ライフサイエンスコーパス: Ricinus communis

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

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

3 e carrier at various developmental stages in Ricinus communis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

18 Fluorescently labeled lectin Ricinus communis agglutinin I detected polysaccharides s

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

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

21 3.5 gestational weeks (g.w.), using lectins, Ricinus communis agglutinin-1 [RCA-1], and Lycopersicon

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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