ライフサイエンスコーパス: gravity sensing

1 to test the effects of starch deficiency on gravity sensing.

2 t that calmodulin plays an intrinsic role in gravity sensing.

3 ing a bioelectric current as an indicator of gravity sensing.

4 cells has been postulated to play a role in gravity sensing.

5 , selective nutrient uptake and storage, and gravity sensing.

6 tarch-statolith sedimentation hypothesis for gravity sensing.

7 e show insecticide resistance and defects in gravity sensing.

8 here a physical separation between sites for gravity sensing and curvature response has facilitated d

9 kinin signaling antagonizes this BR reset of gravity sensing and/or tropism by affecting ethylene bio

10 sedimentation in specialized cells initiates gravity sensing, but the molecular mechanism remains unc

11 lating the transcription of PIN3 and PIN7 in gravity-sensing cells of primary and lateral roots.

12 IAA-ARF-dependent auxin signaling within the gravity-sensing cells of the root and shoot.

13 nced if physiological events associated with gravity sensing could be detected separately from subseq

14 ;4 mutant when expressed specifically in the gravity-sensing endodermal cells of the stem.

15 involvement of a secondary site/mechanism of gravity sensing for gravitropism in roots, and the possi

16 However, recent results suggest that gravity-sensing hair cells in murine utricles may increa

17 formulated a new, tensegrity-based model of gravity sensing in columella cells.

18 Gravity sensing in plants and algae is hypothesized to r

19 The starch statolith hypothesis of gravity sensing in plants postulates that the sedimentat

20 The cap is widely accepted to be the site of gravity sensing in roots because removal of the cap abol

21 The primary site for gravity sensing in roots includes the root cap and appea

22 t that auxin transport is not a component of gravity sensing in the root cap.

23 ls performed on ground, indicating a role of gravity sensing in the tuning of this response.

24 ich corresponds to the presentation time for gravity sensing in this tissue.

25 as well as being a valuable means to detect gravity sensing independently of differential growth.

26 this region of the root where the effect of gravity sensing is executed by differential cell elongat

27 Some characteristics of the gravity sensing mechanism in maize root caps were invest

28 We propose a gravity-sensing mechanism by which LZY translocation to

29 The gravity-sensing mechanism has long been considered a mec

30 ent normally established across stems by the gravity-sensing mechanism.

31 o infection by most pathogens, so growth and gravity sensing often proceed normally even when other s

32 sorder caused by the aberrant development of gravity-sensing organs.

33 The distribution of gravity-sensing, otolith afferent fibers and terminals w

34 Gravity sensing provides a robust verticality signal for

35 e found an electric current generated by the gravity sensing region of the root cap of maize (Zea may

36 ke other senses, the brain lacks a dedicated gravity-sensing region and instead relies on a distribut

37 tropic growth, including impaired touch- and gravity-sensing responses.

38 Gravity sensing takes place in the columella cells of th

39 rchitecture and is specifically expressed in gravity-sensing tissues, including the shoot base, nodes

40 teins control plant architecture by coupling gravity sensing to the formation of auxin gradients that

41 the early signaling events of plants linking gravity sensing to the initiation of the gravitropic res

42 ebrafish, we generated a complete map of the gravity-sensing (utricular) system spanning from the inn

43 t in endocytosis may affect both the initial gravity sensing via amyloplasts sedimentation and the su