戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (left1)

通し番号をクリックするとPubMedの該当ページを表示します
1                                              N-Acylphosphatidylethanolamine phospholipase D (NAPE-PLD
2                                              N-AS then acetylates serine 565 (S565) of COX2, and the
3                                              N-protein condenses with specific RNA genomic elements u
4  CTX-OCT-Alg had a negligible release in 0.1 N HCl, while the CTX-OCT was completely released after 3
5 n the water column ranged between 0 and 1287 N m(-3) and in the sediment from 239 to 13 331 N kg(-1).
6 only (1) H-(15) N dipolar couplings and (15) N chemical shifts have been routinely assessed in orient
7              However, so far only (1) H-(15) N dipolar couplings and (15) N chemical shifts have been
8 ave been routinely assessed in oriented (15) N-labeled samples.
9                                          (15)N-(29)Si coupling constants and (29)Si chemical shifts s
10  side chain fast time-scale dynamics and (15)N backbone fast time-scale dynamics are fully consistent
11 e flux of other labeled tracers (such as (15)N-tracers) in any metabolite detectable by LC-MS/MS and
12 nambiguously assigned using (1)H, (13)C, (15)N, (29)Si, and (1)H DOSY NMR as well as X-ray diffractio
13 e high variability in bulk collagen delta(15)N values observed among cave bears in Romania reflects n
14                 By comparison, mean delta(15)N values were similar across decades for all five specie
15 le isotope analyses (delta(13)C and delta(15)N) indicated that the elephants were not from deep rainf
16                        Using solid-state (15)N NMR spectroscopy, the cis/trans isomerization in a two
17                                 Only the (15)N chemical shift of A280 (the first residue of SP1) chan
18 ted muOR bound to the morphine and D-Ala(2), N-MePhe(4), Gly-ol]-enkephalin (DAMGO) nonbiased agonist
19 and enrolled patients between 2006 and 2016 (N = 1,302).
20 ed a remarkable sensitivity of 2.9 x 10(-24) N m Hz(-1/2) at millikelvin temperatures in a dilution r
21 t-principle calculations based on typical 2D N-doped carbon/RuMo nanoalloys heterostructures demonstr
22 te material by coupling DMASnBr(3) to g-C(3) N(4) , taking advantage from the combination of their op
23                                    The Li(3) N-LiF layer coating on Li(3) PS(4) SSE achieves a record
24                                    The Li(3) N-LiF/Li(3) PS(4) SSE enables LiCoO(2) cathodes to achie
25              Graphitic carbon nitride (g-C(3)N(4)) is a robust organic semiconductor photocatalyst wi
26           The tris- and tetra-adducts of M(3)N@I(h)-C(80) metallofullerenes were synthesized and char
27 95% CI -0.45 to -0.16], P < 0.001, I = 44.3, N = 1398).
28 m(-3) and in the sediment from 239 to 13 331 N kg(-1).
29 mated cranial impact forces to be up to 3400 N during ramming, and prior finite element modeling stud
30 but inhibited by increased drought (-30.4%), N deposition (-31.0%), and combinations of available mul
31       The exopolysaccharide poly-beta-(1->6)-N-acetylglucosamine (PNAG) is a major structural determi
32 to no treatment was 1.17 (95% CI, 0.83-1.64; N = 736).
33  those who screened positive for PTSD (7.9%, N = 42), all had co-morbid depression and/or anxiety.
34 ct conformers at cryogenic temperatures in a N(2) matrix, and subsequent narrow-band near-infrared (N
35 ot elongation is associated with aboveground N content and that overexpression of DWF1 significantly
36 replicated in African Americans from ACCORD (N = 585, P = 0.02) and in external cohorts (ACCORD-BP, O
37 es l-fucose, d-mannose, N-acetylglucosamine, N-acetylgalactosamine, and galactose).
38  for the activation of 4-methylbutyric acid (N-debenzoyl-N-(2-methylbutyryl)taxol side chain), TmAAE1
39 xhibited rapid bactericidal activity against N. gonorrhoeae.
40 ition using an equivalent mixture of 4-amino-N,N,N-trimethylanilinium and 4-aminobenzenesulfonate.
41 te differential expression of aminopeptidase N and other midgut genes in an insect host, diamondback
42 ition in the dynamic self-organization among N individuals within a social system.
43   We show here that the strongly amphipathic N-terminal helix of CPn0678 mediates binding to phosphol
44                                           An N-heterocyclic-carbene-ligated 3-benzoborepin with a bri
45                                           An N-Lip C-Lip fusion of mouse lipin-2 is catalytically act
46 d has switched its coordination mode from an N(2) S(2) (4-) cavity holding a single metal, to a binuc
47 y and functionally modular, consisting of an N-terminal effector domain (NTD) and a C-terminal regula
48                             Here, we show an N. gonorrhoeae diagnostic workflow for analysis of metag
49 benzo[3,4]cycloundec-3-ene-1,5-diyne with an N-heterocyclic carbene borane.
50 ST2 by 4% (95% CI: 1% to 7%; p = 0.002), and N-terminal propeptide of collagen III by 3% (95% CI: 0%
51   The warming-induced rise in soil CH(4) and N(2) O emissions (1.84 Pg CO(2) -equivalent/year) could
52 ositive and negative signs for net CH(4) and N(2) O flux.
53 microsites that produce or consume CH(4) and N(2) O, such that a range of microsites occurs with both
54  were then easily converted into N-alkyl and N-acyl analogues (RX, NaHCO(3)/DMF/100 degrees C) in hig
55 nnect between high-density wetland areas and N hotspots.
56 e close linkage between soil microbial C and N cycling.
57 e associated with decoupling of litter C and N cycling.
58 n (up to 20 transgenes) for increasing C and N flows with the purpose of increasing tomato fruit yiel
59 ble condensation between CBT derivatives and N-terminal cysteine residues has been established as a b
60 yielded spectra with more aliphatic-like and N-containing compounds than toluene-doping.
61                           In contrast, T and N status biomarkers differed between amnestic and non-am
62 c valve replacement, with (N=8098) TAVR and (N=14 778) SAVR referrals.
63 rate that antibodies from patients with anti-N-methyl-d-aspartate receptor (NMDAR) encephalitis alter
64                                    Arylamine N-acetyltransferase 1 (NAT1) is a phase II xenobiotic-me
65 t, one nontarget pollutant was identified as N-methylpyrrolidone.
66 the composition of the five CD16a asparagine(N)-linked carbohydrates (glycans) impacts affinity.
67  truncation of the putatively autoregulatory N terminus of TMEM165.
68          A borinic acid functionalized 1,4-B,N-anthracene 1 was found to display unprecedented reacti
69 access, near-UV-emitting linearly extended B,N-doped heptacene with high thermal stability is designe
70 r selective formation of bromo-substituted B,N,B-benzo[4]helicenes 2 a/2 b via intramolecular borylat
71  in two independent brain collections (BA10, N = 81 and 64).
72  of effect in the second brain tissue (BA25, N = 60) from the same individuals and in two independent
73 arkably mild conditions (25 degrees C, 1 bar N(2)O), together with high turnover numbers (TON, up to
74               However, the interplay between N and P availability with other critical resources on se
75 nase is the enzyme that catalyzes biological N(2) reduction to NH(3).
76 tum >11 mm) and elevated cardiac biomarkers (N-terminal pro-B-type natriuretic peptide [>40 pg/mL] or
77  This is the first research reporting boiled N. nouchali rhizome as an ideal food material to manage
78 that the formation of stable multiply bonded N(2) is usually thermodynamically preferable.
79 Global metabolic changes were driven by both N speciation and diel cycling.
80 localized in a punctate distribution in both N. benthamiana and maize (Zea mays) protoplasts.
81 CP without the necessity of additional bulky N(6)-substituents.
82 irogenic phosphinite moiety was performed by N -> O phosphinyl migration of aminophosphines borane by
83 tion with increasing N/C and is regulated by N/C.
84 a translation factor directly upregulated by N-MYC, is itself a strong predictor of poor clinical out
85 posed faster via the isomer (C(6)H(4), O)(C, N, Ph) formed by P-stereomutation involving a M(B2) perm
86 atomically embedded into an in situ formed C-N network, yielding a stable compound insensitive to O(2
87 functionalization with the construction of C-N, C-S, and C-C bonds under mild conditions.
88 echanism allows access to both traditional C-N adducts at room temperature as well as a large range o
89  chemical oxygen demand (COD) to nitrogen (C/N) ratios.
90 trains postnatally exposed to the carcinogen N-ethyl-N-nitrosourea developed PTMCs, which closely res
91 olds have been enantio- and chemoselectively N-oxidized using an aspartic acid containing peptide cat
92                           The PrOMIS cohort (N = 3308) was recruited from prenatal care clinics at th
93 o truncations and mutations in the conserved N terminus of the Rubisco large subunit.
94 sease-mutations cluster within the conserved N-Lip and C-Lip regions that are separated by 500-residu
95 athway alpha-diversity between CTX-T and CTX-N infants.
96 ose with callous-unemotional traits (DBD+CU, N=198) and without callous-unemotional traits (DBD only,
97 puts and outputs to demonstrate that current N removal by US wetlands (about 860 +/- 160 kilotonnes o
98 undergo a new rearrangement to cyanopyridine N-imide 40 with an activation energy of 43 kcal/mol.
99 he enzyme was highly active with l-cysteine, N-acetyl-l-cysteine, and allyl mercaptan.
100 f CBFbeta counteracted the interference of D/N Vif mutants with A3G degradation by wild-type Vif.
101 ur results provide proof of principle that D/N Vif variants could have therapeutic potential.
102 eloping youths (N=693) and youths with DBDs (N=995), subdivided into those with callous-unemotional t
103 irmed to be the Vi monomer both de-O- and de-N-acetylated by mono- and bidimensional Nuclear Magnetic
104  DspB has increased catalytic activity on de-N-acetylated PNAG oligosaccharides, but the molecular ba
105 ivation of 4-methylbutyric acid (N-debenzoyl-N-(2-methylbutyryl)taxol side chain), TmAAE15 as a highl
106                                           dG(N(1)-H)(*) were formed as a result of the indirect and d
107   Individuals with a primary PTSD diagnosis (N = 66) participated in a randomized clinical trial of p
108 d lack information about the receptor distal N-termini, despite the importance of the latter in signa
109                    Upon IL-6 treatment, Endo-N and Endo-T cells displayed altered expression of the D
110                                   The enzyme N-myristoyltransferase (NMT) is an essential protein, wh
111 ostnatally exposed to the carcinogen N-ethyl-N-nitrosourea developed PTMCs, which closely resembled t
112                      As in other eukaryotes, N (6)-methylation of adenosine is the most abundant and
113 ocycle prevents the formation of a linear Fe-N(2)-Fe unit and leads to orbital interactions that are
114 angstrom X-ray crystal structure of the FigC N-citrylornithine decarboxylase reveals how the larger s
115 eved using rhodium(II) carbenes derived from N-sulfonyltriazoles and aryldiazoacetates as carbene pre
116                                       Fungal N:P varied comparatively less due to simultaneous reduct
117 WV G(N) is different from other bunyavirus G(N) proteins, they all share similar domain connectivity
118         Although the structure of the TSWV G(N) is different from other bunyavirus G(N) proteins, the
119          These findings highlight that CoV G-N-7 MTase may be a novel target for rational design of l
120  the expression of the tumor suppressor gene N-myc downstream-regulated gene 1 (NDRG1) in MCPyV gene-
121 ylated proteins when compared to the general N-glycoproteome.
122 ding activity of EBV gH/gL and the EBV gH/gL-N(69)L/S(71)V mutant.
123 emperatures have a profound impact on global N cycling processes with implications of a positive feed
124 , confirming the generality of the Ni(II) -&gt; N(IV) protocol, either in the presence of bipyridine, or
125 atous visual field loss was "detected" if &gt;= N(theta) clusters had deteriorated with p < p(Cluster),
126 ge number of self-reported Native Hawaiians (N = 3693) a functionally important, Polynesian-specific
127 zer of MEILB2 by binding to an alpha-helical N-terminus of MEILB2 and preventing MEILB2 self-associat
128 a TNF and KYN/TRP yielded subgroups of high (N = 17) and low (N = 55) TNF-KYN/TRP groups.
129 quinone analogue 2-heptyl-4-hydroxyquinoline-N-oxide inhibited C. thermarum NDH-2 activity, and its p
130 week with high-frequency MST (i.e., 100 Hz) (N = 24), medium frequency MST (i.e., 60 or 50 Hz) (N = 2
131 ), medium frequency MST (i.e., 60 or 50 Hz) (N = 26), or low-frequency MST (i.e., 25 Hz MST) (N = 36)
132 mprised exclusively of single-atom Fe(1)(II)-N(4) sites via in-temperature X-ray absorption spectrosc
133       Alternatively, local heating MoS(2) in N(2) produces n-character.
134 that in addition to antigenicity, changes in N-linked glycosylation sites can alter other properties
135 or a significant number of genes involved in N signalling and metabolism.
136 l types of inactivation processes, including N-, C-, and U-types.
137  precipitation, increased drought, increased N deposition, and their combinations).
138 with nitrogen fertilizer exhibited increased N(2)O production, by 74 times in mineral soil and 2 time
139 eclines in tight association with increasing N/C and is regulated by N/C.
140 ng an effective population size of infection N(e) for influenza infection.
141 ine oxalates were then easily converted into N-alkyl and N-acyl analogues (RX, NaHCO(3)/DMF/100 degre
142 eterostructures demonstrate that introducing N and Mo atoms into C and Ru lattices, respectively, tri
143 derivatives olefinated through the isolated (N, O)(Ph, C(6)H(4), C) oxaphosphetanes (Channel A), wher
144 e, which was alleviated upon deletion of its N terminus.
145 e among innate immune sensors because of its N-terminal Zalpha1 and Zalpha2 domains, which bind to nu
146                           Ahnak, through its N-terminal region, scaffolds the L-type pore-forming alp
147 or NEMO in the activation of oncogenic c-Jun N-terminal kinase (JNK) signaling, induced by the latent
148 d by the stress- and immune-responsive c-Jun N-terminal kinase (JNK).
149 expression of TNFalpha and activation of JUN N-terminal kinase (JNK).
150 ary T4, right colon), biological features (K/N-RAS status), and response to chemotherapy (Response Ev
151 vels of application (0, 168, 336, and 672 kg N/ha) were used and replicated three times.
152 ltopyranoside (DDM), and lauryldimethylamine N-oxide (LDAO).
153 performance of an ensemble of QDCs of length N (N-QDCs) to assess the robustness of QDCs as a practic
154                   Moreover, we show that low N-induced root elongation is associated with aboveground
155 tural variation of root elongation under low N.
156  yielded subgroups of high (N = 17) and low (N = 55) TNF-KYN/TRP groups.
157 , which is fundamentally essential to make M-N-C catalysts viable in PEMFC technologies.
158  to the monosaccharides l-fucose, d-mannose, N-acetylglucosamine, N-acetylgalactosamine, and galactos
159 gallium carbenoid Ga(Nacnac) (Nacnac=HC[C(Me)N(2,6-i-Pr(2) C(6) H(3) )](2) ).
160 senting saturated, less oxygenated, and more N-containing compounds than ESI.
161 26), or low-frequency MST (i.e., 25 Hz MST) (N = 36) using 100% stimulator output.
162 s due to simultaneous reductions in mycelial N and P contents.
163 formance of an ensemble of QDCs of length N (N-QDCs) to assess the robustness of QDCs as a practical
164 n using an equivalent mixture of 4-amino-N,N,N-trimethylanilinium and 4-aminobenzenesulfonate.
165 amyloid (A), tau (T), and neurodegeneration (N) status as required by recent biomarker classification
166                                           Ni,N-doped carbon catalysts have shown promising catalytic
167 (2)O production and maintain greater nitrate-N levels in flooded soil.
168 se gases nitrous oxide (N(2)O) and nitrogen (N(2)) in arable soils include high nitrate, moisture and
169 ically limiting nutrients, such as nitrogen (N) and phosphorus (P), which can reduce grassland divers
170          Human release of reactive nitrogen (N) to the environment has increased 10-fold since 1860 a
171 here are an essential link in soil nitrogen (N) cycling and plant N supply.
172 odies targeting spike (S) and nucleoprotein (N).
173 se of complete genome and the nucleoprotein (N) gene.
174                              PC occurrences (N = 36,360) were classified into one or more subtypes: e
175 itu formation and photoinduced activation of N-chloroamines to give aminium radicals that enable effi
176                   Conformational analyses of N-acyl isochalcogenouronium species and comparison with
177 n enzyme responsible for the biosynthesis of N-acylethanolamines (NAEs), a family of bioactive lipid
178 tudies have reported the characterization of N-glycans in rodent brains, but there is a lack of spati
179             We report a novel conjugation of N-terminal cysteines (NCys) that proceeds with fast kine
180        Cross-dehydrogenative C-O coupling of N-hydroxyimides with ketones, esters, and carboxylic aci
181 able to study the spatiotemporal dynamics of N(2) production due to denitrification in riparian groun
182                       Whether the effects of N fertilization vary with bioenergy crop species also re
183 -(diazomethylene)pyridine and elimination of N(2) with a barrier of ca. 26 kcal/mol.
184 data and 5-kilometre grid-scale estimates of N inputs and outputs to demonstrate that current N remov
185 e reduction to Cu(I), under the formation of N(2).
186                         Furthermore, loss of N-WASP reduces the diffusivity of CD19, a stimulatory co
187 he degree to which variation in magnitude of N balance across irrigated maize fields in the US Corn B
188  fertilizer use efficiency and mitigation of N(2) O emissions.
189 s limited by the inert and gaseous nature of N(2).
190 sion preferentially blocked proliferation of N-Myc overexpressing cells, when glutamine levels were r
191 ing (ChIP-seq) was used to assess a range of N-terminal posttranscriptional modifications (marks) to
192 sed on 852 observations from 158 studies) of N fixation across three types of ecosystems with differe
193 toplasmic and nuclear protein by transfer of N-acetylglucosamine (O-GlcNAc) to serine and threonine h
194 orks operating in the glandular trichomes of N. tabacum are of pivotal significance to be undertaken.
195 sults provide a mechanistic understanding of N(2)O production in eukaryotic phototrophs and represent
196 ane depolarization blocks cellular uptake of N-acylethanolamides-lipoprotein-borne Hh pathway inhibit
197 of functional groups, providing a variety of N-H pyrroles in good yields and with high regioselectivi
198 l we sequentially enrolled 1.5-45 year-olds (N=148) into four age-descending groups, randomized 2:1 t
199 ithout callous-unemotional traits (DBD only, N=276).
200  namely Regional Corn (Regional) and Optimum N rate (Optimum N).
201  Corn (Regional) and Optimum N rate (Optimum N).
202 nificantly improves plant growth and overall N accumulation.
203 roduction of greenhouse gases nitrous oxide (N(2)O) and nitrogen (N(2)) in arable soils include high
204 g a diabetes centre in the UAE.Participants (N = 973) with different weight and glucose tolerance cat
205                                    Patients (N = 1817) with untreated, active choroidal neovasculariz
206  slices with nociceptin/orphanin FQ peptide (N/OFQ; 500 nM), an endogenous opioid-like peptide, norma
207                The enzyme phenylethanolamine N-methyltransferase (PNMT, EC 2.1.1.28) catalyzes the fi
208 n that the rate constants of the phthalimide-N-oxyl radicals' self-decay with different electron-with
209 r than that of the unsubstituted phthalimide-N-oxyl radical in most cases.
210  link in soil nitrogen (N) cycling and plant N supply.
211                                         Poly-N-acetyl-lactosamine is involved in the immune system in
212 ides a sustainable alternative for preparing N,O-biaryl compounds that are widely used as ligands and
213 rculating IL6 (interleukin-6) and NT-proBNP (N terminal pro B-type natriuretic peptide) levels were e
214 ng sulfide as an electron donor will promote N(2) O and ammonium production, which is generally not d
215 gy for the selective modification of protein N-termini with mass boosters.
216 e Ab responses to different areas on protein N and S and showed that the IgM, A, and G Ab responses a
217 tures akin to those observed in the putative N(2) complex.
218  over the nighttime O(2) consumption rate (R(N)) in mature leaves of Arabidopsis (Arabidopsis thalian
219 , but have also increased losses of reactive N to the environment.
220 tive site residues have changed to recognize N-citrylornithine.
221 m from recycled human urine; once recovered, N and P can be redirected to fertilizer production.
222 appropriate SOFs applied were able to reduce N(2)O production and maintain greater nitrate-N levels i
223 or acute inhibition of the Arp2/3 regulator, N-WASP, which is associated with enhanced signaling, inc
224 ombine the CsgG nanopore with the 35-residue N-terminal region of its extracellular interaction partn
225 e specifically, we show that acidic residues N-terminal to the substrate pTyr in EGFR and HER2 mediat
226 ide variety of transformations (acylation, S(N)Ar, silylation, solvolysis, Pd catalyzed C-S cross-cou
227  of nucleophilic substitution of hydrogen (S(N)(H)) was first applied for the direct modification of
228 onal group swap) results from a cascade of S(N)Ar reactions, which are facilitated by azidoazomethine
229 ls via nucleophilic aromatic substitution (S(N)Ar).
230 c preference of PH(2)(-) is steered to the S(N)2 reaction channel (less-destabilizing activation stra
231 electrophiles follow a hitherto unexplored S(N)2 pathway for the reaction with large transition state
232                       The signal-to-noise (S/N) for analytes improved up to 19-fold compared to direc
233  FIDs, achieving a further increase in the S/N ratio and more effective denoising also on the transie
234 10 uM with the detection limit of 0.11 uM (S/N = 3).
235                Here, testing a large sample (N = 72) using an established paradigm and a preregistere
236                                  The sample (N = 459, Mean age = 62.43, 58.40% female) was a subset o
237 r treatment of depression (discovery sample, N=30; active replication sample, N=81; sham replication
238 ery sample, N=30; active replication sample, N=81; sham replication sample, N=87).
239 ation sample, N=81; sham replication sample, N=87).
240 (n = 206) and 1 collection of blood samples (N = 1132) of MDD cases and controls, we used epigenomic
241                    Tn-antigen (Tn), a single N-acetylgalactosamine (GalNAc) monosaccharide attached t
242 his study, we identify the vesicular soluble N-ethylmaleimide-sensitive factor attachment protein rec
243 table compounds often with chemically stable N-N bonds but which are thermodynamically unstable in th
244 erein reported a series of novel substituted N-(4-amino-2-chlorophenyl)-5-chloro-2-hydroxybenzamide a
245  emotional well-being, relationship support; N = 54,673).
246 sically stable SACs on traditional supports (N-doped carbon, metal oxides, etc.) remains a formidable
247 e), together accounting for 72% of synthetic N fertilizer-induced NH(3) emissions from croplands in t
248 ere female) were classified into 8 A+/-/T+/-/N+/- categories according to the abnormal (+)/normal (-)
249 ent biomarker classification algorithms (A/T/N).
250                                  Terrestrial N fixation was stimulated by warming (+152.7%), elevated
251  domain (RBD) and those directed against the N-terminal domain (NTD), indicating that both of these r
252              Here we show that, although the N-terminal region of RNF4 bears no secondary structure,
253 alidated the interaction between hTR and the N (6)-methyladenosine (m(6)A) demethylase ALKBH5 and sho
254 cetylates serine 565 (S565) of COX2, and the N-AS-acetylated COX2 induces the production of specializ
255  O-glycopeptides modified exclusively at the N-terminus would enable O-glycoproteomic methods to rely
256 s, synthetic binding proteins, that bind the N-terminal four-helix bundle (4HB) "killer" domain and n
257 se in clusters of polar residues at both the N and C termini, and deletion of up to 11 C-terminal res
258 ered the disordered region that connects the N- and C-terminal halves in many eukaryotic ABC transpor
259           This process appears to follow the N-end rule and is mediated by ClpA/P protease and the Cl
260 residues that project into solution from the N or C-termini of peptide and protein substrates.
261 CTD and the His-Cys-His (HCH) motif from the N-terminal segment of the neighboring subunit.
262   We further explored its application in the N-glycan profile of a biotherapeutic monoclonal antibody
263 ified hemi- and heterozygous variants in the N-terminal domain of the A isoform of FHF2 (FHF2A).
264  differ only by the sequence position of the N terminus.
265 trong triple bond and the nonpolarity of the N(2) molecule pose thermodynamic and kinetic challenges
266    Here we present the first analysis of the N- and O- and glycosphingolipid-glycans from total human
267    Accordingly, deletion or depletion of the N-end rule pathway ubiquitin E3 ligases in NatB mutants
268  activities involved in the synthesis of the N-glycan of the viral major capsid protein in PBCV-1 and
269 onal CI arising from the inactivation of the N-module subunits due to attrition caused by its constan
270 he ring conformations in the vicinity of the N-O bond.
271 effects on the RNA-unwinding activity of the N-terminal cassette, with one configuration enhancing an
272                         Considering that the N-terminal half of TIMP-1 is sufficient for TIMP-1's MMP
273  structural modeling have suggested that the N-terminal myristoylation signal and the C-terminal FXXF
274 etween mixing and freezing, we find that the N-terminal portion of M13 converts from a conformational
275 he sialylation showed selectivity toward the N-glycan compared to another glycan substrate.
276 ngs of C-type lectin-like domains, where the N-terminal cysteine-rich and fibronectin domains reside
277 rin homology (PH) domains interacts with the N-terminal region comprising ARL8- and kinesin-1-binding
278                                 70% of these N-glycans were anionic, carrying either sialic acid, sul
279 dogenous compounds, including IBC, thiamine, N(1)-methylnicotinamide (1-NMN), creatinine, carnitine,
280 gradation of target mRNAs, mediated by three N-terminal Repression Domains (RDs), which are unique to
281 MS) is an important tool for high-throughput N-glycan profiling and, upon use of tandem MS, for struc
282 evised CO(2) limits and (for the first time) N(2) respiration limits for complex life.
283 o the formation of six-membered rings and to N-homoallylindoles.
284 2) administered intravaginally (10 mug/d) to N. gonorrhoeae-colonized mice were equally efficacious.
285                       The reduction of NO to N(2)O by flavodiiron nitric oxide reductases (FNORs) is
286 rates of litter decomposition in response to N deposition.
287 horts (ACCORD-BP, ORIGIN, and TRIUMPH, total N = 3059, P = 0.005).
288 her things, the production of trimethylamine N-oxide, a proinflammatory compound associated with card
289 Wu and colleagues report that trimethylamine N-oxide (TMAO), an intestinal microbiome-dependent metab
290 ts freshness status in comparison to the TVB-N and TVC method which takes many hours to complete invo
291 7 h respectively, highly correlated with TVB-N, TVC, pH and sensory evaluation analysis.
292 obular C-terminal domain and an unstructured N-terminal domain.
293 nism by which the intrinsically unstructured N-terminal translocation domain (IUTD) of the endonuclea
294  comes from the interaction of VP4C and VP4B N-termini.
295 with the broadly neutralizing antibody VRC01-N using a highly reproducible humanized mouse model.
296                  Transcripts associated with N-glycan processing were downregulated while those assoc
297 njugation of 2-cyanobenzothiazole (CBT) with N-terminal cysteines (NCys) typically gives a luciferin
298 tion of small amounts of the Ru complex with N-oxide ligands can significantly activate single-site R
299 eferrals for aortic valve replacement, with (N=8098) TAVR and (N=14 778) SAVR referrals.
300  were compared: typically developing youths (N=693) and youths with DBDs (N=995), subdivided into tho

 
Page Top