ライフサイエンスコーパス: Ulex

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1 subsequent endarterectomy were stained with ULEX and CD-31 antibody to highlight microvessels.

2 l cell markers (Factor VIII-related antigen, Ulex, CD31, CD34, and KDR[Flk-1]).

3 mal controls using endothelial cell markers (ULEX-E and von Willebrand factor [vWF]).

4 s were highly significant (P <.0001 for both ULEX-E and vWF staining).

5 Using ULEX-E staining, AML marrows had (average +/- SEM) 8.3 +

6 ra (elder berry), Arachis hypogaea (peanut), Ulex europaeus (gorse, furze), Triticum vulgaris and Con

7 distribution of two different plant lectins, Ulex europaeus agglutinin (UEA) and Dolichos biflorus ag

8 In labeling studies using the lectin Ulex europaeus agglutinin (UEA), we discovered a novel s

9 2) kinase domain-containing receptor; and 3) Ulex europaeus agglutinin 1, and were able to form cord/

10 ctins Griffonia simplicifolia II (GS II) and Ulex europaeus agglutinin I (UEA I) selectively bind to

11 A), Maackia amurensis lectin II (MALII), and Ulex europaeus agglutinin I (UEA) was utilized in force

12 Ulex Europaeus Agglutinin I (UEA-I) lectin has been used

13 Although the labelling by the fucose-binding Ulex europaeus agglutinin I (UEA-I) was completely abrog

14 nofluorescence for C4d, type IV collagen and Ulex europaeus agglutinin I.

15 Choroidal vasculature was labeled using Ulex europaeus agglutinin lectin and examined using conf

16 (beta)1-4GlcNAc-R epitopes reacting with the Ulex europaeus agglutinin lectin.

17 es keratin 5 (K5) and K14, but fails to bind Ulex europaeus agglutinin-1 (UEA-1) lectin.

18 e-linked lectin assay (ELLA) with the lectin Ulex europaeus agglutinin-1 (UEA-1), Western blot analys

19 cells that express CD80 and bind the lectin Ulex europaeus agglutinin-1, leading to a significant de

20 integrin alpha v beta 3, and bind the lectin ulex europaeus agglutinin-1.

21 binding assay was competitively inhibited by Ulex europaeus agglutinin-I (UEA-I), a lectin specific f

22 he immobilized H blood group-specific lectin Ulex europaeus agglutinin-I (UEA-I), whereas none from p

23 vein injection of human endothelial specific Ulex europaeus agglutinin-I demonstrated an increased nu

24 (type IV collagen+) and in the endothelium (Ulex europaeus agglutinin-I+).

25 Under glasshouse conditions, Ulex europaeus and Acacia paradoxa either uninfected or

26 rtially with the endothelium-specific lectin Ulex Europaeus I in human glomeruli, leaving portions of

27 ific because the NeuAc-unrelated lectin from Ulex europaeus is ineffective on Tat.

28 cetylated low-density lipoprotein uptake and Ulex europaeus lectin binding; (iii) tube-like network f

29 were stained with antibodies against CD31 or Ulex europaeus lectin, smooth muscle alpha-actin, and S-

30 Ulex europaeus supported significantly greater parasite

31 on Willebrand's factor and CD31 with lectins Ulex europaeus, Bandeiraea simplicifolia, peanut aggluti

32 antigen and those recognized by lectins from Ulex europaeus-1 and Tetragonolobus purpureus were enhan

33 Ulex europaeus-1, a membranous (M) cell-specific lectin,

34 ncrease in numbers of bromodeoxyuridine- and Ulex europaeus-positive cells, but there was no evidence

35 expression of the surface mucous cell marker Ulex europaeus.

36 ystyrene beads (Dynabeads M-450) coated with Ulex Europeus 1.

37 chiffs reagent (AB/PAS) and with the lectins Ulex europeus agglutinin I (UEA-I) and Helix pomatia agg

38 The lectin Ulex europeus agglutinin I was used to measure glycoconj

39 To test this, we isolated EPCs (CD133(+)/Ulex europeus- I(+)) and mature ECs (CD133(-)/Ulex europ

40 lex europeus- I(+)) and mature ECs (CD133(-)/Ulex europeus-I(+)) from proliferating hemangiomas and u

41 The majority of acetylated LDL(+)ulex-lectin(+) cells are derived from monocyte/macrophag

42 Our findings suggest that acetylated LDL(+)ulex-lectin(+) cells, commonly referred to as EPCs, do n

43 d by uptake of acetylated LDL and binding of ulex-lectin.

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