ライフサイエンスコーパス: somatic embryo

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1 er, AGL18, show decreased ability to produce somatic embryos.

2 ortholog of AGL15 was isolated from soybean somatic embryos.

3 lus and callus enriched for transition stage somatic embryos.

4 cing conditions, allowing the development of somatic embryos.

5 olecular markers from carrot (Daucus carota) somatic embryos and characterizing the expression and re

6 n transgenic plants induces the formation of somatic embryos and other organ-like structures and ofte

7 he cre gene, conferring Cre functionality in somatic embryos and recombination of lox sites resulting

8 ts expression pattern in banana cell clumps, somatic embryos and regenerated plantlets was characteri

9 f a functional LEC1 promotes viviparous leaf somatic embryos and thus enhances vegetative propagation

10 ture loblolly pine (Pinus taeda) zygotic and somatic embryos, but is undetectable in later-stage embr

11 t that PEG may improve the quality of spruce somatic embryos by promoting normal differentiation of t

12 Globular somatic embryos can be induced from immature cotyledons

13 Somatic embryos develop from the adaxial side of the cot

14 ion of orthologs of AGL15 is able to enhance somatic embryo development in other species, thereby fac

15 ssed the soybean protein was able to enhance somatic embryo development in soybean.

16 h many genes varied in expression throughout somatic embryo development in this study, no statistical

17 aturation phase, and is sufficient to induce somatic embryo development in vegetative cells.

18 -LIKE15 (AGL15) has been reported to enhance somatic embryo development when constitutively expressed

19 NDUCED PROTEIN30 is involved in promotion of somatic embryo development.

20 ays showed significant time variation during somatic embryo development.

21 na ortholog of LEC1 is expressed during leaf somatic embryo development.

22 iosynthesis inhibitor fluridone, which broke somatic-embryo dormancy and promoted their normal develo

23 The soybean somatic embryos expressing ManS cDNA contained high leve

24 Ectopic accumulation of AGL15 also promoted somatic embryo formation after germination from the shoo

25 ssion of either transcription factor induces somatic embryo formation from Arabidopsis (Arabidopsis t

26 induced overexpression caused high-frequency somatic embryo formation in all tissues and organs teste

27 e generation of an unorganized cell mass and somatic embryos from a single root hair.

28 y anionic molecule inhibitory to early-stage somatic embryo growth of loblolly pine (LP) was purified

29 Formation of somatic embryos in plants is known to require high conce

30 caused several developmental defects to leaf somatic embryos, including seed dormancy characteristics

31 opical application of InsP(6) to early-stage somatic embryos indeed inhibits embryonic growth.

32 Our results indicate that the appearance of somatic embryos is preceded by dedifferentiation of the

33 Somatic embryos of jack, a Glycine max (L.) Merrill cult

34 nd subtracted RNA populations of zygotic and somatic embryos of loblolly pine (Pinus taeda L.).

35 f seed germination attributes and effects on somatic embryo production.

36 actors and is related to Medicago truncatula somatic embryo-related factor1 (MtSERF1), which has been

37 an and C. americana DGAT variants in soybean somatic embryos resulted in oil contents as high as 10%

38 D2-1 in Saccharomyces cerevisiae and soybean somatic embryos resulted in the accumulation of the tran

39 We used the P. abies somatic embryo system and a combination of reverse genet

40 lity of the subtracted-probe approach to the somatic embryo system.

41 phenoxyacetic acid can be induced to develop somatic embryos upon their transfer to an auxin-free med

42 Transformation efficiency of carrot somatic embryos was very high, with one transgenic event

43 Upon inducer withdrawal, all these somatic embryos were able to germinate directly, without

44 range of time-points until the emergence of somatic embryos, were compared in a loop design to ident

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