Valeria Casavola
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    Explore the profile of Valeria Casavola including associated specialties, affiliations and a list of published articles.
          
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              Articles
              47
            
            
              Citations
              1390
            
            
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  Recent Articles
          1.
        
    
    Guerra L, Favia M, Di Gioia S, Laselva O, Bisogno A, Casavola V, et al.
  
  
    Expert Opin Drug Discov
    . 2020 Apr;
          15(8):873-891.
    
    PMID: 32290721
  
  
          Introduction: Cystic Fibrosis (CF) is caused by mutations in the  (CFTR) gene. The most common mutation, , induces protein misprocessing and loss of CFTR function. The discovery through  studies of...
      
2.
        
    
    Favia M, Gallo C, Guerra L, De Venuto D, Diana A, Polizzi A, et al.
  
  
    Int J Mol Sci
    . 2020 Apr;
          21(7).
    
    PMID: 32244302
  
  
          The treatment of cystic fibrosis (CF) patients homozygous for the  mutation with Orkambi, a combination of a corrector (lumacaftor) and a potentiator (ivacaftor) of the mutated CFTR protein, resulted in...
      
3.
        
    
    Biondani G, Zeeberg K, Greco M, Cannone S, Dando I, Dalla Pozza E, et al.
  
  
    FEBS J
    . 2019 Sep;
          286(17):3504.
    
    PMID: 31475461
  
  
          No abstract available.
      
4.
        
    
    Biondani G, Zeeberg K, Greco M, Cannone S, Dando I, Dalla Pozza E, et al.
  
  
    FEBS J
    . 2018 Apr;
          285(11):2104-2124.
    
    PMID: 29660229
  
  
          Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal cancers. Its aggressiveness is driven by an intense fibrotic desmoplastic reaction in which the increasingly collagen I-rich extracellular matrix (ECM)...
      
5.
        
    
    Laselva O, Molinski S, Casavola V, Bear C
  
  
    Mol Pharmacol
    . 2018 Apr;
          93(6):612-618.
    
    PMID: 29618585
  
  
          The most common cystic fibrosis causing mutation is deletion of phenylalanine at position 508 (F508del), a mutation that leads to protein misassembly with defective processing. Small molecule corrector compounds: VX-809...
      
6.
        
    
    Carbone A, Zefferino R, Beccia E, Casavola V, Castellani S, Di Gioia S, et al.
  
  
    Stem Cells Int
    . 2018 Mar;
          2018:1203717.
    
    PMID: 29531530
  
  
          We previously found that human amniotic mesenchymal stem cells (hAMSCs) in coculture with CF immortalised airway epithelial cells (CFBE41o- line, CFBE) on Transwell® filters acquired an epithelial phenotype and led...
      
7.
        
    
    Muzzachi S, Guerra L, Martino N, Favia M, Punzi G, Silvestre F, et al.
  
  
    Reproduction
    . 2018 Mar;
          155(5):433-445.
    
    PMID: 29491124
  
  
          Sperm motility, a feature essential for  fertilization, is influenced by intracellular pH (pH) homeostasis. Several mechanisms are involved in pH regulation, among which sodium-hydrogen exchangers (NHEs), a family of integral...
      
8.
        
    
    Guerra L, DOria S, Favia M, Castellani S, Santostasi T, Polizzi A, et al.
  
  
    Pediatr Pulmonol
    . 2017 Apr;
          52(7):900-908.
    
    PMID: 28445004
  
  
          Aim: The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) potentiator ivacaftor (Kalydeco®) improves clinical outcome in G551D cystic fibrosis (CF) patients. Here, we have investigated whether ivacaftor has a clinical impact...
      
9.
        
    
    Castellani S, Favia M, Guerra L, Carbone A, Abbattiscianni A, Di Gioia S, et al.
  
  
    Histol Histopathol
    . 2016 Nov;
          32(5):445-459.
    
    PMID: 27834058
  
  
          Cystic fibrosis (CF), one of the most common genetic disorders affecting primarily Caucasians, is due to mutations in the CF Transmembrane Conductance Regulator (CFTR) gene, encoding for a chloride channel...
      
10.
        
    
    Gorrieri G, Scudieri P, Caci E, Schiavon M, Tomati V, Sirci F, et al.
  
  
    Sci Rep
    . 2016 Oct;
          6:36016.
    
    PMID: 27786259
  
  
          Goblet cell hyperplasia, a feature of asthma and other respiratory diseases, is driven by the Th-2 cytokines IL-4 and IL-13. In human bronchial epithelial cells, we find that IL-4 induces...