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1 long-with ATRA (45 mg/m(2) orally, days 1-15/cycle).
2 a-stable cycling stability (96.6% after 5000 cycles).
3 Maintenance venetoclax was permitted (7 cycles).
4 h cm(-2) ), and long cycle life (over 10 000 cycles).
5 entage of GSCs in M- and S-phase of the cell cycle.
6 ing in the mHsp60-mHsp10 chaperonin reaction cycle.
7 essory factors helps order the transcription cycle.
8 HPV-mediated carcinogenesis and the HPV life cycle.
9 its multifunctional role during the AAV life cycle.
10 zymatic step of the tricarboxylic acid (TCA) cycle.
11 t the expense of transfer to the methylation cycle.
12 ic mechanism of the eukaryotic cell division cycle.
13 ranscription, DNA damage repair and the cell cycle.
14 following the galvanostatic charge-discharge cycle.
15 g a model for the biological water oxidation cycle.
16 tabolic network, was used to close the first cycle.
17 ple lipid substrates may be transported each cycle.
18 two electron transfers within the catalytic cycle.
19 is a critical parameter in the ocean carbon cycle.
20 a coordinated and directional GTP-hydrolysis cycle.
21 for multiple phases of the viral replication cycle.
22 uture investigations of the global marine Si cycle.
23 of the pressure waveform during the cardiac cycle.
24 anges in axial strain throughout the pumping cycle.
25 ructure of PfMyoA in two states of its motor cycle.
26 tty acids all contributed carbons to the TCA cycle.
27 tes rhythmic expression across the day/night cycle.
28 key replication events during the HIV-1 life cycle.
29 ntermediates in the canonical polymerization cycle.
30 ial version of this model across a circadian cycle.
31 symmetry and differentiation during the cell cycle.
32 that play a major role in the global carbon cycle.
33 context of the entire nairovirus replication cycle.
34 scuss implications on the terrestrial carbon cycle.
35 5 intermediate states in the water-splitting cycle.
36 er several consecutive adsorption/desorption cycles.
37 erage Coulombic efficiency of 99.1 % for 350 cycles.
38 levels of redox ratios in synchrony with the cycles.
39 nd time between two consecutive chemotherapy cycles.
40 intravenously once every 3 weeks, in 3-week cycles.
41 te to bridge sylvatic and human transmission cycles.
42 ts initial enzymatic activity after 15 reuse cycles.
43 eceptor CXCR2 and by regulators of circadian cycles.
44 sign of degradation after ~10(10) switching cycles.
45 ) with capacity retention of 97.6% over 2000 cycles.
46 reased further after additional blinatumomab cycles.
47 int was met, with an sCR rate of 60% after 8 cycles.
48 ity following multiple adsorption-desorption cycles.
49 ) cathodes to achieve 101.6 mAh g(-1) for 50 cycles.
50 affecting the step length over multiple gait cycles.
51 close linkage between soil microbial C and N cycling.
52 ant consequences for biogeochemical nitrogen cycling.
53 associated with decoupling of litter C and N cycling.
54 es were driven by both N speciation and diel cycling.
55 lly important consequences for global carbon cycling.
56 the symbiotic lifestyle and aids in nutrient cycling.
57 ule of 4 days on and 3 days off (starting on cycle 1 day 15) until disease progression, unacceptable
58 ry 28 days (plus a loading dose on day 15 of cycle 1) with either capivasertib 400 mg or matching pla
60 ng Cancer 13 (QLQ-LC13) were administered at cycles 1-5, every three cycles thereafter during year 1,
62 s of therapy were offered (cycle 1: CPX-351; cycle 2: FLAG [fludarabine 30 mg/m(2)/dose on days 1-5;
64 Rac family small GTPase 1 and cell division cycle 42 activation, as well as downstream intracellular
66 from lipogenesis toward ketogenesis and TCA cycle, a milieu which can hasten oxidative stress and in
67 er and monomer photoreception, dimer/monomer cycling, abundance of native COP1 and RUP proteins, and
68 e of ATP hydrolysis and blocks the catalytic cycle after formation of the aspartyl phosphate intermed
71 ociated with plasticity/rigidity of the cell cycle and correlated with sensitivity to CDK4/6 inhibiti
74 LuxS is essential for the activated methyl cycle and generates homocysteine for conversion to l-met
75 nce in coordination with the DNA replication cycle and have an important role in segregating genetic
76 s revealed downregulation of matrisome, cell cycle and immune related gene sets in Lcn2(-/-) mice exp
78 ipheral homeostasis in the CD4+ Th cell life cycle and invariant NK (iNK) T cell development and CD8+
79 OX blocks apicoplast biogenesis in the first cycle and is rescued by isopentenyl pyrophosphate, an es
80 ranscriptase (TERT) throughout its catalytic cycle and mapped the active site residues responsible fo
82 and transporter genes, ascorbate-glutathione cycle and nutrient uptake, and lowering in oxidative str
83 line metabolism by up-regulating the proline cycle and proline biosynthesis, and knockdowns of PYCR1
84 h and counteracted EZH2 and SOX2 during cell-cycle and self-renewal regulation to restrain tumorigene
86 cycle continuum to within 14% of the entire cycle and that using more genes did not improve this acc
87 product (RAP) were obtained for each cardiac cycle and their dynamic response to a step change in MAP
89 therapy, with a reciprocal decrease in cell-cycle and WNT signaling pathways in responding biopsies.
91 s given in 21-day cycles for the first eight cycles and 35-day cycles from the ninth cycle until dise
94 ationship between the number of chemotherapy cycles and time between two consecutive chemotherapy cyc
96 methane production drives a cryptic methane cycling and fuels AOM coupled to the reduction of sulfat
98 ion plays an important role in terrestrial N cycling and represents a key driver of terrestrial net p
99 every 3 weeks (8 mg/kg loading dose at first cycle, and 6 mg/kg thereafter) for 18 doses or weekly (4
102 localize to centrosomes throughout the cell cycle, and in interphase cells to the nucleus, and in bo
103 ysis/gluconeogenesis, the tricarboxylic acid cycle, and monosaccharide and disaccharide metabolism.
105 r this and other microalgal species, diurnal cycles are well known to control the metabolism, growth,
106 ominant mechanisms that determine the carbon cycling are different between the consolidated gully and
107 Y cells with PMA and it correlated with cell cycle arrest at G2/M, upregulation of tumor suppressor p
108 nd that overexpression of ABHD5 induces cell cycle arrest at the G1 phase and causes growth retardati
112 ak and trough that correlates with a cardiac cycle as revealed by a reference pulse oximeter (correla
113 very low average voltage decay of 0.8 mV per cycle as well as a capacity retention of 88.4% within 20
114 s able to facilitate wood decay and nutrient cycling as well as tolerate latex and utilize resinous e
116 increasingly predictable over multiple fire cycles, as boundaries are progressively sharpened until
118 n retention of 1-carbon groups in the folate cycle at the expense of transfer to the methylation cycl
121 is is that logging influences phosphorus (P) cycling, because this scarce nutrient is removed in extr
122 or emerges, in which the period of the limit cycles becomes an integer n > 1 multiple of the driving
124 re of the SAT varied with phases of the gape cycle, but gape distance accounted for the majority of d
125 Synthetic trees can mimic this transpiration cycle, but have been confined to pumping water across a
126 eota are important organisms in the nitrogen cycle, but the mechanisms driving their radiation into d
127 s on progression through S phase of the cell cycle, but the molecular nature of this requirement has
128 mproving the harvested energy per mechanical cycle, but they are complicated to implement at such vol
129 a suggest that LGR4 promotes the normal hair cycle by activating HF stem cells and by influencing the
131 to blood pressure variability (BPV)-induced cycle-by-cycle fluctuations in mechanical forces which v
132 scopy to demonstrate that the apparent first-cycle capacity loss is a kinetic effect linked to limite
134 ls show that these extinction-related carbon cycle changes would have allowed the ocean to absorb mas
138 ffects of contact force, scan speed, contact cycles, contact region and charge diffusion on the trans
139 enes predicted a cell's position on the cell cycle continuum to within 14% of the entire cycle and th
140 g tool to facilitate in vivo studies of cell-cycle control in a wide-range of developmental contexts.
141 er, we use cell cycle tags to reinstall cell cycle control to a deregulated version of Yen1, showing
142 tion of Aurora B in interphase leads to cell cycle defects often linked to aberrant chromosomal conde
146 ifically, we find that genes related to cell cycle, DNA repair, cell death, the IGF1 pathway, and imm
147 ange intra-generational correlations in cell-cycle duration, up to second cousins, seem paradoxical b
148 vate neural differentiation and inhibit cell cycle during the transition, whereas epilepsy genes func
150 d key regulatory enzymes that drive the cell cycle, elucidated structural components that underly ess
151 Mammalian cells typically start the cell-cycle entry program by activating cyclin-dependent prote
155 and neurovascular coupling during submaximal cycling exercise and temperature-matched passive heat st
156 end-tidal PCO2 was held constant) Submaximal cycling exercise and temperature-matched passive heat st
157 w uncover that when the epigenetic chromatin cycle falters, a genetically hardwired mechanism offers
161 four genes) and the tricarboxylic acid (TCA) cycle (five genes), and four genes (GmFATB1a, GmPDAT, Gm
162 pressure variability (BPV)-induced cycle-by-cycle fluctuations in mechanical forces which vary consi
166 cycles for the first eight cycles and 35-day cycles from the ninth cycle until disease progression, u
167 , extracted from chest radiographs after the cycle-GAN's texture translation (fake chest radiographs)
168 limate change has intensified the hydrologic cycle globally, increasing the magnitude and frequency o
170 that significant variations existed in life cycle GWP, EU, and AD among counties and across years.
171 services such as water filtration, nutrient cycling, habitat stabilization, and food web enhancement
172 Patients with NMRs >= 5.75 after the first cycle had significantly higher objective response rates
173 Ct value for asymptomatic children was 10.3 cycles higher than for symptomatic children (P < 0.0001)
176 e molecular mechanisms and logic of the cell cycle, identified key regulatory enzymes that drive the
179 2l 1) caused significant effects on the cell cycle in PC3 cells, with the vast majority of treated ce
180 s, we examined key aspects of the viral life cycle in three-dimensional (3-D) human airway tissues.
181 consistent decrease in the C. difficile life cycle in vivo, it was able to attenuate an overly robust
183 s is driven by molecular clock timing, which cycles in anti-phase between day- versus night-biting mo
184 r reduction in NPM1mut TLs after 2 treatment cycles in MRD positive patients by the addition of GO le
186 evidence of EM fungal suppression of C and N cycling in the Pinus-dominated site, but no suppression
187 Each surface loop was evolved by infectious cycling in the presence of a helper adenovirus to yield
189 onal repressor of key regulators of the cell cycle, in turn influencing contact inhibition and tumori
190 inate receptor 1 or GPR91) senses the citric cycle intermediate succinate and is implicated in variou
191 cally reduced intracellular succinate, a TCA cycle intermediate that serves as a direct electron dono
192 atalyst, which introduces a second catalytic cycle into the metabolic network, was used to close the
193 The chromosome breakage-fusion-bridge (BFB) cycle is a mutational process that produces gene amplifi
196 rinciple QTL determining SET (SET1: dormancy cycling) is physically close on chromosome 5, but is dis
199 als were found to be dependent on underlying cycle length in a highly curvilinear fashion with the de
203 able-adjusted HRs between lifetime ovulatory cycles (LOC) and its components and ovarian cancer risk
204 he effect of subduction on the deep nitrogen cycle may be less important than has been suggested by p
205 a quantum system, adiabatically driven in a cycle, may acquire a measurable phase depending only on
206 dation activity and tricarboxylic acid (TCA) cycle metabolites were measured in cells collected from
208 ch enable modeling of kinematic loops (e.g., cycling models) and complex anatomy (e.g., patellar moti
209 Minimizing the number and duration of design cycles needed to optimize hit or lead compounds into hig
212 rmediates, their relevance for the catalytic cycle of [FeFe] hydrogenase, and novel strategies for ex
214 and timings, which would affect the seasonal cycle of atmospheric radiocarbon concentrations recorded
215 gene transcription dynamics, we show that a cycle of fast exodus of nuclear YAP to the cytoplasm fol
216 ntally determined and investigated through a cycle of ligand-FEP calculations, validating the binding
222 17-2018), 1,493 participants with 6 or fewer cycles of attempt time were randomly assigned with 50% p
223 d this percentage increased to 60% after two cycles of blinatumomab; the percentage of patients with
224 (1:1) to either surveillance or four 21-day cycles of chemotherapy, using a minimisation algorithm w
226 ggest Arctic marine biomes persisted through cycles of glaciation, leading to unique assemblages in p
227 LM can be used to describe normal sleep-wake cycles of healthy adult dogs and the effects of physiolo
228 d 30, inhibit early steps of the replicative cycles of HIV-1 and EV-A71 by interacting with their res
229 lations, were employed for sampling multiple cycles of LIV-BPSS clamshell-like conformational changes
230 If >= 100 out of 125 patients completed 4 cycles of paclitaxel without dose delay, the regimen wou
235 torage-temperature, and repeated freeze-thaw cycles on circulating BDNF concentrations was evaluated.
236 (16 mg/kg of bodyweight, once weekly during cycle one, once every 3 weeks in cycles two through nine
237 f diversity at many levels-ranging from cell cycle organization to chromosome ploidy to replication m
241 reased during mitosis relative to other cell cycle phases suggests that redox modifications could pla
243 to permanent state change in biogeochemical cycling, primary production, and biological diversity by
244 tural components that underly essential cell cycle processes, and influenced our thinking about cance
245 peratures have a profound impact on global N cycling processes with implications of a positive feedba
246 The chaperone protein SmgGDS promotes cell-cycle progression and tumorigenesis in human breast and
247 illin also affected networks related to cell cycle progression as well as connective tissue developme
248 loop between appressorium formation and cell cycle progression in U. maydis, which serves as a "toggl
250 paired growth is due to perturbation of cell cycle progression rather than induction of apoptosis.
251 ucial roles in cell differentiation and cell-cycle progression, and kinase dysregulation is associate
252 , increased Tnf expression, decreased a cell cycle regulator (Ccnb1), and increased apoptotic factors
255 rior results, HML and HMR had identical cell-cycle requirements for silencing establishment, with no
260 chromatin and kinetochores at distinct cell-cycle stages, revealing extensive reorganization of kine
261 -life of p53 and uses p53 to initiate a slow-cycling state following stress (DNA damage, targeted the
264 ndent kinases at distinct stages of the cell cycle, suppresses S-phase entry and promotes progression
268 feedbacks, mediated by the oxygen and sulfur cycles, that led to permanent state change in biogeochem
269 k to the original quinone, creating a futile cycle, the byproducts of which are deleterious reactive
270 During interphase of the eukaryotic cell cycle, the microtubule (MT) cytoskeleton serves as both
271 were administered at cycles 1-5, every three cycles thereafter during year 1, and every four cycles d
273 als had an RT-PCR-positive viral test with a cycle threshold (C(T) ) of <35 or seroconverted during t
276 nsistently yielded amplifiable RNA with mean cycle threshold differences of <3 over the various condi
277 f isolation/quarantine, (ii) whether the PCR cycle threshold value should be included on patient repo
280 gens are able to compartmentalize their life cycle to provide favorable conditions for replication an
283 f T-PLL cells evoked higher-than-normal cell-cycle transition and profiles of cytokine release that r
284 lly recurrent prostate cancer (PCa), whereby cycling treatment on and off can reduce cumulative dose
285 ekly during cycle one, once every 3 weeks in cycles two through nine, and once every 4 weeks thereaft
286 ight cycles and 35-day cycles from the ninth cycle until disease progression, unacceptable toxicity,
287 with 40 mg of weekly dexamethasone in 28-day cycles until disease progression or up to 6 cycles after
288 It however suffers from a voltage decay upon cycling, urging for an in-depth understanding of the par
289 Although the ribulose monophosphate (RuMP) cycle used by methylotrophs to assimilate methanol diffe
291 devices; we will illustrate that the thermal cycling variations strongly determine the type of damage
292 echanistic insights into the viral infection cycle, very little is known about the location and foldi
294 d of a simple reductive quenching photoredox cycle, we have successfully harnessed this novel radical
295 ct by the carboxylate anion on the catalytic cycle, whereas 2-ethyl hexanoate minimizes this inhibito
296 stomatal opening and closing across the diel cycle, which conserves water and provides a means of mai
298 ts, which play a key role in trace elemental cycles, with potentially important consequences for glob
301 t studies indicate that the classical visual cycle works together with light-dependent processes in b
302 osystems in modulating global biogeochemical cycles, yet their biological communities and related car