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1 ied at the end of rapid shortening, recovery was accelerated by (1) the introduction of a slow fallin
2  FZR1 undergo passage through meiosis I that is accelerated by ~1 h, and this is due to an earlier on
3 homolysis, while slow for the free cofactor, is accelerated by 12 orders of magnitude when AdoCbl is
4 cation, the kinetics of late gene expression is accelerated by 12 to 24 h and that virus produced fol
5 find the approximate time to full expression is accelerated by 13 min, 48 s in D. simulans and retard
6 approximate time to full expression of hairy is accelerated by 13 min, 48 s in D. simulans.
7                However, charge recombination is accelerated by 2 orders of magnitude in ferrocene-con
8 ereas muscle and hepatic glycogen depletions were accelerated by 27-55%, revealing 2-fold greater car
9 der these conditions the hydrolysis kinetics are accelerated by 40- to 1300-fold over that of d-G.
10 lled water was added and the microextraction was accelerated by 4min sonication.
11 sign of more effective malaria vaccines will be accelerated by a better understanding of the immune e
12          Post-ischemic neurodegeneration may be accelerated by a cytokine-receptor mediated apoptotic
13  that this small batch uptake reaction could be accelerated by a factor of about 5-fold or more, depe
14 ding of riboswitch regulatory function would be accelerated by a high-throughput, quantitative screen
15 ork we demonstrate that closing the gaps can be accelerated by a selective recombinational capture of
16  is combined, with real-time data processing being accelerated by a graphics-processing unit.
17 , because the rate of second-strand cleavage is accelerated by a factor of almost 150 relative to the
18 rin cofactor II (HCII) and antithrombin (AT) is accelerated by a heparin template between the serpin
19                     Flowering in Arabidopsis is accelerated by a reduced ratio of red light to far-re
20   Here, we describe medicinal chemistry that was accelerated by a diversity-oriented synthesis (DOS)
21 ed functional regulatory volume increase and was accelerated by a return of extracellular osmolality
22    Gold particles of radius 0.9+/-0.6 microm were accelerated by a hand-held supersonic device to imp
23 ng antibody response in wild-type mice could be accelerated by ablation of their IFN-gamma response.
24 e hydrolysis of 4-alkoxy-substituted acetals was accelerated by about 20-fold compared to that of ste
25 hered head is slow (0.05 s(-1)), but release is accelerated by added ADP or ATP.
26                            Disease induction was accelerated by adding B:9-23 immunization to PolyIC.
27 receptors, we show that response decay times are accelerated by addition of GABA, a weak partial agon
28                            Guanosine binding is accelerated by addition of residues that form helices
29 In saturating amounts of counterion, folding is accelerated by addition of urea.
30 stabilization via thiosuccinimide hydrolysis were accelerated by addition of N-phenyl or N-fluorophen
31  synthesized SPGP through intrahepatic sites was accelerated by additional administration of cAMP but
32 ation, mechanisms underlying cyst expansion, are accelerated by adenosine 3':5'-cyclic monophosphate
33          Progress in this field has recently been accelerated by advances in computational, molecular
34          We also found that GCNA1 expression was accelerated by agents which promote DNA demethylatio
35  show that the silyl ether exchange rate can be accelerated by almost three orders of magnitude.
36 d with reductions in hippocampal volume that are accelerated by Alzheimer's disease and vascular risk
37                                All reactions are accelerated by an increase in temperature, but the m
38 oembolic pulmonary hypertension (CTEPH) will be accelerated by an animal model that replicates the ph
39 s in adult mice, and this contribution could be accelerated by an induced interferon response.
40 initial quaternary contact (RT intermediate) is accelerated, by an order of magnitude, but the lockin
41                    This phenotypic reversion was accelerated by anti-inflammatory therapy.
42                          Conversely, pruning is accelerated by application of exogenous NMDA.
43  signals return to baseline, although firing is accelerated by approximately 20 Hz for approximately
44 ls (judged by BCR clonality) did not seem to be accelerated by APRIL; both mouse strains were oligocl
45 he aorta stiffens with aging, a process that is accelerated by arterial hypertension.
46     When the Fe(II) is 5C, the O(2) reaction is accelerated by at least 2 orders of magnitude.
47 P to E2-P transition and the enzyme turnover are accelerated by ATP binding to the phosphoenzyme in e
48 er, whereas polymerization of wild-type ParF is accelerated by ATP and inhibited by ADP, filamentatio
49 rough solution, and suggest that binding may be accelerated by atypical structural or dynamic feature
50                                     Carriers were accelerated by band-bending at the suspension inter
51 o the CGI of the INSL6 promoter, which could be accelerated by binding a KRAB-containing transcriptio
52             Moreover, beta-AR maturation can be accelerated by biomechanical stimulation.
53 , death was associated with LD depletion and was accelerated by blocking LD biogenesis after pharmaco
54 wound-induced stellate cell migration, which is accelerated by both exogenous and endogenous ET-1.
55  the G(1)/S transition during the cell cycle is accelerated by both the Kit/Stat5 and Kit/PI3K/Akt pa
56                       Cardiovascular disease is accelerated by both type 1 and type 2 diabetes.
57                           Reaction with H2O2 is accelerated by bound substrate and produces fosfomyci
58  slightly voltage-dependent, and its washout was accelerated by bovine serum albumin.
59 strate that entry of mature vaccinia virions is accelerated by brief low-pH treatment and severely re
60 ocess by promoting migration, a process that is accelerated by cell spreading.
61 iabetic individuals is multifactoral but may be accelerated by changes in the structure and function
62 abetic individuals is multifactorial but may be accelerated by changes in the structure and function
63 refore, the assay optimization process could be accelerated by choosing detection antibodies with the
64 leen cells, and that transformation by c-Rel is accelerated by co-expression of Bc1-2.
65 ltage activation of wild-type ClC-7 subunits was accelerated by co-expressing an excess of ClC-7 subu
66 ced energy deficit and metabolic dysfunction is accelerated by cocaine inducing energy sensor AMPKs,
67                 The degradation of IL-8 mRNA was accelerated by competition for saliva ARE-binding pr
68 nd the d-band theory: Ni and Pt's activities were accelerated by compression, while Cu's activity was
69                Additionally, fiber formation is accelerated by constructs that mimic the intra-sheet
70 rotein synthesis, the loss of CYP3A4 protein was accelerated by cotreatment with either proteasome or
71 response element binding protein (CREB), and are accelerated by CREB overexpression.
72                          Lymphomagenesis can be accelerated by crossing in a further novel allele, wh
73 rite outgrowth in CGNs, determined at 3 DIV, was accelerated by CtxB and suppressed by TRPC5 siRNA an
74 se hydrogen sulfide as the reductant and can be accelerated by Cu(I)-Cu(II) photoredox cycling.
75  occur in the periphery and that their onset is accelerated by decreased thymic output and/or functio
76 longation of dimers to form longer oligomers is accelerated by decreasing polycytidylate (poly(C)) co
77  activity by ceramide was time-dependent and was accelerated by depletion of internal Ca(2+) stores.
78                           Toxin dissociation was accelerated by depolarization and increased by these
79                       Fos-mediated apoptosis was accelerated by deregulated c-Myc.
80                     Such complementation can be accelerated by developing better tools for the effici
81 therosclerosis and restenosis, both of which are accelerated by diabetes mellitus.
82                              Atherosclerosis is accelerated by diabetes and is associated with increa
83                Periodontal wound healing has been accelerated by different low-level laser therapy (L
84 sampling of different protein configurations is accelerated by disruption of the disulfide bond.
85 ome is dependent upon the TPR domain, and it is accelerated by disruption of the TPR organizational s
86 ory, supports a charge transfer process that is accelerated by dissociation of the anion from the oxi
87 inhibited by constitutively active FoxO1 and is accelerated by dominant-negative FoxO1.
88  the safety and quality of surgical care can be accelerated by drawing more heavily upon implementati
89                    Moreover, these processes are accelerated by EBOV infection.
90                                    Apoptosis is accelerated by ectopic expression of c-Myc and blocke
91 pression driven by the rat SREBP-1c promoter was accelerated by ectopic expression of Sp1, and insuli
92 Ca2+ in the presence of TM, but, instead, it was accelerated by EDTA.
93    Shutoff of host RNA and protein synthesis was accelerated by either the 44- single mutant or the 5
94                        Reductive elimination is accelerated by electron-donating substituents (rho =
95                                 The reaction is accelerated by electron-poor ArS ligands, but is unaf
96 (R(2) = 0.996), indicating that the reaction is accelerated by electron-withdrawing aryl rings.
97 profound extent to which very slow reactions are accelerated by elevated temperatures, collapsing the
98                           The latter process is accelerated by elevated proinflammatory responses ass
99      Cognitive decline over 2-year follow-up was accelerated by elevated baseline cerebrovascular res
100  causing polyphosphoinositide breakdown, and was accelerated by elevated intracellular Ca(2+) levels.
101  These sites recover with a time course that is accelerated by elevations of Ca(res).
102 ly, we found that this conformational change is accelerated by elongation factor Ts (EF-Ts), the guan
103 and suggests that dipolar cycloadditions can be accelerated by enzyme catalysis.
104  new drug of abuse, and that this conversion is accelerated by ethanol oxidation.
105 ost importantly, that the oxidative addition is accelerated by ethylene glycol, most likely via hydro
106  results show that the rate of evolution can be accelerated by evolving cell populations in sequentia
107 oleic and low linoleic acid) in peanut could be accelerated by exploiting linked markers through mole
108               The degradation of HDAC4 could be accelerated by exposure of cells to ultraviolet irrad
109                The development of BE and EAC was accelerated by exposure to bile acids and/or nitrosa
110                                   This decay is accelerated by extraerythrocytic thiol (slope, 0.089;
111                   By contrast, melting rates are accelerated by factors of approximately 100 and appr
112        This suggests that the molecules have been accelerated by fast shocks driven into the interste
113 er the development of these immune responses is accelerated by frequent treatment after reinfection.
114 ification was evident, rates of modification were accelerated by GABA co-application, indicating that
115 was not affected by Galpha12, but reassembly was accelerated by Galpha12 depletion.
116 orylation regulates biological function will be accelerated by general methods to biosynthesize defin
117                                   Expression is accelerated by gerontogenic behaviors such as tobacco
118 e product-release step of the B-site mutants is accelerated by glycerol, suggestive of a structural e
119 me, which occurs only after subunit joining, is accelerated by GTP hydrolysis by eIF5B.
120 g proteins, and inhibition of KLK7 by vaspin is accelerated by heparin.
121 o-myc lymphomagenesis, because disease onset was accelerated by heterozygosity for Suz12 or by short
122                     Recovery of function may be accelerated by high dose corticosteroids, and althoug
123  montane forests; the upslope shift may have been accelerated by high turnover in canopy trees that p
124                               Biologic aging is accelerated by high-calorie intake, increased free ra
125 s channel gating, particularly deactivation, was accelerated by histamine.
126                           Whereas forward ET is accelerated by hopping through W122, BET is retarded
127 transport of NaCl across the mTAL epithelium is accelerated by hormones that increase cAMP levels (va
128 We found that the ATPase activity of mtHSP70 is accelerated by HSC20 and further accelerated by HSC20
129                Recruitment of CD8(+) T cells was accelerated by IFN-gamma-dependent production of che
130 localization of RFP-LC3 and LysoSensor Green was accelerated by IGF-I.
131 unstimulated conditions, but its degradation is accelerated by IL-22 treatment.
132                        Further progress will be accelerated by implementing knowledge about the molec
133      INTERPRETATION: National coverage gains were accelerated by important increases among poor and r
134          Progress in these applications will be accelerated by improved sensitivity, specificity, and
135                             Tumor growth may be accelerated by in vivo passage, thus making these tum
136 s and adenocarcinomas, and their growth rate was accelerated by in vivo passages.
137  the 26 S proteasome in vivo, a process that is accelerated by inactivation of S-adenosylmethionine d
138    The importance of tick-borne diseases has been accelerated by increases in animal populations, as
139 ndependently varied, the rate of decay of EG is accelerated by increasing [H2] and slowed by increasi
140 hat the dissociation of Fis protein from DNA is accelerated by increasing the concentration of the Fi
141                            The reaction rate was accelerated by increasing amounts of Mn(III), carbad
142            The exploration of sequence space was accelerated by increasing the mutation rate using mu
143            The macrocycle formations via RCM were accelerated by increasing the pore size and decreas
144 om circulating progenitors in a process that is accelerated by inflammatory stimuli.
145 y stress and cytotoxicity caused by 2-DG can be accelerated by inhibition of eEF-2 kinase, and sugges
146 ansported to the ER by binding to the KDEL-R is accelerated by inhibition or genetic ablation of Src.
147 of mutant host hepatocytes, and repopulation was accelerated by injection of an adenovector expressin
148                                     Cleavage is accelerated by insulin stimulation in 3T3-L1 adipocyt
149  in older subjects, and the encoding process was accelerated by intake of levodopa.
150    Rubella control and prevention of CRS can be accelerated by integrating with current global measle
151 that show that the time course of relaxation is accelerated by interfilamentary movement resulting fr
152 s, (Re126W122Cu(I))2 and that the forward ET is accelerated by intermolecular electron hopping throug
153 ly progressive process that is postulated to be accelerated by intervening diseases, such as diabetes
154       Re-compaction of Von Willebrand factor is accelerated by intramolecular interactions and increa
155                                 The reaction is accelerated by iodine, and HBr effects rearrangement
156 unoassays in which protein-antibody reaction is accelerated by isotachophoresis (ITP).
157  NO dissociation from the heme center of sGC is accelerated by its interaction with one or more cofac
158                         The solution process is accelerated by Krylov subspace methods and a new vers
159               The decay of this intermediate is accelerated by l-ornithine binding.
160  cycle re-entry of quiescent satellite cells is accelerated by lack of Rb1, resulting in the expansio
161 thesis of A2E and its conversion to oxiranes are accelerated by light.
162 ee of hydration w0 (in "drier micelles") and is accelerated by light through NADH photochemistry.
163 ur hypothesis that chondrocyte proliferation is accelerated by mechanical stimuli above natural growt
164 erization of H(2)B horizontal lineNMe(2) can be accelerated by MeCN; and complementary nonclassical B
165  with the lethal triggering of the holin and is accelerated by membrane depolarization.
166 ponse was also voltage dependent, because it was accelerated by membrane hyperpolarization.
167 ysis is slow in the absence of metalloid and is accelerated by metalloid binding.
168 ysis is slow in the absence of metalloid and is accelerated by metalloid binding.
169                         Such redirected flow was accelerated by microtubule depolymerization, showing
170 aled that movement of the hIR through the ER was accelerated by misfolding or by overexpression of ei
171                               Recovery might be accelerated by more effective interventions to increa
172 n with reduced anisotropy, with the velocity being accelerated by more than twice compared with that
173                    Loss of lens transparency was accelerated by more than 50-fold in AQP1-null lenses
174 nce of tumors displaying genomic instability is accelerated by mutant p53172R-H.
175                                 This process was accelerated by N-ethyl-N-nitrosourea-induced mutatio
176                              This trend will be accelerated by new concepts for molecular recognition
177                           Target association is accelerated by nonspecific binding to nearby sites an
178 bservation that the decomposition of an RSNO is accelerated by O(2), mixtures of O(2) and NO, and oth
179  with FADH(2) in the oxidative half-reaction is accelerated by ornithine 80-fold, providing a mechani
180 as part of the normal aging of the aorta but is accelerated by other conditions, including hypertensi
181             EGF-induced receptor degradation is accelerated by overexpression of either wild-type PLD
182 wnstream targets of STAT5-Bcl-X(L) and pim-1 was accelerated by overexpression of SHP-2.
183 ired the left but not right auditory cortex, was accelerated by oxytocin in the left auditory cortex,
184 ed selectivity for specific TLR agonists and was accelerated by P2X7 receptor activation.
185 ediated by ERK activation, and that cleavage is accelerated by p38 MAP kinase activation.
186                          This predisposition was accelerated by p53 deficiency, reducing the earliest
187 ), as measured by unscheduled DNA synthesis, was accelerated by PAF and 5-HT receptor antagonists.
188 he amphipathic N-terminal domain of RGS4 and are accelerated by palmitoylation of cysteine residues i
189 nder normal physiological conditions and can be accelerated by pathological stress, possibly as a cyt
190 s, reflecting synchronous neuronal activity, was accelerated by PbTx-2 treatment.
191     The GTPase activity of Galpha(t)G38D can be accelerated by photoreceptor regulator of G protein s
192                   Uncoupling during ischemia was accelerated by PKC and KATP channel inhibition.
193                                     Shedding is accelerated by PMA activation of protein kinase C, an
194 XIIa or thrombin is a slow reaction that can be accelerated by polyanions.
195 ions between labels, analyte, and antibodies are accelerated by positioning magnets alternately above
196 hanges, suggesting that their divergence has been accelerated by positive Darwinian selection.
197 yloidogenic proteins into ordered fibers can be accelerated by preformed amyloid aggregates derived f
198 ent Goal 4 for child mortality reduction can be accelerated by prevention and treatment of pneumococc
199                 Peripheral axon regeneration is accelerated by prior injury; however, DLK KO neurons
200 g site is extremely slow in resting RyR2 but is accelerated by promoting RyR opening or unzipping (by
201               The decline in crystal binding was accelerated by prostaglandin E(2) (PGE(2)) supplemen
202  under hypoxia occurs via the proteasome and is accelerated by protein acetylation.
203 health scholars believe that this change has been accelerated by public policy interventions to reduc
204 utational events suggests that evolution may be accelerated by punctuated changes in genome architect
205 A) showed that annealing of oligonucleotides is accelerated by Rad52 in the presence of RPA.
206        The acyclic 1,5-dienyl hydrogen shift is accelerated by radical-stabilizing phenyl substituent
207     The reduction from Pu(VI) to Pu(V) could be accelerated by raising the pH of the solution, which
208                In intact cells, AR breakdown was accelerated by raising intracellular Ca(2+) using ca
209 the stage of testing in clinical trials that were accelerated by recent advances in the characterizat
210                     In Arabidopsis flowering is accelerated by reduced red:far-red (R:FR) ratio which
211  to co-ordinate movement of hormogonia might be accelerated by reducing cell volume.
212 ro, which occurs by the reverse process, can be accelerated by removing the alpha-subunit oligosaccha
213                The oxidative degradation can be accelerated by replacing methyl iodide with dimethyl
214 witch, from excitatory to inhibitory action, was accelerated by REST inhibition and slowed by REST ov
215                   The rate of polymerization was accelerated by seeding with polymers of alpha(1)-ant
216            Constitutive neutrophil apoptosis was accelerated by sequestration of Hsp27 from Akt, and
217                         VWF self-association is accelerated by shear stress.
218                Moreover, the in-ice reaction is accelerated by simple amino acids, in particular glyc
219 ng rate determined for these cyclic peptides is accelerated by some two orders of magnitude over the
220 gths, suggesting that relativistic particles are accelerated by strong shocks in the ejecta.
221                                 The reaction is accelerated by substituents in the aromatic ring that
222 ation of 2 into [Ir(CO)(2)I(3)(COMe)](-), 6, is accelerated by substoichiometric amounts of neutral p
223 nes with cell replication and the effect can be accelerated by such factors as inflammation, oxidativ
224  The production of the hydrogen peroxide can be accelerated by superoxide dismutase or redox active m
225 eparate sites, suggesting that tumorigenesis is accelerated by Tat through soluble factors.
226 ffective drug discovery and optimization can be accelerated by techniques capable of deconvoluting th
227 g at 6 hours, a measure of orocecal transit, was accelerated by tegaserod (70.4% +/- 1.3% [mean +/- S
228 elerated by compression, while Cu's activity was accelerated by tension.
229 n inactivation by heparin cofactor II (HCII) is accelerated by ternary complex formation with heparin
230 ) by the serpin, heparin cofactor II (HCII), is accelerated by ternary complex formation with the gly
231 ying the stable B-methallylborinane 1, which was accelerated by tertiary alcohols.
232                        The reporter response was accelerated by tethering to PKA holoenzyme and slowe
233 ted that the carbon-carbon bond-forming step is accelerated by TFA and is a rare example of Bronsted
234 aser-driven accelerators, in which particles are accelerated by the electric field of a plasma wave (
235  events in clathrin-coated vesicle formation are accelerated by the overexpression of dyn(K694A) and
236 play activation energies of 20 kcal/mol, and are accelerated by the peptidyl-prolyl isomerase SlyD.
237 ent, reproducible, and translatable research are accelerated by the rapid growth of "post-publication
238 ing groups showed that these transformations are accelerated by the use of electron-withdrawing direc
239  effective cell therapies against cancer can be accelerated by the adaptation of tools to rapidly qua
240 s model, the rate of fibril formation should be accelerated by the addition of preformed aggregates o
241 monstrate how discovery of new materials can be accelerated by the combination of high-throughput the
242 e-refractory prostate cancer, which tends to be accelerated by the current antiandrogen therapy, we i
243 entation on neurocognitive development could be accelerated by the development of a nonhuman primate
244 ion of novel therapies for FRDA and this can be accelerated by the development of cell models which r
245  future advances in solar fuels science will be accelerated by the development of new methods for mat
246  channels, as initiated by ceramidase, could be accelerated by the direct interaction of the hydrolys
247  showed that the sweep of this variant could be accelerated by the presence of copy number variation
248                           Cycloadditions can be accelerated by the presence of electron-withdrawing g
249 tion of appropriate antifungal therapy could be accelerated by the timely reporting of laboratory tes
250 ently required, and their development should be accelerated by the use of a human challenge model.
251 tions for the separation of new analytes can be accelerated by the use of appropriate theoretical too
252 he mapping of the canine genome has recently been accelerated by the availability of chromosome-speci
253 he interest in adipose tissue remodeling has been accelerated by the current epidemic of obesity and
254  neutral atoms (both hot and cold) that have been accelerated by the electric field in the solar wind
255  mechanisms underlying lymphangiogenesis has been accelerated by the identification of tissue-specifi
256                               In addition to being accelerated by the plasma wakefield, the beam part
257 e autoinhibited and activated conformations, is accelerated by the action of peptidyl-prolyl isomeras
258                                    ER export is accelerated by the alternatively spliced C2' domain o
259 the slow intrinsic rate of transducin GTPase is accelerated by the complex of the ninth member of the
260                                 The reaction is accelerated by the copper(I)-stabilizing ligand batho
261                      The hydrolysis of E-XMP is accelerated by the deprotonation of a residue with a
262 and structural similarity, and loss of Tim10 is accelerated by the disruption of conserved disulfide
263 lyl O- to C-acetyl or carboxyl rearrangement is accelerated by the electron-withdrawing N-diphenylace
264 hich this free energy is transferred to work is accelerated by the free energy of a motor-catalyzed r
265 n by the serpin, heparin cofactor II (HCII), is accelerated by the glycosaminoglycans (GAGs) dermatan
266 t the sequential metabolism of Nile Red (NR) is accelerated by the heterotropic allosteric effector a
267          Proteasome-mediated turnover of p53 is accelerated by the HPV E6 and cellular E6AP proteins.
268 action of the fully reduced enzyme with O(2) is accelerated by the N139D mutation, as shown by a more
269                                           It is accelerated by the PI(3)P- and phosphatidylinositol 3
270       Internal cleavage by this endonuclease is accelerated by the presence of a monophosphate at the
271 n undergoes autocatalytic fragmentation that is accelerated by the presence of the metal cofactor, zi
272 iate to the active Mn(IV)/Fe(III)-R2 complex is accelerated by the presence of the one-electron reduc
273 with the single-stranded DNA-binding protein is accelerated by the RecF, RecO, and RecR (RecFOR) prot
274 e show that degradation of HMG CoA reductase is accelerated by the sterol-induced binding of its ster
275 s replication in T cells expressing 5ptaseIV was accelerated by the 74LR mutation relative to replica
276 eriments involving mutants whose growth rate was accelerated by the addition of lysozyme or autolysin
277 ation of the ferrocytochrome b moiety of SCR was accelerated by the addition of NO, and was inhibited
278 Tgf-beta1-/- phenotype, and disease transfer was accelerated by the depletion of Tgf-beta1-/- CD4+CD2
279 contrast, retinal astrocytic differentiation was accelerated by the exposure of wild-type newborn mic
280                Shutoff of host DNA synthesis was accelerated by the mutants early in infection but de
281           Conversion of fibrinogen to fibrin was accelerated by the prothrombin fragments generated b
282       Formation of the acid SC-buffer system was accelerated by topically applying the LXR activator,
283     In these ligations, amide bond formation is accelerated by transient enforcement of an intramolec
284     Melanosome accumulation in keratinocytes was accelerated by treatment with lysosomal inhibitors o
285                             Network assembly was accelerated by two conserved regulators that control
286 iferating, antigen-specific CD4+ T cells may be accelerated by type I IFN during a secondary response
287 s, the development of immune complex lesions was accelerated by unilateral nephrectomy-induced hyperf
288 at electrons in the tail of a drive beam can be accelerated by up to 27 GeV in a high-ionization-pote
289  Inhibition of several coagulation proteases is accelerated by up to 10,000-fold by heparin, either t
290 n to controls, brucite carbonation using BCA was accelerated by up to 240%.
291 hat entry into the S phase of the cell cycle was accelerated by up to 4 h in AML-1B-expressing 32D.3
292                         Complex PD insertion was accelerated by up to threefold in response to salicy
293 itis, cirrhosis, or both, hepatocyte cycling is accelerated by upregulation of mitogenic pathways, in
294                      This folding transition is accelerated by urea and increased temperature and slo
295 ing of ribozymes containing Alt P1 and Alt 2 was accelerated by urea as long as the native ribozyme f
296 ral induction and caudalization of hPSCs can be accelerated by using a synthetic microengineered subs
297 ogerin with abnormal nuclear shapes may also be accelerated by UV and with that contribute to photoag
298 ation of RCL-mimicking peptides into wtPAI-1 is accelerated by vitronectin, we further propose that v
299 is found to undergo first-order decay, which is accelerated by water.
300 model legume, Medicago truncatula (Medicago) is accelerated by winter cold (vernalisation) followed b

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