ライフサイエンスコーパス: conidiophore

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1 induction of fl expression in the developing conidiophore.

2 t of the asexual reproductive structure, the conidiophore.

3 nd bore lateral and terminal, erect, septate conidiophores.

4 ing phase of development required to produce conidiophores.

5 dia, formed on specialized structures called conidiophores.

6 ation and frequent reinitiation of secondary conidiophores.

7 ptum formation in both hyphae and developing conidiophores.

8 l development, aberrant morphogenesis of the conidiophore and an early block in the sexual cycle.

9 er vegetative growth and the assembly of the conidiophore and spore maturation.

10 AfuvelB results in the abundant formation of conidiophores and highly increased AfubrlA mRNA accumula

11 on of multicellular reproductive structures (conidiophores) and chains of uninucleate conidia (spores

12 n of asexual spore-forming structures called conidiophores but does not hinder vegetative hyphal grow

13 er the temporal development of cell types or conidiophore density.

14 During conidiophore development a 6-fold, brlA-dependent increa

15 lopment was further supported by analysis of conidiophore development and septation in cell cycle spe

16 -like sterigmatal cells during multicellular conidiophore development requires correct StuAp-regulate

17 e genetic background is sufficient to induce conidiophore development.

18 of NIMX(CDC2) during G(1)/S, septation, and conidiophore development.

19 mentous growth to budding growth seen during conidiophore development.

20 opmental regulators to control initiation of conidiophore development.

21 f aerial hyphae formation, and no subsequent conidiophore development.

22 A beta gene, but not brlA alpha, to initiate conidiophore development.

23 e products of these two genes in controlling conidiophore development.

24 mation of the development specific structure conidiophores even at 12 h of liquid culture, and near c

25 diospore to mature and get detached from its conidiophore for the first time.

26 Although several factors required for conidiophore formation have been characterized, the mech

27 Conidiophores formed by sepA mutants exhibit abnormal br

28 Thirteen sfgA and 1 sfgC mutants elaborated conidiophores in liquid submerged culture, indicating th

29 s have reduced growth phenotypes and develop conidiophores in submerged cultures.

30 pression of flbC (OEflbC) does not elaborate conidiophores, it inhibits hyphal growth and activates e

31 and there are morphological abnormalities in conidiophores, leading to reduced conidiation.

32 ores that are remarkably similar to wild-tye conidiophores made by air- exposed colonies.

33 Conidiophore morphogenesis in Aspergillus nidulans occur

34 regulated transcription factor required for conidiophore morphogenesis.

35 Altered stuA expression affected conidiophore morphology and conidial yields quantitative

36 Production of conidiophores on edr1 plants, however, was <16% of that

37 Conidiospores are developed in a single conidiophore one after another.

38 owdery mildew, than wild type as measured by conidiophore production.

39 The Deltaace2 mutant had dysmorphic conidiophores, reduced conidia production and abnormal c

40 oxyurea, while snxC1 causes septation in the conidiophore stalk and aberrant conidiophore structure.

41 ation in the conidiophore stalk and aberrant conidiophore structure.

42 lminates in the formation of a multicellular conidiophore that bears spores known as conidia.

43 ulture and leads to the formation of complex conidiophores that are remarkably similar to wild-tye co

44 ced elaborate sporulation structures, called conidiophores, under environmental conditions that block

45 al modifier medusa (medA) result in aberrant conidiophores with branching chains of reiterated reprod

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