Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Y M, Shuba"'
Publikováno v:
Fiziolohichnyi zhurnal (Kiev, Ukraine : 1994). 61(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f6e7721acdb0e2642200ba098e28c627
https://pubmed.ncbi.nlm.nih.gov/26552306
https://pubmed.ncbi.nlm.nih.gov/26552306
Publikováno v:
Experimental oncology. 37(2)
In recent years gold nanoparticles (AuNPs) have received considerable attention for various biomedical applications including diagnostics and targeted drug delivery. However, more research is still needed to characterize such aspects of their use in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9b29d02216ffb625e7792d29df905ce9
https://pubmed.ncbi.nlm.nih.gov/26112935
https://pubmed.ncbi.nlm.nih.gov/26112935
Publikováno v:
Journal of physiology and pharmacology : an official journal of the Polish Physiological Society. 59(3)
hERG (human ether-a-go-go-related gene) potassium (K+) channels are expressed in a range of tissue types including neuroblastoma cells and the heart, in which hERG K+ current is important for action potential repolarization. Whilst gender differences
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7a0a926fe00443947c5841a54d43b3ab
https://pubmed.ncbi.nlm.nih.gov/18953086
https://pubmed.ncbi.nlm.nih.gov/18953086
Publikováno v:
Biochemical pharmacology. 62(1)
Diverse drugs from many therapeutic classes exert cardiotoxic side effects by inducing torsades de pointes (TdP), a life threatening cardiac arrhythmia, which often results from drug interaction with HERG (human ether-a-go-go related gene) encoded K(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6cb748f40ec955f931310be45851f81b
https://pubmed.ncbi.nlm.nih.gov/11377395
https://pubmed.ncbi.nlm.nih.gov/11377395
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 281(1)
Nonsedating H1 receptor (H1-R) antagonists exert variable effects on QT interval, most likely mediated through modulation of cardiac K+ channels. We examined the effects of a novel H1-R antagonist, ebastine, on a family of K+ currents in isolated rat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ea9dc7e219e0381edc72f640917bd497
https://pubmed.ncbi.nlm.nih.gov/9103502
https://pubmed.ncbi.nlm.nih.gov/9103502
Publikováno v:
General physiology and biophysics. 10(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c39cc47724a537910f4006542ece0f4f
https://pubmed.ncbi.nlm.nih.gov/1650727
https://pubmed.ncbi.nlm.nih.gov/1650727
Publikováno v:
The American journal of physiology. 259(1 Pt 2)
A severalfold increase in calcium current (ICa) is a signal feature of the maximal beta-adrenergic response of the heart. It is generally ascribed to enhanced adenosine 3',5'-cyclic monophosphate (cAMP)-dependent phosphorylation of calcium (Ca) chann
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbecfa1ce97c0b6092524ea7afce31bb
https://pubmed.ncbi.nlm.nih.gov/2165365
https://pubmed.ncbi.nlm.nih.gov/2165365
Publikováno v:
Advances in second messenger and phosphoprotein research. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2a31aad7f032af979d505d962c7a2566
https://pubmed.ncbi.nlm.nih.gov/1976335
https://pubmed.ncbi.nlm.nih.gov/1976335