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1 ons, in comparison to parenchymatic cells in ground tissue.
2 established in the Arabidopsis thaliana root ground tissue.
3 aintenance of the boundary between stele and ground tissue.
4  and OsSHR2) function in patterning the root ground tissue.
5 the formation of supernumerary layers in the ground tissue.
6 ate additional cell divisions outside of the ground tissues.
7  by providing a non-autonomous signal to the ground tissues.
8 s that suppress herbivorous insects in above-ground tissues.
9  ability of seagrasses to aerate their below-ground tissue and immediate rhizosphere to prevent sulfi
10 f development, activity was also detected in ground tissue and parenchyma cells associated with vascu
11                                          The ground tissue and stem cell niche fates soon separate an
12 cts as a suppressor of epidermal fate in the ground tissue, and (2) it is required to repress pericli
13 Ts were generated from aerial tissues, below-ground tissues, and tissues challenged with the late-bli
14 circadian clock, and small RNA regulation in ground tissue; and suberin biosynthesis, iron transporte
15 sis, formative divisions generating the root ground tissue are controlled by SHORTROOT (SHR) and SCAR
16 stem cell niche that gives rise to the above-ground tissues, are crucially involved in regulating dif
17 oot and resulted in Ti accumulation in above ground tissues at a higher level compared to BPs.
18  and SCARECROW (SCR) functions do not form a ground tissue because they do not develop ground tissue
19 on in the Arabidopsis thaliana root meristem ground tissue by tethering and regulating transcriptiona
20 his PLT-mediated regeneration response, leaf ground tissue cells can neither acquire the early vascul
21 control the asymmetric division of the first ground tissue cells.
22 ions that generate the two cell types of the ground tissue - cortex and endodermis.
23 ;1) to drive formative divisions during root ground tissue development.
24 with eukaryotic toxins that persist as above-ground tissue develops.
25      In scz mutants, the subepidermal layer (ground tissue) develops root hairs.
26 dinal asymmetric cell division occurs in the ground tissue earlier than in wild-type plants.
27 c cell division responsible for formation of ground tissue (endodermis and cortex) as well as specifi
28 e regulator SHORT-ROOT from the stele to the ground tissue has been associated with transferring posi
29 that root explants, in addition to the above-ground tissues, have considerable regeneration capacity
30    In contrast, it is completely unknown how ground tissue identity is first specified from totipoten
31                    A symplastic block of the ground tissue impairs regeneration, which is rescued by
32 mechanism regulates the radial patterning of ground tissue in both root and shoot during embryogenesi
33 ing plants by governing radial patterning of ground tissue in roots and cell proliferation in leaves.
34 rs, indicating that mis-specification of the ground tissue in scz mutants is uncoupled to the cell di
35 results in the formation of a single layered ground tissue in the double mutants.
36 blishment of the stem cells that produce the ground tissue in the embryonic root meristem.
37 t stem cells responsible for growth of above-ground tissues in flowering plants.
38      The post-embryonic development of above-ground tissues in plants is dependent upon the maintenan
39 mpounds accumulated in high amounts in above-ground tissues including leaves, petioles, and stems, bu
40 al meristem generate all postembryonic above-ground tissues, including the germline cells.
41 tion in the embryonic root, and reveals that ground tissue initiation and maintenance use different r
42 n of dissolved organic carbon from the below-ground tissue into the rhizosphere.
43  asymmetric cell divisions that separate the ground tissue into two separate layers: the endodermis a
44                                   The middle ground tissue layer comprises the majority of the plant
45  cellular anatomy of the protoderm and outer ground tissue layer is established.
46 ch moves from the stele into the neighboring ground tissue layer to specify endodermis.
47 esults in a radial pattern defect, loss of a ground tissue layer, in the root.
48 show that MP transcriptionally initiates the ground tissue lineage and acts upstream of the regulator
49 ot tip give rise to all the above- and below-ground tissues of a plant.
50 ation potential of these metals in the above ground tissues of Indian mustard plants.
51 s of SHORT-ROOT (SHR) and SCARECROW (SCR) in ground tissue patterning and differentiation have been w
52                                              Ground tissue patterning and maintenance in Arabidopsis
53 ream of the regulatory network that controls ground tissue patterning and maintenance.
54      These data also provide a new model for ground tissue patterning in A. thaliana in which the abi
55 o essential for apical meristem maintenance, ground tissue patterning, vascular differentiation, and
56 te the molecular basis of the role of SCR in ground tissue patterning, we screened for SCR-interactin
57 d SCR expression in cells that contribute to ground tissue radial patterning in both embryonic root a
58          In plants, development of all above-ground tissues relies on the shoot apical meristem (SAM)
59 TERCTING FACTOR 4 (PIF4) regulates the above ground tissue response, the below ground root elongation
60        Here we show that the above and below ground tissue-response to high ambient temperature are m
61                      Transcriptomes of above-ground tissues reveal that, in addition to the predictab
62  suggests that during the development of the ground tissue SCZ has two distinct roles: (1) it acts as
63  identifies auxin response as a regulator of ground tissue specification in the embryonic root, and r
64 nd CYCD6;1 expression, but not SHR-dependent ground tissue specification.
65 signals in apm1-1 knockdown mutants, and the ground tissue specifiers SHORTROOT and SCARECROW are mis
66 rk mutants have excess cell divisions in the ground tissue stem cells and endodermis, indicating IRK
67 actors are postembryonic determinants of the ground tissue stem cells and their lineage.
68 ryo development, the vascular precursors and ground tissue stem cells divide to renew themselves and
69 ar embryos and second asymmetric division of ground tissue stem cells in early-heart embryos are abno
70 division patterns of vascular precursors and ground tissue stem cells, likely via the YDA-MKK4/5 casc
71  a ground tissue because they do not develop ground tissue stem cells.
72 , rapidly reprograms and splits into a mixed ground tissue/stem cell niche fate and a vascular precur
73 rease in the number of cell divisions in the ground tissue that lead to extra cells in the cortex and
74 th gene expression in either above- or below-ground tissue, thus spatially separating the production
75  variation in endophyte assemblages in above-ground tissues varied with host growth habit.