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1 c interneurons and the substantia nigra pars compacta.
2 RRK2 expression in the substantia nigra pars compacta.
3 fused locally into the substantia nigra pars compacta.
4 lase expression in the substantia nigra pars compacta.
5  the thalamus, and the substantia nigra pars compacta.
6 inergic neurons of the substantia nigra zona compacta.
7 ventral tegmental area/substantia nigra pars compacta.
8 arkably, little to the substantia nigra pars compacta.
9  and very few fibers within substantia nigra compacta.
10 inergic neurons of the substantia nigra pars compacta.
11 ne (DA) neurons in the substantia nigra pars compacta.
12 ne (DA) neurons in the substantia nigra pars compacta.
13 x, caudate-putamen and substantia nigra pars compacta.
14 raphe nucleus, and the substantia nigra pars compacta.
15 inergic neurons in the substantia nigra pars compacta.
16 egmental area (VTA) or substantia nigra pars compacta.
17 substantia nigra pars reticulata and/or pars compacta.
18  ventral tegmental area and substantia nigra compacta.
19 of degeneration of the substantia nigra pars compacta.
20 inergic neurons in the substantia nigra pars compacta.
21 nd inflammation in the substantia nigra pars compacta.
22 al tegmental area, and substantia nigra zona compacta.
23 inergic neurons in the substantia nigra pars compacta.
24 ession is noted in the substantia nigra pars compacta.
25 opaminergic neurons in substantia nigra pars compacta.
26 inergic neurons in the substantia nigra pars compacta.
27 inergic neurons in the substantia nigra pars compacta.
28  lesser extent, in the substantia nigra pars compacta.
29 opamine neurons in the substantia nigra pars compacta.
30 inergic neurons of the substantia nigra pars compacta.
31 ral tegmental area and substantia nigra pars compacta.
32 neuron activity in the substantia nigra pars compacta.
33 opamine neurons of the substantia nigra pars compacta.
34 inergic neurons in the substantia nigra pars compacta.
35 ine neurons from mouse substantia nigra pars compacta.
36 sal GL or in the right substantia nigra pars compacta.
37 s. 36+/-2.6 O.D. BMP-7-treated, p<0.05; pars compacta: 29.0+/-4.9 O.D. control vs. 64.4+/-6.9 O.D. BM
38 inergic neurons in the substantia nigra pars compacta 60 days after infection.
39 opamine neurons of the substantia nigra pars compacta, a deficit in dopamine neurotransmission and th
40  of serotonin, and the substantia nigra pars compacta, a major source of dopamine, while monkeys perf
41 inergic neurons of the substantia nigra pars compacta, a susceptible brain region in PD.
42 gmental area (VTA) and substantia nigra pars compacta activates inhibitory postsynaptic D2-receptors
43 ons of 6-OHDA into the substantia nigra pars compacta and 1 week later were tested for startle after
44 nergic (DA) neurons in substantia nigra pars compacta and age-dependent L-DOPA-sensitive motor dysfun
45 oducing neurons in the substantia nigra pars compacta and decreased striatal dopamine levels are the
46 opaminergic neurons of substantia nigra pars compacta and in the CA1/2 pyramidal cells of hippocampus
47 inergic neurons in the substantia nigra pars compacta and intracellular inclusion called Lewy bodies.
48 inergic neurons in the substantia nigra pars compacta and locus ceruleus, without Lewy body pathology
49 gmented neurons of the substantia nigra pars compacta and locus coeruleus in all four DYT1 dystonia c
50 inergic neurons of the substantia nigra pars compacta and locus coeruleus, among other regions.
51 ing cell levels in the substantia nigra pars compacta and nigrostriatal terminal density in vivo, in
52 ergic neurons from the substantia nigra pars compacta and noradrenergic neurons from the locus coerul
53 ons) in neurons of the substantia nigra pars compacta and other brain areas.
54 sion, particularly the substantia nigra pars compacta and other dopamine-synthesizing cell groups.
55 pamine (DA) neurons in substantia nigra pars compacta and restored DA levels in striatum using two di
56  in neurons within the substantia nigra pars compacta and striatum, two regions critically involved i
57 inergic neurons in the Substantia Nigra pars compacta and terminal dopamine fiber density in the stri
58 inergic neurons in the substantia nigra pars compacta and the accumulation of the protein alpha-synuc
59 ergic neurons from the substantia nigra pars compacta and the presence, in affected brain regions, of
60 icking, in vivo in the substantia nigra pars compacta and the serum of 1-methyl-4-phenyl-1,2,3,6-tetr
61 c projections from the substantia nigra pars compacta and the ventral tegmental area to the basal gan
62 neurons located in the substantia nigra pars compacta and the ventral tegmental area, which form the
63 mine by neurons in the substantia nigra pars compacta and ventral tegmental also influences basal gan
64                    The substantia nigra pars compacta and ventral tegmental area contain the two larg
65 nucleus, raphe nuclei, substantia nigra pars compacta and ventral tegmental area homologs, superficia
66 2 were more numerous in the substantia nigra compacta and ventral tegmental area in the Ts65Dn compar
67 opamine neurons in the substantia nigra pars compacta and ventral tegmental area regulate behaviours
68 ic (DA) neurons in the substantia nigra pars compacta and ventral tegmental area regulate extrapyrami
69 nses from cells in the substantia nigra pars compacta and ventral tegmental area.
70 dies of neurons in the substantia nigra pars compacta and ventral tegmental area.
71 ogous to the mammalian substantia nigra pars compacta and was renamed accordingly; a group of gamma-a
72 (PT; homologous to the substantia nigra pars compacta and/or ventral tegmental area of mammals) to th
73 aminergic neurons, A9 (substantia nigra pars compacta) and A10 (ventral tegmental area), have distinc
74  within neurons of the substantia nigra pars compacta, and dual labeling and confocal imaging confirm
75 entral tegmental area, substantia nigra pars compacta, and nucleus of the solitary tract.
76 he ventral tier of the substantia nigra pars compacta, and the lowest levels in the ventral tegmental
77 Mn accumulation in the substantia nigra pars compacta, and thus, can represent a link between Mn expo
78 was upregulated in the substantia nigra pars compacta, and trkB was elevated in the striatum in MDMA-
79 inergic neurons of the substantia nigra pars compacta are autonomous pacemakers.
80 inergic neurons of the substantia nigra pars compacta are defective in Parkinson's disease, but the s
81 ne neurons in the substantia nigra (SN) pars compacta are selectively lost during the progression of
82    Because the VTA and substantia nigra pars compacta are the sole sources of striatal and limbic for
83 mic nucleus (STN), and substantia nigra pars compacta, are conserved throughout vertebrate phylogeny
84  and A10 region of the substantia nigra pars compacta as well as the technical and surgical steps ass
85 ns of the adult rodent substantia nigra pars compacta, as well their development in vitro.
86 inergic neurons of the substantia nigra pars compacta, become transduced.
87 eactive neurons in the substantia nigra pars compacta (both in total and in subregions) were performe
88 in neurons not only in substantia nigra pars compacta but also in other extrastriatal areas of the br
89  ventral tegmental area and substantia nigra compacta but Nts(Dehy) neurons do not.
90 opamine neurons in the substantia nigra pars compacta, but not in the adjacent ventral tegmental area
91 , was observed in the substantia nigra, pars compacta, but not in the ventral tegmental area.
92 eactive neurons in the substantia nigra pars compacta by 2-fold (p < 0.05) in animals lesioned with 6
93 gmental area (VTA) and substantia nigra (SN) compacta (C).
94 ne terminal damage and substantia nigra pars compacta cell loss.
95 ns to the striatum and substantia nigra pars compacta compared with PV-GPe neurons.
96 ventral tegmental area-substantia nigra pars compacta complex.
97 gic neurons within the substantia nigra pars compacta coupled with depletion of striatal dopamine.
98 inergic neurons in the substantia nigra pars compacta coupled with intracytoplasmic inclusions known
99 opamine neurons in the substantia nigra pars compacta, culminating in severe motor symptoms, includin
100 ral tegmental area and substantia nigra pars compacta DA neurons in the post-reward period had a sign
101 neurons of the brain's substantia nigra pars compacta die in Parkinson's disease has been an enduring
102 cordings of identified substantia nigra pars compacta dopamine neurons in R1441C LRRK2 transgenic rat
103 reby properly maintain substantia nigra pars compacta dopaminergic neurons and their innervation in t
104         Studying mouse substantia nigra pars compacta dopaminergic neurons both in brain slice and af
105   We show that, in rat substantia nigra pars compacta dopaminergic neurons, the voltage dependences o
106 e from the soma in rat substantia nigra pars compacta dopaminergic neurons.
107  is expressed in human substantia nigra pars compacta glia as well as tyrosine hydroxylase-positive n
108 forming an ultra-short substantia nigra pars compacta --&gt; SNr dopamine pathway that regulates the fir
109 alpha-synuclein in the substantia nigra pars compacta impacts visual processing in a well-established
110 urodegeneration in the substantia nigra pars compacta in aged VMAT2 LO mice.
111 grostriatal neurons of substantia nigra pars compacta in Parkinson's disease represents the best-stud
112 e vulnerability of the substantia nigra pars compacta in PD, why the disorder is age related, and the
113 ty (TH-ir) in the substantia nigra (SN) pars compacta, in the lesioned hemisphere [31.7+/-5.2 (optica
114 ral tegmental area and substantia nigra pars compacta innervate the majority of the cortex, including
115 inergic neurons of the substantia nigra pars compacta is a cardinal feature of Parkinson's disease (P
116 ation of DA neurons in substantia nigra pars compacta is a key neuropathological feature in Parkinson
117 inergic neurons in the substantia nigra pars compacta is the primary cause for motor symptoms observe
118 onial pterobranch hemichordate, Rhabdopleura compacta, is expressed in a dramatically different patte
119 inergic neurons of the substantia nigra pars compacta leading to abnormal activity within the basal g
120 inergic neurons in the substantia nigra pars compacta, leading to nigrostriatal degeneration.
121 n subtypes outside the substantia nigra pars compacta may be compensating at a molecular level for di
122 ucleus and dorsomedial substantia nigra pars compacta) mesodiencephalic dopaminergic neuron subset, u
123 haracterized by severe substantia nigra pars compacta neuronal loss.
124 kB) receptor occurs in substantia nigra pars compacta neurons and is required for neuroprotection.
125  Unilateral lesions of substantia nigra pars compacta neurons created rats with hyperexcitable trigem
126  spontaneous firing of substantia nigra pars compacta neurons, isolated from transgenic mice in which
127 dopaminergic (DAergic) substantia nigra pars compacta neurons, only select downregulation of the PHD2
128 nger tapping is a clinical correlate of pars compacta nigral degeneration.
129 characterised by the presence of severe pars-compacta nigral-cell loss, and accumulation of aggregate
130 s in culture or in the substantia nigra pars compacta of 5-wk-old mice.
131 ell body counts in the substantia nigra pars compacta of 6-OHDA- and free-3NT-treated mice (injected/
132 ta from the cortex and substantia nigra pars compacta of aged LRRK2 transgenic animals revealed alter
133 le DA neurons from the substantia nigra pars compacta of controls and subjects with idiopathic Parkin
134 opamine neurons of the substantia nigra pars compacta of mice following systemic administration of a
135 opamine neurons in the substantia nigra pars compacta of monkeys (Macaca mulatta) during a reaching t
136 21(ras) in vivo in the substantia nigra pars compacta of MPTP-intoxicated mice.
137 ion of microglia in the substantia nigra par compacta of MPTP-treated mice.
138  of glial cells in the substantia nigra pars compacta of Parkinson's disease.
139 been identified in the substantia nigra pars compacta of patients with sporadic PD.
140 s activated within the substantia nigra pars compacta of PD patients and MPTP-intoxicated mice.
141 so up-regulated in the substantia nigra pars compacta of post-mortem PD brains as compared with age-m
142 so demonstrated in the substantia nigra pars compacta of post-mortem PD brains.
143 gic neurons within the substantia nigra pars compacta of the midbrain.
144 ositive neurons in the substantia nigra pars compacta of wild-type mice.
145 sitive neurons in the substantial nigra pars compacta one week after the first dose of MPTP.
146 opamine neurons of the substantia nigra pars compacta, other regions of the midbrain, and also the hi
147 in injured IL-6 (+/+) and IL-6 (-/-) SN pars compacta (pc), microgliosis was severely compromised in
148  amygdalopallii pars basalis (PoAb) and pars compacta (PoAc), the nucleus taeniae amgygdalae (TnA) an
149 inergic neurons in the substantia nigra pars compacta portion of the brain.
150 inergic neurons of the substantia nigra pars compacta preferentially terminate in patch-like regions
151 leasing neurons of the substantia nigra pars compacta produce an extraordinarily dense and expansive
152  (DA) neurons in their substantia nigra pars compacta, progressing to bilateral degeneration of the n
153 inergic neurons in the substantia nigra pars compacta, reproducing an important pathological feature
154 Neuronal counts in the substantia nigra pars compacta revealed that neuronal loss in the parkin cases
155 ne hydroxylase mRNA in substantia nigra pars compacta (SC) (93%; P<0.05) compared with control rats.
156 l proliferation in the substantia nigra pars compacta (SN(C)) with a time-dependent adoption of a neu
157  the laterally-located substantia nigra pars compacta (SN) and medially-located ventral tegmental are
158 inergic neurons in the substantia nigra pars compacta (SN) leads to debilitating motor dysfunction.
159 n-stained cells in the substantia nigra pars compacta (SN-PC)].
160 inergic neurons in the substantia nigra pars compacta (SNc) and consequent depletion of striatal dopa
161 ks the majority of the substantia nigra pars compacta (SNc) and experiences striatal denervation.
162 ine hydroxylase (TH) in the substantia nigra compacta (SNc) and in two subdivisions of the ventral te
163 nergic neurones in the substantia nigra pars compacta (SNc) and may contribute to excitotoxic cell de
164  ([DA](o)) between the substantia nigra pars compacta (SNc) and striatum.
165 n between the midbrain substantia nigra pars compacta (SNc) and the CeA.
166 opamine neurons of the substantia nigra pars compacta (SNc) and the importance of protein aggregation
167 inergic neurons in the substantia nigra pars compacta (SNc) and the presence of intracytoplasmatic in
168 amine neurons from the substantia nigra pars compacta (SNc) and ventral tegmental area (VTA) are invo
169  dopamine centers, the substantia nigra pars compacta (SNc) and ventral tegmental area (VTA), densely
170 f RET in the maintenance of substantia nigra compacta (SNC) and ventral tegmental area (VTA), we bred
171 opamine neurons in the substantia nigra pars compacta (SNC) and ventral tegmental area (VTA).
172 ns that project to the substantia nigra pars compacta (SNc) are activated by a visual CS for food.
173 gmental area (VTA) and substantia nigra pars compacta (SNc) are not significantly modulated by anesth
174 gmental area (VTA) and substantia nigra pars compacta (SNC) contain dopamine neurons intermixed with
175 gmental area (VTA) and substantia nigra pars compacta (SNc) convey distinct signals.
176 ata (SNr), which in turn inhibits nigra pars compacta (SNc) DAergic neurons.
177 ns (DAs) of the rodent substantia nigra pars compacta (SNc) display varied electrophysiological prope
178 sease characterized by substantia nigra pars compacta (SNc) dopamine (DA) neuron loss and subsequent
179                        Substantia nigra pars compacta (SNc) dopamine neurons and their targets are in
180  have established that substantia nigra pars compacta (SNc) dopamine neurons are a key node in the ci
181 underlying the loss of substantia nigra pars compacta (SNc) dopaminergic neurons in Parkinson's disea
182       Burst spiking in substantia nigra pars compacta (SNc) dopaminergic neurons is a key signaling e
183  increased activity of substantia nigra pars compacta (SNc) dopaminergic neurons, elevated baseline e
184 epend on the firing of substantia nigra pars compacta (SNc) dopaminergic neurons, we identified and c
185 ogous to the mammalian substantia nigra pars compacta (SNc) evokes increasing activation of MLR cells
186 inergic neurons of the substantia nigra pars compacta (SNc) exhibit functional heterogeneity that lik
187 ic (DA) neurons of the substantia nigra pars compacta (SNc) govern movements requires a detailed know
188 ons (TH-IR) within the substantia nigra pars compacta (SNc) in both young and aged animals.
189 tal area (VTA) and the substantia nigra pars compacta (SNc) mDA neurons.
190 receptor in regulating substantia nigra pars compacta (SNc) neuron physiology in both mice and rats.
191 ordings were made from substantia nigra pars compacta (SNC) neurons in horizontal brain slice prepara
192 s differs from that in substantia nigra pars compacta (SNc) neurons, where subthreshold calcium curre
193  much stronger in monkey than in rat SN pars compacta (SNc) neurons, whereas a moderate level of mGlu
194 drites of dopaminergic substantia nigra pars compacta (SNc) neurons.
195 eterogeneity among the substantia nigra pars compacta (SNc) neurons.
196 rAAV2/5 vectors in the substantia nigra pars compacta (SNc) on one side of the brain; the other side
197 as seen in neighboring substantia nigra pars compacta (SNC) or substantia nigra pars reticulata.
198 ave been implicated in substantia nigra pars compacta (SNc) pathology in Parkinson's disease.
199 nt dopamine neurons in substantia nigra pars compacta (SNc) play such roles.
200                    The substantia nigra pars compacta (SNc) projects specifically into the rostral mi
201 ne (DA) release in the substantia nigra pars compacta (SNc) shows a limited dependence on extracellul
202 neurons, including the substantia nigra pars compacta (SNc) subpopulation that preferentially degener
203 e neuron in the monkey substantia nigra pars compacta (SNc) that retains past learned reward values s
204 gmental area (VTA) and substantia nigra pars compacta (SNc) to that of axonal dopamine release in the
205 atal pathway, from the substantia nigra pars compacta (SNc) to the dorsal striatum, and on related fu
206 low or Fluorogold into substantia nigra pars compacta (SNc) were combined with larger injections of T
207  neuron numbers in the substantia nigra pars compacta (SNC) were estimated using stereological method
208 ne (DA) neurons of the substantia nigra pars compacta (SNc) were found to exhibit sustained responses
209 olliculus (SC), to the substantia nigra pars compacta (SNc) where direct synaptic contacts are made w
210 inergic neurons in the substantia nigra pars compacta (SNc), but not in ventral tegmental area or sub
211 stantia nigra pars reticulata (SNr) and pars compacta (SNc), but not the thalamus.
212 rst established in the substantia nigra pars compacta (SNc), but their validity in the VTA is uncerta
213 inergic neurons of the substantia nigra pars compacta (SNc), in addition to many other regions, inclu
214 gmental area (VTA) and substantia nigra pars compacta (SNc), no clear evidence for separate structure
215  neurons (DaNs) of the substantia nigra pars compacta (SNc), resulting in the characteristic hypokine
216 related changes in the substantia nigra pars compacta (SNc), the key pathological loci.
217 suggested that, in the substantia nigra pars compacta (SNc), the pacemaking relies more on Ca(2+) cha
218 he retrorubral field (RRF), substantia nigra compacta (SNc), ventral tegmental area (VTA), and ventro
219 to dopamine neurons in substantia nigra pars compacta (SNc), whereas matrix neurons receive sensorimo
220 ne (DA) neurons in the substantia nigra pars compacta (SNc).
221 inergic neurons in the substantia nigra pars compacta (SNc).
222 inergic neurons in the substantia nigra pars compacta (SNc).
223 ell bodies in the substantia nigra (SN) pars compacta (SNc).
224 ne (DA) neurons in the substantia nigra pars compacta (SNc).
225 t in DA neurons of the substantia nigra pars compacta (SNc).
226 opamine neurons in the substantia nigra pars compacta (SNc).
227 nergic neurones of the substantia nigra pars compacta (SNc).
228 ites of neurons in the substantia nigra pars compacta (SNc).
229 egmental area (VTA) and the substantia nigra compacta (SNc).
230 al tegmental area (VTA) and substantia nigra compacta (SNc).
231 ssed GFRalpha-1 in the substantia nigra pars compacta (SNC).
232 gmental area (VTA) and substantia nigra pars compacta (SNc).
233 ine neurons within the substantia nigra pars compacta (SNc).
234 ine neurons within the substantia nigra pars compacta (SNc).
235 inergic neurons in the substantia nigra pars compacta (SNc).
236 inergic neurons of the substantia nigra pars compacta (SNc).
237 or, a homologue of the substantia nigra pars compacta (SNc)/ventral tegmental area (VTA) is present i
238 inergic neurons of the substantia nigra pars compacta (SNpc) against 6-OHDA and MPTP.
239 nergic neurons of the substantia nigra, pars compacta (SNpc) akin to what is observed in Parkinson di
240 ic (DA) neurons in the substantia nigra pars compacta (SNpc) and of noradrenergic neurons in the locu
241 ntly diminished in the substantia nigra pars compacta (SNpc) and striatum, regions most affected in h
242 ese neurons in the rat substantia nigra pars compacta (SNpc) and ventral tegmental area (VTA), and co
243 opamine neurons in the substantia nigra pars compacta (SNpc) and widespread aggregates of the protein
244 ters, compromising the substantia nigra pars compacta (SNpc) and, later, the cerebral cortex.
245 opamine neurons in the substantia nigra pars compacta (SNpc) are greatly needed to effectively change
246 inergic neurons in the substantia nigra pars compacta (SNpc) as seen in Parkinson's disease.
247 opamine neurons of the substantia nigra pars compacta (SNpc) by regulating the magnitude of the first
248  (THir) neurons in the substantia nigra pars compacta (SNpc) compared with saline treatment.
249 e hydroxylase-immunoreactive (TH-ir) SN pars compacta (SNpc) DA neurons are immunoreactive for estrog
250 DA) neurons within the substantia nigra pars compacta (SNpc) display a differential vulnerability to
251 generation of midbrain substantia nigra pars compacta (SNpc) dopaminergic (DA) neurons contributes to
252 acterized by a loss of substantia nigra pars compacta (SNpc) dopaminergic (DA) neurons, and can be mo
253   Neuronal loss in the substantia nigra pars compacta (SNpc) in Parkinson disease (PD) is not uniform
254 ogenetic activation of substantia nigra pars compacta (SNpc) neurons alleviates parkinsonism in acute
255 inergic neurons of the substantia nigra pars compacta (SNpc) of human PD patients.
256  has been shown in the substantia nigra pars compacta (SNpc) of PD models when there has been a decre
257 sfer of RGS10 into the substantia nigra pars compacta (SNpc) of rats reduced microgliosis and protect
258 's disease (PD), in the substantia nigra par compacta (SNpc) of the brain in a PD mouse model.
259 neurons at the ventral substantia nigra pars compacta (SNpc) preferentially degenerate in Parkinson's
260 ic (DA) neurons in the substantia nigra pars compacta (SNpc) remains to be answered.
261 inergic neurons in the substantia nigra pars compacta (SNpc) undergo natural cell death during develo
262 s containing CR in the substantia nigra pars compacta (SNpc) were relatively spared compared to those
263 Here, we show that the substantia nigra pars compacta (SNpc), a brain region where dopamine (DA) cell
264 opaminergic neurons in substantia nigra pars compacta (SNpc), and SNCA mice were more vulnerable.
265 opaminergic neurons in substantia nigra pars compacta (SNpc), and there was no loss of dopaminergic n
266 ore TH-ir cells in the substantia nigra pars compacta (SNpc), but this difference was significant onl
267  neurons (DANs) in the substantia nigra pars compacta (SNpc), decrease of dopamine (DA) transmitter,
268 degeneration of DNs in substantia nigra pars compacta (SNpc), decreased striatal dopamine levels and
269 neurons located in the substantia nigra pars compacta (SNpc), expression of monoamines and indolamine
270 ensity loss within the substantia nigra pars compacta (SNpc), locus coeruleus, and ventral tegmental
271 g GDF5 into either the substantia nigra pars compacta (SNpc), the lateral ventricle (LV) or the stria
272 aminergic cells in the substantia nigra pars compacta (SNpc), ventral tegmental area (VTA), and retro
273 inergic neurons of the substantia nigra pars compacta (SNpc).
274 ic (DA) neurons in the substantia nigra pars compacta (SNpc).
275 nergic (DA) neurons in substantia nigra pars compacta (SNpc).
276 on was detected in the substantia nigra pars compacta, striatum, hippocampus, or selected regions of
277 ccumulation within the substantia nigra pars compacta, suggesting that nigrostriatal dopamine dysfunc
278 ccumulation within the substantia nigra pars compacta, suppression of microglial activation, and incr
279 the BG, and dopaminergic neurons of the pars compacta that modulate thalamic excitability.
280 inergic neurons in the substantia nigra pars compacta, the exact mechanism involved is still poorly u
281                 In the substantia nigra pars compacta, there was a 50-90% loss of tyrosine hydroxylas
282 rom frontal cortex and substantia nigra pars compacta tissue, isolated by several filtration and cent
283 allidus, thalamus, and substantia nigra pars compacta to various environmental or genetic insults.
284 and a 42% reduction in substantia nigra pars compacta tyrosine hydroxylase-positive neurons at 8 week
285 taining neurons in the substantia nigra pars compacta use pacemaking mechanisms common to neurons not
286 ps of neurons, such as substantia nigra pars compacta, ventral tegmental area and retrorubal field, t
287 pus and dentate gyrus, substantia nigra pars compacta, ventral tegmental area, geniculate nucleus and
288  the SN allowing readers to distinguish pars compacta ventralis and dorsalis from pars reticulata.
289 rminals in the ventral substantia nigra pars compacta (vSNc) or to the ventral tegmental area (VTA),
290  the nucleus tegmenti pedunculopontinus pars compacta was recognized as homologous to the mammalian s
291 TRPM2 and TRPM4mRNA in substantia nigra pars compacta.We propose that ICAN is selectively activated d
292 opamine neurons in the substantia nigra pars compacta were immunonegative.
293 ommissural putamen and substantia nigra pars compacta were processed for tyrosine hydroxylase and dop
294 aminergic cells in the substantia nigra pars compacta were unaffected by METH or haloperidol alone or
295  dorsolaterally in the substantia nigra pars compacta, whereas neurons inhibited by the stimuli were
296 ic (DA) neurons of the substantia nigra pars compacta, which are preferentially lost in human Parkins
297 ify mDA neurons of the substantia nigra pars compacta while the late Shh and Gli1 lineages maintain t
298 inergic neurons in the substantia nigra pars compacta, with more than 40% of these neurons lost by ag
299 oss and gliosis in the substantia nigra pars compacta, without Lewy bodies.
300 d neuron counts in the substantia nigra pars compacta, yet striatal medium spiny neuron dendritic spi

 
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