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Titlebook: Cell Volume and Signaling; Peter K. Lauf,Norma C. Adragna Conference proceedings 2005 The Editor(s) (if applicable) and The Author(s), und

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楼主: vein220
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Effects of Ammonium on Ion Channels and Transporters in Colonic Secretory CellsNH..-2Cl. transport modes. NH.. conducts through most K. channels and thus likely through the apical K. channel present in native crypt cells. This suggests that, similar to the kidney, colonic secretory cells have the capacity to secrete NH.. when in a K.-secreting mode with elevated basolateral NH.. levels.
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Ordinary and Partial Differential Equationsn these two responses. Understanding the mechanisms regulating apoptosis related volume changes and the ion movements resulting in the activation of the cell death program may lead to the development of drugs that target ion channels or transporters and tip the balance between cell life and death.
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Apoptosis and Cell Volume Regulationn these two responses. Understanding the mechanisms regulating apoptosis related volume changes and the ion movements resulting in the activation of the cell death program may lead to the development of drugs that target ion channels or transporters and tip the balance between cell life and death.
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Conference proceedings 2005nal Transduction. As we all recall, this symposium brought together the Doyens of Cellular and Molecular Physiology as well as aspiring young investigators and students in this field. It became a memorable event in an illustrious series of International Symposia on Cell Volume and Signaling. This se
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The Role of the Blood-Brain Barrier Na-K-2Cl Cotransporter in Strokent during cerebral ischemia. Further, our . studies have shown that the cotransporter resides predominantly in the luminal BBB membrane. This is consistent with the hypothesis that a luminal cotransporter works with abluminal Na/K ATPase to secrete NaCl into the brain, and during stroke, BBB cotrans
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Probing of the ICln Channel Pore by Cysteine Mutagenesis and Cadmium-Blocknts revealed E41 and D49 as the amino acids responsible for the Ca.-dependence of the channels’ ion selectivity and G49 to be part of the putative nucleotide binding site of the protein. H64 could be pinpointed within the ion conducting pathway of ICln. In the present study, cysteine mutagenesis and
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