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1 response gene to signals from the organizer (Hensen's node).
2 locally activates Notch on the left side of Hensen's node.
3 cular signals on the left and right sides of Hensen's node.
4 many markers as they initially extend out of Hensen's node.
5 g cells into and out of the chick organizer, Hensen's node.
6 e initiated by signals located in and around Hensen's node.
7 the neurula by stage 7 at levels rostral to Hensen's node.
8 rder to pattern left-sided Shh expression at Hensen's node.
9 ng chick embryogenesis in small domains near Hensen's node.
10 terning normal left-right gene expression at Hensen's node.
11 ndary neuraxis, identical to that induced by Hensen's node.
12 at this density expresses typical markers of Hensen's node.
13 nerated an immortalized cell line from young Hensen's node.
14 esicle (KV), a ciliated structure similar to Hensen's node.
15 crescents flanking the area rostrolateral to Hensen's node.
16 of sonic hedgehog (Shh) in the left side of Hensen's node, a crucial step for specifying the left-ri
17 ric crescents located immediately rostral to Hensen's node and appears to pre-configure the emerging
19 are, therefore, free from the influences of Hensen's node and ingressing axial mesoderm - tissues th
20 Gdf11, and retinoid signals originating from Hensen's node and paraxial mesoderm establish and refine
21 that Pax-3 inductive activities arising from Hensen's node and posterior non-axial mesoderm do not st
25 ordal inducer also induces the reconstituted Hensen's node and, therefore, acts like a Nieuwkoop Cent
26 derm, notochord, neural plate, mesoderm, and Hensen's node, and between cells in different tissues, e
27 rain and neural tube, caudalward movement of Hensen's node, and establishment of normal left-right as
28 prospective notochord cells contained within Hensen's node are able to induce supernumerary digits, w
29 erges from the anterior primitive streak and Hensen's node as a cell monolayer that replaces hypoblas
30 ed asymmetrically, only on the right side of Hensen's node, at the correct time for it to be the endo
31 tablishment of asymmetric gene expression in Hensen's node based on the epistatic interactions observ
32 f4 is expressed in the notochord anterior to Hensen's node before transcripts for the earliest molecu
33 The avian equivalent of Spemann's organizer, Hensen's node, begins to lose its ability to induce a ne
35 Shh, which is initially expressed throughout Hensen's node but becomes restricted to the left side at
36 d medial somite do not originate solely from Hensen's node, but also from the anterior primitive stre
38 sent study it is demonstrated that grafts of Hensen's node can induce the formation of supernumerary
42 hown that TGF-betas can mimic the effects of Hensen's node cells on neural crest differentiation.
43 s are accomplished through an integration of Hensen's node-derived and paraxial mesoderm signaling.
45 forms a density, morphologically similar to Hensen's node, during the first 10-12 hours in culture,
46 or when labeled and transplanted in place of Hensen's node, forms typical derivatives of Hensen's nod
49 imbs that form from the flank in response to Hensen's node grafts often contain elongated, jointed ca
52 a chicken embryo elicit different responses: Hensen's node induces a neural plate whereas the head me
54 revealed asymmetry of Shh expression in the Hensen's node of both vitamin A-sufficient and -deficien
55 ed that Fgf and Gdf11 signals located around Hensen's node of chick embryos have the ability to induc
56 activity was initially apparent posterior to Hensen's node of stage 5-6 embryos and subsequently in s
58 appropriate numbers of progenitor cells from Hensen's node of the chick embryo to the notochord and t
59 metric expression of Sonic hedgehog (Shh) in Hensen's node of the chicken embryo plays a key role in
60 y neurula stage (i.e., stage 3d/4) that lack Hensen's node (organizer) and primitive streak can recon
61 essive relationship between Shh and cMid1 in Hensen's node plays a key role in establishing the avian
63 Hensen's node, forms typical derivatives of Hensen's node such as endoderm, notochord and the floor
64 GF/SF secreting cells can mimic signals from Hensen's node that maintain L5 expression, they cannot r
65 directly from the extreme rostral portion of Hensen's node, the avian equivalent of the Spemann organ
69 cascade moving sequentially from the area of Hensen's node to the somitic mesoderm, the intermediate
70 cascade moving sequentially from the area of Hensen's node to the somitic mesoderm, the intermediate
71 an activin-like factor on the right side of Hensen's node was suggested because ectopic activin prot
72 pressor of notochord reconstitution, as does Hensen's node, when transplanted to other blastoderm iso
73 ast cells flanking the late-phase organizer (Hensen's node), which retains its ability to induce cash
74 ding to Spemann's organizer in amphibians is Hensen's node, which lies at the tip of the primitive st
75 rimitive streak, lateral plate mesoderm, and Hensen's node, while distinct SRF expression was seen la
76 hway controls Nodal expression in and around Hensen's node, without affecting the upstream regulators
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