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1 r localization to sporogenic compartments of aerial hyphae.
2 vision and genome segregation in specialized aerial hyphae.
3 vel compartment, the 'subapical stem' of the aerial hyphae.
4 equisite to sporulation, which occurs in the aerial hyphae.
5 g that sigNP1 activity was restricted to the aerial hyphae.
6 governing the pathway for spore formation in aerial hyphae.
7 utants of S. coelicolor the ability to raise aerial hyphae.
8 s facilitating the emergence of newly formed aerial hyphae.
9 orphogenesis restores their capacity to form aerial hyphae.
10 nown to be required for the morphogenesis of aerial hyphae.
11 e down-regulated in a mutant unable to erect aerial hyphae.
12 strate mycelia, but was completely absent in aerial hyphae.
13  when sporulation septa were observed in the aerial hyphae.
14 on and degradation of FtsZ within individual aerial hyphae.
15  when sporulation septa were observed in the aerial hyphae.
16 yed pleiotropic defects, including shortened aerial hyphae, altered conidiation pattern, female steri
17  resulted in weakened hyphal tips, misshaped aerial hyphae and anucleate spores and demonstrates that
18 nts lacking the chaplins are unable to erect aerial hyphae and differentiate on minimal media.
19           Deletion of gna-3 leads to shorter aerial hyphae and premature, dense conidiation during gr
20 entary osmolyte, an osaB mutant cannot erect aerial hyphae and produces up to fivefold greater antibi
21 eriments demonstrate that the development of aerial hyphae and spores by S. coelicolor is inhibited b
22 nts of the hydrophobic sheath that coats the aerial hyphae and spores in Streptomyces, and mutants la
23 ant and the devA promoter was also active in aerial hyphae and spores in this background, suggesting
24  hydrophobic sheath that covers Streptomyces aerial hyphae and spores.
25 ree developmental stages: vegetative hyphae, aerial hyphae and spores.
26 isea causes severe defects in development of aerial hyphae and spores.
27 e for clavusporins as morphogens in erecting aerial hyphae and thereby advancing sporulation and prol
28 ensitivity, delayed or impaired formation of aerial hyphae, and a block in spore formation.
29 evelopment of reproductive structures called aerial hyphae, and differentiation of these aerial filam
30 ants have reduced growth rate, produce short aerial hyphae, and fail to develop protoperithecia.
31 omyces form multicellular vegetative hyphae, aerial hyphae, and spores.
32           The devA mutant produced only rare aerial hyphae, and those that were produced developed ab
33  when sporulation septa were observed in the aerial hyphae, and transcription from both promoters dep
34 undetermined steps within the spore-yielding aerial hyphae as well.
35  However, analysis of mutants unable to form aerial hyphae (bld mutants) showed that sigHp2 transcrip
36 fferentiation contributes to the erection of aerial hyphae by decreasing the surface tension at the c
37 y B. subtilis that inhibits the formation of aerial hyphae by streptomycetes.
38 signal transduction pathway(s) that regulate aerial hyphae development and sensitivity to heat and ox
39         Reproduction occurs when specialized aerial hyphae differentiate into chains of spores.
40                    These strains form little aerial hyphae during asexual development on solid medium
41 sulted in reduced colony size with increased aerial hyphae, elevated accumulation of brown pigments a
42                                However, such aerial hyphae fail to sporulate, exemplifying the need t
43 se activity of GNA-2 cause subtle defects in aerial hyphae formation and conidial germination.
44 vps27) exhibited a reduction in growth rate, aerial hyphae formation and hydrophobicity.
45 s in conidiogenesis, fruit body development, aerial hyphae formation and infection structure elaborat
46 plin genes examined (chpE, chpH) depended on aerial hyphae formation but not sporulation, and egfp fu
47 tinomycete, Amycolatopsis sp. AA4, inhibited aerial hyphae formation in adjacent colonies of Streptom
48 ts, as illustrated by its ability to restore aerial hyphae formation when applied exogenously to deve
49 ion of chaplin genes caused severe delays in aerial hyphae formation, a phenotype rescued by exogenou
50 ar wild-type growth rates, female fertility, aerial hyphae formation, and hyphal fusion, but not vege
51 leads to restricted colonial growth, loss of aerial hyphae formation, and no subsequent conidiophore
52 d medium, when its activation coincided with aerial hyphae formation.
53 igHp2 is dramatically induced at the time of aerial hyphae formation.
54 rose-free R2YE, where division sites in many aerial hyphae had finished constricting and chains of sp
55                                      Loss of aerial hyphae in developmental mutants can be rescued by
56  fungal proteins involved in the erection of aerial hyphae in the filamentous fungus Schizophyllum co
57 ption is spatially restricted to sporulating aerial hyphae in wild-type S. coelicolor.
58 ase appears to be required for conversion of aerial hyphae into chains of spores, SCO6938 is a probab
59 o the role of whi genes in the conversion of aerial hyphae into chains of spores.
60 quired for the conversion of multinucleoidal aerial hyphae into chains of uninucleoidal spores, altho
61 e differentiation of Streptomyces coelicolor aerial hyphae into mature spore chains, was localized by
62 nvolving the differentiation of reproductive aerial hyphae into spores.
63 inating growth and cytokinesis in sporogenic aerial hyphae, is largely unknown.
64 GFP foci were not uniformly positioned along aerial hyphae, nor were they associated with every conde
65 n substitute for SapB in a mutant that lacks aerial hyphae, not all surfactants have this effect.
66 he orderly multiple sporulation septation of aerial hyphae of Streptomyces coelicolor A3(2) and for t
67 igma factors required for sporulation in the aerial hyphae of Streptomyces coelicolor.
68                   These mutants fail to form aerial hyphae on rich medium and most are defective in a
69 pores within yellow or yellow-green tufts of aerial hyphae on sporulation media.
70 nvolves the formation of a lawn of hair-like aerial hyphae on the colony surface that stands up in th
71 na-1(Q204L) strains elaborate abundant, long aerial hyphae, produce less conidia, and possess lower l
72                              In contrast, in aerial hyphae regularly spaced bright foci accompanied s
73 nscription of nepA originated from a single, aerial hyphae-specific and sigN-dependent promoter.
74 roteins produced by fungi during assembly of aerial hyphae, sporulation, mushroom development and pat
75 s many septa synchronously form in syncytial aerial hyphae such that prespore compartments accurately
76 re defective in macroconidiation, possessing aerial hyphae that are shorter, contain abnormal swellin
77 n involving the formation of a dense lawn of aerial hyphae that grow away from the colony surface int
78 tiates by forming specialized, spore-bearing aerial hyphae that grow into the air.
79 es produce a remarkable cell type called the aerial hyphae that is central to its ability to meet bot
80 the envelope by the chaplins is required for aerial hyphae to grow out of the aqueous environment of
81 he mycelial architecture and the erection of aerial hyphae were affected by the expression of clsA.
82 area constitutes the support for the growing aerial hyphae, which do not have direct contact with the
83   R273 and R318 produce long, tightly coiled aerial hyphae with frequent septation.
84 r A3(2) ftsI- and ftsW-null mutants produced aerial hyphae with no evidence of septation when grown o
85 r ftsL or divIC resulted in the formation of aerial hyphae with partially constricted division sites
86 type; it produces straight, undifferentiated aerial hyphae with very rare short chains of spores.
87 rly spaced, ladder-like arrays in developing aerial hyphae, with an average spacing of about 1.3 micr