ライフサイエンスコーパス: somatic embryogenesis

1 gramming during plant regeneration driven by somatic embryogenesis.

2 ur distinct genotypes using androgenesis and somatic embryogenesis.

3 useful in other species regenerating through somatic embryogenesis.

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

5 s of ethylene synthesis or perception reduce somatic embryogenesis.

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

7 genes putatively involved in the process of somatic embryogenesis.

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

9 were strongly induced during the process of somatic embryogenesis.

10 regenerated from bombarded cell cultures via somatic embryogenesis.

11 ssect the signal transduction pathway during somatic embryogenesis.

12 ansformation through either organogenesis or somatic embryogenesis.

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

14 the formation of a complete plantlet through somatic embryogenesis.

15 ming of gene expression patterns involved in somatic embryogenesis.

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

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

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

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

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

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

22 rk responsible for cell reprogramming during somatic embryogenesis are still largely unclear.

23 ly associated with endosperm development and somatic embryogenesis, are not considered.

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

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

26 Induction of somatic embryogenesis by exogenous auxin requires OsBBM

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

28 Somatic embryogenesis can be induced in vitro by exposin

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

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

31 In somatic embryogenesis, exogenous auxin triggers OsBBM1 e

32 bserved that Tnt1 actively transposed during somatic embryogenesis, generating an average of 6.37 ins

33 Advances in somatic embryogenesis have brought mass clonal propagati

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

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

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

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

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

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

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

41 Propagation by somatic embryogenesis in Theobroma cacao has some issues

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

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

44 Somatic embryogenesis is a major process for plant regen

45 Somatic embryogenesis is a more accessible system, and m

46 Somatic embryogenesis is an example of induced cellular

47 Somatic embryogenesis is an important tissue culture tec

48 Somatic embryogenesis is crucial for plant genetic engin

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

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

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

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

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

54 regions to maintain genome integrity during somatic embryogenesis over the short term, which eventua

55 gistically induce regeneration involving the somatic embryogenesis pathway and can break recalcitranc

56 This study developed somatic embryogenesis protocols for Picea pungens (Engel

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

58 ptors HAESA (HAE) and HAESA-LIKE2 (HSL2) and somatic embryogenesis receptor kinase (SERK) co-receptor

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

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

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

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

63 the association of MIK2 and the coreceptors SOMATIC EMBRYOGENESIS RECEPTOR KINASE 3 (SERK3) and SERK

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

65 inosteroid insensitive 1-associated kinase 1/somatic embryogenesis receptor kinase 3).

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

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

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

69 Somatic embryogenesis receptor kinases (SERKs) are ligan

70 Somatic embryogenesis receptor kinases (SERKs) are trans

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

72 immunomodulatory phytocytokines and recruit SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) co-rec

73 duced interaction with a shape complementary SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) corece

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

75 CLE19 induces the interactions of PXL1 with SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) corece

76 he short leucine-rich repeat (LRR) domain of SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) family

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

78 In complex with members of the SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) family

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

80 this study, we show that loss of function of SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) genes

81 The plasma membrane-resident SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE 1, the BOTRYT

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

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

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

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

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

87 Somatic embryogenesis (SE) is a developmental process re

88 Somatic embryogenesis (SE) is a poorly understood proces

89 Somatic embryogenesis (SE) is a powerful model system fo

90 Maize somatic embryogenesis (SE) requires the induction of emb

91 Tnt1 retro-transposition event occurs during somatic embryogenesis (SE), a pivotal process that trigg

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

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

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

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

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

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

98 rst time the methylome landscape of T. cacao somatic embryogenesis was examined, using whole-genome b

99 rstand the genomic and epigenomic impacts of somatic embryogenesis, we characterized soybean (Glycine

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

101 c trigger in the zygote and can also promote somatic embryogenesis when ectopically expressed in soma

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

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

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

105 Ectopic OsBBM1 initiates somatic embryogenesis without exogenous auxins but requi

106 During somatic embryogenesis, ZmHb2 transcripts are restricted