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1                                              Basipetal [(3)H]IAA transport in Arabidopsis roots was i
2 s, with the mutant roots also having reduced basipetal and acropetal auxin transport.
3                                         Root basipetal and acropetal indole-3-acetic acid (IAA) trans
4 leaf primordium, major leaflet initiation is basipetal, and lobe formation and early vascular differe
5 ansport in Selaginella shoots is exclusively basipetal, as in angiosperms.
6 basal end of hypocotyl cells associated with basipetal auxin flow.
7 hore and is indicative of the redirection of basipetal auxin from the shoot into the rhizophore durin
8 ,N,N',N'-tetraacetic acid, greatly decreased basipetal auxin movement, reducing polarity from 6.3 to
9 ent, but not for the AGR1/PIN2-mediated root basipetal auxin transport and auxin response in CEZ cell
10 volved in regulating AGR1/PIN2-mediated root basipetal auxin transport and gravitropism, as well as a
11                  We demonstrate that reduced basipetal auxin transport and low auxin accumulation at
12 ges in PIN polarity result in increased root basipetal auxin transport and severe defects, including
13 ed gene expression, and acropetal as well as basipetal auxin transport are altered at the root tip of
14 sta4 [tt4(2YY6)] seedlings had elevated root basipetal auxin transport compared with the wild type, c
15 psis thaliana roots shows that MDR4-mediated basipetal auxin transport did not affect root elongation
16 otic rhizobia cannot locally alter acro- and basipetal auxin transport during nodule initiation and t
17 d gene expression, indicating that increased basipetal auxin transport impedes gravitropism.
18 presence of extracellular ATP also decreases basipetal auxin transport in a dose-dependent fashion in
19        This is accompanied by a reduction of basipetal auxin transport in the hypocotyls of d6pk as w
20                  PIN1 localizations identify basipetal auxin transport in the SAM L1 layer at the sit
21                        Although PIN-mediated basipetal auxin transport regulates branching patterns i
22 transport and suggest that the acropetal and basipetal auxin transport streams are differentially reg
23 essary for root gravitropism by facilitating basipetal auxin transport to distal elongation zone tiss
24 rotein phosphatases on root gravitropism and basipetal auxin transport, as well as the expression pat
25 nsistent with the proposed role of AtMDR1 in basipetal auxin transport, we found that expression of t
26 hat quercetin is the flavonol that modulates basipetal auxin transport.
27 roots are also agravitropic and have reduced basipetal auxin transport.
28 x component regulating root gravitropism and basipetal auxin transport.
29                       On the other hand, the basipetal carpels of the 35S::XAL2 lines lose determinac
30 as detected, whereas IAA is transported in a basipetal direction from the meristem tip.
31  both IBA and IAA were transported only in a basipetal direction in the hypocotyl.
32 dular trichomes can selectively secrete in a basipetal direction monoterpenoids, which can reach dist
33 efficiently within the xylem, primarily in a basipetal direction.
34 ource leaves, loading capacity occurred in a basipetal direction.
35 IAA) transport in both the acropetal and the basipetal directions.
36              Mutant eta1 individuals display basipetal displacement of the blade/sheath boundary and
37 ocalized exclusively either to the apical or basipetal end of cells depending on the expansin gene an
38 ant phenotypes consistent with the disrupted basipetal flow of auxin.
39 perception, elevated auxin levels occur in a basipetal gradient away from the cotyledons and that thi
40  apparent across the lamina, whereas a clear basipetal gradient in cell production rate was found.
41                           Leaves exhibited a basipetal gradient of leaf development, investigated by
42 eaf growth in model plants have identified a basipetal growth direction with the highest growth rate
43 ch has agravitropic roots, exhibited reduced basipetal IAA transport but wild-type levels of acropeta
44                                Inhibition of basipetal IAA transport by local application of NPA bloc
45 ux1-7 also has ACC-insensitive acropetal and basipetal IAA transport, as well as altered DR5-GUS expr
46                                              Basipetal indole-3-acetic acid transport and gravitropis
47 rolling gravitropic response, a reduction in basipetal indole-3-acetic acid transport, and a delay in
48 tion seedlings exhibit increased and reduced basipetal indole-3-acetic acid transport, respectively.
49 ID kinase function inhibits gravitropism and basipetal indole-3-acetic acid transport.
50                    Monocot leaf matures in a basipetal manner, and has a well-defined developmental g
51  of plant cell wall and membrane structures, basipetal movement along the vascular parenchyma, and ma
52 lication of calcium to the root cap enhanced basipetal movement of auxin, increasing polarity from 6.
53 istribution of gland initiation reflects the basipetal pattern of leaf maturation, with relatively im
54 rst developing leaf demonstrate a decline in basipetal phloem transport that can be alleviated by the
55 n source, seedling growth rate increases and basipetal phloem transport velocity becomes more stable.
56                     The results suggest that basipetal polar auxin transport occurred in the common a
57 cap is particularly important in maintaining basipetal polarity of auxin transport in primary roots o
58  quercetin derivatives are the inhibitors of basipetal root auxin transport, gravitropism, and elonga
59                          We demonstrate that basipetal secretions can also occur, by addressing the o
60  synthesis in maize endosperm adheres to the basipetal sequence from the apex downwards.
61 illary bud activation and by attenuating the basipetal sequence of bud activation that is triggered f
62  distribution within single leaves along the basipetal sink-source transition trajectory during senes
63 rted by expression analyses of DR5uidA, root basipetal transport assay of auxin, and RSA of the pgp19
64 s preferentially basipetal, with a polarity (basipetal transport divided by acropetal transport) of 6
65                An NPA treatment that reduced basipetal transport in rcn1 and cantharidin-treated wild
66 genous SL synthesis significantly reduce the basipetal transport of a second branch-regulating hormon
67  mutant of Arabidopsis which is defective in basipetal transport of IAA.
68 nt are consistent with a basic disruption in basipetal transport of IAA.
69                                         Root basipetal transport was increased in rcn1 or phosphatase
70 Conversely, mutations in MDR4 blocked 50% of basipetal transport without affecting acropetal transpor
71                               In contrast to basipetal transport, root acropetal transport was normal
72  transport in roots by 80% without affecting basipetal transport.
73                  Arabidopsis petals grow via basipetal waves of cell division, followed by a phase of
74 al region of intact roots was preferentially basipetal, with a polarity (basipetal transport divided