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databases
phosphosite cbn pc11 biopax bel_lc signor biogrid lincs_drug tas hprd trrust ctd virhostnet phosphoelm drugbank omnipath | geneways tees isi trips rlimsp medscan sparser eidos reach
reading

E2 affects KCNQ5
| 10
E2 increases the amount of KCNQ5.
| 8
E2 increases the amount of KCNQ5. 8 / 8
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"As found in NPY neurons, E2 replacement significantly increased the mRNA expression of KCNQ5 in RNA extracted from the arcuate nucleus dissected from wild-type females but failed to alter KCNQ5 expression in ERalpha KO females (XREF_FIG)."
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"Because E2 regulates KCNQ5 and NPY gene expression in the arcuate but fails to increase KCNQ5 expression in NPY neurons in ERalpha KO mice, we determined the expression of ERalpha and ERbeta in single and pooled NPY neurons collected from ovariectomized females."
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"We have previously shown that E2 will increase KCNQ5 expression in the guinea pig arcuate nucleus both after 24 hr and long-term treatment using unbiased microarray analysis followed by quantitative real-time PCR."
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"Because E2 increased the expression of KCNQ5 in NPY neurons, we wanted to determine if this was dependent on ERalpha."
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"E2 treatment increases the mRNA expression of the KCNQ5 channel subunit that underlies the M-current and the inwardly rectifying K + (Kir) channel Kir2.4 subunit."
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"Previously, we have shown that E2 (24 hr and long-term) increases the expression of KCNQ5 in guinea pig arcuate nucleus."
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"In the mouse, E2 replacement also increased the expression of KCNQ5 both in the whole arcuate and specifically in NPY neurons."
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"E2 treatment increased the expression of the KCNQ5 subunit in females but not KCNQ2 or KCNQ3 subunits."
E2 decreases the amount of KCNQ5.
| 1
E2 decreases the amount of KCNQ5. 1 / 1
| 1
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"Because E2 suppresses food intake and NPY neurons are orexigenic, we hypothesized that E2 may suppress feeding behavior by increasing the KCNQ5 expression and activity of the M-current in NPY neurons."
E2 activates KCNQ5.
| 1
E2 activates KCNQ5. 1 / 1
| 1
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"The expression of KCNQ2 and KCNQ3 was not affected by E2 treatment while KCNQ5 was significantly increased by E2 treatment (XREF_FIG; n = 5, p < 0.05)."
| 6
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"We recently discovered that the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) directly activates Kv channels KCNQ3 and KCNQ5."
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"We recently discovered that the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) directly activates Kv channels KCNQ3 and KCNQ5."
reach
"We recently discovered that the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) directly activates Kv channels KCNQ3 and KCNQ5."
reach
"We recently discovered that the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) directly activates Kv channels KCNQ3 and KCNQ5."
reach
"Here, phylogenetic analysis, electrostatic potential mapping, in silico docking, electrophysiology, and radioligand binding assays reveal that the anticonvulsant binding pocket evolved to accommodate endogenous neurotransmitters including gamma-aminobutyric acid (GABA), which directly activates KCNQ5 and KCNQ3 via W265."
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"Here, phylogenetic analysis, electrostatic potential mapping, in silico docking, electrophysiology, and radioligand binding assays reveal that the anticonvulsant binding pocket evolved to accommodate endogenous neurotransmitters including gamma-aminobutyric acid (GABA), which directly activates KCNQ5 and KCNQ3 via W265."
CTCF affects KCNQ5
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CTCF activates KCNQ5.
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CTCF activates KCNQ5. 4 / 4
| 4
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"CTCF Mediates the Cell-Type Specific Spatial Organization of the Kcnq5 Locus and the Local Gene Regulation."
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"By comparing the CTCF binding ability with the interaction frequencies of the kcnq5 locus mediated by CTCF in the different cell lines, we found that the cell-type specific distribution of CTCF binding sites in the kcnq5 locus determined the CTCF mediated cell-type specific organization of the locus."
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"Here, we characterized the CTCF mediated dynamic spatial organization of the kcnq5 gene locus in detail to present a perspective of cell type specific intra-chromosomal interaction networks that are established and maintained by both cis-elements and trans-factors."
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"Correction : CTCF Mediates the Cell-Type Specific Spatial Organization of the Kcnq5 Locus and the Local Gene Regulation."
| PMC
CTCF increases the amount of KCNQ5.
| 1
CTCF increases the amount of KCNQ5. 1 / 1
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"In addition, it has been reported that CTCF is involved in the spatial organization of the KCNQ5 locus, and knockdown of CTCF downregulates KCNQ5 expression 46."
CALM affects KCNQ5
| 2 3
CALM binds KCNQ5.
| 2 1
| 2 1
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"The maximal level of KCNQ5 and CaM interaction was found when photoreceptors had almost completely disappeared; the KCNQ5 and VGluT1 interaction signal decreased and the KCNQ5 and GFAP interaction increased in the inner retina, while degeneration progressed."
sparser
"Retinal degeneration progression in P23H-1 rats can be followed by an interaction between KCNQ5 with CaM in an in situ system."
sparser
"The physical interactions of KCNQ5 with calmodulin (CaM), vesicular glutamate transporter 1 (VGluT1) and glial fibrillary acidic protein (GFAP) were analyzed by in situ proximity ligation assays and were supported by calcium recording."
CALM inhibits KCNQ5.
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CALM inhibits KCNQ5. 2 / 2
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"Moreover, overexpression of CaM reduced current amplitudes of KCNQ2, KCNQ4, and KCNQ5, but not those of KCNQ1 and KCNQ3."
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"Coexpression of CaM in Chinese hamster ovary (CHO) cells strongly reduced currents of KCNQ2, KCNQ4, and KCNQ5, but not KCNQ1 or KCNQ3."
Ezogabine affects KCNQ5
| 4
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"Moreover, KCNQ3 and KCNQ5 channels are potently activated by the anticonvulsant retigabine (Wickenden et al., 2001)."
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"In the present study, retigabine enhanced the KCNQ5 current at -30 and -60 mV, by 3 and 7 fold, respectively."
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"Retigabine activated the KCNQ5 channel by increasing the current in a concentration dependent way."
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"Recently, Wickenden et al. (2001) have also shown that retigabine can activate the KCNQ5 and KCNQ3 heteromer expressed in CHO cells."
PKC affects KCNQ5
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PKC inhibits KCNQ5. 4 / 4
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"These results suggest that despite its ability to directly activate TRPC6 channels (XREF_SUPPLEMENTARY), DAG contributes to the stimulation of Ca 2+ spiking primarily via PKC dependent suppression of KCNQ5 currents."
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"We previously provided evidence that physiological concentrations (10-100 pM) of AVP indeed produce membrane depolarization and Ca 2+ influx in A7r5 rat aortic smooth muscle cells through a protein kinase C (PKC)-dependent suppression of KCNQ5 currents [XREF_BIBR]."
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"These results suggest that the stimulation of Ca (2+) spiking by physiological concentrations of AVP involves PKC dependent inhibition of KCNQ5 channels and increased AP firing in A7r5 cells."
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"We previously provided evidence that physiological concentrations (10-100 pM) of AVP indeed produce membrane depolarization and Ca 2+ influx in A7r5 rat aortic smooth muscle cells through a protein kinase C (PKC)-dependent suppression of KCNQ5 currents [XREF_BIBR]."
KCNQ5 affects calcium(2+)
| 4
KCNQ5 inhibits calcium(2+).
| 2
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"The resulting outward K + current opposes membrane depolarization and prevents E m from reaching the threshold for triggering action potential firing; (2) Suppression of KCNQ5 channel activity by physiological concentrations of AVP will depolarize the membrane and stimulate Ca 2+ influx though voltage sensitive Ca 2+ channels; (3) Activation of TRPC6 non selective cation currents modestly contributes to AVP induced membrane depolarization and generation of Ca 2+ spikes at physiological concentrations of AVP."
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"KCNQ5 knockdown resulted in more positive resting membrane potentials and induced spontaneous action potential firing and Ca 2+ spiking."
KCNQ5 activates calcium(2+).
| 2
| 2
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"Similarly, KCNQ4 and KCNQ5 are key modulators of L-type Ca 2+ channel activity in cardiovascular cells [XREF_BIBR]."
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"Here we examine the relative contributions of KCNQ5 channels and TRPC6 non selective cation channels to AVP stimulated Ca 2+ spiking using patch clamp electrophysiology and fura-2 fluorescence measurements in A7r5 cells."
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Transcriptionally active hsa-miR-6867-5p decreases the amount of KCNQ5. 3 / 3
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-574-5p decreases the amount of KCNQ5. 3 / 3
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
SLC6A1 affects KCNQ5
| 3
SLC6A1 activates KCNQ5. 3 / 3
| 3
sparser
"Here, phylogenetic analysis, electrostatic potential mapping, in silico docking, electrophysiology, and radioligand binding assays reveal that the anticonvulsant binding pocket evolved to accommodate endogenous neurotransmitters including γ-aminobutyric acid (GABA), which directly activates KCNQ5 and KCNQ3 via W265."
sparser
"We recently discovered that the inhibitory neurotransmitter γ-aminobutyric acid (GABA) directly activates Kv channels KCNQ3 and KCNQ5."
sparser
"We recently discovered that the inhibitory neurotransmitter γ-aminobutyric acid (GABA) directly activates Kv channels KCNQ3 and KCNQ5."
| 2 1
sparser
"The M-type current was activated by 1) 10 μM retigabine, an opener of all KCNQ channels except KCNQ1, 2) 10 μM zinc pyrithione, which augments all KCNQ channels except KCNQ3, and 3) 50 μM N-ethylmaleimide, which activates KCNQ2, KCNQ4, and KCNQ5, but not KCNQ1 or KCNQ3, channels."
sparser
"Among these, NEM activates the isothiocyanate-activated cation channel TRPA1 [ xref ] and the voltage-gated K + channels (M channels) Kv7.2, Kv7.4, and Kv7.5 [ xref ] (also activated by H 2 O 2 in a dithiothreitol-reversible manner [ xref ])."
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"The M-type current was activated by 1) 10 muM retigabine, an opener of all KCNQ channels except KCNQ1, 2) 10 muM zinc pyrithione, which augments all KCNQ channels except KCNQ3, and 3) 50 muM N-ethylmaleimide, which activates KCNQ2, KCNQ4, and KCNQ5, but not KCNQ1 or KCNQ3, channels."
KCNQ5 affects CALM
| 2 1
| 2 1
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"The maximal level of KCNQ5 and CaM interaction was found when photoreceptors had almost completely disappeared; the KCNQ5 and VGluT1 interaction signal decreased and the KCNQ5 and GFAP interaction increased in the inner retina, while degeneration progressed."
sparser
"Retinal degeneration progression in P23H-1 rats can be followed by an interaction between KCNQ5 with CaM in an in situ system."
sparser
"The physical interactions of KCNQ5 with calmodulin (CaM), vesicular glutamate transporter 1 (VGluT1) and glial fibrillary acidic protein (GFAP) were analyzed by in situ proximity ligation assays and were supported by calcium recording."
| 2
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"KCNQ1 and KCNE1, KCNQ4, and KCNQ5 channels are also reactivated by PIP 2 after inhibition by polylysine, showing that all KCNQ family members are PIP 2 sensitive."
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"We therefore asked if pharmacological reduction of PIP 2 levels inhibited KCNQ5 current in the calyx."
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Transcriptionally active hsa-miR-7847-3p decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-6797-5p decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-6782-5p decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-675-3p decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-6747-5p decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-6738-5p decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-6515-5p decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
Hsa-miR-543 affects KCNQ5
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Transcriptionally active hsa-miR-543 decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-5194 decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-4455 decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-3650 decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-223-5p decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-1914-3p decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-1249-5p decreases the amount of KCNQ5. 2 / 2
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biopax:mirtarbase
No evidence text available
biopax:mirtarbase
No evidence text available
Diclofenac affects KCNQ5
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"Finally, diclofenac, which activates KCNQ2/3 and KCNQ4 channels but inhibits KCNQ5 channels, inhibited the M-type current in the majority of RPE cells but activated it in others."
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"Diclofenac (100 muM) inhibited KCNQ5 channels, reducing maximum conductance by 53%, but increased maximum conductance of KCNQ4 channels by 38%."
UCL2077 affects KCNQ5
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UCL2077 inhibits KCNQ5.
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UCL2077 inhibits KCNQ5. 1 / 1
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"Among cloned KCNQ subunits, UCL2077 is reported to inhibit all but KCNQ5, which exhibits voltage dependent potentiation by the drug 27."
UCL2077 activates KCNQ5.
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UCL2077 activates KCNQ5. 1 / 1
| 1
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"In contrast, UCL2077 potentiates KCNQ5 channels at more positive membrane potentials, with little effect at negative membrane potentials."
SRC affects KCNQ5
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hprd
No evidence text available
SRC binds KCNQ3, KCNQ4, and KCNQ5. 1 / 1
| 1
sparser
"Immunoprecipitation and immunoblot analysis showed Src-dependent phosphotyrosine signals associated with KCNQ3, KCNQ4, and KCNQ5 but not with KCNQ1 or KCNQ2 that may be tyrosine phosphorylation of the channel subunits."
KCNQ5 affects HCCS
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biogrid
No evidence text available
biogrid
No evidence text available
KCNQ5 affects DISC1
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1 1 |
hprd
No evidence text available
biogrid
No evidence text available
HCCS affects KCNQ5
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biogrid
No evidence text available
biogrid
No evidence text available
DISC1 affects KCNQ5
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1 1 |
hprd
No evidence text available
biogrid
No evidence text available
| 1
| 1
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"The results were comparable after intracochlear TTX injection, which drastically reduced KCNQ5 immunostaining in MNTB calyces and increased immunolabeling in VCN cell bodies."
Pyraclofos affects KCNQ5
| 1
| 1
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"BMS-204352 potentiated the voltage activated KCNQ5 current at all potentials tested."
MiR190 affects KCNQ5
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MiR190 inhibits KCNQ5. 1 / 1
| 1
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"Moreover, KCNQ1 and KCNQ5 are down-regulated by other miRs, namely, miR1/133 and miR190, respectively."
MiR1/133 affects KCNQ5
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MiR1/133 inhibits KCNQ5. 1 / 1
| 1
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"Moreover, KCNQ1 and KCNQ5 are down-regulated by other miRs, namely, miR1/133 and miR190, respectively."
MiR-499 inhibitor affects KCNQ5
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MiR-499 inhibitor increases the amount of modified KCNQ5. 1 / 1
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"Interestingly, the protein expression of KCNQ5 was significantly upregulated by miR-499 mimic (1.41 +/-0.11 vs. 1.0 +/-0.10 relative units in control, n = 3, P < 0.05) and downregulated by miR-499 inhibitor (0.21 +/-0.05 vs. 1.0 +/-0.25 relative units in control, n = 3, P < 0.05) (XREF_FIG), suggesting that miR-499 does not directly regulate KCNQ5 expression but may be regulating a negative inhibitor of KCNQ5 expression."
MiR-499 affects KCNQ5
| 1
MiR-499 increases the amount of KCNQ5. 1 / 1
| 1
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"Interestingly, the protein expression of KCNQ5 was significantly upregulated by miR-499 mimic (1.41 +/-0.11 vs. 1.0 +/-0.10 relative units in control, n = 3, P < 0.05) and downregulated by miR-499 inhibitor (0.21 +/-0.05 vs. 1.0 +/-0.25 relative units in control, n = 3, P < 0.05) (XREF_FIG), suggesting that miR-499 does not directly regulate KCNQ5 expression but may be regulating a negative inhibitor of KCNQ5 expression."
| 1
Isoprenaline phosphorylates KCNQ5. 1 / 1
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sparser
"Correspondingly, proximity ligation assays indicated that isoproterenol induced PKA-dependent phosphorylation of exogenously expressed Kv7.5 channel subunits, but not of Kv7.4 subunits."
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Transcriptionally active hsa-miR-6507-5p decreases the amount of KCNQ5. 1 / 1
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biopax:mirtarbase
No evidence text available
1 |
Transcriptionally active hsa-miR-5693 decreases the amount of KCNQ5. 1 / 1
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biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-5096 decreases the amount of KCNQ5. 1 / 1
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biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-4999-3p decreases the amount of KCNQ5. 1 / 1
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biopax:mirtarbase
No evidence text available
1 |
Transcriptionally active hsa-miR-4282 decreases the amount of KCNQ5. 1 / 1
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biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-194-3p decreases the amount of KCNQ5. 1 / 1
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biopax:mirtarbase
No evidence text available
1 |
Transcriptionally active hsa-miR-190a-5p decreases the amount of KCNQ5. 1 / 1
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biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-144-3p decreases the amount of KCNQ5. 1 / 1
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biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-139-5p decreases the amount of KCNQ5. 1 / 1
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biopax:mirtarbase
No evidence text available
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Transcriptionally active hsa-miR-101-3p decreases the amount of KCNQ5. 1 / 1
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biopax:mirtarbase
No evidence text available
Estrogen affects KCNQ5
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Estrogen increases the amount of KCNQ5. 1 / 1
| 1
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"Previously, we have shown that estrogen replacement in ovariectomized female guinea pigs increased the expression of KCNQ5 in the arcuate nucleus after both 24 hr and long-term treatment."
Celecoxib affects KCNQ5
| 1
| 1
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"We conclude that celecoxib inhibits calcium responses in VSMCs by enhancing KCNQ5 currents and suppressing L-type calcium currents, which ultimately reduces vascular tone."
XE991 affects KCNQ5
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XE991 inhibits KCNQ5. 1 / 1
| 1
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"However, as previously described for the KCNQ4 current (Schroder et al., 2001), a brief transient increase in the amplitude of the tail current measured at -60 mV was observed before deactivation in the absence or presence of the compound, which could be explained as recovery from a very weak inactivation.XE991 is a blocker of M-type currents, and recently Schroeder et al. (2000) have shown that the KCNQ5 current is also blocked by the XE991 in Xenopus oocytes."
TWIST1 affects KCNQ5
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sparser
"In addition to the top significant SNPs rs2917454 and rs6907229, imputation analysis uncovered additional genetic variants in KCNMA1 and in KCNQ5 that were associated with CRS."
PPY affects KCNQ5
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PPY activates KCNQ5. 1 / 1
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"The KCNQ5 potassium channel from mouse : a broadly expressed M-current like potassium channel modulated by zinc, pH, and volume changes."
Kcnq4/5 affects KCNQ5
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Kcnq4/5 activates KCNQ5. 1 / 1
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"This branching pattern can be explained by two duplication events in the vertebrate lineage, where a single proto-orthologue to Kcnq2/3/4/5, duplicated to create two ancestor genes to Kcnq2/3 and Kcnq4/5 which both duplicated again to produce Kcnq2, kcnq3, kcnq4 and kcnq5 genes as conserved in current vertebrate genomes."
Kcnq2/3 affects KCNQ5
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Kcnq2/3 activates KCNQ5. 1 / 1
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"This branching pattern can be explained by two duplication events in the vertebrate lineage, where a single proto-orthologue to Kcnq2/3/4/5, duplicated to create two ancestor genes to Kcnq2/3 and Kcnq4/5 which both duplicated again to produce Kcnq2, kcnq3, kcnq4 and kcnq5 genes as conserved in current vertebrate genomes."
| 1
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"The water channel AQP1 and the main calcium regulated ion channel in chondrocytes TRPV4 are strongly increased in Group B. XREF_BIBR Also increased in Group B are other calcium activated potassium channels including KCNN3, 4, XREF_BIBR the voltage sensitive calcium activated chloride channel ANO1 and potassium channels KCNQ5, KCNS3 and KCTD12, KCNMB4 (XREF_TABLE)."
KCNQ5 affects TWIST1
| 1
| 1
sparser
"In addition to the top significant SNPs rs2917454 and rs6907229, imputation analysis uncovered additional genetic variants in KCNMA1 and in KCNQ5 that were associated with CRS."
KCNQ5 affects PTCH1, and spef1
| 1
| 1
sparser
"In the first, we constructed a mutant tetraethylammonium ion-sensitive KCNQ4 subunit and tested its assembly with KCNQ5 by patch clamp analysis of the tetraethylammonium ion sensitivity of the resulting current; however, those data were not conclusive."
KCNQ5 affects HAUS3
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sparser
"Results of RT-qPCR showed that the levels of lncRNAs MTCO2P12, KCNQ5-IT1 and RP11-83J16.1 were increased, whereas lncRNAs LINC00570, RP11-342M1.6, and REXO1L4P were decreased in RA patients compared to controls."
KCNQ5 affects GFAP
| 1
| 1
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"The maximal level of KCNQ5 and CaM interaction was found when photoreceptors had almost completely disappeared; the KCNQ5 and VGluT1 interaction signal decreased and the KCNQ5 and GFAP interaction increased in the inner retina, while degeneration progressed."
KCNQ5 affects CDH
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KCNQ5 activates CDH. 1 / 1
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"We hypothesized that KCNQ1, KCNQ4, and KCNQ5 expression is altered in the pulmonary vasculature of nitrofen induced CDH rats."
KCNQ5 affects CALM3
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hprd
No evidence text available
KCNQ5 affects CALM2
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hprd
No evidence text available
KCNQ5 affects CALM1
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hprd
No evidence text available
KCNQ3 affects KCNQ4, KCNQ5, and SRC
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SRC binds KCNQ3, KCNQ4, and KCNQ5. 1 / 1
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sparser
"Immunoprecipitation and immunoblot analysis showed Src-dependent phosphotyrosine signals associated with KCNQ3, KCNQ4, and KCNQ5 but not with KCNQ1 or KCNQ2 that may be tyrosine phosphorylation of the channel subunits."
KCNQ channel opener affects KCNQ5
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KCNQ channel opener activates KCNQ5. 1 / 1
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reach
"Zinc pyrithione (ZnPy) is a newly identified KCNQ channel opener, which potently activates KCNQ2, KCNQ4, and KCNQ5."
HAUS3 affects KCNQ5
| 1
| 1
sparser
"Results of RT-qPCR showed that the levels of lncRNAs MTCO2P12, KCNQ5-IT1 and RP11-83J16.1 were increased, whereas lncRNAs LINC00570, RP11-342M1.6, and REXO1L4P were decreased in RA patients compared to controls."
GS26575 affects KCNQ5
| 1
| 1
reach
"KCNQ5 is inhibited by the M1 muscarinic receptor activation and shows pharmacological properties suggesting that it plays a role in generating M currents or M like currents (Lerche et al., 2000; Schroeder et al., 2000)."
GFAP affects KCNQ5
| 1
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reach
"The maximal level of KCNQ5 and CaM interaction was found when photoreceptors had almost completely disappeared; the KCNQ5 and VGluT1 interaction signal decreased and the KCNQ5 and GFAP interaction increased in the inner retina, while degeneration progressed."
EZG affects KCNQ5
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EZG activates KCNQ5. 1 / 1
| 1
reach
"XREF_BIBR However, KCNQ4 and KCNQ5 potassium channels are activated by EZG and may be found in cochlear hair cells XREF_BIBR or smooth muscle."
EB affects KCNQ5
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EB increases the amount of KCNQ5. 1 / 1
| 1
reach
"We found that EB significantly increased the expression of KCNQ5 and Kv4.1 and decreased expression of KCNQ3 and AKAP in the rostral arcuate."
CYP7B1 affects KCNQ5, and PPP3CC
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sparser
"The genetic component highlighted genes including PPP3CC, KCNQ5, and CYP7B1 which are directly associated with brain function or mental disorders."
CALM3 affects KCNQ5
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hprd
No evidence text available
CALM2 affects KCNQ5
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hprd
No evidence text available
CALM1 affects KCNQ5
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hprd
No evidence text available
BMS-204352 affects KCNQ5
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BMS-204352 activates KCNQ5. 1 / 1
| 1
reach
"Application of BMS-204352 also slowed the voltage independent KCNQ5 channel deactivation."
BBR affects KCNQ5
| 1
BBR activates KCNQ5. 1 / 1
| 1
reach
"At 10 muM, BBR potentiated KCNQ1, KCNQ4, and KCNQ5 but not KCNQ3."
AVP affects KCNQ5
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AVP activates KCNQ5. 1 / 1
| 1
reach
"However physiological concentrations of AVP induced additional depolarization and increased Ca 2+ spike frequency in KCNQ5 knockdown cells."
ADRB affects KCNQ5
| 1
ADRB activates KCNQ5. 1 / 1
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sparser
"A phospho-mimic mutation (S53D) exhibited characteristics of βAR-activated Kv7.5."