projections to every lobule of the cerebellum.
59       We observed stronger and more numerous projections to excitatory than inhibitory SC neurons.
60                          Comparison of these projections to experiments in vivo indicates that synerg
61 ed cocaine seeking via functionally distinct projections to forebrain limbic regions.
62 DYT1 mice, PDE10A is upregulated in striatal projections to globus pallidus, preferentially expressin
63 dback to first-order thalamus and also sends projections to higher-order thalamus, yet how it engages
64 how neuromodulation via locus coeruleus (LC) projections to HPC area CA1 (LC-CA1) regulates the overr
65 loping postnatal mouse PCs and used metagene projection to identify the most salient patterns of PC g
66  avenues to improve the usefulness of hazard projections to inform decision-making such as (i) repres
67 opulation of IC cells sends branching axonal projections to innervate the MG bilaterally.
68   D3-receptor-expressing neurons send axonal projections to intratelencephalic (IT) targets, includin
69 l as adjacent nidopallial areas, send axonal projections to ipsilateral Av; Av in turn projects to co
70                                   Orthogonal projection to latent structures by partial least square
71 hical Cluster Analysis (HCA), and Orthogonal Projection to Latent Structures Discriminant Analysis (O
72 is [principal component analysis, orthogonal projections to latent structures (OPLS) and OPLS with di
73 ncer (n = 195) were modelled with orthogonal projections to latent structures (OPLS).
74 etween blanching treatments while Orthogonal Projections to Latent Structures Discriminant Analysis (
75                                   Orthogonal projections to latent structures-discriminant analysis (
76 odelling of class analogies and (orthogonal) projections to latent structures-discriminant analysis t
77 g are assembled from VP cell types and their projections to lateral hypothalamus (LH) and ventral teg
78 but not to relapse during reacquisition, via projections to LH, where they converge with ventral stri
79 ) neurons control relapse during renewal via projections to LH.
80 at aberrant functioning of midbrain dopamine projections to limbic regions causes psychotic symptoms.
81 rastriate regions return stronger descending projections to localized LGd areas.
82 ted by using only two of 984 conventional CT projections to locate and reconstruct the needle, which
83                        We find that residual projections to lumbar MNs are required to produce leg mo
84   CeA(GA) neurons have widespread inhibitory projections to many affective pain-processing centers.
85 n, but little understood, massive cerebellar projection to maps in the superior colliculus.
86 aversive stimuli and sends robust inhibitory projections to midbrain dopamine neurons, leading to the
87 natomic evidence revealing novel cholinergic projections to MNTB arising from pontine and superior ol
88                                     Indirect projections to MOB also originate from the solitary nucl
89  information processing area sends extensive projections to multiple brain centers, but the behaviora
90 tisensory nature of the JO together with its projections to multisensory neuropils in the ant brain l
91 chial (PBN) nuclei and brainstem showed dual projections to muscle + WAT, muscle + BAT, and WAT + BAT
92 of this work was to test the necessity of IC projections to NAc during social affective behavior.
93 rontal cortex as principal sources of CRH(+) projections to NAc.
94 onal contribution of the vmPFC, dmPFC, vmPFC projections to NAcS, or vmPFC projections to basolateral
95                                     While PL projections to nucleus accumbens core have been shown to
96 or rapid post-acquisition alignment of these projections to obtain high quality three-dimensional ima
97 ion of prefrontal cortex that has descending projections to oculomotor control centers.
98 L cells showed that they send profuse axonal projections to olfactory cortical areas, but not to the
99                     We focused on vestibular projections to ON and OFF classes of unipolar brush cell
100 ing specific receptor genes send stereotyped projections to one or two of about 50 morphologically de
101 neurons in a single brain and relating those projections to other properties such as gene or Cre expr
102 urons within the pBNST send dense inhibitory projections to other stress-related brain regions (for e
103 e, we use immunostaining to quantify the MOC projections to outer hair cells and lateral OC (LOC) pro
104 ement tuning is determined by the pattern of projections to output neurons and may even be uncorrelat
105 t, for neurons that only affect movement via projections to output neurons, the relationship between
106 obutyric acid (GABA) neurons or their axonal projections to paraventricular thalamus (PVT) excitatory
107  the olfactory bulb and sends an associative projection to piriform cortex that has potential roles i
108 ) of thalamus, a homolog of pulvinar, or its projection to primary visual cortex (V1), we found that
109               We use CMIP5 local temperature projections to project the impact of future warming, and
110                   We compared the integrated projections to projections from the empirical climatic n
111 orts on a new direct descending dopaminergic projection to reticulospinal neurons that modulates loco
112 n cocaine seeking by implicating PL efferent projections to RMTg in inhibiting cue-induced reinstatem
113 estigated the potential circuit suggested by projections to RSCg layer 1 (L1) from GABAergic CA1 neur
114 propose that granulosa cells use cytoplasmic projections to search for the oocyte, and cumulus cell d
115 ) connects subcortically, sending inhibitory projections to sensorimotor structures, including the su
116 metabolism and reproduction because of their projections to several brain areas both in and outside o
117 lux through TRPV4 channels at myoendothelial projections to smooth muscle cells decreases resting blo
118 en predicts dendrite morphologies and axonal projections to specific tectal layers and extratectal ta
119 RVLM) regulate blood pressure through direct projections to spinal sympathetic preganglionic neurons.
120 r neurons on the basis of their preferential projections to SpVO versus SpVIr.
121 s highlight an unexpected contribution of M2 projections to striatal dysfunction in the Sapap3-KO obs
122  the preoptic nucleus, which send long-range projections to targets throughout the brain, including t
123 not into the auditory AI, revealed a massive projection to tectal layer 13 and other tectal related a
124 fied dendritic arbor and a descending axonal projection to tegmentum.
125 mic neurons of layer 6 send a dense feedback projection to thalamic nuclei that provide input to sens
126 responsive neurons were enriched in the vCA1 projection to the amygdala.
127 f Nrp2(+) MCs to the PV MOB and their axonal projection to the anterior MeA.
128 e movement (NREM) sleep partly through their projection to the caudal medulla.
129 lPAG NTS neurons is partly mediated by their projection to the caudal ventromedial medulla, where the
130                                      The VTA projection to the NAcSh releases dopamine, GABA and glut
131             The ventral tegmental area (VTA) projection to the nucleus accumbens shell (NAcSh) regula
132 t the role of the infralimbic cortex and its projection to the nucleus accumbens shell in suppressing
133 llum largely arises from the lateral LM; the projection to the oculomotor cerebellum largely arises f
134  tectofugal visual system and its descending projection to the optic tectum (TeO) has been less inves
135 irectional activity modulations of LP or its projection to the primary auditory cortex (A1) in awake
136 es that encode spatial relationships and its projection to the primary motor cortex.
137 neurons innervate brown fat via a descending projection to the raphe pallidus (RPa).
138 te that the cMRF provides a dense, bilateral projection to the region of the medial rectus C-group mo
139  on prey, was mediated by a central amygdala projection to the reticular formation in the brainstem.
140         We recently demonstrated a bilateral projection to the supraoculomotor area from the central
141                           In addition to the projection to the TeO, cells in FRLx send, via collatera
142  (PT), which in turn gives rise to bilateral projection to the TeO.
143        In addition, we report a Brn3c(+) RGC projection to the thalamic reticular nucleus, a visual n
144 -fugal visual pathway is a massive bilateral projection to the thalamus originating from a distinct n
145 o each projection, with the exception of the projection to the ventrolateral periaqueductal gray, whe
146                              In pigeons, the projection to the vestibulocerebellum largely arises fro
147               Ventral hippocampal CA1 (vCA1) projections to the amygdala are necessary for contextual
148 o previous report has described overall 5-HT projections to the amygdala in the rat.
149  in part, from claustrum and/or peri-insular projections to the anterior cingulate and medial prefron
150                  Inhibiting dorsal subiculum projections to the anterior thalamic nuclei produced the
151  separate inhibition of the dorsal subiculum projections to the anterior thalamic nuclei.
152 led the key contribution of dorsal subiculum projections to the anteromedial and anteroventral thalam
153 rn of AR immunoreactivity or of the afferent projections to the AR- nucleus were observed.
154 tivity in the ventral CA1 (vCA1) hippocampal projections to the basal amygdala (BA), paired with aver
155 dulate locomotor behavior both via ascending projections to the basal ganglia and through descending
156  locomotor behaviors through their ascending projections to the basal ganglia, which in turn project
157  is observed after the inhibition of CeA CRF projections to the bed nucleus of the stria terminalis (
158 on of PNOC(ARC) neurons in the ARC and their projections to the bed nucleus of the stria terminalis p
159 ed in novel, nonthreatening environments via projections to the BLA but do so as a result of training
160       Our findings show that the ACC and HPC projections to the BLA regulate generalized fear in nont
161                     Inactivating ACC or vHPC projections to the BLA significantly reduced generalized
162 r results highlight how CeAL CRF neurons and projections to the BNSTDL consolidate longer-lasting com
163  to examine the role of CeAL CRF neurons and projections to the BNSTDL during the acquisition of cont
164 mportant roles in the development of retinal projections to the brain and in motion detection, specif
165  to threat and injury through its descending projections to the brainstem.
166 aintenance of opiate-associated memories via projections to the central nucleus of the amygdala (CeA)
167 pe-specific manner, from remodeling of input projections to the characterization of specific molecula
168 lude that most cortical areas send bilateral projections to the claustrum, the majority being denser
169 lian peripheral auditory system through axon projections to the cochlea.
170 opic map presenting topographically discrete projections to the cochlear nuclei.
171 te and the secondary motor areas send denser projections to the contralateral claustrum than to the i
172 dient of Fzd3 in inner ear afferents directs projections to the correct dorsoventral column within th
173 gic positive cells in the IC, and descending projections to the DCN were colabeled with antibodies ag
174 on of Rorb in the wild type showed increased projections to the dLGN and decreased projections to the
175 rved in global and conditional Rorb mutants: projections to the dLGN were strongly decreased, and pro
176 are inconsistent with visual stream-specific projections to the dLGN.
177 ophila appears to be a group of neurons with projections to the dorsal fan-shaped body (dFB neurons)
178 out two dozen sleep-inducing neurons(3) with projections to the dorsal fan-shaped body (dFB) adjust t
179 main segregated within the IPS, and that its projections to the dorsal stream can be further segregat
180 s in the medial prefrontal cortex, including projections to the dorsomedial striatum, maintained pers
181 results support the idea that inhibiting LHb projections to the DRN provides animals with resilience
182  from the mid- and hindbrain, its widespread projections to the forebrain and its role in sharp-wave
183 ficient 5-HT neurons fail to generate axonal projections to the forebrain and spinal cord.
184                   Here, we study subcortical projections to the geniculate from the superior collicul
185  express the neuropeptide somatostatin, send projections to the globus pallidus external segment (GPe
186 , we found that a subset of CeA neurons send projections to the GPe, and the majority of these GPe-pr
187                                              Projections to the hippocampus from L2 of LEC arise from
188 ons to outer hair cells and lateral OC (LOC) projections to the inner hair cell area in humans 0-89 y
189 5-GFP+ subplate cells form long-range axonal projections to the internal capsule or callosum.
190 er pyramidal neurons in the mPFC send direct projections to the IPAC.
191                       Here, we show that CeA projections to the lateral hypothalamus (LH) are prefere
192 e behaviors, but also partially on VTA(Vgat) projections to the lateral hypothalamus (LH).
193  basal forebrain signaling, mediated through projections to the lateral hypothalamus, promotes select
194       While much of this work has focused on projections to the lateral hypothalamus, the role of NAc
195 behavior, with particular focus on accumbens projections to the lateral hypothalamus.
196 rgic and/or dopaminergic neurons and through projections to the lateral hypothalamus.
197 n activates nucleus tractus solitarius (NTS) projections to the lateral parabrachial nucleus (lPBN) a
198           Lastly, we examined the role of DH projections to the lateral septum (LS), a brain region i
199 nstrate that the CeA sends robust inhibitory projections to the lateral substantia nigra (SNL) that c
200  and the former has excitatory glutamatergic projections to the latter.
201 n lineage 7B, Unc-4 promotes proper neuronal projections to the leg neuropil and a specific flight-re
202 ribed functions of IC and CeA through direct projections to the LH.
203 ntial but not exclusive role of rEPN and its projections to the LHb in processing the aversive effect
204                                    Thus, PFC projections to the LHb may represent an important part o
205 ons to the dLGN were strongly decreased, and projections to the LP were increased.
206 reased projections to the dLGN and decreased projections to the LP.
207 licated in cocaine seeking and found that DH projections to the LS govern cocaine seeking on AD30.
208 ndicates that optogenetic stimulation of BLA projections to the medial entorhinal cortex (mEC) enhanc
209                       Descending facial lobe projections to the medial funicular nucleus were also no
210 enhancement of the flight behavior via their projections to the medial posterior complex of thalamus
211 ocomotor movements through direct descending projections to the mesencephalic locomotor region and sp
212           Using it, we have identified major projections to the mesolimbic dopamine circuit from the
213    In contrast, prey pursuit was mediated by projections to the midbrain periaqueductal gray matter.
214                          In contrast, direct projections to the MOB arise from melanin-concentrating
215 tual loss of 5HT neurons in the DRif and its projections to the mPFC as evidenced by fewer labeled ce
216 ecreases in 5HT soma within the DRif and its projections to the mPFC.
217                           To test whether IC projections to the NAc are involved in social decision-m
218             Additionally, the dense VTA-GABA projections to the NAc do not influence the motivational
219 ivating either the VTA-GABA neurons or their projections to the NAc.
220                         Photosilencing vmPFC projections to the NAcS, but not to the basolateral amyg
221  basolateral amygdala (BLA) sends excitatory projections to the nucleus accumbens (NAc) and regulates
222 opamine-producing VTA neurons with divergent projections to the nucleus accumbens (NAc) core and shel
223 bserved when we manipulated the serotonergic projections to the nucleus accumbens (NAc).
224 ) sleep-active, produced wakefulness through projections to the nucleus accumbens and the lateral hyp
225 ne neurons grouped according to their axonal projections to the nucleus accumbens or dorsal striatum
226 gation of these pathways in their subsequent projections to the nucleus ovoidalis (Ov) in the thalamu
227                                              Projections to the nucleus praeeminentialis (nP) arise f
228 hese findings suggest that glutamatergic AON projections to the OB impede early olfactory signaling b
229 0, 360, 480 and 729-day) revealed comparable projections to the observed long-term SOC changes under
230                                 In contrast, projections to the oculomotor cerebellum in hummingbirds
231    Likewise, activation of glutamatergic AON projections to the olfactory bulb (OB) transiently inhib
232                   Basal forebrain long-range projections to the olfactory bulb are important for olfa
233 Brn3b(+) Ret(+) RGCs shows minor ipsilateral projections to the olivary pretectal nucleus and the LGN
234 neity of the BF, we mapped the pattern of BF projections to the orexin neurons across multiple BF reg
235 negative-valence signal is transmitted along projections to the organum vasculosum of the lamina term
236 SSNA), arterial pressure, and heart rate via projections to the paraventricular nucleus (PVN) and dor
237  the area are largely glutamatergic and send projections to the paraventricular nucleus of the hypoth
238 ressing neurons in the hindbrain send robust projections to the paraventricular nucleus of the hypoth
239 eptin receptors in the mouse and send direct projections to the paraventricular nucleus of the hypoth
240 ly overlapped zones previously shown to form projections to the posterior parietal, somatosensory, vi
241            Quantitative analysis of cortical projections to the PPC revealed a significant loss of se
242 ns revealed that while activation of VLM(CA) projections to the pPVT was sufficient to elicit robust
243 We showed that ventral HC (vHC) neurons with projections to the PrL cortex (vHC-PrL projectors) are a
244 nown about the laminar distribution of these projections to the pulvinar across visual cortical areas
245 is view ignores the cortico-thalamo-cortical projections to the pulvinar nucleus in the thalamus, whi
246 ade tracing approach to map direct brainstem projections to the putative location of pF(L) , with RNA
247 find that activation of SF1 neurons or their projections to the PVT elicits a flavor aversive effect,
248 togenetic stimulation of ChR2-expressing SF1 projections to the PVT elicits direct excitatory postsyn
249 n of the PVT-projecting SF1 neurons or their projections to the PVT inhibits food intake, and chemica
250      Taken together with prior studies of IP projections to the raphe, these results form an emerging
251 pothalamicnucleus sends direct oxytocinergic projections to the rostral agranular insular cortex on G
252  the periaqueductal gray, and its descending projections to the rostral ventromedial medulla and spin
253 driving reinstatement of cocaine seeking, PL projections to the rostromedial tegmental nucleus (RMTg)
254 m that this preparation retains intact optic projections to the SCN, thalamus and pretectum and a fun
255 on cell interneurons with superficial axonal projections to the sensory input layer of the MOB.
256 f the lateral recess gave rise to descending projections to the SGN/V and the vagal lobe.
257 ndings reveal a consistent pattern: cortical projections to the somatosensory thalamus target thalamo
258 ord, while other studies demonstrate that CS projections to the spinal cord are eliminated in an acti
259 th the arrival and maturation of supraspinal projections to the spinal cord.
260 l evidence that a circuit involving cortical projections to the striatum and midbrain may underlie th
261 lls, we show that the switching neurons make projections to the substantia nigra (SN), ventral tegmen
262 sults ascribe motor and sensory roles to ACC projections to the superior colliculus and the visual co
263                                     Cortical projections to the thalamus arise from corticothalamic (
264 ation within MB subdivisions and topographic projections to the thalamus.
265 alculate the effect of localizer radiography projections to the total radiation dose, including both
266 duces short-term plasticity in corticospinal projections to the trunk muscle in healthy humans.
267 uts from the nucleus accumbens (NAc) include projections to the ventral pallidum and the ventral tegm
268  of LDTg GLP-1R-expressing neurons and their projections to the ventral tegmental area (VTA) in the r
269  that the cerebellum sends direct excitatory projections to the ventral tegmental area (VTA), one of
270 moment of shock delivery and was mediated by projections to the ventral tegmental area, which is cons
271 with wide dynamic ranges, send glutamatergic projections to the ventrolateral periaqueductal gray (vl
272 p2 and Pdyn cases was a notable lack of Pdyn projections to the ventromedial hypothalamic nucleus.
273                       Activation of efferent projections to the ventromedial hypothalamus (VMH) or la
274                    In all three species, the projections to the vestibulocerebellum were largely from
275 ly, NTS(HSD2) neurons stimulate appetite via projections to the vlBNST, which is also the effector si
276                Activation of locus coeruleus projections to the vPAG or vPAG(DA) neurons induced by D
277 er photometry, we find that medial NAc shell projections to the VTA (mNAc->VTA) are inhibited during
278     These results demonstrate that GABAergic projections to the VTA are a major contributor to the re
279                             We show that NAc projections to the VTA bidirectionally control food inta
280 food reward and consumption; yet, LHA (GABA) projections to the VTA exclusively modulated food consum
281                              Conversely, NAc projections to the VTA have mainly been studied in the c
282 to the lateral hypothalamus, the role of NAc projections to the VTA in the control food intake has be
283 trols feeding: optogenetic activation of NAc projections to the VTA inhibits food-seeking and food in
284  study, we mapped the major neurotransmitter projections to the VTA through cell-type-specific retrog
285 ens (NAc) provides one of the most prominent projections to the VTA; however, recent studies have pro
286 ding the mechanisms that wire retinal axonal projections to their appropriate central targets.
287 axon that exits tectum to form a topographic projection to torus longitudinalis (TL).
288 erneuron populations use specific anatomical projections to transform sensations into reflexive actio
289 eference-based algorithm (called constrained projection) to two non-constrained approaches including
290 l accounted for by a model assuming thalamic projections to two cortical layer-4 cell populations: on
291 4B output neurons, just like their extrinsic projections to V2, preserve CO streams.
292  pyramidal tract neurons (PTs) - send axonal projections to various subcortical areas.
293 ture eye disease burden, causing state-level projections to vary from national levels.
294 major ascending projections, including focal projections to ventral hippocampus, ventrolateral septum
295 risingly, driving excitatory thalamocortical projections to VLO at low frequencies (5-10 Hz) evoked w
296  Bidirectional modulation of avoidance by PL projections to VS and BLA enables the animal to make app
297 ontine tegmental nucleus sends glutamatergic projections to VTA dopamine neurons, and that stimulatio
298  in reinforcement, with an emphasis on their projections to VTA dopamine neurons.
299 se during both renewal and reacquisition via projections to VTA.
300 se during both renewal and reacquisition via projections to VTA.

 
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