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1.
Characterizing the role of Thr352 in the inhibition of the large conductance Ca2+-activated K+ channels by 1-[1-hexyl-6-(methyloxy)-1H-indazol-3-yl]-2-methyl-1-propanone.
J Pharmacol Exp Ther
; 334(2): 402-9, 2010 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-20430843
2.
PTC-174, a positive allosteric modulator of NMDA receptors containing GluN2C or GluN2D subunits.
Neuropharmacology
; 173: 107971, 2020 08 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-31987864
3.
A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance.
Cardiovasc Res
; 77(1): 98-106, 2008 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-18006462
4.
2-[2-(3,4-dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic acid (PD-307243) causes instantaneous current through human ether-a-go-go-related gene potassium channels.
Mol Pharmacol
; 73(3): 639-51, 2008 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-18042732
5.
1-[1-Hexyl-6-(methyloxy)-1H-indazol-3-yl]-2-methyl-1-propanone, a potent and highly selective small molecule blocker of the large-conductance voltage-gated and calcium-dependent K+ channel.
J Pharmacol Exp Ther
; 327(1): 168-77, 2008 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-18591221
6.
N-((1S)-1-{[4-((2S)-2-{[(2,4-dichlorophenyl)sulfonyl]amino}-3-hydroxypropanoyl)-1-piperazinyl]carbonyl}-3-methylbutyl)-1-benzothiophene-2-carboxamide (GSK1016790A), a novel and potent transient receptor potential vanilloid 4 channel agonist induces urinary bladder contraction and hyperactivity: Part I.
J Pharmacol Exp Ther
; 326(2): 432-42, 2008 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-18499743
7.
Acetic acid opens large-conductance Ca2+-activated K+ channels in guinea pig detrusor smooth muscle cells.
Eur J Pharmacol
; 563(1-3): 203-8, 2007 Jun 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-17382925
8.
MPX-004 and MPX-007: New Pharmacological Tools to Study the Physiology of NMDA Receptors Containing the GluN2A Subunit.
PLoS One
; 11(2): e0148129, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-26829109
9.
An orally active TRPV4 channel blocker prevents and resolves pulmonary edema induced by heart failure.
Sci Transl Med
; 4(159): 159ra148, 2012 Nov 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-23136043
10.
Functional TRPV4 channels and an absence of capsaicin-evoked currents in freshly-isolated, guinea-pig urothelial cells.
Channels (Austin)
; 3(3): 156-60, 2009.
Artículo
en Inglés
| MEDLINE | ID: mdl-19411839
11.
1,4-Diazabicyclo[2.2.2]octane derivatives: a novel class of voltage-gated potassium channel blockers.
Mol Pharmacol
; 69(3): 718-26, 2006 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-16317109
12.
Endogenous KCNE subunits govern Kv2.1 K+ channel activation kinetics in Xenopus oocyte studies.
Biophys J
; 90(4): 1223-31, 2006 Feb 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-16326911
13.
RNA interference reveals that endogenous Xenopus MinK-related peptides govern mammalian K+ channel function in oocyte expression studies.
J Biol Chem
; 278(14): 11739-45, 2003 Apr 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-12529362
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