Discovery of CLC transport proteins: cloning, structure, function and pathophysiology
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Therapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug DiscoveryThe Origin of Coupled Chloride and Proton Transport in a Cl(-)/H(+) AntiporterClC-1 chloride channels: state-of-the-art research and future challenges.Revealing an outward-facing open conformational state in a CLC Cl(-)/H(+) exchange transporterMolecular bases of K(+) secretory cells in the inner ear: shared and distinct features between birds and mammalsThe Arabidopsis Thylakoid Chloride Channel AtCLCe Functions in Chloride Homeostasis and Regulation of Photosynthetic Electron Transport.Ubiquitination and the Regulation of Membrane Proteins.ClC Channels and Transporters: Structure, Physiological Functions, and Implications in Human Chloride Channelopathies.Biology of SLAC1-type anion channels - from nutrient uptake to stomatal closure.Alkaline activation of ClC-K2 chloride channels switches renal cells from reabsorbing to secreting.Structure of a CLC chloride ion channel by cryo-electron microscopyMouse models of human ocular disease for translational research.Protein ligands for studying ion channel proteins.Identification and characterization of the three members of the CLC family of anion transport proteins in Trypanosoma brucei.Leukoencephalopathy-causing CLCN2 mutations are associated with impaired Cl- channel function and trafficking.De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females.CLCN2 chloride channel mutations in familial hyperaldosteronism type II.Multiscale Kinetic Modeling Reveals an Ensemble of Cl-/H+ Exchange Pathways in ClC-ec1 Antiporter.Ion Transport at the Vacuole during Stomatal Movements.Depolarization causes the formation of a ternary complex between GlialCAM, MLC1 and ClC-2 in astrocytes: implications in megalencephalic leukoencephalopathy.Identification of Sidt2 as a lysosomal cation-conducting protein.A selective class of inhibitors for the CLC-Ka chloride ion channel.Chloride Ion Transport by the E. coli CLC Cl-/H+ Antiporter: A Combined Quantum-Mechanical and Molecular-Mechanical Study.Chloride Homeostasis in Neurons With Special Emphasis on the Olivocerebellar System: Differential Roles for Transporters and Channels.Suppression of chloride voltage-gated channel 3 expression increases sensitivity of human glioma U251 cells to cisplatin through lysosomal dysfunction.
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P2860
Discovery of CLC transport proteins: cloning, structure, function and pathophysiology
description
2015 nî lūn-bûn
@nan
2015 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Discovery of CLC transport proteins: cloning, structure, function and pathophysiology
@ast
Discovery of CLC transport proteins: cloning, structure, function and pathophysiology
@en
Discovery of CLC transport proteins: cloning, structure, function and pathophysiology
@nl
type
label
Discovery of CLC transport proteins: cloning, structure, function and pathophysiology
@ast
Discovery of CLC transport proteins: cloning, structure, function and pathophysiology
@en
Discovery of CLC transport proteins: cloning, structure, function and pathophysiology
@nl
prefLabel
Discovery of CLC transport proteins: cloning, structure, function and pathophysiology
@ast
Discovery of CLC transport proteins: cloning, structure, function and pathophysiology
@en
Discovery of CLC transport proteins: cloning, structure, function and pathophysiology
@nl
P2860
P3181
P356
P1476
Discovery of CLC transport proteins: cloning, structure, function and pathophysiology
@en
P2093
Thomas J. Jentsch
P2860
P304
P3181
P356
10.1113/JP270043
P407
P577
2015-09-15T00:00:00Z