458 results on '"Galietta, Luis J V"'
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2. Pharmacological rescue of the G85E CFTR variant by preclinical and approved modulators.
3. Assessing the Potential of N-Butyl-l-deoxynojirimycin (l-NBDNJ) in Models of Cystic Fibrosis as a Promising Antibacterial Agent
4. Pharmacoproteomics pinpoints HSP70 interaction for correction of the most frequent Wilson disease-causing mutant of ATP7B
5. TMEM16 Proteins (Anoctamins) in Epithelia
6. Esc peptides as novel potentiators of defective cystic fibrosis transmembrane conductance regulator: an unprecedented property of antimicrobial peptides
7. Putting bicarbonate on the spot: pharmacological insights for CFTR correction in the airway epithelium
8. The Role of Pendrin in the Airways: Links with Asthma and COPD
9. TMEM16 Proteins (Anoctamins) in Epithelia
10. TMEM16 Proteins (Anoctamins) in Epithelia
11. Author Correction: Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis
12. Bioactive Thymosin Alpha-1 Does Not Influence F508del-CFTR Maturation and Activity
13. Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis
14. Easy-to-Build and Reusable Microfluidic Device for the Dynamic Culture of Human Bronchial Cystic Fibrosis Epithelia
15. Analysis of inhibitors of the anoctamin‐1 chloride channel (transmembrane member 16A, TMEM16A) reveals indirect mechanisms involving alterations in calcium signalling
16. Pharmacological potentiators of the calcium signaling cascade identified by high-throughput screening
17. CFTR pharmacology
18. Application of Green Fluorescent Protein-Based Chloride Indicators for Drug Discovery by High-Throughput Screening
19. KCa3.1 differentially regulates trachea and bronchi epithelial gene expression in a chronic-asthma mouse model
20. TMEM16A, a Membrane Protein Associated with Calcium-Dependent Chloride Channel Activity
21. The L467F-F508del Complex Allele Hampers Pharmacological Rescue of Mutant CFTR by Elexacaftor/Tezacaftor/Ivacaftor in Cystic Fibrosis Patients: The Value of the Ex Vivo Nasal Epithelial Model to Address Non-Responders to CFTR-Modulating Drugs
22. Analysis of inhibitors of the anoctamin‐1 chloride channel (transmembrane member 16A, TMEM16A) reveals indirect mechanisms involving alterations in calcium signalling.
23. TMEM16 Proteins (Anoctamins) in Epithelia
24. Esc peptides as novel potentiators of defective cystic fibrosis transmembrane conductance regulator: an unprecedented property of antimicrobial peptides
25. Chloride transport modulators as drug candidates
26. Comprehensive Analysis of Combinatorial Pharmacological Treatments to Correct Nonsense Mutations in the CFTR Gene
27. Managing the Underlying Cause of Cystic Fibrosis: A Future Role for Potentiators and Correctors
28. Partial Rescue of F508del-CFTR Stability and Trafficking Defects by Double Corrector Treatment
29. Ex vivo model predicted in vivo efficacy of CFTR modulator therapy in a child with rare genotype
30. Epithelial Sodium Channel Silencing as a Strategy to Correct the Airway Surface Fluid Deficit in Cystic Fibrosis
31. Association of TMEM16A chloride channel overexpression with airway goblet cell metaplasia
32. The anoctamin family: TMEM16A and TMEM16B as calcium-activated chloride channels
33. Identification, Structure–Activity Relationship, and Biological Characterization of 2,3,4,5-Tetrahydro-1H-pyrido[4,3-b]indoles as a Novel Class of CFTR Potentiators
34. Ionocytes and CFTR Chloride Channel Expression in Normal and Cystic Fibrosis Nasal and Bronchial Epithelial Cells
35. Intrinsic Abnormalities of Cystic Fibrosis Airway Connective Tissue Revealed by an In Vitro 3D Stromal Model
36. Discovery of a picomolar potency pharmacological corrector of the mutant CFTR chloride channel
37. An improved method to obtain highly differentiated monolayers of human bronchial epithelial cells
38. Epithelial Sodium Channel Inhibition in Primary Human Bronchial Epithelia by Transfected siRNA
39. The Importance of Differentiating Gelsolin Isoforms
40. Activation of Ca2+-dependent K+ and Cl− currents by UTP and ATP in CFPAC-1 cells
41. Gelsolin Secretion in Interleukin-4-treated Bronchial Epithelia and in Asthmatic Airways
42. Effect of Inflammatory Stimuli on Airway Ion Transport
43. Characterization of chloride and cation channels in cultured human keratinocytes
44. Modulation of HLA-DR antigen and ICAM-1 molecule expression on airway epithelial cells by sodium nedocromil
45. Two CFTR mutations within codon 970 differently impact on the chloride channel functionality
46. Erratum: High-throughput screening for modulators of ACVR1 transcription: Discovery of potential therapeutics for fibrodysplasia ossificans progressiva (Disease Models & Mechanisms 9 (685-696))
47. The Autophagy Inhibitor Spautin-1 Antagonizes Rescue of Mutant CFTR Through an Autophagy-Independent and USP13-Mediated Mechanism
48. Substituted 2-Acylaminocycloalkylthiophene-3-carboxylic Acid Arylamides as Inhibitors of the Calcium-Activated Chloride Channel Transmembrane Protein 16A (TMEM16A)
49. ANO4 (Anoctamin 4) Is a Novel Marker of Zona Glomerulosa That Regulates Stimulated Aldosterone Secretion.
50. Properties of CFTR activated by the xanthine derivative X-33 in human airway Calu-3 cells
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