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Maria Svelto

Researcher at University of Bari

Publications -  197
Citations -  8331

Maria Svelto is an academic researcher from University of Bari. The author has contributed to research in topics: Aquaporin & Water transport. The author has an hindex of 52, co-authored 188 publications receiving 7471 citations. Previous affiliations of Maria Svelto include University of Basilicata.

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Minireview: aquaporin 2 trafficking.

TL;DR: Recent data support the hypothesis that, in vivo external calcium, through activation of calcium-sensing receptors, modulates the expression/trafficking of AQP2.
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FGF signalling regulates bone growth through autophagy

TL;DR: It is shown that autophagy is induced in growth-plate chondrocytes during post-natal development and regulates the secretion of type II collagen (Col2), the major component of cartilage ECM, and is identified as a novel effector of FGF signalling in bone.
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Role of aquaporin-4 water channel in the development and integrity of the blood-brain barrier.

TL;DR: The results show that aquaporin-4 expression occurs in the chick embryonic brain, in parallel with maturation and functioning of the blood-brain barrier and suggest that there is a close relationship between water transport regulation and brain development.
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Inhibition of aquaporin-4 expression in astrocytes by RNAi determines alteration in cell morphology, growth, and water transport and induces changes in ischemia-related genes

TL;DR: AQP4 seems to be the major factor responsible for the fast water transport of cultured astrocytes, as in skeletal muscle, AQP4 is a protein involved in cell plasticity and RNA interference could be a new potent tool for studying AQP pathophysiology in those organs and tissues where they are expressed.
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Aquaporin‐4 orthogonal arrays of particles are the target for neuromyelitis optica autoantibodies

TL;DR: This study demonstrates that in the CNS, NMO‐IgG is able to pull down both M1‐ and M23‐AQP4 but experiments performed using cells selectively transfected with M1- or M23-AqP4 and native tissues show NMO'G epitope to be intrinsic in AQP4 assemblies into OAPs.