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1 cidification) or discretely (~3 months after acidification).
2 ves under impending global warming and ocean acidification.
3 t protonation, which occurs upon muscle cell acidification.
4 gulation of V-ATPase trafficking and urinary acidification.
5 educed coral calcification rates under ocean acidification.
6 ubcellular location, or changes in endosomal acidification.
7 equestration but delayed lysosomal fusion or acidification.
8 e-mediated processes, microbial activity and acidification.
9 quaculture leases differing in environmental acidification.
10 plies the potential for acclimation to ocean acidification.
11 tive autophagic flux due to reduced lysosome acidification.
12 f this species to contemporary environmental acidification.
13 dy reduces atherosclerosis and blocks lesion acidification.
14 red: de novo protein synthesis and endocytic acidification.
15 ain fatty acid (SCFA)-mediated intracellular acidification.
16 a job-sharing role with V-ATPase in vacuolar acidification.
17 ction as well as by a reduction in lysosomal acidification.
18 tand future climate-driven change to habitat acidification.
19 uires Src phosphorylation and endo/lysosomal acidification.
20 nge effects-in particular, ocean warming and acidification.
21 that are not as plant-available as prior to acidification.
22 elevated seawater CO(2) levels due to ocean acidification.
23 a consequence of recovery from anthropogenic acidification.
24 vations that NCOA7 is required for lysosomal acidification.
25 docytosis, protein maturation, and lysosomal acidification.
26 matter supporting excess respiration driving acidification.
27 greater than atmospheric CO(2)-driven ocean acidification.
28 ting against eutrophication and global water acidification.
29 ing, MVB fusion, exosome uptake and endosome acidification.
30 rete sample analysis at least 3 months after acidification.
31 ceptor, respectively, and impaired lysosomal acidification.
32 oteasome activity but dependent on lysosomal acidification.
33 ure to contemporary and future environmental acidification.
34 ulated via chronic exposure to extracellular acidification.
35 l biomineralization, promoting resilience to acidification.
36 tion of high-latitude populations from ocean acidification.
37 This untimely egress depends on host cell acidification.
38 ncing browning associated with recovery from acidification.
39 global change, particularly increasing ocean acidification.
40 a second mutation in lysosomal biogenesis or acidification.
41 tated further H(+)-ATPase-mediated endosomal acidification.
42 ch as light exposure, temperature, and ocean acidification.
43 ted to end-Triassic global warming and ocean acidification.
44 ied in semiarid grasslands experiencing soil acidification.
45 s to the protection of the brain milieu from acidification.
46 CO(2) can cause intracellular acidification.
47 fied shells and acid/base balance with ocean acidification.
48 C(6) F(5) )(3) ], which releases N(2) O upon acidification.
49 TM3, SLC15A3, and CNP contribute to lysosome acidification.
50 with the complete decay of ECD signals upon acidification.
51 ls reduced autophagic flux and autophagosome acidification.
52 nhibited, so long as cells undergo cytosolic acidification.
53 contrast to the uniform trends of open-ocean acidification (-0.0004 to -0.0026 pH units yr(-1)) drive
55 d a significant reduction in urine pH (i.e., acidification) accompanied by an increase in blood pH an
59 lobal warming (GWP), eutrophication (EU) and acidification (AD) impacts of soybean production in near
60 er increasing pCO(2) , suggesting that ocean acidification alleviates oxidative stress in kelp, which
64 of gold nanostar morphology is induced upon acidification, an effect that depends on both pH and aci
65 emission was positively correlated with soil acidification and an increase in the relative abundances
69 ce extent, increase in riverine input, ocean acidification and changes in primary productivity are cr
72 ver, this regulating service causes warming, acidification and deoxygenation of deep waters, leading
73 stically, Hvcn1 deficiency delayed endosomal acidification and enhanced intracellular reactive oxygen
75 subunit VMA5 expression, impairing lysosome acidification and inhibiting autophagic protein degradat
76 ar et al. show that SIRT1 controls lysosomal acidification and its loss enhances the secretion of pro
77 smegmatis Polyphosphate inhibited phagosome acidification and lysosome activity in D. discoideum and
78 doption of an ecosystem perspective to ocean acidification and multiple stressors in productive aquat
80 nduced aggregation and co-precipitation upon acidification and significantly reduced purity (~71%).
82 o the cell cytosol, which leads to cytosolic acidification and the generation of action potentials.
85 re measured both continuously (4.5 min after acidification) and discretely (repeatedly from 1 to 151
86 tems, such as climate change (warming, ocean acidification) and pollution, with irreversible ramifica
88 an, through warming, oxygen loss, increasing acidification, and changing particulate organic carbon f
89 enario in terms of global warming potential, acidification, and eutrophication in ~63, ~77, and ~100%
90 ssors: rising sea surface temperature, ocean acidification, and increased prevalence of infectious di
92 gh TRPML1 channels is vital for trafficking, acidification, and other basic functions of these organe
93 hat local ecosystem processes modulate ocean acidification, and support the adoption of an ecosystem
96 ulub impact, supporting impact-induced ocean acidification as a mechanism for ecological collapse in
98 s of soil food webs, and highlight that soil acidification, as an anthropogenic stressor, reduced the
101 redicts that pH fluctuations decrease during acidification, but noise analysis of single-vesicle data
103 ts suggest that kelp will benefit from ocean acidification by a reduction in environmental stress how
104 ominance of woody vegetation as well as soil acidification by EM fungi, which are associated with gre
105 erns worldwide, nutrient enrichment and soil acidification can lead to substantial changes in the div
106 c analysis, taking into account growth rate, acidification capacity, proteolytic activity, cell envel
107 uricemia with UA crystalluria due to urinary acidification caused tubular obstruction, inflammation,
109 Island, Australia, we simulated future ocean acidification conditions, and found reduced pH led to a
110 s how species may survive under future ocean acidification conditions, and help to reveal the traits
111 lic costs when exposed to experimental ocean acidification conditions, potentially limiting the energ
113 of impaired PLGA degradation and intestinal acidification confirming an important enterohepatic axis
115 oupled during H(+)-ATPase-mediated endosomal acidification, crucial for ClC-5 activation by depolariz
116 nisms collected on the 2016 West Coast Ocean Acidification cruise in the California Current System.
118 of the histidine 98 residue, which is, after acidification, decoupled from the resting position and i
121 ulture is vulnerable to the impacts of ocean acidification driven by increasing carbon dioxide (CO(2)
122 ermined that Acetobacter species counter the acidification driven by L. plantarum production of lacta
123 bsorption by the ocean as well as to coastal acidification driven by land run off and rising sea leve
124 ults extend evidence that impaired lysosomal acidification drives progressive lysosomal failure in mu
126 cifiers are particularly vulnerable to ocean acidification due to dissolution and a reduction in shel
127 ries and is particularly vulnerable to ocean acidification, due to its natural upwelling of carbon-en
128 suggest that shifts in plant cover and soil acidification during ecosystem development are associate
129 systems (i.e., wetter and warmer), increased acidification during pedogenesis was associated with dec
130 ell-known antiautophagy property of impeding acidification during the late stage of autophagic flux.
131 tic demands of pinto abalone caused by ocean acidification during winter will be exacerbated by seaso
132 r oxygen consumption (OCR) and extracellular acidification (ECAR) are widely used proxies for mitocho
133 ipneustes ventricosus) submitted to a 5 week acidification experiment (pHT of 8.1, 7.7, and 7.4).
134 rgeting Ac45 (AAV-sh-Ac45) impaired cellular acidification, extracellular acidification, and bone res
135 ene inactivations of lysosomal biogenesis or acidification factors causes vitamin B12 deficiency.
136 ycling of ESS is shown to reduce terrestrial acidification, freshwater eutrophication, and particulat
137 er membrane in most impact categories (e.g., acidification, global warming potential, and carcinogeni
138 d as an imminent threat to our oceans, ocean acidification has been documented in all oceanic basins.
139 onoamine transporter function and on vesicle acidification has been reported, a role of CAPS in vesic
140 lution and mechanical chip removal and ocean acidification has been shown to accelerate bioerosion ra
142 en (N) and phosphorus (P) contents, and soil acidification have greatly increased in grassland ecosys
143 mbined result of projected ocean warming and acidification, highlighting the susceptibility of coral
144 ave catastrophic biotic effects due to ocean acidification hindering biogenic carbonate production, w
145 re further suggested by media and apoplastic acidification, hygromycin B tolerance and changes in rel
146 patterns are important for predicting ocean acidification impacts, but are lacking in coastal oceans
147 , revealed specific requirements for luminal acidification in apical, but not basolateral, membrane p
148 -ATF4 hyperactivation and impaired lysosomal acidification in beta-cells lacking Furin, causing beta-
149 on, whereas increasing productivity enhances acidification in bottom waters of stratified coastal eco
150 observation, the importance of extracellular acidification in cancer is now considered a hallmark of
151 nitude over time, especially because of soil acidification in low diversity communities and especiall
153 osomal-delivered MPO also disrupts lysosomal acidification in RPE cells, which coincides with nuclear
156 PLGA nanoparticles accumulate and cause gut acidification in the cecum, accompanied by significant c
158 of hypoxia are stronger than the effects of acidification in weakening these grazing interactions ov
159 melanoma cells, in response to intracellular acidification induced by ammonium chloride prepulse.
161 abolished lysosome enlargement and lysosome acidification induced by wild-type TMEM106B overexpressi
162 s from this study suggest that environmental acidification induces drug resistance and extracellular
164 through lantibiotic expression or intestinal acidification, influence host mucosal immune cells and e
169 s phenomenon, commonly referred to as "Ocean Acidification", is endangering coral reefs and the broad
170 zation during neurotransmission, rather than acidification, is a generalizable phenomenon across conv
171 le in the sugar metabolism and environmental acidification (key virulence traits associated with cari
174 proportional to light-driven thylakoid lumen acidification, manipulating thylakoid ion and proton flu
175 a novel mechanism linking impaired lysosomal acidification, mitochondrial malfunction and inflammatio
176 ced dormant model-organism cultures using an acidification model and characterized those by a multila
177 l skeletons' resilience to ocean warming and acidification must take into account the dual formation
178 tigated how predicted ocean warming (OW) and acidification (OA) affect key ecological behaviours (loc
179 investigated the cumulative effects of ocean acidification (OA) and hypoxia on the organic carbon fat
180 test of coral parental conditioning to ocean acidification (OA) and tracking of offspring for 6 month
182 -fixing cyanobacteria Trichodesmium to ocean acidification (OA) is critical to understanding future o
191 ial pH, suggesting a possible involvement of acidification of airway fluid and/or tissue generated by
192 equired for cell migration and extracellular acidification of breast cancer cells in response to HER2
193 iphosphatase is not only responsible for the acidification of CG, but also contributes to the maturat
195 trafficking required microtubular transport, acidification of endosomes, and a functional redox envir
197 n bronchopulmonary C-fibres was generated by acidification of fluid and/or tissue in the lung and air
199 ng Trypanosoma brucei brucei Endocytosis and acidification of high-density lipoprotein-associated APO
203 e again use the reduced DS model explore the acidification of large, lysosome-like vesicles to determ
205 osensors for evaluation of the extracellular acidification of microorganisms in various biotechnologi
206 esults of this study show that the impact of acidification of natural waters on Fe availability will
207 of dissolution of iron oxyhydroxides on the acidification of natural waters will also have implicati
209 es to marine ecosystems globally, with ocean acidification of particular concern for coral reefs.
212 , starter cultures are needed for successful acidification of the cheese and proteolytic strains like
213 cid-activated proton channel responsible for acidification of the inside of the virus, a critical ste
214 and is part of a feedback loop that ensures acidification of the luminal compartment These results h
215 al complex I during acute hypoxia(11) drives acidification of the matrix and the release of free Ca(2
216 porated into solid medium, with accompanying acidification of the media, and extensive precipitation
218 he bacteria, but cannot be explained through acidification of the phagosome or calcium limitation.
220 c aspects of frustule biosynthesis involving acidification of the silica deposition vesicle (SDV) by
221 cers, mammary carcinoma progression involves acidification of the tumor microenvironment, which is an
222 lar ATPases as the likely mechanisms driving acidification of the venom gland lumen during venom prod
223 eviously underappreciated role for localized acidification of tumor microenvironment in the expressio
224 taste of Citrus fruits is due to the extreme acidification of vacuoles in juice vesicle cells via a m
226 ., sediment, low salinity, anoxia, and ocean acidification), offering an alternative approach for der
228 em nucleus that mediates the effect of brain acidification on breathing, also contributes to arousal
231 aluated fundamental effects of environmental acidification on mammary carcinoma cells in standard two
232 nic activities, and the consequences of this acidification on marine fauna and ecosystems are the sub
233 previous attempts to quantify the effect of acidification on planktonic calcifying organisms has rel
235 is study aims to determine the role of dough acidification on the nutritional pattern of Chlorella vu
236 ations that did not interfere with lysosomal acidification or degradation and were nontoxic in primar
237 cally is analyzed continuously (<5 min after acidification) or discretely (~3 months after acidificat
240 nd 25-64% in eutrophication potential, while acidification potential ranged between a 24% decrease to
241 s generated in vitro either using the common acidification procedure or primed by limited selective c
243 dinal patterns, implying that the phagosomal acidification process was a stochastic dynamical system.
245 , IFN-I signaling modified the localization, acidification, protease activity, and proteomic profile
247 oxygen consumption rate (OCR), extracellular acidification rate (ECAR) and proton production rate (PP
248 oxygen consumption rate (OCR), extracellular acidification rate (ECAR), and fatty acid beta-oxidation
249 onse, as evidenced by elevated extracellular acidification rate and increased expression of key glyco
250 se in oxygen consumption rate, extracellular acidification rate and spare respiratory capacity, chang
251 we prospectively screened the extracellular acidification rate as a measure of glycolysis and the ox
253 CBCs had a very low glycolytic extracellular acidification rate but consumed oxygen in response to FA
254 s in the parasite nor impaired extracellular acidification rate, but resulted in specific defects in
255 colytic function with enhanced extracellular acidification rate, glycolytic metabolites, and lactate
257 th of which work in concert with IRT1 in the acidification-reduction-transport strategy of iron uptak
262 n collections as a tool to investigate ocean acidification since the early Industrial Revolution.
266 an be induced to perforate membranes through acidification, such as would occur within maturing phago
267 knockout HeLa cells increased autophagosome acidification, suggesting a therapeutic approach to over
269 radients of temperature, salinity, and ocean acidification, then model growth rate and duration of Ol
270 ecursor protein (APP) gene impairs lysosomal acidification, thereby depressing lysosomal hydrolytic a
271 alyses indicate that increased use of slurry acidification, thermal drying, incineration and pyrolysi
272 ydroxybilobalide is found to rely on lactone acidification through lone-pair delocalization, which le
273 A two-component system CpxRA directly senses acidification through protonation of CpxA periplasmic hi
277 nsequences of eutrophication versus those of acidification, to maintain biodiversity and ecosystem se
278 lucose and linoleic acid, restored lysosomal acidification, TOR activation, and survival with refeedi
279 anion currents are detectable, whereas upon acidification transport of the neutral, protonated monoa
280 tCLCa loss of function mutant, the cytosolic acidification triggered by extracellular NO(3) (-) and t
281 We show here that inhibition of lysosomal acidification triggers cellular iron deficiency, which r
282 four common grazers under hypoxia and ocean acidification using short-term laboratory experiments an
283 a, resident in habitats subjected to coastal acidification, using high-resolution electron backscatte
284 enilin-1 (PSEN1) function causing AD impedes acidification via defective vacuolar ATPase (vATPase) V0
288 Using a mouse model of impaired lysosomal acidification, we observed a robust iron deficiency resp
290 us K(m) estimates based on substrate-induced acidification were severely biased by confounding pH-reg
291 e antioxidant defence system and rhizosphere acidification were up-regulated in Si and SA treatments
292 productivity can improve resistance to ocean acidification, whereas increasing productivity enhances
293 been known to cause transient intracellular acidification which, for reasons which have remained unc
294 and then accelerated with ocean warming and acidification (which increased per capita lethal grazing
295 2) is absorbed by oceans, resulting in ocean acidification, which is a threat to calcifying algae.
296 otency of MSA-2 increased upon extracellular acidification, which mimics the tumor microenvironment.
297 ing, increased dissolved carbon dioxide, and acidification will affect the distribution and relative
298 Because of findings that endolysosome de-acidification with, for example, the weak-base anti-mala
299 NaC is profoundly activated by extracellular acidification within biologically relevant ranges (pH 8.
300 Our findings of alkalinization, rather than acidification, within the cleft of two different neurona