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1 ry networks and with cellular processes of a growing cell.
2 the demand for membrane expansion of rapidly growing cells.
3 bosomes are stably maintained even in slowly growing cells.
4 e only partially methylated in exponentially growing cells.
5 entially to the synthesis of TAG in actively growing cells.
6 was not substantially methylated in actively growing cells.
7 sphatase is strongly active in exponentially growing cells.
8  equivalents and synthetic materials in fast-growing cells.
9 rowing bacteria among populations of rapidly growing cells.
10 are viable but have reduced expansion of tip-growing cells.
11 hh1 and Pat1 from ribosomes in exponentially growing cells.
12 I localization to chromatin in exponentially growing cells.
13 asmid ColE1 in a population of exponentially growing cells.
14 om a TA (toxin-antitoxin) operon in normally growing cells.
15 n RpoS-independent promoter in exponentially growing cells.
16  ratio and temporal resolution in individual growing cells.
17 ential for chromosome segregation in rapidly growing cells.
18 e phospholipid metabolism in logarithmically growing cells.
19 rized growth, For2 are apically localized in growing cells.
20 regulon in a DNA damage response in actively growing cells.
21 in the observed variability in shapes of tip-growing cells.
22 ng domain in the chromosome of exponentially growing cells.
23 ase is a component of the division septum in growing cells.
24  de novo synthesis by 75% in logarithmically growing cells.
25 tolytic enzymes must be tightly regulated in growing cells.
26 vation but not when CDC2 is highly active in growing cells.
27  their environment differently from actively growing cells.
28 results from changes in peptidoglycan in non-growing cells.
29 p positively regulates sigD transcription in growing cells.
30 tgrowth from the ER maintains peroxisomes in growing cells.
31 curred that was not evident in exponentially growing cells.
32 and predominantly at the regions of actively growing cells.
33 Escherichia coli chromosome in exponentially growing cells.
34 as only E2F3 is necessary for the S phase in growing cells.
35  salt but at lower levels than in comparable growing cells.
36 nown to be involved in turgor maintenance in growing cells.
37 Here, we investigate bypassing in unstarved, growing cells.
38 depletion is toxic to virtually all actively growing cells.
39 most of the gene expression in exponentially growing cells.
40  expressed higher p66(Shc) protein than slow-growing cells.
41 B(-) strain in sessile, planktonic, and free-growing cells.
42 s higher in confluent cells than in actively growing cells.
43 by mechanisms distinct from those in rapidly growing cells.
44 ation products generated by Hin catalysis in growing cells.
45 se are around 55% of those in asynchronously growing cells.
46 ramatically more Cln protein than did slowly growing cells.
47 eflect non-stress-specific processes in rare growing cells.
48 delivery of a subset of vacuolar proteins in growing cells.
49 following the irradiation of logarithmically growing cells.
50 d reduction of phosphorylated Rb in normally growing cells.
51 ibonucleases are more toxic for more rapidly growing cells.
52 nterorganelle lipid transfer is extensive in growing cells.
53 (cephalexin, aztreonam, and piperacillin) in growing cells.
54 inducible hsp70 promoter, into exponentially growing cells.
55 l tension along cell junctions within faster-growing cells.
56 lk to meet the need for protein synthesis in growing cells.
57 t such a gradient is absent in exponentially growing cells.
58 re of transcription factors expressed in tip-growing cells.
59 onger distances in quiescence as compared to growing cells.
60 d effectively reduces fluorescence signal in growing cells.
61  which are mainly effective against actively growing cells.
62 aining genetically identical to the actively growing cells.
63 e ethanol in mitochondria as opposed to slow growing cells.
64 h pseudopod orientation during chemotaxis of growing cells.
65  were mapped by UV cross-linking in actively growing cells.
66 centrioles and aberrant assembly of cilia in growing cells.
67  differently in those cells than in actively growing cells.
68 origin and terminus domains in exponentially growing cells.
69  the idea of chemotherapy targeting actively growing cells.
70 ate the ClpP protease, resulting in death of growing cells.
71 dmark is a broadly conserved strategy in tip-growing cells.
72 nificantly increases plasmalemma in normally growing cells.
73 articipation of myosin XI and F-actin in tip growing cells.
74 lipid composition is very similar to that of growing cells?
75 mine the particularly simple geometry of tip-growing cells [1, 3, 15, 16], which elongate via the ass
76 rigenic in forming bone metastases than fast-growing cells (55 vs. 15%) and had a unique gene express
77  the half-lives of total mRNA in resting and growing cells (about 9 h).
78 rays are the major sites of transcription in growing cells, accounting for as much as 50% of RNA synt
79                           How populations of growing cells achieve cell-size homeostasis remains a ma
80 ls or by protein phosphatase M1A in normally growing cells activates CDK9.
81 elopmental differences between P. patens tip-growing cells and A. thaliana pollen tubes and root hair
82 tion are only slightly increased compared to growing cells and are 10-fold below the levels observed
83 CC2, and XRCC3) are expressed in mitotically growing cells and are thought to play mediating roles in
84 natural populations, selection is imposed on growing cells and can detect the more common mutations t
85  activity is partially suppressed by cdk2 in growing cells and derepressed upon cell confluence.
86 the unique metabolic requirements of rapidly growing cells and geminivirus-infected cells that have b
87 ces transcriptional slippage within actively growing cells and in vitro.
88 ent cells would mechanically isolate rapidly growing cells and limit their impact on organ shape.
89  between polarization mechanisms in moss tip-growing cells and multicellular tissues of seed plants.
90 enotypic switching occurred between normally growing cells and persister cells having reduced growth
91 ls are known to be very low in exponentially growing cells and rise sharply as cells enter stationary
92                              Logarithmically growing cells and spores were each harvested from the cu
93 pXP localize in foci often near the poles of growing cells and that ClpP and the ATPase are each capa
94 rall accuracy of DNA replication in normally growing cells and that repair pathways may exist primari
95 chastically in a population of exponentially growing cells and that the high (p)ppGpp level in rare c
96 ls to correct DNA replication errors both in growing cells and under nongrowing conditions.
97 in differentiated stationary-phase (not rare growing) cells and, second, that transient genetic insta
98 or CP110 promotes primary cilia formation in growing cells, and enforced expression of CP110 in quies
99 ng protein synthetic capacity in dividing or growing cells, and requires coordinated production of ri
100 sm regulates cellulase expression in rapidly growing cells, and that the presence of hemicelluloses h
101 evealed nucleolin at the surface of actively growing cells, and these cells bound and internalized fl
102 1 and Pom1 were enriched at opposite ends of growing cells, and they phosphorylated largely non-overl
103                                           In growing cells, apurinic/apyrimidinic (AP) sites generate
104 , while, conversely, certain types of faster-growing cells are able to eliminate adjacent wild-type c
105                                     Many tip-growing cells are capable of responding to guidance cues
106  that macropinosomes, but not pseudopods, in growing cells are dependent on PIP(3).
107                            Viable but slower growing cells are eliminated during embryonic developmen
108 pression of HIF-1alpha results in death when growing cells are exposed to hypoxia.
109 cally switch into slow growth, that the slow-growing cells are multidrug tolerant, and that they are
110 of Hg transformations suggests that actively growing cells are primarily responsible for methylation,
111                  We further found that while growing cells are rapidly killed by iron starvation, sta
112 ecular composition of isogenic, steady-state growing cells arises spontaneously from the inherent sto
113 which old OMPs are displaced to the poles of growing cells as new OMPs take their place.
114          The problem was easily rectified by growing cells at a low glucose concentration.
115 t ABCC4/Abcc4 proteins are mostly rescued by growing cells at subphysiological temperatures.
116  associated with a constant-thickness rim of growing cells at the cluster edge, as well as the emerge
117 mophila, highly phosphorylated histone H1 of growing cells becomes partially dephosphorylated when ce
118 n to that of cells grown in suspension (free-growing cells), bfr mRNA expression by sessile cells on
119 adaption of the ontology to the continuously growing cell biological knowledge.
120  The enzyme is extremely unstable in rapidly growing cells but becomes stabilized under conditions of
121  RNA and protein can be detected in actively growing cells but decline sharply when the replicon cell
122 yogenes SF370 is functional in exponentially growing cells but defective when resources are limiting.
123           Conversely, Fis levels are high in growing cells but fall to nearly zero in stationary-phas
124 nced by the repressive Polycomb complexes in growing cells but is activated in response to oncogenic
125  cell wall-derived muropeptides derived from growing cells but not lysed cells.
126 pathway affected the cell length of actively growing cells but not their growth rate.
127 ave features not required for mRNA export in growing cells but which enhance the ability of mRNAs to
128 tion of protein homeostasis in exponentially growing cells, but ERAD became relevant when the gene do
129 t Mdm2 inhibits the p53 response in normally growing cells by binding to chromatin-associated p53.
130       Conversely, growth suppression of fast-growing cells by cellular form of prostatic acid phospha
131 ed the redox state of the C-terminal HRMs in growing cells by thiol-trapping experiments using the is
132 ) isolation of synchronous subpopulations of growing cells by zonal centrifugation.; (ii) fractionati
133 enome content, responded to Fe starvation in growing cells characterized by low photosynthetic effici
134 overall data revealed that, in exponentially growing cells, CodY and CovRS act in opposite directions
135 ugh HNP-3 were bound to the periphery of the growing cell colonies.
136                        We show that moss tip growing cells contain a prominent subapical cortical F-a
137 ospores, it was determined that vegetatively growing cells contain one to two copies of the genome, b
138                                              Growing cells coordinate protein translation with metabo
139 P signals that locally reduce Anillin at the growing cell cortex.
140 d mRNA expression profiling of synchronously growing cell cultures progressing through the cell cycle
141    In both sucrose-starved and exponentially growing cells, CYCD3;1 protein abundance increases in re
142 wn of p66(Shc) expression by RNAi in rapidly growing cells decreased their proliferation as evidenced
143                                         Slow-growing cells deep in the biofilms had little expression
144  proteins (Twis) preferentially expressed in growing cells differ in their genetic essentiality and s
145                          A wide range of tip-growing cells display highly polarized cell growth, and
146                                          Tip-growing cells do not display neighbor-induced growth con
147 % of ribosomal proteins expressed in rapidly growing cells does not contribute to translation.
148 have reexamined the cidal activity of bSi on growing cells, dormant and germinated spores of B. subti
149 ed diversity of 23- to 24-nt sRNA classes in growing cells, each with distinct genetic requirements f
150 residues seem to mediate crystal adhesion to growing cells, either directly or via linkage to other c
151 ver, the engineered expression of CuZnSOD in growing cells eliminated superoxide release, confirming
152 g new proteins can be enforced after rapidly growing cells encounter energy limitation.
153 n monopolar distribution of GTP-Cdc42 to the growing cell end.
154 lished, POs and LDs drift slowly towards the growing cell end.
155 owth with abnormal Tea1 aggregate at the non-growing cell end; this abnormal aggregate fails to recru
156 t GTP-bound, active Cdc42 is concentrated to growing cell ends accompanied by developed F-actin struc
157 n further detail and show that exponentially growing cells exhibit Ca(2+) elevation resulting exclusi
158 ass, which are specifically expressed in tip-growing cells, exhibited exocytosis-related functional e
159 tion with cell proliferation, that is, rapid-growing cells expressed higher p66(Shc) protein than slo
160                                         Free-growing cells expressed more sspA-specific mRNA and sspB
161                                         Free-growing cells expressed the same levels of sspA and sspB
162                                      Rapidly growing cells expressed, and required, dramatically more
163 eous transformation are selected in vitro by growing cells for many low density passages at maximal e
164 n, while a small fraction of elongated, slow-growing cells formed colicin-expressing hotspots, placin
165                                           In growing cells, H2A.Y is incorporated into micronuclei on
166  trigger intracellular responses in actively growing cells have not yet been experimentally character
167                                          Tip-growing cells have the unique property of invading livin
168                          Because the rapidly growing cells have very different geometry from that of
169 stoma protein (Rb), whereas in exponentially growing cells, HIN-1 induces apoptosis without apparent
170 so generate variable resistance levels among growing cells in a population.
171 ct of pH on cell viability was determined by growing cells in broth at various initial glucose concen
172 Bacillus subtilis, we analyzed exponentially growing cells in different media.
173        Enhancing CtBP-mediated repression by growing cells in low oxygen increased the association of
174                          The method involves growing cells in multiwell plates, incubating cells with
175 rowth are likely similar to those of non-tip growing cells in seedlings.
176 of FGF-induced MAPK activation than actively growing cells in sparse culture.
177 kton blooms, we mimicked those conditions by growing cells in the presence of increased amounts of di
178                                        After growing cells in the presence of labeled palmitate compl
179 ion," which manifests in apoptosis of slower-growing cells in the vicinity of faster growing tissue,
180 and limitations on the technologies used for growing cells in vitro, perturbing them, and measuring t
181                               In aerobically growing cells, in which reactive oxygen species are prod
182 this phenomenon occurs ubiquitously for fast-growing cells, including bacteria, fungi and mammalian c
183  was observed only in the presence of nearby growing cells, indicating cross-inhibition.
184 ed from polysomal complexes in exponentially growing cells, indicating that they may not be associate
185  RpoS, RpoS must regulate Pol IV activity in growing cells indirectly via one or more intermediate fa
186                                   In rapidly growing cells, initiation of replication occurs before t
187                          The conversion of a growing cell into an endospore in Bacillus subtilis invo
188 (the major vegetative holoenzyme) in rapidly growing cells is engaged in transcribing the rrn operons
189                 Metabolite exchange among co-growing cells is frequent by nature, however, is not nec
190      Temporal increase in EB fluorescence of growing cells is indicative for toxic but reversible eff
191  by TORC1, whose inhibition in exponentially growing cells is shown to match an interruption in endom
192                                           In growing cells, it is found in active and inactive forms.
193 Because aerobic glycolysis is only useful to growing cells, it is tightly regulated in a proliferatio
194 to push old OMP islands towards the poles of growing cells, leading to a binary distribution when cel
195 nSOD by adenovirus transfection in the rapid growing cell line MIA PaCa-2 increased MnSOD immunoreact
196 tic RanGTP gradients were present in rapidly growing cell lines and were required for chromosome cong
197                                 Aggressively growing cell lines displayed ERK1/2 activation, which st
198                            How exponentially growing cells maintain size homeostasis is an important
199 e genes are highly expressed in vegetatively growing cells, many pombe-specific genes are expressed a
200 ate sources, which are incorporated into the growing cell mass; PKA signaling responds to the availab
201 show via computational modeling that rapidly growing cells may distort organ shape.
202  progeny cells, and cell wall homeostasis in growing cells, may also be essential for Mtb's survival
203 B concentration was about 122 microM in 4HPA-growing cells, much higher than the total intracellular
204           Malignant cells, like all actively growing cells, must maintain their telomeres, but geneti
205 -599 site, suggesting that in asynchronously growing cells NF-Y functions only to stimulate expressio
206                                              Growing cells of Bacillus subtilis are a bistable mixtur
207 hromosome replication origin and terminus in growing cells of Escherichia coli have been visualized s
208 tors in live cells by artificially deforming growing cells of Escherichia coli in curved agar microch
209 t the perturbation of cell wall synthesis in growing cells of S. aureus induces strong repression of
210 re and organization of the S layer on intact growing cells of the Gram-negative bacterium Caulobacter
211               When starved for nitrogen, non-growing cells of the photosynthetic bacterium Rhodopseud
212                               In the rapidly growing cells of the root elongation zone, we found MAP6
213 d application of GA to the relatively slowly growing cells of the unexpanded light-grown Arabidopsis
214                                         When growing cells on these substrates, it is found that cell
215 re stored in LDs, are typically mobilized in growing cells or upon hormonal stimulation by LD-associa
216                                           In growing cells, P-TEFb exists in active and inactive form
217 cipitation indicates that, in asynchronously growing cells, p53 occupies this element.
218         The CPAM, which is found only around growing cell plate regions, is suggested to be responsib
219 ects vesicles to the CPAM and thereby to the growing cell plate.
220 onsible for the majority of transcription in growing cells, Pol I regulation is poorly understood com
221 oriented Z rings and not by deformation of a growing cell pole or emergence of new tips from the side
222 the Rv1422 protein localizes uniquely to the growing cell pole, the site of peptidoglycan synthesis i
223  (SILAC) can be used to differentially label growing cell populations for quantitation of protein lev
224                                         Slow-growing cell populations located within solid tumors are
225 n alterations in their relative abundance in growing cell populations that have been transduced with
226 and competition that maximizes the health of growing cell populations.
227                     We suggest that steadily growing cells prepare for conditions that demand increas
228                                     Normally growing cells prevent this response through constitutive
229 ce correlates with growth rate, where faster growing cells produce more flagella.
230                                      Rapidly growing cells produce thousands of new ribosomes each mi
231         Even when deformations are acquired, growing cells progressively recover their original shape
232  exert more severe cytotoxic effects on fast growing cells, providing an important molecular basis fo
233   Rather, Spo0A is present at high levels in growing cells, rapidly rising to yet higher levels under
234 ind that addition of hydrogen sulfide gas to growing cells recapitulates all aspects of reversible MT
235                Our results show that rapidly growing cells require significant methylation, likely fo
236                                           In growing cells, Sav1866 expression conferred resistance t
237                            We found that non-growing cells shifted their metabolism to use the tricar
238                        Wall expansion in tip-growing cells shows variations according to position and
239                     Indeed, in exponentially growing cells, sprE deletion mutants exhibit significant
240                                           In growing cells, Ste11p is present in low levels and is pa
241 cond messenger, plays essential roles in tip-growing cells, such as animal neurons, plant pollen tube
242 which are normally repressed in vegetatively growing cells, such as targets of the Clr6 histone deace
243 are present in approximately 11% of actively growing cells, suggesting that the low frequency of Z ri
244                                      Rapidly growing cell suspension and adherent cells were effectiv
245 erium that is capable of differentiating non-growing cells that constitute gliding filaments termed h
246                          However, in rapidly growing cells the prophage excises and replicates as an
247                                           In growing cells, the circuit gives rise to an occasional r
248      While BRI1 is ubiquitously expressed in growing cells, the expression of BRL1 and BRL3 is restri
249                               In intercalary growing cells, the normal actin organization is disrupte
250                             In exponentially growing cells, the nucleoid-binding protein H-NS downreg
251 anical signals are propagated around rapidly growing cells, the resistance to stress in adjacent cell
252                                       In tip-growing cells, the tip-high Ca(2+) gradient is thought t
253  with the high secretory dynamics of the tip growing cell; they show a pattern to the endoplasmic ret
254                                     For fast-growing cells, this necessitates rapid recycling of DNA
255 in the GTP pool within 10 min of addition to growing cells; this response does not result from the re
256 adjacent cells mechanically isolates rapidly growing cells, thus contributing to organ shape reproduc
257  collar of endocytic activity encircling the growing cell tip, which elongates through directed membr
258 rexpression leads to reduced diameter of the growing cell tip.
259 nthesized by membrane-bound synthases at the growing cell tip.
260 c42, found in a cap at the inner membrane of growing cell tips, as an important regulator of local ce
261 teins are interdependent for localization to growing cell tips.
262              Mitochondria must grow with the growing cell to ensure proper cellular physiology and in
263                    Exposure of exponentially growing cells to iron-limited media, oxidative stress, a
264  single cyanobacteria enable a population of growing cells to maintain synchrony for weeks.
265 uction systems that are adapted to allow non-growing cells to sense and respond to their environment
266 nversely correlated with the capacity of non-growing cells to synthesize protein.
267  a function of acute and chronic exposure of growing cells to the drug.
268 ddition to increasing genetic instability in growing cells, Top1 activity in transcriptionally active
269                             In exponentially growing cells translating ribosomes are interspersed amo
270 mply that PolIV can also promote mutation in growing cells under genome stress due to excess single-s
271                                         Slow-growing cells upregulate transposons and express more ch
272 resting cells and about 8 h in exponentially growing cells, values which are similar to the half-live
273 ates the activity of Pol IV in exponentially growing cells via a second, indirect pathway.
274 te that splicing is prevented in mitotically growing cells via inhibition, in contrast to the positiv
275 cks from Lipid II carrier molecules onto the growing cell wall scaffold during growth and division.
276  of the major load-bearing mechanisms of the growing cell wall.
277  Arabidopsis thaliana as a model of primary, growing cell wall.
278  of cross-links between peptide stems in the growing cell wall.
279 -mediated delivery of new polysaccharides to growing cell walls.
280 program with this array, an RNA extract from growing cells was compared with one prepared from develo
281 ion angle on the affected area of adherently growing cells was investigated both theoretically and ex
282 ddition to a 3.5-fold higher H2 yield by non-growing cells we also observed an accumulation of polyhy
283                            For exponentially growing cells we observe high levels of inter-centromeri
284                                   In rapidly growing cells, we show that the major sites of RNA polym
285 uidic lab-on-a-chip device developed for tip-growing cells, we tested the ability to exert penetrativ
286                                Exponentially growing cells were infected with the adenovirus vector,
287 gnal for the release, although only actively growing cells were proficient eDNA donors.
288  sHA, surrounding planktonic cells, and free-growing cells were recovered separately.
289      Similar changes were also observed when growing cells were treated with rapamycin, which is know
290  Most RNase R is sequestered on ribosomes in growing cells where it is stable and participates in tra
291 E conferred acid resistance to exponentially growing cells, whereas GadX overexpression did not.
292 sigma(S) is highly unstable in exponentially growing cells, whereas its stability increases dramatica
293 d cycle to metabolize acetate in contrast to growing cells, which used the glyoxylate cycle exclusive
294  While single cellular organisms and rapidly growing cells with high protein production have short NR
295 ested in both synchronized and exponentially growing cells with only one replicating chromosome.
296 network that controls the development of tip-growing cells with rooting functions among most extant l
297                   Treatment of exponentially growing cells with the protein synthesis inhibitor cyclo
298    The distribution shifted to that found in growing cells within 3 h after serum stimulation.
299                              We predict that growing cells without MreB exhibit an instability that f
300                                           In growing cells, xyloglucan is thought to connect cellulos

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