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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 be associated to the development of abnormal somatic embryos.
6 o explain the morphological abnormalities of somatic embryos.
7 thylene and its precursor involvement in the somatic embryo abnormalities in cacao are discussed.
8 he aim to understand the epigenetic basis of somatic embryo abnormalities.
9 olecular markers from carrot (Daucus carota) somatic embryos and characterizing the expression and re
10 n transgenic plants induces the formation of somatic embryos and other organ-like structures and ofte
11 he cre gene, conferring Cre functionality in somatic embryos and recombination of lox sites resulting
12 ts expression pattern in banana cell clumps, somatic embryos and regenerated plantlets was characteri
13 f a functional LEC1 promotes viviparous leaf somatic embryos and thus enhances vegetative propagation
14 ture loblolly pine (Pinus taeda) zygotic and somatic embryos, but is undetectable in later-stage embr
15 t that PEG may improve the quality of spruce somatic embryos by promoting normal differentiation of t
16                                     Globular somatic embryos can be induced from immature cotyledons
17                                              Somatic embryos develop from the adaxial side of the cot
18 ion of orthologs of AGL15 is able to enhance somatic embryo development in other species, thereby fac
19 ssed the soybean protein was able to enhance somatic embryo development in soybean.
20 h many genes varied in expression throughout somatic embryo development in this study, no statistical
21 aturation phase, and is sufficient to induce somatic embryo development in vegetative cells.
22 profiling gene expression during zygotic and somatic embryo development to support studies aiming to
23 -LIKE15 (AGL15) has been reported to enhance somatic embryo development when constitutively expressed
24 NDUCED PROTEIN30 is involved in promotion of somatic embryo development.
25 ays showed significant time variation during somatic embryo development.
26  AATP1 and DOX2, in the regulation of cotton somatic embryo development.
27 na ortholog of LEC1 is expressed during leaf somatic embryo development.
28 iosynthesis inhibitor fluridone, which broke somatic-embryo dormancy and promoted their normal develo
29                                  The soybean somatic embryos expressing ManS cDNA contained high leve
30  Ectopic accumulation of AGL15 also promoted somatic embryo formation after germination from the shoo
31 ssion of either transcription factor induces somatic embryo formation from Arabidopsis (Arabidopsis t
32 induced overexpression caused high-frequency somatic embryo formation in all tissues and organs teste
33 ograms a stomatal precursor to a totipotent, somatic embryo founder cell.
34 e generation of an unorganized cell mass and somatic embryos from a single root hair.
35     A total of 69.9% or more of cotyledonary somatic embryos germinated normally and developed into n
36 y anionic molecule inhibitory to early-stage somatic embryo growth of loblolly pine (LP) was purified
37                                 Formation of somatic embryos in plants is known to require high conce
38 caused several developmental defects to leaf somatic embryos, including seed dormancy characteristics
39 opical application of InsP(6) to early-stage somatic embryos indeed inhibits embryonic growth.
40  Our results indicate that the appearance of somatic embryos is preceded by dedifferentiation of the
41                                              Somatic embryos of jack, a Glycine max (L.) Merrill cult
42 nd subtracted RNA populations of zygotic and somatic embryos of loblolly pine (Pinus taeda L.).
43 f seed germination attributes and effects on somatic embryo production.
44 actors and is related to Medicago truncatula somatic embryo-related factor1 (MtSERF1), which has been
45 an and C. americana DGAT variants in soybean somatic embryos resulted in oil contents as high as 10%
46 D2-1 in Saccharomyces cerevisiae and soybean somatic embryos resulted in the accumulation of the tran
47  several steps during the development of the somatic embryo (Sem) that are suboptimal compared to zyg
48                         We used the P. abies somatic embryo system and a combination of reverse genet
49 lity of the subtracted-probe approach to the somatic embryo system.
50  be solved, as many morphologically abnormal somatic embryos that do not germinate into plants are fr
51 phenoxyacetic acid can be induced to develop somatic embryos upon their transfer to an auxin-free med
52          Transformation efficiency of carrot somatic embryos was very high, with one transgenic event
53           Upon inducer withdrawal, all these somatic embryos were able to germinate directly, without
54  range of time-points until the emergence of somatic embryos, were compared in a loop design to ident
55 between zygotic embryos, normal and abnormal somatic embryos, with important roles in development, pr