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1 but more frequent in participants who are BE-reactive.
2 ion, even when the C-H bond is intrinsically reactive.
3                                     The less reactive 2-substituted ethynylphosphonates required gold
4  orthogonal acetalization of substrates with reactive, acid-sensitive functional groups.
5 ex" of the shrinking baby lung is opposed by reactive, adaptive, and reparative processes.
6                                              Reactive alkoxy radicals are proposed as key intermediat
7 ates under Curtin-Hammett control via a more reactive alpha,alpha-bisboryl tertiary allylcopper speci
8 ring-chain isomerization to produce uniquely reactive alpha-diazoimines.
9 rreversible labeling species that are highly reactive and footprint broadly several amino acid residu
10 ses and an increase in the expression of HAf reactive and inflammatory markers.
11 that is, a subpopulation acquires a ductular reactive and proliferative phenotype, while another subp
12 ularly since catechol metabolites are likely reactive and toxic.
13            SARS-CoV-2 spike glycoprotein (S)-reactive antibodies were detectable using a flow cytomet
14 re important in elicitation of these broadly reactive antibodies.
15 le enhanced the elicitation of these broadly reactive antibodies.
16         Small reductions in calculated panel-reactive antibody (cPRA) are associated with increased k
17 99%, complement-dependent cytotoxicity panel reactive antibody [CDC PRA+], C1q+) heart transplant can
18     Four highly sensitized (calculated panel reactive antibody [cPRA] class I and/or II >99%, complem
19 obacillus casei over-expressing myosin-cross-reactive antigen (LC(+mcra)).
20 hage in stools and expression of a TMP-cross-reactive antigen by tumors correlated with long-term ben
21                                    The CO(2)-reactive ashes embodied significant amounts of CO(2) (14
22 K-STAT3 signaling pathway, as well as the A2 reactive astrocyte phenotype after ischemia.
23 europrotective and critical for induction of reactive astrocytes and their ability to produce astrocy
24  of macrophages linked to subacute infarcts, reactive astrocytes, and damaged blood vessels in multi-
25 iderosis was associated with upregulation of reactive astrocytes.
26 strate an unexpected mixed phenotype of apoB-reactive autoimmune T cells in atherosclerosis and sugge
27 his study presents a new model of peripherin-reactive B lymphocyte-dependent autoimmune neuritis.
28 nput into motor decision processes eliciting reactive behaviour.
29                      The highly strained and reactive beta-lactone products are versatile linchpins f
30  cells has accompanied the use of covalently reactive beta5i inhibitors, whose activity against the c
31 y relies on in situ generation of a uniquely reactive Bi(V) arylating agent from a bench-stable Bi(II
32 onditions, highly active catalysts or highly reactive bonding groups, as is done in classical DCC, is
33       Overall, 33% of samples with VLVL were reactive by antigen testing.
34  23 (45.1%), 24 (47.1%), and 22 (43.1%) were reactive by the Abbott IgG, Roche total antibody, and Ab
35 es, constituting a protective system against reactive carbonyl compounds in B. pseudomallei..
36                          Reactions involving reactive carbonyls, creatinine, and ammonia-producing co
37          To study the clonality of flagellin-reactive CD4 cells in Crohn patients, we used a common C
38 lowing short-term Ag exposure to identify Ag-reactive CD4 cells.
39 o the gene expression patterns of SARS-CoV-2-reactive CD4(+) T cells in distinct disease severities.
40 they evolved resistance by developing a more reactive cellular immune response.
41           Recent animal experiments detected reactive changes in (18)F-FET uptake at the rim of the r
42 ngle strain-specific clone, a single broadly reactive clone or both clones.
43                                    In the BE-reactive comparator group, 7 of 39 participants (17.9%)
44 ycobiota) represent a highly immunologically reactive component of the gut microbiota.
45 t can be generated when water interacts with reactive components of mineral surfaces such as silicate
46 greenhouse gases, odorous/toxic species, and reactive compounds can affect net climate and air qualit
47     The preparation of pure samples of these reactive compounds enables measurement of their laborato
48 isfavors desorption into gas phase under the reactive conditions.
49 re then adjuvanted by a co-administered cell reactive CpG adjuvant.
50 mation, as well as its accommodation of more-reactive diazoalkane species, vastly improve the accessi
51 successfully integrated into the trapping of reactive dicarbonyls by one-pot heterocyclization and in
52 opropargyl sulfonamides to generate a highly reactive dihydropyrrole intermediate in situ followed by
53      In cholestatic liver diseases, ductular reactive (DR) cells extend into the hepatic parenchyma a
54  nanoparticles' formation and evolution in a reactive environment and identify classical evaporation-
55         After unblinding, a Leishmania cross-reactive epitope was identified and removed from the pan
56 5 h) might lead to the exposure of new IgE - reactive epitopes.
57  of magnitude greater for PeBr, 2.0 x 10(-7) reactive events per electron, than for PhBr with a yield
58 ge mitigation, yet little is known about how reactive Fe and Al minerals affect C cycling in restored
59 nd nanoSIMS) that organic carbon is bound to reactive Fe primarily in the transition between organic
60 w-progressive feedforward process and a fast-reactive feedback-driven process.
61    We aimed to evaluate the effectiveness of reactive focal mass drug administration (rfMDA) and reac
62 e focal mass drug administration (rfMDA) and reactive focal vector control (RAVC) in the low malaria-
63                                        Those reactive for hepatitis C were further tested for HCV RNA
64 servation demonstrates the utility of highly reactive fragment ions for selective bond formation proc
65 cine peptides accurately distinguishes cross-reactive from non-cross-reactive peptides.
66 )](-) occurred in the presence of other more reactive functional groups.
67 e of their intriguing carbogenic frameworks, reactive functionalities, and emerging anticancer profil
68 obe lithography (tc-SPL) with a flow-through reactive gas cell to achieve nanoscale control of defect
69 ng and to extensive postprocessing, e.g. via reactive gas plasmas, organic solvents, and photolithogr
70 rate the potential of the 2-sulfonylpyridine reactive group with the discovery of a selective covalen
71 thesis of polysubstituted thiophenes bearing reactive groups is difficult because of high reactivity
72            2H-Azirine-2-carbonyl azides, new reactive heterocyclic building blocks, were synthesized
73 0) to the atmosphere where it is oxidized to reactive Hg(II) compounds, which efficiently deposit to
74                      We report three broadly reactive human MAbs targeting N1 NA.
75             However, the exact nature of the reactive hydrogen species and the role of electride supp
76  output displayed stronger correlations with reactive hyperemia index (r = -0.63 vs. r = -0.31; Meng
77      So far, no precise information on cross-reactive IgE-epitopes of cyclophilins is available.
78 JM17 from L. longipalpis-elicited DSG1-cross-reactive IgG4 antibodies may lead to FS in genetically p
79 l serovar, Salmonella Typhi, generates cross-reactive immune responses, which provide far greater res
80  potential to avert more HIV infections than reactive implementation after the detection of an outbre
81  as HIV viral load positive or serologically reactive in National Centers for Clinical Laboratories (
82 ping styles, while high resting HRV typifies reactive individuals.
83             Some antiviral drugs and broadly reactive influenza vaccines that target the HA protein h
84 lambda3-iodane (PhIBr(2)) is proposed as the reactive intermediate.
85 upled with EPR is broadly applicable to trap reactive intermediates at low temperature and creates a
86 mmonia synthesis showed that the coverage of reactive intermediates increased significantly when the
87 ides multiple pathways for the generation of reactive intermediates, including mixed carboxylic acid-
88 e nature of the energy landscape of a highly reactive, intrinsically disordered library peptide befor
89                                              Reactive iron phases promote stabilizing interactions be
90 ent labeling of the Cys residues using a Cys-reactive label that masks epitope residues, followed by
91 s of adult T cells but instead are a broadly reactive layer of T cells poised to quickly develop into
92                 This approach makes use of a reactive linker to form cyclic peptides on the phage sur
93 n, ranging from narrowly reactive to broadly reactive mAbs.
94                                              Reactive malaria strategies are predicated on the assump
95 and further refining the process of managing reactive metabolite issues in drug development.
96 ance was evaluated by trapping acetaminophen reactive metabolite N-acetyl-p-benzoquinoneimine (NAPQI)
97 abolic enzymes were used to make potentially reactive metabolites that can react with test protein in
98 eversed, suggesting that signals provided by reactive microglia influence how NF-kappaB impacts Mulle
99                   As an important basis for 'reactive' ML, we establish a first-principles database (
100 e precracked beam method and simulated using reactive molecular dynamics.
101                                              Reactive molecular oxygen (O(2)) plays important roles i
102 in yields, but have also increased losses of reactive N to the environment.
103 ibitory, highly reactive (supportive) or non-reactive (neutral).
104 dies demonstrated that the most potent cross-reactive neutralizing mAbs, HENV-26 and HENV-32, protect
105 olated, characterized, and humanized a cross-reactive, neutralizing anti-F mAb (h5B3.1).
106                             Human release of reactive nitrogen (N) to the environment has increased 1
107 we observe a 60% linear decrease in volatile reactive nitrogen gas flux (NO(y) = NO, NO(2) , HONO) as
108   Major host insults are reactive oxygen and reactive nitrogen species as well as cellular stress ind
109  precursors include reactive oxygen species, reactive nitrogen species, and sulfur dioxide.
110 molecules, can also lead to the formation of reactive nitrogen species.
111 ses, suggesting that the formation of highly reactive nitroso intermediates is essential for target i
112 ns showing that the lifetime of the putative reactive NO(2) dimer on the surface of pure water drople
113 in the presence of sub-neutralizing or cross-reactive non-neutralizing antiviral antibodies.
114 a previously undiscovered Serpina3n(+)C4b(+) reactive oligodendrocyte population in mice.
115  lipase (MAGL) were synthesized and the most reactive one was applied to the labeling of endogenous M
116                                 The multiple reactive oxidants produced during chlorine photolysis ef
117 phil-mediated immunity via the generation of reactive oxidation products.
118  onto well plates for live cell, fluorescent reactive oxidative species (ROS) and viability observati
119 vation is driven by a, so far, not-described reactive oxidative species (ROS)-regulated calcium influ
120                       Major host insults are reactive oxygen and reactive nitrogen species as well as
121 n plays a critical role in the generation of reactive oxygen intermediates during immunity and has be
122                               ROS are highly reactive oxygen molecules that can interact with cellula
123                   Contrary to common belief, reactive oxygen species (ROS) accumulation did not appea
124 eceptor pathway controls the distribution of reactive oxygen species (ROS) along the developmental zo
125 t sleep deprivation leads to accumulation of reactive oxygen species (ROS) and consequent oxidative s
126                  Clearance and adaptation to reactive oxygen species (ROS) are crucial for cell survi
127  consumption relative to mammals, increasing reactive oxygen species (ROS) formation.
128 nsin II (Ang II)-induced AAA by facilitating reactive oxygen species (ROS) formation.
129 d endothelium-dependent vasodilation through reactive oxygen species (ROS) formation.
130                           Here, we show that reactive oxygen species (ROS) function as signaling mole
131 dynamic therapy (CDT), resulting in enhanced reactive oxygen species (ROS) generation.
132                                   Oxygen and reactive oxygen species (ROS) have been co-opted during
133 e structure helped in the photogeneration of reactive oxygen species (ROS) in water.
134                                              Reactive oxygen species (ROS) increased in human donor l
135                                              Reactive oxygen species (ROS) inflict multiple types of
136                                Production of reactive oxygen species (ROS) is critical for successful
137                                        Since reactive oxygen species (ROS) is vitally involved in tis
138 om a PBMT-mediated increase of intracellular reactive oxygen species (ROS) levels and Src protein pho
139                 As results, cellular ATP and reactive oxygen species (ROS) levels are elevated, mTOR
140                                              Reactive oxygen species (ROS) oxidize nucleotide triphos
141          Singlet oxygen ((1)O(2)), the major reactive oxygen species (ROS) produced in chloroplasts,
142  shifting glycolytic pathways and inhibiting reactive oxygen species (ROS) production in PM-activated
143                We previously identified that reactive oxygen species (ROS) signal to SI-PCD.
144            Hydrogen peroxide (H(2)O(2)) is a reactive oxygen species (ROS) that mediates essential si
145 regulation, calcium signaling, generation of reactive oxygen species (ROS), and additional determinan
146 l role in cellular metabolism, generation of reactive oxygen species (ROS), and the initiation of apo
147 on of N-acetylcysteine (NAC), a scavenger of reactive oxygen species (ROS), diminished the morphologi
148 n attributed to the AMP sensitizing cells to reactive oxygen species (ROS), making them more suscepti
149                                              Reactive oxygen species (ROS), mitochondrial dysfunction
150 neration of NADPH oxidase 2 (NOX2)-dependent reactive oxygen species (ROS), signals we term X-ROS.
151 regions by specific demethylase(s) generates reactive oxygen species (ROS), which oxidize DNA and oth
152 these inflammatory responses is the burst of reactive oxygen species (ROS), with hydrogen peroxide (H
153  against oxidative stress while serving as a reactive oxygen species (ROS)-activated persulfide donor
154 r (EGFR), locally increases the abundance of reactive oxygen species (ROS).
155 ectly reduce the dissolved oxygen (O(2) ) to reactive oxygen species (ROS).
156 o chilling stress with accumulation of extra reactive oxygen species (ROS).
157 toxic and organelle stress, and elevation of reactive oxygen species (ROS).
158 hypothesized that an increase in calcium and reactive oxygen species activate a large conductance cha
159 ndings underscore prolific marine sources of reactive oxygen species and a complex and dynamic oxygen
160  energy as heat and limits the production of reactive oxygen species and cellular damage.
161 cts of alphaSyn that form in the presence of reactive oxygen species and cytochrome c, a proapoptotic
162 dation of the substrates, which is caused by reactive oxygen species and leads to a mixture of produc
163  and resulted in generation of mitochondrial reactive oxygen species and p38 MAPK-dependent upregulat
164               Importantly, the production of reactive oxygen species and the subsequent stress respon
165                                              Reactive oxygen species are centrally involved in the pa
166                                              Reactive oxygen species are linked to the induction of o
167 ynergistically with doxorubicin by producing reactive oxygen species but also provide catechol moieti
168 tolerance, low adiponectin levels, increased reactive oxygen species damage, and elevated GDF15 and F
169  site IQ electron leak, decreased myocardial reactive oxygen species generation and improved postcard
170 ron leak, which inhibits complex I-dependent reactive oxygen species generation by suppression of sit
171 tered mitochondrial respiratory function and reactive oxygen species generation.
172                                  LBL favored reactive oxygen species homeostasis and metabolic activi
173                                          The reactive oxygen species hydrogen peroxide and the polyun
174 n and membrane potential, and an increase of reactive oxygen species in A549 cells and fibroblasts, b
175 d aPS contributed to efficient generation of reactive oxygen species including singlet oxygen and sup
176  the inherited ability of TiO(2) to generate reactive oxygen species is used as a strategy to avoid a
177 ial, adenosine 5'-triphosphate contents, and reactive oxygen species levels in hepatoma cells (Hepa1-
178 Dual inhibition resulted in reduced cellular reactive oxygen species production compared with negativ
179 precipitates cardiomyocyte apoptosis through reactive oxygen species production in an aryl hydrocarbo
180  in neutrophil extracellular trap formation, reactive oxygen species production, and released human n
181 g on ectotherm ageing through its effects on reactive oxygen species production, oxidative damage, an
182 ivation, as well as downstream intracellular reactive oxygen species production.
183                             In addition, the reactive oxygen species scavenger glutathione (GSH) was
184  from its potential to catalyze formation of reactive oxygen species that, in addition to causing dam
185 plays an important role in the resistance to reactive oxygen species through the regulation of mangan
186                                     Further, reactive oxygen species were produced in both endoperoxi
187                                             'Reactive oxygen species' (ROS) is an umbrella term for a
188 NA can be damaged by spontaneous hydrolysis, reactive oxygen species, aberrant cellular metabolism or
189 nerative diseases, including neural fibrils, reactive oxygen species, and cofilin-actin rods, present
190 fects, decreased survival factors, increased reactive oxygen species, and excessive neuroinflammation
191  mitochondrial depolarization, generation of reactive oxygen species, and PARP cleavage.
192 lism and ATP production, such as calcium and reactive oxygen species, are also key regulators of mito
193  collagen produces radicals and subsequently reactive oxygen species, essential biological signaling
194 ate accumulation and increased production of reactive oxygen species, highlighting fumarate as an onc
195                  These OH precursors include reactive oxygen species, reactive nitrogen species, and
196  tumor cell death, associated with increased reactive oxygen species, S-adenosyl-methionine depletion
197 domain is responsible for the Fls3-sustained reactive oxygen species, suggesting involvement of multi
198 ools, thereby allowing toxic accumulation of reactive oxygen species.
199 and fusion of mitochondria and production of reactive oxygen species.
200 s, reduced aerobic respiration and increased reactive oxygen species.
201 s poor photosensitizers for (1)O(2) or other reactive oxygen species.
202 ial function trigger release of DNA damaging reactive oxygen species.
203 cle, the byproducts of which are deleterious reactive oxygen species.
204 ic reprogramming, mitochondrial dysfunction, reactive-oxygen species generation, and DNA-replicative
205 this study, we found that the 2019 dissolved reactive P (DRP) load from March-July was 29% lower than
206  that ice sheets create highly geochemically reactive particulates in subglacial environments, which
207  distinguishes cross-reactive from non-cross-reactive peptides.
208 ntiating between strain-specific and broadly reactive plasma cell production during infections.
209   Our data show that a general assignment of reactive positions for reactions of ozone with aromatic
210 as nontrivial due to challenges in assigning reactive positions in the probe compounds for the monode
211 nally circulating coronaviruses induce cross-reactive, potentially even cross-neutralizing, antibodie
212  and the potential pathogenic roles of these reactive proliferative and senescent cholangiocyte subpo
213  counts (15.8 vs 7 x 10(3) /uL, P = .019), C-reactive protein (198 vs. 107 mg/L, P = .010) and D-dime
214 compared with that of measurement of serum C-reactive protein (CRP) and fecal calprotectin.
215                Additionally, the impact of C-reactive protein (CRP) and platelet count was also analy
216 udy was to assess the sensitivity of blood C-reactive protein (CRP) and procalcitonin (PCT) measured
217 t triglycerides, interleukin-6 (IL-6), and C-reactive protein (CRP) are likely causal risk factors fo
218 tection was explored as a new approach for C-reactive protein (CRP) determination in serum and preter
219 e, reproducible and immediate detection of C-reactive protein (CRP) in the wide concentration range o
220                           Peripheral blood C-reactive protein (CRP) is a biomarker used clinically to
221 tory years (LOY) and circulating levels of C-reactive protein (CRP), counter to their hypothesis.
222 bable association with older age; elevated C-reactive protein (CRP), D-dimer, and fibrinogen levels;
223 sma ANGPTL5, and obesity, high sensitivity C-reactive protein (HsCRP) and oxidized low-density lipopr
224 or alpha (TNF-alpha), and high-sensitivity C-reactive protein (hsCRP) concentrations.
225 rising baseline levels of high-sensitivity C-reactive protein (hsCRP), and both hsCRP and IL-6 decrea
226 t serum concentrations of high-sensitivity C-reactive protein (hsCRP), z-inflammation composite score
227 seases (OR, 4.54; 95% CI, 1.36-15.10), and C-reactive protein (OR, 1.01; 95% CI, 1.01-1.02) increased
228 edictors of deterioration or death; as was C-reactive protein (OR, 2.1; 95% CI: 1.3, 3.4 per doubling
229                                     Median C-reactive protein [138 mg/L (IQR: 83-179) vs 73 mg/L (IQR
230 emic inflammation (as shown by an elevated C-reactive protein [CRP] level).
231 udged by significant decrease of fever and C-reactive protein at day 3.
232                            In some persons C-reactive protein clearly dropped only after the second l
233 ting the recent observations that IL-6 and C-reactive protein could be used as markers for COVID-19 s
234 ur (normal range, 0-30 mm per hour), and a C-reactive protein level of 203.8 mg/L (1940.9 nmol/L) (no
235 ur (normal range, 0-30 mm per hour), and a C-reactive protein level of 203.8 mg/L (1940.9 nmol/L) (no
236                 White blood cell count and C-reactive protein level were elevated, and hepatic enzyme
237 vel, 36 mg/dL; and median high-sensitivity C-reactive protein level, 2.1 mg/L), 12 633 (96.6%) comple
238 esity, an elevated d-dimer value, elevated C-reactive protein level, and a rising d-dimer value over
239                           High IL-6 level, C-reactive protein level, lactate dehydrogenase (LDH) leve
240              Last, we showed that IL-6 and C-reactive protein serum concentrations were higher in pat
241 omplexes streptavidin, concanavalin A, and C-reactive protein under charge reducing conditions.
242 le biomarkers (troponin, procalcitonin and C-Reactive Protein) in parallel in undiluted urine samples
243                            Lower levels of C-reactive protein, white blood cell count, absolute neutr
244 omarkers were HbA1c, total cholesterol and C-reactive protein.
245  effects of parental Holocaust exposure on C-reactive protein.
246 , many of these target a handful of the most reactive proteinogenic amino acids.
247                                          IgE-reactive proteins were purified from almond kernels.
248                      Their mother had poorly reactive pupils with asymptomatic cerebral arteriopathy
249 can enable Fenton-like chemistry and produce reactive radicals from hydrogen peroxide activation have
250 ree structural epitopes: two partially cross-reactive regions around alpha-helices 2 and 4 as well as
251 ferences may contribute to the broadly cross-reactive response elicited by HN13.
252 ein have been hampered by concerns for cross-reactive responses that induce antibody-dependent enhanc
253   And while depth, or the frequency of cross-reactive responses, did not correlate with viral loads i
254 posed to enable catalysis by stabilizing the reactive Rh(-I) species, which is responsible for cleavi
255 single sensor device integrated in the cross-reactive sensor matrix exhibits multimodal detection of
256             Here, a highly stretchable cross-reactive sensor matrix is demonstrated, which can detect
257 uence precisely dictated by the placement of reactive side chains during the reductive amination reac
258 e bifunctional analog, CDDO-Im, has a second reactive site (imidazolide) and can covalently bind to a
259           Interestingly, the most stable and reactive sites were those that were partially buried, pr
260 advanced oxidation processes generate highly reactive SO(4)(*-) and are promising for water treatment
261 DMPO) were tested to determine if any of the reactive species were involved in the degradation of nor
262 he chemical factors in CAP, particularly the reactive species.
263     The AlN waveguide device was prepared by reactive sputtering deposition and complementary-metal-o
264 es astrocyte counts in the MEA, alters their reactive status, and attenuates proliferation and/or inf
265 he widespread programmatic implementation of reactive strategies, little empirical evidence exists as
266  hydroperoxides (PV) and thiobarbituric acid reactive substances (TBARS).
267 ng Conjugated Dienes and Thiobarbituric acid reactive substances assays.
268 logy, which can be either inhibitory, highly reactive (supportive) or non-reactive (neutral).
269 en we accounted for the effect it had on the reactive surface area of goethite.
270                     Quantum-state control of reactive systems has enabled microscopic probes of under
271 rate PESs for relatively large molecular and reactive systems.
272                            We identified all reactive T cell epitopes in the HIV-1 proteome for each
273                                Spike-protein-reactive T cell lines generated from SARS-CoV-2-naive he
274                             All patients had reactive T cells against at least 1 of 12 analyzed viral
275 ells play a pivotal role in suppressing auto-reactive T cells and maintaining immune homeostasis.
276 ntify patient specific neoepitopes and tumor reactive T cells ex vivo.
277 ce to a model of celiac disease where gluten-reactive T cells provide help to autoreactive TG2-specif
278 gerous effect of enabling the escape of self-reactive T cells.
279 d repeated screening and panning for antigen-reactive TCRs using peptide major histocompatibility com
280 tis results in generation of oral pathobiont-reactive Th17 cells in the oral cavity.
281 the assumption that HULIS is equally or less reactive than the humic acid used in these experiments,
282                We report a proximity-enabled reactive therapeutics (PERx) approach to generate covale
283  space-time dynamics of transport times with reactive timescales of denitrification in soil indicate
284                      Participants who became reactive to 4 g of peanut 13 weeks off active OIT exhibi
285 dth of HA recognition, ranging from narrowly reactive to broadly reactive mAbs.
286 IV A(H3N2)v vaccine induced antibodies cross-reactive to cluster 2010.1 viruses in approximately one-
287 es, including the presence of autoantibodies reactive to fetal brain proteins in nearly a quarter of
288 ive, prone to photodecomposition, and poorly reactive towards sterically bulky alkene substrates.
289 rogeochemical campaigns allowed developing a reactive transport model capable of reproducing the redo
290                                  Geochemical reactive transport modelling, constrained by elemental b
291 icting and controlling the vast diversity of reactive transport processes in natural and synthetic po
292 iated by two distinct S(1) decay pathways: a reactive twisting pathway and an unreactive planar pathw
293  be inert in the absence of force but highly reactive under applied tension.
294 measures, based on profiling neoepitopes for reactive viral epitope similarity, have been proposed to
295 d fragrances are among the most abundant and reactive VOCs associated with VCP emissions.
296 harmacophores-a zinc binding group and a Cys-reactive warhead-were designed to leverage both affinity
297 t photolysis alters DOM such that it is more reactive with chlorine, which also contributes to enhanc
298 ctional groups or reagents that are mutually reactive with one another, but unreactive with biopolyme
299 o identify immunoglobulin G (IgG) antibodies reactive with Rickettsia rickettsii.
300     Here, we used direct labeling of B cells reactive with the N-acetyl-D-glucosamine (GlcNAc)-contai

 
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