ライフサイエンスコーパス: seed storage protein

1 crease of 1% to 4%, mostly at the expense of seed storage protein.

2 the glb1 locus, which encodes a nonessential seed storage protein.

3 ure and polypeptide composition of the grape seed storage proteins.

4 zelnut and almond, in contrast to nsLTPs and seed storage proteins.

5 achin, the major allergen Ara h 1, and other seed storage proteins.

6 elated proteins include foliage proteins and seed storage proteins.

7 ative structural homology with globulin-like seed storage proteins.

8 patial and temporal expression patterns with seed storage proteins.

9 zymes, coinciding with the remobilization of seed storage proteins.

10 id sequence of Ara h 3 shows homology to 11S seed-storage proteins.

11 ng seeds and test the role(s) of all VPEs in seed storage protein accumulation by systematically stac

12 used as a model to understand regulation of seed-storage protein accumulation.

13 hey were shown to bind the major Arabidopsis seed storage proteins albumin and globulin (14 to albumi

14 opic LEC2 expression induces accumulation of seed storage protein and oil bodies in vegetative and re

15 Two-dimensional [(13)C, (1)H] NMR spectra of seed storage protein and starch hydrolysates were acquir

16 constitute merely one pathway for processing seed storage protein and that other proteolytic enzymes

17 een shown to belong to the vicilin family of seed storage proteins and to contain 23 linear IgE bindi

18 otease inhibitors, alpha-amylase inhibitors, seed storage proteins, and lipid transfer proteins.

19 es in senescing silique wall tissues encoded seed storage proteins, and the significance of this find

20 Seed storage proteins are both an important source of nu

21 11S seed storage proteins are synthesized as precursors that

22 e tissue in which the majority of starch and seed storage proteins are synthesized.

23 ght glutenin subunits (HMW-GS), one class of seed storage proteins, are important determinants of the

24 its prolamin gene family, encoding the major seed storage proteins, as a model for gene evolution by

25 These allergens include certain seed storage proteins, Bet v 1-like and nonspecific lipi

26 eagents for the detection of the Arabidopsis seed storage proteins by ELISA.

27 eanut allergen genes and their corresponding seed storage proteins can provide the basic information

28 Vigna mungo SHEP) which are also involved in seed storage protein degradation.

29 The complete lack of seed storage protein expression in vegetative tissues an

30 ssed in a pattern similar to the Arabidopsis seed storage protein genes.

31 AG-3') found in the promoters of many cereal seed storage protein genes.

32 A comparison to the major soybean seed storage proteins, glycinin and beta-conglycinin est

33 Ara h 2, a peanut seed storage protein, has been identified as the most po

34 2S albumins of peanuts are seed storage proteins, highly homologous in structure an

35 aseolin (phas) gene, which encodes the major seed storage protein in bean (Phaseolus vulgaris), is ac

36 he successful deposition and mobilization of seed storage protein in the protein storage vacuoles of

37 Globulins are an important group of seed storage proteins in dicotyledonous plants.

38 pecific lipid transfer proteins (nsLTPs) and seed storage proteins in hazelnut, almond, cashew nut, B

39 ential for post-translational proteolysis of seed storage proteins in the protein storage vacuole of

40 xpanded to encode different classes of major seed storage proteins in Triticeae species.

41 allergen belonging to the vicilin family of seed storage proteins, is recognized by serum IgE from >

42 mutation, rendering the signal peptide of a seed storage protein kafirin resistant to processing, in

43 tor or the promoter/terminator of a Brassica seed storage protein (napin) gene.

44 ta-phaseolin gene (phas), encoding the major seed storage protein of bean (Phaseolus vulgaris) is con

45 Phaseolin is the major seed storage protein of common bean, Phaseolus vulgaris

46 Zeins, the major seed storage proteins of maize, are of four distinct typ

47 MS/MS as homologous to the 11S globulin-like seed storage proteins of other plant species, while a mo

48 (phas) gene, which encodes one of the major seed storage proteins of P. vulgaris, is tightly regulat

49 Although seed storage proteins of poplar share some similarities

50 The influence of prominently expressed seed storage proteins on relative quantification data is

51 is, and two having significant homology to a seed storage protein or a yeast secretory protein.

52 omoter/terminator of Brassica, or equivalent seed storage protein regulatory elements of other plant

53 rkers, including RFLP DNA markers, isozymes, seed storage proteins, rRNA, and morphological loci, is

54 f endosperm (ES) specificity, several cereal seed storage protein (SSP) promoters were isolated and s

55 g wild-type seed germination, mRNAs encoding seed storage proteins (SSPs) are translationally repress

56 responsible for activating the synthesis of seed storage proteins (SSPs) during seed development, SS

57 th a role for bspA in vegetative rather than seed storage protein storage.

58 loping Arabidopsis seeds accumulate oils and seed storage proteins synthesized by the pathways of pri

59 Zeins are seed storage proteins that form accretions called protei

60 nd structural homology with the vicilin-like seed storage proteins that organize into homotrimers.

61 uence-specific signal was needed to target a seed storage protein to the vacuoles of a vegetative cel

62 Trafficking of seed storage proteins to protein storage vacuoles is med

63 ndance proteins revealed that two classes of seed storage proteins, vicilins and legumins, compose th

64 Sensitization to seed storage proteins was observed in less than 10%, mai

65 In all four methods, seed storage proteins were well separated by 2D-PAGE wit

66 prt6 seedlings, including cruciferins, major seed storage proteins, which were regulated by Group VII

67 The major maize seed storage proteins, zeins, are deficient in lysine an