ライフサイエンスコーパス: embryogenic

1 Genes encoding heat shock proteins, late embryogenic-abundant proteins, enzymes from the aromatic

2 , and the critical role of angiopoietin-1 in embryogenic angiogenesis was demonstrated by targeted ge

3 bacterium-mediated transformation of friable embryogenic calli (FEC) is the most widely used method t

4 ormants, probably because mass production of embryogenic calli and longer callus growth periods were

5 Molecular analysis of paromomycin-resistant embryogenic calli and of plants regenerated from these c

6 ocol relies on the transformation of compact embryogenic calli derived from immature embryos using vi

7 Gene expression profiles were generated from embryogenic calli induced to undergo embryo maturation a

8 in the establishment of putative transgenic embryogenic calli.

9 1 in roots, leaves, reproductive tissues and embryogenic calli.

10 gene integration and genome editing, friable embryogenic callus (FEC).

11 pression changes were detected between total embryogenic callus and callus enriched for transition st

12 oped based on microprojectile bombardment of embryogenic callus and hygromycin selection.

13 (picloram) inducing the formation of friable embryogenic callus from which highly totipotent embryoge

14 ransformed by microprojectile bombardment of embryogenic callus.

15 id embryo development in culture, also forms embryogenic cell clusters after TSA treatment.

16 ecame nuclear localized before or soon after embryogenic cell divisions began.

17 astid transformation to nongreen plastids in embryogenic cells of cereal crops.

18 amous-like15 (GmAGL15) and GmAGL18 increased embryogenic competence of explants from these transgenic

19 the production of a new and highly prolific embryogenic culture system have been developed in cassav

20 those plant species that utilize dark-grown embryogenic cultures and for characterizing the steps th

21 Transformed plants were regenerated from embryogenic cultures of three Virginia peanut cultivars

22 Somatic embryogenic cultures of white spruce (Picea glauca) repr

23 ms form well-developed suspensors in somatic embryogenic cultures.

24 genesis, and cellular differentiation during embryogenic development.

25 es the somatic initiation of organogenic and embryogenic developmental programs in the leaves.

26 hat recapitulates multiple post-implantation embryogenic events centered around amniotic sac developm

27 amniotic sac embryoid, to recapitulate early embryogenic events of human amniotic sac development.

28 ts roles for chemokine signaling in multiple embryogenic events.

29 n of Apaf-1 into the Apaf-1-containing mouse embryogenic fibroblasts (MEFs; Apaf-1+/- MEFs) or Apaf-1

30 Embryogenic growth is enhanced by, but not dependent on,

31 oportion of cells that switch from pollen to embryogenic growth.

32 ally up-regulates RBR3, but not RBR1, RNA in embryogenic maize calli.

33 ranscript of this gene was only expressed in embryogenic microspores, pollen embryoids, and developin

34 h CDK1 and play partially redundant roles in embryogenic mitosis .

35 These plants were then subjected to embryogenic pollen culture to separate independently int

36 ell and its decendents normally suppress the embryogenic potential of the basal cell and its decenden

37 tion and maintenance of embryo identity, the embryogenic potential of transgenic plants that constitu

38 Xist clouds and H3K27me3 foci, and have full embryogenic potential.

39 ndicated that nuclear extracts isolated from embryogenic rice suspension cells treated with the phyto

40 id screen in yeast using a cDNA library from embryogenic rice suspension cultures and the plant trans

41 lexes were formed when nuclear extracts from embryogenic rice suspension cultures or maize embryos we

42 eared to be developmentally regulated in all embryogenic situations.

43 moter (alpha'-subunit) was used to transform embryogenic soybean cultures.

44 lters leaf morphology and anatomy and causes embryogenic structures to form subcellularly in leaves o

45 ne showed preferential expression in BMS and embryogenic suspension cell cultures vs. endosperm-deriv

46 ryogenic callus from which highly totipotent embryogenic suspension cultures could be established.

47 The availability of embryogenic suspension cultures is considered to have im

48 e (GUS) were generated from rapidly dividing embryogenic suspension-cultured cells co-cultivated with

49 established for the introduction of DNA into embryogenic suspension-derived tissues of cassava via mi

50 y to determine the developmental fate of the embryogenic tissue during somatic embryogenesis through

51 gulating the growth of vegetative as well as embryogenic tissue in a mechanism involving ABA and suga

52 ells anchoring the embryos to the subtending embryogenic tissue, whereas ZmHb1 transcripts extend to

53 in in controlling the development of cassava embryogenic tissues has been demonstrated, with culture

54 e plants were regenerated after cobombarding embryogenic tissues with a mixture of 14 different pUC-b

55 s, presumably by promoting the vegetative-to-embryogenic transition and/or maintaining the identity o

56 ar mechanism that mediates the vegetative-to-embryogenic transition.

57 A-containing transgenic maize calli remained embryogenic, were readily regenerable, and produced fert