about
Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathyHigher order structure of aquaporin-4AQP4-dependent water transport plays a functional role in exercise-induced skeletal muscle adaptationsAquaporin-4 autoantibodies in Neuromyelitis Optica: AQP4 isoform-dependent sensitivity and specificityDevelopment of an Aquaporin-4 Orthogonal Array of Particle-Based ELISA for Neuromyelitis Optica Autoantibodies Detection.A novel human aquaporin-4 splice variant exhibits a dominant-negative activity: a new mechanism to regulate water permeability.Role of the H-bond between L53 and T56 for Aquaporin-4 epitope in Neuromyelitis Optica.AQP5 is expressed in type-B intercalated cells in the collecting duct system of the rat, mouse and human kidney.Aquaporin-4 orthogonal arrays of particles are the target for neuromyelitis optica autoantibodies.Glio-vascular modifications caused by Aquaporin-4 deletion in the mouse retina.Massive transcriptome sequencing of human spinal cord tissues provides new insights into motor neuron degeneration in ALSIdentification 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.Tapia's syndrome secondary to laterocervical localization of diffuse large cell lymphoma.Unusual trigeminal autonomic pain heralding hemichorea due to zoster sine Herpete vasculopathy.Patterns of Novel Alleles and Genotype/Phenotype Correlations Resulting from the Analysis of 108 Previously Undetected Mutations in Patients Affected by Neurofibromatosis Type I.Correction: AQP4-Dependent Water Transport Plays a Functional Role in Exercise-Induced Skeletal Muscle Adaptations.Potential role of the methylation of VEGF gene promoter in response to hypoxia in oxygen-induced retinopathy: beneficial effect of the absence of AQP4.Aquaporin-1 inhibition reduces metastatic formation in a mouse model of melanoma.Supramolecular aggregation of aquaporin-4 is different in muscle and brain: correlation with tissue susceptibility in neuromyelitis optica.Translational readthrough generates new astrocyte AQP4 isoforms that modulate supramolecular clustering, glial endfeet localization, and water transport.D184E mutation in aquaporin-4 gene impairs water permeability and links to deafness.A new gating site in human aquaporin-4: Insights from molecular dynamics simulationsAquaporin-4 orthogonal arrays of particles from a physiological and pathophysiological point of viewAQP4 Aggregation State Is a Determinant for Glioma Cell Fate
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description
researcher ORCID: 0000-0001-8511-117X
@en
name
Francesco Pisani
@ast
Francesco Pisani
@en
Francesco Pisani
@es
Francesco Pisani
@nl
type
label
Francesco Pisani
@ast
Francesco Pisani
@en
Francesco Pisani
@es
Francesco Pisani
@nl
prefLabel
Francesco Pisani
@ast
Francesco Pisani
@en
Francesco Pisani
@es
Francesco Pisani
@nl
P106
P1153
55458095800
P21
P31
P496
0000-0001-8511-117X