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1     Genes encoding heat shock proteins, late embryogenic-abundant proteins, enzymes from the aromatic
2 n the human connectome is a product of their embryogenic age, such that early-born nodes should becom
3  structural centrality correlated with their embryogenic age, supporting our hypothesis.
4    Using a human brain segmentation based on embryogenic age, we observed that nodes' structural cent
5 , and the critical role of angiopoietin-1 in embryogenic angiogenesis was demonstrated by targeted ge
6 bacterium-mediated transformation of friable embryogenic calli (FEC) is the most widely used method t
7 ormants, probably because mass production of embryogenic calli and longer callus growth periods were
8  Molecular analysis of paromomycin-resistant embryogenic calli and of plants regenerated from these c
9 ocol relies on the transformation of compact embryogenic calli derived from immature embryos using vi
10 Gene expression profiles were generated from embryogenic calli induced to undergo embryo maturation a
11 ed in ROS generation were upregulated in the embryogenic calli of GP.
12 1 in roots, leaves, reproductive tissues and embryogenic calli.
13  in the establishment of putative transgenic embryogenic calli.
14 gene integration and genome editing, friable embryogenic callus (FEC).
15 pression changes were detected between total embryogenic callus and callus enriched for transition st
16 embryogenesis (SE) requires the induction of embryogenic callus and establishment of proliferation be
17 oped based on microprojectile bombardment of embryogenic callus and hygromycin selection.
18 (picloram) inducing the formation of friable embryogenic callus from which highly totipotent embryoge
19 ransformed by microprojectile bombardment of embryogenic callus.
20 ene function and improvement due to its high embryogenic capacity and many contrasting traits to the
21 id embryo development in culture, also forms embryogenic cell clusters after TSA treatment.
22 ecame nuclear localized before or soon after embryogenic cell divisions began.
23                                       Banana embryogenic cell suspensions (ECSs) treated with FSA exh
24 astid transformation to nongreen plastids in embryogenic cells of cereal crops.
25 amous-like15 (GmAGL15) and GmAGL18 increased embryogenic competence of explants from these transgenic
26  the production of a new and highly prolific embryogenic culture system have been developed in cassav
27  those plant species that utilize dark-grown embryogenic cultures and for characterizing the steps th
28     Transformed plants were regenerated from embryogenic cultures of three Virginia peanut cultivars
29                                      Somatic embryogenic cultures of white spruce (Picea glauca) repr
30 ms form well-developed suspensors in somatic embryogenic cultures.
31 regulate the expression of genes involved in embryogenic development as well as adult life.
32 genesis, and cellular differentiation during embryogenic development.
33 es the somatic initiation of organogenic and embryogenic developmental programs in the leaves.
34 hat recapitulates multiple post-implantation embryogenic events centered around amniotic sac developm
35 amniotic sac embryoid, to recapitulate early embryogenic events of human amniotic sac development.
36 ts roles for chemokine signaling in multiple embryogenic events.
37 n of Apaf-1 into the Apaf-1-containing mouse embryogenic fibroblasts (MEFs; Apaf-1+/- MEFs) or Apaf-1
38                                              Embryogenic growth is enhanced by, but not dependent on,
39 oportion of cells that switch from pollen to embryogenic growth.
40 ally up-regulates RBR3, but not RBR1, RNA in embryogenic maize calli.
41 e conifer species, including needles and pro-embryogenic mass (PEM), is also present in Arabidopsis c
42 evelopmental stages of SE, starting with pro-embryogenic masses (PEMs) up until germination, revealed
43 ranscript of this gene was only expressed in embryogenic microspores, pollen embryoids, and developin
44 h CDK1 and play partially redundant roles in embryogenic mitosis .
45 ere, we report that KIF2A is dispensable for embryogenic neurogenesis but critical in postnatal stage
46             NODAL, a morphogen essential for embryogenic patterning, is often reexpressed in breast c
47          These plants were then subjected to embryogenic pollen culture to separate independently int
48 l stages and displaying contrasting in vitro embryogenic potential and morphology.
49   The molecular mechanisms underlying callus embryogenic potential are not well understood.
50 ell and its decendents normally suppress the embryogenic potential of the basal cell and its decenden
51 tion and maintenance of embryo identity, the embryogenic potential of transgenic plants that constitu
52 Xist clouds and H3K27me3 foci, and have full embryogenic potential.
53 uccessfully conducted genome modification of embryogenic protoplast cells and epicotyl tissues.
54 n within 10 months through transformation of embryogenic protoplasts with Cas12a/crRNA ribonucleoprot
55 ndicated that nuclear extracts isolated from embryogenic rice suspension cells treated with the phyto
56 id screen in yeast using a cDNA library from embryogenic rice suspension cultures and the plant trans
57 lexes were formed when nuclear extracts from embryogenic rice suspension cultures or maize embryos we
58 eared to be developmentally regulated in all embryogenic situations.
59 moter (alpha'-subunit) was used to transform embryogenic soybean cultures.
60 lters leaf morphology and anatomy and causes embryogenic structures to form subcellularly in leaves o
61 ne showed preferential expression in BMS and embryogenic suspension cell cultures vs. endosperm-deriv
62 ryogenic callus from which highly totipotent embryogenic suspension cultures could be established.
63                          The availability of embryogenic suspension cultures is considered to have im
64 e (GUS) were generated from rapidly dividing embryogenic suspension-cultured cells co-cultivated with
65 established for the introduction of DNA into embryogenic suspension-derived tissues of cassava via mi
66 y to determine the developmental fate of the embryogenic tissue during somatic embryogenesis through
67 gulating the growth of vegetative as well as embryogenic tissue in a mechanism involving ABA and suga
68 ells anchoring the embryos to the subtending embryogenic tissue, whereas ZmHb1 transcripts extend to
69                                              Embryogenic tissues (ET) from 13 clones of three familie
70 in in controlling the development of cassava embryogenic tissues has been demonstrated, with culture
71                                      Somatic embryogenic tissues were induced from mature zygotic emb
72 e plants were regenerated after cobombarding embryogenic tissues with a mixture of 14 different pUC-b
73 ss of cystic proliferation was observed from embryogenic to adult stages, impacting the success of ga
74 s, presumably by promoting the vegetative-to-embryogenic transition and/or maintaining the identity o
75 ar mechanism that mediates the vegetative-to-embryogenic transition.
76 OsBBM1) transcription factor functions as an embryogenic trigger in the zygote and can also promote s
77 A-containing transgenic maize calli remained embryogenic, were readily regenerable, and produced fert