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Search Results to David A Schwartz

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Schwartz, David

One or more keywords matched the following items that are connected to Schwartz, David

Item Type	Name
Academic Article	Genetic regulation of rejection and survival following human lung transplantation by the innate immune receptor CD14.
Academic Article	A common MUC5B promoter polymorphism and pulmonary fibrosis.
Academic Article	The genetic and environmental causes of pulmonary fibrosis.
Academic Article	Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis.
Academic Article	The role of the E2F1 transcription factor in the innate immune response to systemic LPS.
Concept	Promoter Regions, Genetic
Academic Article	The MUC5B variant is associated with idiopathic pulmonary fibrosis but not with systemic sclerosis interstitial lung disease in the European Caucasian population.
Academic Article	A comparison of visual and quantitative methods to identify interstitial lung abnormalities.
Academic Article	MUC5B and Idiopathic Pulmonary Fibrosis.
Academic Article	MUC5B expression and location in surfactant protein C mutations in children.
Academic Article	MUC5B Promoter Variant rs35705950 Affects MUC5B Expression in the Distal Airways in Idiopathic Pulmonary Fibrosis.
Academic Article	CT Imaging Phenotypes of Pulmonary Fibrosis in the MUC5B Promoter Site Polymorphism.
Academic Article	IDIOPATHIC PULMONARY FIBROSIS IS A COMPLEX GENETIC DISORDER.
Academic Article	Regulation of MUC5B Expression in Idiopathic Pulmonary Fibrosis.
Grant	Genetic and Epigenetic Changes in MUC5B and Fibrosing Interstitial Lung Disease
Academic Article	The MUC5B promoter polymorphism is associated with specific interstitial lung abnormality subtypes.
Academic Article	The relationship between complement C3 expression and the MUC5B genotype in pulmonary fibrosis.
Academic Article	MUC5B Promoter Polymorphism and Development of Acute Respiratory Distress Syndrome.
Academic Article	MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease.
Academic Article	Idiopathic Pulmonary Fibrosis Is a Genetic Disease Involving Mucus and the Peripheral Airways.
Academic Article	Muc5b overexpression causes mucociliary dysfunction and enhances lung fibrosis in mice.
Academic Article	Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis.
Academic Article	Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis.
Academic Article	MUC5B variant is associated with visually and quantitatively detected preclinical pulmonary fibrosis.
Academic Article	MUC5B promoter variant rs35705950 and rheumatoid arthritis associated interstitial lung disease survival and progression.
Academic Article	Evolution of the Gain-of-Function MUC5B Promoter Variant.
Academic Article	Dysregulated Cell-Cell Communication Characterizes Pulmonary Fibrosis.

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Promoter Regions Genetic