ライフサイエンスコーパス: somatic embryogenesis

1 ur distinct genotypes using androgenesis and somatic embryogenesis.

2 useful in other species regenerating through somatic embryogenesis.

3 g61590 is essential for AGL15's promotion of somatic embryogenesis.

4 s of ethylene synthesis or perception reduce somatic embryogenesis.

5 or, that may underlie its ability to promote somatic embryogenesis.

6 genes putatively involved in the process of somatic embryogenesis.

7 the maturation phase and in the induction of somatic embryogenesis.

8 were strongly induced during the process of somatic embryogenesis.

9 regenerated from bombarded cell cultures via somatic embryogenesis.

10 ssect the signal transduction pathway during somatic embryogenesis.

11 ansformation through either organogenesis or somatic embryogenesis.

12 d a high capacity for plant regeneration via somatic embryogenesis.

13 ction similar to zygotic development, making somatic embryogenesis a valuable model for the study of

14 We also uncover functional redundancy for somatic embryogenesis among other Arabidopsis BBM-like p

15 impact of HbCuZnSOD gene over-expression in somatic embryogenesis and in plant development are prese

16 ome genetic conservation between apogamy and somatic embryogenesis and that such asexual reproduction

17 pression patterns correlated with zygotic or somatic embryogenesis, and one gene encodes a putative L

18 ds and inadequate tissue culture systems via somatic embryogenesis are major challenges.

19 Using Zea mays somatic embryogenesis as a model system, we report that

20 main transcriptional regulator that promotes somatic embryogenesis by binding DNA and regulating gene

21 , unlike normal embryogenesis in seeds, leaf somatic embryogenesis bypasses seed dormancy to form via

22 Somatic embryogenesis can be induced in vitro by exposin

23 is with an efficient regeneration system via somatic embryogenesis, cotton plastid transformation was

24 r AGAMOUS-Like15 (AGL15) in the promotion of somatic embryogenesis, direct target genes were identifi

25 Advances in somatic embryogenesis have brought mass clonal propagati

26 ene expression patterns were profiled during somatic embryogenesis in a regeneration-proficient maize

27 enesis in oilseed rape (Brassica napus), and somatic embryogenesis in alfalfa (Medicago sativa).

28 etic similarity between apogamy in ferns and somatic embryogenesis in angiosperms.

29 re significantly up or down-regulated during somatic embryogenesis in Hi II maize line regeneration.

30 F1), which has been shown to be required for somatic embryogenesis in M. truncatula.

31 xpression patterns during the progression of somatic embryogenesis in potato.

32 , we investigated the effects of ethylene on somatic embryogenesis in soybean (Glycine max).

33 cant differential expression patterns during somatic embryogenesis 'induction' phase, 524 during 'emb

34 global gene expression patterns during true somatic embryogenesis initiated from mature and complete

35 Somatic embryogenesis is a more accessible system, and m

36 Somatic embryogenesis is an example of induced cellular

37 y identified genes during critical stages of somatic embryogenesis is discussed.

38 se changes to the ability of LEC2 to promote somatic embryogenesis is discussed.

39 BBM-mediated somatic embryogenesis is dose and context dependent, and

40 We have used the gymnosperm, Picea abies, somatic embryogenesis model system to address this quest

41 NASE (SERK) gene plays a fundamental role in somatic embryogenesis of angiosperms, and is associated

42 rns of a large number of genes during potato somatic embryogenesis (PSE).

43 We report here that the SOMATIC EMBRYOGENESIS RECEPTOR KINASE (SERK) family RLKs

44 In this study, we identify SOMATIC EMBRYOGENESIS RECEPTOR KINASE (SERK)3/brassinost

45 ere we report the isolation of OsSERK2 (rice somatic embryogenesis receptor kinase 2) and demonstrate

46 ands Avr4 and Avr9, BRI1-ASSOCIATED KINASE 1/SOMATIC EMBRYOGENESIS RECEPTOR KINASE 3 (BAK1/SERK3) ass

47 The plant receptor-like kinase somatic embryogenesis receptor kinase 3 (SERK3)/brassino

48 VE 1-associated receptor kinase 1 (BAK1) and somatic embryogenesis receptor kinase 4 (SERK4) redundan

49 tical function in anther development for the SOMATIC EMBRYOGENESIS RECEPTOR KINASE1 (SERK1) and SERK2

50 Somatic embryogenesis receptor kinases (SERKs) are ligan

51 Somatic embryogenesis receptor kinases (SERKs) are trans

52 e factor (ARF ), Leafy cotyledon1 (LEC1) and somatic embryogenesis receptor-like kinase (SERK ) known

53 on requires the interaction of BRI1 with its SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) corece

54 s that non-ligand-binding coreceptors of the SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) family

55 The SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) gene p

56 the leucine-rich repeat receptor-like kinase SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE1 (SERK1) acts

57 Here, we show that SERK1 (SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE1) and SERK2 L

58 Another pair of LRR-RLKs, EVERSHED (EVR) and SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE1, act as inhi

59 EROID INSENSITIVE1-ASSOCIATED KINASE1 (BAK1)/SOMATIC-EMBRYOGENESIS RECEPTOR-LIKE KINASE3, which is a

60 (Glycine max), GmAGL15, are able to promote somatic embryogenesis (SE) in these plants when ectopica

61 Somatic embryogenesis (SE) is a poorly understood proces

62 t growth and development, including in vitro somatic embryogenesis (SE).

63 lved in processes which are more relevant to somatic embryogenesis such as apoptosis, development, re

64 cell survival/death decision that influences somatic embryogenesis through their cell-specific locali

65 mental fate of the embryogenic tissue during somatic embryogenesis through their effect on PCD.

66 ation has recently been accomplished through somatic embryogenesis using species-specific chloroplast

67 Demonstration of plastid transformation via somatic embryogenesis utilizing non-green tissues as rec

68 sponse factor family, effects of ethylene on somatic embryogenesis were investigated.

69 Precursors to ethylene stimulate somatic embryogenesis, whereas inhibitors of ethylene sy

70 M) genes in angiosperms are known to promote somatic embryogenesis, which like apogamy produce sporop

71 nd ABI3 quantitatively regulate BBM-mediated somatic embryogenesis, while FUS3 and LEC1 are essential

72 During somatic embryogenesis, ZmHb2 transcripts are restricted