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 nd the generation of multilineage HSPCs from hemogenic endothelium.
2 ll signaling to control the emergence of the hemogenic endothelium.
3 or 1) is indispensable for the generation of hemogenic endothelium.
4  GATA2 might function at early stages within hemogenic endothelium.
5 cification necessitates an earlier marker of hemogenic endothelium.
6 atopoiesis and vascular specification of the hemogenic endothelium.
7 s, just prior to their emergence from aortic hemogenic endothelium.
8 imilar to those found later in the embryonic hemogenic endothelium.
9 te to regulate the neighboring precursors of hemogenic endothelium.
10 d a role for SP3 and MAZ in the formation of hemogenic endothelium.
11 fies distinct subpopulations of hESC-derived hemogenic endothelium.
12 fies distinct subpopulations of hESC-derived hemogenic endothelium.
13 generation of hematopoietic progenitors from hemogenic endothelium.
14 enitor cells arise directly from YS and P-Sp hemogenic endothelium.
15 n the generation of hematopoietic cells from hemogenic endothelium.
16 luding the concepts of the hemangioblast and hemogenic endothelium.
17 port the emergence of HSPCs from neighboring hemogenic endothelium.
18 rimes them to switch fate towards definitive hemogenic endothelium, a pre-requisite to specify HSPCs.
19 , AIBP, orchestrates HSPC emergence from the hemogenic endothelium, a type of specialized endothelium
20 een shown to direct the specification of the hemogenic endothelium and emergence of hematopoietic ste
21 ulated a rich ensemble of genes that control hemogenic endothelium and HSCs, as well as genes not imp
22 tory pathway leading to increased numbers of hemogenic endothelium and HSPCs.
23      We found that the formation of yolk sac hemogenic endothelium and its hematopoietic potential we
24 the hematopoietic transcriptional program in hemogenic endothelium and preventing its misspecificatio
25 hematopoietic stem and progenitor cells from hemogenic endothelium and revealed a YS-specific acceler
26 ord, suggesting that the former programs the hemogenic endothelium and the latter drives EHT.
27 treak, lateral mesoderm, artery endothelium, hemogenic endothelium, and >90% pure hematopoietic proge
28 S) cells to identify Sox17 as a regulator of hemogenic endothelium, and use conditional expression of
29 nd placenta; however, the precursor cells to hemogenic endothelium are not defined phenotypically.
30 ls that control HSPC fate decisions from the hemogenic endothelium are not fully understood.
31 s located in the yolk sac and intraembryonic hemogenic endothelium before the initiation of circulati
32  small number of HSPCs are produced from the hemogenic endothelium, before they colonize a transient
33          Runx1 expression marks the putative hemogenic endothelium between embryonic days (E) 8.5 to
34 ells (HSCs) emerge during embryogenesis from hemogenic endothelium, but it remains unclear how the HS
35 , the hematopoietic lineage transits through hemogenic endothelium, but the signaling pathways effect
36 s (ECs) through an intermediate stage called hemogenic endothelium by a process known as endothelial-
37 enta and other sites has been tracked to the hemogenic endothelium by using novel genetic and imaging
38 d in vivo the proximal Runx1 isoform marks a hemogenic endothelium cell population, whereas the subse
39 rise from the unique transdifferentiation of hemogenic endothelium comprising the floor of the dorsal
40 Nr4a1 and Nr4a2 expression is upregulated in hemogenic endothelium during EHT.
41 Ps) and hematopoietic stem cells (HSCs) from hemogenic endothelium during embryogenesis.
42 ence of hematopoietic stem cells (HSCs) from hemogenic endothelium during embryogenesis.
43 on, and distinguish unique subpopulations of hemogenic endothelium during hESC differentiation.
44 eveals a phenotype for in vivo precursors to hemogenic endothelium, establishing that direct in vitro
45 embryo are specified independently, and that hemogenic endothelium first appears in the YS and produc
46 esults indicate that Gata2b functions within hemogenic endothelium from an early stage, whereas Gata2
47 e embryonic day 10.5 (E10.5) endothelium and hemogenic endothelium from the major arteries, an enrich
48 s (HSPC) in zebrafish emerge from the aortic hemogenic endothelium (HE) and migrate towards the cauda
49  hydrochloride increases blood flow, expands hemogenic endothelium (HE) cells and promotes HSPC emerg
50 topoietic stem cells (HSCs) develop from the hemogenic endothelium (HE) in the aorta- gonads-and meso
51 ogenitor cells (HSPCs), first specified from hemogenic endothelium (HE) in the ventral dorsal aorta (
52                     Loss of EZH2 activity in hemogenic endothelium (HE) leads to the generation of ph
53       Although the factors regulating EHT in hemogenic endothelium (HE) of the dorsal aorta have been
54 ood formation, progenitor specification from hemogenic endothelium (HE), and generates hematopoietic
55 poietic differentiation, including mesoderm, hemogenic endothelium (HE), and multipotent hematopoieti
56 a specialized endothelial population, termed hemogenic endothelium (HE), located in the ventral wall
57 n, where a rare subset of endothelial cells, hemogenic endothelium (HE), undergoes an endothelial-to-
58 iverse population of immune cells, including hemogenic endothelium (HE)-like cells and erythromyeloid
59 ls from specialized endothelial cells called hemogenic endothelium (HE).
60 ryo from an aortic-derived tissue called the hemogenic endothelium (HE).
61 ly, Tie2-Cre-mediated ablation of Rpl22l1 in hemogenic endothelium impairs the emergence of embryonic
62 g hematopoietic stem cell emergence from the hemogenic endothelium in both zebrafish and mice.
63 topoietic stem cells (HSCs) develop from the hemogenic endothelium in cluster structures that protrud
64  These data establish that Cdh5, a marker of hemogenic endothelium in the AGM, is dispensable for the
65 s (collectively known as HSPCs), emerge from hemogenic endothelium in the floor of the embryonic dors
66                Across phyla, HSCs arise from hemogenic endothelium in the ventral floor of the dorsal
67 t that Vegfc regulates HSPC emergence in the hemogenic endothelium, in part by suppressing a myeloid
68                         HSPCs arise from the hemogenic endothelium of the dorsal aorta (DA) during de
69 rogenitors and stem cells are generated from hemogenic endothelium precursors through a process terme
70  acetate, through HOXA-patterned mesoderm to hemogenic endothelium specified by bone morphogenetic pr
71  role for RA signaling in the development of hemogenic endothelium that contributes to definitive hem
72 anism that controls stem cell emergence from hemogenic endothelium to establish the adult hematopoiet
73 f the +9.5 element abrogated the capacity of hemogenic endothelium to generate HSC-containing cluster
74 veals dynamics of gene expression during the hemogenic endothelium to HSC transition, identifying sur
75 iles of AGM-derived cells transitioning from hemogenic endothelium to HSCs, and AGM-derived endotheli
76 he AGM, is dispensable for the transition of hemogenic endothelium to HSCs.
77 ine a role for Hh signaling in patterning of hemogenic endothelium, we assessed the effect of altered
78 ad that mesodermal precursors first generate hemogenic endothelium, which then generate blood cells i
79 Hematopoietic stem cells (HSCs) develop from hemogenic endothelium within embryonic arterial vessels
80 tion of hematopoietic stem cells (HSCs) from hemogenic endothelium within the aorta, gonad, mesonephr
81 d from specialized endothelial cells, termed hemogenic endothelium, within the yolk sac, placenta, an