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1 k1-ts diploids failed to undergo meiosis and spore formation.
2 H, ytrI, ytvI and yunB) exhibited defects in spore formation.
3 d-type for most vegetative functions and for spore formation.
4 s that had not been previously implicated in spore formation.
5 he time and location of SpoIIIE synthesis on spore formation.
6 s(4)P 5-kinase, Mss4p, also is essential for spore formation.
7 lipase D (PLD), is essential for meiosis and spore formation.
8 grew slowly and exhibited severely impaired spore formation.
9 ate vegetative growth, swarming and glycerol spore formation.
10 hypersensitive to caffeine and defective in spore formation.
11 e expression that is essential for efficient spore formation.
12 atase 1 interacting protein, is required for spore formation.
13 in1p, plays important roles in mating and in spore formation.
14 the meiotic plaque and is thus essential for spore formation.
15 tilis, a developmental program distinct from spore formation.
16 so-called meiotic plaque, a prerequisite for spore formation.
17 d formation of aerial hyphae, and a block in spore formation.
18 s required for chromosome segregation during spore formation.
19 n5-21, was isolated as a mutant defective in spore formation.
20 surface but had not commenced the process of spore formation.
21 prospore membrane, a prerequisite event for spore formation.
22 pression in the mother cell to ensure proper spore formation.
23 re returning to the nuclear periphery during spore formation.
24 (whiG, whiH and whiB), which are blocked in spore formation.
25 s2-Cdc10 complex is required for meiosis and spore formation.
26 uclear divisions and coordinates meiosis and spore formation.
27 t these proteins regulate multiple stages of spore formation.
28 cells are indeed defective in both stalk and spore formation.
29 which plays an essential role in meiosis and spore formation.
30 tially redundant roles during the process of spore formation.
31 mutant cells were blocked at a late stage of spore formation.
32 enes for roles in chromosome segregation and spore formation.
33 ntial for class II activity, did not improve spore formation.
34 f spore-specific gray pigment and a delay in spore formation.
35 on identifying small genes activated during spore formation.
36 at controls exit from prophase, meiosis, and spore formation.
37 on of sigma(E) activity is not essential for spore formation.
38 the completion of the nuclear divisions, and spore formation.
39 to feed the community, effectively delaying spore formation.
40 (MAPK) in budding yeast that is required for spore formation.
41 es related to cell growth, cell division and spore formation.
42 ole is directly in germination or perhaps in spore formation.
43 efects in meiotic chromosome segregation and spore formation.
44 direct transcription of genes necessary for spore formation.
45 r cell compartments of the sporangium during spore formation.
46 ng development causing dramatic reduction in spore formation.
47 the cell to accumulate resources to support spore formation.
48 xit from pachytene, meiotic progression, and spore formation.
49 icial induction of csfB severely compromised spore formation.
50 rminus (ter) region of the chromosome during spore formation.
51 dergoes a highly distinctive division during spore formation.
52 genes, SSP2 and OSW1, which are required for spore formation.
53 f a four-gene operon that may be involved in spore formation.
54 her than from slower kinetics of meiosis and spore formation.
55 ae that regulates the postmeiotic program of spore formation.
56 on and indicates a direct role for DdCdk8 in spore formation.
57 n is not the cause of their being blocked in spore formation.
58 st highly expressed gene during C. difficile spore formation, a previous study reported that Alr2 has
59 l mutant of SM101 showed decreased levels of spore formation, along with lower levels of CPE producti
63 y hydroxyurea resulted in a 90% reduction in spore formation and decreased the germination viability
66 ed that SpoIIQ processing is dispensable for spore formation and for activation of late forespore and
67 onmental and physiological conditions during spore formation and for modeling the inhalation and disp
68 findings contribute to our understanding of spore formation and function and will be useful in the d
69 tivity by changes in intracellular pH during spore formation and germination in Bacillus species.
72 called CotE assembles into the coat early in spore formation and plays a morphogenetic role in the as
73 80p coordinately controls genes that mediate spore formation and progression through the two meiotic
74 with nutrient gradients may allow efficient spore formation and spore dispersal in natural environme
75 ical for correct localization of BclB during spore formation and that the N-terminal domains of the B
77 wn molecular manifestation of the process of spore formation, and its discovery provides insight into
80 n the stationary phase and gave rise to 3.2% spore formation as opposed to 100% attained with DZF1.
82 to production of Cho and Ptd-butanol, blocks spore formation at concentrations where the inert isomer
86 rotein (MAP) kinase plays a critical role in spore formation, but the proteins that interact with Smk
93 t limitation but delay becoming committed to spore formation by killing nonsporulating siblings and f
96 , a circadian rhythm of conidiation (asexual spore formation) can be seen on the surface of agar medi
97 clear visualization of circadianly regulated spore formation (conidial banding), has remained an inte
98 4-kinase, suppressed the sec14-1 meiosis and spore formation defects; conversely, pik1-ts diploids fa
99 but later stages (chromosome segregation and spore formation) did not, suggesting that Snf1 controls
102 or sigma(G) ordinarily becomes active during spore formation exclusively in the prespore upon complet
103 is concluded that SpoIIIE is required during spore formation for chromosome separation as well as for
106 se results indicate that SpoVT levels during spore formation have a major impact on the germination a
107 developmental pathway, YnzD and YisI inhibit spore formation if over-expressed, while a chromosomal d
117 Following asymmetric cell division during spore formation in Bacillus subtilis, a forespore expres
125 apparent competitive dominance hierarchy of spore formation in chimera is partly due to a fixed stra
130 f HtrC did not stabilize YpeB or SleB during spore formation in the absence of the partner protein, i
131 st-cytokinetic DNA segregation occurs during spore formation in the bacterium Bacillus subtilis, wher
132 on of the polar septum during the process of spore formation in the bacterium Bacillus subtilis.
139 n bacterial physiology including biofilm and spore formation involve signaling by the cyclic dinucleo
141 ating feature of biofilm formation, and that spore formation is coupled to the formation of an archit
143 s-specific SASPs vary depending upon whether spore formation is induced by starvation inside cell agg
148 ers have shown that the phase angle at which spore formation occurs depends on the entrainment period
150 stage of engulfment in the Bacillus subtilis spore formation pathway, the larger mother cell engulfs
151 of parameters) was then used to investigate spore formation patterns under constant conditions and r
152 minal domain of Ime2, exacerbated the smk1-2 spore formation phenotype and prevented cyr1 mutations f
153 development and growth and is important for spore formation, possibly by providing dNTPs for mitocho
154 sults in partial suppression of the block to spore formation resulting from the loss of the prestalk
155 DNA transcription and DNA protection during spore formation, spore dormancy, and spore germination a
156 th, whereas epl2 was mainly expressed during spore formation, suggesting that the respective proteins
158 The mutations of interest confer a defect in spore formation that is dependent upon a gene required f
159 in in sporulating diploid cells also blocked spore formation, underscoring the importance of this cha
161 aits, e.g.: spore size versus viability; and spore-formation (via aggregation) versus staying vegetat
162 med heat-resistant, phase-refractile spores, spore formation was blocked in the sigF- and sigG-null m
163 , surface-associated communities (biofilms), spore formation was discovered to have heretofore unsusp
166 uring sexual differentiation, at the time of spore formation, was enriched in yeast-specific genes, i
167 in new insights into meiotic development and spore formation, we followed differential expression of
168 We propose that ridges are formed early in spore formation, when the spore volume likely decreases,
169 btilis chooses between matrix production and spore formation, which are both controlled by the regula
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