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1 ction being selectively inhibited by soluble EphB receptor.
2 ty peptides antagonize ephrin binding to the EphB receptors.
3  mediates high-affinity interaction with the EphB receptors.
4 nd NMDA receptors as prolonged activation of EphB receptors.
5 embrane-anchored presynaptic ligands for the EphB receptors.
6 emonstrate that melanoblasts express several EphB receptors.
7 und to be remarkably conserved between these EphB receptors.
8        In mice lacking ephrin-B3 or multiple EphB receptors, a significant number of axons followed a
9 nd that ephrin-B2-mediated activation of the EphB receptors accelerates dendritic spine development.
10 g within the retina is partially mediated by EphB receptors acting in a kinase-independent manner.
11       Recombinant ephrinB1-Fc, which induces EphB receptor activation, enhanced bFGF-induced tube for
12   Dominant-negative inhibition of endogenous EphB receptor activities blocks clustering of endogenous
13 B localized to the midline, together with an EphB receptor and a zinc-finger transcription factor exp
14 inhibitors of the pathological activities of EphB receptors and as targeting agents for imaging probe
15 more fully document the presence of specific EphB receptors and B-ephrins in embryonic mouse retina a
16       Contact-dependent interactions between EphB receptors and ephrin-B ligands mediate a variety of
17 be the spatiotemporal expression patterns of EphB receptors and ephrin-B1 in the vertebrate spinal co
18         At this age, ephrin-B2, a ligand for EphB receptors and for EphA4, is expressed in NL cell bo
19  through an association between postsynaptic EphB receptors and presynaptic B-ephrins are necessary f
20 s-synaptic interactions between postsynaptic EphB receptors and presynaptic B-ephrins are necessary f
21        These functions require processing of EphB receptors and removal of EphB-ephrinB complexes fro
22                                              EphB receptors and their ephrin-B ligands are required f
23         These observations indicate that the EphB receptors and their ligand regulate hippocampal axo
24  are phosphorylated upon interaction with an EphB receptor, and may transduce signals that regulate a
25                            Here we show that EphB receptors, and especially EphB4, regulate the migra
26                                 At this age, EphB receptors are expressed at the ventral floor plate.
27                                              EphB receptors are expressed in a low to high DV gradien
28                                          The EphB receptors are expressed in the hippocampus, and the
29 yonic mouse retina and provide evidence that EphB receptors are involved in RGC axon pathfinding to t
30 on of the embryonic mouse spinal cord, while EphB receptors are present on decussated segments of com
31 as RGC axons begin this pathfinding process, EphB receptors are uniformly expressed along the dorsal-
32                      These data suggest that EphB receptors are upstream regulators of FAK in dendrit
33 ed in the dorsal spinal cord, and decussated EphB receptor-bearing commissural axons navigate between
34  however, are significantly inhibited by the EphB receptor blocker.
35                  Spinal administration of an EphB receptor blocking reagent EphB2-Fc prevents and/or
36 the retina to the optic disc is dependent on EphB receptors, but independent of their kinase activity
37               We show that the expression of EphB receptors by motor axons, and ephrin-B ligands by l
38          Overexpression of dominant-negative EphB receptor, catalytically inactive kalirin, or domina
39                       These results indicate EphB receptor cell autonomous forward signaling is respo
40                               We report that EphB receptors direct unique axonal behaviors required f
41         There are 10 EphA receptors, and six EphB receptors, distinguished on sequence difference and
42 role of Eph proteins signaling as receptors, EphB receptor ECDs can also function in the opposite rol
43 proteins including cadherins, integrins, and EphB receptor/ephrinB significantly reduced the presynap
44 ll-to-cell contact, engagement of EphrinB by EphB receptors expressed on another cell, and Src-depend
45  thus grow across the midline at a time when EphB receptor expression levels are low.
46 on and post-transcriptional up-regulation of EphB receptor expression through relief of endocytosis a
47 ritic spines, and is accomplished through an EphB receptor-focal adhesion kinase (FAK) pathway.
48 jor recent advance is the demonstration that EphB receptor forward signaling and ephrin-B reverse sig
49                         We show in vivo that EphB receptor forward signaling and the ephrinB1 ligand
50                   Furthermore, inhibition of EphB receptor forward signaling by overexpression of a f
51  increases RhoA activity, whereas inhibiting EphB receptor forward signaling decreases RhoA activity.
52 llowing ephrinB(+) cells to trans-endocytose EphB receptors from opposing cells.
53 idirectional signaling between ephrin-B2 and EphB receptors impairs morphogenetic cell-cell septation
54 te the well-established roles of ephrins and EphB receptors in axon pathfinding, expression of these
55 dies demonstrate that FAK acts downstream of EphB receptors in hippocampal neurons and EphB2-FAK sign
56  that signaling occurs between B-ephrins and EphB receptors in the adult CNS in response to injury.
57 ults indicate that the role of ephrin-B2 and EphB receptors in these processes involves Crk-p130(CAS)
58 on assays, engagement of ephrin-B ligands to EphB receptors increases melanoblast attachment to fibro
59 with Connector Enhancer of KSR1 (CNK1) in an EphB receptor-independent manner.
60  of ephrinB2 to EphB4, these data suggest an EphB-receptor-independent blocking mechanism.
61                            Activation of the EphB receptor induces translocation of the Rho-GEF kalir
62 e activated by ephrin-A ligands, whereas the EphB receptors interact with ephrin-B ligands.
63 reported high ventral-low dorsal gradient of EphB receptors later in development when RGC axons map t
64                           We report that the EphB receptor ligand, ephrin-B1, may act bifunctionally
65 ervations provide a mechanistic link between EPHB receptor mutations and metastasis in colorectal can
66                                              EphB receptors provide crucial adhesive and repulsive si
67 in is specifically required for EphA and not EphB receptor signaling in mouse and chick spinal motor
68                               Alternatively, EphB receptor signaling may act as a 'ligand-density sen
69                          This novel role for EphB receptor signaling suggests that these molecules ma
70                 These findings indicate that EphB receptor signaling, probably by interacting with NR
71                       Peptides with the same EphB receptor specificity compete with each other for bi
72  that dorsal retinal axons prefer to grow on EphB receptor stripes supporting an attractive guidance
73 hosphorylation sites identified here for the EphB receptors suggest a complex regulation of their fun
74 wever, because VT RGCs express more than one EphB receptor, the sufficiency and specificity of the Ep
75 r protein for kinesin-dependent transport of EphB receptors to dendrites.
76                                   Binding of EphB receptors to ephrinB ligands on the surface of adja
77         Signaling is initiated by binding of EphB receptors to ephrinB ligands, stimulating their tyr
78                           The ability of the EphB receptors to regulate cell migration and promote an
79                We have identified an ephrinB-EphB receptor trans-synaptic signaling pathway which reg
80                                              EphB receptor tyrosine kinase signaling has been implica
81 pse development until EphrinB binding to the EphB receptor tyrosine kinase triggers Ephexin5 phosphor
82 nd antibodies that interfere with binding of EphB receptor tyrosine kinases (EphRs) to the PDZ protei
83                                              EphB receptor tyrosine kinases are enriched at synapses,
84                                          The EphB receptor tyrosine kinases are localized at excitato
85          Recent evidence supports a role for EphB receptor tyrosine kinases as tumour suppressors in
86                                              EphB receptor tyrosine kinases control multiple steps in
87          Here we show that activation of the EphB receptor tyrosine kinases in cultured hippocampal n
88  a genetic approach, we dissect the roles of EphB receptor tyrosine kinases in dendritic spine develo
89                                  In neurons, EphB receptor tyrosine kinases mediate excitatory synapt
90 rinB transmembrane ligands and their cognate EphB receptor tyrosine kinases regulate vascular develop
91          EphrinB2, a transmembrane ligand of EphB receptor tyrosine kinases, is specifically expresse
92                     We investigated roles of EphB receptor tyrosine kinases--which play important rol
93 l studies have reported the up-regulation of EphB receptor-tyrosine kinases and ephrin-B ligands in a
94                                     Notably, EphB receptors utilize the Tiam1-Bcr complex to control

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