GALIETTA, Luis Juan Vicente
 Distribuzione geografica
Continente #
NA - Nord America 1.912
EU - Europa 634
AS - Asia 359
AF - Africa 5
Continente sconosciuto - Info sul continente non disponibili 3
OC - Oceania 2
SA - Sud America 1
Totale 2.916
Nazione #
US - Stati Uniti d'America 1.868
CN - Cina 323
IT - Italia 235
NL - Olanda 155
SE - Svezia 50
UA - Ucraina 44
CA - Canada 42
DE - Germania 39
IE - Irlanda 30
GB - Regno Unito 21
FR - Francia 15
FI - Finlandia 12
SG - Singapore 9
BE - Belgio 7
AT - Austria 5
CI - Costa d'Avorio 4
IL - Israele 4
IN - India 4
TR - Turchia 4
VN - Vietnam 4
ES - Italia 3
EU - Europa 3
HR - Croazia 3
BG - Bulgaria 2
JP - Giappone 2
RO - Romania 2
TH - Thailandia 2
AF - Afghanistan, Repubblica islamica di 1
AU - Australia 1
BD - Bangladesh 1
BR - Brasile 1
BT - Bhutan 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
GR - Grecia 1
HK - Hong Kong 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
PL - Polonia 1
PT - Portogallo 1
SI - Slovenia 1
TW - Taiwan 1
ZA - Sudafrica 1
Totale 2.916
Città #
Chandler 490
Lawrence 166
Amsterdam 155
Ashburn 143
Nanjing 142
Des Moines 131
Boston 111
Millbury 108
Naples 93
Napoli 51
Ottawa 36
Hebei 33
Shenyang 33
Nanchang 29
Wilmington 26
Jiaxing 22
Dublin 21
Changsha 20
Washington 16
Tianjin 15
Jacksonville 13
Beijing 11
Edinburgh 10
Frankfurt am Main 8
Brussels 7
Stockholm 7
Kronberg 6
Chicago 5
Fairfield 5
Ningbo 5
Vienna 5
Dong Ket 4
Fremont 4
Helsinki 4
Lappeenranta 4
Norwalk 4
Piacenza 4
Princeton 4
Tel Aviv 4
Bournemouth 3
Brescia 3
Houston 3
Izmir 3
Metz 3
Milan 3
Taizhou 3
Woodbridge 3
Zagreb 3
Agazzano 2
Andover 2
Antigonish 2
Atlanta 2
Carpi 2
Dallas 2
Hefei 2
Indiana 2
Islington 2
Jinan 2
Los Angeles 2
Madrid 2
Miami 2
Montezuma 2
Nakhon Pathom 2
New York 2
Nocera Inferiore 2
Nociglia 2
Paris 2
Qualiano 2
Rome 2
San Giuseppe Vesuviano 2
Seattle 2
Singapore 2
Sofia 2
Toronto 2
Viadanica 2
Appignano 1
Arzano 1
Athens 1
Auckland 1
Avellino 1
Bad Durrheim 1
Boardman 1
Bucharest 1
Budapest 1
Camponogara 1
Caserta 1
Catanzaro 1
Cologne 1
Como 1
Dhaka 1
Edison 1
Esslingen am Neckar 1
Frattamaggiore 1
Giugliano In Campania 1
Hangzhou 1
Istanbul 1
Johannesburg 1
Kabul 1
Kuala Lumpur 1
Lauria 1
Totale 2.061
Nome #
Light-responsive microRNA miR-211 targets Ezrin to modulate lysosomal biogenesis and retinal cell clearance 90
3-(2-Benzyloxyphenyl)isoxazoles and isoxazolines: synthesis and evaluation as CFTR activators 47
A chloride conductance evoked by hypotonic shock in epithelial cells 47
Proinflammatory cytokine secretion is suppressed by TMEM16A or CFTR channel activity in human cystic fibrosis bronchial epithelia 39
Altered expression of ano1 variants in human diabetic gastroparesis 35
Volume-sensitive chloride currents in four epithelial cell lines are not directly correlated to the expression of the MDR-1 gene 35
Two CFTR mutations within codon 970 differently impact on the chloride channel functionality 33
Activation of Ca(2+)-dependent K+ and Cl- currents by UTP and ATP in CFPAC-1 cells 32
Activation of G551D CFTR channel with MPB-91: regulation by ATPase activity and phosphorylation 32
High-throughput screening identifies FAU protein as a regulator of mutant cystic fibrosis transmembrane conductance regulator channel 31
Rheological Properties of Cystic Fibrosis Bronchial Secretion and in Vitro Drug Permeation Study: The Effect of Sodium Bicarbonate 31
Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis 31
The Autophagy Inhibitor Spautin-1 Antagonizes Rescue of Mutant CFTR Through an Autophagy-Independent and USP13-Mediated Mechanism 30
The role of functional studies in the diagnosis and treatment of Cystic Fibrosis: comparing the case of the G970D and G970R mutation. 30
Substituted 2-Acylaminocycloalkylthiophene-3-carboxylic Acid Arylamides as Inhibitors of the Calcium-Activated Chloride Channel Transmembrane Protein 16A (TMEM16A) 28
Altered channel gating mechanism for CFTR inhibition by a high-affinity thiazolidinone blocker 28
A large conductance Cl- channel revealed by patch-recordings in human fibroblasts 28
An overview on chemical structures as ΔF508-CFTR correctors 28
Effect of inflammatory stimuli on airway ion transport 27
Alternative splicing at a NAGNAG acceptor site as a novel phenotype modifier 26
Antihypertensive 1,4-dihydropyridines as correctors of the cystic fibrosis transmembrane conductance regulator channel gating defect caused by cystic fibrosis mutations 26
Ex vivo model predicted in vivo efficacy of CFTR modulator therapy in a child with rare genotype 26
Airway microenvironment alterations and pathogen growth in cystic fibrosis 25
Combination potentiator (‘co-potentiator’) therapy for CF caused by CFTR mutants, including N1303K, that are poorly responsive to single potentiators 25
Regulation of taurine transport in murine macrophages 25
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) 25
A minimal isoform of the TMEM16A protein associated with chloride channel activity 24
ATP and A1 adenosine receptor agonists mobilize intracellular calcium and activate K+ and Cl- currents in normal and cystic fibrosis airway epithelial cells 24
Thiazolidinone CFTR inhibitor identified by high-throughput screening blocks cholera toxin-induced intestinal fluid secretion 24
High-affinity activators of cystic fibrosis transmembrane conductance regulator (CFTR) chloride conductance identified by high-throughput screening 24
Association of TMEM16A chloride channel overexpression with airway goblet cell metaplasia 24
CFTR chloride channel drug discovery--inhibitors as antidiarrheals and activators for therapy of cystic fibrosis 24
A class of non-selective cation channels in human fibroblasts 24
Autocrine regulation of volume-sensitive anion channels in airway epithelial cells by adenosine 23
Speeding up the identification of cystic fibrosis transmembrane conductance regulator-targeted drugs: An approach based on bioinformatics strategies and surface plasmon resonance 23
Epithelial sodium channel inhibition in primary human bronchial epithelia by transfected siRNA 23
Biophysical characteristics of swelling-activated Cl- channels in human tracheal 9HTEo-cells 23
DOG1 regulates growth and IGFBP5 in gastrointestinal stromal tumors 23
A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree 23
Gelsolin secretion in interleukin-4-treated bronchial epithelia and in asthmatic airways 23
Correction of delF508-CFTR activity with benzo(c)quinolizinium compounds through facilitation of its processing in cystic fibrosis airway cells 23
Evidence for direct CFTR inhibition by CFTRinh-172 based on Arg347 mutagenesis 23
Small-molecule correctors of defective ΔF508-CFTR cellular processing identified by high-throughput screening 23
Unravelling druggable signalling networks that control F508del-CFTR proteostasis 22
Lectin Conjugates as Potent, Nonabsorbable CFTR Inhibitors for Reducing Intestinal Fluid Secretion in Cholera 22
Cl- currents activated by extracellular nucleotides in human bronchial cells 22
Rescue of the mutant CFTR chloride channel by pharmacological correctors and low temperature analyzed by gene expression profiling 22
α-aminoazaheterocyclic-methylglyoxal adducts do not inhibit cystic fibrosis transmembrane conductance regulator chloride channel activity 21
Proteomic analysis of the airway surface liquid: Modulation by proinflammatory cytokines 21
Regulation of transepithelial ion transport by two different purinoceptors in the apical membrane of canine kidney (MDCK) cells 21
Regulation of TMEM16A chloride channel properties by alternative splicing 21
Why is the cystic fibrosis gene so frequent? 21
Lack of Kcnn4 improves mucociliary clearance in muco-obstructive lung disease 21
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 20
Insensitivity of volume-sensitive chloride currents to chromones in human airway epithelial cells 20
Non-canonical translation start sites in the TMEM16A chloride channel 20
Dual activity of aminoarylthiazoles on the trafficking and gating defects of the cystic fibrosis transmembrane conductance regulator chloride channel caused by cystic fibrosis mutations 20
Extracellular 2-chloroadenosine and ATP stimulate volume-sensitive Cl- current and calcium mobilization in human tracheal 9HTEo- cells 20
ANO4 (Anoctamin 4) Is a Novel Marker of Zona Glomerulosa That Regulates Stimulated Aldosterone Secretion 20
Modulation of HLA-DR antigen and ICAM-1 molecule expression on airway epithelial cells by sodium nedocromil 19
High-throughput screening for modulators of ACVR1 transcription: Discovery of potential therapeutics for fibrodysplasia ossificans progressiva 19
Startle disease in an Italian family by mutation (K276E): The alpha-subunit of the inhibiting glycine receptor 19
Synthesis of 4-thiophen-2′-yl-1,4-dihydropyridines as potentiators of the CFTR chloride channel 19
TRPV4 and purinergic receptor signalling pathways are separately linked in airway epithelia to CFTR and TMEM16A chloride channels 19
Influence of cell background on pharmacological rescue of mutant CFTR 19
A volume-sensitive chloride conductance revealed in cultured human keratinocytes by 36Cl- efflux and whole-cell patch clamp recording 18
Anoctamin-1/TMEM16A is the major apical iodide channel of the thyrocyte 18
Phenylhydrazones as Correctors of a Mutant Cystic Fibrosis Transmembrane Conductance Regulator 18
The extracellular calcium-sensing receptor regulates human fetal lung development via CFTR 18
Development of the olfactory epithelium and Nasal Glands in TMEM16A-/-and TMEM16A+/ +Mice 18
TMEM16 Proteins: Membrane Channels with Unusual Pores 18
Evidence against the rescue of defective ΔF508-CFTR cellular processing by curcumin in cell culture and mouse models 18
Alternative Splicing of In-Frame Exon Associated with Premature Termination Codons: Implications for Readthrough Therapies 18
An improved method to obtain highly differentiated monolayers of human bronchial epithelial cells 18
Thiocyanate transport in resting and IL-4-stimulated human bronchial epithelial cells: role of pendrin and anion channels 18
Analysis of ion transport in the airway epithelium using RNA interference 18
Low Ca2+-sensitive maxi-K+ channels in human cultured fibroblasts 18
Intrinsic Abnormalities of Cystic Fibrosis Airway Connective Tissue Revealed by an In Vitro 3D Stromal Model 18
Goblet Cell Hyperplasia Requires High Bicarbonate Transport to Support Mucin Release 17
Upregulation of TMEM16A protein in bronchial epithelial cells by bacterial pyocyanin 17
Ion channel and lipid scramblase activity associated with expression of TMEM16F/ANO6 isoforms 17
Targeting ion channels in cystic fibrosis 17
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 17
Mutation-specific potency and efficacy of cystic fibrosis transmembrane conductance regulator chloride channel potentiators 17
Green fluorescent protein-based halide indicators with improved chloride and iodide affinities 17
Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis 17
The anoctamin family: TMEM16A and TMEM16B as calcium-activated chloride channels 17
Contribution of CFTR to apical-basolateral fluid transport in cultured human alveolar epithelial type II cells 17
Asymmetric 4-Aryl-1,4-dihydropyridines Potentiate Mutant Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) 16
Evaluation of a systems biology approach to identify pharmacological correctors of the mutant CFTR chloride channel 16
The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophy 16
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) 16
Functional analysis of acid-activated Cl- channels: Properties and mechanisms of regulation 16
Genetic Inhibition of the Ubiquitin Ligase Rnf5 Attenuates Phenotypes Associated to F508del Cystic Fibrosis Mutation 16
Volume regulatory taurine release in human tracheal 9HTEo- and multidrug resistant 9HTEo-/Dx cells 16
Phenylglycine and sulfonamide correctors of defective ΔF508 and G551D cystic fibrosis transmembrane conductance regulator chloride-channel gating 16
High-throughput screening of libraries of compounds to identify CFTR modulators 16
Nanomolar affinity small molecule correctors of defective ΔF508-CFTR chloride channel gating 16
IL-12 can target human lung adenocarcinoma cells and normal bronchial epithelial cells surrounding tumor lesions 16
Normal calcium-activated anion secretion in a mouse selectively lacking TMEM16A in intestinal epithelium 16
Totale 2.302
Categoria #
all - tutte 13.031
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 13.031


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201928 0 0 0 0 0 0 0 0 2 0 3 23
2019/2020398 289 2 9 4 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
2022/20231.304 176 48 12 129 140 152 12 154 227 123 110 21
2023/2024521 36 145 116 73 38 48 27 32 6 0 0 0
Totale 3.133