Luis J. V. Galietta mainly focuses on Cystic fibrosis transmembrane conductance regulator, Chloride channel, Cystic fibrosis, Biochemistry and Biophysics. His biological study spans a wide range of topics, including Epithelial sodium channel, Green fluorescent protein, Molecular biology, Apical membrane and Pharmacology. Chloride channel is a subfield of Cell biology that Luis J. V. Galietta tackles.
His Cell biology research incorporates themes from Secretion, Lung and Pathology. His study in Cystic fibrosis is interdisciplinary in nature, drawing from both Channel blocker, Forskolin, Genetic heterogeneity, Pancreatic disease and Haplotype. His research in Biophysics focuses on subjects like Structure–activity relationship, which are connected to Signal transduction, In vivo and Inhibitory postsynaptic potential.
His main research concerns Cystic fibrosis transmembrane conductance regulator, Chloride channel, Cystic fibrosis, Cell biology and Biochemistry. As a part of the same scientific family, Luis J. V. Galietta mostly works in the field of Cystic fibrosis transmembrane conductance regulator, focusing on Molecular biology and, on occasion, Cell culture. His study explores the link between Chloride channel and topics such as Potentiator that cross with problems in Gating, Binding site and ΔF508.
His Cystic fibrosis study combines topics in areas such as Cancer research, Immunology, Endoplasmic reticulum, Small molecule and Pharmacology. The concepts of his Cell biology study are interwoven with issues in Respiratory epithelium, Lung, Mucociliary clearance, Transmembrane protein and Ion channel. His biological study deals with issues like Biophysics, which deal with fields such as Ion transporter, Intracellular and Extracellular.
His primary areas of study are Cystic fibrosis, Cell biology, Cystic fibrosis transmembrane conductance regulator, Chloride channel and Mutation. The study incorporates disciplines such as Cell culture, Inflammation, Potentiator, Molecular biology and Small molecule in addition to Cystic fibrosis. His Cell biology research incorporates elements of Autophagy, Epithelium, Respiratory epithelium and Ex vivo.
By researching both Cystic fibrosis transmembrane conductance regulator and Surface plasmon resonance, Luis J. V. Galietta produces research that crosses academic boundaries. His research integrates issues of Purinergic receptor and Subcellular localization in his study of Chloride channel. His research in Mutation intersects with topics in Thiazole and Mutant.
The scientist’s investigation covers issues in Cystic fibrosis, Mutation, Cystic fibrosis transmembrane conductance regulator, Cell culture and Chloride channel. His Cystic fibrosis study integrates concerns from other disciplines, such as Inflammation, Molecular biology, Disease and Intensive care medicine. Luis J. V. Galietta works mostly in the field of Mutation, limiting it down to topics relating to Mutant and, in certain cases, Pharmacology, Structure–activity relationship, Agonist and Small molecule, as a part of the same area of interest.
In his works, Luis J. V. Galietta undertakes multidisciplinary study on Cystic fibrosis transmembrane conductance regulator and Induced pluripotent stem cell. Luis J. V. Galietta combines subjects such as Purinergic receptor, TRPV4, Intracellular, Calcium signaling and Activator with his study of Chloride channel. As a part of the same scientific study, he usually deals with the Cytokine, concentrating on Respiratory epithelium and frequently concerns with Cell biology.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
TMEM16A, A Membrane Protein Associated with Calcium-Dependent Chloride Channel Activity
Antonella Caputo;Emanuela Caci;Loretta Ferrera;Nicoletta Pedemonte.
Thiazolidinone CFTR inhibitor identified by high-throughput screening blocks cholera toxin–induced intestinal fluid secretion
Tonghui Ma;Jay R. Thiagarajah;Hong Yang;Nitin D. Sonawane.
Journal of Clinical Investigation (2002)
Small-molecule correctors of defective ΔF508-CFTR cellular processing identified by high-throughput screening
Nicoletta Pedemonte;Gergely L. Lukacs;Kai Du;Emanuela Caci.
Journal of Clinical Investigation (2005)
Chloride channels as drug targets
Alan S. Verkman;Luis J. V. Galietta.
Nature Reviews Drug Discovery (2009)
Green fluorescent protein-based halide indicators with improved chloride and iodide affinities.
Luis J.V Galietta;Peter M Haggie;A.S Verkman.
FEBS Letters (2001)
Structure and Function of TMEM16 Proteins (Anoctamins)
Nicoletta Pedemonte;Luis J. V. Galietta.
Physiological Reviews (2014)
Discovery of Glycine Hydrazide Pore-occluding CFTR Inhibitors: Mechanism, Structure–Activity Analysis, and In Vivo Efficacy
Chatchai Muanprasat;N.D. Sonawane;Danieli Salinas;Alessandro Taddei.
The Journal of General Physiology (2004)
Nanomolar Affinity Small Molecule Correctors of Defective ΔF508-CFTR Chloride Channel Gating
Hong Yang;Anang A. Shelat;R. Kiplin Guy;Vadiraj S. Gopinath.
Journal of Biological Chemistry (2003)
High-affinity activators of cystic fibrosis transmembrane conductance regulator (CFTR) chloride conductance identified by high-throughput screening.
Tonghui Ma;L. Vetrivel;Hong Yang;Nicoletta Pedemonte.
Journal of Biological Chemistry (2002)
Novel CFTR Chloride Channel Activators Identified by Screening of Combinatorial Libraries Based on Flavone and Benzoquinolizinium Lead Compounds
Luis J.V. Galietta;Mark F. Springsteel;Masahiro Eda;Edmund J. Niedzinski.
Journal of Biological Chemistry (2001)
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