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1 ylyl cyclase is responsive to both CO(2) and bicarbonate ion.
2 hanism by which diverse organisms can detect bicarbonate ion.
3 lectron density that we believe represents a bicarbonate ion.
4 th's carbon cycle, we focus on carbonate and bicarbonate ions.
5 orm of solid carbonate minerals or dissolved bicarbonate ions.
6 lin stimulation and is uniquely modulated by bicarbonate ions.
7 cal species such as hydroxide, carbonate and bicarbonate ions.
8 G proteins, and its activity is regulated by bicarbonate ions.
9 tely alkaline solutions rich in carbonate or bicarbonate ions.
10 d drop in oxygen affinity in the presence of bicarbonate ions.
11 nd innocuous carbonate minerals or dissolved bicarbonate ions(3,6,7).
12                  However, in the presence of bicarbonate ions, a significantly higher photoreduction
13 gulates the active transport of chloride and bicarbonate ions across membranes.
14                                              Bicarbonate ions activated both sAC forms and increased
15 fer via a carbocation mechanism in which the bicarbonate ion acts as a general base.
16 pH recovery was dependent on the presence of bicarbonate ion and was blocked by the addition of the e
17 ngle components of pancreatic juice, such as bicarbonate ions and calcium carbonate crystals, induce
18 ium, sodium, chloride, calcium, hydrogen and bicarbonate ions and carbon dioxide across an ischemic b
19 he gas-particle partitioning of pH buffering bicarbonate ions and carbon dioxide is a significant fac
20  water (NBIW) bathing enhances blood flow by bicarbonate ions and described the underlying mechanism.
21 ermeability of the GABAA chloride channel to bicarbonate ions and NMDA receptor activation do not med
22 der removes atmospheric CO(2) in the form of bicarbonate ions and secondary carbonates.
23  reveal the precise interactions between two bicarbonate ions and the crocodilian protein at symmetry
24       sAC activity is uniquely stimulated by bicarbonate ions, and in cells, sAC functions as a physi
25 ations, the latter of which is stabilized by bicarbonate ion binding to a non-catalytic site.
26 F) is caused by a nonfunctional chloride and bicarbonate ion channel (CF transmembrane regulator [CFT
27               Previous work indicates that a bicarbonate ion does not bind reversibly close to the OE
28 catalyst that was specifically stimulated by bicarbonate ion (EC50 9.6 mm).
29 nterface, while the remaining 10 chains bind bicarbonate ion exclusively at the allosteric site.
30 two of 12 chains in the asymmetric unit bind bicarbonate ion exclusively at the dimerization interfac
31 the hydration of CO2 to generate protons and bicarbonate ions for cellular ion transport and pH homeo
32 that the overlayers suppress HER by blocking bicarbonate ions from reaching the buried active sites.
33 e OEC, which would release any tightly bound bicarbonate ions from the active site, and mass spectrom
34 n a further set of experiments by removal of bicarbonate ions from the perfusate at this point, which
35 ces the second messenger cAMP in response to bicarbonate ions (HCO(3)(-)).
36 bonic anhydrase 4 catalyzes the formation of bicarbonate ions (HCO[Formula: see text]), for accumulat
37  (W39F and Y181F) involved in the binding of bicarbonate ion in the non-catalytic site and an active-
38 results strongly argue against tightly bound bicarbonate ions in the OEC.
39 we show that a uniform local distribution of bicarbonate ions increases the accessibility of reverted
40 serendipitously found to bind sulfate ion or bicarbonate ion near pairs of Glu50 and Arg64 residues l
41 esses, we have chosen as an example hydrogen-bicarbonate ion pair diffusion within the mammalian corn
42    The diffusion coefficient of the hydrogen-bicarbonate ion pair in corneal stroma and epithelium is
43 s C, a diffusion coefficient of the hydrogen-bicarbonate ion pair of 2.5 x 10(-6) cm2/s in the stroma
44 ults suggested that phosphate, ammonium, and bicarbonate ions reduced hydroxyl radical availability,
45 ped into this extracellular compartment, one bicarbonate ion remains in the cytoplasm.
46 f Hb-O(2) affinity via allosteric binding of bicarbonate ions represents a croc-specific innovation t
47                    In the case of HICA-V47A, bicarbonate ions simultaneously bind to both the dimeriz
48                                              Bicarbonate ions stabilize the clusters and even promote
49 lance of nutrient precursors of hydrogen and bicarbonate ions that induces a lifelong, low-grade, pat
50  protein that is regulated by the binding of bicarbonate ion to a non-catalytic (inhibitory) site tha
51 ediate along the ingress and egress route of bicarbonate ion to and from the allosteric binding site,
52 ssisted rate constants for carbonic acid and bicarbonate ion were estimated for the monochloramine re