ライフサイエンスコーパス: Ricinus

1 ly two defensins had been identified from I. ricinus.

2 ersity of the defensin family in the tick I. ricinus.

3 that the alpha-Gal epitope is present in I. ricinus and imply host exposure to alpha-Gal during a ti

4 Trichomonas vaginalis, the hard tick Ixodes ricinus, and the flatworm Schistosoma mansoni.

5 tion of six novel putative defensins from I. ricinus at the genomic and transcriptional levels.

6 y and midgut tissues of nymphal and adult I. ricinus at various time points after attachment on the v

7 The hard-bodied tick Ixodes ricinus (castor bean tick) is the most common tick speci

8 the functional diversity of multiple Ixodes ricinus cathepsin D forms (IrCDs).

9 stinct proteins, but also in the case of the Ricinus communis ("ricin") agglutinins (RCA(60) and RCA(

10 roteins present in the sieve-tube exudate of Ricinus communis (castor bean) seedlings, a cDNA was clo

11 two higher plants, Arabidopsis thaliana and Ricinus communis (Castor bean).

12 to permit its use with authentic extracts of Ricinus communis (castor beans) and Abrus precatorius (j

13 imilarity to an oleate hydroxylase gene from Ricinus communis (L.).

14 rotein, 18:0-ACP) on the diferric centers of Ricinus communis 18:0-ACP Delta(9) desaturase.

15 iculus of mice by injecting the toxic lectin Ricinus communis agglutinin (RCA) I into the sciatic ner

16 Sambucus nigra agglutinin type I (SNA), and Ricinus communis agglutinin (RCA) on polycrystalline gol

17 tect glycoproteins from 1 fM (Con A), 10 fM (Ricinus communis agglutinin (RCA), or 100 fM (SNA) with

18 enine-specific RNA N-glycosidases, including Ricinus communis agglutinin (RCA), saporin, and abrin II

19 al fibrillary acidic protein for astrocytes, Ricinus communis agglutinin (RCA)-l for macrophage/micro

20 , Vicia villosa isolectin B4 (VVL-B(4)), and Ricinus communis agglutinin (RCA120).

21 Ricinus communis agglutinin I (RCA I), a galactose-bindi

22 lectins concanavalin agglutinin (Con A) and Ricinus communis agglutinin I (RCA) to delineate carbohy

23 However, the binding of Ricinus communis agglutinin I (RCA) to sCJD and vCJD sam

24 The binding specificity of lectins Ricinus communis agglutinin I (RCA), peanut (Arachis hyp

25 Fluorescently labeled lectin Ricinus communis agglutinin I detected polysaccharides s

26 e accompanied by parenchymal infiltration of Ricinus communis agglutinin I(+) microglia/macrophages,

27 ntiation of ricin from the highly homologous Ricinus communis agglutinin which is currently not feasi

28 3.5 gestational weeks (g.w.), using lectins, Ricinus communis agglutinin-1 [RCA-1], and Lycopersicon

29 icin is a potent toxin found in the beans of Ricinus communis and is often lethal for animals and hum

30 tein (ACP) desaturase (DS) from castor plant Ricinus communis catalyzes the dioxygen- and NADPH-depen

31 Half-tipped primary and lateral roots of Ricinus communis cv Hale bend toward the side of the roo

32 The reaction of recombinant Ricinus communis Delta9D with natural and nonnatural cha

33 Expression of the Ricinus communis FA hydroxylase reduced the flux of de n

34 organization of a PLD gene from castor bean (Ricinus communis L. cv. Hale).

35 storage vacuoles of developing castor bean (Ricinus communis L.) endosperm.

36 the oleate 12-hydroxylase from castor bean (Ricinus communis L.) has previously been shown to direct

37 The expression of a castor bean (Ricinus communis L.) phospholipase D (PLD; EC 3.1.4.4) g

38 The injury model employs the injection of Ricinus communis lectin into a cranial or peripheral ner

39 c fluorescence, increased molecular mass and Ricinus communis lectin recognition.

40 The targeting of the castor bean (Ricinus communis) 2S albumin precursor has been investig

41 In developing castor oil seeds (Ricinus communis) a novel, allosterically desensitized 9

42 are found naturally in seed oils of castor (Ricinus communis) and tung tree (Vernicia fordii), respe

43 pped glyoxysomal membranes from castor bean (Ricinus communis) endosperm that bind the peptide YHKHLK

44 s in the triacylglycerol fraction of castor (Ricinus communis) endosperm, even though it is synthesiz

45 ates in the storage vacuoles of castor bean (Ricinus communis) endosperm.

46 example, seed-specific expression of castor (Ricinus communis) fatty acid hydroxylase (RcFAH) in Arab

47 nd Camelina sativa expressing a castor bean (Ricinus communis) hydroxylase were analyzed.

48 Castor bean (Ricinus communis) is an oilseed crop that belongs to the

49 elds of HFA compared with the native castor (Ricinus communis) plant and caused undesirable effects,

50 centrations for the recombinant castor bean (Ricinus communis) PLD alpha expressed in Escherichia col

51 fatty acid hydroxylase (FAH12) from castor (Ricinus communis) was expressed in Arabidopsis seeds, th

52 da), squash (Cucurbita maxima), castor bean (Ricinus communis), and tomato (Solanum lycopersicum).

53 process, although oilseeds, such as castor (Ricinus communis), are capable of accumulating oil witho

54 diterpenoid biosynthetic genes from castor (Ricinus communis), including casbene synthases and cytoc

55 rotein toxin extracted from the castor bean (Ricinus communis).

56 ESTs from four stages of developing seeds of Ricinus communis, Brassica napus, Euonymus alatus and Tr

57 doxin and cystatin, phloem sap proteins from Ricinus communis, established that these proteins can al

58 Ricin produced from the castor oil plant, Ricinus communis, is a well-known toxin.

59 y toxic protein produced by the castor plant Ricinus communis.

60 e carrier at various developmental stages in Ricinus communis.

61 acid carrier cDNAs, RcAAP1 and RcAAP2, from Ricinus communis.

62 complicate the mating systems of the Ixodes ricinus complex of species.

63 e borreliosis (LB) are acquired after Ixodes ricinus-complex tick bites.

64 yses show that these novel members of the I. ricinus defensin family differ phylogenetically and stru

65 Saliva from I. ricinus did not affect NET formation by human neutrophil

66 ut transcriptome composition in adult Ixodes ricinus females during early and late phase of engorgeme

67 acificus, from western North America, and I. ricinus, from Europe, have no sequence variation indicat

68 ilum infection on an enclosed area of Ixodes ricinus-infested pasture in North Wales, United Kingdom,

69 ma mansoni (SmAE), and the hard tick, Ixodes ricinus (IrAE).

70 Ixodes ricinus is a tick that transmits the pathogens of Lyme a

71 I. ricinus is a vector of the causative agents of diseases

72 gE responses to alpha-Gal by the tick Ixodes ricinus is demonstrated.

73 Differential expression of these I. ricinus lipocalins during feeding at distinct developmen

74 enerated robust predictions showing these I. ricinus lipocalins have the potential to bind monoamines

75 ysis using 803 sequences places the three I. ricinus lipocalins with tick lipocalins that sequester m

76 idues at position 148 of FAD2, LFAH, and the Ricinus oleate hydroxylase prompted us to rationally eng

77 ted on an arthropod species (the tick Ixodes ricinus) on which de novo sequencing was performed.

78 er characterized the expression of RcAAP1 in Ricinus roots by in situ hybridization.

79 his study was initiated by mining the Ixodes ricinus salivary gland transcriptome for specific, uncha

80 I. ricinus-secreted proteins are encoded by genes that have

81 iological role of the sucrose carrier in the Ricinus seedling and to the pathways of sucrose movement

82 A clone, RcSUT1, was isolated by RT-PCR from Ricinus seedling RNA.

83 es the phosphorylation of actin in an Ixodes ricinus tick cell line and Ixodes scapularis ticks, to a

84 the authentic virus isolated from the Ixodes ricinus tick reservoir.

85 ilencing of virus replication in live Ixodes ricinus ticks and abolished virus neurotropism in highly

86 They are transmitted mainly by Ixodes ricinus ticks.

87 rthermore, using cryostat-cut sections of I. ricinus, we show that both a monoclonal and a polyclonal

88 A total of 7215 novel sequences from I. ricinus were deposited in public databases as an additio

89 IRE/CTVM20 cell lines, both derived from I. ricinus, were susceptible to the virus rescued from plas