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6 ra (elder berry), Arachis hypogaea (peanut), Ulex europaeus (gorse, furze), Triticum vulgaris and Con
7 d several lectins but was weak to absent for Ulex europaeus 1 (alpha1,2 fucose-binding) and Sambucus
8 distribution of two different plant lectins, Ulex europaeus agglutinin (UEA) and Dolichos biflorus ag
11 A close association of acino-ductal markers (Ulex europaeus agglutinin 1, amylase, cytokeratin-19) an
12 2) kinase domain-containing receptor; and 3) Ulex europaeus agglutinin 1, and were able to form cord/
13 ctins Griffonia simplicifolia II (GS II) and Ulex europaeus agglutinin I (UEA I) selectively bind to
14 A), Maackia amurensis lectin II (MALII), and Ulex europaeus agglutinin I (UEA) was utilized in force
16 Although the labelling by the fucose-binding Ulex europaeus agglutinin I (UEA-I) was completely abrog
21 e-linked lectin assay (ELLA) with the lectin Ulex europaeus agglutinin-1 (UEA-1), Western blot analys
22 cells that express CD80 and bind the lectin Ulex europaeus agglutinin-1, leading to a significant de
24 binding assay was competitively inhibited by Ulex europaeus agglutinin-I (UEA-I), a lectin specific f
25 he immobilized H blood group-specific lectin Ulex europaeus agglutinin-I (UEA-I), whereas none from p
26 vein injection of human endothelial specific Ulex europaeus agglutinin-I demonstrated an increased nu
27 pithelium degeneration) were evaluated using Ulex europaeus agglutinin-I labeling to discriminate bet
30 rtially with the endothelium-specific lectin Ulex Europaeus I in human glomeruli, leaving portions of
32 cetylated low-density lipoprotein uptake and Ulex europaeus lectin binding; (iii) tube-like network f
33 were stained with antibodies against CD31 or Ulex europaeus lectin, smooth muscle alpha-actin, and S-
35 nd nitrogen (N) availability on both a host (Ulex europaeus) and its parasite (Cassytha pubescens).
36 on Willebrand's factor and CD31 with lectins Ulex europaeus, Bandeiraea simplicifolia, peanut aggluti
37 antigen and those recognized by lectins from Ulex europaeus-1 and Tetragonolobus purpureus were enhan
39 ncrease in numbers of bromodeoxyuridine- and Ulex europaeus-positive cells, but there was no evidence
42 chiffs reagent (AB/PAS) and with the lectins Ulex europeus agglutinin I (UEA-I) and Helix pomatia agg
44 To test this, we isolated EPCs (CD133(+)/Ulex europeus- I(+)) and mature ECs (CD133(-)/Ulex europ
45 lex europeus- I(+)) and mature ECs (CD133(-)/Ulex europeus-I(+)) from proliferating hemangiomas and u
47 Our findings suggest that acetylated LDL(+)ulex-lectin(+) cells, commonly referred to as EPCs, do n