FAVIA, MARIA
 Distribuzione geografica
Continente #
NA - Nord America 3.086
EU - Europa 756
AS - Asia 361
OC - Oceania 7
AF - Africa 1
SA - Sud America 1
Totale 4.212
Nazione #
US - Stati Uniti d'America 3.079
CN - Cina 300
SE - Svezia 252
IT - Italia 136
DE - Germania 120
FI - Finlandia 72
UA - Ucraina 56
GB - Regno Unito 51
SG - Singapore 31
FR - Francia 19
RU - Federazione Russa 16
BE - Belgio 15
IN - India 11
IE - Irlanda 9
CA - Canada 7
AU - Australia 5
KR - Corea 4
VN - Vietnam 4
AT - Austria 3
NL - Olanda 3
HK - Hong Kong 2
IR - Iran 2
JP - Giappone 2
NZ - Nuova Zelanda 2
AE - Emirati Arabi Uniti 1
BG - Bulgaria 1
CH - Svizzera 1
CL - Cile 1
EG - Egitto 1
ES - Italia 1
PK - Pakistan 1
RO - Romania 1
SA - Arabia Saudita 1
TH - Thailandia 1
TR - Turchia 1
Totale 4.212
Città #
Chandler 405
Fairfield 358
Woodbridge 302
Ashburn 225
Nyköping 211
Houston 193
Seattle 165
Cambridge 156
Jacksonville 148
Ann Arbor 140
Wilmington 133
Dearborn 91
Nanjing 75
Lawrence 71
Roxbury 67
Beijing 63
Bari 61
Princeton 42
Des Moines 38
New York 36
Brooklyn 35
Inglewood 30
San Diego 22
Singapore 18
Boardman 17
Helsinki 17
Shenyang 17
Guangzhou 16
Hebei 15
Brussels 14
Nanchang 14
Falls Church 13
Kunming 13
Jiaxing 11
Changsha 9
Hefei 9
Paris 9
Dublin 8
Los Angeles 8
San Francisco 7
Milan 6
Norwalk 6
Pune 6
Redwood City 6
San Mateo 6
Washington 6
Shanghai 5
Carosino 4
Catania 4
Dong Ket 4
Foggia 4
Hounslow 4
Melbourne 4
Tianjin 4
Zhengzhou 4
Bremen 3
Jinan 3
Jinhua 3
Leawood 3
London 3
Ningbo 3
Strasbourg 3
Toronto 3
Wuhan 3
Acireale 2
Alberobello 2
Auburn Hills 2
Austin 2
Bitonto 2
Cerignola 2
Chongqing 2
Edinburgh 2
Fuzhou 2
Grafing 2
Gragnano 2
Haikou 2
Hangzhou 2
Hong Kong 2
Kilburn 2
Mola Di Bari 2
Parma 2
Perg 2
Prescot 2
Shaoxing 2
Silvi 2
Triggiano 2
Turin 2
Wuxi 2
Yellow Springs 2
Acquaviva Delle Fonti 1
Amsterdam 1
Ardabil 1
Auckland 1
Augusta 1
Baotou 1
Brindisi 1
Cairo 1
Canberra 1
Chengdu 1
Christchurch 1
Totale 3.443
Nome #
Correctors of mutant CFTR enhance subcortical cAMP-PKA signaling through modulating ezrin phosphorylation and cytoskeleton organization 149
Cftr gene targeting in mouse embryonic stem cells mediated by Small Fragment Homologous Replacement (SFHR) 128
Characterization of mitochondrial function in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function 123
Antibiotic therapy affects functional behaviour in cystic fibrosis blood mononuclear cells 121
Trimethylangelicin promotes the functional rescue of mutant F508del CFTR protein in cystic fibrosis airway cells 116
G-CSF and GM-CSF Modify Neutrophil Functions at Concentrations found in Cystic Fibrosis 111
NHERF1 and CFTR restore tight junction organisation and function in cystic fibrosis airway epithelial cells: Role of ezrin and the RhoA/ROCK pathway 110
NHE3 inhibits PKA-dependent functional expression of CFTR by NHERF2 PDZ interactions 107
Pseudomonas aeruginosa reduces the expression of CFTR via post-translational modification of NHERF1 98
Extracellular adenine nucleotides regulate Na/H exchanger NHE3 activity in A6-NHE3 transfectants by a cAMP/PKA-dependent mechanism 96
CFTR-dependent chloride efflux in cystic fibrosis mononuclear cells is increased by ivacaftor therapy 93
Hematopoietic Stem/Progenitor Cells Express Functional Mitochondrial Energy-Dependent Cystic Fibrosis Transmembrane Conductance Regulator 93
Beyond the big five: Investigating myostatin structure, polymorphism and expression in Camelus dromedarius 88
Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells. 87
Aberrant GSH reductase and NOX activities concur with defective CFTR to pro-oxidative imbalance in cystic fibrosis airways 83
Combined effects of furocoumarin compounds as anti-inflammatory and CFTR potentiator in Calu-3 epithelial cells. 82
Goblet Cell Hyperplasia Requires High Bicarbonate Transport to Support Mucin Release 81
CFTR Regulation in Human Airway Epithelial Cells Requires Integrity of the Actin Cytoskeleton and Compartmentalized cAMP and PKA Activity. 81
Na+/H+ exchanger regulatory factor 1 overexpression-dependent increase of cytoskeleton organization is fundamental in the rescue of F508del CFTR in human airway CFBE41o- cells 80
null 78
null 78
Pharmacological targets of metabolism in disease: Opportunities from macrophages 70
Role of small molecule F508del CFTR correctors on the cAMP/PKA/ezrin compartmentalization in primary CF-BE cells. 69
Ruolo dei correttori VX-809 e TMA nella riorganizzazione del citoscheletro actinico e della compartimentazione dell’AMPc in cellule primarie CF-BE omozigoti per la mutazione F508del-CFTR. 66
Homing to the lung, mitochondrial content and CFTR expression in hematopoietic stem cells. 64
Mitochondria and cystic fibrosis transmembrane conductance regulator dialogue: Some news. 63
Trimethylangelicin reduces IL-8 transcription and potentiates CFTR function 62
null 59
Stimulation of Xenopus P2Y1 receptor activates CFTR in A6 cells 58
The purinergic receptor P2Y1 regulates CFTR-dependent chloride in a renal cellular model 57
null 54
CFBE41o- cells have a different compartmentalization of ezrin and cAMP/PKA than their normal counterpart 16HBE14o- cells. 53
The preclinical discovery and development of the combination of ivacaftor + tezacaftor used to treat cystic fibrosis 51
Combined effects of furocoumarin compounds as anti-inflammatoty and CFTR potentiator in Calu-3 epithelial cells. 49
Co-colture di cellule staminali amniotiche e cellule epiteliali respiratorie con la mutazione F508del: correzione del difetto di base della fibrosi cistica 49
The purinergic receptor P2Y1 regulates CFTR-dependent chloride efflux in a renal cellular model. 49
Energetic metabolism and CFTR expression and function in murine hematopoietic stem cells 48
Human amniotic mesenchymal stem cells can partially correct the cystic fibrosis phenotype upon coculture with F508del airway epithelial cells. 48
Trimethylangelicin (TMA) interacts directly with F508del-CFTR protein and rescues the F508del-CFTR-dependent chloride secretion. 47
Amniotic mesenchymal stem cells can correct the defective CFTR/ENaC function and tightness of CF airway epithelial cells upon cocolture: involvement of gap junctions. 46
Role of NHERF1 in rescuing of F508del-CFTR activity 44
Ezrin phosphorylation and activation of RhoA play a role in the rescue of F508del CFTR in CFBE41o- cells by NHERF1. 44
Human amniotic mesenchimal stem cells can partially correct the cystic fibrosis phenotype upon co-culture with F508del airway epithelial cells. 43
β-estradiol rescues ∆F508-CFTR functional expression in cystic fibrosis cells by the up-regulation of NHERF 42
Rescue of ∆F508 CFTR in CFBE41o- is dependent on actin cytoskeleton interaction with ezrin and NHERF1. 41
Decreased apical expression of CFTR by Pseudomonas aeruginosa infection in respiratory cells: role of NHERF1 phosphorylation 40
null 40
Phosphorylation of ezrin on threonine T567 plays a crucial role in the rescue of F508del CFTR functional expression 39
Spatial cAMP/PKA compartmentalization and activity in primary airway cells. 37
The purinergic receptor P2Y1 regulates CFTR-dependent chloride efflux in a renal cellular model 37
Glufosinate constrains synchronous and metachronous metastasis by promoting anti‐tumor macrophages 37
Ezrin phosphorylation and activation of RhoA play a role in the NHERF1 overexpression-dependent rescue of F508del-CFTR in human airway CFBE41o- cells 36
Beta-oestradiol rescues DeltaF508CFTR functional expression in human cystic fibrosis airway CFBE41o- cells through the up-regulation of NHERF1 35
NHERF1 overexpression-dependent increase of cytoskeleton organization is fundamental in the rescue of F508del-CFTR in CF human airway cells 35
Trimethylangelicin modulates neutrophil chemotaxis in murine model of Pseudomonas aeruginosa acute lung infection. 34
Gap Junctions Are Involved in the Rescue of CFTR-Dependent Chloride Efflux by Amniotic Mesenchymal Stem Cells in Coculture with Cystic Fibrosis CFBE41o- Cells 34
Rescue of ΔF508CFTR in CFBE41o- cells is dependent on actin cytoskeleton interaction with Ezrin and NHERF1. 34
Ruolo dei domini PDZ di entrambe le isoforme di NHERF nella regolazione del CFTR 33
CFTR regulation of ion transporters by protein-protein interactions 32
Correzione in vitro del difetto di base della Fibrosi cistica mediante co-colture di cellule staminali amniotiche e cellule epiteliali respiratory con fibrosis cistica 32
NHERF1 over-expression modulates CFTR expression and activity in human airway 16HBE14o- cells and rescues ∆F508 CFTR functional expression in cystic fibrosis cells 31
Differentiation of human embryonic stem cells into alveolar epithelial type II pneumocytes. 29
The J2-Immortalized Murine Macrophage Cell Line Displays Phenotypical and Metabolic Features of Primary BMDMs in Their M1 and M2 Polarization State 29
Involvement of gap junctions in the recovery of cystic fibrosis-associated defects upon co-culture of human amniotic mesenchymal stem cells with F508del airway epithelial cells. 26
Differential Expression of ADP/ATP Carriers as a Biomarker of Metabolic Remodeling and Survival in Kidney Cancers 24
null 24
Mitochondrial membranes of human SH-SY5Y neuroblastoma cells express serotonin 5-HT7 receptor 23
Trimethylangelicin modulates neutrophil chemotaxis in murine model of Pseudomonas aeruginosa acute lung infection. 23
N‐acetylaspartate release by glutaminolytic ovarian cancer cells sustains protumoral macrophages 22
Energetic metabolism and CFTR expression and function in murine hematopoietic stem cells 22
Reactive Oxygen Species in Macrophages: Sources and Targets 21
Design, Synthesis, Biological Evaluation, and Computational Studies of Novel Ureidopropanamides as Formyl Peptide Receptor 2 (FPR2) Agonists to Target the Resolution of Inflammation in Central Nervous System Disorders 20
Differentiation of human embryonic stem cells into alveolar epithelial type II pneumocytes 20
CFTR regulation in human airway epithelial cells requires integrity of the actin cytoskeleton and compartmentalized cAMP and PKA activity. 19
null 19
The Non-Gastric H+/K+ ATPase (ATP12A) Is Expressed in Mammalian Spermatozoa 18
Metabolic Features of Brain Function with Relevance to Clinical Features of Alzheimer and Parkinson Diseases 18
null 16
MED1101: a new dialdehydic compound regulating P2×7 receptor cell surface expression in U937 cells 14
The hyperchromatic supranuclear stria corresponds to the golgi apparatus in nasal ciliated cells 13
Emerging relationship between CFTR, actin and tight junction organization in cystic fibrosis airway epithelium. 12
Small-molecule drugs for cystic fibrosis: Where are we now? 11
null 4
Cellular redox state acts as switch to determine the direction of nnt-catalyzed reaction in cystic fibrosis cells 2
Totale 4.354
Categoria #
all - tutte 18.651
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 18.651


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.037 162 45 34 74 92 119 141 94 103 61 82 30
2020/2021546 45 30 39 34 69 32 73 28 43 72 56 25
2021/2022616 23 64 5 26 31 35 26 49 42 30 96 189
2022/2023938 143 133 79 75 94 127 8 110 119 5 21 24
2023/2024394 21 70 19 24 64 80 23 24 7 7 5 50
2024/202518 18 0 0 0 0 0 0 0 0 0 0 0
Totale 4.354