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1 gonads, and reproductive ductal systems: the intermediate mesoderm.
2 erived from an embryonic germ layer known as intermediate mesoderm.
3 hesis that nephron epithelia derive from the intermediate mesoderm.
4 sis, three kidney structures form within the intermediate mesoderm.
5 anephric developmental program in responsive intermediate mesoderm.
6 alian metanephric kidney is derived from the intermediate mesoderm.
7 tion in the lateral mesoderm, but not in the intermediate mesoderm.
8 n kidney is derived from progenitor cells in intermediate mesoderm.
9 level tissue-specific expression within the intermediate mesoderm.
10 in the formation of organs derived from the intermediate mesoderm.
11 on of lamprey FoxC genes in the paraxial and intermediate mesoderms.
12 tor in acquiring metanephric fate within the intermediate mesoderm and as a key regulator of Gdnf exp
13 pment, Fgf-8 transcripts are detected in the intermediate mesoderm and subsequently in the prelimb fi
14 ons: nephrogenic mesenchyme derived from the intermediate mesoderm and tailbud-derived mesoderm, whic
15 are responsible for the establishment of the intermediate mesoderm and the induction of the embryonic
17 tions in the development of the paraxial and intermediate mesoderm and the neural crest in Xenopus.
18 such as Pax2/8, which are essential for the intermediate mesoderm and the renal epithelial lineage,
19 lopment are both believed to derive from the intermediate mesoderm and to be specified as the kidney
21 nown Wnt11 gene is expressed in paraxial and intermediate mesoderm, and in differentiated myocardial
22 f Hensen's node to the somitic mesoderm, the intermediate mesoderm, and then to the prospective limb-
23 f Hensen's node to the somitic mesoderm, the intermediate mesoderm, and then to the prospective limb-
24 rast, their misexpression in the prospective intermediate mesoderm appears to drive cells to acquire
25 n the surface ectoderm, lateral mesoderm and intermediate mesoderm are essential for nephric duct for
27 imb formation and that its expression in the intermediate mesoderm at the appropriate time and place
28 pecifies the metanephric blastema within the intermediate mesoderm at the caudal end of the nephrogen
29 is model, ablation of Fgf8 expression in the intermediate mesoderm before limb bud initiation had no
30 egulate the establishment of paraxial versus intermediate mesoderm cell fates in the vertebrate embry
32 an differentiate into multiple cell types of intermediate mesoderm-derived organs in vitro and in viv
33 the ureteropelvic junction were derived from intermediate mesoderm-derived renal progenitors and were
34 tutively active Hedgehog signaling in murine intermediate mesoderm-derived renal progenitors results
35 useful system to elucidate the mechanisms of intermediate mesoderm development and potentially provid
36 r analyses show that key regulators of early intermediate mesoderm development, including Lhx1, Pax2,
38 se embryonic day 8.5 (E8.5) in the region of intermediate mesoderm fated to become the nephric duct,
39 important role in regulating the balance of intermediate mesoderm fates by attenuating Fgf activity.
40 on along the medio-lateral axis, its role in intermediate mesoderm formation has not been well charac
43 s high levels of Bmp repress both medial and intermediate mesoderm gene expression and activate later
44 tterning in which low levels of Bmp activate intermediate mesoderm gene expression by inhibition of r
45 riments in the chick, Fgf8 expression in the intermediate mesoderm (IM) has been proposed to play a c
46 erning of zebrafish renal progenitors in the intermediate mesoderm (IM) involves the formation of ros
47 ining as markers for the conversion of chick intermediate mesoderm (IM) to pronephric tissue and Lmx-
48 Amniote kidney tissue is derived from the intermediate mesoderm (IM), a strip of mesoderm that lie
49 onic red blood cells (RBCs) develop in trunk intermediate mesoderm (IM), and early macrophages develo
51 (UBs) in mutants emerge as doublets from the intermediate mesoderm (IM)-derived nephric duct (ND) wit
52 tly expressed in multiple derivatives of the intermediate mesoderm, implicating the cell of origin as
53 owed a strong beta-galactosidase activity in intermediate mesoderm in an embryonic day 10 embryo and
55 1), the earliest known gene expressed in the intermediate mesoderm, is blocked by cyclohexamide, indi
58 cking both Foxc1 and Foxc2 show expansion of intermediate mesoderm markers into the paraxial domain,
59 class homeobox gene Lim1 is expressed in the intermediate mesoderm, nephric duct, mesonephric tubules
61 ndoderm and subsequently in the endoderm and intermediate mesoderm, prior to the expression of defini
63 irst epithelial tubule to differentiate from intermediate mesoderm that is essential for all further
64 there was a bounded contiguous region of the intermediate mesoderm that provides pronephric progenito
65 etanephric mesenchyme or blastema within the intermediate mesoderm, the earliest step of metanephric
67 Odd1 is the earliest known marker of the intermediate mesoderm, the precursor to all kidney tissu
68 riction of the Eya1(+) population within the intermediate mesoderm to nephron-forming cell fates and
69 ox11 paralog expression is restricted in the intermediate mesoderm to the posterior, metanephric leve
70 established a robust induction protocol for intermediate mesoderm, which produces up to 90% OSR1(+)
71 kidney markers are expressed in a stripe of intermediate mesoderm, with distinct, overlapping antero
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