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1 ruptive effect of the E2F-ETS interaction on cell cycle control.
2 in-associated transcriptional regulation and cell cycle control.
3 r the Golgi as a ubiquitylation platform for cell cycle control.
4 d exhibited downstream effects distinct from cell cycle control.
5 mmalian tissues such as immune responses and cell cycle control.
6 a candidate oncogene involved in Rb-mediated cell cycle control.
7 ffecting a link between hypoxia pathways and cell cycle control.
8 ular proteins in genomic DNA replication and cell cycle control.
9 rucial roles in transcription modulation and cell cycle control.
10 tic stimulus, steroid metabolic process, and cell cycle control.
11 and can be dissociated from its function in cell cycle control.
12 s with a fundamental requirement for precise cell cycle control.
13 through regulation of targets distinct from cell cycle control.
14 t plays pivotal roles in gene regulation and cell cycle control.
15 s in the cellular response to DNA damage and cell cycle control.
16 n the beta-cell has no discernible effect on cell cycle control.
17 arding miRNA function and their influence on cell cycle control.
18 n, suggesting an obligatory role for TRF1 in cell cycle control.
19 sistance to oxidative stress, DNA repair and cell cycle control.
20 is a disease that results from inappropriate cell cycle control.
21 th a parallel redundancy in their effects on cell cycle control.
22 some biogenesis, chromosome segregation, and cell cycle control.
23 stigated whether this enzyme plays a role in cell cycle control.
24 dence linking nucleocytoplasmic transport to cell cycle control.
25 lular signaling, DNA topological change, and cell cycle control.
26 and repair, transcriptional regulation, and cell cycle control.
27 events and are involved in several facets of cell cycle control.
28 atase, these proteins are likely involved in cell cycle control.
29 s that have previously not been connected to cell cycle control.
30 e-TCR and IL-7 signaling with DNA damage and cell cycle control.
31 n ligase APC/C-Cdh1 is central to eukaryotic cell cycle control.
32 which have not previously been connected to cell cycle control.
33 elf-renewal is intrinsically associated with cell cycle control.
34 Xenopus laevis oocytes, suggesting a role in cell cycle control.
35 deubiquitylase USP11, which is itself under cell cycle control.
36 ell-supported consensus model for eukaryotic cell cycle control.
37 ddition to their well-characterized roles in cell cycle control.
38 gi reassembly, transcription activation, and cell cycle control.
39 CycC, the cognate cyclin partner of Cdk8, in cell cycle control.
40 moting acetylation, leading to disruption of cell cycle control.
41 likely to apply to signaling pathways beyond cell-cycle control.
42 res c-Kit, notch signaling, and p27-mediated cell-cycle control.
43 al molecular link between oxygen sensing and cell-cycle control.
44 aberrations, rather than simply by affecting cell-cycle control.
45 erium Caulobacter crescentus, a paradigm for cell-cycle control.
46 d in brain and involved in DNA synthesis and cell-cycle control.
47 cluding inflammation, immune regulation, and cell-cycle control.
48 umulation of DNA damage secondary to loss of cell-cycle control.
49 upon parasite virulence, differentiation and cell-cycle control.
50 sponse and are likely to be also involved in cell-cycle control.
51 or CHD4 in the DNA-damage response (DDR) and cell-cycle control.
52 or the structure and evolution of eukaryotic cell-cycle control.
53 o mechanisms of epithelial cell polarity and cell-cycle control.
54 pecificity and efficiency required for tight cell-cycle control.
55 A replication increase the robustness of the cell-cycle control.
56 progression mechanism driven by failures in cell-cycle control.
57 op a systems-level perspective of eukaryotic cell cycle controls.
58 to-S transition, and this process is tightly cell cycle controlled.
59 n conjunction with additional alterations of cell cycle control, a situation that might be reminiscen
61 es suggest that JNKs may also play a role in cell cycle control, although the underlying mechanisms a
62 s preliminary analysis, 12 genes involved in cell cycle control and 9 genes involved in apoptosis wer
63 n revealed upregulated genes associated with cell cycle control and activation of the Wingless and in
64 ulator of transcription networks that govern cell cycle control and apoptosis throughout development.
65 act as a transcription factor affecting both cell cycle control and apoptosis, and we have previously
66 SMC phenotype in vitro, linked to changes in cell cycle control and bone morphogenic protein receptor
67 t a passive marker, but actively changed the cell cycle control and cell death process motifs of T ce
68 Network analysis of these data revealed that cell cycle control and cell death were the most altered
69 ates the transformation process by impairing cell cycle control and cellular response to DNA damage.
70 at Skp2, an E3 ubiquitin ligase that affects cell cycle control and death, plays a critical role in t
71 ily of pocket proteins play central roles in cell cycle control and development, and the regulatory n
73 subfamily, which are known to be involved in cell cycle control and DNA repair, among other functions
75 tional strategies for metabolic programming, cell cycle control and functional polarization following
77 ts of all metazoan body plans, and comprises cell cycle control and growth, development, somatic- and
78 stigated the coordinate impact of RB-loss on cell cycle control and immune function in the liver.
79 errant miR expression results in deregulated cell cycle control and impaired apoptotic responses, and
81 a demonstrate a novel function of APC beyond cell cycle control and implicate critical role of ubiqui
82 factors involved in histone methylation and cell cycle control and include Ash2L, RbBP5, WDR5, HCF-1
83 -CDK6 conjugation constitutes a mechanism of cell cycle control and inhibition of this SUMOylation pa
84 odes a transcriptional regulator involved in cell cycle control and mother-daughter cell separation.
86 ble for regulation of many genes involved in cell cycle control and proliferation, and it has recentl
87 regulation via miRNAs-confers robustness to cell cycle control and provides a molecular basis to und
88 inhibitors, which play critical roles in the cell cycle control and regulation of cell transcription.
89 o human, pescadillo homologs are involved in cell cycle control and ribosome biogenesis, and are esse
90 en the hypothesis that BRCA1 plays a role in cell cycle control and show that BRCA1 is a marker of cl
91 tes the expression of many genes involved in cell cycle control and that a mutation which disrupts th
92 HV genes regulated by CTCF-cohesin are under cell cycle control and that mutation of the CTCF binding
93 We propose that the p63 C-terminus links cell cycle control and the proliferative potential of ep
97 etwork of cellular processes that integrates cell-cycle control and DNA repair or apoptosis, which se
100 oss of these hypoxia-driven lncRNAs impaired cell-cycle control and inhibited capillary formation.
101 ppression of DNA damage signaling is key for cell-cycle control and needed for normal development.
102 signaling and p27 expression, which restored cell-cycle control and rescued hemogenic endothelial cel
103 pression analysis revealed downregulation of cell-cycle control and survival pathways and upregulatio
104 portance of pRB's LxCxE-interacting motif in cell-cycle control and tumor suppression, we generated m
105 solved how HPV-infected keratinocytes escape cell-cycle control and whether their cross-talk with imm
106 ression of a cdc12p fragment bypasses normal cell-cycle controls and induces contractile ring assembl
107 tor tyrosine kinase signalling pathways, and cell cycle control) and emerging (for example, histone,
108 tumour suppressor gene), CDC14B (involved in cell cycle control) and NTRK3 (tyrosine receptor kinase
112 the AR to maintain AR activity, AR-dependent cell cycle control, and continued cell proliferation.
113 ss, impaired checkpoint signaling, defective cell cycle control, and genomic instability, which was r
114 with enhanced expression of DNA replication, cell cycle control, and liver-specific genes, indicating
115 at are involved in pigmentation, DNA repair, cell cycle control, and melanocyte proliferation pathway
116 4L, we characterized B cell differentiation, cell cycle control, and mitotic gene expression in GON4L
118 functions in ribosome biogenesis and export, cell cycle control, and response to stress stimuli.
119 transcription, translation, DNA replication, cell cycle control, and signal transduction, to name but
121 se results confirm that B-Myb is involved in cell cycle control, and that its dysregulation may contr
125 ssociated with pathways of Wnt signaling and cell-cycle control, and most were conserved between mous
126 ved in cell invasion, metastasis, apoptosis, cell-cycle control, and tumor-related angiogenesis.
127 pression could dysregulate the expression of cell cycle control- and metastasis-related molecules by
130 tory proteins, leading to the loss of normal cell-cycle control, are a hallmark of many cancers, incl
131 determines its ability to bind DNA and exert cell cycle control as well as its subcellular localizati
133 y sub-dynamics that are essential for viable cell cycle control, as well as identifying the sub-dynam
134 between autophagy components, apoptosis and cell cycle control at different stages of autophagic ves
138 mphasize differences in the cytoskeleton and cell cycle control between two life cycle stages of the
140 of mitotic gene expression is a key issue in cell cycle control but is poorly understood in most orga
142 ssive functions of RB that are distinct from cell cycle control, but also demonstrate that the molecu
143 diated protein degradation is fundamental to cell cycle control, but the precise degradation order at
144 ally-derived SBF may have initially hijacked cell cycle control by activating transcription via the c
147 onic fibroblasts, and osteoblasts shows that cell-cycle control by matrix stiffness is widely conserv
148 al regulator of the cell cycle, and abnormal cell-cycle control can lead to oncogenesis, aberrancies
149 y of mRNA transcribed from genes involved in cell-cycle control, cell proliferation, and apoptosis ha
150 B and p53 were revealed; their loss affected cell cycle control, checkpoint response, and genome stab
152 sregulation of multiple genes that influence cell cycle control (cyclin b1 and p21), apoptosis (Bcl-2
154 ys that underlie higher order events such as cell cycle control, development, innate immune response
155 rphase chromosome-LINC contacts constitute a cell-cycle control device linking nucleoplasmic and cyto
157 pates in multiple cellular functions such as cell cycle control, DNA repair and regulation of gene tr
158 r cellular growth and has been implicated in cell cycle control, DNA replication, and gene rearrangem
159 lved in sensitive cellular processes such as cell cycle control, DNA replication, control of gene exp
160 ctions as a transcription factor involved in cell-cycle control, DNA repair, apoptosis and cellular s
161 veral canonical signalling pathways, such as cell-cycle control, DNA-damage and -repair responses, p5
162 (Cdk5) contributes to neuronal migration and cell cycle control during embryogenesis, and to the diff
164 and provides insights into the importance of cell-cycle control during host-pathogen interactions.
166 Transcripts involved in cell signaling, cell cycle control, energy production/metabolism, microt
168 complex structures and processes, including cell cycle control, flagella and basal bodies, ribosome
170 Deletions of key B-cell differentiation and cell cycle control genes are highly prevalent but vary i
171 causes concerted upregulation of a cadre of cell cycle control genes, including those encoding cycli
175 systematic evaluation of the association of cell-cycle control genes with endometrial cancer risk.
176 n in cancer cells results in a disruption of cell cycle control, genetic instability, enhanced cell m
177 thesis, which may contribute to its roles in cell cycle control, genomic maintenance, and tumor suppr
178 f p53 in cellular metabolism, apoptosis, and cell cycle control has led to increasing interest in def
180 er G2-M transition, and its contributions to cell cycle control have been modeled based on studies us
181 se of the feedback-first motif in eukaryotic cell-cycle control, implemented by nonorthologous protei
182 levels in dDP-deficient fat bodies restores cell-cycle control, improves tissue morphology, and exte
185 dings in the context of broader knowledge of cell cycle control in normal and abnormal development.
186 way, which may be explored to restore proper cell cycle control in p53-deficient tumors via p21.
187 and important dimension to the robustness of cell cycle control in particular and to biological signa
189 flowering time and suggest an involvement of cell cycle control in the timing of reproductive transit
190 ve imaging to assess mitotic progression and cell cycle control in these cells, yielding new insights
191 sential cell functions such as apoptosis and cell-cycle control in addition to their role as efficien
193 Although current textbook explanations of cell-cycle control in eukaryotes emphasize the periodic
194 formation, the role for SOX10 in maintaining cell-cycle control in melanocytes suggests a rational ne
197 ese findings provide a global perspective on cell-cycle control in vivo, and they highlight a critica
199 the tumor suppressor function of pRb during cell cycle control, in part by creating a better substra
200 nate vesicular trafficking, cytokinesis, and cell cycle control independent of GTPase-activating prot
203 l established, whereas their contribution to cell cycle control is only beginning to be understood.
208 lysis of the digital circuit showed that the cell-cycle control is robust to intrinsic stochastic var
209 ch occurs in cancers as a result of aberrant cell cycle control, is sufficient to cause PCS and gross
210 ses various diseases associated with loss of cell cycle control, leading to uncontrolled cell prolife
214 stemic perturbation for mutations within the cell cycle control mechanisms (G2 to mitosis transition)
217 hins provide an excellent model for studying cell cycle control mechanisms governing DNA replication
218 we show this is the result of cooperation of cell cycle control mechanisms that limit E2F-CycE positi
219 eslin is a key positive-regulatory target of cell-cycle control mechanisms; activation of Treslin by
220 luding epigenetic regulation, DNA damage and cell cycle control, microRNA silencing, signal transduct
221 Significant alterations of genes involved in cell cycle control, mitotic checkpoints, and DNA repair
222 allows unbiased integration of the consensus cell cycle control model with innovations specific to th
223 reveals that almost all of the critical G1/S cell cycle control molecules are located in the cytoplas
224 icative of telomere dysfunction and abnormal cell-cycle control, namely dysregulated G1-to-S-phase tr
225 on of single isogenic cells reveals that the cell cycle control network of this bacterium generates a
226 eukaryotic cell divisions before the current cell-cycle control network evolved in all its complexity
227 during DNA licensing, with implications for cell cycle control of DNA replication and genome stabili
228 Our study establishes a mechanism for direct cell cycle control of ECM remodeling during cytokinesis.
229 actor P (HiNF-P; gene symbol Hinfp) mediates cell cycle control of histone H4 gene expression to supp
231 during latency and that failure to maintain cell cycle control of latent transcripts inhibits host c
232 kinase 2 (CDK2) is a known regulator in the cell cycle control of the G1/S and S/G2 transitions.
234 plex plays a critical role in regulating the cell cycle control of viral gene expression during laten
237 gs therefore provide a mechanistic basis for cell-cycle control of DSB repair and highlight the impor
241 ired for hemogenic specification, as well as cell-cycle control, of endothelium during embryogenesis.
242 n of genes associated with proliferation and cell cycle control only in the acute liver-specific Hnf4
243 erogeneity represents distinct mechanisms of cell-cycle control or whether a common mechanism can acc
244 ns involved in replication licensing (CDT1), cell cycle control (p21), and chromatin modification (SE
247 gene known to be involved in DNA repair and cell cycle control, plays a role in the effect of metfor
254 phosphorylated Cx43 forms complexes with the cell cycle control proteins cyclin E and cyclin-dependen
255 ng pathway and down-regulates several G(2)-M cell cycle control proteins, resulting in enhanced G(2)-
256 itically involved in processes as diverse as cell cycle control, protooncogene expression, cellular d
257 actors (E2Fs) have a clearly defined role in cell cycle control, recent work has uncovered new functi
258 r the transcriptional regulation of multiple cell cycle control-related genes, including E2F-responsi
259 E2 and TopBP1 would allow E2 to bypass this cell cycle control, resulting in DNA replication more th
262 ion of a variety of target genes involved in cell cycle control, senescence, and apoptosis in respons
263 rs that are involved in generic processes of cell-cycle control, signal transduction, and stress resp
264 enomena as diverse as circadian rhythmicity, cell cycle control, stress and damage responses, and ste
265 uiescent state include factors essential for cell cycle control, stress response and survival pathway
266 n translation, global transcription control, cell-cycle control, stress response, DNA topology, DNA r
267 enes participate in chromatin regulation and cell cycle control, supporting the concept that the esta
271 We report a hybrid simulation of the coupled cell-cycle control system, including asymmetric cell div
272 key regulatory pathways involved, including cell cycle control, Tgf-beta signaling, Pten/Akt signali
273 E2F axis is an important pathway involved in cell-cycle control that is deregulated in a number of ca
274 downstream effector of the Hippo pathway of cell-cycle control that plays important roles in tumorig
277 Despite the well established role of RB in cell cycle control, the deletion of RB had no impact on
279 n structure of a key regulatory interface in cell-cycle control: the destruction box sequence bound t
281 s regulating diverse cellular processes from cell cycle control to developmental fate, deregulation o
286 eir importance to critical functions such as cell cycle control, transcription, and translation, as w
287 es the evolutionarily conserved processes of cell cycle control, transcription, DNA replication and m
289 functions of the BAF57 subunit of SWI/SNF in cell cycle control via transcriptional regulation of cel
292 n keeping with its previous association with cell cycle control, we demonstrate that FOXM1 binds and
293 central role in the DNA damage response and cell cycle control, we directly tested the hypothesis th
294 Despite a potential role for Geminin in cell cycle control, we found no evidence of proliferatio
295 To explore the mechanisms and evolution of cell-cycle control, we analyzed the position and conserv
296 gulators, establishing a mechanistic link to cell cycle control which provides sustained mitotic acti
297 sistent with defects in proliferation and/or cell cycle control while accumulating higher levels of r
298 but the mechanisms coupling cell growth and cell cycle control with cell size regulation are poorly
299 let-7/miR-98 family play a critical role in cell cycle control with respect to differentiation and t
300 sh a link that intertwines the mechanisms of cell-cycle control with the mechanisms underlying the ac
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