ライフサイエンスコーパス: radicle

1 nd in the micropylar tissues surrounding the radicle.

2 l polarity, and endogenous initiation of the radicle.

3 tion after germination, the emergence of the radicle and lateral roots, and the transition to floweri

4 mpleted following enhanced growth within the radicle and lower axis.

5 get PXMT1 are predominantly expressed in the radicle, and the expression patterns of the two genes ar

6 he endosperm cap and radicle tip, and in the radicle appears as a distinct band possibly associated w

7 nsplanted cells were observed in portal vein radicles, as well as in liver sinusoids, albeit integrat

8 ferently within cotyledons and the hypocotyl/radicle axis in embryos of the oilseed crop Camelina sat

9 In optimal conditions, radicle cell divisions occur only after the completion o

10 re seeds but accumulated specifically in the radicle cortex during and after germination.

11 ecause of impediment of the mutant testae to radicle egress.

12 completion of germination is blocked by ABA, radicle elongation and cell divisions occurred in these

13 e balance between the two opposing forces of radicle elongation and mechanical resistance of the endo

14 level of SHAM + CN but inhibited subsequent radicle elongation, thereby decreasing germination when

15 ations of osmoticum and measuring subsequent radicle elongation.

16 l components that reflect the future site of radicle emergence and abundant heteromannan.

17 oM abscisic acid, which delayed or prevented radicle emergence but not endosperm cap weakening.

18 ty contributes to the temporal regulation of radicle emergence in endospermic seeds by altering the m

19 (Lycopersicon esculentum) seeds just before radicle emergence through this tissue to complete germin

20 pression of LeEXP4 was not reduced, although radicle emergence was inhibited.

21 Completion of germination (radicle emergence) by gibberellin (GA)-deficient (gib-1)

22 ssed in tomato endosperm cap tissue prior to radicle emergence, we found no evidence that they were d

23 ciated with endosperm cap weakening prior to radicle emergence, whereas LeMAN1 mobilizes galactomanna

24 ndosperm cap tissue of tomato seeds prior to radicle emergence, whereas LeMAN1 was expressed only in

25 m cap', and is specifically activated before radicle emergence.

26 ycopersicon esculentum Mill.) seeds prior to radicle emergence.

27 ute to tissue weakening that is required for radicle emergence.

28 ight dependent and limited to the process of radicle emergence.

29 xpressed only in the lateral endosperm after radicle emergence.

30 y abundant in the micropylar region prior to radicle emergence.

31 nation, coincident with the emergence of the radicle from the seed coat.

32 icted that the outer cotyledon and hypocotyl/radicle generate the bulk of plastidic reductant/ATP via

33 vealed their enrichment within the embryonic radicle, identifying the presence of a decision-making c

34 fference between hepatocytes and portal vein radicles, intrasplenically transplanted cells were distr

35 cell wall extensibility changes in both the radicle itself and in the micropylar tissues surrounding

36 Radicle meristem activation and extension can therefore

37 tants complete germination in the absence of radicle meristem activation and growth.

38 soids, along with attenuation of portal vein radicles on angiography.

39 ed for the outer cotyledon and the hypocotyl/radicle only.

40 artments CAP (micropylar endosperm) and RAD (radicle plus lower hypocotyl).

41 Radicle protrusion from tomato (Lycopersicon esculentum

42 all loosening of the endosperm necessary for radicle protrusion from tomato seeds and in subsequent e

43 ring seed development and remained high when radicle protrusion was blocked by abscisic acid (ABA), w

44 nd weakening in the endosperm cap leading to radicle protrusion, and jasmonate is involved in the sig

45 by enabling embryo cell expansion leading to radicle protrusion, as well as endosperm weakening prior

46 is resistant to external ABA at the stage of radicle protrusion.

47 associated with endosperm cap weakening and radicle protrusion.

48 Upward orientation of the micropyle/radicle reduced the number of graviresponding roots to a

49 tly highlight the fates of the endosperm and radicle: senescence and growth, respectively.

50 glycerols was observed within the embryo and radicle, showing correlation with the heterogeneous dist

51 of several module (cotyledon, hypocotyl, and radicle)-specific factor-DNA interactions has been explo

52 , and -237 to -231 were found to orchestrate radicle-specific repression.

53 arated from other hepatocytes in portal vein radicles that failed to exhibit bile canalicular reconst

54 in the micropylar endosperm cap covering the radicle tip and subsequently in the remaining lateral en

55 it is not responsible for expression in the radicle tip during embryo development.

56 m growth factors is first induced within the radicle tip of the embryo.

57 kening of the endosperm tissue enclosing the radicle tip requires GA.

58 hitinase localized to both endosperm cap and radicle tip tissues.

59 nation predominates in the endosperm cap and radicle tip, and in the radicle appears as a distinct ba

60 ermal lipid gap, which channels water to the radicle tip, from whence it is distributed via embryonic

61 ndosperm in a seed, which is adjacent to the radicle tip, is called the 'endosperm cap', and is speci

62 ses, LeGOLS-1 mRNA was most prevalent in the radicle tip.

63 ly in the endosperm cap tissue enclosing the radicle tip.

64 akening of the endosperm tissue opposite the radicle tip.

65 tems, and distributed computation within the radicle underlies this signal integration mechanism.