ライフサイエンスコーパス: pulvinus

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1 D-Fru) accumulated asymmetrically across the pulvinus.

2 crease in acid invertase activity across the pulvinus.

3 ghly specialized region, the stem internodal pulvinus.

4 ifferential cell elongation across the maize pulvinus.

5 sured pH(c) in the cells composing the maize pulvinus.

6 The size of the pulvinus affects the angle of the lateral branches that

7 Starch in pulvinus amyloplasts of barley (Hordeum vulgare cv Larke

8 s to contain the graviresponsive leaf-sheath pulvinus and gibberellin-sensitive internodal tissue.

9 Changes in InsP(3) were confined to the pulvinus and were not detected in internodal tissue, hig

10 e cell proliferation in a lateral organ, the pulvinus, and influences inflorescence architecture by i

11 h before the cells on the lower side of the pulvinus are committed to elongation.

12 BAD1 is expressed in the developing pulvinus as well as in other developing tissues, includi

13 PLP is specifically expressed in the pulvinus, as demonstrated by quantitative reverse-transc

14 y a significant reduction in the size of the pulvinus compared with normal plants.

15 he perceiving to the responding cells in the pulvinus, coordinating a synchronized growth response.

16 plays a crucial role in the determination of pulvinus development.

17 Optimum pulvinus elongation growth (millimeters) and segment cur

18 r a range of concentrations had no effect on pulvinus elongation growth or segment curvature in verti

19 l tissue, highlighting the importance of the pulvinus for both graviperception and response.

20 recessive mutants in maize having defects in pulvinus formation.

21 The effect of this loss on the pulvinus graviresponse was evaluated by following change

22 f horizontal segments significantly enhanced pulvinus growth and segment curvature, although exogenou

23 ravistimulation, InsP(3) levels in the lower pulvinus half increased 3-fold over the upper.

24 l 4-phosphate 5-kinase activity in the lower pulvinus half increased transiently within 10 min of gra

25 ld over vertical controls in upper and lower pulvinus halves and fluctuated in both pulvinus halves o

26 lower pulvinus halves and fluctuated in both pulvinus halves over the first minutes.

27 In the graviresponding pulvinus, hexose sugars (D-Glc and D-Fru) accumulated as

28 of gravistimulation in the lower half of the pulvinus, indicating that the positional change was sens

29 te of both graviperception and response, the pulvinus is an ideal system to study how organisms sense

30 ation time for gravistimulation in the maize pulvinus is not yet complete.

31 rass inflorescences, a structure called the "pulvinus" is found between the inflorescence main stem a

32 suggest that cells at opposite sides of the pulvinus mediate leaf or leaflet movements by swelling a

33 cular tissue of roots and nodules and in the pulvinus of petioles.

34 ibosomes occurred predominantly in the lower pulvinus one-half during the first 4 h when the presenta

35 of Medicago truncatula, four petiolule-like pulvinus (plp) mutant lines with defects in leaf movemen

36 The internodal maize pulvinus responds to gravistimulation with differential

37 te that gravistimulation produces changes in pulvinus responsiveness to both IAA and GA3 and that the

38 in plants with the so-called motor organ or pulvinus suggest that cells at opposite sides of the pul

39 ominantly in the lower one-half of the maize pulvinus; the association of transcripts for vacuolar in

40 nhibit gravitropic responses when applied to pulvinus tissue after the free IAA gradient peak has occ

41 and calmodulin were elevated 5-fold in maize pulvinus total RNA.

42 f free indole-3-acetic acid (IAA) across the pulvinus was apparent shortly after initiation of gravis

43 yctinastic leaf movement is generated by the pulvinus, which is a specialized motor organ located at

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