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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
14 riodic oscillations, anti-correlated between Phi = 0 and Phi0/2.
15  = pi) to that of a perfect magnetic mirror (phi = 0).
16  The sole isolated interlocked photoproduct (Phi = 0.06) is a [2]rotaxane, with the dimerized anthrac
17 ity and adaptive functioning groups was low (phi = 0.13, P < .05).
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
20 g with visual sensations (chi-square, 34.22; Phi = 0.45; df, 1; P < 0.001).
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
25 2730 m(2) einstein(-1)), and quantum yields (Phi) (0.03-0.95 mol einstein(-1)).
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
30                                          The Phi(2)GFP10 reporter phage showed high sensitivity for d
31 developed a more powerful mycobacteriophage (Phi(2)GFP10) with a fluorescent reporter.
32                    Sputum was incubated with Phi(2)GFP10, in the presence and absence of RIF, and bac
33 The model we used is a square lattice with a phi(4) potential between next-nearest-neighbour sites, w
34 errupt open bursts, was greatly increased at pHi 5.8 and 6.3.
35 D all abolished the prolongation of taucf at pHi 6.3.
36              When compared with the control (pHi 7.3), acidifying pHi to 6.3 or alkalinizing pHi to 8
37 een pCO2 (a function of tumor perfusion) and pHi (a potent modulator of cancer cell physiology).
38 onstrated clinically relevant utility of the PHI across threshold probabilities of 5-30%.
39 : 1) complex 2, originating from the initial PhI activation with 3, is roughly as reactive toward PhI
40                              In summary, the PHI adds predictive performance to image-guided detectio
41 ast to the trends in the metal work function Phi(Ag)<Phi(Au).
42                   In mpMRI negative men, the PHI again improved prediction of significant cancers; AU
43                                    Increased pHi also occurs with mESC differentiation and, when prev
44                                              Phi and %p2PSA have a high diagnostic accuracy rates and
45                                              Phi and %p2PSA may be useful as tumor markers in predica
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
50 ied by the MCT1 inhibitor decreasing further pHi and glycolysis.
51 IKSper in human sperm is activated weakly by pHi and more strongly by Ca(2+).
52  four deep learning architectures to predict phi and psi angles of protein backbone.
53             The mean absolute error (MAE) of phi and psi angles predicted by DRNN, DReRBM, DRBM and D
54 lomycin had only a small effect upon resting pHi and recovery following an acid load.
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
58 ccurred in a large fraction of patients with PHI and were associated with substantial morbidity.
59 31-45 to 15-23 events; a shorter duration of PHI and/or a lower testing frequency reduces the number
60 s to screen, select, and characterize anti-1-pHis and anti-3-pHis mAbs.
61 is a powerful regulator of intracellular pH (pHi) and extracellular pH (pHo), and contributes to solu
62 ll-interfering RNA lowered intracellular pH (pHi) and induced apoptosis.
63 n one season by individuals of the same age (phi) and lifetime variance in reproductive success of in
64 at three constant pH levels: the initial pH (pHi) and pH 6.5 and 5.5.
65  during (acute/early) primary HIV infection (PHI) and up to one year post-infection (p.i).
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
68                                   The MAE of phi angle is comparable to the existing methods, but the
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
74        Parallel measurements of [Cl(-)]i and pHi at the single-cell level in the mouse cortex showed
75 he trends in the metal work function Phi(Ag)<Phi(Au).
76 toxin C5a as a master switch of the delicate pHi balance in neutrophils resulting in profound inflamm
77          Additional data types included into PHI-base 4 are the direct targets of pathogen effector p
78  (PHI-base) is available at www.phi-base.org PHI-base contains expertly curated molecular and biologi
79                        Genes with associated PHI-base data can be easily identified across all plant
80 o associated with pathogenicity based on the PHI-base database.
81                             Future plans for PHI-base include development of tools facilitating commu
82                                              PHI-base phenotypes were mapped via their associated gen
83 encountered and the future directions of the PHI-base project are briefly discussed.
84                   Here we describe a revised PHI-base Version 4 data platform with improved search, f
85                           The new release of PHI-base Version 4.2 (October 2016) has an increased dat
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
89 irectly curate their own published data into PHI-base.
90 ions database (PHI-base) is available at www.phi-base.org PHI-base contains expertly curated molecula
91        The contents of short B-chains of the phi, beta-LDs of amylopectins from the outer pericarp we
92 e higher (by approximately 3%) than those of phi, beta-LDs of the core amylopectins.
93 r unit chains of both amylopectins and their phi, beta-limit dextrins (LDs) than those of the outer p
94                                              PHIS billing data had higher sensitivity (> 50% for nine
95 view of Pediatric Health Information System (PHIS) billing and microbiology data were compared with c
96 al role of Slc26a6 in regulation of not only pHi, but also cardiac excitability.
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
101 the two-electrode voltage-clamp technique or pHi changes using Vm/pH-sensitive microelectrodes.
102 ffect on tauo , taucf and their responses to pHi changes.
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
106 iability was moderate (G-coefficient = 0.67, Phi-coefficient = 0.52).
107 ar HCO3(-) concentrations and elevated brain pHi compared to control fish, providing evidence of CO2
108  with DeltaG() approximately 24 kcal/mol for PhI (computed DeltaG() = 21.9 kcal/mol).
109 ns LC-MS/MS spectra for potential matches to pHis-containing peptides based on their neutral loss pat
110 orkflow for the identification of endogenous pHis-containing proteins in cellular lysates.
111 ation, leading to putative identification of pHis-containing proteins.
112 ivation reactions involve PPh3 dissociation, PhI coordination to Ru through I, rearrangement to a eta
113                                              PHI could change according to the application time, beca
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
116                              With 3 years of PHIS data on 48887 children, an asthma template was cons
117 mpared with EMR and PHIS data, while EMR and PHIS data were comparable in magnitude of savings.
118 estimated cost savings compared with EMR and PHIS data, while EMR and PHIS data were comparable in ma
119 ata, $1184336 for EMR data, and $2117522 for PHIS data.
120                      Costs obtained from the PHIS database also showed reduction with CPG-directed ca
121 g data and pre-existing cost data within the PHIS database provided similar results.
122  the Pediatric Hospital Information Systems (PHIS) database, all normalized to patient census.
123 o the Pediatric Hospital Information System (PHIS) database.
124 tial acidification, but limits the extent of pHi decrease in neurons and astrocytes.
125                       Calculation of psi and phi dihedral angles from the chemical shift assignments
126                The reaction of 3 with excess PhI displays striking kinetics which initially appears z
127 n in the 3 months after infection depends on PHI duration and testing frequency.
128 ngs reveal a previously unrecognized role of pHi dynamics for the differentiation of two distinct typ
129                            Intracellular pH (pHi) dynamics is increasingly recognized as an important
130                ADCC was documented in 80% of PHI enrollment samples and in 100% of PHI 12-month, chro
131 f the high infectivity but short duration of PHI, even short-term behavior change can significantly r
132 e critical roles of Slc26a6 in regulation of pHi, excitability, and contractility.
133   The conductance versus axial magnetic flux Phi exhibits Aharonov-Bohm oscillations with maxima occu
134       However, the significance of increased pHi for cancer in vivo remains unresolved.
135         The estimated pre-harvest intervals (PHI) for fipronil and difenoconazole were 15 and 19.5day
136 ow pass filtering would "buffer" cancer cell pHi from non-steady-state extracellular pCO2.
137  The series exhibits quantum yields of up to phi = &gt;4%, with emission maxima ranging from 725 to 820
138                                      Using a PHI&gt;/=35, only 1/21 significant cancers was missed and 3
139 lumns form a 3D hexagonal crystalline phase, Phi(h)(k) (P6(3) symmetry), that can be obtained only fr
140                            The highest order Phi(h)(k) consists of enantiopure single-handed columns
141  and a columnar hexagonal 2D liquid crystal, Phi(h).
142                                   Thus, ptxD/Phi has proven to be a very efficient, positive selectio
143 uman immunodeficiency virus (HIV) infection (PHI) have not been published.
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
155                         In contrast, resting pHi in RON astrocytes was 7.10 +/- 0.04, significantly l
156  encoded biosensor we also confirm increased pHi in situ.
157 fusion, giving rise to an electric potential Phi in the 100 muV range on the micrometer scale.
158         We included patients enrolled during PHI in the Agence Nationale de Recherche sur le Sida PRI
159 tively enrolled 290 patients with documented PHI in the Zurich Primary HIV Infection Study.
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
162                                 We show that pHi increases with differentiation from FSCs to prefolli
163 B and -C outward currents and NBCe1-mediated pHi increases, and changes in NBCe1 activity paralleled
164 n to Ru through I, rearrangement to a eta(2)-PhI intermediate, and Ph-I oxidative addition.
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
167                                              pHi is a critical regulator of other membrane and contra
168   We find that the stationary noise strength Phi is close to its baseline limit 1 when the mRNA level
169                                Additionally, pHi is elevated in Slc26a6(-/)(-) cardiomyocytes with sl
170                           Notably, increased pHi is now acknowledged as a conserved characteristic of
171 sophila melanogaster, we show that increased pHi is sufficient to induce dysplasia in the absence of
172                            Intracellular pH (pHi) is critical to cardiac excitation and contraction;
173 report that an increase in intracellular pH (pHi) is necessary for the efficient differentiation of D
174                   Histidine phosphorylation (pHis) is well studied in bacteria; however, its role in
175 ross-react with phosphotyrosine or the other pHis isomer.
176 ationic I(III) oxidants of the general form [PhI(L)2](2+) (L = pyridine, 4-DMAP, 4-cyanopyridine) all
177                                           If PHI lasts for 3 months and testing is performed monthly,
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 &lt; 120 degrees , 45 degrees < theta < 80 degrees ), w
180 BPMA-PAAm gels in a reaction-limited regime (Phi &lt;< 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
184 ect, and characterize anti-1-pHis and anti-3-pHis mAbs.
185                                              PHI manifested with typical ARS in 202 (70%) and with at
186 f amphiphile required to form microemulsion (Phi(ME)), which was the analytical signal of the method.
187                         A simple taxonomy of Phi-measures is presented where they are each characteri
188                           When requiring the Phi-measures to satisfy a minimum of attractive properti
189 Viridans group streptococcal detection using PHIS microbiology data had high sensitivity (92.3%) and
190              The high sensitivity and PPV of PHIS microbiology data suggest that using external data
191                    Using regular and reverse-phi motion in a rapid adaptation paradigm, we investigat
192                     At a threshold of >/=35, PHI + mpMRI demonstrated a NPV of 0.97 for excluding sig
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
197                                              Phi-O-Me-cAMP is a weak partial agonist for purified Epa
198                                              Phi-O-Me-cAMP readily entered intact myocytes, but did n
199                              Fluorescence of Phi-O-Me-cAMP was enhanced by binding to Epac.
200 -methyladenosine-3',5'-cyclic monophosphate (Phi-O-Me-cAMP) in mice lacking either one or both isofor
201                         Reaction of 1-X with PhI(O2CCF3)2 facilitates I(-)/CF3CO2(-) ligand exchange
202 urylamines or thiophen-2-ylmethanamines with PhI(OAc)2 in the presence of the Pd(OAc)2 catalyst, succ
203                 A N,N-ligand (1,10-Phen) and PhI(OAc)2 were identified as crucial factors to promote
204       Here, we use the common combination of PhI(OAc)2 with BF3.Et2O as a model to fully explore this
205 tructed from 2-(arylamino)benzamides through PhI(OAc)2-mediated oxidative C-N bond formation.
206 has been developed from ethynylcarbinols and PhI(OAc)2.
207 in self-assembled structures was found using PhI(OCOR)2.
208  and excellent correlation was found between Phi of 5a-g and sigmap(-) of the substituent on the phen
209               In experimental murine sepsis, pHi of blood neutrophils was analogously alkalinized, wh
210                                           No PHI of imidacloprid is required, while for oxamyl it was
211 ce of fluopyram at the pre-harvest interval (PHI) of 7-21 d was between 0.0108 and 0.1603 mg/kg, and
212 formation of peroxynitrite, corresponding to Phi(ONOO(-)) < 0.26%.
213              With moderate depletion of P at pHi or pH 6.5, CaP minerals became more prominent in the
214 ibodies (mAbs) that specifically recognize 1-pHis or 3-pHis; they do not cross-react with phosphotyro
215 hosphorylated, forming 1-phosphohistidine (1-pHis) or 3-phosphohistidine (3-pHis).
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
218 1 complex in an inhibited state known as the phi-particle.
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
228                      In contrast, increasing pHi promotes excess pFC cell differentiation toward a po
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
236                Using ammonia pulse recovery, pHi recovery in RON astrocyte was achieved largely via V
237 s HCO3(-) efflux) enhances intracellular pH (pHi ) recovery (decrease) from alkali loads in neurons a
238 ellular enzyme in HCO3- transport, and hence pHi regulation in the heart.
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
241 eral ion transporters participate in cardiac pHi regulation.
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
247  and 0.17 (95% CI, 0.14-0.19) for %p2PSA and Phi, respectively.
248 ly after removal of plasma IgA from 12-month PHI samples: the magnitude of ADCC not only increased af
249                                              PHI scores were measured in men undergoing re-biopsy wit
250  to a membrane, whereas the poorly conserved phi segments play no role in binding or protection.
251                               Under the ptxD/Phi selection, an average of 3.43 transgenic events per
252 pHi, suggesting that H155 is responsible for pHi sensitivity of Orai1/STIM1.
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
261                                           If Phi stays well above 1, then the gene is infrequently ac
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
264 selection efficiency of 97% under the ptxD/Phi system.
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
271                         In this study adding PHI to mpMRI improved overall and significant cancer pre
272 nflux, nor for maintaining intracellular pH (pHi) uniformity.
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
279                                  Then, using Phi-value analysis we show that the structural differenc
280                                        Every phi-value was less than 0.4, indicating the transition s
281                  Furthermore, the calculated PHI values, according to the maximum residue levels set
282 of human CFTR at different intracellular pH (pHi ) values.
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
285                                          The PHI was assessed for ability to add value to mpMRI in pr
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
289   Okra samples harvested after the estimated PHIs were found safe for human consumption.
290      Both permeability and intracellular pH (pHi) were found to be significantly improved for 14 comp
291  were studied and the pre-harvest intervals (PHIs) were calculated.
292 rt limitations, we employed Weisz's modulus (Phi), which compares observed enzyme-catalyzed reaction
293 red sequences derived from the bacteriophage phi X 174 genome.
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
298 ic tail of each cargo, with Wls using tandem Phi-X-[L/M] motifs and beta2AR using a PDZ motif.
299                   We identified a common D-Q-Phi-X0,1-G-K-N-zeta-E motif in CsgC client proteins that
300 uman immunodeficiency virus (HIV) infection (PHI) yields a larger decrease in cell-associated HIV-DNA

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