IRIS
GALIETTA, Luis Juan Vicente
 Distribuzione geografica
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Continente #
NA - Nord America 2.171
AS - Asia 827
EU - Europa 677
AF - Africa 5
Continente sconosciuto - Info sul continente non disponibili 3
OC - Oceania 2
SA - Sud America 2
Totale 3.687
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Nazione #
US - Stati Uniti d'America 2.127
SG - Singapore 450
CN - Cina 346
IT - Italia 256
NL - Olanda 156
SE - Svezia 50
UA - Ucraina 44
CA - Canada 42
DE - Germania 40
GB - Regno Unito 34
IE - Irlanda 29
FR - Francia 18
FI - Finlandia 15
BE - Belgio 7
IN - India 6
AT - Austria 5
CI - Costa d'Avorio 4
IL - Israele 4
TR - Turchia 4
VN - Vietnam 4
ES - Italia 3
EU - Europa 3
HR - Croazia 3
BG - Bulgaria 2
BR - Brasile 2
CZ - Repubblica Ceca 2
HK - Hong Kong 2
JP - Giappone 2
PL - Polonia 2
RO - Romania 2
TH - Thailandia 2
AF - Afghanistan, Repubblica islamica di 1
AU - Australia 1
BD - Bangladesh 1
BT - Bhutan 1
CH - Svizzera 1
DK - Danimarca 1
GR - Grecia 1
HU - Ungheria 1
IR - Iran 1
LT - Lituania 1
MK - Macedonia 1
MX - Messico 1
MY - Malesia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PA - Panama 1
PT - Portogallo 1
SA - Arabia Saudita 1
SI - Slovenia 1
TW - Taiwan 1
ZA - Sudafrica 1
Totale 3.687
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Città #
Chandler 490
Singapore 363
Lawrence 166
Amsterdam 155
Ashburn 147
Nanjing 142
Des Moines 131
Boston 111
Millbury 108
Naples 100
Santa Clara 100
Napoli 51
Ottawa 36
Shenyang 34
Hebei 33
Nanchang 29
Wilmington 26
Jiaxing 22
Changsha 20
Dublin 20
Washington 18
Tianjin 15
Jacksonville 13
Brighton 12
Beijing 11
Edinburgh 10
Frankfurt am Main 9
Brussels 7
Helsinki 7
Milan 7
Stockholm 7
Kronberg 6
Boardman 5
Chicago 5
Fairfield 5
Ningbo 5
Vienna 5
Dong Ket 4
Fremont 4
Lappeenranta 4
Los Angeles 4
Norwalk 4
Piacenza 4
Princeton 4
Springfield 4
Tel Aviv 4
Bournemouth 3
Brescia 3
Houston 3
Izmir 3
Kunming 3
Metz 3
Rome 3
Taizhou 3
Woodbridge 3
Zagreb 3
Agazzano 2
Andover 2
Antigonish 2
Atlanta 2
Carpi 2
Dallas 2
Fort Worth 2
Hefei 2
Indiana 2
Islington 2
Jinan 2
London 2
Madrid 2
Miami 2
Montezuma 2
Nakhon Pathom 2
New York 2
Nocera Inferiore 2
Nociglia 2
Paris 2
Qualiano 2
San Giuseppe Vesuviano 2
Seattle 2
Shanghai 2
Sofia 2
Toronto 2
Viadanica 2
Warsaw 2
Appignano 1
Arzano 1
Athens 1
Auckland 1
Avellino 1
Bad Durrheim 1
Brno 1
Bucharest 1
Budapest 1
Buffalo 1
Camponogara 1
Caserta 1
Catanzaro 1
Cologne 1
Como 1
Dhaka 1
Totale 2.569
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Nome #
Light-responsive microRNA miR-211 targets Ezrin to modulate lysosomal biogenesis and retinal cell clearance 99
3-(2-Benzyloxyphenyl)isoxazoles and isoxazolines: synthesis and evaluation as CFTR activators 56
A chloride conductance evoked by hypotonic shock in epithelial cells 50
Proinflammatory cytokine secretion is suppressed by TMEM16A or CFTR channel activity in human cystic fibrosis bronchial epithelia 42
Two CFTR mutations within codon 970 differently impact on the chloride channel functionality 40
Altered expression of ano1 variants in human diabetic gastroparesis 38
A large conductance Cl- channel revealed by patch-recordings in human fibroblasts 38
The role of functional studies in the diagnosis and treatment of Cystic Fibrosis: comparing the case of the G970D and G970R mutation. 38
Volume-sensitive chloride currents in four epithelial cell lines are not directly correlated to the expression of the MDR-1 gene 37
High-throughput screening identifies FAU protein as a regulator of mutant cystic fibrosis transmembrane conductance regulator channel 36
Rheological Properties of Cystic Fibrosis Bronchial Secretion and in Vitro Drug Permeation Study: The Effect of Sodium Bicarbonate 36
Why is the cystic fibrosis gene so frequent? 36
Substituted 2-Acylaminocycloalkylthiophene-3-carboxylic Acid Arylamides as Inhibitors of the Calcium-Activated Chloride Channel Transmembrane Protein 16A (TMEM16A) 35
Activation of Ca(2+)-dependent K+ and Cl- currents by UTP and ATP in CFPAC-1 cells 34
Activation of G551D CFTR channel with MPB-91: regulation by ATPase activity and phosphorylation 34
Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis 33
An overview on chemical structures as ΔF508-CFTR correctors 33
The Autophagy Inhibitor Spautin-1 Antagonizes Rescue of Mutant CFTR Through an Autophagy-Independent and USP13-Mediated Mechanism 32
ATP and A1 adenosine receptor agonists mobilize intracellular calcium and activate K+ and Cl- currents in normal and cystic fibrosis airway epithelial cells 31
Alternative splicing at a NAGNAG acceptor site as a novel phenotype modifier 31
Effect of inflammatory stimuli on airway ion transport 30
Altered channel gating mechanism for CFTR inhibition by a high-affinity thiazolidinone blocker 30
Airway microenvironment alterations and pathogen growth in cystic fibrosis 29
Regulation of TMEM16A chloride channel properties by alternative splicing 29
Antihypertensive 1,4-dihydropyridines as correctors of the cystic fibrosis transmembrane conductance regulator channel gating defect caused by cystic fibrosis mutations 29
A minimal isoform of the TMEM16A protein associated with chloride channel activity 28
Combination potentiator (‘co-potentiator’) therapy for CF caused by CFTR mutants, including N1303K, that are poorly responsive to single potentiators 28
Biophysical characteristics of swelling-activated Cl- channels in human tracheal 9HTEo-cells 28
Novel Hits in the Correction of δf508-Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Protein: Synthesis, Pharmacological, and ADME Evaluation of Tetrahydropyrido[4,3-d]pyrimidines for the Potential Treatment of Cystic Fibrosis 27
Epithelial sodium channel inhibition in primary human bronchial epithelia by transfected siRNA 27
Thiazolidinone CFTR inhibitor identified by high-throughput screening blocks cholera toxin-induced intestinal fluid secretion 27
High-affinity activators of cystic fibrosis transmembrane conductance regulator (CFTR) chloride conductance identified by high-throughput screening 27
DOG1 regulates growth and IGFBP5 in gastrointestinal stromal tumors 27
Association of TMEM16A chloride channel overexpression with airway goblet cell metaplasia 27
Correction of delF508-CFTR activity with benzo(c)quinolizinium compounds through facilitation of its processing in cystic fibrosis airway cells 27
Regulation of taurine transport in murine macrophages 27
A class of non-selective cation channels in human fibroblasts 27
Ex vivo model predicted in vivo efficacy of CFTR modulator therapy in a child with rare genotype 27
High-throughput screening for modulators of ACVR1 transcription: Discovery of potential therapeutics for fibrodysplasia ossificans progressiva 26
Volume regulatory taurine release in human tracheal 9HTEo- and multidrug resistant 9HTEo-/Dx cells 26
Regulation of transepithelial ion transport by two different purinoceptors in the apical membrane of canine kidney (MDCK) cells 26
Evidence for direct CFTR inhibition by CFTRinh-172 based on Arg347 mutagenesis 26
CFTR chloride channel drug discovery--inhibitors as antidiarrheals and activators for therapy of cystic fibrosis 26
Small-molecule correctors of defective ΔF508-CFTR cellular processing identified by high-throughput screening 26
Author Correction: Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis (Scientific Reports, (2019), 9, 1, (6516), 10.1038/s41598-019-42751-4) 26
Autocrine regulation of volume-sensitive anion channels in airway epithelial cells by adenosine 25
Unravelling druggable signalling networks that control F508del-CFTR proteostasis 25
Speeding up the identification of cystic fibrosis transmembrane conductance regulator-targeted drugs: An approach based on bioinformatics strategies and surface plasmon resonance 25
Lectin Conjugates as Potent, Nonabsorbable CFTR Inhibitors for Reducing Intestinal Fluid Secretion in Cholera 25
Phenylglycine and sulfonamide correctors of defective ΔF508 and G551D cystic fibrosis transmembrane conductance regulator chloride-channel gating 25
A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree 25
Dual activity of aminoarylthiazoles on the trafficking and gating defects of the cystic fibrosis transmembrane conductance regulator chloride channel caused by cystic fibrosis mutations 25
Gelsolin secretion in interleukin-4-treated bronchial epithelia and in asthmatic airways 25
TMEM16 Proteins: Membrane Channels with Unusual Pores 24
Characterization of the human gene coding for the swelling-dependent chloride channel ICln at position 11q13.5-14.1 (CLNS1A) and further characterization of the chromosome 6 (CLNS1B) localization 24
α-aminoazaheterocyclic-methylglyoxal adducts do not inhibit cystic fibrosis transmembrane conductance regulator chloride channel activity 24
Proteomic analysis of the airway surface liquid: Modulation by proinflammatory cytokines 24
Non-canonical translation start sites in the TMEM16A chloride channel 24
Cl- currents activated by extracellular nucleotides in human bronchial cells 24
Rescue of the mutant CFTR chloride channel by pharmacological correctors and low temperature analyzed by gene expression profiling 24
Extracellular 2-chloroadenosine and ATP stimulate volume-sensitive Cl- current and calcium mobilization in human tracheal 9HTEo- cells 24
Ionocytes and CFTR Chloride Channel Expression in Normal and Cystic Fibrosis Nasal and Bronchial Epithelial Cells 24
Lack of Kcnn4 improves mucociliary clearance in muco-obstructive lung disease 24
Modulation of HLA-DR antigen and ICAM-1 molecule expression on airway epithelial cells by sodium nedocromil 23
Phenylhydrazones as Correctors of a Mutant Cystic Fibrosis Transmembrane Conductance Regulator 23
Development of the olfactory epithelium and Nasal Glands in TMEM16A-/-and TMEM16A+/ +Mice 23
Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis 23
ANO4 (Anoctamin 4) Is a Novel Marker of Zona Glomerulosa That Regulates Stimulated Aldosterone Secretion 23
TRPV4 and purinergic receptor signalling pathways are separately linked in airway epithelia to CFTR and TMEM16A chloride channels 23
Anoctamin-1/TMEM16A is the major apical iodide channel of the thyrocyte 22
Evaluation of a systems biology approach to identify pharmacological correctors of the mutant CFTR chloride channel 22
Upregulation of TMEM16A protein in bronchial epithelial cells by bacterial pyocyanin 22
The extracellular calcium-sensing receptor regulates human fetal lung development via CFTR 22
Functional analysis of acid-activated Cl- channels: Properties and mechanisms of regulation 22
Targeting ion channels in cystic fibrosis 22
Insensitivity of volume-sensitive chloride currents to chromones in human airway epithelial cells 22
Green fluorescent protein-based halide indicators with improved chloride and iodide affinities 22
Startle disease in an Italian family by mutation (K276E): The alpha-subunit of the inhibiting glycine receptor 22
Analysis of ion transport in the airway epithelium using RNA interference 22
Synthesis of 4-thiophen-2′-yl-1,4-dihydropyridines as potentiators of the CFTR chloride channel 22
Low Ca2+-sensitive maxi-K+ channels in human cultured fibroblasts 22
Influence of cell background on pharmacological rescue of mutant CFTR 22
Goblet Cell Hyperplasia Requires High Bicarbonate Transport to Support Mucin Release 21
The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophy 21
Ion channel and lipid scramblase activity associated with expression of TMEM16F/ANO6 isoforms 21
CFTR pharmacology 21
Evidence against the rescue of defective ΔF508-CFTR cellular processing by curcumin in cell culture and mouse models 21
Mutation-specific potency and efficacy of cystic fibrosis transmembrane conductance regulator chloride channel potentiators 21
Normal calcium-activated anion secretion in a mouse selectively lacking TMEM16A in intestinal epithelium 21
Intrinsic Abnormalities of Cystic Fibrosis Airway Connective Tissue Revealed by an In Vitro 3D Stromal Model 21
A volume-sensitive chloride conductance revealed in cultured human keratinocytes by 36Cl- efflux and whole-cell patch clamp recording 20
Asymmetric 4-Aryl-1,4-dihydropyridines Potentiate Mutant Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) 20
Identification and characterization of a novel promoter for the human ANO1 gene regulated by the transcription factor signal transducer and activator of transcription 6 (STAT6) 20
Genetic Inhibition of the Ubiquitin Ligase Rnf5 Attenuates Phenotypes Associated to F508del Cystic Fibrosis Mutation 20
Pharmacological analysis of epithelial chloride secretion mechanisms in adult murine airways 20
Alternative Splicing of In-Frame Exon Associated with Premature Termination Codons: Implications for Readthrough Therapies 20
An improved method to obtain highly differentiated monolayers of human bronchial epithelial cells 20
Nanomolar CFTR Inhibition by Pore-Occluding Divalent Polyethylene Glycol-Malonic Acid Hydrazides 20
Thiocyanate transport in resting and IL-4-stimulated human bronchial epithelial cells: role of pendrin and anion channels 20
The anoctamin family: TMEM16A and TMEM16B as calcium-activated chloride channels 20
Totale 2.724
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Categoria #
all - tutte 20.567
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 20.567
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202094 0 0 0 0 0 0 4 2 23 8 35 22
2020/2021137 0 1 20 11 10 15 10 5 30 11 14 10
2021/2022560 5 1 2 8 30 28 4 23 20 7 57 375
2022/20231.300 176 48 12 129 140 152 12 154 224 122 110 21
2023/2024723 36 145 116 73 34 48 27 32 6 6 128 72
2024/2025583 235 263 20 23 42 0 0 0 0 0 0 0
Totale 3.914