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1 s of capsaicin-responsive neurons in primate dorsal root ganglion.
2 a the release of substance P in the skin and dorsal root ganglion.
3 ressed in a subset of sensory neurons of the dorsal root ganglion and in cutaneous mechanoreceptors k
4 antly over time, a number of changes, in the dorsal root ganglion and in dorsal horn observed after t
5 ion and expression in sensory neurons of the dorsal root ganglion and spinal cord.
6 NR2B receptor protein expression in both the dorsal root ganglion and spinal dorsal horn ipsilateral
7 mpairs channel slow inactivation within both dorsal root ganglion and superior cervical ganglion neur
8 the peripheral nervous system within sensory dorsal root ganglion and sympathetic ganglion neurons an
9 m channel is preferentially expressed within dorsal root ganglion and sympathetic ganglion neurons an
10  is preferentially expressed in nocioceptive dorsal root ganglion and sympathetic ganglion neurons.
11                              The survival of dorsal root ganglion and sympathetic neurons is promoted
12 be responsible for pathology observed in the dorsal root ganglion and the sensory ganglionopathy docu
13 s: cortical (embryonic rat), embryonic chick dorsal root ganglion, and P-19 (mouse embryonic carcinom
14  integrin transport and traffic in adult rat dorsal root ganglion axons and PC12 cells.
15 al JNK substrate, is lost rapidly from mouse dorsal root ganglion axons following axotomy.
16 ple host axons when co-cultured with primary dorsal root ganglion cells and formed myelin after trans
17 n the plasma membrane of pancreatic beta and dorsal root ganglion cells and link steroid hormone sign
18             These results may be relevant to dorsal root ganglion cells and to other neurons that coe
19 ficantly suppressed 5-HT-evoked responses in dorsal root ganglion cells from wild-type mice.
20  contrast to its effect on the hair cell and dorsal root ganglion cells in culture; (iv) SLV recyclin
21                               Experiments on dorsal root ganglion cells show that, for each of a grou
22  sensory terminals of primary mechanosensory dorsal root ganglion cells, so the presence of such a sy
23 le for the PGE2-induced sensitization of rat dorsal root ganglion cells.
24 tion of lymphoid cell kinase in Schwann cell-dorsal root ganglion cocultures and dorsal root ganglion
25   hVariant 3 is more abundantly expressed in dorsal root ganglion compared with brain and shows basic
26   The administration of NO donors to primary dorsal root ganglion cultures prevents axonal degenerati
27                        Treatment of isolated dorsal root ganglion cultures with myocilin stimulates c
28 y of glial cells and reduced spinal cord and dorsal root ganglion cytokine levels without affecting p
29                         To determine whether dorsal root ganglion damage was associated with altered
30 oop L1 reduces Na(v)1.6 current density in a dorsal root ganglion-derived cell line, without changing
31 hat CXCL12 and CXCR4 were upregulated in the dorsal root ganglion (DRG) after chronic compression of
32 injury causes down-regulation of MORs in the dorsal root ganglion (DRG) and diminishes the opioid eff
33 most prominent subtypes expressed in the rat dorsal root ganglion (DRG) and dorsal spinal cord.
34 ed and manipulated MrgprA3(+) neurons in the dorsal root ganglion (DRG) and found that they exclusive
35 titutive autophagosome biogenesis in primary dorsal root ganglion (DRG) and hippocampal cultures.
36 KChIP2, KChIP3, DPP6, and DPP10 in adult rat dorsal root ganglion (DRG) and spinal cord by immunohist
37 parts in two major pain-related regions, the dorsal root ganglion (DRG) and spinal cord dorsal horn.
38 hannel NaV1.7 is preferentially expressed in dorsal root ganglion (DRG) and sympathetic ganglion neur
39 1.7 which is preferentially expressed within dorsal root ganglion (DRG) and sympathetic ganglion neur
40 tion after axotomy was abolished in both the dorsal root ganglion (DRG) and the distal sciatic nerve.
41 ncreases in osmolality excite isolated mouse dorsal root ganglion (DRG) and trigeminal ganglion (TG)
42                          Here we study mouse dorsal root ganglion (DRG) axons and show that their ext
43 port that stimulated membrane enlargement in dorsal root ganglion (DRG) axons is triggered by intra-a
44                            Ca(2+) imaging in dorsal root ganglion (DRG) cells confirmed LY enhanced C
45 tigate mRNA expression in colonic tissue and dorsal root ganglion (DRG) cells isolated from 3- and 24
46                  It is well established that dorsal root ganglion (DRG) cells synthesize prostaglandi
47                    Using live myelinated rat dorsal root ganglion (DRG) cultures, we investigated whe
48                 The treatment of myelinating dorsal root ganglion (DRG) explant cultures from neuropa
49  at a dose of 100 mpk PO due to insufficient dorsal root ganglion (DRG) exposure attributed to poor m
50 ge-diameter (>30 mum) sensory neurons of the dorsal root ganglion (DRG) express distinct combinations
51 pression and functional role of Panx1 in the dorsal root ganglion (DRG) in the development of chronic
52 ion of HIV infection and is characterized by dorsal root ganglion (DRG) inflammation and intraepiderm
53     The T-junction of sensory neurons in the dorsal root ganglion (DRG) is a potential impediment to
54 gated potassium channel subunit Kcna2 in the dorsal root ganglion (DRG) is critical for DRG neuronal
55 d texture is the activation of trigeminal or dorsal root ganglion (DRG) mechanosensory neurons, which
56  elevation, activation of cGMP increases rat dorsal root ganglion (DRG) neurite outgrowth on a polyly
57 ing sodium channels, thus acutely regulating dorsal root ganglion (DRG) neuron excitability.
58 nsgenic mice lacking Merkel cells had normal dorsal root ganglion (DRG) neuron numbers, but fewer DRG
59  EGABA and kinetics into acutely dissociated dorsal root ganglion (DRG) neuron somata.
60 hondrial trafficking plays a central role in dorsal root ganglion (DRG) neuronal cell survival and ne
61  that STOML1 is expressed in at least 50% of dorsal root ganglion (DRG) neurones.
62 nduced spontaneous pain and axonal injury of dorsal root ganglion (DRG) neurons and inhibited CCI-evo
63 the Na(+)/K(+)-ATPase (alpha3) in some large dorsal root ganglion (DRG) neurons and large intrafusal
64 um channel that is specifically expressed in dorsal root ganglion (DRG) neurons and peripheral nerve
65 satellite glial cells (SGCs) surrounding the dorsal root ganglion (DRG) neurons appears to play a rol
66                             We used cultured dorsal root ganglion (DRG) neurons as a model of axotomi
67 norepinephrine and sensitizes colon-specific dorsal root ganglion (DRG) neurons by increasing express
68 fast-inactivating Kv3.4 potassium current in dorsal root ganglion (DRG) neurons contributes to the hy
69         We demonstrate that monkey and human dorsal root ganglion (DRG) neurons do not express apprec
70 v5 are expressed by developing TrkA-positive dorsal root ganglion (DRG) neurons during the period of
71                                  Nociceptive dorsal root ganglion (DRG) neurons express tetrodotoxin-
72 s axon growth from neurons; adult miR-155 KO dorsal root ganglion (DRG) neurons extend 44% longer neu
73 en implicated in the hyperexcitable state of dorsal root ganglion (DRG) neurons following direct inju
74 arization-evoked Ca2+ transient is larger in dorsal root ganglion (DRG) neurons from tumor-bearing mi
75                                              Dorsal root ganglion (DRG) neurons from wild-type or fat
76 e firing frequency and spontaneous firing of dorsal root ganglion (DRG) neurons have recently been id
77                        These variants render dorsal root ganglion (DRG) neurons hyperexcitable.
78 tion mutations of sodium channel NaV1.7 make dorsal root ganglion (DRG) neurons hyperexcitable.
79 GKIalpha) that regulates axon bifurcation of dorsal root ganglion (DRG) neurons in the spinal cord.
80 hormones in regulating axonal development of dorsal root ganglion (DRG) neurons in the spinal cord.
81                                 We show that dorsal root ganglion (DRG) neurons in transgenic mice ex
82  electroporation approach to transfect adult dorsal root ganglion (DRG) neurons in vivo that enables
83 gnitude and properties by voltage clamp from dorsal root ganglion (DRG) neurons in vivo, after classi
84 -expression network analysis, we categorized dorsal root ganglion (DRG) neurons into different subtyp
85 hat the activity of TRPM3 expressed in mouse dorsal root ganglion (DRG) neurons is inhibited by agoni
86 nduced current with activation of ASIC(3) in dorsal root ganglion (DRG) neurons of control rats and r
87 cell patch-clamp recordings from dissociated dorsal root ganglion (DRG) neurons revealed enhanced tet
88 rophysiological characterization of isolated dorsal root ganglion (DRG) neurons revealed that RPRFami
89       Calcium-imaging studies on dissociated dorsal root ganglion (DRG) neurons revealed the peptide'
90           We identified the subpopulation of dorsal root ganglion (DRG) neurons that are activated by
91      Nociceptors are a particular subtype of dorsal root ganglion (DRG) neurons that detect noxious s
92 t IgG-IC directly excited a subpopulation of dorsal root ganglion (DRG) neurons through the neuronal
93 luence the electrophysiological responses of dorsal root ganglion (DRG) neurons to mechanical stimula
94 ciatic nerve allows the central processes of dorsal root ganglion (DRG) neurons to spontaneously rege
95                                              Dorsal root ganglion (DRG) neurons transmit sensory info
96 nhanced green fluorescent protein-expressing dorsal root ganglion (DRG) neurons transplanted into the
97  after axonal injury, Nogo-A is increased in dorsal root ganglion (DRG) neurons unable to regenerate
98 4-well format axon degeneration assay in rat dorsal root ganglion (DRG) neurons using a trophic facto
99     Depolarization-induced calcium influx in dorsal root ganglion (DRG) neurons was inhibited by both
100                          Porcine lumbosacral dorsal root ganglion (DRG) neurons were neurochemically
101 hat voltage-gated sodium channels (VGSCs) in dorsal root ganglion (DRG) neurons were sensitized in a
102 that reduction of GRK2 or increased EPAC1 in dorsal root ganglion (DRG) neurons would promote the tra
103 mature rat retinal ganglion cells (RGCs) and dorsal root ganglion (DRG) neurons, and is essential for
104 s in the up-regulation of alpha(2)delta-1 in dorsal root ganglion (DRG) neurons, and there is a conse
105                For KOR(-/-) or KOR-knockdown dorsal root ganglion (DRG) neurons, EGF can no longer ef
106                                       In rat dorsal root ganglion (DRG) neurons, exposure to E-2 in a
107 hosphatase (PAP) is expressed in nociceptive dorsal root ganglion (DRG) neurons, functions as an ecto
108  expressed in a subpopulation of nociceptive dorsal root ganglion (DRG) neurons, where it acts as a s
109 thereby producing hyperexcitability of small dorsal root ganglion (DRG) neurons, which include nocice
110 ury induces changes in gene transcription in dorsal root ganglion (DRG) neurons, which may contribute
111 pid inward currents and action potentials in dorsal root ganglion (DRG) neurons.
112 ked Ca(2+) transient in putative nociceptive dorsal root ganglion (DRG) neurons.
113 rade Rab7-vesicles within axons of rat E15.5 dorsal root ganglion (DRG) neurons.
114 racterized in cocultures of OECs and primary dorsal root ganglion (DRG) neurons.
115 ignals induced by PregS and CIM0216 in mouse dorsal root ganglion (DRG) neurons.
116 rease of ATF-3 and TRPV1 immunoreactivity in dorsal root ganglion (DRG) neurons.
117 tally regulated and governs axonal growth in dorsal root ganglion (DRG) neurons.
118 vels of Tet3 and 5-hydroxylmethylcytosine in dorsal root ganglion (DRG) neurons.
119 esults in increased NKCC1 phosphorylation in dorsal root ganglion (DRG) neurons.
120 ed potassium (K(Na)) channels in nociceptive dorsal root ganglion (DRG) neurons.
121 l vanilloid type 1 (TRPV1) currents in L6-S2 dorsal root ganglion (DRG) neurons.
122 nels are expressed in the plasma membrane of dorsal root ganglion (DRG) neurons.
123   We characterized KNa channels in adult rat dorsal root ganglion (DRG) neurons.
124 two GsMTx-4-sensitive SACs, are expressed in dorsal root ganglion (DRG) neurons.
125 m involved in regulation of TRPM8 in sensory dorsal root ganglion (DRG) neurons.
126  potential (TRP) channel V1 (TRPV1)-positive dorsal root ganglion (DRG) neurons.
127 s significantly reinforced in Pirt-deficient dorsal root ganglion (DRG) neurons.
128  with microglia BV-2 cells exposed to G-CSF, dorsal root ganglion (DRG) nociceptors become hyperexcit
129 melanoma and normal neural tissues including dorsal root ganglion (DRG) produce PD-L1 that can potent
130  studied pancreatic nodose ganglion (NG) and dorsal root ganglion (DRG) sensory neurons (identified b
131 ort functional expression of SHANK3 in mouse dorsal root ganglion (DRG) sensory neurons and spinal co
132 pplied to their distal axons, in contrast to dorsal root ganglion (DRG) sensory neurons in which GDNF
133 analyze the detailed molecular signatures of dorsal root ganglion (DRG) sensory neurons.
134 ge-gated sodium channels (Navs) expressed in dorsal root ganglion (DRG) sensory neurons.
135 AP7) during collateral branch development of dorsal root ganglion (DRG) sensory neurons.
136  of BMP signaling, highly expressed in adult dorsal root ganglion (DRG) sensory neurons.
137 otential (TRPV1) receptors, respectively, on dorsal root ganglion (DRG) sensory neurons.
138            Pharmacological studies in rodent dorsal root ganglion (DRG) show their analgesic effect i
139 and the potential target ion channels in rat dorsal root ganglion (DRG) slices.
140             Primary sensory afferents of the dorsal root ganglion (DRG) that innervate the skin detec
141 of rodent embryonic sensory neurons from the dorsal root ganglion (DRG) to demonstrate the role of cG
142                       VZV infection of human dorsal root ganglion (DRG) xenografts in immunodeficient
143  neurons infected in vivo was examined using dorsal root ganglion (DRG) xenografts maintained in mice
144 dent outgrowth and traction forces from PNS (dorsal root ganglion (DRG)) and CNS (hippocampal) neuron
145 set of nonpeptidergic nociceptors within the dorsal root ganglion (DRG), and knockdown of Kv4.3 selec
146  reduction in K(+) channel expression in the dorsal root ganglion (DRG), but little is known about th
147                Lumbosacral and thoracolumbar dorsal root ganglion (DRG), lumbar sympathetic chain (LS
148 icular pain model, local inflammation of the dorsal root ganglion (DRG), we observed marked increases
149  in nociceptor (pain-sensing) neurons of the dorsal root ganglion (DRG), where they transmit the larg
150 Kcna2, in first-order sensory neurons of rat dorsal root ganglion (DRG).
151  80% reduction in the sensory neurons of the dorsal root ganglion (DRG).
152  of heterogeneous expression of ASIC3 in the dorsal root ganglion (DRG).
153 l V1 expressed in the nociceptive neurons of dorsal root ganglion (DRG).
154 200 in large-diameter A-fiber neurons in the dorsal root ganglion (DRG).
155 vivo forepaw muscles/median and ulnar nerves/dorsal root ganglion (DRG)/spinal cord (SC) recording pr
156 n in capsaicin-sensitive nociceptors using a dorsal root ganglion (DRG)/spinal cord neuron co-culture
157 ar CFA injection and in the ipsilateral L4/5 dorsal root ganglions (DRGs) 1 and 3 days after CFA inje
158 ly by small-sized primary sensory neurons in dorsal root ganglions (DRGs) that coexpress the itch sig
159               Coculture of cancer cells with dorsal root ganglion extracts revealed that Schwann cell
160 ann cell-dorsal root ganglion cocultures and dorsal root ganglions from Lck(-/-) mice show a reductio
161 ongation of actin-based filopodia from mouse dorsal root ganglion growth cones.
162  at the Ascl1 promoter, isolated from murine dorsal root ganglion (hypermethylated) and striated cell
163 plotted global expression changes in the rat dorsal root ganglion in three peripheral neuropathic pai
164 permeant cAMP analog, 8-bromo cAMP, into the dorsal root ganglion induced mechanical hyperalgesia and
165 that signals emanating from within the mouse dorsal root ganglion mediated partly by early-born neuro
166 imulated oligodendrocytes was validated in a dorsal root ganglion microfluidics chamber platform.
167 city, nerve amplitude, and sciatic nerve and dorsal root ganglion morphology at 0.25 x MTD, 0.5 x MTD
168 rsal column lesions and reduced in models of dorsal root ganglion neuron (DRGN) axon regeneration.
169 n of the effects of the Del-L955 mutation on dorsal root ganglion neuron hyperexcitability with those
170 ng a CD4-Na(v)1.2/L2 reporter protein in rat dorsal root ganglion neuron-Schwann cell myelinating coc
171 single K562 erythroleukemic cell or a single dorsal root ganglion neuron.
172 adapting, mechanically activated currents in dorsal root ganglion neuronal cultures are absent in Pie
173            We therefore established a robust dorsal root ganglion neuronal model that mirrors key cel
174 that TLRs 3, 7, and 9 are expressed by human dorsal root ganglion neurons (DRGNs) and in cultures of
175              Here we show in adult mice that dorsal root ganglion neurons (DRGs) and CST neurons fail
176 , PKCdelta, and PKC was also observed in the dorsal root ganglion neurons after chronic treatment wit
177 receptor that increases cAMP, in a subset of dorsal root ganglion neurons and also within neurons of
178 bility of single TRPV1 molecules in isolated dorsal root ganglion neurons and cell lines.
179 ase ion transporter in both cultured primary dorsal root ganglion neurons and injured peripheral nerv
180  for PKCepsilon was found in the majority of dorsal root ganglion neurons and intensely labeled lamin
181 e-collapsing molecule than Nogo-66 for chick dorsal root ganglion neurons and mature cortical neurons
182 t channels enhance resurgent currents within dorsal root ganglion neurons and show by current-clamp t
183                                  ROCKII(-/-) dorsal root ganglion neurons are less sensitive to inhib
184                                 In contrast, dorsal root ganglion neurons are stiffer than P-19 and c
185  and biochemical modulation of T-channels in dorsal root ganglion neurons as measured by a large incr
186                        However, conditioning dorsal root ganglion neurons by first lesioning their pe
187 f3r gene expression could not be detected in dorsal root ganglion neurons by single-cell RT-PCR.
188 diated local expression of erythropoietin in dorsal root ganglion neurons can protect in vivo as well
189  that in small PLCdelta4(-/-) TRPM8-positive dorsal root ganglion neurons cold, menthol and WS-12, a
190 n; and (5) electrophysiology recordings from dorsal root ganglion neurons collected during remission
191 tion of the alpha2delta-1 subunit in sensory dorsal root ganglion neurons contributes to the generati
192                             Correspondingly, dorsal root ganglion neurons cultured in G-CSF failed to
193 iated inhibition of M current in nociceptive dorsal root ganglion neurons did not reduce the efficacy
194                                              Dorsal root ganglion neurons displayed a fall in resting
195    Here, we show that only 43% of CQ-excited dorsal root ganglion neurons expressed TRPA1; as expecte
196 mazepine normalized the hyperexcitability of dorsal root ganglion neurons expressing S241T.
197 pic screen, we find that CAST/Ei mouse adult dorsal root ganglion neurons extend axons more on CNS my
198 tion of NFATc3 and NFATc4 in hippocampal and dorsal root ganglion neurons following electrically evok
199  A-type K(+) current (I(AHV)) in nociceptive dorsal root ganglion neurons from 7-day-old rats.
200 m photoactivated axonal segments in cultured dorsal root ganglion neurons from DLS/LeJ and dl20J dilu
201 ratching behavior and activation of cultured dorsal root ganglion neurons from mice.
202 between TRPV1 and Pirt, and that dissociated dorsal root ganglion neurons from Pirt knock-out mice ha
203 ne also acts on endogenous TRPA1 in cultured dorsal root ganglion neurons from rats and in the entero
204 erior cervical ganglion neurons, and renders dorsal root ganglion neurons hyperexcitable and superior
205 ons in sodium channel Na(V)1.7, which render dorsal root ganglion neurons hyperexcitable, are present
206  neonatal-short, isoform of Na(v)1.7 renders dorsal root ganglion neurons hyperexcitable, reducing th
207 ant channels; each of the mutations rendered dorsal root ganglion neurons hyperexcitable.
208 and show by current-clamp that R185H renders dorsal root ganglion neurons hyperexcitable.
209  from synaptic vesicles along axons of mouse dorsal root ganglion neurons in culture promotes myelin
210 , enables siRNA to gain entry into adult rat dorsal root ganglion neurons in culture.
211                                              Dorsal root ganglion neurons in vitro express a number o
212      We now find that treatment of adult rat dorsal root ganglion neurons in vitro with LRP1 agonists
213 c or optogenetic depolarization of GABAergic dorsal root ganglion neurons in vivo reduced acute and c
214 activation does not depend on the age of the dorsal root ganglion neurons in which the mutant is expr
215               We find that FMRP knockdown in dorsal root ganglion neurons increases Ca(V) channel den
216 K-2 channels was also demonstrated in native dorsal root ganglion neurons indicating that heterodimer
217         However, if the peripheral branch of dorsal root ganglion neurons is lesioned before lesionin
218 -alpha2A cross-desensitization was absent in dorsal root ganglion neurons lacking beta-arrestin 2.
219                           Accordingly, mouse dorsal root ganglion neurons lacking TRPV1 only responde
220 examined micro-receptor coupling to VDCCs in dorsal root ganglion neurons of delta(+/+), delta(+/-),
221                         Approximately 45% of dorsal root ganglion neurons of transgenic mice were EGF
222 channels in rat endocrine GH(3) cells, mouse dorsal root ganglion neurons or cardiac myocytes, and re
223                          Similar analyses of dorsal root ganglion neurons revealed a salutary effect
224 .2/Kv7.3 heteromers and native M currents in dorsal root ganglion neurons suggest the following concl
225 at dorsal root injury model, transduction of dorsal root ganglion neurons to express kindlin-1 promot
226                    Current-clamp analysis of dorsal root ganglion neurons transfected with G856D muta
227 teers, sensitized TRPV1 in mouse nociceptive dorsal root ganglion neurons via HRH1; this effect could
228 ratching behavior and activation of cultured dorsal root ganglion neurons was dependent on Mrgprs rat
229 a(2+) channels expressed in HEK293 cells and dorsal root ganglion neurons were abolished by blocking
230  two distinct types of cutaneous nociceptive dorsal root ganglion neurons were identified as respondi
231          Approximately 90% of 5-HT-sensitive dorsal root ganglion neurons were immunoreactive for an
232 n prostate cells, PC3 prostate cancer cells, dorsal root ganglion neurons, and hippocampal neurons.
233 eurons, chemotherapy-induced cytotoxicity of dorsal root ganglion neurons, and retinal ganglion cells
234 similar expression levels in spinal cord and dorsal root ganglion neurons, and that both kinases part
235  is transiently expressed in a wide range of dorsal root ganglion neurons, and that its expression is
236 PV1 current (IC(50) = 0.4 nm) in dissociated dorsal root ganglion neurons, and this IC(50) is approxi
237 s hTRPM8, and rTRPM3, which are expressed in dorsal root ganglion neurons, are insensitive toward apo
238 1 x 10(12) vg of AAV-PHP.S transduced 82% of dorsal root ganglion neurons, as well as cardiac and ent
239 age-gated K(+) channel robustly expressed in dorsal root ganglion neurons, becomes dysfunctional upon
240 el, depolarize resting membrane potential of dorsal root ganglion neurons, enhance spontaneous firing
241  including altered ion channel expression in dorsal root ganglion neurons, enhanced dorsal horn gluta
242                                  In isolated dorsal root ganglion neurons, EP3 receptor activation co
243                     In transfected small rat dorsal root ganglion neurons, expression of L1302F and L
244 ed sustained ASIC currents in both groups of dorsal root ganglion neurons, independent of mu opioid r
245 llular signal-regulated kinase expression in dorsal root ganglion neurons, induced by co-cultured MRM
246                            When expressed in dorsal root ganglion neurons, mutant p.Arg222His channel
247  that maintain the position of postmigratory dorsal root ganglion neurons, neural crest derivatives f
248                                       Unlike dorsal root ganglion neurons, Nf1 heterozygous (Nf1+/-)
249 physiology and Ca(2+) imaging experiments on dorsal root ganglion neurons, NGF- and IL-6-induced incr
250 nic spinal commissural neurons, motoneurons, dorsal root ganglion neurons, retinal ganglion cells, an
251 ppressed spontaneous activity in dissociated dorsal root ganglion neurons, reversed hypersensitivity
252 g calcium imaging in cultured primary murine dorsal root ganglion neurons, the response of neurons af
253 een TLR4 and TRPV1 is shown in rat and human dorsal root ganglion neurons, TLR4/TRPV1-coexpressing HE
254 tion and inhibits neurite outgrowth in adult dorsal root ganglion neurons, validating Slit2 signaling
255                         Using cultured mouse dorsal root ganglion neurons, we found that myosin II (M
256 tion in both male and female embryonic mouse dorsal root ganglion neurons, we show that MAP4K4, MINK1
257                 NKCC1 is highly expressed in dorsal root ganglion neurons, where it is involved in ga
258 duced robust neurite outgrowth by cocultured dorsal root ganglion neurons, which was prevented by neu
259 sed TRPV1 activity after TRPA1 activation in dorsal root ganglion neurons.
260 -type (primarily Cav3.2) channels in sensory dorsal root ganglion neurons.
261 of TRPV1 receptor expression to medium sized dorsal root ganglion neurons.
262 ant inhibition of TRPM8 in 48.8% of TRPM8(+) dorsal root ganglion neurons.
263 l imaging of cargo motility in primary mouse dorsal root ganglion neurons.
264  a subpopulation of large-diameter Nav1.8(+) dorsal root ganglion neurons.
265 of the injured central branch of conditioned dorsal root ganglion neurons.
266 used the growth cone collapse assay on chick dorsal root ganglion neurons.
267  stages results in loss of pigment cells and dorsal root ganglion neurons.
268 nvestigate autophagosome dynamics in primary dorsal root ganglion neurons.
269 um, potassium, and calcium channels in mouse dorsal root ganglion neurons.
270  support neurite growth of co-cultured adult dorsal root ganglion neurons.
271 onatal-short splicing isoform of Na(v)1.7 in dorsal root ganglion neurons.
272 ncy of kinases in the regulation of NKCC1 in dorsal root ganglion neurons.
273 ens was assessed by calcium imaging of mouse dorsal root ganglion neurons.
274 a sensory neuronal cell line and primary rat dorsal root ganglion neurons.
275 d stable in oligodendrocytes cocultured with dorsal root ganglion neurons.
276  cultured either alone or in the presence of dorsal root ganglion neurons.
277 on-induced intracellular Ca(2+) signaling in dorsal root ganglion neurons.
278                   In this study, dissociated dorsal-root ganglion neurons from mice were exposed to v
279 pound elicited responses in only a subset of dorsal-root ganglion neurons.
280                         The sensitization of dorsal root ganglion nociceptors in BDL rats was associa
281  currents recorded from small neurons in the dorsal root ganglion of normal rats are potentiated by e
282  apoptosis was observed in the forebrain and dorsal root ganglions of mutant embryos.
283 lymer, following inflammatory exposures in a dorsal root ganglion organotypic coculture system.
284 ore variable across cultures than in primary dorsal root ganglion, particularly for genes related to
285        Intracellular recordings from ex vivo dorsal root ganglion preparations revealed that Kv9.1 kn
286  capsaicin-induced calcium uptake in a mouse dorsal root ganglion primary cell culture assay.
287 y processes characterized by spinal cord and dorsal root ganglion production of proinflammatory cytok
288 fer elevated intracellular calcium levels in dorsal root ganglion pruriceptors, and (iii) injection o
289 ly ( approximately 71%) expressed in Nppb(+) dorsal root ganglion pruriceptors.
290                          Using a nociceptive dorsal root ganglion sensory neuronal cell line, which e
291 P that binds and regulates multiple mRNAs in dorsal root ganglion sensory neurons and thereby promote
292 ated virus (AAV) has been shown to transduce dorsal root ganglion sensory neurons following direct in
293 r microtubule-associated protein 7 (MAP7) in dorsal root ganglion sensory neurons.
294 ta from an in vitro preparation of small rat dorsal root ganglion somata showing a reduction in the m
295 ptor found on select immune, epithelial, and dorsal root ganglion/spinal cord neuronal cells.
296                                       In the dorsal root ganglion, subpopulations of cells express co
297 peripheral immune cell infiltration into the dorsal root ganglion, suggesting that adaptive immune re
298     We show here that synaptic contacts from dorsal root ganglions to a small number of dorsal column
299 evidence indicates that gene transfer to the dorsal root ganglion using replication-defective herpes
300           Noting the prevalence of Slo2.2 in dorsal root ganglion, we find that KO of Slo2.2, but not

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