Tamsulosin ameliorates bone loss by inhibiting the release of Cl- through wedging into an allosteric site of TMEM16A. [PDF]
Li S +19 more
europepmc +1 more source
Characterization of TMEM16F-Specific Affibodies and Their Cellular Effects. [PDF]
Kim E, Bang J, Kim S, Lee BC.
europepmc +1 more source
Beyond the mutations: spatiotemporal regulation of CFTR by cAMP and calcium signaling in epithelial physiology and cystic fibrosis. [PDF]
Varga A +5 more
europepmc +1 more source
The roles and functions of TMEM protein family members in cancers, cardiovascular and kidney diseases (Review). [PDF]
Xu H +9 more
europepmc +1 more source
Spontaneous Calcium Signalling in the Developing Mammalian Cochlea. [PDF]
Ceriani F, Marcotti W.
europepmc +1 more source
Distinct modulation of calcium-activated chloride channel TMEM16A by drug-binding sites. [PDF]
Roh JW +5 more
europepmc +1 more source
TMEM16A Activation Inhibits Autophagy in Dorsal Root Ganglion Cells, Which is Associated with the p38 MAPK/mTOR Pathway. [PDF]
Yang S +9 more
europepmc +1 more source
The multifaceted role of TMEM16A in cancer
The calcium-activated chloride channel TMEM16A is intimately linked to cancers. Over decades, TMEM16A over-expression and contribution to prognosis have been widely studied for multiple cancers strengthening the idea that TMEM16A could be a valuable biomarker and a promising therapeutic target.
David Crottès, Lily Jan
exaly +7 more sources
Pharmacological characterization of TMEM16A currents [PDF]
Recent studies have shown that transmembrane protein 16 A (TMEM16A) is a subunit of calcium-activated chloride channels (CACCs). Pharmacological agents have been used to probe the functional role of CACCs, however their effect on TMEM16A currents has not been systematically investigated.
Gérard sergeant +2 more
exaly +3 more sources
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Emerging Modulators of TMEM16A and Their Therapeutic Potential
Journal of Membrane Biology, 2021Calcium-activated chloride channels (CaCCs) are widespread chloride channels which rely on calcium activation to perform their functions. In 2008, TMEM16A (also known as anoctamin1, ANO1) was identified as the molecular basis of the CaCCs, which provided the possibility to study the physiological function of CaCCs.
Xuzhao Wang, Yafei Chen, Hailong An
exaly +3 more sources

