196 results on '"Karp, Philip H."'
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2. CFTR-rich ionocytes mediate chloride absorption across airway epithelia
3. Mitochondrial uncoupling proteins protect human airway epithelial ciliated cells from oxidative damage
4. Amphotericin B induces epithelial voltage responses in people with cystic fibrosis
5. Mitochondrial uncoupling proteins protect human airway epithelial ciliated cells from oxidative damage.
6. Motile cilia of human airway epithelia contain hedgehog signaling components that mediate noncanonical hedgehog signaling
7. Inflammatory cytokines TNF-[alpha] and IL-17 enhance the efficacy of cystic fibrosis transmembrane conductance regulator modulators
8. A Shortened Adeno-Associated virus Expression Cassette for CFTR Gene Transfer to Cystic Fibrosis Airway Epithelia
9. 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
10. The Osmolyte Xylitol Reduces the Salt Concentration of Airway Surface Liquid and May Enhance Bacterial Killing
11. Lack of cystic fibrosis transmembrane conductance regulator disrupts fetal airway development in pigs
12. Relationships among CFTR expression, HCO 3 − secretion, and host defense may inform gene- and cell-based cystic fibrosis therapies
13. Airway acidification initiates host defense abnormalities in cystic fibrosis mice
14. Aggregates of mutant CFTR fragments in airway epithelial cells of CF lungs: New pathologic observations
15. WNK Inhibition Increases Surface Liquid pH and Host Defense in Cystic Fibrosis Airway Epithelia
16. Acidic pH increases airway surface liquid viscosity in cystic fibrosis
17. A microRNA network regulates expression and biosynthesis of wild-type and ∆F508 mutant cystic fibrosis transmembrane conductance regulator
18. Human cystic fibrosis airway epithelia have reduced Cl − conductance but not increased Na + conductance
19. Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR -/- mice
20. Disruption of the CFTR Gene Produces a Model of Cystic Fibrosis in Newborn Pigs
21. Processing and Function of CFTR-ΔF508 Are Species-Dependent
22. Inflammatory cytokines TNF-α and IL-17 enhance the efficacy of cystic fibrosis transmembrane conductance regulator modulators
23. CYSTIC FIBROSIS: Airway acidification initiates host defense abnormalities in cystic fibrosis mice
24. Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs
25. A Genomic Signature Approach to Rescue ΔF508-Cystic Fibrosis Transmembrane Conductance Regulator Biosynthesis and Function
26. Chemosensory Functions for Pulmonary Neuroendocrine Cells
27. microRNA REGULATION OF CFTR EXPRESSION AND FUNCTION IN AIRWAY EPITHELIA: S8.2
28. EXPLOITING A microRNA-REGULATED GENE NETWORK TO RESCUE FUNCTION OF CFTR-DeltaF508: S1.1
29. Post-Transcriptional Regulation of Cystic Fibrosis Transmembrane Conductance Regulator Expression and Function by MicroRNAs
30. Processing and function of CFTR-[DELTA]F508 are species-dependent
31. Gene transfer of CFTR to airway epithelia: low levels of expression are sufficient to correct [Cl.sup.-] transport and overexpression can generate basolateral CFFR
32. Heterogeneous expression of the SARS-Coronavirus-2 receptor ACE2 in the human respiratory tract
33. TNFα and IL-17 alkalinize airway surface liquid through CFTR and pendrin
34. Heterogeneous expression of the SARS-Coronavirus-2 receptor ACE2 in the human respiratory tract
35. Cellular Localization and Activity of Ad-Delivered GFP-CFTR in Airway Epithelial and Tracheal Cells
36. Thixotropic Solutions Enhance Viral-Mediated Gene Transfer to Airway Epithelia
37. Small-molecule ion channels increase host defences in cystic fibrosis airway epithelia
38. Defective Fluid Transport by Cystic Fibrosis Airway Epithelia
39. Nominal carbonic anhydrase activity minimizes airway-surface liquid pH changes during breathing
40. Electrolyte transport properties in distal small airways from cystic fibrosis pigs with implications for host defense
41. Motile cilia of human airway epithelia contain hedgehog signaling components that mediate noncanonical hedgehog signaling.
42. Nominal carbonic anhydrase activity minimizes airwaysurface liquid pH changes during breathing.
43. Medical reversal of chronic sinusitis in a cystic fibrosis patient with ivacaftor
44. An In Vitro Model of Differentiated Human Airway Epithelia: Methods for Establishing Primary Cultures
45. Integrin α6β4 Identifies Human Distal Lung Epithelial Progenitor Cells with Potential as a Cell-Based Therapy for Cystic Fibrosis Lung Disease
46. Multicenter Intestinal Current Measurements in Rectal Biopsies from CF and Non-CF Subjects to Monitor CFTR Function
47. Adenoviral Gene Transfer Corrects the Ion Transport Defect in the Sinus Epithelia of a Porcine CF Model
48. Relationships among CFTR expression, HCO3- secretion, and host defense may inform gene- and cell-based cystic fibrosis therapies.
49. Electrolyte transport properties in distal small airways from cystic fibrosis pigs with implications for host defense.
50. A microRNA network regulates expression and biosynthesis of wild-type and ΔF508 mutant cystic fibrosis transmembrane conductance regulator
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