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1 response gene to signals from the organizer (Hensen's node).
2  organizer (the tip of the primitive streak, Hensen's node).
3  locally activates Notch on the left side of Hensen's node.
4 cular signals on the left and right sides of Hensen's node.
5 many markers as they initially extend out of Hensen's node.
6 g cells into and out of the chick organizer, Hensen's node.
7 e initiated by signals located in and around Hensen's node.
8  the neurula by stage 7 at levels rostral to Hensen's node.
9 rder to pattern left-sided Shh expression at Hensen's node.
10 ng chick embryogenesis in small domains near Hensen's node.
11 terning normal left-right gene expression at Hensen's node.
12 ndary neuraxis, identical to that induced by Hensen's node.
13 at this density expresses typical markers of Hensen's node.
14 nerated an immortalized cell line from young Hensen's node.
15 esicle (KV), a ciliated structure similar to Hensen's node.
16 crescents flanking the area rostrolateral to Hensen's node.
17  of sonic hedgehog (Shh) in the left side of Hensen's node, a crucial step for specifying the left-ri
18 avian embryos, organizer cells reside within Hensen's node, a transient structure located at the tip
19 ric crescents located immediately rostral to Hensen's node and appears to pre-configure the emerging
20 of BMP-4 also arrests further development of Hensen's node and axial structures.
21  are, therefore, free from the influences of Hensen's node and ingressing axial mesoderm - tissues th
22 Gdf11, and retinoid signals originating from Hensen's node and paraxial mesoderm establish and refine
23 that Pax-3 inductive activities arising from Hensen's node and posterior non-axial mesoderm do not st
24                                      Second, Hensen's node and posterior non-axial mesoderm which und
25 12-14), the tailbud contains the remnants of Hensen's node and the primitive streak.
26 d using cultured blastoderm isolates lacking Hensen's node and the primitive streak.
27 ordal inducer also induces the reconstituted Hensen's node and, therefore, acts like a Nieuwkoop Cent
28 derm, notochord, neural plate, mesoderm, and Hensen's node, and between cells in different tissues, e
29 rain and neural tube, caudalward movement of Hensen's node, and establishment of normal left-right as
30 prospective notochord cells contained within Hensen's node are able to induce supernumerary digits, w
31 erges from the anterior primitive streak and Hensen's node as a cell monolayer that replaces hypoblas
32 ed asymmetrically, only on the right side of Hensen's node, at the correct time for it to be the endo
33 tablishment of asymmetric gene expression in Hensen's node based on the epistatic interactions observ
34 f4 is expressed in the notochord anterior to Hensen's node before transcripts for the earliest molecu
35 The avian equivalent of Spemann's organizer, Hensen's node, begins to lose its ability to induce a ne
36 espond to neural induction by the organizer (Hensen's node) between stages 4 and 4+.
37 Shh, which is initially expressed throughout Hensen's node but becomes restricted to the left side at
38 d medial somite do not originate solely from Hensen's node, but also from the anterior primitive stre
39          We have shown previously that young Hensen's node can act in vitro to regulate the expressio
40 sent study it is demonstrated that grafts of Hensen's node can induce the formation of supernumerary
41                                 In contrast, Hensen's node can promote formation of IM in the lateral
42                  These results indicate that Hensen's node can provide a limb-forming signal to the l
43                  It is well established that Hensen's nodes can induce the formation of supernumerary
44 hown that TGF-betas can mimic the effects of Hensen's node cells on neural crest differentiation.
45 s are accomplished through an integration of Hensen's node-derived and paraxial mesoderm signaling.
46 left-right asymmetric genes are expressed at Hensen's node during chick gastrulation.
47  forms a density, morphologically similar to Hensen's node, during the first 10-12 hours in culture,
48 or when labeled and transplanted in place of Hensen's node, forms typical derivatives of Hensen's nod
49                         Here, we report that Hensen's node from vitamin A-deficient quail embryo indu
50 ecreting cells, the competence to respond to Hensen's node grafts is retained.
51 imbs that form from the flank in response to Hensen's node grafts often contain elongated, jointed ca
52  time of action of these signals to and from Hensen's node in establishing left-right asymmetry.
53 Activin-betaB and Bmp4, in the right side of Hensen's node in the developing embryo.
54 a chicken embryo elicit different responses: Hensen's node induces a neural plate whereas the head me
55 as a responding tissue, late, but not early, Hensen's node induces Pax-3 expression.
56                           Here, we show that Hensen's node is composed of two transcriptionally and f
57  revealed asymmetry of Shh expression in the Hensen's node of both vitamin A-sufficient and -deficien
58 ed that Fgf and Gdf11 signals located around Hensen's node of chick embryos have the ability to induc
59 activity was initially apparent posterior to Hensen's node of stage 5-6 embryos and subsequently in s
60                                              Hensen's node of the chick embryo contains multipotent s
61 appropriate numbers of progenitor cells from Hensen's node of the chick embryo to the notochord and t
62 metric expression of Sonic hedgehog (Shh) in Hensen's node of the chicken embryo plays a key role in
63 y neurula stage (i.e., stage 3d/4) that lack Hensen's node (organizer) and primitive streak can recon
64 essive relationship between Shh and cMid1 in Hensen's node plays a key role in establishing the avian
65            Additionally, the architecture of Hensen's node raises doubts as to whether Ca(i)(2+) asym
66 strulation, the cellular architecture of the Hensen's node remains poorly understood.
67  Hensen's node, forms typical derivatives of Hensen's node such as endoderm, notochord and the floor
68 GF/SF secreting cells can mimic signals from Hensen's node that maintain L5 expression, they cannot r
69 directly from the extreme rostral portion of Hensen's node, the avian equivalent of the Spemann organ
70                                         Both Hensen's node, the organizer center in chick embryo, and
71 del system was preceded by reconstitution of Hensen's node, the organizer of the avian neuraxis.
72 eft-side enriched Ca(i)(2+) asymmetry across Hensen's node to govern its lateral identity.
73 cascade moving sequentially from the area of Hensen's node to the somitic mesoderm, the intermediate
74 cascade moving sequentially from the area of Hensen's node to the somitic mesoderm, the intermediate
75  an activin-like factor on the right side of Hensen's node was suggested because ectopic activin prot
76 pressor of notochord reconstitution, as does Hensen's node, when transplanted to other blastoderm iso
77 ast cells flanking the late-phase organizer (Hensen's node), which retains its ability to induce cash
78 ody form from a growth zone at the tail end, Hensen's node, which generates neural, mesodermal, and e
79 ding to Spemann's organizer in amphibians is Hensen's node, which lies at the tip of the primitive st
80 rimitive streak, lateral plate mesoderm, and Hensen's node, while distinct SRF expression was seen la
81 hway controls Nodal expression in and around Hensen's node, without affecting the upstream regulators