SCUDIERI, PAOLO
 Distribuzione geografica
Continente #
EU - Europa 2.300
Totale 2.300
Nazione #
IT - Italia 2.300
Totale 2.300
Città #
Genova 1.395
Genoa 472
Rapallo 397
Vado Ligure 24
Bordighera 12
Totale 2.300
Nome #
Association of TMEM16A chloride channel overexpression with airway goblet cell metaplasia 141
Upregulation of TMEM16A protein in bronchial epithelial cells by bacterial pyocyanin 126
Goblet Cell Hyperplasia Requires High Bicarbonate Transport To Support Mucin Release 124
TMEM16A-TMEM16B chimaeras to investigate the structure-function relationship of calcium-activated chloride channels 120
The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophy 120
Intermolecular Interactions in the TMEM16A Dimer Controlling Channel Activity 116
Non-canonical translation start sites in the TMEM16A chloride channel 108
A minimal isoform of the TMEM16A protein associated with chloride channel activity 103
The danger signal extracellular ATP is involved in the immunomediated damage of α-sarcoglycan deficient muscular dystrophy 101
Ion channel and lipid scramblase activity associated with expression of TMEM16F/ANO6 isoforms 96
High-throughput screening identifies FAU protein as a regulator of mutant cystic fibrosis transmembrane conductance regulator channel 67
ANO4 (Anoctamin 4) is a novel marker of zona glomerulosa that regulates stimulated aldosterone secretion 61
Ionocytes and CFTR Chloride Channel Expression in Normal and Cystic Fibrosis Nasal and Bronchial Epithelial Cells 60
The anoctamin family: TMEM16A and TMEM16B as calcium-activated chloride channels 57
Discovery of a picomolar potency pharmacological corrector of the mutant CFTR chloride channel 55
Intermolecular interactions in the TMEM16A dimer controlling channel activity 48
The Autophagy Inhibitor Spautin-1 Antagonizes Rescue of Mutant CFTR Through an Autophagy-Independent and USP13-Mediated Mechanism 45
Pharmacological rescue of mutant CFTR protein improves the viscoelastic properties of CF mucus 43
Clinical and Genetic Features in Patients With Reflex Bathing Epilepsy 43
An overview on chemical structures as ΔF508-CFTR correctors 41
Peripheral localization of the epithelial sodium channel in the apical membrane of bronchial epithelial cells 40
SLC26A9 as a Potential Modifier and Therapeutic Target in Cystic Fibrosis Lung Disease 40
Two CFTR mutations within codon 970 differently impact on the chloride channel functionality 39
Epilepsy Course and Developmental Trajectories in STXBP1-DEE 36
TRPV4 and purinergic receptor signalling pathways are separately linked in airway epithelia to CFTR and TMEM16A chloride channels 36
Increased expression of ATP12A proton pump in cystic fibrosis airways 35
Normal calcium-activated anion secretion in a mouse selectively lacking TMEM16A in intestinal epithelium 34
Brain Organoids as Model Systems for Genetic Neurodevelopmental Disorders 34
P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular Dystrophy 34
Comprehensive analysis of combinatorial pharmacological treatments to correct nonsense mutations in the cftr gene 33
Genotype-phenotype correlations in neurofibromatosis type 1: A single-center cohort study 32
null 31
Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders 30
Hyperkinetic stereotyped movements in a boy with biallelic CNTNAP2 variants 30
A Phenotypic-Driven Approach for the Diagnosis of WOREE Syndrome 29
Vesicular glutamate release from feeder-free hiPSC-derived neurons 28
Light-responsive microRNA miR-211 targets Ezrin to modulate lysosomal biogenesis and retinal cell clearance 26
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Epilepsy Patients With KCNC2 Pathogenic Variants 26
De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes 24
Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development 20
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture 18
Mapping the human genetic architecture of COVID-19 17
Somatic Double Inactivation of NF1 Associated with NF1-Related Pectus Excavatum Deformity 16
Generation of an induced pluripotent stem cell line (IGGi002A) from nasal cells of a cystic fibrosis patient homozygous for the G542X-CFTR mutation 14
TMEM16A alternative splicing coordination in breast cancer 10
ATP12A Proton Pump as an Emerging Therapeutic Target in Cystic Fibrosis and Other Respiratory Diseases 7
Role of ANO4 in regulation of aldosterone secretion in the zona glomerulosa of the human adrenal gland 6
Airway surface hyperviscosity and defective mucociliary transport by IL-17/TNF-α are corrected by β-adrenergic stimulus 6
Take a big sip and shrink it with ASOR 4
KCa3.1 differentially regulates trachea and bronchi epithelial gene expression in a chronic-asthma mouse model 3
Totale 2.413
Categoria #
all - tutte 11.895
article - articoli 11.153
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 23.048


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020334 0 11 8 29 34 40 61 31 32 46 32 10
2020/2021478 6 9 79 119 12 16 36 37 25 74 45 20
2021/2022357 12 14 19 29 19 12 11 85 24 39 29 64
2022/2023478 42 41 14 39 86 63 9 35 68 3 72 6
2023/2024397 19 52 8 49 31 59 20 29 16 16 33 65
2024/202551 41 10 0 0 0 0 0 0 0 0 0 0
Totale 2.413