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1 pheral nervous system, developing liver, and surface ectoderm.
2 the lens fails to detach completely from the surface ectoderm.
3 istent adhesion of the lens to the overlying surface ectoderm.
4 luding retinal cells, lens cells, and ocular-surface ectoderm.
5 m depends on its interaction with overlaying surface ectoderm.
6 m, neural crest, ocular-surface ectoderm, or surface ectoderm.
7 on, cells retained the expression profile of surface ectoderm.
8  mouse line, which expresses Cre in the head surface ectoderm.
9 gression in the urethral endoderm and in the surface ectoderm.
10 r midline transition between neural tube and surface ectoderm.
11 imary mechanism for lens separation from the surface ectoderm.
12   In the mouse, the lens forms from the head surface ectoderm.
13 ation of beta-catenin expression in the head surface ectoderm.
14 ed in an overlapping manner with Wise in the surface ectoderm.
15 ese tissues, a crucial source of Edn1 is the surface ectoderm.
16  with more focused QSulf1 expression in r2/3 surface ectoderm.
17 on arising from the border of the neural and surface ectoderm.
18 maintained independently of r5, but requires surface ectoderm.
19 a tissue explant containing neural plate and surface ectoderm.
20  antagonistic signals from the notochord and surface ectoderm.
21 estigate the divergence between amniotic and surface ectoderms.
22 tocols were used to replace FGF secretion by surface ectoderm: (1) implantation of FGF-secreting fibr
23   To test this hypothesis in vivo we removed surface ectoderm, a rich source of FGFs.
24 differentiation of pluripotent stem cells to surface ectoderm and cranial neural crest cells, which g
25 teins mediate the dorsalizing effects of the surface ectoderm and dorsal neural tube on somites.
26 irecting sclerotome development, whereas the surface ectoderm and dorsal neural tube provide a dorsal
27 y the sclerotome, while the dorsally located surface ectoderm and dorsal neural tube provide the dors
28 at the surrounding extraocular tissues - the surface ectoderm and extraocular mesenchyme - are necess
29 th factors, which emanate from the overlying surface ectoderm and induce the adjacent neuroepithelium
30 cial tissue-specific functions in patterning surface ectoderm and its appendages by controlling divis
31 gnals from the axial tissues, as well as the surface ectoderm and lateral plate mesoderm, together ac
32 g their activation by Wnt signaling from the surface ectoderm and neural tube.
33 araxial mesoderm and in arch epithelia, both surface ectoderm and pharyngeal endoderm, but not in ske
34 development proceeds, including those of the surface ectoderm and placental vasculature.
35  the lens vesicle fails to separate from the surface ectoderm and the maturing lens is smaller and sh
36 inductive interactions between the embryonic surface ectoderm and the underlying neuroepithelium of t
37 g is ectopically activated in central ocular surface ectoderm and underlying mesenchyme in Pitx2- and
38 d, Brn-3.0 neurons develop in the absence of surface ectoderm and ventral midline tissue, suggesting
39 gen were expressed from E12 posterior to the surface ectoderm, and became widespread from E14.
40 ate eye is derived from the neuroepithelium, surface ectoderm, and extracellular mesenchyme.
41 A levels are detected in somites, the dorsal surface ectoderm, and in vertebral cartilage primordia.
42              Par1 and Par2 were expressed in surface ectoderm, and Par2 was expressed selectively alo
43 The lens vesicle failed to separate from the surface ectoderm, and prospective lens and corneal epith
44 tic FGF10 with progressive maturation of the surface ectoderm, and show that full expression of somit
45 ad domain, including tissues in the foregut, surface ectoderm, and the head ganglion of the central n
46 ally exit it, thereby colonizing the ventral surface ectoderm anterior to the VER.
47 expressed in both the dorsal neural tube and surface ectoderm are also potent inhibitors of myogenesi
48  we propose that human amniotic ectoderm and surface ectoderm are specified along a common nonneural
49  Mechanisms specifying amniotic ectoderm and surface ectoderm are unresolved in humans due to their c
50 nterface between the neuroepithelium and the surface ectoderm, are required for completion of neural
51 d that PAA formation requires the pharyngeal surface ectoderm as a key signalling centre from which G
52 phalic neuroblasts which delaminate from the surface ectoderm as individual cells, cells of the dorso
53  hpf, before separation of the lens from the surface ectoderm, as evidenced by cell elongation, exit
54  strong regional expression in ventrolateral surface ectoderm at E10.5, much earlier than previously
55  is patterned molecularly, with dorsolateral surface ectoderm at the levels of r2/3 and r7 expressing
56 rsal neural tube and of Wnt4 and Wnt6 in the surface ectoderm at the time of dermomyotome specificati
57  crest cells that arise at the neuroectoderm/surface ectoderm border, but not for their initial forma
58 ting in a lateral shift of the neuroectoderm/surface ectoderm border.
59 have ablated the lens precursor cells of the surface ectoderm by generation of transgenic mice that e
60                             We observed that surface ectoderm cells surrounding the mouse HNP assembl
61 ion of integrin beta1 and focal anchorage of surface ectoderm cells to a shared point of fibronectin-
62                                Attachment of surface ectoderm cells to the neural plate is required f
63                                              Surface ectoderm cells undergo proximal junction shorten
64 ese results indicate that, in the absense of surface ectoderm, cells of the optic vesicles display bo
65           Mechanistically, TFAP2C primes the surface ectoderm chromatin landscape and induces p63 exp
66 tgrowth involve coordinated morphogenesis of surface ectoderm, cloacal mesoderm and hindgut endoderm.
67 t contact between pharyngeal pouches and the surface ectoderm coincides with the onset of neurogenesi
68  During skin development, the single-layered surface ectoderm covering the mouse embryo must initiate
69 ed cranial neural tissue and reduced cranial surface ectoderm culminating in a lateral shift of the n
70  corneal morphogenesis, we deleted Cited2 in surface ectoderm derived ocular structures including cor
71  we deleted the Klf4 gene selectively in the surface ectoderm-derived structures of the eye (cornea,
72 AP2C, but not p63, is sufficient to initiate surface ectoderm differentiation, and TFAP2C-initiated p
73 porters, we showed that Wnt ligands from the surface ectoderm directly or indirectly elicit a Wnt/bet
74          The mammary gland develops from the surface ectoderm during embryogenesis and proceeds throu
75 F can mimic one of the earliest functions of surface ectoderm during eye development, namely the dema
76             Lack or excess expression of the surface ectoderm-expressed transcription factor Grainyhe
77                                          The surface ectoderm expresses BMP-4 and we show that it is
78                                          The surface ectoderm expresses FGFs and the optic vesicles e
79  NC development, while blocking placodal and surface ectoderm fates.
80 chyme/BMP specifies pigmented epithelium and surface ectoderm/FGF specifies neural retina.
81  however, from the hindbrain forward, little surface ectoderm forms and the forebrain is enlarged and
82 led an intermediate cell state with enhanced surface ectoderm gene expression.
83 and weakly in the surrounding mesenchyme and surface ectoderm, has crucial roles during lens inductio
84 vative, while the dorsal neural tube and the surface ectoderm have been shown to direct somite cells
85      Cells lacking Bmpr1a also contribute to surface ectoderm; however, from the hindbrain forward, l
86                               General ocular surface ectoderm identity is maintained during developme
87 on by signals from neural tube/notochord and surface ectoderm in cultured presomitic mesoderm (PSM),
88 inhibits separation of the lens vesicle from surface ectoderm in mice heterozygous or homozygous for
89 Thus, BMP-4 signaling can substitute for the surface ectoderm in supporting nephric duct morphogenesi
90 d in the arch mesenchyme, pouch endoderm and surface ectoderm in the pharyngeal region of Eya1(-/-) e
91 ally fated to give rise to neuroectoderm and surface ectoderm, in a serum-free, chemically defined me
92 ndance of Grhl2 generates a super-epithelial surface ectoderm, in which up-regulation of cell-cell ju
93 te that r3 neuroepithelium and its overlying surface ectoderm independently help maintain the NCC-fre
94 found two critical chromatin networks during surface ectoderm initiation and keratinocyte maturation,
95                                   The facial surface ectoderm is essential for normal development of
96   Finally, we demonstrate that avian cranial surface ectoderm is patterned molecularly, with dorsolat
97 to the nephric duct and demonstrate that the surface ectoderm is required for its differentiation.
98  tissue explants in vitro and confirmed that surface ectoderm is sufficient to induce paraxis express
99 gest that inductive interactions between the surface ectoderm, lateral mesoderm and intermediate meso
100 s indicative of lineage, spanning the ocular surface ectoderm, lens, neuro-retina, and retinal pigmen
101 ults also suggest that the lens cells of the surface ectoderm may be critical for the proper differen
102 gonistic signals from the dorsal neural tube/surface ectoderm, mediated by WNTs, and from the ventral
103 sensory neurons originate in placodes in the surface ectoderm, migrating to form ganglia that connect
104 c basis for the known synergistic actions of surface ectoderm/neural tube and notochord signaling in
105                                         This surface ectoderm/neural tube Wnt signaling has both nega
106 mesenchyme, pouch endoderm, and possibly the surface ectoderm of 3rd pharyngeal clefts.
107 RA) synthesized by Raldh3 in the frontonasal surface ectoderm of chick embryos has been suggested to
108                   Acvr1 was deleted from the surface ectoderm of mouse embryos on embryonic day 9 usi
109                   Finally, we found that the surface ectoderm of the 3rd and 4th pharyngeal region sh
110  placode which normally invaginates from the surface ectoderm of the embryo and gives rise to two sep
111 hat associated with Raldh3 expression in the surface ectoderm of the eye field.
112 ion of five pairs of mammary placodes in the surface ectoderm of the mouse embryo.
113 amined the influence of axial structures and surface ectoderm on paraxis expression by performing mic
114 sembling neuroectoderm, neural crest, ocular-surface ectoderm, or surface ectoderm.
115  that Wise, a Wnt modulator expressed in the surface ectoderm overlying the trigeminal ganglion, play
116 lly programmed events involving induction of surface ectoderm, preliminary morphogenesis, specificati
117 trix (ECM) between the optic vesicle and the surface ectoderm prevents the prospective lens cells fro
118 that the dermal progenitor cells beneath the surface ectoderm process canonical Wnt signaling at the
119 n and close a subset of the TFAP2C-initiated surface ectoderm program.
120 signals from the neural tube, notochord, and surface ectoderm promote somitic myogenesis.
121                           We showed that the surface ectoderm region that includes the lens placode e
122 ung mice (<P30), which derive from embryonic surface ectoderm remain undifferentiated and serve as co
123                                    Following surface ectoderm removal, mainly r4 NCCs enter r3 mesenc
124 f a BMP-4-coated bead to embryos lacking the surface ectoderm restored normal levels of Sim-1 and Pax
125                               Removal of the surface ectoderm resulted in decreased levels of Sim-1 a
126               Conversely, the removal of the surface ectoderm results in the maintenance of MITF in t
127                                              Surface ectoderm (SE) cells give rise to structures incl
128 re key epigenomes of cell types derived from surface ectoderm (SE), including keratinocytes and breas
129                                   Grhl2 null surface ectoderm shows a shift from epithelial to neuroe
130 ation by signals from dorsal neural tube and surface ectoderm stimulates the development of the dermo
131 n regulating biomechanical properties of the surface ectoderm that are essential for spinal neurulati
132  the neuroectoderm that forms the retina and surface ectoderm that forms the lens.
133 riginate from Pax3-expressing regions of the surface ectoderm that normally contribute to the ophthal
134  synergise with dorsalising signals from the surface ectoderm to induce the formation of the hypaxial
135 ns with the commitment of the single-layered surface ectoderm to initiate a stratification program, a
136 AP-2alpha is required for signaling from the surface ectoderm to the underlying mesoderm for proper d
137  it, in conjunction with DiI labeling of the surface ectoderm, to analyze some of the mechanisms unde
138 En1-expressing cells directly underneath the surface ectoderm transduce Wnt signals.
139 e co-Smad Smad4 were deleted from the ocular surface ectoderm using Cre recombinase.
140 mbryos, the persistent connection of lens to surface ectoderm was associated with aborted lens develo
141 actor, Pax6 was conditionally deleted in the surface ectoderm was associated with greatly diminished
142 es, but Raldh3 expression in the frontonasal surface ectoderm was found to be needed for normal Fgf8
143 to the ECM between the optic vesicle and the surface ectoderm was sufficient to explain lens placode
144 e of separation of the lens vesicle from the surface ectoderm was the earliest structural defect obse
145 c42 in the dorsal neuroepithelium, or in the surface ectoderm, we show that these protrusions origina
146 ess of somite formation and signals from the surface ectoderm, whereas upregulation of patched and ac
147 patial development of cells derived from the surface ectoderm, which become corneal epithelium and le
148 le, the corneal epithelium is descended from surface ectoderm, while the iris and collagen-rich strom
149                             Wnt-modulator in surface ectoderm (WISE) is a secreted modulator of Wnt s
150 r plate (Shh), dorsal neural tube (Wnt1) and surface ectoderm (Wnt1-like signalling activity) but neg

 
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