about
Biogenesis and transmembrane topology of the CHIP28 water channel at the endoplasmic reticulumAquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathiesHigher order structure of aquaporin-4Cloning of a water channel homolog expressed in brain meningeal cells and kidney collecting duct that functions as a stilbene-sensitive glycerol transporterAutomated cell-based assay for screening of aquaporin inhibitors.Absence of aquaporin-4 in skeletal muscle alters proteins involved in bioenergetic pathways and calcium handling.Bone marrow angiogenesis in patients with active multiple myeloma.AQP4-dependent water transport plays a functional role in exercise-induced skeletal muscle adaptationsAquaporin-4 autoantibodies in Neuromyelitis Optica: AQP4 isoform-dependent sensitivity and specificityA multidisciplinary evaluation of the effectiveness of cyclosporine a in dystrophic mdx mice.Aquaporin-4 expression during development of the cerebellum.The role of aquaporin-4 in the blood-brain barrier development and integrity: studies in animal and cell culture models.Expression, functional analysis, and in situ hybridization of a cloned rat kidney collecting duct water channel.Transepithelial water permeability in microperfused distal airways. Evidence for channel-mediated water transport.Expression of aquaporin-4 in fast-twitch fibers of mammalian skeletal muscle.A novel human aquaporin-4 splice variant exhibits a dominant-negative activity: a new mechanism to regulate water permeability.The speed of swelling kinetics modulates cell volume regulation and calcium signaling in astrocytes: A different point of view on the role of aquaporins.Aquaporin-4 orthogonal arrays of particles are the target for neuromyelitis optica autoantibodies.Actin cytoskeleton remodeling governs aquaporin-4 localization in astrocytes.Structure and function of kidney water channels.A heterotrimeric G protein of the Gi family is required for cAMP-triggered trafficking of aquaporin 2 in kidney epithelial cells.Expression and functional analysis of water channels in a stably AQP2-transfected human collecting duct cell line.Localization and functional analysis of CHIP28k water channels in stably transfected Chinese hamster ovary cells.Effects of chronic treatment with statins and fenofibrate on rat skeletal muscle: a biochemical, histological and electrophysiological study.Identification of a point mutation impairing the binding between aquaporin-4 and neuromyelitis optica autoantibodies.Detection of anti-aquaporin-4 autoantibodies in the sera of Chinese neuromyelitis optica patients.Effect of microgravity on gene expression in mouse brain.The KATP channel is a molecular sensor of atrophy in skeletal muscle.Tissue distribution and membrane localization of aquaporin-9 water channel: evidence for sex-linked differences in liver.DNA adducts, benzo(a)pyrene monooxygenase activity, and lysosomal membrane stability in Mytilus galloprovincialis from different areas in Taranto coastal waters (Italy).The alteration of calcium homeostasis in adult dystrophic mdx muscle fibers is worsened by a chronic exercise in vivo.Gentamicin treatment in exercised mdx mice: Identification of dystrophin-sensitive pathways and evaluation of efficacy in work-loaded dystrophic muscle.Potential role of the methylation of VEGF gene promoter in response to hypoxia in oxygen-induced retinopathy: beneficial effect of the absence of AQP4.Altered blood-brain barrier development in dystrophic MDX mice.Supramolecular aggregation of aquaporin-4 is different in muscle and brain: correlation with tissue susceptibility in neuromyelitis optica.Response to 'The evolving mystery of why skeletal muscle is spared in seropositive neuromyelitis optica'.Translational readthrough generates new astrocyte AQP4 isoforms that modulate supramolecular clustering, glial endfeet localization, and water transport.Functional down-regulation of volume-regulated anion channels in AQP4 knockdown cultured rat cortical astrocytes.Change of chloride ion channel conductance is an early event of slow-to-fast fibre type transition during unloading-induced muscle disuse.Altered aquaporin-4 expression in human muscular dystrophies: a common feature?
P50
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wetenschapper
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հետազոտող
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A Frigeri
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A Frigeri
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A Frigeri
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A Frigeri
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A Frigeri
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A Frigeri
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A Frigeri
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A Frigeri
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A Frigeri
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A Frigeri
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A Frigeri
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P106
P1153
7003582574
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0000-0002-5284-2934