41 results on '"Kropski, J. A."'
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2. Spatial Transcriptomics Analysis Reveals Pathology-specific Alveolar Niches in Pulmonary Fibrosis
3. The MUC5B Genotype and Other Common Variants Are Associated With Computational Imaging Features of Usual Interstitial Pneumonia Pattern Among Patients With Idiopathic Pulmonary Fibrosis
4. NF-κB Activation During Alveolar Epithelial Regeneration
5. Impact of the COVID-19 Pandemic on a Longitudinal Program to Screen for Subclinical Familial Pulmonary Fibrosis
6. Sustained Activation of Yap/Taz After Injury Leads to Aberrant Alveolar Differentiation and Failure of Alveolar Repair
7. Using Single Nuclei Multiomics and Spatial Transcriptomics to Identify Drivers of Early Pulmonary Fibrosis
8. Epithelial HIF Inhibition Enables Adaptive Repair and Alveolar Regeneration in Chronic Lung Injury
9. Genetically-informed Single-cell Genomic Analysis of Discordantly Affected Regions of IPF Lungs
10. Epithelial Yap-Taz Deletion Promotes Maladaptive Alveolar Repair
11. Epithelial Outgrowth Through Mesenchymal Rings Drives Alveologenesis
12. GPR87 Regulates Epithelial Repair During Pulmonary Fibrosis
13. Reporting of Exposures by Patients With Interstitial Lung Disease During an Unstructured Clinician Interview or on a Questionnaire
14. Association between cytomegalovirus seropositivity and severity of pulmonary fibrosis
15. Chemically Defined Basement Membrane Mimetic Hydrogels for the Culture of Type 2 Pneumocytes
16. Epithelial Deletion of Yap-Taz Promotes Fibroblast Activation and Potentiates Experimental Pulmonary Fibrosis
17. Integrating Gene Expression with Genome-Wide Association Summary Statistics to Identify Genes Associated with Idiopathic Pulmonary Fibrosis Survival
18. Functional T Cell Subsets in Idiopathic Pulmonary Fibrosis
19. Single-Cell Analysis of Airway and Alveolar-Derived Progenitors During Recurrent Injury-Repair
20. S65 Genome-wide association study of survival times after diagnosis of idiopathic pulmonary fibrosis
21. Detection and Early Referral of Patients With Interstitial Lung Abnormalities: An Expert Survey Initiative
22. SARS-CoV-2 Entry Factors are Highly Expressed in Nasal Epithelial Cells Together with Innate Immune Genes
23. Alveolar Basement Membrane and Transitional Cell Dynamics Identified by Single Cell RNA Sequencing
24. Fibroblast Heterogeneity in Interstitial Lung Disease
25. Self-Reported Exposure to Organic Dust Is Associated with Earlier Symptom Onset in Individuals with Familial Pulmonary Fibrosis
26. Thromboxane-Prostanoid Receptor Signaling in Fibroblasts Is a Potential Interventional Target for Pulmonary Fibrosis
27. Fibroblast Subtypes Identified by Single Sell RNA Sequencing in Pulmonary Fibrosis
28. Enhanced Wnt Signaling in Adult Mesenchymal Vascular Progenitors Alters Adaptive Angiogenesis and Exacerbates the Development of Pulmonary Fibrosis
29. Single Cell RNA Sequencing Reveals Altered T-Cell Repertoire and Gene Expression in the Peripheral Blood and Lungs of Patients with Idiopathic Pulmonary Fibrosis
30. PET Imaging of Glutamine Uptake in Lymphangioleiomyomatosis
31. Single-Cell RNA Sequencing Identifies a Novel Profibrotic Epithelial Cell Population in Pulmonary Fibrosis
32. The Polymeric Immunoglobulin Receptor Is Highly Expressed in Secretory Cells in the Airway Epithelium and Is Reduced in COPD
33. Occupational and Environmental Exposures Associated with Increased Risk of Interstitial Lung Abnormalities in Individuals at Risk for Familial Interstitial Pneumonia
34. Among Individuals At-Risk, Pre-Clinical Pulmonary Fibrosis Occurs Commonly and Is Progressive
35. The Effects of Tobacco Smoking Intensity and Cessation on Idiopathic Pulmonary Fibrosis Incidence and Progression
36. Role of Regulator of Telomere Elongation Helicase 1 (RTEL1) in Experimental Models of Pulmonary Fibrosis
37. The Prognostic Value of Monocyte Count in Idiopathic Pulmonary Fibrosis: A Multi-Omic Cohort Study
38. Single Cell Analysis of Pulmonary Fibrosis Phenotypes
39. The Prevalence and Progression of Early Interstitial Lung Disease in First-Degree Relatives of Patients with Familial Interstitial Pneumonia
40. Circulating Plasma Proteins Differentially Detected in Idiopathic Pulmonary Fibrosis and in Subjects with Pre-Clinical Pulmonary Fibrosis
41. T Cell Phenotype in Peripheral Blood of Patients with Idiopathic Pulmonary Fibrosis
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