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1 ase in the expression of a plasticity marker growth-associated protein 43.
2 n and microtubules as well as synapsin I and growth-associated protein 43.
3  between alcohol dependence and a SNP in the growth-associated protein 43.
4 t into neurites by a targeting sequence from growth-associated protein-43.
5 th FTD and AD than in controls, but those of growth-associated protein 43 and synapsin 1 were reduced
6       Both stellate ganglia were stained for growth-associated protein 43 and synaptophysin.
7                  Staining with antibodies to growth-associated protein-43 and microtubule-associated
8 ially due to significantly higher amounts of growth-associated protein-43 and/or beta1 integrin than
9  cytoskeletal proteins, neurofilament-M, and growth-associated protein-43 as well as the dendrite-spe
10 eeks after lesion judging from the return in growth associated protein-43 expression to control level
11               We previously showed increased growth associated protein 43 (GAP-43) expression in brai
12  antibodies to tyrosine hydroxylase (TH) and growth associated protein-43 (GAP-43) in the L5 DRG 1 we
13                                              Growth-associated protein 43 (GAP 43) is a presynaptic p
14                       Neuronal expression of growth-associated protein 43 (GAP-43) and the cell adhes
15         We have analyzed a promoter from the growth-associated protein 43 (GAP-43) gene and found tha
16 identify a novel repressive element from the growth-associated protein 43 (GAP-43) gene that can cont
17            In this study, we have identified Growth-associated protein 43 (Gap-43) mRNA as a novel ta
18             Alterations in the expression of growth-associated protein 43 (GAP-43) were examined in l
19 marker protein gene product 9.5 (PGP9.5) and growth-associated protein 43 (GAP-43), a marker of regen
20                           Immunostaining for growth-associated protein 43 (GAP-43), a molecular marke
21 AP1B), its phosphorylated isoform (MAP1B-P), growth-associated protein 43 (GAP-43), and polysialylate
22               Here, we dissected the role of growth-associated protein 43 (GAP-43; also known as neur
23 lament 200 kd (NF200; sensory nerve fibers), growth-associated protein 43 (GAP-43; sprouted nerve fib
24  Here we show a preferential upregulation of growth-associated protein-43 (GAP-43) and enhanced Fluor
25 the dendritic associated protein, MAP-2, the growth-associated protein-43 (GAP-43) and the dendritic
26                                              Growth-associated protein-43 (GAP-43) is a major growth
27 element in the 3'-untranslated region of the growth-associated protein-43 (GAP-43) mRNA.
28 f ATPgammaS into the sciatic nerve increased growth-associated protein-43 (GAP-43), a marker for axon
29    Further, we demonstrate that the level of growth-associated protein-43 (GAP-43), a palmitoylated n
30 f membrane-anchored, palmitoylated H-Ras and growth-associated protein-43 (GAP-43), respectively.
31 w that the INCL brain contains high level of growth-associated protein-43 (GAP-43), which is known to
32 oteins, postsynaptic density-95 (PSD-95) and growth-associated protein-43 (GAP-43).
33 The expression of nerve growth factor (NGF), growth associated protein 43 (GAP43), and other nerve ma
34 g of cardiac nerves was performed using anti-growth-associated protein 43 (GAP43) and anti-tyrosine h
35 nsport was visualized by the accumulation of growth-associated protein 43 (GAP43) at the ligation sit
36 We also identify the cytoskeleton-associated growth-associated protein 43 (GAP43) mRNA as a new targe
37 lex gene expression profiling, we found that growth-associated protein 43 (GAP43) RNA and protein exp
38                                              Growth-associated protein 43 (GAP43), a protein kinase C
39 udy, we demonstrated for the first time that growth-associated protein 43 (GAP43), a well known growt
40 in levels of KOR and axon extension markers, growth-associated protein 43 (GAP43), and transient axon
41 n and local translation of the mRNA encoding growth-associated protein 43 (GAP43).
42 tor, p75NGFR), postmitotic immature neurons (growth-associated protein 43 [GAP43]), and mature olfact
43 and a protein expressed during axonogenesis (growth-associated protein 43 [GAP43]).
44 nctions, including somatostatin, enkephalin, growth-associated protein 43, glutamate acid decarboxyla
45 was assessed 4 and 8 d after implantation by growth-associated protein-43 immunolabeling.
46 tress, activating transcription factor 3 and growth-associated protein 43 in DRGs, whereby the latter
47 ceptors, dendritic spines, and expression of growth-associated protein-43 in the cornu ammonis 1 regi
48 r expression of olfactory marker protein and growth-associated protein 43, indicating decreases in bo
49 n, below ACC there was overexpression of the growth-associated protein 43 kDa accompanied by excessiv
50 easured levels of neuronal-specific enolase, growth-associated protein 43, nerve growth factor (NGF),
51 /mm(2) and 20,623 +/- 4,926 mum(2)/mm(2) for growth-associated protein 43 (p < 0.05) and were 32,116
52 ecific enolase-positive (57.7% increase) and growth-associated protein 43-positive fibers (56.1% incr
53 ecause a number of presynaptic marker mRNAs (growth-associated protein-43, synapsin, synaptophysin, s
54  to tyrosine hydroxylase, synaptophysin, and growth-associated protein-43 than those of normal contro
55 , betaIII-tubulin, protein gene product 9.5, growth associated protein 43, trkA, and calcitonin gene-
56 ing by tyrosine hydroxylase fibers, mRNA for growth associated protein-43 was upregulated in dopamine
57 promoted neurite outgrowth and expression of growth-associated protein-43, whereas FP3 antagonized th
58 ion of brain-derived neurotrophic factor and growth-associated protein-43, which was inhibited by PD9

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