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1 ence and settles proportionally to exp(-mu/D Phi).
2 H in the intracellular side of the membrane (pHI).
3 rter NBCn1 which regulates intracellular pH (pHi).
4 h stages on the Pre-harvest Interval Period (PHI).
5 ohistidine (1-pHis) or 3-phosphohistidine (3-pHis).
6 in the Pediatric Health Information System (PHIS).
7 are jointly considered with respect to d and phi.
8 strongly regulated by Ca(2+) and less so by pHi.
9 ed randomised population of individuals with PHI.
10 hen performing dissipation studies to define PHI.
11 eleases two virus-encoded peptides, mu1N and Phi.
12 peptides, myristoylated mu1N (myr-mu1N) and Phi.
13 emissive than cytidine (lambdaem 398-420 nm, Phi 0.009-0.687), and excellent correlation was found be
16 The sole isolated interlocked photoproduct (Phi = 0.06) is a [2]rotaxane, with the dimerized anthrac
18 in with visual sensations (chi-square, 3.91; Phi = 0.15; df, 1; P < 0.05) and seeing with visual sens
19 eing were intercorrelated (chi-square, 5.47; Phi = 0.18; df, 1; P < 0.05), pain with visual sensation
21 nol, which is slightly lower than that of 1, Phi = 0.88(2), in the same solvent (lambdairr = 460 nm).
22 Phi(0), is given by (chi1((3))-ichi2((3))) x Phi(0), and that the interference between this product a
23 ty and the interfacial potential, chi((3)) x Phi(0), is given by (chi1((3))-ichi2((3))) x Phi(0), and
24 that this newly identified term, ichi((3)) x Phi(0), which is out of phase from the surface terms, is
26 e sintered into porous, bulk nanocomposites (phi 10 mmxh 10 mm) with low kappa (0.48 W m(-1) K(-1) )
27 jects enrolled during primary HIV infection (PHI), 10 chronically infected subjects (chronic), and 7
28 80% of PHI enrollment samples and in 100% of PHI 12-month, chronic, and EC samples; it peaked after a
29 t spherical carbonate concretions (diameters phi : 14 ~ 37 mm) around tusk-shells (Fissidentalium spp
33 The model we used is a square lattice with a phi(4) potential between next-nearest-neighbour sites, w
39 : 1) complex 2, originating from the initial PhI activation with 3, is roughly as reactive toward PhI
46 ative energy differences between the 5fdelta/phi and 5fpi*/5fsigma* orbitals as a qualitative measure
47 l to simultaneously determine the changes of pHi and [Cl(-)]i in response to hypercapnia and seizure
48 nction as reflected in elevated steady-state pHi and accelerated recovery from intracellular acidosis
49 a relationship between the HOMO-LUMO gap and Phi and explained the loss of fluorescence in the nitro
55 ptation duration was short (188 ms), reverse-phi and regular motion led to similar adaptation effects
56 on duration was increased to 752 ms, reverse-phi and regular motion showed distinct adaptation effect
57 reservoir in patients initiating cART during PHI and to assess the impact of the timing of cART initi
59 31-45 to 15-23 events; a shorter duration of PHI and/or a lower testing frequency reduces the number
61 is a powerful regulator of intracellular pH (pHi) and extracellular pH (pHo), and contributes to solu
63 n one season by individuals of the same age (phi) and lifetime variance in reproductive success of in
66 he lipid-facing interface (DeltaDeltaG(0)w,i(phi)) and the protein-facing interface (DeltaDeltaG(0)w,
67 largely due to an enhanced dynamic response (PHId), and a more than twofold improvement in glucose to
69 und in conformations that require a positive phi angle such as helical C-capping motifs or type I' an
70 structure (estimated space-filling fraction phi approximately 0.59) which has not been anticipated b
71 Intracellular chloride ([Cl(-)]i) and pH (pHi) are fundamental regulators of neuronal excitability
72 vation with 3, is roughly as reactive toward PhI as 3 itself; and 2) the Ph-I bond cleavage with the
73 rotocol based on selection medium containing Phi, as the sole source of phosphorus (P), can serve as
76 toxin C5a as a master switch of the delicate pHi balance in neutrophils resulting in profound inflamm
78 (PHI-base) is available at www.phi-base.org PHI-base contains expertly curated molecular and biologi
86 The Pathogen-Host Interactions database (PHI-base) catalogues experimentally verified pathogenici
87 The pathogen-host interactions database (PHI-base) is available at www.phi-base.org PHI-base cont
88 at integrates phenotypic data for genes from PHI-base, an expertly curated catalog of genes with expe
90 ions database (PHI-base) is available at www.phi-base.org PHI-base contains expertly curated molecula
93 r unit chains of both amylopectins and their phi, beta-limit dextrins (LDs) than those of the outer p
95 view of Pediatric Health Information System (PHIS) billing and microbiology data were compared with c
97 combined two-photon imaging of [Cl(-)]i and pHi, but this has never been performed at the cellular l
98 n neutrophils to C5a significantly increased pHi by selective activation of the sodium/hydrogen excha
99 ST search function is provided and a link to PHI-Canto, a tool for authors to directly curate their o
100 otassium thioacetate (KSAc) and iodobenzene (PhI) catalyzed by CuI associated with 1,10-phenanthrolin
103 sults, researchers have proposed that a phi (Phi)-clamp composed of phenylalanine (Phe)427 residues o
104 ture reveals the long-sought-after catalytic Phi-clamp and the membrane-spanning translocation channe
105 s propargylic or homopropargylic, react with PhI(+)CN(-)OTf (Stang's reagent) or 3,5-(CF3)2C6H3I(+)CN
107 ar HCO3(-) concentrations and elevated brain pHi compared to control fish, providing evidence of CO2
109 ns LC-MS/MS spectra for potential matches to pHis-containing peptides based on their neutral loss pat
112 ivation reactions involve PPh3 dissociation, PhI coordination to Ru through I, rearrangement to a eta
114 activated by Ca(2+) rather than by alkaline pHi; current-voltage relations of human Slo3 and human I
115 rs per 1000 patient-days), while the EMR and PHIS data endorsed a decrease of $12785 and $21380 per 1
118 estimated cost savings compared with EMR and PHIS data, while EMR and PHIS data were comparable in ma
128 ngs reveal a previously unrecognized role of pHi dynamics for the differentiation of two distinct typ
131 f the high infectivity but short duration of PHI, even short-term behavior change can significantly r
133 The conductance versus axial magnetic flux Phi exhibits Aharonov-Bohm oscillations with maxima occu
137 The series exhibits quantum yields of up to phi = >4%, with emission maxima ranging from 725 to 820
139 lumns form a 3D hexagonal crystalline phase, Phi(h)(k) (P6(3) symmetry), that can be obtained only fr
144 c MRI (mpMRI) and the Prostate Health Index (PHI) have shown promise in predicting a positive biopsy
145 (-/-) mice to investigate the role of AE3 in pHi homeostasis in HC neurons, co-cultured with astrocyt
146 The effects of AE3 knockout on astrocytic pHi homeostasis in MAc-related assays require the presen
147 tumors require energy and intracellular pH (pHi) homeostasis through the activity of two major monoc
148 reaction of 1(P1) with N-nosyl iminoiodane (PhI horizontal lineNNs) 4(Ns) led to the formation of a
149 ato moieties, mediates nitrene-transfer from PhI horizontal lineNR sources to a wide variety of aliph
150 ents, Rx(3)Wx(3-8)PhixGxzetax(P/A) (motif A; Phi, hydrophobic; zeta, hydrophilic), (Y/W)PhiGSxT (moti
151 on and contraction; uncompensated changes in pHi impair cardiac function and trigger arrhythmia.
152 ffects has been unclear because the starting pHi in AE3(-/-) and wild-type neurons is indistinguishab
153 In agreement with previous studies, resting pHi in cultured astrocytes was 6.82 +/- 0.06 and inhibit
154 Drosophila Na(+)-H(+) exchanger DNhe2 lowers pHi in differentiating cells, impairs pFC differentiatio
160 between complement activation and neutrophil pHi In this article, we demonstrate that in vitro exposu
161 Still, the detection of phosphohistidine (pHis) in the proteome has remained difficult due to the
163 B and -C outward currents and NBCe1-mediated pHi increases, and changes in NBCe1 activity paralleled
165 -assembly strategy to organize Mdh, Hps, and Phi into an engineered supramolecular enzyme complex usi
166 s to cells the ability to convert phosphite (Phi) into orthophosphate (Pi) offers an alternative sele
168 We find that the stationary noise strength Phi is close to its baseline limit 1 when the mRNA level
171 sophila melanogaster, we show that increased pHi is sufficient to induce dysplasia in the absence of
173 report that an increase in intracellular pH (pHi) is necessary for the efficient differentiation of D
176 ationic I(III) oxidants of the general form [PhI(L)2](2+) (L = pyridine, 4-DMAP, 4-cyanopyridine) all
178 , AE3 contributes to braking the decrease in pHi later during MAc in both neurons and astrocytes.
179 can scan in the end-fire area (60 degrees < phi < 120 degrees , 45 degrees < theta < 80 degrees ), w
180 BPMA-PAAm gels in a reaction-limited regime (Phi << 0.15 for all measurements), allowing us to isolat
181 ate can lead to non-classical Phi(M)-values (Phi(M) > 1) in the rate-determining loop 1 substructure,
182 ngineering and report mutational Phi-values (Phi(M)) as indicators for folding transition-state struc
183 n the native-state can lead to non-classical Phi(M)-values (Phi(M) > 1) in the rate-determining loop
186 f amphiphile required to form microemulsion (Phi(ME)), which was the analytical signal of the method.
189 Viridans group streptococcal detection using PHIS microbiology data had high sensitivity (92.3%) and
193 ent iodine reagents of the general structure PhI[N(SO2R)(SO2R')]2 promote the selective direct C-H-am
194 ned model to evaluate the correction factor (Phi) needed for chamber SOA mass yields due to losses of
195 We measure an average nitrite quantum yield (Phi(NO2(-))) of (1.1 +/- 0.2)% (313 nm, 50 muM nitrate,
196 ike several Epac-specific antibodies tested, Phi-O-Me-cAMP exhibited dramatically reduced signals in
200 -methyladenosine-3',5'-cyclic monophosphate (Phi-O-Me-cAMP) in mice lacking either one or both isofor
202 urylamines or thiophen-2-ylmethanamines with PhI(OAc)2 in the presence of the Pd(OAc)2 catalyst, succ
208 and excellent correlation was found between Phi of 5a-g and sigmap(-) of the substituent on the phen
211 ce of fluopyram at the pre-harvest interval (PHI) of 7-21 d was between 0.0108 and 0.1603 mg/kg, and
214 ibodies (mAbs) that specifically recognize 1-pHis or 3-pHis; they do not cross-react with phosphotyro
216 ze phosphorylation of nitrogens at the N1 (1-pHis) or N3 (3-pHis) positions of the imidazole ring, we
217 )2 (0-5 mol %) catalyzed hypervalent iodine [PhI(OTf)2] mediated oxidative coupling of 4-anilinoquina
219 Samples from 14 healthy donors (HDs), 40 PHI patients, 17 Chronics, and 13 Elite controllers (ECs
220 c strategy based on mechanistic insight into pHis peptide gas-phase fragmentation during LC-MS/MS.
221 ins, combining selective immunoenrichment of pHis peptides and a bioinformatic strategy based on mech
222 n illustration of this strategy, we analyzed pHis peptides from glycerol-fed and mannitol-fed Escheri
223 c effect on net base uptake and steady-state pHi persisted only in vascular smooth muscle cells but n
224 al results, researchers have proposed that a phi (Phi)-clamp composed of phenylalanine (Phe)427 resid
225 able from that of a perfect electric mirror (phi = pi) to that of a perfect magnetic mirror (phi = 0)
226 ion of nitrogens at the N1 (1-pHis) or N3 (3-pHis) positions of the imidazole ring, we detect for the
227 mpared to an implementation using Intel Xeon Phi processor with off-chip memory (with hypothetical on
229 eport the first global proteomic analysis of pHis proteins, combining selective immunoenrichment of p
230 This study lays the groundwork for future pHis proteomics studies in bacteria and other organisms.
231 ation of the activation segment, measured by phi, psi, chi1, and pseudo-dihedral angles more accurate
232 opyranosyloxy)-3',4'-didehydro-1',2'-dihydro-phi,psi-caroten -2'-ol, is novel and has been given the
233 r MAc removal in neurons and astrocytes, and pHi recovery from an ammonium prepulse-induced acid load
234 neurons and astrocytes, and speeds neuronal pHi recovery from an ammonium prepulse-induced acid load
235 eases the acidification rate constant during pHi recovery from intracellular alkaline loads imposed b
237 s HCO3(-) efflux) enhances intracellular pH (pHi ) recovery (decrease) from alkali loads in neurons a
239 genotypic influence on SLC4A7 expression and pHi regulation in vascular smooth muscle cells provides
240 degree upon V-ATPase for HCO3(-)-independent pHi regulation than do cultured astrocytes, with importa
242 astrocytes, contributes to intracellular pH (pHi ) regulation by facilitating the exchange of extrace
243 astrocytes, contributes to intracellular pH (pHi ) regulation by facilitating the exchange of extrace
244 sms of HCO3(-)-independent intracellular pH (pHi) regulation were examined in fibrous astrocytes with
245 two potential sorting motifs, YXXPhi (where Phi represents a bulky hydrophobic amino acid) and LL, t
246 and 0.90 (95% CI, 0.87-0.92) for %p2PSA and Phi respectively, and the specificity was low, only 0.09
248 ly after removal of plasma IgA from 12-month PHI samples: the magnitude of ADCC not only increased af
253 he molecular mechanism for intracellular pH (pHi) sensitivity of Orai1/STIM1 is not fully understood.
254 ase (Hps) and 6-phospho-3-hexuloseisomerase (Phi) serves as the key driving force to pull the pathway
255 ABAergic currents (EGABA) and NH4(+)-induced pHi shifts enabled an estimate of the range of chloride
256 ation mimics were created and NH4(+)-induced pHi shifts were used in cultured hippocampal neurons to
257 nsiderably in magnitude (from -0.02 to -1.00 pHi shifts) depending on the combination of alanine muta
258 known and a number of previously speculative pHis sites inferred by homology, predominantly in the ph
259 eadily integrate data collected in the 'fine phi-slicing' mode (in which the rotation angle per image
260 emains largely unexplored due to the lack of pHis-specific antibodies and the lability of the phospho
262 ould be broadly useful for identification of pHis substrates and functional study of pHis using a var
263 minishes the response to acidic and alkaline pHi, suggesting that H155 is responsible for pHi sensiti
265 free PSA (%p2PSA) and prostate health index (Phi) tests for PCa and to evaluate their ability in disc
266 it is crucial to understand the begin-state phi (the "self") - a state that is shaped by early socia
267 likewise exhibited a significantly increased pHi These data suggest a novel role for the anaphylatoxi
268 Abs) that specifically recognize 1-pHis or 3-pHis; they do not cross-react with phosphotyrosine or th
269 pared with the control (pHi 7.3), acidifying pHi to 6.3 or alkalinizing pHi to 8.3 and 8.8 caused sma
270 7.3), acidifying pHi to 6.3 or alkalinizing pHi to 8.3 and 8.8 caused small reductions in the open-t
273 n of pHis substrates and functional study of pHis using a variety of immunological, proteomic, and bi
274 e functional effects of these residues using phi value analysis revealed a steep negative slope.
275 g of a hydrolysis-deficient mutant and apply Phi value analysis to compare timing of opening-associat
276 core include hydrogen-deuterium exchange and Phi-value analysis and can be expensive and time consumi
277 lding pathway of this protein we carry out a Phi-value analysis and use the resulting structural info
278 kinetics of a panel of mutants prepared for Phi-value analysis has now revealed a bimolecular reacti
283 degradation rates, the pre-harvest interval (PHI) values and the half-life values of the three pestic
284 th protein engineering and report mutational Phi-values (Phi(M)) as indicators for folding transition
286 ctivity, acid loading from a highly alkaline pHi was rate-limited by HCO3(-) supply from spontaneous
287 ing highly infectious primary HIV infection (PHI), we developed a stochastic individual-based model t
288 ity is highly dependent on intracellular pH (pHi), we propose a direct mechanistic link between compl
290 Both permeability and intracellular pH (pHi) were found to be significantly improved for 14 comp
292 rt limitations, we employed Weisz's modulus (Phi), which compares observed enzyme-catalyzed reaction
294 h, which can be unambiguously aligned to the phi X 174 reference genome, and demonstrate proof-of-con
295 ermore, we show nanopore sequencing reads of phi X 174 up to 4,500 bases in length, which can be unam
296 f DNA from two viruses (Human adenovirus 41, Phi X 174) and the bacterium Enterococcus faecalis, whic
297 t of detection (LOD) determined for HAdV 41, Phi X 174, and E. faecalis was 35 GU/muL, 1 GU/muL, and
300 uman immunodeficiency virus (HIV) infection (PHI) yields a larger decrease in cell-associated HIV-DNA
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