ライフサイエンスコーパス: pseudohyphae

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1 ed cells were viable and formed constitutive pseudohyphae.

2 cut molecular distinction between hyphae and pseudohyphae.

3 The Deltatup1 mutant formed only pseudohyphae.

4 G1 cyclin genes in strains competent to form pseudohyphae.

5 o serum or to a serum filtrate but does form pseudohyphae.

6 yeast form cells to multicellular, invasive pseudohyphae.

7 ents and the TEC1 gene during development of pseudohyphae.

8 bud-site selection cues in the formation of pseudohyphae.

9 a cellular yeast form or in filaments called pseudohyphae.

10 tes cell cycle dependent growth in yeast and pseudohyphae.

11 Germ tubes of hyphae and pseudohyphae also have different widths.

12 rrelate with the ability of yeast to produce pseudohyphae and hyphae and to invade corneal tissue.

13 Pseudohyphae and hyphae are both elongated and sometimes

14 Cellular differences between pseudohyphae and hyphae are further revealed by septin l

15 t least three different morphologies: yeast, pseudohyphae and hyphae.

16 ogen, displays three modes of growth: yeast, pseudohyphae and true hyphae, all of which differ both i

17 r yeast or as filamentous forms that include pseudohyphae and true hyphae.

18 to determine whether the cells are hyphae or pseudohyphae and we suggest some simple experimental cri

19 Gin4-depleted pseudohyphae are unable to form hyphae when challenged w

20 gma1278b with deletions of FLO11 do not form pseudohyphae as diploids nor invade agar as haploids.

21 ced PMNL-mediated damage of Candida albicans pseudohyphae by 33% (P=.007) on day 2 and by 44% (P=.04)

22 at both gin4Delta and hsl1Delta mutants form pseudohyphae constitutively, in a fashion that in the ca

23 is critically required for both invasion and pseudohyphae formation in response to nitrogen starvatio

24 filamentous growth, unable to form hyphae or pseudohyphae in response to many stimuli, including seru

25 Diploid yeast develop pseudohyphae in response to nitrogen starvation, while h

26 phogenetic transition from the yeast form to pseudohyphae in Saccharomyces cerevisiae may be regulate

27 In pseudohyphae induced by growth at 35 degrees C in YEPD o

28 DC with T. rubrum (but not with C. albicans pseudohyphae) induced phosphorylation of DC-HIL, but not

29 est, C. albicans was able to bud and develop pseudohyphae inside human BMEC without apparent morpholo

30 This dimorphic transition from yeast to pseudohyphae is induced by starvation for nitrogen.

31 eiosis aberrantly, and their ability to form pseudohyphae is significantly diminisehd.

32 ins localized to a tight ring at the bud and pseudohyphae necks and as a more diffuse array in emergi

33 by compromise of Hsp90 function are neither pseudohyphae nor hyphae but closely resemble filaments f

34 ilamentation as ste12 mutants rarely produce pseudohyphae on nitrogen depleted media.

35 C was defined as the presence of yeast buds, pseudohyphae, or both on a wet preparation (including po

36 ptional profiling that genes associated with pseudohyphae represent a subset of those associated with

37 Yeast or pseudohyphae that undergo a cell cycle delay also exhibi

38 ted to sequentially transition from yeast to pseudohyphae to hyphae in the absence of complex environ

39 4 may regulate the developmental switch from pseudohyphae to hyphae.

40 he germ tubes of Candida albicans hyphae and pseudohyphae was studied using an antibody to Saccharomy

41 Filamentation (pseudohyphae) was associated with DB colonies.

42 grow only in the yeast form and fail to form pseudohyphae when starved for nitrogen.

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