ライフサイエンスコーパス: acropetal

1 ation and early vascular differentiation are acropetal.

2 ulating auxin transport and suggest that the acropetal and basipetal auxin transport streams are diff

3 aux1-7 also has ACC-insensitive acropetal and basipetal IAA transport, as well as altere

4 le-3-acetic acid (IAA) transport in both the acropetal and the basipetal directions.

5 attern of auxin-induced gene expression, and acropetal as well as basipetal auxin transport are alter

6 Importantly, BRs promote acropetal auxin transport (from the base to the tip) in

7 However, impaired acropetal auxin transport due to mutation of the MDR1 ge

8 in Multidrug Resistance-Like1 (MDR1) reduced acropetal auxin transport in roots by 80% without affect

9 Thus, acropetal auxin transport maintains straight growth but

10 This tracheid curvature is consistent with acropetal auxin transport previously documented in the r

11 The mdr1 deficit was explained by 40% less acropetal auxin transport within the mdr1 lateral roots.

12 omote lateral root development by increasing acropetal auxin transport.

13 tant roots also having reduced basipetal and acropetal auxin transport.

14 Inhibition of acropetal IAA transport by application of NPA at the roo

15 Acropetal IAA transport was also elevated in roots of tt

16 ein2-5 and etr1-3 have less acropetal IAA transport, and transport is no longer regu

17 ipetal IAA transport but wild-type levels of acropetal IAA transport.

18 Root basipetal and acropetal indole-3-acetic acid (IAA) transport increase

19 arly leaf primordium, thereby conferring the acropetal leaflet formation.

20 psis thaliana, anthocyanins accumulate in an acropetal manner, with the highest level at the junction

21 lored the molecular mechanisms underlying an acropetal mode of leaflet initiation in chickpea pinnate

22 rotophloem cells, is proposed to promote the acropetal, post-phloem movement of auxin to the root ape

23 Arabidopsis, AtABCG14, is essential for the acropetal (root to shoot) translocation of the root-synt

24 e restricted factors of PAHs and heavy metal acropetal translocation by maize when they co-exist at w

25 ropism are reduced in pid-9 seedlings, while acropetal transport and lateral root development are unc

26 t auxin levels established by MDR1-dependent acropetal transport control lateral root growth rate to

27 nsitivity in rcn1 seedlings, consistent with acropetal transport controlling lateral root growth.

28 e and present in the tissues responsible for acropetal transport in the primary root.

29 sed in the dark, as were differences in root acropetal transport in tt4(2YY6).

30 f aluminum to the root cap strongly promoted acropetal transport of auxin reducing polarity from 6.3

31 In contrast to basipetal transport, root acropetal transport was normal in phosphatase-inhibited

32 dia and later in the tissues responsible for acropetal transport within the lateral root, fully suppo

33 h a polarity (basipetal transport divided by acropetal transport) of 6.3.

34 50% of basipetal transport without affecting acropetal transport.