The cystic fibrosis transmembrane conductance regulator is an extracellular chloride sensor.
about
Structural Changes Fundamental to Gating of the Cystic Fibrosis Transmembrane Conductance Regulator Anion Channel Pore.Architecture and functional properties of the CFTR channel pore.CFTR channel in oocytes from Xenopus laevis and its regulation by xShroom1 protein.Ca(2+) signals mediated by bradykinin type 2 receptors in normal pancreatic stellate cells can be inhibited by specific Ca(2+) channel blockade.Regulation of TMEM16A/ANO1 and TMEM16F/ANO6 ion currents and phospholipid scrambling by Ca2+ and plasma membrane lipid.Gating modes of calcium-activated chloride channels TMEM16A and TMEM16B.
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The cystic fibrosis transmembrane conductance regulator is an extracellular chloride sensor.
description
2014 nî lūn-bûn
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2014年の論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年论文
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2014年论文
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2014年论文
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name
The cystic fibrosis transmembr ...... extracellular chloride sensor.
@en
type
label
The cystic fibrosis transmembr ...... extracellular chloride sensor.
@en
prefLabel
The cystic fibrosis transmembr ...... extracellular chloride sensor.
@en
P2093
P2860
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The cystic fibrosis transmembr ...... extracellular chloride sensor.
@en
P2093
Barry E Argent
Christine E Bear
Michael A Gray
Mohabir Ramjeesingh
P2860
P2888
P304
P356
10.1007/S00424-014-1618-8
P577
2014-10-04T00:00:00Z