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1 ination, but stimulates asexual sporulation (conidiation).
2 ingle locus, designated rco-1 (regulation of conidiation).
3  biosynthesis but also vegetative growth and conidiation.
4 microtubule-depolymerizing agent benomyl for conidiation.
5 ting the idea that GanB signalling represses conidiation.
6 luG function but also results in hyperactive conidiation.
7  compartmentation, nuclear distribution, and conidiation.
8 ern, suggesting that VIB-1 is a regulator of conidiation.
9 on of Mr-OPY2 elicits saprophytic growth and conidiation.
10 arget of FadA activity, in ST production and conidiation.
11 cated a role for NIMX(CDC2) in septation and conidiation.
12 mX, affects nuclear division, septation, and conidiation.
13 velopmentally regulated and expressed during conidiation.
14  fl gene to determine its role in regulating conidiation.
15 opmentally regulated, being expressed during conidiation.
16 egetative hyphae and to undergo constitutive conidiation.
17 lular signal and regulates the initiation of conidiation.
18  accessions permitted some fungal growth and conidiation.
19 tion of unicellular sterigmata and inhibited conidiation.
20 tation genes exercise feedback regulation of conidiation.
21 dicating a direct repressive role of NsdD in conidiation.
22  distinct positive roles of FlbC and FlbD in conidiation.
23  mutant strains showed a severe reduction in conidiation.
24 n virulence, deoxynivalenol biosynthesis and conidiation.
25 ed in pathogenesis, secondary metabolism and conidiation.
26 AfSUN1 negatively affected hyphal growth and conidiation.
27 e, suggesting that they act as repressors of conidiation.
28 e of the key environmental factors affecting conidiation.
29  regulation of phialide morphogenesis during conidiation.
30 B expression during the mid to late phase of conidiation.
31 viously identified genetic locus controlling conidiation.
32 rhythm is visible and cultures show constant conidiation.
33 SPB and is required for timely septation and conidiation.
34 , FlbC, FlbB, and BrlA) necessary for normal conidiation.
35 nases SEPH and SIDB for septum formation and conidiation.
36 st the SIN pathway to regulate septation and conidiation.
37 alities in conidiophores, leading to reduced conidiation.
38  sfg mutants show varying levels of restored conidiation, all recovered the ability to produce ST at
39 ative growth to induced asexual sporulation (conidiation) along a decreasing phenazine gradient.
40 ediated suppression of host pigmentation and conidiation, although to a lesser extent, and is dispens
41 pecifically in differentiating tissue during conidiation and acon-2 plays a role in this induction.
42 ese results demonstrate that GNA-3 modulates conidiation and adenylyl cyclase levels in N. crassa.
43                                          The conidiation and aerial hypha defects of the Deltagna-3 s
44 V29 severely affected the vegetative growth, conidiation and biotrophic invasion of the fungus in sus
45 ed hyphal growth and differential effects on conidiation and cyclosporine resistance.
46 le of SfgA, overexpression of sfgA inhibited conidiation and delayed/reduced expression of conidiatio
47 found that MoGlo3 is highly expressed during conidiation and early infection stages and is required f
48 e wild-type strain, and circadian rhythms of conidiation and FRQ protein oscillation were observed to
49 show severe growth inhibition, repression of conidiation and hyphal compartmentation and death (HCD).
50 t delay in mycelial growth, complete loss of conidiation and inability to penetrate the host surface
51 was identified and its functions involved in conidiation and mycoparasitism were studied.
52 hat CmNox1, but not CmNox2, is necessary for conidiation and parasitism, and its expression could be
53 ulatory factor of CmNox1 and was involved in conidiation and parasitism.
54 egulates CmNox1-CmSlt2 pathway in regulating conidiation and pathogenicity of C. minitans.
55 servative signal modulator, dictates growth, conidiation and pathogenicity of M. oryzae.
56 e phenotypes, and advances our insights into conidiation and pigmentation in this fungus.
57 sfgA mutations bypassed the need for fluG in conidiation and production of ST.
58 Loss of fluG results in the blockage of both conidiation and production of the mycotoxin sterigmatocy
59 f peanut seeds as reflected by a decrease in conidiation and production of the seed degradative enzym
60 velopmental defects included reduced (> 90%) conidiation and reduced dimorphic transition to the prod
61 ent roles of the velvet regulators governing conidiation and sporogenesis in A. fumigatus is presente
62                          Filamentous growth, conidiation and the differentiation of PH-like asexual r
63 le mutant had more severe defects in growth, conidiation and virulence than the Fgatf1 or Fgskn7 muta
64 etion mutant was slightly reduced in growth, conidiation and virulence.
65 ons in hyphal polarity, marked activation of conidiation and yeast-like growth.
66 ttern formation during asexual reproduction (conidiation) and for initiation of the sexual reproducti
67 velB causes hyperactive asexual development (conidiation) and precocious and elevated accumulation of
68 ssary for activation of asexual sporulation (conidiation) and production of the carcinogenic mycotoxi
69    The Fgcdc14 mutant was reduced in growth, conidiation, and ascospore formation.
70 ecrease in growth rate, drastic reduction in conidiation, and complete loss of sexual development.
71 and myoE are necessary for proper septation, conidiation, and conidial germination, but only myoB is
72 etion resulted in reduced vegetative growth, conidiation, and conidial germination.
73 nt, resolution of iron starvation, increased conidiation, and enhanced resistance to oxidative stress
74 on factor necessary for proper activation of conidiation, and its balanced activity is crucial for go
75  is detectable during both hyphal growth and conidiation, and its gene product is similar to the Myb
76      Taken together, FgSRP1 is important for conidiation, and pathogenesis and alternative splicing i
77 molog, also plays important roles in growth, conidiation, and pathogenicity.
78  resulted in identical phenotypes in growth, conidiation, and ST production, indicating that the prim
79 onidiation and delayed/reduced expression of conidiation- and ST-specific genes.
80                       Loss of BcJAR1 impairs conidiation, appressorium formation and stress adaptatio
81 omoter resulted in defects in hyphal growth, conidiation, appressorium penetration and pathogenicity,
82 both wc-1 and fluffy show that regulators of conidiation are elevated in ras-1(bd).
83  commencement, progression and completion of conidiation are regulated by multiple positive and negat
84 cadian rhythms in asexual spore development (conidiation) are abolished in constant conditions, yet c
85 pharmacological treatment, but also affected conidiation, ascospore formation and pathogenicity.
86  In Neurospora crassa, a circadian rhythm of conidiation (asexual spore formation) can be seen on the
87 lts from Northern analysis support light and conidiation-based regulation of nop-1 gene expression, a
88 ortant for cellular division, branching, and conidiation both pre- and postmitotically.
89 n the promoter of the essential activator of conidiation brlA, indicating a direct repressive role of
90 deletion of flbC causes a delay/reduction in conidiation, brlA and vosA expression, and conidial germ
91 md1 deletion mutant was normal in growth and conidiation but defective in ascospore discharge due to
92 Uvhog1 mutant was reduced in growth rate and conidiation but had increased sensitivities to SDS, Cong
93 enes, including con-10, are expressed during conidiation but not during mycelial growth.
94 f the Fgimd1 mutant in vegetative growth and conidiation but not sexual reproduction, whereas additio
95  MOBA protein was required for septation and conidiation, but was not essential for hyphal extension
96 It was found that Hog1-MAPK regulates fungal conidiation by controlling the conidiation regulatory pa
97 iated suppression of fungal pigmentation and conidiation by providing an accessory function in hypovi
98  phosphorylation state in regulating growth, conidiation, calcium and cell wall stress tolerance, and
99  mycelial phase included several involved in conidiation, cell polarity, and melanin production in ot
100                                    About 287 conidiation, colony sectorization or pathogenicity loci,
101 relieved growth inhibition and repression of conidiation conferred by het-c vegetative incompatibilit
102 normal in the Tox2(+) ccsnf1 mutant, as were conidiation, conidial morphology, conidial germination,
103 ound that N. crassa rca-1 can complement the conidiation defect of an A. nidulans flbD mutant and tha
104 en-starved cultures, but does not bypass the conidiation defect of the acon-3 mutant.
105 with exogenous cAMP suppresses the premature conidiation defect, but aerial hypha formation is still
106 and ETFDH mutations led to severe growth and conidiation defects, which could be largely rescued by e
107 ted in the ability to control entry into the conidiation developmental program were isolated.
108 ates that multiple genes negatively regulate conidiation downstream of fluG and that the activity of
109 he circadian rhythm is expressed as rhythmic conidiation driven by a feedback loop involving the prot
110 o shorter aerial hyphae and premature, dense conidiation during growth on solid medium or in standing
111 ene has been named nrc-1, for nonrepressible conidiation gene #1.
112 ocus is referred to as nrc-2 (nonrepressible conidiation gene #2).
113 ed vegetative repression of con-10 and other conidiation genes.
114         Mutants were examined for effects on conidiation, hyphal growth, cyclosporine and stress resi
115  in F.verticillioides (Deltaubl1) influenced conidiation, hyphal morphology, pigmentation and amyloly
116 metabolites, etc., which may be required for conidiation, IFS formation, host penetration and virulen
117      A genetic model depicting regulation of conidiation in A. nidulans is presented.
118 this study, we report that the FluG-mediated conidiation in A. nidulans occurs via derepression.
119 idence that NIMX(CDC2) affects septation and conidiation in addition to nuclear division, and cloning
120 causes enhanced and precocious activation of conidiation in Aspergillus fumigatus or Aspergillus flav
121                                              Conidiation in Aspergillus nidulans is induced by exposu
122 spora crassa gene called rca-1 (regulator of conidiation in Aspergillus) based on its sequence simila
123                                The defect of conidiation in DeltaCmRac1 could be partially restored b
124                                              Conidiation in filamentous fungi involves many common th
125  Overexpression of rgsA caused inappropriate conidiation in liquid submerged culture, supporting the
126        However, carbon limitation can induce conidiation in mycclia submerged in an aerated liquid me
127 inase that functions to repress the onset of conidiation in N. crassa.
128  and that induced expression of rca-1 caused conidiation in submerged A. nidulans cultures just as wa
129 tanding liquid cultures and to inappropriate conidiation in submerged culture.
130 g alternate carbon sources does not suppress conidiation in submerged culture.
131 hialide morphogenesis and/or function during conidiation in the aspergilli.
132          A FRQ-independent oscillator drives conidiation in the csn-2 mutant, resulting in a 2-d coni
133 ct this factor under conditions that promote conidiation in the veA1 suppressors.
134                                              Conidiation in this DeltaFWO strain was still synchroniz
135                         Asexual development (conidiation) in Aspergillus is governed by multiple regu
136                         Asexual sporulation (conidiation) in the ascomycetous filamentous fungi invol
137                         Asexual sporulation (conidiation) in the filamentous fungus Aspergillus nidul
138                         Asexual development (conidiation) in the filamentous fungus Aspergillus nidul
139        Here, we summarize genetic control of conidiation including the light-responding mechanisms in
140 culture, and near constitutive activation of conidiation, indicating that acquisition of developmenta
141                                              Conidiation induction in A. nidulans by another microbia
142                    NsdD's role in repressing conidiation is conserved in other aspergilli, as deletin
143                            Submerged-culture conidiation is refractory to cAMP but is suppressed by p
144 f TRX2 caused pleiotropic defects in growth, conidiation, light sensing, responses to stresses and pl
145 eover, loss of SEP4 severely impaired mutant conidiation, melanin and chitin accumulation in hyphal t
146          The four rco-1 mutants had distinct conidiation morphologies, suggesting that conidiation wa
147                                       During conidiation Mr-BlrA up-regulates Mr-AbaA, which in turn
148 sn2 proliferation in the host haemolymph and conidiation on the host cadaver was reduced.
149 and GAS2 had no defect in vegetative growth, conidiation, or appressoria formation, but they were red
150 BbSiRNA30 strains were unaffected in growth, conidiation, or under osmotic or cell wall perturbing st
151  and branched and remained totally devoid of conidiation over a period of 2 years on all mycological
152 , including shortened aerial hyphae, altered conidiation pattern, female sterility, slow growth rate,
153        The vib-1 mutants displayed a profuse conidiation pattern, suggesting that VIB-1 is a regulato
154 not vegetative incompatibility and wild-type conidiation pattern.
155  surface hydrophobicity, hyphal polarity and conidiation pattern.
156 were isolated; several of these had abnormal conidiation phenotypes and were trans-acting, i.e., they
157 tors of the SIN suppressed the septation and conidiation phenotypes due to the loss of SNAD.
158  constitutively enter, but not complete, the conidiation program.
159 kinase is required to repress entry into the conidiation program.
160                                  A conserved conidiation regulatory pathway containing Mr-BrlA, Mr-Ab
161 ulates fungal conidiation by controlling the conidiation regulatory pathway, and that all three pigme
162 urthermore, HxtB was shown to be involved in conidiation-related processes and may play a role in dow
163 n) are abolished in constant conditions, yet conidiation remains rhythmic in temperature cycles.
164                                          The conidiation rhythm in L/L in vvd is therefore driven by
165                                          The conidiation rhythm in the fungus Neurospora crassa is a
166 icities of the earth's 24-hour rotation, the conidiation rhythm of the fungus Neurospora crassa was m
167 tion in the csn-2 mutant, resulting in a 2-d conidiation rhythm that persists in constant darkness (D
168 ight-induced phase shifting of the circadian conidiation rhythm.
169 rhythms of gene expression and the circadian conidiation rhythms are abolished in these fwd1 mutants.
170 w short period, low amplitude, or arrhythmic conidiation rhythms in constant darkness.
171 ceptor involved in photo-adaptation, exhibit conidiation rhythms in L/L as well as in D/D.
172 ase gene have pleiotropic effects on growth, conidiation, sexual development, and appressorium format
173  overlapping functions in vegetative growth, conidiation, sexual reproduction and plant infection, de
174         The three key negative regulators of conidiation SfgA, VosA, and NsdD act at different contro
175                                    Phenazine conidiation signaling was conserved in the genetic model
176  clock output, yielding a pattern of asexual conidiation similar to a ras-1 mutant that is used in ci
177 n activation of the previously characterized conidiation-specific (con) genes, con-6 and con-10.
178 sion of stuA alpha, but not stuAbeta, by the conidiation-specific Bristle (BrlAp) transcriptional act
179 tE-AS was increased significantly during the conidiation stage, while GzmetE was upregulated in the l
180  7-kb transcript is detected only during the conidiation stage.
181 t and be affected by RAS signaling, increase conidiation, suggesting a link between generation of ROS
182 ergoes a well-defined developmental program, conidiation, that culminates in the production of numero
183 shown that the veA1 (velvet) mutation allows conidiation to occur in the absence of light.
184 n, HHK3 is involved in hyphal morphogenesis, conidiation, virulence, and cellular adaptation to oxida
185 ct conidiation morphologies, suggesting that conidiation was blocked at different stages.
186 opic examination indicated that the restored conidiation was concomitant with restored septation in t
187                                              Conidiation was reduced > 80%; however, conidia produced
188 esis of an extracellular factor that directs conidiation, we do not detect this factor under conditio
189 he regulatory pathway to brlA activation and conidiation, we isolated suppressor mutations that rescu
190 ate suppressor (smo) mutations that restored conidiation when MOBA was not expressed.
191    In general, low stuA:brlA ratios promoted conidiation while high ratios caused proliferation of un

 
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