| Q43759026 | (Xeno)estrogen sensitivity of smooth muscle BK channels conferred by the regulatory beta1 subunit: a study of beta1 knockout mice |
| Q36868080 | A marriage of convenience: beta-subunits and voltage-dependent K+ channels. |
| Q40384021 | Activation of large-conductance, Ca2+-activated K+ channels by cannabinoids |
| Q44540518 | Acute modulation of adrenal chromaffin cell BK channel gating and cell excitability by glucocorticoids |
| Q37385468 | Alcohol modulation of BK channel gating depends on β subunit composition |
| Q64071356 | Anti-diarrheal effect of is associated with suppression of smooth muscle in the rat colon |
| Q34311824 | BK channel activators and their therapeutic perspectives |
| Q37555406 | BK channels in rat and human pulmonary smooth muscle cells are BKα-β1 functional complexes lacking the oxygen-sensitive stress axis regulated exon insert. |
| Q51787407 | BKCa channel activity and vascular contractility alterations with hypertension and aging via β1 subunit promoter methylation in mesenteric arteries. |
| Q47754486 | Beta 1-subunits are required for regulation of coupling between Ca2+ transients and Ca2+-activated K+ (BK) channels by protein kinase C. |
| Q46911452 | Beta2 and beta4 subunits of BK channels confer differential sensitivity to acute modulation by steroid hormones |
| Q39029227 | Bisphenol A activates BK channels through effects on α and β1 subunits |
| Q33812793 | Bisphenol A activates Maxi-K (K(Ca)1.1) channels in coronary smooth muscle |
| Q33997624 | Cholesterol depletion alters amplitude and pharmacology of vascular calcium-activated chloride channels |
| Q36273589 | Chronic fetal exposure to caffeine altered resistance vessel functions via RyRs-BKCa down-regulation in rat offspring |
| Q38262896 | Current understanding of iberiotoxin-resistant BK channels in the nervous system |
| Q34596930 | Defining the BK channel domains required for beta1-subunit modulation. |
| Q36923791 | DiBAC₄(3) hits a "sweet spot" for the activation of arterial large-conductance Ca²⁺-activated potassium channels independently of the β₁-subunit. |
| Q37000197 | Diabetes downregulates large-conductance Ca2+-activated potassium beta 1 channel subunit in retinal arteriolar smooth muscle |
| Q37788327 | Dietary isoflavones and vascular protection: Activation of cellular antioxidant defenses by SERMs or hormesis? |
| Q39578530 | Differential efficacy of GoSlo-SR compounds on BKα and BKαγ1-4 channels. |
| Q47449758 | Downregulation of the BK Channel β1 Subunit in Genetic Hypertension |
| Q42653362 | Dual effect of tamoxifen on arterial KCa channels does not depend on the presence of the beta1 subunit. |
| Q44423212 | Effect of 17β-Estradiol on mRNA Expression of Large- Conductance, Voltage-Dependent, and Calcium-Activated Potassium Channel α and β Subunits in Guinea Pig |
| Q42637131 | Effect of exercise training volume on arterial contractility and BK(Ca) channel activity in rat thoracic aorta smooth muscle cells |
| Q35538521 | Effects of the novel BK (KCa 1.1) channel opener GoSlo-SR-5-130 are dependent on the presence of BKβ subunits |
| Q46516424 | Estrogen regulates {beta}1-subunit expression in Ca(2+)-activated K(+) channels in arteries from reproductive tissues |
| Q46054861 | Heterogeneity in function of small artery smooth muscle BKCa: involvement of the beta1-subunit |
| Q42745852 | High glucose alters apoptosis and proliferation in HEK293 cells by inhibition of cloned BK Ca channel |
| Q40663741 | IKCa1 activity is required for cell shrinkage, phosphatidylserine translocation and death in T lymphocyte apoptosis |
| Q48787258 | Individual variation and hormonal modulation of a sodium channel beta subunit in the electric organ correlate with variation in a social signal |
| Q37376966 | Inhibition of vascular calcium-gated chloride currents by blockers of KCa1.1, but not by modulators of KCa2.1 or KCa2.3 channels |
| Q41791327 | Keeping you healthy: BK channel activation by omega-3 fatty acids |
| Q37308093 | Large conductance Ca2+-activated K+ channels contribute to vascular function in nonpregnant human uterine arteries |
| Q36439617 | Large conductance Ca2+-activated and voltage-activated K+ channels contribute to the rise and maintenance of estrogen-induced uterine vasodilation and maintenance of blood pressure |
| Q34475162 | Large conductance, Ca2+-activated K+ channels (BKCa) and arteriolar myogenic signaling |
| Q46567498 | Large-conductance Ca2+-dependent K+ channels regulate basal uteroplacental blood flow in ovine pregnancy |
| Q46864156 | Mechanisms underlying regional differences in the Ca2+ sensitivity of BK(Ca) current in arteriolar smooth muscle |
| Q37032053 | Modulation of BK Channel Function by Auxiliary Beta and Gamma Subunits |
| Q35679204 | Modulation of the molecular composition of large conductance, Ca(2+) activated K(+) channels in vascular smooth muscle during hypertension |
| Q38997044 | Molecular Determinants of BK Channel Functional Diversity and Functioning |
| Q37406412 | Mutation of protein kinase C phosphorylation site S1076 on alpha-subunits affects BK(Ca) channel activity in HEK-293 cells |
| Q44720800 | Non-genomic effects of tamoxifen on the activation of membrane-bound guanylate cyclase GC-A. |
| Q41160541 | Nongenomic modulation of the large conductance voltage- and Ca2+-activated K+ channels by estrogen: A novel regulatory mechanism in human detrusor smooth muscle |
| Q38262897 | Pharmacological consequences of the coexpression of BK channel α and auxiliary β subunits |
| Q44326160 | Potentiation of glycine responses by dideoxyforskolin and tamoxifen in rat spinal neurons |
| Q34356206 | Prolonged uterine artery nitric oxide synthase inhibition modestly alters basal uteroplacental vasodilation in the last third of ovine pregnancy |
| Q36864691 | Raloxifene, tamoxifen and vascular tone. |
| Q37057980 | Rapid estrogen actions on ion channels: A survey in search for mechanisms |
| Q33820422 | Regulation of cerebral arterial BKCa channels by angiotensin II signaling in adult offspring exposed to prenatal high sucrose diets |
| Q36691916 | Review article: steroid hormones and uterine vascular adaptation to pregnancy |
| Q35601325 | Role of caveolin-1 in endothelial BKCa channel regulation of vasoreactivity |
| Q41481833 | Smooth muscle relaxation and activation of the large conductance Ca(++)-activated K+ (BK(Ca)) channel by novel oestrogens |
| Q24684666 | Structural determinants for functional coupling between the beta and alpha subunits in the Ca2+-activated K+ (BK) channel |
| Q30480699 | Tamoxifen inhibits BK channels in chick cochlea without alterations in voltage-dependent activation |
| Q89724523 | Targeting BKCa Channels in Migraine: Rationale and Perspectives |
| Q55272783 | The G protein–coupled estrogen receptor agonist, G‐1, attenuates BK channel activation in cerebral arterial smooth muscle cells. |
| Q44359182 | The anti-breast cancer drug tamoxifen alters Ca2+ movement in Chinese hamster ovary (CHO-K1) cells |
| Q33484494 | The large-conductance Ca(2+)-activated K(+) channel interacts with the apolipoprotein ApoA1 |
| Q91776559 | The molecular nature of the 17β-Estradiol binding site in the voltage- and Ca2+-activated K+ (BK) channel β1 subunit |
| Q35044494 | The pure anti-oestrogen ICI 182,780 (Faslodex) activates large conductance Ca(2+)-activated K(+) channels in smooth muscle. |
| Q44038456 | Triphenylethylene antiestrogen-induced acute relaxation of mouse duodenal muscle. Possible involvement of Ca2+ channels |
| Q46578017 | Voltage-dependent K+ channel acts as sex steroid sensor in endocrine cells of the human ovary |
| Q42514789 | Voltage-dependent open-channel block of G protein-gated inward-rectifying K(+) (GIRK) current in rat atrial myocytes by tamoxifen. |
| Q34503545 | Volume-regulated anion channel--a frenemy within the brain |