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1 (pCa unit)-1, (about 250 times less than for hydrogen ions).
2 d enzymes that convert endogenous glucose to hydrogen ion.
3 d with a linked function model involving the hydrogen ion.
4 ted by the reversible transfer of oxygen and hydrogen ions.
5 the response of sensory afferent neurons to hydrogen ions.
6 attempt to restore the effect of lactate and hydrogen ions.
7 ch can dramatically suppress the detrimental hydrogen ions.
8 eractions, particularly between sulphate and hydrogen ions.
9 ional to block the production of lactate and hydrogen ions.
10 the alginate beads; prompting the release of hydrogen ions.
11 to the transfer of electrons from NAD(P)H to hydrogen ions.
12 ed autocatalytic production and diffusion of hydrogen ions.
13 enium(II), tetramethylammonium, ferrous, and hydrogen ions.
14 dissociate to form an ammonia molecule and a hydrogen ion (a proton), which then pass through the cel
18 est was used to estimate correlation between hydrogen ion and individual cytokine concentrations.
19 first detected herein to react with several hydrogen ions and electrons for the formation of CH3OH.
20 ctive filaments through interactions between hydrogen ions and photogenerated electrons within the en
21 atory responses to osmotic stress; and (iii) hydrogen-ion and charge imbalance underlie transcription
22 tory control of sodium, potassium, chloride, hydrogen ion, and water homeostasis through its effects
23 With the Stewart approach bicarbonate and hydrogen ions are dependent variables that represent the
26 This is explained by the local depletion of hydrogen ions at the sample-membrane interface as a resu
27 shown to correlate with the basicity of the hydrogen ion carrier doped within the membrane phase.
29 zaldehyde acetals, PhCH(OR)(2), are specific hydrogen-ion catalyzed when R = methyl, n-butyl, but wit
30 extracellular sodium ions for intracellular hydrogen ions, causing a release of hydrogen ions at the
31 ormer system functions according to an anion-hydrogen ion coextraction mechanism and shows a Hofmeist
32 anges in partial pressure of CO(2) (pCO(2)), hydrogen ion concentration ([H(+)]), pH, aragonite satur
33 An inverse relationship was found between hydrogen ion concentration and concentrations of tumor n
34 d to determine if changes in gastric mucosal hydrogen ion concentration are associated with liver and
37 simulated for oxygenation or oxygenation and hydrogen ion concentration together performed worse than
38 hermore, an increase in gastric intramucosal hydrogen ion concentration was associated with a concomi
40 ecies also allows an in situ estimate of the hydrogen ion concentration, or pCH(+) values, of the rea
41 group was increased by raising the external hydrogen ion concentration, responses became outward rec
43 stants of these arsenic species in different hydrogen ions concentration leading to the arsine format
44 generally enhanced at low pH in the range of hydrogen ion concentrations found in the endosomal compa
45 nge in leukotriene B4, hydrogen peroxide, or hydrogen ion concentrations in exhaled breath condensate
47 solution as a function of the dihydrogen and hydrogen ion concentrations through direct measurement o
49 imited by uncertainties in synaptic zinc and hydrogen ion concentrations, both of these being known t
53 esent DR studies of the deuterated triatomic hydrogen ion D(2)H(+), where the molecular ions were sto
54 that in organic media through exploiting the hydrogen ion dependence for the equilibrium distribution
55 at Lake occurred between 1920 and 1930, when hydrogen ion deposition was approximately 74 eq ha(-1) y
56 state at elevated temperatures, in which the hydrogen ions diffuse through a stable sublattice that i
58 ction method for directly measuring released hydrogen ions during nucleotide incorporation rather tha
60 ariants in CLCN4, which encodes the chloride/hydrogen ion exchanger CIC-4 prominently expressed in br
61 observe wedge-like dispersion structures of hydrogen ions exhibiting butterfly-shaped distributions
63 anistic target of rapamycin activity and net hydrogen ion exporters, particularly sodium bicarbonate
64 to be depleted owing to the constant imposed hydrogen ion flux from the membrane, and a local pH chan
65 t deuterium isotope effects originating from hydrogen ion fractionation at multiple sites on the enzy
67 e same sensor by imposing an outward flux of hydrogen ions from an ion-selective membrane to the samp
68 is determined by imposing a defined flux of hydrogen ions from the membrane to the sample with an ap
70 he events of capturing and emitting a single hydrogen ion (H(+)) at the solid/liquid interface are di
73 cle fatigue and inorganic phosphate (Pi) and hydrogen ions (H(+)) in women and men, and (2) whether t
74 cle fatigue and inorganic phosphate (Pi) and hydrogen ions (H(+)) in women and men, and (2) whether t
75 ghly conserved process to transfer cytosolic hydrogen ions (H+) across plasma membranes in exchange f
76 aracteristics of emission from the triatomic hydrogen ion H3+ are key to understanding the auroral en
81 nvolves the net generation or consumption of hydrogen ions in aqueous solutions over the pH range of
82 s exist about the role played by lactate and hydrogen ions in evoking the exercise pressor reflex.
83 exaggerated the concentration of lactate and hydrogen ions in pygm(+/+) but not in pygm(-/-) rats.
84 on elevated the concentration of lactate and hydrogen ions in pygm(+/+) but not in pygm(-/-) rats.
85 r their reactions, changes in the binding of hydrogen ions in these reactions, and standard apparent
86 g the insertion and extraction of oxygen and hydrogen ions independently of each other can direct rev
87 oenvironment; consisting of oxygen, glucose, hydrogen ions, inhibitory factors and growth factors.
88 The carbonate ion is extracted together with hydrogen ions into a polymeric film that contains the an
94 s, indicating a higher concentration of free hydrogen ions near the extracellular surface of the cell
98 ormation of these two products resulted from hydrogen ion or hydride transfer from C1' and C5' positi
99 5-MF for dsDNA was attributed to the ease of hydrogen ion (or hydride transfer) from the C5' compared
100 aicin, the potent vanilloid resiniferatoxin, hydrogen ions (pH 6.2), or noxious thermal stimuli (50 d
103 me, and they suggest that factors other than hydrogen ion production during ischemia are responsible
104 ia, contraction increased muscle lactate and hydrogen ion production in pygm(+/+) rats (P < 0.0134),
108 , the high activity of the anatase phase for hydrogen ion reduction when compared to that of the ruti
110 r findings argue against the hypothesis that hydrogen ions released by horizontal cells normally act
113 r H+-ATPases have an essential role in renal hydrogen ion secretion in the proximal tubule, collectin
114 etermination of the degree of protonation of hydrogen ion-selective chromoionophores incorporated int
115 surfactants on the EMF response function of hydrogen ion-selective polymeric membrane electrodes are
116 e sample phase on the response properties of hydrogen ion-selective polymeric membrane electrodes con
117 O3), although associations with sulfates and hydrogen ion suggest a possible role by fine particles a
118 elective electrode containing a receptor for hydrogen ions that provided a favorable selectivity for
119 are impermeable to atoms and molecules, but hydrogen ions (thermal protons) penetrate through them.
121 us 100 muM formic acid to provide sufficient hydrogen ions to ionize the protein without dislodging m
125 he concentrations of calcium, phosphate, and hydrogen ions were also determined in the same solutions
126 Enteral feeding stimulates the secretion of hydrogen ions, which are then buffered by ionized bicarb
128 tor was used to image high concentrations of hydrogen ions, which were generated in the electrooxidat
129 ning species that result from replacement of hydrogen ions with sodium or potassium ions at multiple