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1 phosphates via sample digestion (heating and acidifying).
2 sitol-3-kinase from these organelles as they acidify.
3 lifespan, but that daughter cell vacuoles re-acidify.
4 deficient NC cells remain immature but still acidify.
5  promoted by the failure of M1 phagosomes to acidify.
6 , failure to acquire LAMP-1 and inability to acidify.
7 rm activity, whereas neurons are observed to acidify.
8 S stained intensely for the vATPase and were acidified.
9 ely open, the cytosol of sour taste cells is acidified.
10  ocean impacts narrow as the ocean warms and acidifies.
11 ctrospray ionization (ESI) of ubiquitin from acidified (0.1%) aqueous solution produces abundant ubiq
12 fast UHPLC separation (5min separation using acidified 10% MeOH isocratic flow in a CORTECS C18 colum
13 long and 5 mm diameter) and then eluted with acidified 5 M NaCl solution directly into a sodium aceta
14                                          The acidified 70% acetone was identified as the ideal solven
15 sted samples and haem Fe was extracted using acidified 80% acetone for 60 min.
16 V-ATPase) activity, accounts for the reduced acidifying ability of peripheral lysosomes.
17                Extraction was performed with acidified acetonitrile (acetic acid 1% (v/v)), and addit
18  includes a prior protein precipitation with acidified acetonitrile for all samples and an additional
19                Extraction was performed with acidified acetonitrile, followed by a cleanup step with
20 in pfk2Delta, and the vacuolar lumen was not acidified after reassembly.
21 rsely, expressing ATP12A in CF mouse airways acidified airway surface liquid, impaired defenses, and
22  H(+)/K(+) adenosine triphosphatase (ATP12A) acidified airway surface liquid, which impaired airway h
23 M2 ion channel causes the virion interior to acidify also.
24      This effect is demonstrated by exposing acidified ammonium sulfate particles to 250 parts per bi
25 tion domain) as the lumen of the endosome is acidified and 2) low pH, in conjunction with acidic lipi
26                  Milk samples were initially acidified and centrifuged, and then the supernatant was
27                 Some endocytic vesicles were acidified and colocalized with LysoTracker.
28 uently, vesicles can be locally recycled, re-acidified and re-used.
29 ltasecA2 mutant of M. tuberculosis were more acidified and showed greater association with markers of
30  with phagocytosis because phagosomes become acidified and the average fluorescence lifetime of EGFP
31                  The milks were subsequently acidified and the distribution of protein between colloi
32 pbo-4 mutants the extracellular space is not acidified and the muscles fail to contract.
33                                    Urine was acidified and the organic acids were extracted by revers
34 limate change as oceans continue to warm and acidify and thermal anomalies grow in frequency and inte
35 whole blood was added to the sample chamber, acidified, and the HCN gas evolved was actively transfer
36 ria-containing vacuoles quickly (</= 15 min) acidify, and that this was coincident with greater virul
37 phagosomes in murine cftr(-/-) AMs failed to acidify, and the cells were deficient in bacterial killi
38       The method involved mixing sample with acidified aqueous acetonitrile, followed by salt-out liq
39 brils upon incubation at room temperature in acidified aqueous solution at peptide concentrations >10
40  ions is produced by nanoESI from a slightly acidified aqueous solution with the micron outer diamete
41                                              Acidified aqueous solutions containing unfolded proteins
42 e intramitochondrial pH of astrocytes, which acidifies as a consequence of glutamate uptake, with the
43 orter of acidified mitochondria reveals that acidified axonal mitochondria originating from the retin
44 act with early and late endosomes and become acidified before the onset of phagosomal disruption.
45 utophagic membranes, and that YCVs failed to acidify below pH 7 in naive macrophages.
46 experiments to determine whether exposure to acidified bile salts causes esophageal epithelial cells
47                Exposure of squamous cells to acidified bile salts significantly increased the secreti
48 ophageal squamous cell lines were exposed to acidified bile salts to evaluate their effects on cytoki
49 at addition of moderate amounts of pepsin to acidified bovine insulin at close to physiological tempe
50      Solution chemistry indicated that CO(2)-acidified brine preferentially dissolved dolomite until
51 nt with an experimental study in which a CO2-acidified brine was injected into a fracture in the Dupe
52 omography before and after exposure to CO(2)-acidified brine, allowing mineral phase and voidspace di
53                           We studied two CO2-acidified brines having the same pH (3.3) and comparable
54 ed intradermally to nape or cheek skin, (ii) acidified buffer elevated intracellular calcium levels i
55                                     In cells acidified by 5 minutes of exposure to 20 mM ammonium chl
56 croglia also degrade fAbeta if lysosomes are acidified by an ammonia pulse-wash or by treatment with
57 a persistent ozonide in airway-lining fluids acidified by preexisting pathologies or inhaled particul
58                  The intestinal cytoplasm is acidified by proton influx from the lumen during defecat
59 milieu into an endosome, whose contents then acidify, causing changes in the viral matrix protein (M1
60  in TEs increased significantly following an acidified chlorite treatment.
61 ression of all IFITMs expanded vesicular and acidified compartments within cells, there were marked p
62  on the exudation of reducing, ligating, and acidifying compounds.
63  ascidians and 29% sponges after 100 days in acidified conditions (pH 7.7).
64                        Long-term exposure to acidified conditions predicted for the year 2100 and bey
65 ariability found among samples maintained in acidified conditions relative to controls, suggests a po
66 communities maintained in or transplanted to acidified conditions, and altered community structure in
67 cyanobacterium Trichodesmium decreased under acidified conditions, notwithstanding a beneficial effec
68 berrant shapes being observed only under the acidified conditions.
69  increase in the abundance of Padina spp. in acidified conditions.
70  current and predicted stability under ocean acidifying conditions.
71 y undergo maturation and become increasingly acidified, consistent with the formation of an autolysos
72 sive increase in oxidative ATP supply during acidifying contractions.
73                                 Lactobacilli acidify CVM to pH approximately 4 by continuously produc
74  dissolution of calcite particles by flow of acidified desalinated water through a bed packed with mi
75 y flow of micron-size calcite particles with acidified desalinated water.
76                                           In acidified dough the pattern of volatile metabolites allo
77 were investigated and compared to chemically acidified dough.
78 an; rescue can also be achieved by providing acidified drinking water to sublytic homozygotes.
79 elevated summer temperatures in historically acidified ecosystems.
80 ngly enhanced AN-PEP activity because of its acidifying effect.
81 ecovery from acidification, due to decreased acidifying emissions and deposition, has led to an incre
82  V-ATPase activity are avirulent and fail to acidify endomembrane compartments, exhibiting pleiotropi
83 r structures that colocalize with markers of acidified endosomal compartments.
84 esting RGS4 traffics through PM recycling or acidified endosome pathways.
85 transfer of Wg to DFz2 within the merged and acidified endosome to initiate Wg signaling.
86 of cellular entry requires trafficking to an acidified endosome, which promotes translocation across
87 serving as a route of export of folates from acidified endosomes and (ii) provide a functional role f
88 dendritic cells (pDCs) detect viruses in the acidified endosomes by means of Toll-like receptors (TLR
89 diphtheria toxin catalytic domain (DTA) from acidified endosomes into the cytoplasm of eukaryotic cel
90  facilitates egress of the viral genome from acidified endosomes, and the L2/DNA complex accumulates
91 gests hosts may need to adapt not only to an acidified environment, but also to changes in their Symb
92 e also display enhanced expression of the SC acidifying enzyme, secretory phospholipase A2f (sPLA2f).
93               The blueberries were soaked in acidified ethanol, filtered, and the filtrate was cleane
94 one concentration (%), time of extraction in acidified ethanolic solution (min) and ethanol concentra
95                  Samples were extracted with acidified ethyl acetate, MgSO4 and CH3COONa and cleaned
96 resorb mineralized tissue and cannot form an acidified, extracellular resorption compartment.
97 eactions in fractured basalts exposed to CO2-acidified fluids.
98 g acid stress, bacteria internal pH promptly acidifies, followed by recovery.
99 E. ictaluri-containing vacuoles (ECV) became acidified following ingestion by head kidney-derived mac
100                     This compartment must be acidified for Salmonella to survive within macrophages,
101                    Decades of acid rain have acidified forest soils and freshwaters throughout montan
102 eystone organism in a more nutrient-limited, acidified future ocean.
103           Specimens were demineralized using acidified gel (pH = 4.5) for 5 wk and scanned every week
104 nant protein and electron cryo-microscopy of acidified hantavirus allows us to propose a model for en
105 of the bacteria-containing phagosome into an acidified, hydrolytically active compartment.
106        By contrast, M2 phagosomes proceed to acidify immediately in order to clear apoptotic bodies r
107 n 5days and then approximately pH 8.5) to be acidified in PLGA MS for 9weeks, unlike CM2-free PLGA MS
108 mers that undergo conformational change when acidified in the endosome.
109 reasoned that the Salmonella cytoplasm might acidify in the macrophage vacuole to activate OmpR-depen
110 trongly diminish the ability of lysosomes to acidify in vivo, demonstrating that ClC-7 is a Cl-/H+ an
111 into the intestinal lumen and are lacking in acidified intestinal V-ATPase-containing compartments.
112  either genetic or pharmaceutical approaches acidified intracellular pH and reduced cell growth.
113  vesicular adenosine triphosphatase (ATPase) acidifies intracellular compartments, including synaptic
114 phosphatase (v-ATPase) is a proton pump that acidifies intracellular compartments.
115 ase (V-ATPase) is a rotary motor enzyme that acidifies intracellular organelles and the extracellular
116 -ATPases are ATP-dependent proton pumps that acidify intracellular compartments and, in some cases, t
117            Vacuolar H(+)-ATPases (V-ATPases) acidify intracellular organelles and help to regulate ov
118 e) is a multisubunit complex responsible for acidifying intracellular organelles and is highly regula
119 tes the V-ATPase proton pump responsible for acidifying intracellular organelles.
120 or 9 (TLR9) is activated by DNA presented in acidified, intracellular compartments.
121  of GlcNAc raises the ambient pH rather than acidifying it, as occurs after dextrose catabolism.
122 ication of the host cell vacuole, Salmonella acidifies its own cytoplasm in response to the low extra
123       Polyacetylenes were retained better in acidified juices and cold storage temperatures (4 degree
124 pace between the intestine and the muscle is acidified just prior to muscle contraction and that the
125 -524) is sufficient to pilot the effector to acidified LAMP1-positive lysosomal compartments, where W
126                      Despite localization to acidified late phagosomes, viable G. bethesdensis cells
127 ) cortical neurons, the GA is severely under-acidified, leading to osmotic swelling.
128 could account for enhanced function, because acidifying lightly pigmented human SC resets barrier fun
129 mes via the TAT moiety and to respond to the acidifying lumen of endosomes to cause membrane leakage
130 l pathogen that replicates exclusively in an acidified, lysosome-like vacuole.
131  compartment defects in resistance; V-ATPase acidifies lysosomes and related organelles, whereas adap
132 r H(+)-ATPase (V-ATPase), a proton pump that acidifies lysosomes.
133 GA core and released specifically within the acidifying macrophage phagosomes.
134 e CiaRH, ComDE, or VicRK grew more slowly in acidified media and were more sensitive to killing at le
135 ltaBbPacC mutant showed a reduced ability to acidify media during growth due to failure to produce ox
136  mutants showed a reduced ability to grow in acidified medium.
137                               The epsilon in acidified MeOH and buffer pH 1 ranged between ~16,000-30
138 hilized fruit samples were extracted with an acidified MeOH mixture assisted by ultrasound.
139 ic-lipophilic balanced resin and eluted with acidified methanol (0.1% formic acid), resulting in anal
140  and to evaluate their spectral behaviors in acidified methanol (MeOH) and buffers pH 1-9.
141       Major anthocyanins were extracted with acidified methanol and characterised in powdered berry e
142 udes cell lysis, protein precipitation using acidified methanol and HPLC analysis of the lysate.
143        Compared with methanol solvent, using acidified methanol led to increased extraction yield by
144 om minced muscle samples involved the use of acidified methanol, ultrasound treatment and centrifugat
145                                           An acidified methanol-water mixture was used as an effectiv
146    The method is based on extraction with an acidified methanol-water mixture.
147 s commonly used for phenols, extraction with acidified methanol-water was chosen as the best to quant
148 y with its potent inhibitor HOE 642 not only acidified microglia, abolished the BK-triggered dynamic
149     Sample preparation improvements included acidified, microwave-accelerated, PNGase F N-glycan rele
150 ubjects were randomly assigned to receive an acidified milk drink containing >/=10(9) colony-forming
151 duced tandem fluorophore protein reporter of acidified mitochondria reveals that acidified axonal mit
152        Selective oxidation of a-PhobPH in an acidified mixture of a-PhobPH and s-PhobPH is an efficie
153  feature of these key species in the reduced acidified molybdate solutions and to observe the templat
154 ncentrations increase considerably in gypsum-acidified must, although they fell markedly after fermen
155 nced precipitation was, however, observed in acidified NaHCO(3) solutions (pH 5, DIC approximately 25
156                        The photoactivatable, acidifying nanoparticles (paNPs) demonstrate lysosomal u
157 cales and that as coastal oceans continue to acidify, negative effects on these populations may becom
158 ollowing topical application of the NO donor-acidified nitrite (NO2(-)), has set the paradigm of NO b
159 e nitrogen species produced biochemically as acidified nitrite and by bone marrow-derived macrophages
160 and a treatment arm that received 3 doses of acidified nitrite applied topically for 12 weeks with an
161                               We report that acidified nitrite caused a 3-log-increased kill of C. je
162 nitrosylation upon exposure of Salmonella to acidified nitrite, a signal encountered by this enteropa
163                                  In contrast acidified nitrite, releasing equal quantities of NO (mea
164 gest that the potent inflammation induced by acidified NO2(-) is secondary to the release of addition
165 daptive capacity of species to respond to an acidified ocean, and, as a result, predictions regarding
166 ed to parental care are more protected in an acidifying ocean compared to their relatives employing b
167 ng seawater CO(2) concentrations and thereby acidifying ocean water.
168 coral health and resilience in a warming and acidifying ocean.
169 egional weather patterns, rising sea levels, acidifying oceans, changed nutrient loads and altered oc
170 S stained intensely for the vATPase and were acidified, only 20 to 30% of phagosomes containing live
171 ke of anthropogenic carbon dioxide (CO2) has acidified open-ocean surface waters by 0.1 pH units sinc
172 ectrical current through the system tends to acidify (or basify) the anolyte (or catholyte), their ef
173 are ubiquitous, ATP-driven proton pumps that acidify organelles or the extracellular space.
174 s are conserved ATP-driven proton pumps that acidify organelles.
175  H(+)-ATPase (V-ATPase) enzyme complex is to acidify organelles; this process is critical for a varie
176 inetics in Cd-Zn cocontaminated alkaline and acidified paddy soils, under various flooding periods an
177 intracellular pathogen that replicates in an acidified parasitophorous vacuole derived from host lyso
178 n, the pathogen replicates exclusively in an acidified (pH 4.5 to 5) phagolysosome-like parasitophoro
179 gote stage of the parasite that lives within acidified phagolysomal vesicles of mammalian macrophages
180 Intracellularly, the organism prospers in an acidified, phagolysosome-like vacuole.
181 e normal process of phagosomes maturing into acidified phagolysosomes.
182 7-positive stage, but do not mature to fully acidified phagolysosomes.
183 bility to acid pH and reduced survival in an acidified phagosomal vacuole.
184  How the bacterium resists the low pH of the acidified phagosome is incompletely understood.
185 iplasmic protease MarP for Mtb to survive in acidified phagosomes and establish and maintain infectio
186   Activated macrophages produce NO, which in acidified phagosomes is converted to NO(2).
187 ce are metabolically inactive, reside within acidified phagosomes that have fused with Texas red dext
188 ence are metabolically active, reside in non-acidified phagosomes that have not fused with Texas red
189 esistance, and intracellular survival within acidified phagosomes.
190    When compared with the control (pHi 7.3), acidifying pHi to 6.3 or alkalinizing pHi to 8.3 and 8.8
191  base-poor, parent materials is sensitive to acidifying processes on millennial timescales.
192 SA300 clone, the USA300-containing phagosome acidified rapidly and acquired the late endosome and lys
193              Here we show that NHE5 potently acidifies recycling endosomes in PC12 cells.
194 ires osteoclasts to generate and maintain an acidified resorption compartment between the apical memb
195 r polarization and formation of an isolated, acidified resorptive microenvironment.
196 ve flow-through CO2 equilibration between an acidified sample and an indicator solution with a fast r
197 ve flow-through CO2 equilibration between an acidified sample and an indicator solution with a respon
198 ydrides were generated in the reaction of an acidified sample with NaBH4 after pre-reduction with KI-
199 reviewed experimental data on the effects of acidified seawater on calcifying species growth, reprodu
200 s of PNH erythrocytes in a modified extended acidified serum assay, and also prevents C3 fragment dep
201 opment, allowing serpulids to do best at the acidified site by the end of the experiment, although ea
202               We show that succession at the acidified site was initially delayed (less community cha
203  pH(i) recovery was significantly greater in acidified slc4a10-transfected cells than in control cell
204                      Nitrite addition to the acidified sludge at a concentration of 20 mg NO2(-)-N/L
205 d to grow at higher rates in the presence of acidified sodium nitrite (ASN), a model system used to g
206 othesis that calcium limits forest growth in acidified soils.
207 77-83% moisture content) were conditioned in acidified solution at 5, 15 and 25 degrees C, absence of
208 t of carbonate mineral reactivity with CO(2)-acidified solution is voidspace generation through physi
209                             Microinfusion of acidified solutions into the rhythmically active pre-Bot
210 hm as small as 3.7% achieved in desalted and acidified solutions.
211 nvironmental problem, but efforts to restore acidified streams and biota have had limited success.
212       The secondary production of culturally acidified streams is low, with a few species of generali
213 TPase) is a multisubunit enzyme complex that acidifies subcellular organelles and the extracellular s
214 ta vacuoles were alkalinized and the cytosol acidified, suggestive of impaired V-ATPase proton transp
215  This claim is based on the beliefs that (i) acidified sulfanilamide pretreatment, required to remove
216 ations were only enhanced in the presence of acidified sulfate aerosol, consistent with prior work.
217 Additionally, we show reactive uptake on the acidified sulfate aerosols supports a previously unrepor
218 ich form during the BVOC oxidation, into the acidified sulfate particles is shown to explain the latt
219 low-NO(x) SOA is enhanced in the presence of acidified sulfate seed aerosol (mass yield 28.6%) over t
220 facility in the presence of nonacidified and acidified sulfate seed aerosol.
221 otons (coreleased with neurotransmitter from acidified synaptic vesicles).
222  Remarkably, low concentrations of glutamate acidify synaptic vesicles more slowly but to a greater e
223   These findings suggest the existence of an acidifying synaptic force that is overcome by commonly u
224                                  CS exposure acidified the airspaces and induced localization of the
225 Inhibition of extramitochondrial CA activity acidified the matrix (as determined by fluorescence meas
226                Illumination with amber light acidified the surrounding interstitium and led to activa
227                                         They acidified the yeast cytosol and caused pH-sensitive grow
228 t occurs via a gas channel (aquaporin 1) and acidifies the cell.
229     The gastric proton pump H(+),K(+)-ATPase acidifies the gastric lumen, and thus its inhibitors, in
230 d the vacuolar H(+)-ATPase (V-ATPase), which acidifies the lysosome-like vacuole.
231  expresses vacuolar H(+)-ATPase (VHA), which acidifies the symbiosome space down to pH approximately
232                       Conductance of protons acidifies the viral interior and thereby facilitates dis
233 tetrameric transmembrane proton channel that acidifies the virion after endocytosis.
234 ctivating process in which proton permeation acidifies the virion to release the viral RNA and core p
235 sed, whereby auxin promotes proton efflux to acidify the apoplast and facilitate the uptake of solute
236 nzymes' catalytic power and their ability to acidify the C alpha of amino acids remains unknown.
237          The ability of the mutant strain to acidify the defined medium during growth in the presence
238 tes expand in volume, releasing protons that acidify the developing enamel.
239 ides, could grow faster at pH 5.5, and could acidify the environment more rapidly and to a greater ex
240 tional sclerotia and have reduced ability to acidify the environment.
241  (V-ATPases) are essential proton pumps that acidify the lumen of subcellular organelles in all eukar
242 y-stimulating factor (MCSF) or interleukin-6 acidify the lysosomes of microglia and enable them to de
243 anthropogenic carbon dioxide (CO2) emissions acidify the oceans, calcifiers generally are expected to
244 gs, with roots that have reduced capacity to acidify the rhizosphere.
245                 The sample preparation steps acidify the sample, decompose organics, and convert all
246 rotein lipocalin 2 (LCN2) and protons, which acidify the urine.
247 4, distinct genes, such as PH1 and PH5, that acidify the vacuole.
248 hemical library to search for compounds that acidify the yeast cytosol in vivo using pHluorin-based f
249 effect of acidic medium could be mimicked by acidifying the cytosol with bafilomycin A1, a proton pum
250 cent muscle cells to contract by transiently acidifying the extracellular space between the intestine
251 id and protons to maintain intracellular pH, acidifying the extracellular space.
252 ng in the activation of the O2' nucleophile, acidifying the general acid C75, and stabilizing the non
253                                              Acidifying the host tissue enhanced virulence of the oxa
254             Most plant species acquire Fe by acidifying the rhizosphere and reducing ferric to ferrou
255 abnormalities were normalized by exogenously acidifying the SC, suggesting a basis for the well-known
256 bound uropathogenic E. coli and responded by acidifying the urine and secreting the bacteriostatic pr
257 east cells grown in abundant glucose tend to acidify their extracellular environment, they raise the
258                                         They acidify their microenvironment hence membrane voltage is
259 and 52.4% of p.E161K carriers were unable to acidify their urine below pH 5.3 and thus, can be consid
260 s of V-ATPase function; cells were unable to acidify their vacuoles and exhibited growth defects typi
261 /endosomal network and vacuolar membrane and acidified these compartments as part of a hybrid V-ATPas
262 mes, within a C. neoformans-containing cell, acidified to a lesser extent and failed to recruit CD63
263             In the first hour, DC phagosomes acidified to a pH that was, on average, half a point hig
264                        Sample water is first acidified to convert all DIC to carbon dioxide (CO2).
265  total dissolved iron analysis, samples were acidified to pH 2.0 in the presence of 30 muM DHN and le
266 intained around -120 mV, and the apoplast is acidified to pH 3.
267 is can persist in macrophage phagosomes that acidify to a pH of approximately 4.5 after activation of
268                     A combination of effects acidifies tumor cell interiors, and cells pump out lacti
269 ed that without amelogenins the enamel would acidify unless ameloblasts were buffered by alternative
270  mobilization of metal contaminants by brine acidified upon contact with CO2 during geologic carbon s
271 ns remain regarding how bacteria survive the acidified vacuole and how acidification affects bacteria
272 of macrophages, where Brucella resides in an acidified vacuole at a pH of 4-4.5 during the early phas
273 ts growth medium in vitro, and resided in an acidified vacuole within macrophages.
274  virulence mechanisms differentially rely on acidified vacuoles and that the loss of both vacuolar (V
275 lar proton pump, blocked MDP accumulation in acidified vesicles and cytokine responses, suggesting th
276 c machinery to discriminate fully loaded and acidified vesicles from vesicles undergoing neurotransmi
277                     MDP is internalized into acidified vesicles in macrophages.
278 ation, labeled MDP was rapidly released from acidified vesicles into the cytosol, a process that requ
279 et cells triggers toxin internalization into acidified vesicles, whereupon cryptic segments from with
280  blocking the fusion of early endosomes with acidified vesicles.
281  proteolipid pore of a vesicular ATPase that acidifies vesicles.
282   The desolvated solutions were dispersed in acidified water (pH 3) immediately after desolvation.
283        A gradient method was developed using acidified water and acetonitrile combined with high colu
284                             Extractions with acidified water and ultrasound were not effective to rec
285 ects of the extraction methods and solvents (acidified water pH 2.0, ethanol+water 50% v/v and ethano
286 ite electrode readily produces hydrogen from acidified water when functionalized with the modified cl
287 terials and with a diffusion-limited rate in acidified water, is efficient as well as oxygen tolerant
288 bly linked to a pyrite electrode immersed in acidified water.
289 5) degradation over 2 weeks when prepared in acidified water.
290 sistent spatial mosaic in the penetration of acidified waters into ecologically-important nearshore h
291                             The cytoplasm is acidified when V-ATPase is inhibited; thus we conducted
292 sion, vesicles deep in the egg center slowly acidify, whereas cortical vesicles undergo a rapid alkal
293 se the oceanic surface water to continuously acidify, which has multiple and profound impacts on coas
294  extraction with primary secondary amine and acidified with 0.1% formic acid.
295  modified QuEChERS technique in acetonitrile acidified with acetic acid (1%, v/v) and citrate-buffere
296  extraction was performed using acetonitrile acidified with formic acid (1%, v/v).
297          Samples were dissolved in water and acidified with HNO3.
298                          Winemaking of musts acidified with up to 3g/L of gypsum (CaSO4 2H2O) and tar
299                        Failure of the ECV to acidify would prevent both upregulation of the T3SS and
300                     Inclusion of MTGase into acidified yogurt drinks reduces the serum separation wit

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