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1 lia are polarized coordinately and display a planar cell polarity.
2 the apical membrane during the initiation of planar cell polarity.
3 protein (BMP) signaling, cell migration, and planar cell polarity.
4 g pathway that regulates Hippo signaling and planar cell polarity.
5 suggest that Dchs1-Fat4 signaling influences planar cell polarity.
6 but not directly in MET channel function or planar cell polarity.
7 fluid flow and the developmental process of planar cell polarity.
8 ing network regulates both transcription and planar cell polarity.
9 and gene expression but not its influence on planar cell polarity.
10 that regulates growth, gene expression, and planar cell polarity.
11 on, synaptogenesis, and the establishment of planar cell polarity.
12 nopus oocyte contains components of both the planar cell polarity and apical-basal polarity pathways,
13 d on the embryo have been used in studies on planar cell polarity and as models for the cytoskeletal
15 mutant hair cells also displayed defects in planar cell polarity and morphogenesis of the stereocili
16 TK7 pseudo-kinase plays an essential role in planar cell polarity and the non-canonical Wnt pathway i
18 larize cells in the plane of the epithelium (planar cell polarity) and to affect growth via the Warts
21 oliferation but instead resulted in aberrant planar cell polarity as manifested by abnormalities in t
24 cal cadherin Fat is a conserved regulator of planar cell polarity, but the mechanisms by which Fat co
25 a signaling pathway that controls growth and planar cell polarity by regulating the membrane localiza
27 nd that 5-HT and mdDA axons express the core planar cell polarity components Frizzled3, Celsr3, and V
29 , interactions and functions of the maternal planar cell polarity core protein Vangl2 and the apical-
32 the CNV showed discrete contributions of the planar cell polarity effector SCRIB and the splicing fac
34 eractions between three proteins involved in planar cell polarity: Flamingo, Frizzled and Van Gogh.
38 be in detail two of these: a mutation in the planar cell polarity gene scribbled homolog (Drosophila)
40 When combined with a mutant allele of the planar cell polarity gene Vangl2 (Vangl2(Lp)), Fz1 and/o
41 roles for planar polarity and for the novel planar cell polarity gene, Ptk7, as essential regulators
43 the cue, and reoriented mitosis required the planar cell polarity genes dachsous, fat, and atrophin.
44 ctorin-based matrix, epithelial cilia or the planar cell polarity genes Vangl2 and Ptk7 In wild-type
48 The frizzled/starry night pathway regulates planar cell polarity in a wide variety of tissues in man
49 he conserved frizzled (fz) pathway regulates planar cell polarity in both vertebrate and invertebrate
50 gnaling/signal transduction pathway controls planar cell polarity in both vertebrates and invertebrat
53 ry cilia are required for the maintenance of planar cell polarity in the mammalian kidney and that ac
54 ommatidial rotation, functional readouts of planar cell polarity in the wing and eye respectively, a
57 g and genetic analysis of proteins linked to planar cell polarity (Inturned, Fuzzy and Wdpcp), we ide
64 on CE is robust to relatively high levels of planar cell polarity misalignment and to the presence of
65 ements of cell polarity suggest that classic planar cell polarity molecules are not directly influenc
66 cts at least partially independently of core planar cell polarity molecules at the plasma membrane, a
67 egulation of Kif12 may underlie the abnormal planar cell polarity observed in cystic kidney diseases.
68 ling during kidney morphogenesis affects the planar cell polarity of the epithelium and leads to tubu
69 xpansion of satellite stem cells through the planar cell polarity pathway and by activating the Akt/m
71 g in a novel pathway, independently from the planar cell polarity pathway and in parallel to lin-17/f
72 eover, we demonstrate that components of the planar cell polarity pathway colocalize to recycling end
74 ry sensory organ, the Usher complex, and the planar cell polarity pathway in the formation and polari
76 Medio-lateral cell intercalation and the planar cell polarity pathway play a role during this ear
77 ng satellite stem cell expansion through the planar cell polarity pathway, as well as myofiber hypert
79 molecular control via the non-canonical Wnt/planar cell polarity pathway, Shh/BMP signalling, and th
83 tion between genes of the non-canonical Wnt (planar cell polarity) pathway and NTDs provides candidat
85 et genes not by signalingviathe WNT/Ca(2+)or planar cell polarity pathways, but rather by inhibiting
86 nts of the highly conserved apical-basal and planar cell polarity pathways, suggesting a possible reg
87 vertebrate neural tube formation, connecting planar cell polarity patterning to contraction of specif
88 hs1 signalling has been proposed to regulate planar cell polarity (PCP) and activity of the Hippo eff
89 f cells form as a result of coupling between planar cell polarity (PCP) and anisotropic tissue-scale
93 ila protocadherin Fat (Ft) regulates growth, planar cell polarity (PCP) and proximodistal patterning.
95 The PCP effector gene Inturned regulates planar cell polarity (PCP) and wing hair formation in Dr
96 e demonstrate that several components of the planar cell polarity (PCP) arm of non-canonical Wnt sign
102 he two mouse homologues of a Drosophila core planar cell polarity (PCP) gene Van Gogh (Vang), we reve
111 gnaling/signal transduction pathway controls planar cell polarity (PCP) in both vertebrates and inver
115 tracellular molecular machinery that directs planar cell polarity (PCP) in epithelial tissues, includ
117 Ft, Ds, and Fj are also required for normal planar cell polarity (PCP) in the wing, abdomen, and eye
118 led/starry night (fz/stan) pathway regulates planar cell polarity (PCP) in vertebrates and invertebra
123 In dividing cells of the mammalian skin, planar cell polarity (PCP) is maintained through the bul
125 fish morphants are similar to those found in planar cell polarity (PCP) mutants, a pathway suggested
126 ensory organ to exhibit a particular form of planar cell polarity (PCP) necessary for mechanotransduc
129 Here, we provide evidence implicating the planar cell polarity (PCP) pathway as the downstream com
135 ong et al. add to mounting evidence that the planar cell polarity (PCP) pathway coordinates posterior
136 n by regulating the evolutionarily conserved planar cell polarity (PCP) pathway during embryonic morp
137 including beta-catenin and non-canonical Wnt/planar cell polarity (PCP) pathway factors, such as Daam
138 Recent work implicates a non-canonical Wnt/planar cell polarity (PCP) pathway in the regulation of
149 importance in development and physiology the planar cell polarity (PCP) pathway remains one of the mo
151 facilitate a switch to the non-canonical Wnt planar cell polarity (PCP) pathway that is involved in c
153 Additionally, glypicans function in the planar cell polarity (PCP) pathway, and several PCP gene
154 at Celsr3 and Vangl2, core components of the planar cell polarity (PCP) pathway, are localized at dev
157 of Vangl2, a transmembrane component of the planar cell polarity (PCP) pathway, rescued recessive Da
159 y-Legs (Pk) is an essential component of the planar cell polarity (PCP) pathway, together with Frizzl
160 d PAH pericytes for abnormalities in the Wnt/planar cell polarity (PCP) pathway, which has been shown
162 ochord taper involves three main mechanisms: Planar Cell Polarity (PCP) pathway-independent sibling c
177 ermis whereupon cell division, transmembrane planar cell polarity (PCP) proteins are removed from the
182 increased levels of transcripts encoding the planar cell polarity (PCP) proteins SCRIB and VANGL1 cor
183 nization and require the concerted action of planar cell polarity (PCP) proteins that regulate cell e
184 ir cell bundle alignment is mediated by core planar cell polarity (PCP) proteins, such as Vangl2, tha
185 symmetric subcellular localization of 'core' planar cell polarity (PCP) proteins, we find that altern
192 orientation are manifestations of epithelial planar cell polarity (PCP) required for proper perceptio
199 et of signaling pathways and the role of Wnt/Planar cell polarity (PCP) signaling in adult neurogenes
202 work has implicated Frizzled6 (Fz6)-mediated planar cell polarity (PCP) signaling in the initial spec
216 wingless (Wnt)-beta-catenin (betaC) and Wnt-planar cell polarity (PCP) signaling pathways to facilit
218 o worms, whether and how this is mediated by planar cell polarity (PCP) signaling remain elusive.
222 polarity is controlled by non-canonical Wnt/planar cell polarity (PCP) signaling, the hair cell-intr
223 g a candidate approach for genes involved in planar cell polarity (PCP) signaling, we identified Dros
232 show that Scribble, a protein implicated in planar cell polarity (PCP) signalling, is necessary for
233 ateral polarization was under the control of planar cell polarity (PCP) signalling, was necessary for
236 n the ASP was dependent on components of the planar cell polarity (PCP) system in the disc, and neith
237 nd physiology of tissues and organs requires planar cell polarity (PCP) systems that orient and coord
238 PTK7 regulates epithelial morphogenesis and planar cell polarity (PCP) through modulation of actomyo
239 n of this flow requires the establishment of planar cell polarity (PCP) whereby MCCs align hundreds o
240 ntation within the plane of a tissue, termed planar cell polarity (PCP), appear to be crucial for the
242 lls within the plane of the tissue, known as planar cell polarity (PCP), is a recurring theme in biol
243 n of cells across the tissue plane, known as planar cell polarity (PCP), is manifested by the segrega
244 d identified genes required for PR survival, planar cell polarity (PCP), patterning and differentiati
246 ften coexists, and sometimes intersects with planar cell polarity (PCP), which orients cells in the e
248 mmon pathway suggestive of activation of wnt-planar cell polarity (PCP)-c-Jun N-terminal kinase (JNK)
262 ts of canonical and noncanonical (Ca(2+) and planar cell polarity [PCP]) Wnt pathways, including IWP-
264 restingly, dyl mutants also display a unique planar cell polarity phenotype that is distinct from tha
265 PTK7, a tyrosine kinase receptor involved in planar cell polarity, plays a role in epithelial Wnt sig
270 this ciliopathy that (i) implicate ALMS1 in planar cell polarity signaling and (ii) suggest that the
273 LIN-17 phosphorylation and is antagonized by planar cell polarity signaling components Van Gogh (VANG
274 ata suggest an important role for Ryk in Wnt/planar cell polarity signaling during vertebrate develop
277 Here we reveal a novel requirement for Wnt/planar cell polarity signaling in the anterior-posterior
281 e reporters, that WNT11 strongly induced JNK/planar cell polarity signaling while repressing the beta
285 ase 1 gene (ROCK1) is a key component of the planar cell polarity signalling pathway, which plays an
286 nother non-canonical Wnt pathway involved in planar cell polarity, suggesting that these two pathways
290 he non-canonical Wnt-dependent regulation of planar cell polarity through the Formin homology protein
291 is an evolutionarily conserved regulator of planar cell polarity, tissue size and cell adhesion.
294 onent of both the canonical and noncanonical/planar cell polarity Wnt pathways, modulates cell polari
298 the Wnt/calcium (Wnt/Ca) pathway and the Wnt/planar cell polarity (Wnt/PCP) pathway, in certain cellu
300 orphogenesis (in particular the emergence of planar cell polarity), wound healing, and disease-progre
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