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1                                              H. jecorina Cel7A, cellobiohydrolase I, from glycoside h
2                                              H. naledi casts the fossil and archaeological records in
3 e characterized by both one-dimensional ((1) H, (13) C, (31) P) and two-dimensional (COSY, NOESY, DOS
4                                           (1)H chemical shifts up to 11.8 ppm revealed that certain c
5                                           (1)H HR-MAS NMR metabolite profiling was achieved from a sm
6                                           (1)H HR-MAS NMR spectroscopy was used to track the metaboli
7                                           (1)H NMR analysis and computational investigation of the al
8  combination of MS, isotope labeling, and (1)H and (13)C NMR techniques, we established that the majo
9 o measure these interactions through both (1)H nuclear Overhauser enhancement (NOE) and paramagnetic
10 ChB host systems, we also demonstrate, by (1)H NMR and DFT calculations, that the chalcogen atoms ori
11 s, we carried out metabolomic analysis by (1)H NMR spectroscopy of media from astrocyte-spinal neuron
12 nt amide fragments are detected either by (1)H or (13)C NMR.
13 MR setup showing one- and two-dimensional (1)H, (13)C and heteronuclear NMR experiments under continu
14 a 1.5-T hospital scanner has an effective (1)H polarization level of just 0.0005% this strategy shoul
15 ctions are validated against experimental (1)H NMR data, demonstrating that model-driven engineering
16 e delta1 methyl groups, which facilitated (1)H/(13)C methyl TROSY NMR measurements with opposing liga
17 PCR (A2AR) that are deuterated apart from (1)H/(13)C NMR probes at isoleucine delta1 methyl groups, w
18 the compounds were confirmed by MS, FTIR &(1)H NMR; and their properties were characterized by Temper
19 gate whether changes of (13)C/(12)C, (2)H/(1)H, and (15)N/(14)N ratios of NDMA give rise to isotope f
20 at low temperature and features a hydride (1)H NMR signal (in solution 35.61 ppm; in the solid state
21                                    HR-MAS (1)H NMR and neutron scattering experiments reveal that thi
22                              By measuring (1)H-(15)N dipolar-coupling as well as (15)N R1 and R1rho r
23         This work highlights the power of (1)H photo-CIDNP for characterizing, at the atomic level, t
24 ltidimensional single- and double-quantum (1)H solid-state NMR spectroscopy with density functional t
25 on of UV-vis absorption, resonance Raman, (1)H NMR, EPR, and X-ray absorption (near-edge) spectroscop
26  FAMEs was achieved based on the recorded (1)H NMR spectra.
27        Proton Nuclear Magnetic Resonance ((1)H NMR) was employed to study monovarietal commercial Spa
28 3,4-tetrahydroqui noline is reported, the (1)H and (13)C NMR data of which are in excellent agreement
29  chemical marker has been identified, the (1)H NMR chemometrics approach may contribute in the choice
30 e used to measure with high precision the (1)H(alpha)-(13)C(alpha) dipolar tensor and carboxylate che
31 m of conduction has been determined using (1)H and (7)Li solid-state nuclear magnetic resonance spect
32                                     Using (1)H Nuclear Magnetic Resonance spectroscopy (NMR) and Gas
33 PFC) of awake rats as measured by ex vivo (1)H-[(13)C]-nuclear magnetic resonance spectroscopy.
34                       Using a multi-voxel (1)H MRS approach at 3 Tesla with high spatial resolution a
35 andard addition of water is combined with (1)H magic angle spinning (MAS) NMR detection, absolute qua
36 erning formation of aggregates (1604cm(-1)), H-bonded parallel- and antiparallel-beta-sheets (1690cm(
37 3 orders of magnitude longer than that for 1-H, which decays via 1,5-HAT (tau1/2 = 48 s, DeltaH(doubl
38  (6) obtained from 4,4',5,5'-tetranitro-2H,2'H-3,3'-bipyrazole (4) by N-amination and N-azo coupling
39 ents, we measured hydrogen isotope (delta(2) H) values of metabolically inert feathers and metabolica
40 lasma lumican FSR were measured based on (2) H labeling using tandem mass spectrometry.
41                                           (2)H uptake in helix 1 was suppressed in the Ni(II)- and Co
42                    Furthermore, (31)P and (2)H solid-state NMR spectra show that liquid crystalline 1
43 vestigate whether changes of (13)C/(12)C, (2)H/(1)H, and (15)N/(14)N ratios of NDMA give rise to isot
44 r thousand to +0.54 per thousand for delta(2)H, delta(13)C, and delta(37)Cl values, respectively.
45 onbulk(H)/epsilonbulk(C), where Deltadelta(2)H and Deltadelta(13)C are changes in isotope ratios duri
46 H isotope approach (LambdaC-H = Deltadelta(2)H/Deltadelta(13)C approximately epsilonbulk(H)/epsilonbu
47 nation it is shown that ions arising from (2)H-labeled tracers are completely differentiated from tho
48 tial scanning calorimetry, and sequential (2)H and (31)P solid-state nuclear magnetic resonance spect
49 were investigated by variable-temperature (2)H solid-state NMR spectroscopy to reveal the reorientati
50                                   We used (2)H/(13)C metabolic flux analysis to quantify intermediary
51 or intramolecular cross-coupling of C(sp(2))-H and N-H bonds using N-iodosuccinimide (NIS) has been d
52 rtho-specific nitration of aromatic C(sp(2))-H bonds using chelation-assisted removable vicinal diami
53 re of the C-H bond being activated (C(sp(2))-H or C(sp(3))-H), the nature of the process involved (in
54 ted by means of oral gavage with 200 stage 3 H polygyrus larvae.
55 , hyperglycaemia significantly enhanced [(3) H]ryanodine binding and Ca(2+) /calmodulin-dependent pro
56 t dioxazolone amidating agents via C(sp(3) )-H bond activation to generate the desired amidated produ
57  for determining T cell responses (i.e., [(3)H]thymidine incorporation and the use of cell proliferat
58             Furthermore, sodium enhanced [(3)H]rauwolscine's interactions with the BiOctR, but not at
59 decrease (30%) in IC50 for inhibition of [(3)H]DA uptake by cocaine in WT hDAT.
60 he 9-aminoacridines increase the rate of [(3)H]prazosin dissociation from the alpha1A- and alpha1B-ad
61         To demonstrate the robustness of [(3)H]RO6957022 binding, affinity studies were carried out f
62 ile not inhibiting DNA biosynthesis using (3)H-radiolabeled precursors in macromolecular synthesis in
63 en to be effective for accelerating C(sp(3))-H activation directed by weakly coordinating auxiliaries
64 es the advancements in Pd-catalyzed C(sp(3))-H activation via various redox manifolds, including Pd(0
65 port a silver-free Pd(II)-catalyzed C(sp(3))-H arylation of saturated bicyclic and tricyclic amine sc
66  to 48-70 h led to successive gamma-C(sp(3))-H arylation/intramolecular amidation and the constructio
67 n/intramolecular amidation of gamma-C(sp(3))-H bonds.
68 bond being activated (C(sp(2))-H or C(sp(3))-H), the nature of the process involved (intramolecular w
69 clic ring-closing of Z-hexatriene, the [1,5]-H shift in Z-pentadiene, and the Cope rearrangement.
70 y)-6,7-dihydropyrimido[2,1-c][1,4]oxazin-4(9 H)-one (PF-06462894, 8), possessed favorable properties
71 omplex 2, while 3 itself is able to abstract H-atoms from weaker X-H bonds such as TEMPO-H to re-form
72 els to examine host determinants that affect H. pylori BabA expression.
73 3 knockdown abolished the protection against H/R-induced myocytes injury by AS-1.
74  Three-dimensional structures for almost all H. jecorina cellulose-degrading enzymes are available, e
75 pe in mice expressing the MHC class I allele H-2D(b).
76 the formation of intramolecular phenol-amide H-bonds as a function of solvent composition.
77 (2) AChRs respond strongly to ACh because an H-bond positions the QA to interact optimally with the r
78 ted fucosylation mechanism facilitated by an H-bonded network, which is corroborated by mutagenesis e
79                   This variable domain of an H chain-only Ab (VHH or nanobody) significantly inhibite
80 nd antiparallel-beta-sheets (1690cm(-1)) and H-bonded beta-turns (1664cm(-1)).
81  with DOM molecules of above-average O/C and H/C ratios.
82  with the plasma membrane anion channels and H(+)-ATPase and with the tonoplast TPK K(+) channel.
83 scriptionally active microbial community and H. pylori gene expression were determined using metatran
84 orometry were used to characterize Na(+) and H(+) transport, charge translocation, and thermal stabil
85     Validation of probe targets and "G" and "H" site specificity was carried out using a series of co
86   Here the authors show that in ants such as H. saltator, the 9-exon subfamily of odorant receptors (
87 magnitude of the magnetostriction anomaly at H*.
88 ) mass spectrometry (MS) reports on backbone H-bond fluctuations.
89 the cell surface in association with the BCR H chain.
90                            For example, beta-H elimination of (Phebox)Ir(OAc)(n-octyl) (2-Oc) proceed
91 SH binding "G site" and a substrate binding "H site".
92            Cellular removal was evaluated by H&E, DAPI and DNA quantification.
93  XB hemispheres, geometrically rigidified by H-bonding to eight MeOH molecules and encapsulation of t
94                   Elemental compositions (C, H, N, O, S), Py-GC/FID, Py-GC/MS and SEM imaging reveal
95                           The behavior of C, H, and S in the solid Earth depends on their oxidation s
96 er fashion through photochemically induced C,H insertion reactions and consists of a protective layer
97                                            C-H bonds are ubiquitous structural units of organic molec
98 onstruct triaryl(heteroaryl)methanes via a C-H functionalization in good to excellent yield, and repr
99 ve been engineered to catalyze abiological C-H bond amination reactions, but the yields of these reac
100 explain the unique features of the aerobic C-H imidoylation of N-methoxybenzamides and have important
101 mplications for other Pd-catalyzed aerobic C-H oxidation reactions.
102 ted hydrocarbons and unactivated aliphatic C-H bonds via a metal-hydride pathway.
103 trategies known to enable remote aliphatic C-H oxidations.
104  a Pd(II)-catalysed enantioselective alpha-C-H coupling of a wide range of amines, which include ethy
105 ionships between the functional groups and C-H bonds of a substrate has been exploited to achieve met
106 ropargylamines, such as A(3) couplings and C-H functionalization of alkynes, have been described and
107 itrobenzoate where the halogen bonding and C-H...O hydrogen bonding are well-matched.
108 heory indicate that differential pi-pi and C-H...pi interactions within a scaffold organized by multi
109 in reactivity toward tertiary and benzylic C-H bonds are observed.
110                         The enzymatic beta-C-H hydroxylation of the feedstock chemical isobutyric aci
111  flow protocol has been developed for bond C-H activation which promotes the alpha-cyanation of secon
112 ected activation of carbon-hydrogen bonds (C-H) is important in the development of synthetically usef
113                                       Both C-H activation and transmetalation influence the reaction
114 es H2 under mild conditions, and catalyses C-H hydride abstraction plus H2 generation from a model su
115 and development for rhodium(III)-catalyzed C-H activation reactions has largely been limited to cyclo
116             The mechanisms of Ni-catalyzed C-H arylation, alkylation, and sulfenylation with N,N-bide
117 itionally, many transition-metal-catalyzed C-H bond additions to polarized pi bonds occur within casc
118 luding enantioselectivity) in Pd-catalyzed C-H functionalization reactions.
119 ighly Lewis acidic borane with concomitant C-H or C-C bond formation.
120  to palladium and accelerates non-directed C-H functionalization with arene as the limiting reagent.
121 echols, employing an oxyacetamide-directed C-H hydroxylation on phenols.
122                           The dual-element C-H isotope approach (LambdaC-H = Deltadelta(2)H/Deltadelt
123                            While the first C-H functionalization could involve Ru-N covalent bond, th
124                   The chemoselectivity for C-H bond amination is greater than 20:1 in all cases.
125  among the mildest conditions reported for C-H cleavage at a Ni center.
126 erein, we discovered a mild and metal-free C-H sulfenylation/intramolecular rearrangement cascade rea
127 three catalytic cycles to achieve hydridic C-H bond abstraction (enabled by polarity matching), alkyl
128 fects as tools to implement selectivity in C-H oxidation reactions are briefly discussed.
129                                The initial C-H bond activation remains as the sole kinetically releva
130 provide a "bottom-up" fundamental insight, C-H bond cleavage in methane over Ni-based catalysts was i
131 )methane at 20 K reveals an intermolecular C-H...H-C distance of only 1.566(5) A, which is the shorte
132 ty for insertion of the nitrene units into C-H bonds over reduction of the azides to the sulfonamides
133 e catalyze enantioselective intramolecular C-H bond amination reactions of sulfonyl azides.
134 pic studies establish that Pd(II)-mediated C-H activation is the turnover-limiting step.
135         Notably, neither H2 activation nor C-H hydride abstraction was observed in the analogous comp
136 classes of enantioselective silylations of C-H bonds have been reported recently, but little mechanis
137  low chemoselectivity for the amination of C-H bonds over competing reduction of the azide substrate
138 -type species (O(MeAN)-LA) able to oxidize C-H and O-H bonds.
139 adical approaches, such as a facile remote C-H HAT step, with that of transition-metal-catalyzed chem
140 uld involve Ru-N covalent bond, the second C-H functionalization most likely involves Ru-O coordinate
141 s been exploited to achieve meta-selective C-H activation by using a covalently attached, U-shaped te
142 sed catalysis proceeds through five steps: C-H bond activation; C-C coupling via a concerted 1,2-aryl
143 olecular), and the context (stoichiometric C-H activation or within a variety of catalytic processes)
144             Recently, it was reported that C-H bonds in aromatic heterocycles were converted to C-Si
145 xperimental and theoretical studies of the C-H amination reaction mediated by the iron dipyrrinato co
146                From the SFG spectra in the C-H and O-H regions, we found that the surface layers of A
147 hen surveyed in terms of the nature of the C-H bond being activated (C(sp(2))-H or C(sp(3))-H), the n
148 vage step is not rate-determining, but the C-H bond cleavage and C-Si bond-forming steps together inf
149 f I2 and TBHP as the green oxidant via the C-H bond cleavage of the benzylic carbon under mild reacti
150 Kinetic isotope effects indicated that the C-H bond cleavage step is not rate-determining, but the C-
151  Cp*RhCl to accelerate the cleavage of the C-H bond of N-pentafluorophenylbenzamides, providing a new
152 zontal lineO oriented perpendicular to the C-H bond of substrate) was found to lead to the S = 2 five
153 e reactivity of compound I with respect to C-H bond activation.
154 he direct functionalization of unactivated C-H bonds is ushering in a paradigm shift in the field of
155 aphthylamines with azoles is developed via C-H functionalization and C-N bond formation.
156 mI2(H2O)n should be able to form very weak C-H bonds.
157 rosthesis type II implanted by 2 surgeons (C.H.D. and J.C.).
158 eaction with fluorobenzene afforded the CAr -H bond activation product [1-F-2-IMe -C6 H4 ](+) I(-) (3
159                 In addition to the catalytic H-cluster, CpI contains four accessory iron-sulfur [FeS]
160 a an E1 mechanism with the cleavage of Cbeta-H bond being rate determining.
161 d CF2H groups and the important roles of CF2-H...O hydrogen bonds in influencing intermolecular inter
162              ClC-4 is an intracellular Cl(-)/H(+) exchanger that is highly expressed in the brain and
163 he chemosensitive response to changes in CO2/H+ than previously thought.
164  and 2-pyridone react with nitride complex [(H-PNP)RuN](+) (H-PNP = HN(CH2CH2P(t)Bu2)2) to generate o
165 odes of the diatomic ligands for conceivable H-cluster structures.
166 r34 maintains solvent exclusion and the core H-bond network in the active site by relocating to repla
167 etrahydropyran moiety of (+)-cryptoconcatone H were assembled through catalytic asymmetric methodolog
168 sorption of water via the electron-deficient H atom and the subsequent dissociation of the electron-r
169 lial cells with wild-type and VacA-deficient H. pylori strains, treatment of cells with purified VacA
170 ) of the hydroalane adducts as well as DIBAL-H in its aggregation states support this experimental fi
171 rings, and weakly to Cho because a different H-bond tethers the ligand to misalign the QA and form we
172 sy specimens from individuals with different H. pylori infection statuses and premalignant tissue cha
173 n of Homo sapiens from a group called either H. heidelbergensis or H. rhodesiensis.
174 ycoproteins using sequential endoglycosidase H and peptide:N-glycosidase-F digestions.
175 )H/Deltadelta(13)C approximately epsilonbulk(H)/epsilonbulk(C), where Deltadelta(2)H and Deltadelta(1
176 unprecedented intermolecular aliphatic C-F...H-C interaction was observed in the X-ray crystal struct
177 tic variants in inhibitory complement factor H (CFH) are also features of both ARMD and TMA, we hypot
178       Rare variants in the complement factor H (CFH) gene and their association with age-related macu
179 bind the complement regulator protein factor H.
180 he nitrite reductase gene (aniA), the factor H-binding protein gene (fHbp), and the capsule biosynthe
181 gma-bond metathesis mechanism in which an Fe-H intermediate is postulated to be a key reactive specie
182  bulk CeO2, and identifies surface features, H(+) binding sites, Ce(3+) locations, and O vacancies on
183  LSSE), magnetocrystalline anisotropy field (H K) and surface perpendicular magnetic anisotropy field
184 ace perpendicular magnetic anisotropy field (H KS) in the same Pt/YIG system.
185                               Correction for H-D exchange is required for accurate assessment of biol
186         We report spectroscopic evidence for H-tunneling in the gas phase at temperatures around 320-
187 ed human remains are the oldest reported for H. sapiens.
188 rs), 614 had tumor tissue samples scored for H&E sTILs and 427 for CD8 biomarker assessments.
189                        The pi-trajectory for H atom abstraction (Fe(IV) horizontal lineO oriented per
190 CITES enforcement for distinguishing it from H. indicus.
191  more subtypes, including subtypes A1, F, G, H, J, and K and unclassified fragments, including one su
192           In addition, the presence of Globo H, SSEA-3 and SSEA-4 in some HCC tissues and their absen
193 hane at 20 K reveals an intermolecular C-H...H-C distance of only 1.566(5) A, which is the shortest r
194 ommon mtDNA package comprised of haplogroups H/H5, U5a, A, D/D4, and F1/F2.
195 es, sulfenic acids), which tend to have high H-bond acidities.
196 n the molecular composition of NOM to higher H/C and lower O/C ratios.
197 sequent dissociation of the electron-rich HO-H bond via H transfer to N on the nickel surface, benefi
198                                     However, H doping is a challenge to WO3, the relevant mechanisms
199  unveil two novel mitochondrial effectors in H. pylori-host interaction with links on gastric pathoge
200 s of IL-17 family cytokines was performed in H. pylori-infected and uninfected gastric biopsy specime
201 olar solvent for formation of intramolecular H-bonds.
202 ng catalyst [kappa(5) -((15c5) NCOP(iPr) )Ir(H)](+) exhibiting modest activity.
203  described to do this at an adequate rate is H(+)-coupled lactate efflux on monocarboxylate transport
204 ontact (SC) ion-selective electrodes (ISEs) (H(+), K(+), and Na(+)) have outstanding performance char
205      A systematic structure search in the La-H and Y-H systems under pressure reveals some hydrogen-r
206 e dual-element C-H isotope approach (LambdaC-H = Deltadelta(2)H/Deltadelta(13)C approximately epsilon
207 ation) resulted in clearly different LambdaC-H values: 28 +/- 4 (oxidation), 0.7 +/- 0.1 and 0.9 +/-
208 ls (56%) are produced in diverse landscapes (H>1.5).
209 tra- and intermolecular C horizontal lineO...H-N and C horizontal lineO...H2O hydrogen bonds, elucida
210        HPLC chromatograms of the expected [M-H](-) ion and UV absorption revealed the presence of fiv
211 recognize known major antigenic sites in MeV-H, we identified a D4 genotype variant that escapes neut
212 lorectal cancer locally assessed as dMMR/MSI-H from 31 sites (academic centres and hospitals) in eigh
213 ontrol in pre-treated patients with dMMR/MSI-H metastatic colorectal cancer, and could be a new treat
214 less crowded Sn(II) hydride [Ar((i)Pr4)Sn(mu-H)]2 (Ar((i)Pr4) = C6H3-2,6(C6H3-2,6-(i)Pr2)2) (1b) reac
215 molecular cross-coupling of C(sp(2))-H and N-H bonds using N-iodosuccinimide (NIS) has been demonstra
216 harge centralized on the pyridyl nitrogen, N-H(+).
217 re, we demonstrate the use of bench-stable N-H and N-alkyl oxaziridines derived from readily availabl
218                Significantly, the weakened N-H bonds in ((iPr)PDI)Mo(NH3)2(eta(2)-C2H4) enabled hydro
219 females had greater phosphorylation of Na(+)/H(+) exchanger isoform 3 (NHE3), distribution of NHE3 at
220 ily and a model system for all related Na(+)/H(+) exchangers, including eukaryotic representatives.
221 coli is the best studied member of the Na(+)/H(+) exchanger family and a model system for all related
222                 In human melanoma, the Na(+)/H(+) exchanger NHE1 is an important modifier of the tumo
223 ression of CtBP, or transfection with an NAD(H) insensitive CtBP, and are replicated by a synthetic p
224 ecies (O(MeAN)-LA) able to oxidize C-H and O-H bonds.
225        From the SFG spectra in the C-H and O-H regions, we found that the surface layers of Avicel ar
226 es approaching the surface, activating the O-H bonds and inducing deprotonation.
227              This species reacts with weak O-H bonds in TEMPO-H and 4-dimethylaminophenol ((NMe2)PhOH
228 nteraction on the water nanodroplet (SO2)O...H(H2O) may incur effects on the SO2 chemistry in atmosph
229                                 The observed H-shift rate coefficients are sufficiently fast that, as
230                            Rok, an analog of H-NS from gamma-proteobacteria that affects chromosome a
231                          Higher densities of H. influenzae were observed in both microbiologically co
232                        However, detection of H. pylori infection at any point up to age 6.5 years was
233 d direct method for the in situ detection of H. pylori remains a challenge, mainly due to the strong
234 ogic assays confirmed a protective effect of H. pylori.
235 , the least characterized mobile elements of H. pylori.
236                                  A ladder of H-bond donating residues creates a 'polar track' demarki
237 demonstrated a clear birth-cohort pattern of H. pylori infection in the Japanese population.
238 s of CD8(+) T cells revealed the presence of H-2L(d)/AH1-specific T cells and an expansion of sequenc
239                  The decreased prevalence of H. pylori infection in successive generations should be
240 *CHO formation produced via an ER process of H* with nonadsorbed CO (a unique result).
241                 The calculated trajectory of H indicates that proton has a good mobility in MC, oxyge
242  a group called either H. heidelbergensis or H. rhodesiensis.
243                               However, NAD(P)H FLIM has not been established as a metabolic proxy in
244                  Here we discover that NAD(P)H oxidase 4 (NOX4), an enzyme known to catalyse the oxid
245  a peptide that blocks the activity of NAD(P)H oxidase.
246 yme known to catalyse the oxidation of NAD(P)H, is upregulated when p16 is inactivated by looking at
247 nd electron and ADP-ribosyl transfers (NAD(P)H/NAD(P)(+)) to drive metabolic transformations in and a
248  of steric selection and the presence of a P-H...pi interaction between the ligand and a conserved ar
249 is optimally done by interrogation of paired H chain V region (VH) and L chain V region (VL) sequence
250  elongation growth and play a key role in PM H(+)-ATPase activation by inhibiting PP2C.D family prote
251 -catalyzed proton transfer shows a prominent H/D kinetic isotope effect, which is determined to be 8.
252  reviewed for demographics, Hanifin & Rajka (H&R) and United Kingdom Working Party (UKWP) criteria.
253       Oncogenic KRas, HRas, and NRas (K-Ras, H-Ras, and N-Ras) differentially populate distinct cance
254 lves O-O homolysis, where the phenol remains H-bonding to the peroxo OCu in the transition state (TS)
255                               Here we report H c2 data for epitaxial thin films extracted from the el
256  that the absence of Topoisomerase and RNase H activity in Escherichia coli or Saccharomyces cerevisi
257 on ligation, bind together to the Prp8 RNase H-like domain.
258 most similar to the RuvC family of the RNase H-like endonucleases.
259              Subsequent treatment with RNase H releases RNA-templated ligation products into solution
260 ysis of R-loops in vivo, we develop an RNase-H-based approach; this reveals predominant R-loop format
261  react with nitride complex [(H-PNP)RuN](+) (H-PNP = HN(CH2CH2P(t)Bu2)2) to generate octahedral ammin
262  selection in the same class as Fay and Wu's H and discuss its interpretation and power.
263 w that values of Tajima's D and Fay and Wu's H depend in a direct way on a peculiar measure of tree b
264 e anisotropic mechanical behavior of C-(A-)S-H.
265 ange on the mechanical properties of C-(A-)S-H.
266 ne frameworks, using the building blocks [S=(H)P(mu-NR)]2 .
267                                   Segregated H is used as a means to emphasize differences in the sel
268 loped to catalytic O-transfer from N2O to Si-H bonds.
269 rophobic burial include shorter and stronger H-bonds, and increased entropy in the folded state.
270 l analysis of a prototypical Vbeta8.1(+) TCR-H-2D(b)-GAP5040-48 ternary complex revealed that germlin
271  H-atoms from weaker X-H bonds such as TEMPO-H to re-form 2.
272  species reacts with weak O-H bonds in TEMPO-H and 4-dimethylaminophenol ((NMe2)PhOH), the latter yie
273 and infection of a mouse model, we show that H. pylori deregulates mitochondria by two novel mechanis
274                                          The H. rubrisubalbicans rice interactions were further chara
275         The mutant R411A(alpha) disrupts the H-bonding environment and conformation of Y731, ostensib
276 occurrence of 691.8, 29.9% and 30.8% met the H&R and UKWP criteria, respectively.
277  were significantly higher than those of the H group (P <0.001).
278 2FeH) site for different redox states of the H-cluster.
279 31 in R411A-alpha2 is dynamic, reforming the H-bond between Y731 and Y730 to allow RT to propagate to
280  was examined by using RNA-seq to search the H. pylori transcriptome for RNAs whose 5'-phosphorylatio
281 h the redox state, hence suggesting that the H channel could play a more general role as a dielectric
282 he V LSSE peak at 75 K is attributed to the H KS and M S (saturation magnetization) whose peaks also
283 e additional accessory [FeS] clusters to the H-cluster is thermodynamically favorable.
284  the transition state (TS) and transfers the H(+) after the barrier.
285 been confirmed independently by dating three H. naledi teeth with combined U-series and electron spin
286 ethylome of Arabidopsis roots in response to H. schachtii infection.
287 ent evidence that susceptibility of trees to H. fraxineus is associated with their iridoid glycoside
288 tudied in view of its ability to form triply H-bonded complexes with a suitably complementary 2,6-dia
289 tains, at the same time, no less than twenty H-atoms available for either alpha- or beta-hydride elim
290 turally similar to more potent vacuolar-type H(+)-ATPase inhibitors, which all inhibited LGR5 interna
291 ls (ICs) express the proton pumping vacuolar H(+)-ATPase (V-ATPase) and are extensively involved in a
292                                 The vacuolar H(+) ATPase (V-ATPase) is a complex multisubunit machine
293 r cation channel SlTPC1 and the two vacuolar H(+)-pumps, SlAVP1 and SlVHA-A1, which in turn are revea
294 sociation of the electron-rich HO-H bond via H transfer to N on the nickel surface, beneficial to the
295                         3 is also formed via H-atom abstraction from the corresponding mu-1,1-hydrope
296                                      Whereas H-Ras(G12V) elicited papillomas and hematopoietic tumors
297 onsist of an atomic hydrogen sublattice with H-H distances of about 1.1 A, which are close to predict
298  We identified a centrin-binding site within H. sapiens Prp40 homolog A (HsPrp40A), which contains a
299 lf is able to abstract H-atoms from weaker X-H bonds such as TEMPO-H to re-form 2.
300 ystematic structure search in the La-H and Y-H systems under pressure reveals some hydrogen-rich stru

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