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1 fuses laterally, functioning as a long-range chemorepellent.
2 In addition to AprA, cells secrete a <10 kDa chemorepellent.
3 he localized secretion of a diffusing T cell chemorepellent.
4 nd female neutrophils to be attracted to the chemorepellent.
5 itudinal axon guidance by the Slit family of chemorepellents.
6 ears to be regulated by chemoattractants and chemorepellents.
7 signaling by semaphorins, a family of axonal chemorepellents.
8 g and/or degrading lipid chemoattractants or chemorepellents.
9 mbers that can function as diffusible axonal chemorepellents.
10 chia coli) to different chemoattractants and chemorepellents.
11  relatively little is known about neutrophil chemorepellents.
12                                    Using the chemorepellent acetate to phosphorylate and acetylate Ch
13                                   The rectal chemorepellent activity is blocked by anti-collapsin-1 a
14 rom melanomas expressing CXCL12 confirms the chemorepellent activity of high concentrations of CXCL12
15 s support the thesis that the CXCR4-mediated chemorepellent activity of intrathymic SDF-1 contributes
16 entration, has been shown to act as a T-cell chemorepellent and abrogate T-cell infiltration into a s
17  emigration, and, in vitro, netrin 1 acts as chemorepellent and antagonizes platelet-derived growth f
18 he medial part of ventral telencephalon, and chemorepellent and chemoattractant activities expressed
19 ed male neutrophils to be more repelled by a chemorepellent and female neutrophils to be attracted to
20  fragments, and these fragments are neuronal chemorepellents and inhibit chemoattraction of many cell
21  the class 3 semaphorins, which are neuronal chemorepellents, and plays a role in the directional gui
22 ort that Slit proteins, a family of secreted chemorepellents, are crucial for the proper development
23 eems to act both at close range as a contact chemorepellent, by affecting insect gustatory receptors,
24                   These results suggest that chemorepellents can prevent the premature innervation of
25                         In the presence of a chemorepellent, compared with male neutrophils, female n
26 hanism whereby a cell-surface receptor for a chemorepellent confers specificity of intercellular fusi
27  crossing of the midline and as a long-range chemorepellent controlling mesoderm migration away from
28 innervation require both chemoattractive and chemorepellent cues for precise spatiotemporal regulatio
29 les growth cone (GC) collapse in response to chemorepellent factor semaphorin 3 A (Sema 3 A) by stabi
30                                 Gradients of chemorepellent factors released from myelin may impair a
31 kDa N-terminal Slit2 fragment (Slit2-S) is a chemorepellent for human neutrophils.
32 oduced by microbiota and thought to act as a chemorepellent for invading pathogens, thereby protectin
33 ation assays demonstrated that netrin-1 is a chemorepellent for migrating adult OPCs.
34                 Functionally, Slit acts as a chemorepellent for olfactory bulb axons.
35 several classes of developing axons and as a chemorepellent for other classes of axons, apparently de
36      Collapsin-1 can function as a selective chemorepellent for sensory neurons, however, its early e
37 of Slit containing only the LRRs function as chemorepellents for axons projecting from the olfactory
38    Here, we show that slit1 and slit2, known chemorepellents for RGC axons expressed in specific regi
39 network describes the underlying pathways of chemorepellent gradient sensing in D. discoideum.
40  Furthermore, the secreted protein Slit is a chemorepellent guiding the migratory direction of GABAer
41 acellular glycoproteins that may function as chemorepellents in axon guidance and neuronal cell migra
42 e second idea; i.e., there exists a possible chemorepellent inside tumor cell clusters, which prevent
43               Here, we show that the <10 kDa chemorepellent is a polymer of phosphates (polyphosphate
44     8-CPT-cAMP, widely described as a simple chemorepellent, is inactive on its own and only repels c
45 (Sema3E), initially identified as a neuronal chemorepellent, is involved in the regulation of cell mi
46                             Semaphorin 3A, a chemorepellent known to inhibit integrin activation, was
47                 We also found that Sema3a, a chemorepellent ligand for Nrp1, is expressed by type I a
48                  Moreover, FLRT proteins are chemorepellent ligands for developing interneurons in vi
49 ay from the roof plate (RP) in response to a chemorepellent mediated by the bone morphogenetic protei
50 y because both glial populations express the chemorepellent molecule slit-2, and cortical axons expre
51 ate that combinations of chemoattractant and chemorepellent molecules are involved in this ventricle-
52                 In addition to their role as chemorepellent netrin-1 receptors, UNC5 proteins may med
53 e results indicate that DPPIV functions as a chemorepellent of human and mouse neutrophils, and they
54 ocument for the first time that Slit2-N is a chemorepellent of VSMCs.
55 le of Semaphorin3A (Sema3A), a cell guidance chemorepellent, on angioblast migration and corneal avas
56 hat pathway tissues might secrete diffusible chemorepellents or chemoattractants that guide cranial m
57 ce is provided for a distinct trochlear axon chemorepellent produced by floor plate cells.
58 a Dictyostelium discoideum secretes a 60 kDa chemorepellent protein called AprA to cause cells at the
59           We previously found that AprA is a chemorepellent protein secreted by Dictyostelium cells.
60 hat allogeneic cells engineered to express a chemorepellent protein would not be rejected.
61 em cell-derived OPCs to be unresponsive to a chemorepellent released from chronic MS lesions, and tra
62 1 was also shown to elicit a CXCR4-dependent chemorepellent response from fetal SP thymocytes.
63 s from their localized origin is guided by a chemorepellent response to netrin 1.
64 romeric netrin-receptor complex to mediate a chemorepellent response.
65 wth may be due to a chemoattractant and/or a chemorepellent secreted by intermediate targets of corti
66 he response of Drosophila motoneurons to the chemorepellent Sema-2a during synaptic refinement.
67                                          The chemorepellent Sema3F is required for IPT axon pruning,
68 from the dura into the brain by cleaving the chemorepellent semaphorin 3a.
69                                   Similarly, chemorepellent semaphorin-3a binds neuropilin-1 to activ
70 udy examines the possible role of a secreted chemorepellent, Semaphorin 3E (Sema3E), in neutrophil mi
71             Mapping along this axis requires chemorepellent signalling from tectal cells, expressing
72 ns remain concerning how chemoattractant and chemorepellent signals are integrated within the cell an
73 t) or away from the source (in the case of a chemorepellent)--such migration is termed chemotaxis.
74 maphorin 3A (SEMA3A)-encoded semaphorin is a chemorepellent that disrupts neural patterning in the ne
75 ceptor for semaphorin3A (Sema3A), a secreted chemorepellent that facilitates axon guidance during neu
76 e responsible for the graded distribution of chemorepellents that drive the directed migration of neu
77  proteins (BMPs) appear to act as RP-derived chemorepellents that guide the early trajectory of the a
78 rating D. discoideum cells use two different chemorepellents, that one of the repellents is the unusu
79 epelling axons, including the Slit family of chemorepellents via their Robo receptors, and Netrin1 vi