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1  are reciprocally expressed in rat brain and sympathetic ganglia ().
2  acids suppresses cFos expression in the gut sympathetic ganglia.
3 analysis of rapidly frozen neurons from frog sympathetic ganglia.
4 ly reconstructed nerve terminals in bullfrog sympathetic ganglia.
5  neural crest-derived cells from the gut and sympathetic ganglia.
6 lly along the sympathetic trunk to innervate sympathetic ganglia.
7  All three genes are expressed in peripheral sympathetic ganglia.
8 ations in the ganglionic neurons of bullfrog sympathetic ganglia.
9 vertebral celiac/superior mesenteric (C/SMG) sympathetic ganglia.
10 as formed in the adrenal gland and preaortic sympathetic ganglia.
11 gnate 3.1 kb mRNA is highly enriched in frog sympathetic ganglia.
12 o by nonneuronal cells neighboring embryonic sympathetic ganglia.
13 ion potentials was tested in intact bullfrog sympathetic ganglia.
14  complex neurocircuits may be present within sympathetic ganglia.
15  function of motor neurons in the peripheral sympathetic ganglia.
16 ions arise from noradrenergic neurons within sympathetic ganglia.
17  myenteric neurons that project to abdominal sympathetic ganglia.
18 ion of Lin28B and Let-7a in developing chick sympathetic ganglia.
19  by E8 are more than 100-fold higher than in sympathetic ganglia.
20 ic axonal ingrowth from the spinal cord into sympathetic ganglia.
21  of activated Ret in neuroblastoma cells and sympathetic ganglia.
22 with hyperplastic lesions in early postnatal sympathetic ganglia.
23 differentiate into metameric dorsal root and sympathetic ganglia.
24        Ang II directly activates neurones in sympathetic ganglia.
25 ological role of hand2 in the development of sympathetic ganglia.
26 by N-cadherin, coordinate to sculpt discrete sympathetic ganglia.
27  of elavl3 (HuC) is not reduced in hands off sympathetic ganglia.
28 luding the branchial arches, dorsal root and sympathetic ganglia.
29 catecholaminergic and cholinergic neurons in sympathetic ganglia.
30 ects in condensing cranial sensory and trunk sympathetic ganglia.
31 the trunk of host chick embryos colonise the sympathetic ganglia.
32 +) NCCs to contribute to sensory rather than sympathetic ganglia.
33 ventral horn, in dorsal root ganglia, and in sympathetic ganglia.
34 sed, as was the amount of NT3 present within sympathetic ganglia.
35 ession in the brain, the spinal cord and the sympathetic ganglia.
36 ic development, it is strikingly absent from sympathetic ganglia.
37 incident with BMPR-IB mRNA expression in the sympathetic ganglia.
38 cillators regulate synaptic amplification in sympathetic ganglia.
39 s studied in preparations of bullfrog lumbar sympathetic ganglia 7-10 and the dorsal aorta.
40  from isolated preparations of paravertebral sympathetic ganglia 9 and 10.
41 unoreactivity (SN-LI) was studied in the rat sympathetic ganglia/adrenal gland, enteric and sensory g
42 rophy in diabetic or age-matched control rat sympathetic ganglia after 7 or 10 months of continuous a
43 opment, sympathetic axons grow from thoracic sympathetic ganglia along rib periosteum to reach the st
44 how that this pathway is conserved, as human sympathetic ganglia also contain SAMs expressing the ana
45 renal medulla, enlargement of the associated sympathetic ganglia and a male reproductive defect.
46                               NB develops in sympathetic ganglia and adrenal medulla and is elicited
47  in neuroblastoma (NB), a childhood tumor in sympathetic ganglia and adrenal medulla.
48 lop profound neuroglial hyperplasia of their sympathetic ganglia and adrenal medullae.
49 rom bullfrog (Rana catesbiana) paravertebral sympathetic ganglia and characterized functional propert
50                Sequencing of cDNA from human sympathetic ganglia and colon revealed processed transcr
51 tebral LVs connect to peripheral sensory and sympathetic ganglia and form metameric vertebral circuit
52 nscription factor is expressed in neurons of sympathetic ganglia and has previously been shown to ind
53      NAD did not develop in diabetic ZDF rat sympathetic ganglia and ileal mesenteric nerves as asses
54                                              Sympathetic ganglia and innervation of target tissues ap
55                The elk1 gene is expressed in sympathetic ganglia and is also expressed in sciatic ner
56 ent, PSS1 is transiently expressed in lumbar sympathetic ganglia and is detectable at low levels thro
57 adipose tissue (SAT) via its actions both on sympathetic ganglia and on the SAT itself.
58 3+ neurons that populate the dorsal root and sympathetic ganglia and several ectopic sites, including
59                 NGF and NT3 were measured in sympathetic ganglia and skin (a major target of sympathe
60 1B subunit of the N channel are expressed in sympathetic ganglia and that alternative splicing within
61 cal ganglion is absent, while more posterior sympathetic ganglia and the adrenal medulla are unaffect
62 p NAD in nerve terminals in the prevertebral sympathetic ganglia and the distal portions of noradrene
63  Exon-containing alpha(1B) mRNA dominated in sympathetic ganglia and was present in approximately 50%
64 s found throughout dorsal root, cranial, and sympathetic ganglia and within kidney glomeruli.
65  H2S is endogenously generated in peripheral sympathetic ganglia and, if so, its effect on synaptic t
66 t is destined to form the neural core of the sympathetic ganglia, and (2) the CXCR4 ligand, SDF-1, is
67  trunk neural crest forms the more posterior sympathetic ganglia, and also contributes to the foregut
68 The development of other parasympathetic and sympathetic ganglia appears to be largely unaffected ind
69 llenge the prevailing dogma that posits that sympathetic ganglia are a gnathostome innovation, instea
70 her or not subsets of neurons within complex sympathetic ganglia are predetermined to innervate selec
71                                              Sympathetic ganglia are primarily composed of noradrener
72                   Our findings indicate that sympathetic ganglia are sources of reactivating virus, h
73                                     Discrete sympathetic ganglia arise as a consequence of intermixin
74 he segmental pattern of neural-crest-derived sympathetic ganglia arises as a direct result of signals
75 c neurons that comprise a chain of vertebral sympathetic ganglia, arises developmentally is incomplet
76 BMPR-IB mRNA was expressed in the primordial sympathetic ganglia at stage 17, soon after the first ex
77      BMPR-IA mRNA was first expressed in the sympathetic ganglia at stage 18.
78 of mouse cervical and thoracic paravertebral sympathetic ganglia at stages throughout embryonic and p
79 ts encoding dHAND and eHAND are expressed in sympathetic ganglia beginning at Hamburger and Hamilton
80  satellite glia after the initial seeding of sympathetic ganglia by neural crest.
81 cotinic transmission was studied in bullfrog sympathetic ganglia by recording synaptic currents from
82 l and neuronal progenitor cells in postnatal sympathetic ganglia, by using mouse superior cervical ga
83      The results support the hypothesis that sympathetic ganglia can produce a 2.4-fold amplification
84   Demethylation with azacytidine in cultured sympathetic ganglia cells led to increased GATA3 express
85                                 In all these sympathetic ganglia, clusters of small diameter (< 10 mi
86 with ARSB restored axon outgrowth from mouse sympathetic ganglia co-cultured with cardiac scar tissue
87 efore, we assayed beta43' in dissociated rat sympathetic ganglia cultures, which contain nAchR-positi
88 phalic neural crest cells that is TH+ in the sympathetic ganglia decreases with time, while the propo
89 ecially complex given the vertebral chain of sympathetic ganglia derive secondarily from the dorsal m
90                                 Prevertebral sympathetic ganglia develop markedly enlarged argyrophil
91   In contrast, blood flow in dorsal root and sympathetic ganglia did not vary with changes in pressur
92   The synaptic organization of paravertebral sympathetic ganglia enables them to relay activity from
93  SN-LI in nerve fibers and somata of various sympathetic ganglia, enteric plexus and adrenal medulla
94  Satellite glia are the major glial cells in sympathetic ganglia, enveloping neuronal cell bodies.
95 c neurons of the superior cervical and other sympathetic ganglia exhibited low-to-moderate levels of
96 wed that the spatiotemporal pattern of chick sympathetic ganglia formation is a two-phase process.
97 ratory behaviors that lead to alterations in sympathetic ganglia formation using a recently developed
98                          Motor, sensory, and sympathetic ganglia from 1-, 2-, and 4-month-old P0-GGFb
99  neural crest-derived cells from the gut and sympathetic ganglia had initiated neuronal differentiati
100                           The hypertrophy of sympathetic ganglia in the transgenic mice was correlate
101 athetically innervated peripheral organs, in sympathetic ganglia, in adrenal glands, and in brains.
102 on of ERbeta in the nuclei of neurons in the sympathetic ganglia, increase in tyrosine hydroxylase in
103    However, the number of neurons in DRG and sympathetic ganglia increases continuously at least up t
104 rat superior mesenteric or superior cervical sympathetic ganglia indicating that apoptotic neuronal c
105                           Individual DRG and sympathetic ganglia initially contain few neurons.
106 ations suggest that increased NGF content in sympathetic ganglia innervating the diabetic alimentary
107                                       LTP of sympathetic ganglia is 5-HT(3) receptor-dependent and ha
108                                              Sympathetic ganglia lacking protein tyrosine phosphatase
109 ten extensive in the dorsal root ganglia and sympathetic ganglia, leading to atrophy of Schwann cells
110 clude an increase in nerve, dorsal root, and sympathetic ganglia lipid hydroperoxides and conjugated
111 ylase in both nerve terminals in the SAT and sympathetic ganglia neurons and an increase of beta3-adr
112 y expressed in dorsal root ganglia (DRG) and sympathetic ganglia neurons, have recently been identifi
113 s when heterologously expressed in adult rat sympathetic ganglia neurons.
114                   Neuron number is normal in sympathetic ganglia of adult p75NTR-/- mice.
115 synaptic origin of neuritic dystrophy in the sympathetic ganglia of aged and diabetic human subjects.
116 y AP-2beta is predominantly expressed in the sympathetic ganglia of developing mouse embryos, support
117  the rate of neuroblast proliferation in the sympathetic ganglia of mice lacking the GFRalpha3 subuni
118  in several developing and adult sensory and sympathetic ganglia of the peripheral nervous system.
119    We plated dissociated cells from neonatal sympathetic ganglia on immobilized anti-CD9 antibodies o
120 ing, nor for the formation of dorsal root or sympathetic ganglia, or the adrenal medulla.
121  signals in the gut and in the region of the sympathetic ganglia play a role in the choice of cell fa
122 c potentiation and long-term potentiation in sympathetic ganglia, probably by activation of presynapt
123  the rat model to findings in diabetic human sympathetic ganglia provide promise for the development
124 s and MYCN overexpression in embryonic mouse sympathetic ganglia results in NB-like tumors.
125 mRNA were detected in both superior cervical sympathetic ganglia (SCG) and dorsal root ganglia (DRG)
126 ngly, Nrp/Sema signaling is not required for sympathetic ganglia segmentation.
127 uctures as the dorsal root ganglia (DRG) and sympathetic ganglia (SG), which form in a metameric patt
128 ent during NC cell aggregation into discrete sympathetic ganglia (SG).
129 rete structures, the dorsal root ganglia and sympathetic ganglia (SGs), are unknown.
130 nglia and cryosections of DRG and the sacral sympathetic ganglia (SSG) from latently infected guinea
131 eover, BMP-4 ligand mRNA was detected in the sympathetic ganglia starting at stage 18.
132  EAG genes were found to be expressed in rat sympathetic ganglia, suggesting an important functional
133 ation of both paravertebral and prevertebral sympathetic ganglia targets in vivo independently of its
134  preganglionic sympathetic neurons and their sympathetic ganglia targets.
135 arily from the dorsal migration of 'primary' sympathetic ganglia that are initially located several h
136  of connectivity between the spinal cord and sympathetic ganglia through retrograde control of synaps
137 expression in superior cervical and stellate sympathetic ganglia tissue.
138 n Fz3(-/-) ganglia are able to extend out of sympathetic ganglia toward distal targets, but fail to f
139  Alphaherpesvirus reactivation from thoracic sympathetic ganglia (TSG) and transaxonal spread to targ
140 ne transporter in rat peripheral sensory and sympathetic ganglia was investigated using polymerase ch
141                       Neurite outgrowth from sympathetic ganglia was significantly greater at post-li
142 ts of adenosine on long-term potentiation of sympathetic ganglia was studied in the isolated superior
143 current (IM) of single neurons isolated from sympathetic ganglia were studied.
144 c autonomic neuropathy in mouse prevertebral sympathetic ganglia, were increased 14.8-fold and 17.2-f
145 pes, including gut enteroendocrine cells and sympathetic ganglia, where it may play a role in the mai
146 estigators first characterized the enzyme in sympathetic ganglia wherein dopamine-producing cells lin
147 ute to NC derivatives, with the exception of sympathetic ganglia, which appeared to be 'filled' by th
148                   The actions of estrogen on sympathetic ganglia, which are key players in the browni
149 st cells fails to express dHAND or TH in the sympathetic ganglia, while a further subset initiates bu
150  sympathetic outgrowth, we co-cultured adult sympathetic ganglia with peri-infarct explants.
151 ilure of neurotransmission through abdominal sympathetic ganglia, with retention of neuronal viabilit

 
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