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1 nd gamma, contribute to the formation of the epithelial Na+ channel.
2 bunits of the vertebrate amiloride-sensitive epithelial Na+ channel.
3 bunits of the vertebrate amiloride-sensitive epithelial Na+ channel.
4 is that ENaCs form a core conduction unit of epithelial Na+ channels.
5 m for examining the interactions of CFTR and epithelial Na+ channels.
6 ial cells in culture overexpressing CFTR and epithelial Na+ channels.
7 cation or activity but not the expression of epithelial Na(+) channel.
8 e and processing of the gamma isoform of the epithelial Na(+) channel.
9 he epithelial Na(+) channel (ENaC) family of epithelial Na(+) channels.
10 membrane conductance regulator regulation of epithelial Na(+) channel activity and an absence of expr
11 onductance regulator (CFTR) directly affects epithelial Na+ channel activity by co-incorporating into
14 arge part by increasing transcription of the epithelial Na(+) channel alpha-subunit (alpha-ENaC) expr
16 CFTR and either heterologously expressed rat epithelial Na+ channel ( alpha,b eta,gamma-rENaC) or an
18 which has loss-of-function mutations of the epithelial Na+ channel and an increased volume of airway
19 ,gamma-rENaCs form a core conduction unit of epithelial Na+ channels and that interaction of these ch
20 amiloride, an inhibitor of Na/H exchange and epithelial Na channels, and resuscitation with hypertoni
21 dinated regulation of (a) absorption, by the epithelial Na+ channel, and (b) secretion, by the Ca2+-a
25 ecific proteases have been shown to activate epithelial Na+ channels by cleaving channel subunits at
26 with the pore-forming 150-kDa subunit of an epithelial Na+ channel complex initially purified by Ben
27 n (INa2), with properties consistent with an epithelial Na+ channel current in some cells, and a calc
28 thway involving three factors: the degenerin/epithelial Na(+) channel (DEG/ENaC) class of mechanosens
29 ICs) are H(+)-gated members of the degenerin/epithelial Na(+) channel (DEG/ENaC) family in vertebrate
30 channel (BASIC) is a member of the degenerin/epithelial Na(+) channel (Deg/ENaC) family of ion channe
31 he mechanically gated depolarizing degenerin/epithelial Na+ channels (DEG/ENaC), but it inhibits two
32 hannels (ASICs), newly discovered members of epithelial Na+ channels/degenirin superfamily, are widel
34 As a pathway for Na(+) reabsorption, the epithelial Na(+) channel ENaC is critical for Na(+) home
36 eater expression of the alpha-subunit of the epithelial Na channel (ENaC) compared with age-matched c
37 ns of thiazide-sensitive NaCl cotransporter, epithelial Na channel (ENaC), aquaporin-2, ROMK, and NaK
42 erone-sensitive distal nephron downregulates epithelial Na(+) channel (ENaC) activity, we tested whet
43 orter (NCC), claudin-7, and cleaved forms of epithelial Na(+) channel (ENaC) alpha and gamma subunits
44 a(+) currents that depend on both the apical epithelial Na(+) channel (ENaC) and basolateral Na(+),K(
45 uptake of sodium via the amiloride-sensitive epithelial Na(+) channel (ENaC) and nonselective cyclic-
46 was consistent with Na(+) absorption by the epithelial Na(+) channel (ENaC) and was blocked by the E
48 quitin ligase that reduces expression of the epithelial Na(+) channel (ENaC) at the cell surface.
51 unction implications of loss of function for epithelial Na(+) channel (ENaC) containing a pseudohypoa
54 y overstimulation of the amiloride-sensitive epithelial Na(+) channel (ENaC) expressed by epithelial
56 he hypothesis that subunits of the mammalian epithelial Na(+) channel (ENaC) family are expressed in
57 ent whose characteristics match those of the epithelial Na(+) channel (ENaC) family of epithelial Na(
61 uggests that the extracellular domain of the epithelial Na(+) channel (ENaC) functions as a sensor th
62 acts in large part through induction of the epithelial Na(+) channel (ENaC) gene in the renal collec
67 anscriptional repression of alpha-subunit of epithelial Na(+) channel (ENaC) in lung and salivary epi
68 4-2) binds to and regulates stability of the epithelial Na(+) channel (ENaC) in salt-absorbing epithe
74 dosterone-sensitive distal nephron where the epithelial Na(+) channel (ENaC) is expressed, we hypothe
89 In the current study, domains within the epithelial Na(+) channel (ENaC) reactive at the plasma m
96 e if this apical entry step occurred via the epithelial Na(+) channel (ENaC), studies were performed
97 now demonstrate that WNK4 also inhibits the epithelial Na(+) channel (ENaC), the major mediator of a
98 d triggers Na(+) hyperabsorption through the epithelial Na(+) channel (ENaC), which contribute to red
99 elial clone 1 (SPLUNC1) effectively inhibits epithelial Na(+) channel (ENaC)-dependent Na(+) absorpti
112 e signature biophysical properties of cloned epithelial Na(+) channels (ENaC) (conductance, ion selec
113 cells, Na(+) crosses the apical membrane via epithelial Na(+) channels (ENaC) and is extruded into th
115 colonic Na(+) absorption is mediated by both epithelial Na(+) channels (ENaC) and Na-H exchangers (NH
117 vivo and the activity of amiloride-sensitive epithelial Na(+) channels (ENaC) by measuring AFC in mic
121 h Gi(alpha-3) and PIP(2) bind beta and gamma epithelial Na(+) channels (ENaC), but not alpha ENaC.
122 resent data that TI cells contain functional epithelial Na(+) channels (ENaC), pimozide-sensitive cat
129 ated that CFTR-dependent changes in apparent epithelial Na+ channel (ENaC) activity could be accounte
130 Airway epithelia absorb Na+ through the epithelial Na+ channel (ENaC) and secrete Cl- through th
133 paB kinase-beta (IKKbeta) interacts with the epithelial Na+ channel (ENaC) beta-subunit and enhances
136 ic tails of the mouse alpha, beta, and gamma epithelial Na+ channel (ENaC) important to protein-prote
137 We investigated purinergic regulation of the epithelial Na+ channel (ENaC) in mammalian collecting du
142 is hypertransport is that the activity of an epithelial Na+ channel (ENaC) is inversely related to th
147 enic hypertension caused by mutations in the epithelial Na+ channel (ENaC) that interfere with its ub
148 sor AMP-activated kinase (AMPK) inhibits the epithelial Na+ channel (ENaC) through decreased plasma m
149 s were infected in vivo for determination of epithelial Na+ channel (ENaC) total and cell surface pro
151 on is available regarding domains within the epithelial Na+ channel (ENaC) which participate in amilo
152 regulated genes--including that encoding the epithelial Na+ channel (ENaC), a key arbiter of Na+ tran
158 sensing ion channels (ASICs), members of the epithelial Na+ channel (ENaC)/degenerin (DEG) family of
159 eteromeric combinations of subunits from the epithelial Na+ channel (ENaC)/degenerin superfamily, whi
160 dd4L gene) regulates the amiloride-sensitive epithelial Na+ channel (ENaC/SCNN1) to mediate Na+ homeo
163 lement formed by the alpha-subunit of cloned epithelial Na+ channels (ENaC) was studied in planar lip
164 ms by which RSV inhibits amiloride-sensitive epithelial Na+ channels (ENaC), the main pathways throug
171 (+) absorption and Scnn1g mRNA (encoding the epithelial Na(+) channel ENaCgamma) expression through a
175 TS: A growing body of evidence suggests that epithelial Na(+) channels (ENaCs) in the brain play a si
177 lar fluid clearance because of inhibition of epithelial Na(+) channels (ENaCs) promotes cardiogenic l
187 e transient receptor potential and degenerin/epithelial Na+ channel families are likely to be transdu
188 e alphabetagamma trimer dramatically reduces epithelial Na(+) channel function and surface expression
189 rmine the subunit stoichiometry of the human epithelial Na+ channel (hENaC), we expressed the three w
190 Similarly, coexpression of KS-WNK1 and the epithelial Na(+) channel in Fischer rat thyroid epitheli
191 died the pharmacological responses of native epithelial Na(+) channels in human Clara cells and human
192 wing beta-adrenoceptor-mediated control over epithelial Na(+) channels in the apical plasma membrane.
195 ses in ASL height and MCC, via inhibition of epithelial Na(+)-channel-mediated Na(+) absorption and s
197 tain the alpha-, beta-, and gamma-rENaC (rat epithelial Na+ channels) mRNAs; reconstitution of an ATI
199 e vasopressin-sensitive, and actin-regulated epithelial Na+ channel of A6 cells, including a 6-7 pS s
200 sporter of the distal convoluted tubule, the epithelial Na+ channel of the collecting duct, and the b
201 lieved to be mediated by DEG/ENaC (degenerin/epithelial Na+ channel) proteins in nematodes and mammal
203 eotide-gated cation (pacemaker) channels nor epithelial Na+ channels, respectively, transduce sour ta
204 nopus oocytes with the three subunits of the epithelial Na+ channel results in a significantly enhanc
206 type 2 airway inflammation in juvenile beta-epithelial Na(+) channel (Scnn1b)-transgenic (Tg) mice.
207 a.AF9 complex represses transcription of the epithelial Na(+) channel subunit alpha (alpha-ENaC) gene
208 says showed that no activation of the -ENaC (epithelial Na+ channel -subunit) promoter was discernibl
212 -zipper protein and the alpha-subunit of the epithelial Na(+) channel, supporting impaired MR signali
213 mily that includes subunits of the mammalian epithelial Na+ channel, the Caenorhabditis elegans degen
214 ly up-regulated colonic H(+),K(+)-ATPase and epithelial Na(+) channel to mediate electrolyte and flui
217 in degradation of membrane proteins, such as epithelial Na(+) channel, we examined the effect of Nedd
219 conclude that PKGII is an activator of lung epithelial Na(+) channels, which may expedite the resolu
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