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1 red and reversed by the products of the gene prickle.
2 polarity proteins including Dishevelled and Prickle.
3 wo other tissue polarity genes, flamingo and prickle.
4 and the cytoplasmic proteins Dishevelled and Prickle.
5 interactions with mutations in frizzled and prickle.
7 of NTD prevalence in humans and ascribes to Prickle-1 a critical role in lower spinal cord formation
8 Moreover, the planar-cell-polarity member, Prickle-1, is recruited specifically during junctional n
9 de-mediated knockdown of PCP genes including prickle-1a (pk1a) led to developmental biliary abnormali
11 ed by mutations in disheveled, inturned, and prickle all make hair patterns globally irregular yet lo
12 rast the cytoplasmic components Dishevelled, Prickle and Diego are not needed for intercellular commu
16 nts, including Frizzled, Van Gogh, Flamingo, Prickle, and Dishevelled, to establish their characteris
19 that isoforms of the Fz PCP pathway protein Prickle are differentially required for the two PCP Phas
22 evel is similar to frizzled, dishevelled and prickle, as many cells form a single hair of abnormal po
27 that basal cells predominantly expressed m3, prickle cells had equally high levels of m4 and m5, and
28 We show that a VANG-1/Van Gogh and PRKL-1/Prickle containing PCP pathway and a Slit-independent SA
29 type is similar to frizzled, dishevelled and prickle, dachsous mutant wings display a unique and dist
31 last DNA phylogeny indicates that thorn-like prickles evolved at least four times and leaf dimorphism
33 r data suggest that Strabismus, Flamingo and Prickle function together to regulate the establishment
34 , dishevelled (dsh), Van Gogh/strabismus and prickle, function to regulate wing hair, bristle and omm
35 subdomains within r4, with one gene, a novel prickle homolog (pk1b), expressed specifically within th
39 merely altering the balance of the two adult prickle isoforms in neurons can predispose flies to seiz
41 ns is required for the other's localization, Prickle localization is influenced by Strabismus functio
42 mesoderm C&E, the noncanonical Wnt component Prickle localizes at the anterior cell edge, whereas Dis
44 more generalized cellular mechanism whereby Prickle mediates polarity by influencing microtubule-med
45 Additionally, we show that seizure-prone prickle mutant flies have electrophysiological defects s
46 ar, we show that the stabilizing function of Prickle on Frizzled requires Prickle activity in neighbo
47 s or signs were experienced by 27 patients; 'prickling' or 'asleep numbness' in 20, mild pain in 13 a
48 ed for a gradient of frizzled, starry night, prickle, or spiny-legs expression to repolarize wing cel
50 brafish, and humans showed that mutations in prickle orthologs result in epileptic phenotypes, althou
51 ebrafish homologs of the Drosophila PCP gene prickle (pk) [8], both of which show discrete and dynami
52 the planar cell polarity (PCP) gene products prickle (pk) and dishevelled (dsh) show M/L polarization
57 Here we show that the tissue polarity gene prickle (pk) encodes a protein with a triple LIM domain
58 acterise a zebrafish homologue of Drosophila prickle (pk), a gene that is implicated in the regulatio
59 One of the key members of this pathway is Prickle (Pk), a protein that regulates cell movement thr
60 ed (Fz)/PCP core components, Diego (Dgo) and Prickle (Pk), and screened these against the DrosDel gen
61 We study four polarity genes, frizzled (fz), prickle (pk), Van gogh/strabismus (Vang/stbm) and starry
62 ity (PCP) proteins, we find that alternative Prickle (Pk-Sple) protein isoforms control the polarity
65 in ascidians, the planar cell polarity gene prickle regulates sequential establishment of cell polar
66 t simultaneous depletion of Xtes and Xenopus Prickle results in axial defects that are more severe th
68 ugh characterization of the contributions of Prickle, Spiny-legs, Dachsous, Fat, and Dachs to PCP in
73 d/Dishevelled/Diego (Fz/Dsh/Dgo) or Van Gogh/Prickle (Vang/Pk) complexes within the same cell, stabil
74 im), a mutation in the PCP pathway component Prickle, which has a severe defect in early mediolateral
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