戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ding appropriate pancreas formation from the foregut endoderm.
2 s, we identified 363 lncRNAs in the lung and foregut endoderm.
3 ive domain for Wnt signaling activity in the foregut endoderm.
4 helial lineages that arise from the anterior foregut endoderm.
5 rise in close proximity from the multipotent foregut endoderm.
6  swim bladder development from a multipotent foregut endoderm.
7 lishment of respiratory progenitors in mouse foregut endoderm.
8 of both trachea and lung, initiates from the foregut endoderm.
9 vates a transcriptional program of embryonic foregut endoderm.
10 ce, Sonic hedgehog (Shh) is downregulated in foregut endoderm.
11 id-lineage specification, respectively, from foregut endoderm.
12 diac mesoderm are involved in patterning the foregut endoderm.
13 mits the right and left sides of the ventral foregut endoderm.
14 ition of pancreatic fate by undifferentiated foregut endoderm.
15 participate in liver and lung formation from foregut endoderm.
16 n of buds at specific sites in the embryonic foregut endoderm.
17 ufficient to induce the liver in the ventral foregut endoderm.
18 iation in a larger region of PDX1-expressing foregut endoderm.
19  pulmonary epithelium is a derivative of the foregut endoderm.
20 wnt2/2b, which induces pulmonary fate in the foregut endoderm.
21         Approaches to study human pharyngeal foregut endoderm-a developmental intermediate that is li
22 ifferentiate pluripotent cells into anterior foregut endoderm (AFE) derivatives would expand their ut
23           Subsequently, lung-biased anterior foregut endoderm (AFE) is specified by sequential inhibi
24                                 However, the foregut endoderm also expresses the Wnt-receptor Frizzle
25 ctive signal for posterior neuroectoderm and foregut endoderm and a permissive signal for trunk mesod
26          In addition, we find defects in the foregut endoderm and a reduction in Hex expression, whic
27 on factor Islet1 (Isl1) is expressed in both foregut endoderm and cardiogenic mesoderm and is require
28 blishing the developmental competence of the foregut endoderm and in initiating liver specification.
29 scription factor, FOXA2, is expressed in the foregut endoderm and in subsets of respiratory epithelia
30 ic hedgehog (Shh) is widely expressed in the foregut endoderm and is specifically upregulated in the
31 c prechordal plate (consisting of the dorsal foregut endoderm and mesoderm) and the brain.
32 d for robust osr1 and osr2 expression in the foregut endoderm and surrounding lateral plate mesoderm
33 r the establishment of competence within the foregut endoderm and the onset of hepatogenesis.
34    Therefore, Hhex expression in the ventral foregut endoderm and/or the endothelium is necessary for
35  light onto how the multipotent cells of the foregut endoderm, and subsequently those of the hepatopa
36 drive their lineage diversification from the foregut endoderm are not fully understood.
37 ung epithelial primordial progenitors of the foregut endoderm are thought to be the developmental pre
38 yngeal pouches, which form by budding of the foregut endoderm, are essential for segmentation of the
39 N family protein Cerberus within presumptive foregut endoderm as essential for differentiation of car
40  most mammals the pancreas develops from the foregut endoderm as ventral and dorsal buds.
41 re and heart at E9.0-9.5, and in the ventral foregut endoderm at E8.5-9.0, it has been postulated to
42         Although T1alpha is expressed in the foregut endoderm before the lung buds, T1alpha mRNA and
43 ased cell death in ventral neuroectoderm and foregut endoderm, but normal cranial neural crest produc
44 alian pulmonary progenitors from the ventral foregut endoderm, but their epistatic relationship and d
45    Although the PI3K pathway is activated in foregut endoderm cells, its inhibition does not block he
46                           In contrast, other foregut endoderm-derived organs, including the thyroid,
47  which is known to require an interplay with foregut endoderm development.
48 e notochordal plate, prechordal mesoderm and foregut endoderm during gastrulation.
49     The notochord was adjacent to the dorsal foregut endoderm during the fourth week of development b
50  In the absence of cardiac mesoderm, ventral foregut endoderm explants respond to exogenous fibroblas
51 ely, RA receptor function is required in the foregut endoderm for insulin expression, but not in meso
52  by GATA factors, is critical in presumptive foregut endoderm for normal heart tube morphogenesis.
53 h the establishment of competence within the foregut endoderm for responding to organ-specific signal
54                        Treatment of isolated foregut endoderm from mouse embryos with FGF1 or FGF2, b
55 ntiation method to generate human pharyngeal foregut endoderm from pluripotent stem cells.
56 , we propose that the S1P-dependent anterior foregut endoderm functions primarily through Shh to regu
57 s of Nkx2-1(+) progenitors in the developing foregut endoderm give rise to the entire postnatal lung
58                    During organogenesis, the foregut endoderm gives rise to the many different cell t
59 ng early respiratory system development, the foregut endoderm gives rise to the tracheal and lung cel
60  marker for developing liver and pancreas in foregut endoderm has recently been shown to interact wit
61  tissues are both derived from the posterior foregut endoderm, however, the interdependence of these
62 egulating thyroid lineage specification from foregut endoderm in mouse and Xenopus.
63 loss of hdac1 results in an expansion of the foregut endoderm in the domain from which the liver and
64                     Differentiation of early foregut endoderm into pancreatic endocrine and exocrine
65 ates with evagination of two ventral buds of foregut endoderm into the underlying splanchnic mesoderm
66 iver and biliary primordium emerges from the foregut endoderm, invades the septum transversum mesench
67     The onset of pancreas development in the foregut endoderm is marked by activation of the homeobox
68 we find that the default fate of the ventral foregut endoderm is to activate the pancreas gene progra
69 tion of beta-Catenin (also termed Ctnnb1) in foregut endoderm leads to absence of both the trachea an
70                 Loss of Sin3a in mouse early foregut endoderm led to a specific and profound defect i
71  anterior foregut endoderm, ventral anterior foregut endoderm, lung bud organoids and finally lung or
72   In embryos deficient for both genes in the foregut endoderm, no liver bud is evident and expression
73 ding indicates that Pdx-1 is required in the foregut endoderm prior to Ptf1a for pancreatic MPC speci
74 s that result in lung specification from the foregut endoderm, prior to lung bud formation, are poorl
75   However, the molecular pathways specifying foregut endoderm progenitors are poorly understood.
76 ion of the expression domains of several key foregut endoderm regulators.
77                                     When the foregut endoderm removal is delayed until stage 6, later
78           The stomach, an organ derived from foregut endoderm, secretes acid and enzymes and plays a
79 ung development, is expressed in the ventral foregut endoderm shortly after albumin and Pdx1, early m
80 uired for development of organs derived from foregut endoderm such as lung, liver, gall bladder, and
81 lls are derived from cell progenitors in the foregut endoderm that subsequently differentiate into th
82 blished that the fetal liver originates from foregut endoderm, the identity of the mechanisms that ma
83  When the pancreatic epithelium buds off the foregut endoderm, the pancreatic mesenchyme diffusely ex
84 bryonic stem cells (ESCs) was converted into foregut endoderm, then into replicating Nkx2.1+ lung end
85 , AmphiNk2-tin is expressed first within the foregut endoderm, then transiently in muscle precursor c
86  activates shh transcription in the adjacent foregut endoderm through a conserved MACS1 enhancer.
87 he liver and pancreas are specified from the foregut endoderm through an interaction with the adjacen
88 lecularly distinct anterior versus posterior foregut endoderm tissues and a vascular network.
89 rowth factors (FGFs) 1, 2, and 8, causes the foregut endoderm to develop into the liver.
90  stem cells to definitive endoderm, anterior foregut endoderm, ventral anterior foregut endoderm, lun
91 n implicated in the definition of liver from foregut endoderm where FGFR4 is expressed and stimulatio
92  is derived from the anterior portion of the foregut endoderm, which also gives rise to the respirato
93  with differentiation of cells into anterior foregut endoderm, which is followed by their lineage spe
94 re regulated by hedgehog expression from the foregut endoderm, which is required for connection of th
95              Sox2 is expressed in developing foregut endoderm, with highest levels in the future esop