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1 vates a transcriptional program of embryonic foregut endoderm.
2 helial lineages that arise from the anterior foregut endoderm.
3 rise in close proximity from the multipotent foregut endoderm.
4 id-lineage specification, respectively, from foregut endoderm.
5 swim bladder development from a multipotent foregut endoderm.
6 lishment of respiratory progenitors in mouse foregut endoderm.
7 of both trachea and lung, initiates from the foregut endoderm.
8 ce, Sonic hedgehog (Shh) is downregulated in foregut endoderm.
9 diac mesoderm are involved in patterning the foregut endoderm.
10 mits the right and left sides of the ventral foregut endoderm.
11 ition of pancreatic fate by undifferentiated foregut endoderm.
12 participate in liver and lung formation from foregut endoderm.
13 n of buds at specific sites in the embryonic foregut endoderm.
14 s, we identified 363 lncRNAs in the lung and foregut endoderm.
15 ufficient to induce the liver in the ventral foregut endoderm.
16 iation in a larger region of PDX1-expressing foregut endoderm.
17 ive domain for Wnt signaling activity in the foregut endoderm.
18 pulmonary epithelium is a derivative of the foregut endoderm.
19 ifferentiate pluripotent cells into anterior foregut endoderm (AFE) derivatives would expand their ut
22 ctive signal for posterior neuroectoderm and foregut endoderm and a permissive signal for trunk mesod
24 on factor Islet1 (Isl1) is expressed in both foregut endoderm and cardiogenic mesoderm and is require
25 blishing the developmental competence of the foregut endoderm and in initiating liver specification.
26 scription factor, FOXA2, is expressed in the foregut endoderm and in subsets of respiratory epithelia
27 ic hedgehog (Shh) is widely expressed in the foregut endoderm and is specifically upregulated in the
29 d for robust osr1 and osr2 expression in the foregut endoderm and surrounding lateral plate mesoderm
31 Therefore, Hhex expression in the ventral foregut endoderm and/or the endothelium is necessary for
32 light onto how the multipotent cells of the foregut endoderm, and subsequently those of the hepatopa
33 yngeal pouches, which form by budding of the foregut endoderm, are essential for segmentation of the
34 N family protein Cerberus within presumptive foregut endoderm as essential for differentiation of car
36 re and heart at E9.0-9.5, and in the ventral foregut endoderm at E8.5-9.0, it has been postulated to
38 ased cell death in ventral neuroectoderm and foregut endoderm, but normal cranial neural crest produc
39 alian pulmonary progenitors from the ventral foregut endoderm, but their epistatic relationship and d
40 Although the PI3K pathway is activated in foregut endoderm cells, its inhibition does not block he
43 The notochord was adjacent to the dorsal foregut endoderm during the fourth week of development b
44 In the absence of cardiac mesoderm, ventral foregut endoderm explants respond to exogenous fibroblas
45 ely, RA receptor function is required in the foregut endoderm for insulin expression, but not in meso
46 by GATA factors, is critical in presumptive foregut endoderm for normal heart tube morphogenesis.
47 h the establishment of competence within the foregut endoderm for responding to organ-specific signal
49 , we propose that the S1P-dependent anterior foregut endoderm functions primarily through Shh to regu
50 s of Nkx2-1(+) progenitors in the developing foregut endoderm give rise to the entire postnatal lung
52 ng early respiratory system development, the foregut endoderm gives rise to the tracheal and lung cel
53 marker for developing liver and pancreas in foregut endoderm has recently been shown to interact wit
54 tissues are both derived from the posterior foregut endoderm, however, the interdependence of these
56 loss of hdac1 results in an expansion of the foregut endoderm in the domain from which the liver and
58 ates with evagination of two ventral buds of foregut endoderm into the underlying splanchnic mesoderm
59 iver and biliary primordium emerges from the foregut endoderm, invades the septum transversum mesench
60 The onset of pancreas development in the foregut endoderm is marked by activation of the homeobox
61 we find that the default fate of the ventral foregut endoderm is to activate the pancreas gene progra
62 tion of beta-Catenin (also termed Ctnnb1) in foregut endoderm leads to absence of both the trachea an
64 In embryos deficient for both genes in the foregut endoderm, no liver bud is evident and expression
65 ding indicates that Pdx-1 is required in the foregut endoderm prior to Ptf1a for pancreatic MPC speci
66 s that result in lung specification from the foregut endoderm, prior to lung bud formation, are poorl
71 ung development, is expressed in the ventral foregut endoderm shortly after albumin and Pdx1, early m
72 uired for development of organs derived from foregut endoderm such as lung, liver, gall bladder, and
73 lls are derived from cell progenitors in the foregut endoderm that subsequently differentiate into th
74 blished that the fetal liver originates from foregut endoderm, the identity of the mechanisms that ma
75 When the pancreatic epithelium buds off the foregut endoderm, the pancreatic mesenchyme diffusely ex
76 bryonic stem cells (ESCs) was converted into foregut endoderm, then into replicating Nkx2.1+ lung end
77 , AmphiNk2-tin is expressed first within the foregut endoderm, then transiently in muscle precursor c
78 he liver and pancreas are specified from the foregut endoderm through an interaction with the adjacen
80 n implicated in the definition of liver from foregut endoderm where FGFR4 is expressed and stimulatio
81 re regulated by hedgehog expression from the foregut endoderm, which is required for connection of th
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