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1 d increased endogenous erythropoiesis damage vascular endothelia.
2     During metastasis, tumor cells adhere to vascular endothelia.
3 roteins to both pulmonary and extrapulmonary vascular endothelia.
4 wn to affect eNOS expression and activity in vascular endothelia.
5 mportant for leukocyte extravasation through vascular endothelia and for T-cell activation.
6 aced by bone marrow transplantation, such as vascular endothelia and microglia, to transduce microgli
7 ted mice displayed leukocyte adhesion to the vascular endothelia and petechial hemorrhages throughout
8 iferation, migration, and differentiation of vascular endothelia and smooth muscle cells.
9 pression waned in most areas but remained in vascular endothelia and the dentate gyrus.
10 leukocytes (PMN, neutrophils) migrate across vascular endothelia, and such transmigration has the pot
11 f the population of plasmalemmal vesicles of vascular endothelia are described.
12 herefore studied whether PTPmu, in pulmonary vascular endothelia, associates with and/or regulates bo
13 rated clearing of globotriaosylceramide from vascular endothelia but little effect on proteinuria or
14 D(4) receptor (CysLT(1)) is induced in human vascular endothelia by interleukin-1beta.
15     The identification of IL-6 production in vascular endothelia cells after alloimmune activation re
16  between renal Ent1 and Adora2b expressed on vascular endothelia effectively prevented a postischemic
17  deletion of Adora2b in tubular epithelia or vascular endothelia implicated endothelial Adora2b signa
18  panning to identify peptides that bound the vascular endothelia in diseased and wild-type mice.
19                                We found that vascular endothelia in inflamed areas of lacrimal gland
20 formed a knockout of the receptor for ANP in vascular endothelia in order to distinguish the effects
21 nd nitrergic nerve terminals and by NOS-3 in vascular endothelia, is probably a physiological vasodil
22 a2b deletion in different tissues--including vascular endothelia, myeloid cells, and hepatocytes--rev
23 ssing the power of phage display for mapping vascular endothelia natively in tissue and for achieving
24 yes, NOS-3 was constitutively present in the vascular endothelia of large and small vessels.
25 bes and their cognate antigens for targeting vascular endothelia of specific organs in vivo.
26 e understanding of endorepellin signaling in vascular endothelia, providing insight into the temporal
27 e in mechanotransduction mechanisms by which vascular endothelia respond to local atherorelevant hemo
28                                     However, vascular endothelia, retinal pigment epithelia, Muller c
29  opens the paracellular pathway in pulmonary vascular endothelia through protein tyrosine phosphoryla
30 gene was conditionally deleted in restricted vascular endothelia using a novel endothelial Cre transg
31 efore, PTPmu is expressed in human pulmonary vascular endothelia where it directly binds to VE-cadher
32  a water channel protein expressed widely in vascular endothelia, where it increases cell membrane wa
33  enzyme expressed in, and secreted from, the vascular endothelia will be endocytosed by underlying ne