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1. Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants.

3. Colocalization of Gene Expression and DNA Methylation with Genetic Risk Variants Supports Functional Roles of MUC5B and DSP in Idiopathic Pulmonary Fibrosis.

4. Common idiopathic pulmonary fibrosis risk variants are associated with hypersensitivity pneumonitis.

5. Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease

6. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

8. Chronic Hypersensitivity Pneumonitis, an Interstitial Lung Disease with Distinct Molecular Signatures.

9. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

10. Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

11. Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis

15. Nasal DNA methylation profiling of asthma and rhinitis

16. Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

17. FUT2 Variants Confer Susceptibility to Familial Otitis Media

18. Supervised learning of enhancer–promoter specificity based on genome-wide perturbation studies highlights areas for improvement in learning.

19. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

23. An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels

24. Aberrant Multiciliogenesis in Idiopathic Pulmonary Fibrosis

26. Epithelial ER stress enhances the risk of Muc5b associated lung fibrosis.

27. Molecular Signatures of Idiopathic Pulmonary Fibrosis

28. Colocalization of Gene Expression and DNA Methylation with Genetic Risk Variants Supports Functional Roles of and in Idiopathic Pulmonary Fibrosis.

29. Aberrant Multiciliogenesis in Idiopathic Pulmonary Fibrosis.

30. The MUC5B-associated variant rs35705950 resides within an enhancer subject to lineage- and disease-dependent epigenetic remodeling

31. Preclinical Pulmonary Fibrosis Circulating Protein Biomarkers

32. Epigenome-wide association study of DNA methylation and adult asthma in the Agricultural Lung Health Study

33. Nasal DNA methylation profiling of asthma and rhinitis

34. Nasal DNA methylation profiling of asthma and rhinitis

35. Chronic Hypersensitivity Pneumonitis (CHP), an Interstitial Lung Disease (ILD) with Distinct Molecular Signatures

36. A2ML1and otitis media: novel variants, differential expression, and relevant pathways

37. Common idiopathic pulmonary fibrosis risk variants are associated with hypersensitivity pneumonitis.

38. Chronic Hypersensitivity Pneumonitis, an Interstitial Lung Disease with Distinct Molecular Signatures.

40. A2ML1 and otitis media: novel variants, differential expression, and relevant pathways.

41. Whole Genome Sequencing Identifies CRISPLD2as a Lung Function Gene in Children With Asthma

42. A Review of Apomixis and Differential Expression Analyses Using Microarrays

43. A genetic-association study of circulating coagulation factor VIII and von Willebrand factor levels

44. An APOOPseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels

49. Single Cell Transcriptome Signatures of Sarcoidosis in Lung Immune Cell Populations.

50. MUC5B Genotype and Other Common Variants are Associated with Computational Imaging Features of UIP.

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