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1 nto the brain by cleaving the chemorepellent semaphorin 3a.
2 n leads to ischemia and angiogenesis through Semaphorin 3A.
3 d myelin-associated glycoprotein, but not to semaphorin 3A.
4 chemia and pathological angiogenesis through Semaphorin 3A.
5 ve guidance molecules, such as ephrin-A2 and semaphorin 3A.
6 towards the retina is guided by netrin-1 and semaphorin 3a.
7 h cone collapse in response to ephrin-A2 and semaphorin 3A.
10 required for growth cone steering away from semaphorin-3a, a guidance cue that does not activate ER-
14 teracts cell migration inhibitory signals by Semaphorin 3A and Semaphorin 3F, generating aberrant neu
16 ce neuropilin-1 (NRP1), a receptor shared by semaphorin 3A and vascular endothelial growth factor (VE
18 ntiates the signaling pathways stimulated by semaphorin 3A and VEGF-A in neuronal and endothelial cel
22 helly et al. show that the axon guidance cue Semaphorin 3A can promote dendrite growth by inhibiting
23 ), cell migration (Ret and EdnrB signalling, semaphorin 3A, cell adhesion molecules, Rho GTPases), an
25 evealed that decorin-mediated suppression of semaphorin 3A critically depends on erythroblastic leuka
26 nistration of a ligand of plexin-A4, Sema3A (semaphorin 3A), exacerbates the cytokine storm caused by
28 how that decorin has the ability to suppress semaphorin 3A expression within adult rat cerebral corte
31 nse of dorsal root ganglion (DRG) neurons to Semaphorin 3A gradients can be divided into two steps: g
32 stem scar associated axon growth inhibitors, semaphorin 3A has been shown to be strongly expressed by
33 glycans, decorin has the ability to suppress semaphorin 3A in the injured central nervous system.
36 In the present study, we first showed that semaphorin 3A-induced growth cone collapse in cultured h
40 orrespondingly, Ndr2-null mutant mice show a Semaphorin 3A(-/-)-like phenotype of premature dendritic
44 ridization and immunostaining confirmed that semaphorin 3A messenger RNA expression and protein level
45 days resulted in a significant reduction of semaphorin 3A messenger RNA expression within injury sit
46 ecorin treatment decreased the expression of semaphorin 3A messenger RNA in cultured rat leptomeninge
47 y into avascular tumor areas is regulated by Semaphorin 3A/Neuropilin-1 signaling; interference with
48 on cultured retinal ganglion cell axons, of semaphorin 3A on dorsal root ganglion sensory axons, and
50 d in axonal outgrowth and a component of the semaphorin 3A pathway, in switching GTPase signaling whe
51 However, myelin-associated glycoprotein and semaphorin 3A regulate axonal levels of different mRNAs
52 ; in fact, treatment of primary neurons with Semaphorin 3A rescues Ndr2 knock-down-induced dendritic
56 linear regression model, rs139438618 at the semaphorin 3A (SEMA3A [OMIM 603961]) locus was significa
57 d in TGF-beta-treated AEECs, which decreased semaphorin 3A (Sema3A) and increased EndMT markers, and
59 ressed genes and we investigated the role of semaphorin 3A (Sema3A) and neuropilin-1 (Nrp-1) in lymph
60 Neuropilin-1 (Npn-1) is a receptor for both semaphorin 3A (Sema3A) and vascular endothelial growth f
62 he growth-promoting NGF or growth-inhibitory semaphorin 3A (Sema3a) compared with control green fluor
68 ic genes, and that ventral astrocyte-encoded semaphorin 3a (Sema3a) is required for proper motor neur
69 our laboratory has shown that VEGF-A165 and semaphorin 3A (Sema3A) promote vessel maturation through
70 molecule close homolog of L1 (CHL1) and the semaphorin 3A (Sema3A) receptor, neuropilin 1 (Npn1), im
71 d to produce cell type-specific responses to Semaphorin 3A (Sema3A), a guidance cue that would be pre
73 h factor (VEGF), an angiogenesis factor, and semaphorin 3A (Sema3A), a mediator of axonal guidance.
79 d FGF-2 increased branching by >50%, whereas semaphorin 3A (Sema3A), which repels cortical axons, inh
88 (rs277470) located in a region encoding the semaphorin-3A (SEMA3A) binding domain (meta-analysis p v
93 ystal structure of a secreted 65 kDa form of Semaphorin-3A (Sema3A), containing the full semaphorin d
96 Exposure of growing neurons to thrombin or semaphorin 3A stimulates a receptor-mediated signaling c
97 copies of A22p, a peptide derived from human semaphorin-3a, that exhibits substantially improved edit
101 n superficial laminas, adenovirus expressing semaphorin 3A was injected into the ventral spinal cord
102 either of these receptors or the addition of semaphorin 3A (which blocks VEGF-165 binding to Nrp-1) p