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1 or 1) is indispensable for the generation of hemogenic endothelium.
2 GATA2 might function at early stages within hemogenic endothelium.
3 cification necessitates an earlier marker of hemogenic endothelium.
4 atopoiesis and vascular specification of the hemogenic endothelium.
5 s, just prior to their emergence from aortic hemogenic endothelium.
6 imilar to those found later in the embryonic hemogenic endothelium.
7 te to regulate the neighboring precursors of hemogenic endothelium.
8 fies distinct subpopulations of hESC-derived hemogenic endothelium.
9 fies distinct subpopulations of hESC-derived hemogenic endothelium.
10 generation of hematopoietic progenitors from hemogenic endothelium.
11 enitor cells arise directly from YS and P-Sp hemogenic endothelium.
12 n the generation of hematopoietic cells from hemogenic endothelium.
13 luding the concepts of the hemangioblast and hemogenic endothelium.
14 ll signaling to control the emergence of the hemogenic endothelium.
15 een shown to direct the specification of the hemogenic endothelium and emergence of hematopoietic ste
16 ulated a rich ensemble of genes that control hemogenic endothelium and HSCs, as well as genes not imp
18 the hematopoietic transcriptional program in hemogenic endothelium and preventing its misspecificatio
20 S) cells to identify Sox17 as a regulator of hemogenic endothelium, and use conditional expression of
21 nd placenta; however, the precursor cells to hemogenic endothelium are not defined phenotypically.
22 s located in the yolk sac and intraembryonic hemogenic endothelium before the initiation of circulati
24 ells (HSCs) emerge during embryogenesis from hemogenic endothelium, but it remains unclear how the HS
25 , the hematopoietic lineage transits through hemogenic endothelium, but the signaling pathways effect
26 s (ECs) through an intermediate stage called hemogenic endothelium by a process known as endothelial-
27 enta and other sites has been tracked to the hemogenic endothelium by using novel genetic and imaging
28 d in vivo the proximal Runx1 isoform marks a hemogenic endothelium cell population, whereas the subse
29 rise from the unique transdifferentiation of hemogenic endothelium comprising the floor of the dorsal
33 eveals a phenotype for in vivo precursors to hemogenic endothelium, establishing that direct in vitro
34 embryo are specified independently, and that hemogenic endothelium first appears in the YS and produc
35 esults indicate that Gata2b functions within hemogenic endothelium from an early stage, whereas Gata2
37 a specialized endothelial population, termed hemogenic endothelium (HE), located in the ventral wall
40 These data establish that Cdh5, a marker of hemogenic endothelium in the AGM, is dispensable for the
41 s (collectively known as HSPCs), emerge from hemogenic endothelium in the floor of the embryonic dors
43 rogenitors and stem cells are generated from hemogenic endothelium precursors through a process terme
44 role for RA signaling in the development of hemogenic endothelium that contributes to definitive hem
45 anism that controls stem cell emergence from hemogenic endothelium to establish the adult hematopoiet
46 f the +9.5 element abrogated the capacity of hemogenic endothelium to generate HSC-containing cluster
48 ine a role for Hh signaling in patterning of hemogenic endothelium, we assessed the effect of altered
49 ad that mesodermal precursors first generate hemogenic endothelium, which then generate blood cells i
50 tion of hematopoietic stem cells (HSCs) from hemogenic endothelium within the aorta, gonad, mesonephr
51 d from specialized endothelial cells, termed hemogenic endothelium, within the yolk sac, placenta, an
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