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1 ncentrations of dissolved carbon dioxide and carbonic acid (H(2)CO(3)).
2                                              Carbonic acid (H2CO3), highly unstable at ambient condit
3 hydrolytic process that generates protonated carbonic acid (PCA) as the precursor of CO2.
4 the general acid-assisted rate constants for carbonic acid and bicarbonate ion were estimated for the
5         It has been known for some time that carbonic acid can be separated from strong acids by ion
6 ot find evidence for centrosymmetric (C(2h)) carbonic acid dimers here.
7 -H2CO3 adds a new aspect to the chemistry of carbonic acid in astrophysical environments, especially
8  have succeeded in isolation of undecomposed carbonic acid in the matrix and recondensation after rem
9 molecules unambiguously reveal two different carbonic acid monomer conformers (C(2v) and C(s)).
10  fixed carbon includes respiratory CO(2) and carbonic acid that propagate to the base of the critical
11 Twenty years ago two different polymorphs of carbonic acid, alpha- and beta-H2CO3, were isolated as t
12 n potential generated by the dissociation of carbonic acid, colloidal particles move either away from
13 ticipates, on the basis of its aquation into carbonic acid, in hydrogen evolution.
14 bon dioxide system, previously identified as carbonic acid, was observed in the high-pressure diamond
15 ransition of bicarbonate into nondissociated carbonic acid, which reduces the total concentration of
16 n, despite partial equilibration of CO2 with carbonic acid-a low pKa acid.
17 c rate because of the accelerating effect of carbonic acid.
18 similar role through its prior conversion to carbonic acid.
19 alization by calcite slurry dissolution with carbonic and sulfuric acids.
20 ubiquitin (8.6 kDa), myoglobin (17 kDa), and carbonic anhydrase (29 kDa) upon higher energy collision
21    This study examined the effects of bovine carbonic anhydrase (BCA) and CO2-rich gas streams on the
22 y measuring the affinity of unlabeled bovine carbonic anhydrase (BCA) for a variety of ligands (most
23 g: ribonuclease (Rnase) A, myoglobin, bovine carbonic anhydrase (BCA) II, hemoglobin (Hb), and the he
24 cs of CO(2) hydration, we first measured the carbonic anhydrase (CA) activity of the bladder epitheli
25               The process employs the enzyme carbonic anhydrase (CA) as a catalyst to accelerate the
26 in interactions of these inhibitors into the carbonic anhydrase (CA) catalytic site, thus highlightin
27                                              Carbonic anhydrase (CA) catalyzes the first biochemical
28 intraocular pressure (IOP) by inhibiting the carbonic anhydrase (CA) enzyme to reduce aqueous humor p
29                                              Carbonic anhydrase (CA) enzymes catalyze the chemical eq
30                                              Carbonic anhydrase (CA) enzymes have gained considerable
31                                              Carbonic anhydrase (CA) enzymes, expressed at various si
32 hough many inhibitors are reported for human carbonic anhydrase (CA) enzymes, few may be considered u
33 ective inhibition of cancer-associated human carbonic anhydrase (CA) enzymes, specifically CA IX and
34 es, which act as effective inhibitors of the carbonic anhydrase (CA) from Trypanosoma cruzi (TcCA).
35 etic sequestration based on a self-propelled carbonic anhydrase (CA) functionalized micromotor.
36 , pepsin, maltose binding protein (MBP), and carbonic anhydrase (CA) in the presence of hundreds of n
37 : see text] Finally, we show that the enzyme carbonic anhydrase (CA) increases the dissolution rate a
38                           Prior studies with carbonic anhydrase (CA) inhibitors implicated mitochondr
39 g of the possibility of developing selective carbonic anhydrase (CA) inhibitors, interactions between
40                                              Carbonic anhydrase (CA) is one of nature's fastest enzym
41 itizing agent targeting the tumor-associated carbonic anhydrase (CA) isoforms IX and XII.
42 mplementary DNAs encoding four distinct beta-carbonic anhydrase (CA) isoforms were characterized from
43 ion profile against therapeutically relevant carbonic anhydrase (CA) zinc metalloenzymes.
44 eft protons: (1) generation by extracellular carbonic anhydrase (CA), (2) release from acidic synapti
45 hosphate carboxylase/oxygenase (RuBisCO) and carbonic anhydrase (CA), in an engineered protein cage b
46                                     However, carbonic anhydrase (CA), the enzyme that hydrolyses COS,
47 This enhancement was completely abolished in carbonic anhydrase (CA)-deficient antisense lines of bot
48  phosphoenolpyruvate carboxylase (PEPc), and carbonic anhydrase (CA).
49  hydrolyzed to H2 S by the ubiquitous enzyme carbonic anhydrase (CA).
50 iency only ~100-fold less than that of human carbonic anhydrase (CA)II and at least 550-fold better t
51                                       A beta-carbonic anhydrase (CA, EC 4.2.1.1) from the fungal path
52 cloned, purified, and characterized an alpha-carbonic anhydrase (CA, EC 4.2.1.1) from the human patho
53                                     An alpha-carbonic anhydrase (CA, EC 4.2.1.1) has been identified,
54 ized from three established aminosulfonamide carbonic anhydrase (CA, EC 4.2.1.1) inhibitor pharmacoph
55 nging to the underexposed sulfamate class of carbonic anhydrase (CA, EC 4.2.1.1) inhibitors was gener
56 rimary/secondary amines and COS as potential carbonic anhydrase (CA, EC 4.2.1.1) inhibitors, using th
57 4-sulfamoylphenyl-omega-aminoalkyl ethers as carbonic anhydrase (CA, EC 4.2.1.1) inhibitors.
58 arbamates (DTCs) were recently discovered as carbonic anhydrase (CA, EC 4.2.1.1) inhibitors.
59  constitute a novel class of mechanism-based carbonic anhydrase (CA, EC 4.2.1.1) inhibitors.
60 esulfonamide derivatives acting as effective carbonic anhydrase (CA, EC 4.2.1.1) inhibitors.
61 re thus obtained, which showed an increasing carbonic anhydrase (CA, EC 4.2.1.1) inhibitory action wi
62 ity/selectivity against the tumor associated carbonic anhydrase (CA, EC 4.2.1.1) isoforms hCA IX and
63 gent of Chagas disease, encodes for an alpha-carbonic anhydrase (CA, EC 4.2.1.1) possessing high cata
64                                       A beta-carbonic anhydrase (CA, EC 4.2.1.1) was cloned and chara
65 vant human (h) isoforms of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1).
66 d assayed as inhibitors of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1).
67  reported as inhibitors of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1).
68                                D8 features a carbonic anhydrase (CAH) fold that has evolved to bind t
69                  In this study, we show that carbonic anhydrase (Car) enzymes are up-regulated in typ
70            In the hippocampus, extracellular carbonic anhydrase (Car) speeds the buffering of an acti
71                                          The carbonic anhydrase (Cpb) from Clostridium perfringens st
72      Many microalgae induce an extracellular carbonic anhydrase (eCA), associated with the cell surfa
73 ndogenous metal affinity of Escherichia coli carbonic anhydrase (ECCA).
74 a subcomplex, containing the ancestral gamma-carbonic anhydrase (gamma-CA), gamma-carbonic anhydrase-
75 defined system of protein and ligands--human carbonic anhydrase (HCA) and a series of benzothiazole s
76 oldamer 2 was synthesized and bound to human carbonic anhydrase (HCA) using a nanomolar active site l
77 ss-coupling reactions and evaluated as human carbonic anhydrase (hCA, EC 4.2.1.1) inhibitors against
78 lly and pharmacologically relevant human (h) carbonic anhydrase (hCA, EC 4.2.1.1) isoforms, the cytos
79             This study uses mutants of human carbonic anhydrase (HCAII) to examine how changes in the
80         A panel of metalloenzymes, including carbonic anhydrase (hCAII), several matrix metalloprotei
81 Arg160His mutation of Haemophilus influenzae carbonic anhydrase (HICA), which mimics the endogenous m
82                      The murine inhibitor of carbonic anhydrase (mICA), a member of the transferrin (
83 from small molecules to proteins as large as carbonic anhydrase (molecular weight ca. 29,000).
84  beta-lactoglobulin (five peptides), 25% for carbonic anhydrase (six peptides), and 51% for bovine se
85 ed when buffering was augmented by exogenous carbonic anhydrase (XCAR).
86                             We characterized CARBONIC ANHYDRASE 1 (CAH1) as an essential component of
87 globin, Apolipoprotein E, Apolipoprotein A1, Carbonic anhydrase 1, and Hemoglobin subunit alpha upon
88  of plasma creatine kinase M-type (CK-M) and carbonic anhydrase 3 (CA-3) in the blood, more than 90%
89 s, anti-salivary gland protein 1 (SP1), anti-carbonic anhydrase 6 (CA6) and anti-parotid secretory pr
90 s, anti-salivary gland protein 1 (SP1), anti-carbonic anhydrase 6 (CA6) and parotid secretory protein
91 S-PLA2 (secreted phospholipase A2), and CA6 (carbonic anhydrase 6).
92                             Another protein, carbonic anhydrase 6, is initially imported normally int
93 ion of hypoxia-regulated genes (for example, carbonic anhydrase 9 (CA9) and vascular endothelial grow
94                           Immunostaining for carbonic anhydrase 9 (CAIX), reportedly an endogenous ma
95                                              Carbonic anhydrase activity emerges in the same region o
96 ations, photosynthetic attributes along with carbonic anhydrase activity whereas its higher concentra
97 cable for rapid and simple quantification of carbonic anhydrase activity which is very important to p
98  half-saturation constants for CO2 fixation, carbonic anhydrase activity, CO2 /HCO3 (-) uptake, delta
99  in zinc deficiency, probably due to reduced carbonic anhydrase activity, validated by quantitative p
100 ganic carbon species preference and external carbonic anhydrase activity.
101  by the Ag NPs with no discernible effect on carbonic anhydrase activity.
102 ng the rate constants of interaction between carbonic anhydrase and acetazolamide.
103 stem, using the well-defined model system of carbonic anhydrase and aryl sulfonamides.
104 is dependent on H(+) V-ATPase, together with carbonic anhydrase and five further transporters or chan
105 al hundred molecules of RuBisCO, and contain carbonic anhydrase and other accessory proteins.
106                                              Carbonic anhydrase and phosphoenolpyruvate carboxylase i
107 c carbon into the cell and colocalization of carbonic anhydrase and RuBisCO inside proteinaceous micr
108  CO2 better than any small molecule model of carbonic anhydrase and with an efficiency within 1400-fo
109 fically in a kappa(2)-fashion to the protein carbonic anhydrase as a ligand.
110 revisiae as the folding modulators and human carbonic anhydrase as a model protein, we demonstrate th
111             We demonstrate this system using carbonic anhydrase as the target and a library of 144,00
112                                              Carbonic anhydrase buffers tissue pH by catalyzing the r
113                             We find that the carbonic anhydrase CAH6 is in the flagella, not in the s
114 5-bisphosphate carboxylase/oxygenase and the carbonic anhydrase CcaA, whereas the C-terminal peptide
115                                              Carbonic anhydrase converts COS into H2S, allowing NTAs
116   For comparison we assayed recessive ca1ca4 carbonic anhydrase double mutant plants, based on their
117  recently isolated Arabidopsis thaliana beta-carbonic anhydrase double mutants (ca1 ca4) exhibit an i
118  Clostridium perfringens strain 13, the only carbonic anhydrase encoded in the genome, was characteri
119 eties were investigated as inhibitors of the carbonic anhydrase enzyme (CA; EC 4.2.1.1).
120                                              Carbonic anhydrase enzymes (CAs) catalyse the reversible
121  possible clinical benefits of inhibitors of carbonic anhydrase enzymes and the water channel Aquapor
122 onic anhydrase gene (ca19) beyond the single carbonic anhydrase gene (ca18) that was known previously
123                   We have identified a novel carbonic anhydrase gene (ca19) beyond the single carboni
124 LCI1, CCP1, CCP2 and LCIA) and mitochondrial carbonic anhydrase genes (CAH4 and CAH5) are up regulate
125 alysis and synteny studies suggest that both carbonic anhydrase genes form one or two independent gen
126                       Benzenesulfonamide and carbonic anhydrase have been chosen as the ligand and pr
127                                              Carbonic anhydrase I (Car1) is a gene expressed uniquely
128 ral stability and unfolding process of human carbonic anhydrase I (HCA-I).
129  Tryptic digestion of differentially labeled carbonic anhydrase I and hemoglobin allowed the identifi
130 ng these proteins, the strict association of carbonic anhydrase I and S100A8 with ECM was verified by
131 , human serum albumin, hemoglobin, and human carbonic anhydrase I were successfully labeled.
132 s, which was demonstrated by modification of carbonic anhydrase I with electrochemically generated re
133                                Expression of carbonic anhydrase I, glucosaminyl (N-acetyl) transferas
134  of residual mobility in complexes of bovine carbonic anhydrase II (BCA) and para-substituted benzene
135                 We present a new approach to carbonic anhydrase II (CA II) inhibitor design that enab
136 r binding affinity to the zinc metalloenzyme carbonic anhydrase II (CA II).
137  a fragment screening campaign against human carbonic anhydrase II (CA II).
138 ts to analyze the direct interaction between carbonic anhydrase II (CAII) and MCT1, MCT2, and MCT4, r
139 P1 has two acidic motifs homologous to known carbonic anhydrase II (CAII) binding sequences.
140            In nature, the zinc metalloenzyme carbonic anhydrase II (CAII) efficiently catalyzes the c
141 f MCT1 and MCT4 is enhanced by the cytosolic carbonic anhydrase II (CAII) independent of its catalyti
142                                              Carbonic anhydrase II (CAII)(Cre);Pdx1(Fl) mice were eug
143                   TFGs containing CB[6]- and carbonic anhydrase II (CAII)-binding domains were synthe
144                                        Human carbonic anhydrase II (HCA II) uses a Zn-bound OH(-)/H2O
145                            Variants of human carbonic anhydrase II (HCA II) with amino acid replaceme
146 onic acid, TPMA) to the active site of human carbonic anhydrase II (hCAII) has been investigated.
147 ione (1,2-HOPTO) in the active site of human carbonic anhydrase II (hCAII) has been investigated.
148 e corresponding inhibitor complexes of human carbonic anhydrase II (HCAII) indicated that HpalphaCA p
149         The binding of sulfonamides to human carbonic anhydrase II (hCAII) is a complex and long-deba
150 nvestigation of the CD spectrum of the Human Carbonic Anhydrase II (HCAII), with main focus on the ne
151  This paper uses the binding pocket of human carbonic anhydrase II (HCAII, EC 4.2.1.1) as a tool to e
152             We have reported previously that carbonic anhydrase II augments transport activity of MCT
153 res rapid conversion between CO2 and HCO3(-) Carbonic anhydrase II facilitates this reversible reacti
154  K, tartrate-resistant acid phosphatase, and carbonic anhydrase II in bone marrow macrophages (BMMs),
155         Deprotonation of zinc-bound water in carbonic anhydrase II is the rate-limiting step in the c
156 lls arise mainly from extrainsular PDX-1(+), carbonic anhydrase II(-) (mature ductal), elastase 3a (a
157 three proteins (ubiquitin, cytochrome c, and carbonic anhydrase II) were investigated.
158 of the selected scFvs was shown to recognize carbonic anhydrase II, an up-regulated enzyme involved i
159 rker tartrate-resistant acid phosphatase, or carbonic anhydrase II.
160 lated known genes, whereas Srpx2, Cd200, and carbonic anhydrase III (CAIII) were identified as novel
161                                              Carbonic anhydrase III protects osteocytes from oxidativ
162     Carbonic anhydrase XII (CA12) is the key carbonic anhydrase in epithelial fluid and HCO3 (-) secr
163 e-1,5-bisphosphate carboxylase/oxygenase and carbonic anhydrase in the microcompartment shell.
164 roportion of Rubisco and the thylakoid lumen carbonic anhydrase in the pyrenoid rose substantially, c
165                         MTZ is known to be a carbonic anhydrase inhibitor (CAI); however, CAIs acetaz
166 ich was sensitive to Na(+)withdrawal, to the carbonic anhydrase inhibitor acetazolamide and to H2DIDS
167 tment of B. pertussis-infected mice with the carbonic anhydrase inhibitor acetazolamide reduced lung
168                Given methazolamide, a potent carbonic anhydrase inhibitor, can penetrate the blood-br
169 icarbonate co-transporter (P </= 0.0001) and carbonic anhydrase inhibitors (P = 0.0021).
170                       Azide derivatives of 2 carbonic anhydrase inhibitors, 4-(2-aminoethyl)benzenesu
171 In this connection, we report a new class of carbonic anhydrase inhibitors, based on the thiopyrano-f
172 ation, use of topical beta blockers, topical carbonic anhydrase inhibitors, daily dose of BAK, and gl
173   Other glaucoma medications (beta blockers, carbonic anhydrase inhibitors, parasympathomimetics, and
174  the dye were more potent agents with higher carbonic anhydrase inhibitory action than the parent dye
175 ished nitrite bioactivation, but the role of carbonic anhydrase is abrogated when physiological conce
176  was also observed, in line with patterns of carbonic anhydrase isoform expression in those tissues.
177 vatives have been developed as inhibitors of carbonic anhydrase isoform IX.
178 n efficiency within 1400-fold of the fastest carbonic anhydrase isoform, CAII, and 11-fold of CAIII.
179                                While several carbonic anhydrase isoforms have been identified in nume
180 luated as inhibitors of the ubiquitous human carbonic anhydrase isoforms I, II, IX, XII, and XIV usin
181 t that the human genome encodes 15 different carbonic anhydrase isoforms that have a high degree of h
182 rs (encoded by Slc26a4, Slc4a8, and Slc4a9), carbonic anhydrase isoforms, and V-type H(+)-ATPase subu
183 ed for the inhibition of some selected human carbonic anhydrase isoforms.
184 -the-haystack" screen for inhibitors against carbonic anhydrase isozyme II is performed, in which kno
185                                              Carbonic anhydrase IV (Car4) was a top dysregulated gene
186                                              Carbonic anhydrase IX (CA IX) is a target for hypoxic ca
187                                              Carbonic anhydrase IX (CA IX) is a transmembrane protein
188                                              Carbonic anhydrase IX (CA IX) is an extracellular transm
189                                        Human carbonic anhydrase IX (CA IX) is highly expressed in tum
190                                        Human carbonic anhydrase IX (CA IX) is overexpressed in a numb
191 n of hypoxic tumors is possible by targeting carbonic anhydrase IX (CA IX), an enzyme overexpressed i
192                                              Carbonic anhydrase IX (CA-IX) is upregulated in cancer i
193                                              Carbonic anhydrase IX (CA-IX), a transmembrane enzyme, m
194                                              Carbonic anhydrase IX (CA9) is a transmembrane glycoprot
195  of tumor hypoxia is activated expression of carbonic anhydrase IX (CA9), a regulator of pH and tumor
196 chemical technique, using antibodies against carbonic anhydrase IX (CAIX) and copper pumps (Ctr1 and
197 body-mediated therapy with the chimeric anti-carbonic anhydrase IX (CAIX) antibody girentuximab (cG25
198 t vascularization and acid-extruding protein carbonic anhydrase IX (CAIX) expression.
199                            It was induced by carbonic anhydrase IX (CAIX) overexpression and inhibite
200 MCT4 remained unchanged, while expression of carbonic anhydrase IX (CAIX) was greatly enhanced.
201 CC tumors, which also express high levels of carbonic anhydrase IX (CAIX), a HIF1-dependent protein.
202 o facilitate the intraoperative detection of carbonic anhydrase IX (CAIX)-expressing tumor lesions wi
203                                              Carbonic anhydrase IX (CAIX, CA9) expression is highly u
204                          Inhibition of human carbonic anhydrase IX (hCA IX) has shown to be therapeut
205 armacodynamics from tumor biomarkers such as carbonic anhydrase IX and topoisomerase I by immunohisto
206  beta-catenin) and function (aquaporin 1 and carbonic anhydrase IX).
207 is a chimeric monoclonal antibody that binds carbonic anhydrase IX, a cell surface glycoprotein ubiqu
208 escribed a novel acetazolamide derivative, a carbonic anhydrase ligand with high affinity for the tum
209         We find that expression of the Cd/Zn carbonic anhydrase makes no difference to the Cd isotope
210                                              Carbonic anhydrase members in this class of exofacial mo
211                                        alpha-Carbonic anhydrase of Helicobacter pylori (HpalphaCA) pl
212                                              Carbonic anhydrase plays a key role in CO2 transport, ac
213  of incubation at 750 microatm pCO2, reduced carbonic anhydrase protein activity and shell growth occ
214          Moreover, kinetic analysis of human carbonic anhydrase refolding showed that 6AP decreased t
215  1,5-bisphosphate carboxylase/ oxygenase and carbonic anhydrase to facilitate carbon fixation in cyan
216                                Intracellular carbonic anhydrase transcript abundance increased with t
217 68 and mannose receptor-positive, expressing carbonic anhydrase type II, but relatively low levels of
218                                              Carbonic anhydrase VA (CA-VA) was absent in liver in the
219 lective inhibitors of five isoforms of human carbonic anhydrase was also explored.
220                   The reactions of apo human carbonic anhydrase with [Rh(nbd)2]BF4 or [M(CO)2(acac)]
221 robenzoarylsulfonamide ligands bind to human carbonic anhydrase with a conserved binding geometry, an
222                                              Carbonic anhydrase XII (CA XII) is a membrane-tethered c
223                                              Carbonic anhydrase XII (CA12) is the key carbonic anhydr
224 n of one specific gene in the FLC signature, carbonic anhydrase XII (CA12), at the protein level by w
225   Here we describe variants in CA12 encoding carbonic anhydrase XII in two pedigrees exhibiting CF-li
226                                   Panning on carbonic anhydrase yielded a potent ligand, sulfonamide-
227 ditions we find dorzolamide (an inhibitor of carbonic anhydrase) results in diminished nitrite bioact
228    This paper describes a synthetic dimer of carbonic anhydrase, and a series of bivalent sulfonamide
229               Ion channels and transporters, carbonic anhydrase, and aquaporins were abundantly expre
230 BisCO reaction, staying below saturation for carbonic anhydrase, and avoiding wasteful oxygenation re
231                Assays for actin, AMP-kinase, carbonic anhydrase, and lysozyme are shown to demonstrat
232 genes including: green fluorescent proteins, carbonic anhydrase, and oxidative stress proteins; and f
233 ncorporating 6- and 7-substituted coumarins (carbonic anhydrase, CA inhibitors) derivatized with clin
234 en alga Chlamydomonas reinhardtii, a luminal carbonic anhydrase, CrCAH3, was suggested to improve pro
235  H(+)-extrusion mechanisms and extracellular carbonic anhydrase, is responsible for active transport-
236 ient CO2 We identified CAH1 as an alpha-type carbonic anhydrase, providing a biochemical role in CCM
237 aria susceptibility in the murine model, and carbonic anhydrase, reflecting the blood's abnormal acid
238 showed reduced expression of colonic villin, carbonic anhydrase, secretory mucin muc2, and increased
239 e, biotin, mannose) against matched targets (carbonic anhydrase, streptavidin, concanavalin A) to ide
240        Carbon acquisition enzymes, primarily carbonic anhydrase, stress, degradation and signaling pr
241 ely conserved proteins containing domains of carbonic anhydrase, Sushi, Von Willebrand factor type A,
242 cyclen, a small molecule mimic of the enzyme carbonic anhydrase, was evaluated under rigorous conditi
243 died: ribonuclease A, trypsin inhibitor, and carbonic anhydrase, where the latter had impurities of s
244 on of NP markers FoxF1, Pax-1, keratin-8/18, carbonic anhydrase-12, and NC markers brachyury, galecti
245 glycoprotein hormone luteinizing hormone and carbonic anhydrase-6 (CA6).
246 r than for a DMSO-free sample in the case of carbonic anhydrase-chlorothiazide binding.
247 , in particular for the tight binding system carbonic anhydrase-chlorothiazide.
248 lysozyme-tri-N-acetylchitotriose (NAG3), and carbonic anhydrase-chlorothiazide.
249 ty to CO(2), native extra- and intracellular carbonic anhydrase-like activities, the non-CO(2)/HCO(3)
250 l gamma-carbonic anhydrase (gamma-CA), gamma-carbonic anhydrase-like, and 20.9-kDa subunits, had a si
251 munoisolated from mouse brain, we identified carbonic anhydrase-related proteins CA10 and CA11, two h
252  determines enzyme activity of chloroplastic carbonic anhydrase.
253 ts reveal that the pH gradient is created by carbonic anhydrase.
254 iochemical function for Cd, an unusual Cd/Zn carbonic anhydrase.
255 luding human serum albumin, beta-casein, and carbonic anhydrase.
256 e 1,5-bisphosphate carboxylase/oxygenase and carbonic anhydrase.
257 - by first converting it to CO2 via external carbonic anhydrase.
258 cy to be competitive with the native enzyme, carbonic anhydrase.
259 ed urea channel, UreI; and periplasmic alpha-carbonic anhydrase.
260 onstants for proton transfer in catalysis by carbonic anhydrase.
261 ription of the urease gene cluster and alpha-carbonic anhydrase.
262 ly converted to H2S by the ubiquitous enzyme carbonic anhydrase.
263 ulfide, which is rapidly converted to H2S by carbonic anhydrase.
264 osphate carboxylase/oxygenase (RuBisCO) with carbonic anhydrase.
265 ivity which is very important to prevent the carbonic-anhydrase-associated disorders in human.
266 ing atmospheric CO2 elevation, including the carbonic-anhydrase-encoding genes CA1 and CA4 and the se
267            We examined mechanisms regulating CARBONIC ANHYDRASE4 (CA4) in C4 Gynandropsis gynandra.
268 consist of inorganic carbon transporters and carbonic anhydrases (and other supporting components) th
269 ged from the immunohistochemical analysis of carbonic anhydrases (CA) IX and XII expression in thyroi
270                                              Carbonic anhydrases (CA), which catalyze the reversible
271                                 Two putative carbonic anhydrases (CAs) are encoded in the genome of C
272 on between different Ci species catalyzed by carbonic anhydrases (CAs) are key components in the CCM,
273                            Soluble cytosolic carbonic anhydrases (CAs) are well known to participate
274 mechanisms (CCMs) involving transporters and carbonic anhydrases (CAs) are well known, but the contri
275                                              Carbonic anhydrases (CAs) are zinc metalloenzymes that c
276                                              Carbonic anhydrases (CAs) are zinc metalloenzymes that i
277                                              Carbonic anhydrases (CAs) catalyze the hydration of CO(2
278                                              Carbonic anhydrases (CAs) comprise a family of zinc-cont
279 cotransporter, suggesting that inhibition of carbonic anhydrases (CAs) confers the beneficial thiazid
280 version between CO2 and HCO3(-) catalyzed by carbonic anhydrases (CAs), and active inorganic carbon (
281  HCO3 (-) availability that is determined by carbonic anhydrases (CAs).
282                                              Carbonic anhydrases (CAs, EC 4.2.1.1) are ubiquitous iso
283 ent inhibitors of the tumor-associated human carbonic anhydrases (hCAs) IX and XII.
284  against four physiologically relevant human carbonic anhydrases (hCAs, EC 4.2.1.1), isoforms hCA I,
285 tified in key C4 metabolism genes, including carbonic anhydrases and a malate transporter.
286 esults suggest that intra- and extracellular carbonic anhydrases can work in concert to ensure rapid
287 we investigate the repertoire of cytoplasmic carbonic anhydrases in the sea lamprey (Petromyzon marin
288    Contrastingly, transcripts of chloroplast carbonic anhydrases namely CAH6, CAH3 and LCIB are up re
289                            Overexpression of carbonic anhydrases on cell surfaces further contributes
290 rey metamorphosis resulting in distinct gill carbonic anhydrases reflecting the contrasting life mode
291 ctive inorganic carbon transport components, carbonic anhydrases, and aggregation of Rubisco in the c
292                    The presence of cytosolic carbonic anhydrases, the basolateral Na(+) bicarbonate c
293 larly sodium bicarbonate co-transporters and carbonic anhydrases, which were also expressed in LAM lu
294 eature not previously observed in alpha-type carbonic anhydrases.
295 on of CO2-controlled stomatal development by carbonic anhydrases.
296 isotopic fractionation reaction regulated by carbonic anydrase (CA) metalloenzyme.
297 ogic markers of tumor hypoxia (pimonidazole, carbonic anydrase 9 [CA9]) and vascular perfusion (Hoech
298 ophobic interactions between the analyte and carbonic chain of surfactant, the retention of cationic
299 odelling daily anthocyanin extraction during carbonic maceration, particularly from the sixth day.
300 lp of Gamay winegrapes during twelve days of carbonic maceration.

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