戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 lacodes, with emphasis on the trigeminal and epibranchial.
2 y occupy within the embryo, dorsolateral and epibranchial.
3 ified as being respectively equivalent to an epibranchial and ceratobranchial.
4 ons largely derive from neurogenic placodes (epibranchial and dorsolateral), which are ectodermal thi
5  ganglia in the dogfish, with a focus on the epibranchial and lateral line placodes.
6 x2 is a conserved pan-gnathostome marker for epibranchial and otic placodes, and confirm that Phox2b
7  contributions to cranial ganglia, including epibranchial and trigeminal ganglia, and sensory structu
8     Knockdown of fgf24 or sox3 causes severe epibranchial deficiencies but has little effect on otic
9                                              Epibranchial (EB) placodes generate neurons of the dista
10 vate otic expression of fgf24, which induces epibranchial expression of sox3.
11 ted that Fgf initially induces a common otic/epibranchial field, which later subdivides in response t
12     A common feature of chick trigeminal and epibranchial ganglia is the expression of N-cadherin and
13 nings that contribute sensory neurons to the epibranchial ganglia.
14  whereas low levels increase cell numbers in epibranchial ganglia.
15 we show that the pharyngeal endoderm induces epibranchial neurogenesis in zebrafish, and that BMP sig
16 onents of the endodermal signals that induce epibranchial neurogenesis.
17  it can modulate the BMP signals that induce epibranchial neurogenesis: a gain of PRDC function resul
18 rons in the nodose ganglion that express the epibranchial neuron marker Phox2a on the same schedule a
19 e neuroglial hindbrain crest cells guide the epibranchial neuronal cells inward to establish their ce
20 m explants, it will promote the formation of epibranchial neuronal cells.
21 essary for the number and positioning of the epibranchial neurons.
22 centrate particles near the entrances of the epibranchial organs.
23 ensory neuron development in the trigeminal, epibranchial, otic, and olfactory placodes coincides wit
24 ix regulatory hierarchy also operates in the epibranchial placodal development.
25 nderlying the delamination of cells from the epibranchial placodal ectoderm.
26 xi1 is an important determination factor for epibranchial placodal progenitor cells to acquire both n
27 onal fate and neuronal subtype identity from epibranchial placodal progenitors.
28 e hindbrain neural crest and the neighboring epibranchial placodal tissues, without the need for a pr
29 al crest cell migration and ectoderm-derived epibranchial placode development are affected, leading t
30 ed on these findings, we propose a model for epibranchial placode development in which Fgf3 is a majo
31 factor, Foxi1, is required for both otic and epibranchial placode development.
32 expressed correctly and pharyngeal pouch and epibranchial placode formation are unaffected.
33 to neurons of the jugular ganglia, while the epibranchial placode gives rise to neurons of the nodose
34 etween the cranial neural crest (NC) and the epibranchial placode is critical for the formation of pa
35  grafted ectoderm are induced to express the epibranchial placode marker Pax2 and form neurons in the
36  a major endodermal determinant required for epibranchial placode neurogenesis.
37                       Initially, a subset of epibranchial placode precursors lie lateral to otic prec
38 ctodermal foxi1 expression, a marker for the epibranchial placode precursors, is present in both endo
39                    During the development of epibranchial placode-derived distal cranial sensory gang
40 2b is a conserved pan-gnathostome marker for epibranchial placode-derived neurons.
41  ectoderm is grafted in place of the nodose (epibranchial) placode, Pax3-expressing cells form Pax3-p
42  that innervate the face and jaws, while the epibranchial placodes (geniculate, petrosal and nodose)
43 Mis-expression of Pax3 in the Pax2+ otic and epibranchial placodes also downregulates Pax2 and disrup
44          We identify specific defects in the epibranchial placodes and neural crest, which contribute
45 t in the chick head, integration between the epibranchial placodes and the hindbrain is achieved as t
46                                          The epibranchial placodes are cranial, ectodermal thickening
47 hat the zebrafish mutation no soul, in which epibranchial placodes are defective, disrupts the fork h
48 ngside the central nervous system, while the epibranchial placodes are located close to the top of th
49 govern the induction and neurogenesis of the epibranchial placodes are only now being elucidated.
50                              In vertebrates, epibranchial placodes are transient ectodermal thickenin
51                                 We find that epibranchial placodes do not require neural crest for th
52 actor Pax3 from very early stages, while the epibranchial placodes express Pax2.
53               However, we find that otic and epibranchial placodes form at different times and by dis
54                      Thus, both the otic and epibranchial placodes form in a common region of ectoder
55                                          The epibranchial placodes generate the neurons of the genicu
56 mapping approach to test the hypothesis that epibranchial placodes give rise to gustatory neurons, wh
57                                   Vertebrate epibranchial placodes give rise to visceral sensory neur
58                           The trigeminal and epibranchial placodes of vertebrate embryos form differe
59 c placode forms the inner ear whereas nearby epibranchial placodes produce sensory ganglia within bra
60 eby the otic placode forms first and induces epibranchial placodes through an Fgf-relay.
61        We find that Bmp4 is expressed in the epibranchial placodes while Bmp7 and PRDC are expressed
62 on in directing the later development of the epibranchial placodes, and how this signalling is regula
63 ding question regarding the induction of the epibranchial placodes, and represents the first elucidat
64 statory neurons were generated from cultured epibranchial placodes, and when cultured alone, axon out
65 e signals that trigger neurogenesis from the epibranchial placodes, this represents the first demonst
66  of the nodose ganglion are derived from the epibranchial placodes, whereas jugular ganglion neurons
67  specifically, gustatory neurons derive from epibranchial placodes, whereas neural crest-derived neur
68 s derived from both cranial neural crest and epibranchial placodes.
69 pment is required for the development of the epibranchial placodes.
70  coincides with the onset of neurogenesis in epibranchial placodes.
71 ventually contribute to the otic vesicle and epibranchial placodes.
72 s required for neurogenesis of the zebrafish epibranchial placodes.
73 des, including trigeminal, lateral line, and epibranchial placodes.
74 ctive signal underlying the formation of the epibranchial placodes.
75 ordia and posterior (otic, lateral line, and epibranchial) placodes of vertebrates probably evolved f
76                                   The mutant epibranchial progenitor cells fail to express Neurog2 th
77 for the segregation of the otic lineage from epibranchial progenitors.
78                         We further show that epibranchial sox3 expression is unaffected in mutants in