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1 rovided by secreted Netrin-B and Frazzled, a netrin receptor.
2 ctions, suggesting that Dscam could act as a Netrin receptor.
3 surface of retinal fibers, possibly another Netrin receptor.
4 opulations, according to their expression of Netrin receptors.
5 nd as heterophilic repulsive ligands of Unc5/Netrin receptors.
6 hat this stimulation is independent of known netrin receptors.
7 ans counterpart, define a family of putative netrin receptors.
8 hypothesis that UNC-5 and its relatives are netrin receptors.
10 , in transcriptional regulation of the unc-5 netrin receptor and zmp-1 zinc matrix metalloprotease, a
13 binding allows for the association of other netrin receptors at the generic binding site, eliciting
14 onal link between the expression of distinct Netrin receptor combinations and the transcriptional con
15 that expression and requirement of different Netrin receptor combinations correlate with distinct dor
16 homologs are proposed to form a heteromeric netrin-receptor complex to mediate a chemorepellent resp
18 es have shown that the direct interaction of netrin receptor DCC and DSCAM with polymerized TUBB3, a
20 observation, tyrosine phosphorylation of the Netrin receptor DCC or its Drosophila ortholog, Frazzled
21 at localizes to filopodia tips and binds the netrin receptor DCC, interacts with and ubiquitinates th
24 and express apparently normal levels of the Netrin receptors DCC (deleted in colorectal carcinoma) a
26 otype was observed in B6 embryos lacking the netrin receptors DCC or Neogenin1, or the ligand netrin1
27 exiting RGC axons, and RGC axons express the netrin receptor, DCC (deleted in colorectal cancer).
29 action complex that included DOCK180 and the netrin receptor deleted in colorectal carcinoma (DCC).
30 ns-1 and -3 mice and netrin-2 in chicks) and netrin receptors [deleted in colorectal cancer (DCC), ne
31 y this year provide evidence that in humans, Netrin receptor, Deleted in Colorectal Cancer (DCC), is
33 we characterize two netrin homologs and one netrin receptor family member from Schmidtea mediterrane
35 etic knockout of the two Dscam genes and the Netrin receptor fra produces a midline crossing defect t
37 t the timely and threshold expression of the Netrin receptor Frazzled triggers the initiation of glia
38 cts both physically and genetically with the Netrin receptor Frazzled, and that disrupting this inter
39 mutation, T835M (rs137875858), in the UNC5C netrin receptor gene that segregated with disease in an
41 suggest that Frazzled does not function as a Netrin receptor in attracting retinal fibers to the targ
47 cytoplasmic domain) functions as a repulsive Netrin receptor; neurons expressing Fra-Robo avoid the N
50 to netrins is dictated by the composition of netrin receptors on the cell surface and the internal st
52 to glial biology: we show unc-5 (a repulsive netrin receptor) orients glial migrations and the draper
55 obo4 specifically binds to UNC5B, a vascular Netrin receptor, revealing unexpected interactions betwe
56 in receptor heterodimer INA-1/PAT-3 promotes netrin receptor UNC-40 (DCC) localization to the invasiv
58 ole in AC invasion, in part by targeting the netrin receptor UNC-40 (DCC) to the AC's plasma membrane
60 Here we identify a mechanism by which the Netrin receptor UNC-40/DCC instructs synaptic vesicle cl
63 that MAX-2 functions downstream of the UNC-6/netrin receptor UNC-5 during axon repulsion and is an in
68 rally similar to the ZU5 domain found in the netrin receptor UNC5b supramodule, suggesting that it co
70 nd Netrin-1 integration demonstrate that the Netrin receptor Unc5c and the ephrin receptor EphB2 can
71 strate that mice with a null mutation in the netrin receptor Unc5c on the inbred C57BL/6J (B6) geneti
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