IRIS
SCUDIERI, PAOLO
 Distribuzione geografica
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Continente #
EU - Europa 2.588
Totale 2.588
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Nazione #
IT - Italia 2.588
Totale 2.588
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Città #
Genova 1.395
Genoa 472
Rapallo 397
Vado Ligure 312
Bordighera 12
Totale 2.588
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Nome #
Association of TMEM16A chloride channel overexpression with airway goblet cell metaplasia 146
Goblet Cell Hyperplasia Requires High Bicarbonate Transport To Support Mucin Release 135
The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophy 133
Upregulation of TMEM16A protein in bronchial epithelial cells by bacterial pyocyanin 130
TMEM16A-TMEM16B chimaeras to investigate the structure-function relationship of calcium-activated chloride channels 125
Intermolecular Interactions in the TMEM16A Dimer Controlling Channel Activity 120
Non-canonical translation start sites in the TMEM16A chloride channel 112
A minimal isoform of the TMEM16A protein associated with chloride channel activity 112
The danger signal extracellular ATP is involved in the immunomediated damage of α-sarcoglycan deficient muscular dystrophy 104
Ion channel and lipid scramblase activity associated with expression of TMEM16F/ANO6 isoforms 101
High-throughput screening identifies FAU protein as a regulator of mutant cystic fibrosis transmembrane conductance regulator channel 74
Ionocytes and CFTR Chloride Channel Expression in Normal and Cystic Fibrosis Nasal and Bronchial Epithelial Cells 68
ANO4 (Anoctamin 4) is a novel marker of zona glomerulosa that regulates stimulated aldosterone secretion 66
The anoctamin family: TMEM16A and TMEM16B as calcium-activated chloride channels 62
Discovery of a picomolar potency pharmacological corrector of the mutant CFTR chloride channel 60
SLC26A9 as a Potential Modifier and Therapeutic Target in Cystic Fibrosis Lung Disease 55
Intermolecular interactions in the TMEM16A dimer controlling channel activity 54
The Autophagy Inhibitor Spautin-1 Antagonizes Rescue of Mutant CFTR Through an Autophagy-Independent and USP13-Mediated Mechanism 51
Pharmacological rescue of mutant CFTR protein improves the viscoelastic properties of CF mucus 49
An overview on chemical structures as ΔF508-CFTR correctors 47
Clinical and Genetic Features in Patients With Reflex Bathing Epilepsy 47
TRPV4 and purinergic receptor signalling pathways are separately linked in airway epithelia to CFTR and TMEM16A chloride channels 45
Peripheral localization of the epithelial sodium channel in the apical membrane of bronchial epithelial cells 43
Two CFTR mutations within codon 970 differently impact on the chloride channel functionality 43
Epilepsy Course and Developmental Trajectories in STXBP1-DEE 42
P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular Dystrophy 41
Increased expression of ATP12A proton pump in cystic fibrosis airways 39
Brain Organoids as Model Systems for Genetic Neurodevelopmental Disorders 39
Genotype-phenotype correlations in neurofibromatosis type 1: A single-center cohort study 39
A Phenotypic-Driven Approach for the Diagnosis of WOREE Syndrome 38
Comprehensive analysis of combinatorial pharmacological treatments to correct nonsense mutations in the cftr gene 38
Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders 37
Normal calcium-activated anion secretion in a mouse selectively lacking TMEM16A in intestinal epithelium 36
Hyperkinetic stereotyped movements in a boy with biallelic CNTNAP2 variants 35
Vesicular glutamate release from feeder-free hiPSC-derived neurons 34
null 31
De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes 30
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Epilepsy Patients With KCNC2 Pathogenic Variants 30
Light-responsive microRNA miR-211 targets Ezrin to modulate lysosomal biogenesis and retinal cell clearance 28
Somatic Double Inactivation of NF1 Associated with NF1-Related Pectus Excavatum Deformity 25
Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development 25
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture 23
Generation of an induced pluripotent stem cell line (IGGi002A) from nasal cells of a cystic fibrosis patient homozygous for the G542X-CFTR mutation 22
Mapping the human genetic architecture of COVID-19 20
TMEM16A alternative splicing coordination in breast cancer 14
mGlu5 receptor negative allosteric modulation reduces the aberrant cellular reactivity and neurotoxicity of reactive human astrocytes differentiated from fibroblast of SOD1 and C9orf72 ALS patients 14
ATP12A Proton Pump as an Emerging Therapeutic Target in Cystic Fibrosis and Other Respiratory Diseases 13
Airway surface hyperviscosity and defective mucociliary transport by IL-17/TNF-α are corrected by β-adrenergic stimulus 12
Role of ANO4 in regulation of aldosterone secretion in the zona glomerulosa of the human adrenal gland 8
Take a big sip and shrink it with ASOR 6
KCa3.1 differentially regulates trachea and bronchi epithelial gene expression in a chronic-asthma mouse model 6
Totale 2.707
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Categoria #
all - tutte 13.843
article - articoli 12.997
book - libri 0
conference - conferenze 42
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 26.882
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020286 0 0 0 0 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
2024/2025345 41 68 21 79 136 0 0 0 0 0 0 0
Totale 2.707