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1  to the human colonic T84 epithelial cell Na-K-Cl cotransporter.
2 that it would be distantly related to the Na-K-Cl cotransporter.
3 o examine the effect on O2 dependency of the K+-Cl- cotransporter.
4 rter, and NKCC, the chloride accumulator Na+-K+-Cl- cotransporter.
5 nd increased gene expression of NKCC1--a Na+-K+-Cl- cotransporter.
6 ial homology to KCC2, the mammalian neuronal K(+)-Cl(-) cotransporter.
7 been suggested that the electroneutral Na(+)-K(+)-Cl(-) cotransporter 1 (NKCC1) can play a role in gl
8                                    The Na(+)-K(+)-Cl(-) cotransporter 1 (NKCC1) is particularly relev
9       Alternatively, inhibition of the Na(+)-K(+)-Cl(-) cotransporter 1 (NKCC1), a Cl(-) importer exp
10  is accompanied by down-regulation of the Na-K-Cl cotransporter 1 (Nkcc1) and the Ca(2+)-activated an
11 t colonic basolateral membrane suggests that K-Cl cotransporter: 1) is involved in transepithelial po
12      The VP neurons lacked expression of the K(+)-Cl(-) cotransporter 2 (KCC2), the predominant Cl(-)
13 he Na(+)-K(+)-2Cl(-) cotransporter 1 and the K(+)-Cl(-) cotransporter 2 (KCC2).
14                                              K(+)/Cl(-) cotransporter 2 (KCC2) is selectively express
15                            Expression of the K+Cl- cotransporter 2 (KCC2) also increased across these
16  evidence indicates that the neuron-specific K-Cl cotransporter 2 (KCC2) is the major chloride extrus
17 and GABA(A) receptor alpha1 subunit, but not K-Cl cotransporter 2, are colocalized at the presumed po
18 a(+)-K(+)-2Cl(-) cotransporter-1 (NKCC1) and K(+)-Cl(-) cotransporter-2 (KCC2), critically influence
19 n the absence of water transport through the K(+)-Cl(-) cotransporter, a large osmotic gradient build
20 d with a monoclonal antibody to mammalian Na-K-Cl cotransporter and a fluorescent secondary antibody
21 mportant new insights into the regulation of K-Cl cotransporters and provides in vivo evidence that i
22 +)/Pi co-transporter 2, phosphorylated Na(+)/K(+)/Cl(-) cotransporter, and phosphorylated Na(+)/Cl(-)
23 sion patterns of KCC2, the chloride extruder K+-Cl- cotransporter, and NKCC, the chloride accumulator
24  P (sickle), Ca 2+ -sensitive K channel, and K:Cl cotransporter, and of therapies targeted at these t
25  in using bumetanide, a chloride importer Na-K-Cl cotransporter antagonist, for treatment of neurolog
26                           Electroneutral Na-(K)-Cl cotransporters are present in most cell types, whe
27                                       The Na-K-Cl cotransporters are a class of ion transport protein
28 n chloride cotransporters, e.g. Na-K-2Cl and K-Cl cotransporters, are activated to maintain fluid/ion
29                            Regulation of the K+-Cl- cotransporter by O2 is very similar in equine, sh
30                   Expression of NKCC1, an Na-K-Cl cotransporter characteristic for ductal epithelia,
31 the expected functional characteristics of a K+Cl- cotransporter: Cl--dependent uptake of 86Rb+ which
32   Here we review what is known about the Na-(K)-Cl cotransporters cloned to date and what can be dedu
33 ced monoclonal antibody (T4) specific for Na-K-Cl cotransporter displays the same localization.
34 ing the chloride gradient by blocking the Na-K-Cl cotransporter eliminated responses to light moving
35                                       Two Na-K-Cl cotransporters encoded by different genes have been
36                    KCC2 is a neuron-specific K(+)-Cl(-) cotransporter essential for establishing the
37                                           Na-K-Cl cotransporter fluorescence patterns showed more var
38 ve no effect on total KCC2 protein level and K-Cl cotransporter function.
39                    The other members of this K(+)-Cl(-) cotransporter gene family are exclusively swe
40 KCC2 is the neuron-specific member of the of K(+)-Cl(-) cotransporter gene family.
41                                        Na(+)-K(+)-Cl(-) cotransporter has been proposed to play an im
42  mutations that reduce the level of the sole K+/Cl- cotransporter in the fruitfly Drosophila melanoga
43 m tight junctions supports a role for the Na-K-Cl cotransporter in ciliary epithelium as a chloride e
44 dertaken to determine the location of the Na-K-Cl cotransporter in fixed sections of bovine eye.
45 assing a total of seven Na-Cl, Na-K-2Cl, and K-Cl cotransporters, in addition to two related transpor
46                      The pharmacology of the K-Cl cotransporter is dominated by loop diuretics such a
47 t the behavior of the endogenous HEK cell Na-K-Cl cotransporter is unlike either of the two forms whi
48 that pharmacological inhibition of the Na(+)-K(+)-Cl(-) cotransporter isoform 1 (NKCC1) during ischem
49 , which inhibit Cl- influx through the Na(+)-K(+)-Cl- cotransporter isoform-1 (NKCC-1) and efflux thr
50 er isoform-1 (NKCC-1) and efflux through the K(+)-Cl- cotransporter isoform-2, were unable to inhibit
51 2 is 67% identical to the widely distributed K-Cl cotransporter isoform (KCC1) identified in rat brai
52 ary screening, we have identified a putative K-Cl cotransporter isoform (KCC2) in rat brain that is s
53 at cation-dependent Cl- transport protein Na-K-Cl cotransporter isoform 1 (NKCC1) plays a role in the
54                                           Na-K-Cl cotransporter isoform 1 (NKCC1) plays an important
55                              To date, two Na-K-Cl cotransporter isoforms have been identified: NKCC1,
56 o includes Na-Cl cotransporters and multiple K-Cl cotransporter isoforms.
57          While animals lacking ABTS-1 or the K(+)-Cl(-) cotransporter KCC-2 display only mild behavio
58 ed K(+) channel (the Gardos channel) and the K(+)-Cl(-) cotransporter (KCC) - it would have a synergi
59                                          The K(+):Cl(-) cotransporter (KCC) activity is modulated by
60 ects of CDNB (1 mM) on the activities of the K+-Cl- cotransporter (KCC; measured as Cl--dependent K+
61 s among the polypeptide products of the four K-Cl cotransporter (KCC) genes are little understood.
62                                          The K-Cl cotransporter (KCC) regulates red blood cell (RBC)
63 cells (VSMCs) express at least two mRNAs for K-Cl cotransporters (KCC): KCC1 and KCC3.
64 2Cl cotransporter NKCC1 and Cl(-) efflux via K-Cl cotransporters, KCC1 or KCC2.
65                          The neuron-specific K(+)-Cl(-) cotransporter KCC2 plays a crucial role in de
66                     Diminished levels of the K(+)/Cl(-) cotransporter KCC2 and a depolarizing GABAA r
67                                          The K(+)/Cl(-) cotransporter KCC2 is the main mechanism by w
68 d postsynaptic activity acts on the neuronal K+/Cl- cotransporter KCC2 to shift the reversal potentia
69  larger in mature neurons, which express the K-Cl cotransporter KCC2 at high levels, and inhibition o
70                                          The K-Cl cotransporter KCC2 establishes the low intraneurona
71   Targeted deletion of the neuronal-specific K-Cl cotransporter KCC2 generates mice with a profound s
72 pmental fall in [Cl(-)]i and the role of the K-Cl cotransporter KCC2 in this process.
73                                 The neuronal K-Cl cotransporter KCC2 maintains the low intracellular
74                                          The K-Cl cotransporter KCC2 plays a crucial role in neuronal
75  in Cl(-) homeostasis is the neuron-specific K(+)-Cl(-) cotransporter (KCC2).
76                                          The K(+)/Cl(-) cotransporter (KCC2) allows adult neurons to
77 n caused a progressive downregulation of the K+-Cl- cotransporter (KCC2), which may have contributed
78                          The neuron-specific K-Cl cotransporter (KCC2) is hypothesized to function as
79 o test this, we immunostained retina for the K-Cl cotransporter (KCC2) that normally extrudes chlorid
80 ess-induced functional downregulation of the K(+), Cl(-) cotransporter, KCC2.
81 ted E(GABA), expression of the Cl- extruding K+/Cl- cotransporter, KCC2 was decreased.
82 ted that the protein product of Slc12a6, the K(+)-Cl(-) cotransporter Kcc3, was not detectable in gax
83 dates for Mendelian human disorders, and the K-Cl cotransporter KCC3, in particular, may be involved
84  EAAT1(P>R) mutation, the chloride-extruding K(+)-Cl(-) cotransporter KccB also caused astroglial mal
85                                              K(+)-Cl(-) cotransporters (KCCs) play a fundamental role
86 ires a Cl(-) gradient established in part by K(+)-Cl(-) cotransporters (KCCs).
87                                          The K+-Cl- cotransporters (KCCs) belong to the gene family o
88                               Cl(-) exit via K-Cl cotransporters (KCCs) is a major determinant of [Cl
89 -sensitive K channel, and the electroneutral K:Cl cotransporter-leading to sickle cell dehydration.
90 s, particularly R(+)-butylindazone-sensitive K-Cl cotransporters, may have a synapse- and/or cell typ
91                       In contrast, the Na(+)-K(+)-Cl(-) cotransporter Ncc69, which normally allows ch
92 tes this variation, presumably via an Na(+), K(+), Cl(-) cotransporter (NKCC) and the Shaw K(+) chann
93 mbrane conductance regulator (CFTR) or Na(+)-K(+)-Cl(-) cotransporters (NKCC) blocked alveolar fluid
94 tanide and furosemide, two blockers of Na(+)/K(+)/Cl(-) cotransporters (NKCC), inhibited all capacita
95 25% identity) to the bumetanide-sensitive Na-K-Cl cotransporter (NKCC or BSC) and the thiazide-sensit
96                                       The Na-K-Cl cotransporter (NKCC) mediates the coupled movement
97                                       The Na-K-Cl cotransporter (NKCC) plays a key role in electrolyt
98                                       The Na-K-Cl cotransporter (NKCC) plays central roles in cellula
99 at normally extrudes chloride and for the Na-K-Cl cotransporter (NKCC) that normally accumulates chlo
100                       The human and shark Na-K-Cl cotransporters (NKCC), although 74% identical in am
101                                       The Na-K-Cl cotransporter NKCC1 is activated by phosphorylation
102                             The secretory Na-K-Cl cotransporter NKCC1 is activated by secretagogues t
103 um preparation, AqF026 did not affect the Na-K-Cl cotransporter NKCC1.
104 osphorylation-dependent activation of the Na-K-Cl cotransporter (NKCC1) has been previously well docu
105          In particular, activation of the Na-K-Cl cotransporter (NKCC1) has been shown to be involved
106                                       The Na-K-Cl cotransporter (NKCC1) is expressed in most vertebra
107 re we report that a substrate of PP1, the Na-K-Cl cotransporter (NKCC1), bears this motif in its N te
108 at kidney, the "secretory" isoform of the Na-K-Cl cotransporter, NKCC1 (BSC-2), localizes to the baso
109 examine the structure and function of the Na-K-Cl cotransporter, NKCC1, we tagged the transporter wit
110        Three splice variants of the renal Na-K-Cl cotransporter (NKCC2 F, A, and B) are spatially dis
111 ternatively spliced variants of the renal Na-K-Cl cotransporter (NKCC2) are found in distinct regions
112                                 The renal Na-K-Cl cotransporter (NKCC2) is selectively expressed in t
113                                           Na-K-Cl cotransporter (NKCC2)-mediated sodium chloride reab
114 esence of furosemide, an inhibitor of the Na,K,Cl-cotransporter, NMDA-induced edema were reduced by 6
115  ID cell formation, as did inhibitors of the K:Cl cotransporter, okadaic acid, and [(dihydroindenyl)
116                    KCC2, a neuronal-specific K-Cl cotransporter, plays a major role in maintaining in
117 er BSC2, one of the two major isoforms of Na-K-Cl cotransporters present in mammalian cells, can be d
118 hat a time-dependent expression of the Na(+)-K(+)-Cl(-) cotransporter protein occurs not only in cort
119 vealed that an intense staining of the Na(+)-K(+)-Cl(-) cotransporter protein was observed in dendrit
120                                           Na-K-Cl cotransporter protein was detected on immunoblots o
121 dient by ion substitution or by blocking the K-Cl cotransporter resulted in the starburst cells respo
122 use line expressing an activated form of the K-Cl cotransporter Slc12a4 (Kcc1), which results in a se
123                          The neuron-specific K(+)-Cl(-) cotransporter SLC12A5, also known as KCC2, he
124 turally similar shark and human secretory Na-K-Cl cotransporters (sNKCC1 and hNKCC1).
125 al membrane transport systems, including the K+-Cl- cotransporter (termed KCC), cause HbS-containing
126                    KCC2 is a neuron-specific K(+)-Cl(-) cotransporter that is essential for Cl(-) hom
127 ch is mediated primarily by KCC2, a neuronal K+/Cl- cotransporter that determines the intracellular c
128 ility and the activities of the Na-K-2Cl and K-Cl cotransporters, the Na/H exchanger, and the Gardos
129                       Localization of the Na-K-Cl cotransporter to the plasma membrane on the blood s
130                      The structure of the Na-K-Cl cotransporter transport protein is not known, but f
131  double staining demonstrates that the Na(+)-K(+)-Cl(-) cotransporter was expressed in astrocytes wit
132 lyculin A, consistent with mediation via the K+-Cl- cotransporter, was revealed by depleting deoxygen
133 erogeneous; some cells that expressed the Na-K-Cl cotransporter were weakly stained with the anti-ROM
134       We report here that kcc functions as a K(+)-Cl(-) cotransporter when expressed heterologously i
135 ctivity modulated the mRNA levels of KCC2, a K(+)-Cl(-) cotransporter whose expression correlates wit
136 de the primary link coupling activity of the K+-Cl- cotransporter with O2 tension.
137 hat the KCC1 cDNAs encode a widely expressed K-Cl cotransporter with the characteristics of the K-Cl

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