PubRank

Emanuela Caci

Author PubWeight™ 32.93‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 TMEM16A, a membrane protein associated with calcium-dependent chloride channel activity. Science 2008 8.74
2 Small-molecule correctors of defective DeltaF508-CFTR cellular processing identified by high-throughput screening. J Clin Invest 2005 4.19
3 Gelsolin secretion in interleukin-4-treated bronchial epithelia and in asthmatic airways. Am J Respir Crit Care Med 2005 1.45
4 Thiocyanate transport in resting and IL-4-stimulated human bronchial epithelial cells: role of pendrin and anion channels. J Immunol 2007 1.35
5 IL-4 is a potent modulator of ion transport in the human bronchial epithelium in vitro. J Immunol 2002 1.18
6 Cytokines induce tight junction disassembly in airway cells via an EGFR-dependent MAPK/ERK1/2-pathway. Lab Invest 2012 1.15
7 Association of TMEM16A chloride channel overexpression with airway goblet cell metaplasia. J Physiol 2012 1.09
8 A minimal isoform of the TMEM16A protein associated with chloride channel activity. Biochim Biophys Acta 2011 1.08
9 Correction of G551D-CFTR transport defect in epithelial monolayers by genistein but not by CPX or MPB-07. Br J Pharmacol 2002 1.05
10 Rescue of the mutant CFTR chloride channel by pharmacological correctors and low temperature analyzed by gene expression profiling. Am J Physiol Cell Physiol 2011 0.98
11 Dual activity of aminoarylthiazoles on the trafficking and gating defects of the cystic fibrosis transmembrane conductance regulator chloride channel caused by cystic fibrosis mutations. J Biol Chem 2011 0.97
12 TMEM16A-TMEM16B chimaeras to investigate the structure-function relationship of calcium-activated chloride channels. Biochem J 2013 0.97
13 Antihypertensive 1,4-dihydropyridines as correctors of the cystic fibrosis transmembrane conductance regulator channel gating defect caused by cystic fibrosis mutations. Mol Pharmacol 2005 0.95
14 Effect of inflammatory stimuli on airway ion transport. Proc Am Thorac Soc 2004 0.94
15 Non-canonical translation start sites in the TMEM16A chloride channel. Biochim Biophys Acta 2013 0.90
16 IL-12 can target human lung adenocarcinoma cells and normal bronchial epithelial cells surrounding tumor lesions. PLoS One 2009 0.89
17 A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree. Eur J Hum Genet 2012 0.89
18 Functional human CFTR produced by a stable minichromosome. EMBO Rep 2002 0.88
19 Mutation-specific potency and efficacy of cystic fibrosis transmembrane conductance regulator chloride channel potentiators. J Pharmacol Exp Ther 2009 0.86
20 Block of CFTR-dependent chloride currents by inhibitors of multidrug resistance-associated proteins. Eur J Pharmacol 2007 0.81
21 2-(dialkylamino)-4H-1-benzopyran-4-one derivatives modify chloride conductance in CFTR expressing cells. Farmaco 2003 0.78
22 Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis. Am J Respir Cell Mol Biol 2013 0.77
23 Functional analysis of acid-activated Cl⁻ channels: properties and mechanisms of regulation. Biochim Biophys Acta 2015 0.76