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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.
6 MBV also prevented IOP-induced decreases in growth associated protein-43 and IOP-induced increases i
7 omography, and 28% beyond CSF neurofilament, growth-associated protein 43 and neurogranin in Abeta(+)
8 th FTD and AD than in controls, but those of growth-associated protein 43 and synapsin 1 were reduced
11 ially due to significantly higher amounts of growth-associated protein-43 and/or beta1 integrin than
12 cytoskeletal proteins, neurofilament-M, and growth-associated protein-43 as well as the dendrite-spe
13 eeks after lesion judging from the return in growth associated protein-43 expression to control level
16 antibodies to tyrosine hydroxylase (TH) and growth associated protein-43 (GAP-43) in the L5 DRG 1 we
21 identify a novel repressive element from the growth-associated protein 43 (GAP-43) gene that can cont
25 marker protein gene product 9.5 (PGP9.5) and growth-associated protein 43 (GAP-43), a marker of regen
27 AP1B), its phosphorylated isoform (MAP1B-P), growth-associated protein 43 (GAP-43), and polysialylate
28 manifesting in increases in the presynaptic growth-associated protein 43 (GAP-43), which is closely
30 lament 200 kd (NF200; sensory nerve fibers), growth-associated protein 43 (GAP-43; sprouted nerve fib
31 Here we show a preferential upregulation of growth-associated protein-43 (GAP-43) and enhanced Fluor
32 the dendritic associated protein, MAP-2, the growth-associated protein-43 (GAP-43) and the dendritic
35 f ATPgammaS into the sciatic nerve increased growth-associated protein-43 (GAP-43), a marker for axon
36 Further, we demonstrate that the level of growth-associated protein-43 (GAP-43), a palmitoylated n
37 f membrane-anchored, palmitoylated H-Ras and growth-associated protein-43 (GAP-43), respectively.
38 NeuN, MAP-2, betaIII-tubulin in addition to growth-associated protein-43 (GAP-43), Synapsin-I and th
39 w that the INCL brain contains high level of growth-associated protein-43 (GAP-43), which is known to
41 alcitonin gene-related peptide (CGRP(+)) and growth associated protein 43 (GAP43(+)) fibers occurs co
42 ost synaptic density-95 (PSD-95) (p < 0.05), growth associated protein 43 (GAP43) (p < 0.05), glial f
43 The expression of nerve growth factor (NGF), growth associated protein 43 (GAP43), and other nerve ma
44 g of cardiac nerves was performed using anti-growth-associated protein 43 (GAP43) and anti-tyrosine h
45 nsport was visualized by the accumulation of growth-associated protein 43 (GAP43) at the ligation sit
46 We also identify the cytoskeleton-associated growth-associated protein 43 (GAP43) mRNA as a new targe
47 lex gene expression profiling, we found that growth-associated protein 43 (GAP43) RNA and protein exp
49 udy, we demonstrated for the first time that growth-associated protein 43 (GAP43), a well known growt
50 in levels of KOR and axon extension markers, growth-associated protein 43 (GAP43), and transient axon
52 tor, p75NGFR), postmitotic immature neurons (growth-associated protein 43 [GAP43]), and mature olfact
54 (synaptosomal-associated protein 25, SNAP25; growth-associated protein 43, GAP43), postsynaptic (neur
55 nctions, including somatostatin, enkephalin, growth-associated protein 43, glutamate acid decarboxyla
57 tress, activating transcription factor 3 and growth-associated protein 43 in DRGs, whereby the latter
58 d mice exhibited higher expression of axonal growth-associated protein 43 in the ipsilesional thalamu
59 ceptors, dendritic spines, and expression of growth-associated protein-43 in the cornu ammonis 1 regi
60 r expression of olfactory marker protein and growth-associated protein 43, indicating decreases in bo
61 n, below ACC there was overexpression of the growth-associated protein 43 kDa accompanied by excessiv
62 easured levels of neuronal-specific enolase, growth-associated protein 43, nerve growth factor (NGF),
63 proteins (synaptosome-associated protein 25, growth-associated protein 43 or synaptotagmin-1) had sig
64 /mm(2) and 20,623 +/- 4,926 mum(2)/mm(2) for growth-associated protein 43 (p < 0.05) and were 32,116
65 ecific enolase-positive (57.7% increase) and growth-associated protein 43-positive fibers (56.1% incr
66 ecause a number of presynaptic marker mRNAs (growth-associated protein-43, synapsin, synaptophysin, s
67 to tyrosine hydroxylase, synaptophysin, and growth-associated protein-43 than those of normal contro
68 , betaIII-tubulin, protein gene product 9.5, growth associated protein 43, trkA, and calcitonin gene-
69 ing by tyrosine hydroxylase fibers, mRNA for growth associated protein-43 was upregulated in dopamine
70 promoted neurite outgrowth and expression of growth-associated protein-43, whereas FP3 antagonized th
71 ion of brain-derived neurotrophic factor and growth-associated protein-43, which was inhibited by PD9