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1 ipes depend on light-reflecting cells called iridophores.
2 ophores, yellow xanthophores, and iridescent iridophores.
3  with light interstripes of xanthophores and iridophores.
4 d those cells instruct the patterning of the iridophores.
5  foxd3, a mitfa repressor, resulted in fewer iridophores.
6 ophores, yellow xanthophores, and iridescent iridophores.
7 ophores, yellow xanthophores, and iridescent iridophores.
8  melanocytes, yellow xanthophores and silver iridophores.
9 ut development but have increased numbers of iridophores.
10  crest differentiation into melanophores and iridophores.
11 ent cells: black melanophores and reflective iridophores.
12 region shows specific enhancer activities in iridophores, a type of pigment cells found in egg-spots,
13 from two MTOCs located near the poles of the iridophore and run parallel to, and in between, individu
14 bryogenesis: yellow xanthophores, iridescent iridophores and black melanophores.
15 compare them to guanine crystal formation in iridophores and pterin formation in xanthophores.
16 ee to four pigment cell types (melanophores, iridophores and xanthophores, plus leucophores e.g. in m
17 c skin, we confirm that PAX7 is expressed in iridophores and xanthophores, suggesting that it plays a
18 e stripes, alternating with light stripes of iridophores and xanthophores.
19 consisting of alternating dark (melanophore, iridophore) and light (xanthophore, iridophore) horizont
20 ring embryogenesis, and cells of melanocyte, iridophore, and xanthophore lineages all express this ge
21 pigment cells (chromatophores)-xanthophores, iridophores, and melanophores-in calcium phosphate.
22 inct adult pigment cell types: melanophores, iridophores, and xanthophores.
23  melanocytes and a corresponding decrease in iridophores, another neural crest-derived pigment cell t
24 ures, indicating that stripe and interstripe iridophores are different cell types.
25 With our histological analyses, we show that iridophores are present in the white and yellow bands of
26 oducing founding stem cells (mFSCs), whereas iridophores arise from distinct precursors.
27 ophores, yellow xanthophores, and shimmering iridophores arranged in a characteristic pattern of gold
28 anthosomes in xanthophores and iridosomes in iridophores as lysosome-related organelles.
29 hat their skin is devoid of xanthophores and iridophores at both stages.
30 es indicate that Tjp1a is expressed in dense iridophores but down-regulated in the loose form.
31 xd3 expression in xanthophore precursors and iridophores, but not in terminally differentiated melano
32 ifferentiation, especially in the context of iridophore cell fate, is poorly understood.
33 premature guanine crystals in underdeveloped iridophore cells.
34 tionally demonstrated that iridescent cells (iridophores) containing Bragg reflectors with sinusoidal
35 in patterning in zebrafish in which distinct iridophore crystallotypes containing specialized, physio
36 vidence for a model whereby melanophores and iridophores descend from a common precursor whose fate i
37 , EosFP, revealed that both melanophores and iridophores develop from a mitfa+ precursor.
38 1 and aug-alpha2 are essential for embryonic iridophore development and adult body coloration.
39 ocalized with pnp4a, a novel marker of early iridophore development, and was necessary for its expres
40 oxd3's roles is to suppress mitfa to promote iridophore development.
41 sary and sufficient transcription factor for iridophore differentiation and present evidence on alx4a
42 e Ltk in a tissue-specific context to induce iridophore differentiation from neural crest-derived cel
43 a multipotent stage, with signalling driving iridophore differentiation through repression of fate-sp
44                   However, here we find that iridophores do not migrate between stripes and interstri
45 anization of crystal arrays within zebrafish iridophores during norepinephrine (NE)-induced color cha
46 to develop normal numbers of melanocytes and iridophores during pigment pattern metamorphosis and exh
47 - and/or carotenoid-containing vesicles, and iridophores filled with light-reflecting platelets gener
48 t, aug-alpha2 and aug-beta are essential for iridophore formation in the adult eye.
49  further reveals that stripe and interstripe iridophores have different transcriptomic states, while
50 nophore, iridophore) and light (xanthophore, iridophore) horizontal stripes.
51 bit simple stripes of melanocytes and silver iridophores in a background of yellow xanthophores, this
52 tfec affect coloration and lead to a loss of iridophores in Anolis, indicating that tfec is required
53 e findings for the design and development of iridophore-inspired multispectral composite materials wi
54         We hypothesize that the melanophores-iridophores interactions give rise to the banded pattern
55 including epidermis, melanocyte/xanthophore, iridophore, intraray glia, lateral line, osteoblast, der
56 s, the dark stripes are interrupted by dense iridophores invading as coherent sheets.
57 s color pattern arises from a single type of iridophore migrating differentially to stripes and inter
58 tent pigment precursor will attain either an iridophore or a melanophore fate.
59 at leucophores share molecular pathways with iridophores, particularly those connected to organelle o
60 and aug-beta results in strong impairment in iridophore patterning of embryonic and adult zebrafish t
61 cartilage, peripheral neurons, and glia, and iridophore pigment cells.
62 igmentation defects in which xanthophore and iridophore pigmentation is almost completely absent, and
63                                              Iridophores play a crucial part in this process by switc
64 ett (sbr) mutants exhibit delayed changes in iridophore shape and organisation caused by truncations
65  work led to the discovery and validation of iridophore-specific alx4a transcription factor.
66 g the roles of domain growth and the initial iridophore stripe, and to generate hypotheses about the
67 , comprising a series of dark melanocyte and iridophore stripes, alternating with light stripes of ir
68 in xanthophores and melanophores, but not in iridophores, suggest that both connexins form heteromeri
69       Double mutants showed a restoration of iridophores, suggesting that one of Foxd3's roles is to
70 ed only by a subset of adult melanocytes and iridophores, these analyses also reveal variation among
71  crest differentiation into melanophores and iridophores to identify epigenetic determinants shaping
72 is effort, in the relatively uncharacterized iridophores, we validate alx4a as a necessary and suffic
73 hores for interactions with xanthophores and iridophores, which cause location-specific pigment cell
74 velopment, resulted in supernumerary ectopic iridophores while loss of foxd3, a mitfa repressor, resu
75 tripe pattern is a complex tissue containing iridophores, xanthophores and multiple melanocyte types.