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1 e in suppressing embryo development from the suspensor.
2 s of the whole embryo, the proembryo and the suspensor.
3 d by initially unorganized embryos lacking a suspensor.
4  an embryonic lineage and an extra-embryonic suspensor.
5  expressed either in the proembryo or in the suspensor.
6 oper establishment in the absence of a basal suspensor.
7 cell and a basal cell that gives rise to the suspensor.
8 aughter cell forms the mostly extraembryonic suspensor.
9 ent developmental domains, the proembryo and suspensor.
10 basal daughter cell into the extra-embryonic suspensor.
11  pole from its normal position on top of the suspensor.
12 roper and abnormal cell divisions within the suspensor.
13 stead of differentiating the extra-embryonic suspensor.
14 al mass towards the distal end of the embryo suspensor.
15 tion suggests preferential expression in the suspensor.
16 ryo proper and the supporting extraembryonic suspensor.
17 pmental delay in another mutant with shorter suspensors.
18 in giant scarlet runner bean and common bean suspensors.
19                               Defects in the suspensor, a normally transient structure derived from t
20 tion alleles cause exaggerated growth of the suspensor and can suppress embryonic development to a de
21 rn the differentiation of plant embryos into suspensor and embryo proper regions following fertilizat
22  Cell division was also aberrant both in the suspensor and embryo proper.
23  These results confirm the importance of the suspensor and suspensor-driven auxin transport in patter
24           The defective embryos have shorter suspensors and reduced growth along the longitudinal axi
25 proper formation from the distal cell of the suspensor, and a pathway characterized by initially unor
26  from double fertilization (i.e. the embryo, suspensor, and endosperm) and in apomictic, somatic, and
27 zation in flowering plants (i.e. the embryo, suspensor, and endosperm).
28  sufficient to activate transcription in the suspensor, and that a sequence (TTGGT) between the 10-bp
29                        We uncovered a set of suspensor- and embryo proper-specific transcription fact
30 ize a root independent of MONOPTEROS and the suspensor around a new boundary marked by the auxin maxi
31        This creates a useful system to study suspensor biology.
32 protein, was shifted in the basal embryo and suspensor but does not support a strong direct link to a
33 aspase mcII-Pa, a key protease essential for suspensor cell death.
34                      Yet, normally quiescent suspensor cells can develop a second embryo when the ini
35  embryonal mass cells to thick cables in the suspensor cells in which the microtubule network is comp
36 n one pole and the terminally differentiated suspensor cells on the other, separated by the embryonal
37  cells and the microtubules disrupted in the suspensor cells.
38 g embryonal mass, while it was absent in the suspensor cells.
39 ike" cellular protuberances with an enlarged suspensor characteristic of other raspberry embryo mutan
40                                          The suspensor degenerates as the development of the embryo p
41 rom less specialized soybean and Arabidopsis suspensors demonstrated that fewer genes encoding metabo
42  stage embryo proper development, triggering suspensor-derived embryogenesis.
43 -1 (mrl-1), which shows a high penetrance of suspensor-derived polyembryony due to delayed developmen
44 ntry into a regulatory network important for suspensor development irrespective of morphology.
45 r to necrotic death, resulting in failure of suspensor differentiation and embryonic arrest.
46  confirm the importance of the suspensor and suspensor-driven auxin transport in patterning, but also
47  genes are activated specifically within the suspensor during early embryo development.
48  how genes are activated specifically in the suspensor during early embryo development.
49 eptor-like kinase SHORT SUSPENSOR to promote suspensor elongation through the YODA mitogen-activated
50 us during early stages of development in the suspensor, embryo, and endosperms.
51                 Here we used auxin-dependent suspensor embryogenesis as a model to determine transcri
52      Cells of the embryo proper, but not the suspensor, exhibit abnormalities in size and shape.
53 gotic-like pathway, characterized by initial suspensor formation followed by embryo proper formation
54 er simple Arabidopsis (Arabidopsis thaliana) suspensor has on embryogenesis.
55  nutrient transport has been ascribed to the suspensor in species with prominent suspensor structures
56 es and other gymnosperms form well-developed suspensors in somatic embryogenic cultures.
57 es required to activate transcription in the suspensor, including the 10-bp motif (GAAAAGCGAA) and a
58           We conclude that the length of the suspensor is crucial for fast developmental progression
59 ell divisions in the basal embryo domain and suspensor led to diverse defects during embryogenesis in
60 cts in the early embryo and markedly reduced suspensor length.
61     Eventually, embryos from both apical and suspensor lineages successfully develop into normal plan
62                Until the globular stage, the suspensor maintains embryonic potential and can form emb
63      LEC2 is required for the maintenance of suspensor morphology, specification of cotyledon identit
64                                          The suspensor needs the lowest levels, followed by the root
65 re required to activate transcription in the suspensor of a plant embryo after fertilization.
66 541, that accumulate specifically within the suspensor of globular-stage embryos.
67 r, we show that vacuolar death in the embryo suspensor of Norway spruce requires autophagy.
68 ar mechanisms by which the embryo proper and suspensor of plant embryos activate specific gene sets s
69 ted specifically within the basal region and suspensor of preglobular tobacco embryos.
70 ody organization are up-regulated within the suspensors of these plants as well, strengthening the vi
71 e basal cells that normally give rise to the suspensor proliferate abnormally, giving rise to multipl
72 ts that vary in embryo morphology within the suspensor region.
73 e to the embryo proper and an extraembryonic suspensor, respectively.
74 sion, leading to defects in the cells of the suspensor, root and hypocotyl precursors, and provascula
75 trengthening the view that giant specialized suspensors serve as a hormone factory and a conduit for
76 of the 5 tandem repeats is required to drive suspensor-specific transcription.
77                                Subsequently, suspensor-specific WOX8 expression disappears while proe
78 d kinase (IRAK)/Pelle-like kinase gene SHORT SUSPENSOR (SSP) regulates this pathway through a previou
79 y the membrane-associated pseudokinase SHORT SUSPENSOR (SSP) through an unusual parent-of-origin effe
80  pattern formation and associated PCD in the suspensor, strongly suggesting that the actin network is
81 d to the suspensor in species with prominent suspensor structures.
82 unner bean and soybean WOX9, an up-regulated suspensor TF, gained entry into a regulatory network imp
83 er level within the large basal cells of the suspensor that anchor the embryo to the surrounding seed
84 domain required for transcription within the suspensor that contains several copies of a conserved mo
85 g plant embryogenesis is the extra-embryonic suspensor that positions the embryo in the lumen of the
86  of PtNIP1;1 transcript in embryo proper and suspensor tissues by reverse transcription-polymerase ch
87 originating from the proembryo instructs the suspensor to generate the root stem cell niche.
88 stically with the receptor-like kinase SHORT SUSPENSOR to promote suspensor elongation through the YO
89 roper to prevent direct reprogramming of the suspensor toward embryonic fate.
90 f the G564 upstream region is sufficient for suspensor transcription and contains at least three requ
91 Region 2 and Fifth motifs) is sufficient for suspensor transcription, and represents a cis-regulatory
92 letion of these repeats results in a loss of suspensor transcription.
93  the 10-bp-like motifs is also necessary for suspensor transcription.
94  comparing motif sequences shown to activate suspensor transcription.
95 regulatory module that are required for G564 suspensor transcription: the Fifth motif (5'-GAGTTA-3')
96                We compared embryo proper and suspensor transcriptomes of four plants that vary in emb
97 64 mRNA accumulates uniformly throughout the suspensor, whereas C541 mRNA accumulates to a higher lev
98 ort for embryo proper specification from the suspensor, while the suspensorless pathway is polar auxi