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 The hard tick, Ixodes ricinus, a main Lyme disease vector, harbors an intracel

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

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

6 zard of diseases vectored by the tick Ixodes ricinus at different scales.

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

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

9 a human skin explant model mimicking Ixodes ricinus bites and tick-borne pathogen infection.

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

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

12 Ixodes scapularis cell line ISE18 and Ixodes ricinus cell lines IRE/CTVM19 and IRE/CTVM20 had modal c

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

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

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

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

17 The expression of Ricinus communis (castor) OLEATE 12-HYDROXYLASE (RcFAH12

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

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

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

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

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

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

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

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

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

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

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

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

30 Fluorescently labeled lectin Ricinus communis agglutinin I detected polysaccharides s

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

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

33 3.5 gestational weeks (g.w.), using lectins, Ricinus communis agglutinin-1 [RCA-1], and Lycopersicon

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

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

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

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

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

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

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

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

42 Castor bean (Ricinus communis L.) is an important oil crop, which bel

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

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

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

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

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

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

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

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

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

52 psis thaliana) plants expressing the castor (Ricinus communis) FAH12 hydroxylase.

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

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

55 through transgenic expression of the castor (Ricinus communis) hydroxylase.

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

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

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

59 we identified a triple mutant of the castor (Ricinus communis) stearoyl-Acyl Carrier Protein desatura

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

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

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

63 ymes from soybean (Glycine max), and castor (Ricinus communis), followed by isotopic tracing of glyce

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

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

66 anning the Pentapetalae (Phaseolus vulgaris, Ricinus communis, Arabidopsis [Arabidopsis thaliana], He

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

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

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

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

71 e carrier at various developmental stages in Ricinus communis.

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

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

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

75 Ixodes ricinus contact phase inhibitor (Ir-CPI) is a protein ex

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

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

78 livary gland type II and III acini of Ixodes ricinus female.

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

80 eoretical evidence show that the tick Ixodes ricinus (Figure 1A) can close the gap to their hosts usi

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

82 Multiple non-natural hosts of I. ricinus have shown to develop immunity after repeated ti

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

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

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

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

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

88 In Europe, Ixodes ricinus is the most important vector of human infectious

89 amotoi, including Ixodes persulcatus, Ixodes ricinus, Ixodes pacificus and Ixodes scapularis, was pro

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

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

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

93 allenge with B. afzelii CB43-infected Ixodes ricinus nymphs.

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

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

96 e 3D images of wild-type and aposymbiotic I. ricinus oocytes generated with focused ion beam-scanning

97 erited and resides in the mitochondria of I. ricinus oocytes, but the consequences of this endosymbio

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

99 surface display library (YSD) of nymphal I. ricinus salivary gland genes expressed at 24, 48 and 72

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

101 s revealed the detailed ultrastructure of I. ricinus salivary glands, and provides a solid baseline f

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

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

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

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

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

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

108 grouped with Sulina virus detected in Ixodes ricinus ticks in Romania.

109 ibitor (Ir-CPI) is a protein expressed by I. ricinus ticks, which specifically inhibits both factors

110 They are transmitted mainly by Ixodes ricinus ticks.

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

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

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