1,342 results on '"Welsh, Michael J."'
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2. Development and Initial Characterization of Pigs with DNAI1 Mutations and Primary Ciliary Dyskinesia
3. A pilot dose-finding study of terazosin in humans
4. CFTR-rich ionocytes mediate chloride absorption across airway epithelia
5. Mitochondrial uncoupling proteins protect human airway epithelial ciliated cells from oxidative damage
6. A model for stimulation of enzyme activity by a competitive inhibitor based on the interaction of terazosin and phosphoglycerate kinase 1
7. INJECTABLE LONG-ACTING IVACAFTOR-LOADED POLY (LACTIDE-CO-GLYCOLIDE) MICROPARTICLE FORMULATIONS FOR THE TREATMENT OF CYSTIC FIBROSIS: IN VITRO CHARACTERIZATION AND IN VIVO PHARMACOKINETICS IN MICE
8. Cystic fibrosis carriers are at increased risk for a wide range of cystic fibrosis-related conditions
9. Amphotericin B induces epithelial voltage responses in people with cystic fibrosis
10. Mitochondrial uncoupling proteins protect human airway epithelial ciliated cells from oxidative damage.
11. Small heat shock protein speciation: novel non-canonical 44 kDa HspB5-related protein species in rat and human tissues
12. Enhancing glycolysis attenuates Parkinson's disease progression in models and clinical databases
13. Motile cilia of human airway epithelia contain hedgehog signaling components that mediate noncanonical hedgehog signaling
14. Induction of Hsp22 (HspB8) by Estrogen and the Metalloestrogen Cadmium in Estrogen Receptorpositive Breast Cancer Cells
15. Conformational Changes Resulting from Pseudophosphorylation of Mammalian Small Heat Shock Proteins: A Two-Hybrid Study
16. Inflammatory cytokines TNF-[alpha] and IL-17 enhance the efficacy of cystic fibrosis transmembrane conductance regulator modulators
17. RNA Interference Improves Motor and Neuropathological Abnormalities in a Huntington's Disease Mouse Model
18. A Shortened Adeno-Associated virus Expression Cassette for CFTR Gene Transfer to Cystic Fibrosis Airway Epithelia
19. ADP Inhibits Function of the ABC Transporter Cystic Fibrosis Transmembrane Conductance Regulator via Its Adenylate Kinase Activity
20. Normal Gating of CFTR Requires ATP Binding to Both Nucleotide-Binding Domains and Hydrolysis at the Second Nucleotide-Binding Domain
21. Self-Generated Diversity Produces "Insurance Effects" in Biofilm Communities
22. Extracellular Acidosis Increases Neuronal Cell Calcium by Activating Acid-Sensing Ion Channel 1a
23. Inactivation of a Pseudomonas aeruginosa Quorum-Sensing Signal by Human Airway Epithelia
24. Overexpression of Acid-Sensing Ion Channel 1a in Transgenic Mice Increases Acquired Fear-Related Behavior
25. Propagation of Infectious Human Papillomavirus Type 16 by Using an Adenovirus and Cre/LoxP Mechanism
26. Gel-forming mucins form distinct morphologic structures in airways
27. Inflammation as a Regulator of the Airway Surface Liquid pH in Cystic Fibrosis
28. The Sperm Outer Dense Fiber Protein Is the 10th Member of the Superfamily of Mammalian Small Stress Proteins
29. Effects of C-Terminal Deletions on Cystic Fibrosis Transmembrane Conductance Regulator Function in Cystic Fibrosis Airway Epithelia
30. Drosophila DEG/ENaC Pickpocket Genes Are Expressed in the Tracheal System, Where They May Be Involved in Liquid Clearance
31. cAMP-Dependent Protein Kinase Phosphorylation of the Acid-Sensing Ion Channel-1 Regulates Its Binding to the Protein Interacting with C-Kinase-1
32. CFTR with a Partially Deleted R Domain Corrects the Cystic Fibrosis Chloride Transport Defect in Human Airway Epithelia in vitro and in Mouse Nasal Mucosa in vivo
33. Heteromultimers of DEG/ENaC Subunits Form H + -Gated Channels in Mouse Sensory Neurons
34. Discovery of Five Conserved β-Defensin Gene Clusters Using a Computational Search Strategy
35. DEG/ENaC Ion Channels Involved in Sensory Transduction Are Modulated by Cold Temperature
36. A Conditional Probability Analysis of Cystic Fibrosis Transmembrane Conductance Regulator Gating Indicates That ATP Has Multiple Effects during the Gating Cycle
37. The Osmolyte Xylitol Reduces the Salt Concentration of Airway Surface Liquid and May Enhance Bacterial Killing
38. Regulation of CFTR Cl - Channel Gating by ATP Binding and Hydrolysis
39. A Functional R Domain from Cystic Fibrosis Transmembrane Conductance Regulator Is Predominantly Unstructured in Solution
40. Disruption of the β Subunit of the Epithelial Na + Channel in Mice: Hyperkalemia and Neonatal Death Associated with a Pseudohypoaldosteronism Phenotype
41. Production of β -defensins by Human Airway Epithelia
42. A C-Terminal Motif Found in the β 2 -adrenergic Receptor, P2Y1 Receptor and Cystic Fibrosis Transmembrane Conductance Regulator Determines Binding to the Na + /H + Exchanger Regulatory Factor Family of PDZ Proteins
43. Ripped Pocket and Pickpocket, Novel Drosophila DEG/ENaC Subunits Expressed in Early Development and in Mechanosensory Neurons
44. Lack of cystic fibrosis transmembrane conductance regulator disrupts fetal airway development in pigs
45. Protein Phosphatase 2C Dephosphorylates and Inactivates Cystic Fibrosis Transmembrane Conductance Regulator
46. Relationships among CFTR expression, HCO 3 − secretion, and host defense may inform gene- and cell-based cystic fibrosis therapies
47. Airway acidification initiates host defense abnormalities in cystic fibrosis mice
48. WNK Inhibition Increases Surface Liquid pH and Host Defense in Cystic Fibrosis Airway Epithelia
49. Pulmonary neuroendocrine cells sense succinate to stimulate myoepithelial cell contraction
50. Use of Glycolysis‐Enhancing Drugs and Risk of Parkinson's Disease
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