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Tao Zheng

Researcher at Johns Hopkins University School of Medicine

Publications -  60
Citations -  6547

Tao Zheng is an academic researcher from Johns Hopkins University School of Medicine. The author has contributed to research in topics: Inflammation & Cytokine. The author has an hindex of 34, co-authored 51 publications receiving 6062 citations. Previous affiliations of Tao Zheng include Yale University.

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Acidic Mammalian Chitinase in Asthmatic Th2 Inflammation and IL-13 Pathway Activation

TL;DR: It is shown that acidic mammalian chitinase (AMCase) is induced via a T helper-2 (Th2)–specific, interleukin-13 (IL-13)–mediated pathway in epithelial cells and macrophages in an aeroallergen asthma model and expressed in exaggerated quantities in human asthma.
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Inducible targeting of IL-13 to the adult lung causes matrix metalloproteinase– and cathepsin-dependent emphysema

TL;DR: It is demonstrated that IL-13 is a potent stimulator of MMP and cathepsin-based proteolytic pathways in the lung and causes emphysema with enhanced lung volumes and compliance, mucus metaplasia, and inflammation, when inducibly overexpressed in the adult murine lung.
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The Atopic March: Progression from Atopic Dermatitis to Allergic Rhinitis and Asthma.

TL;DR: Recent studies support the idea of a causal link between AD and later onset atopic disorders and suggest that a dysfunctional skin barrier serves as a site for allergic sensitization to antigen and colonization of bacterial super antigens.
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New insights into the pathogenesis of asthma

TL;DR: It is reasonable to think of asthma as a pul-monary disorder characterized by the generalized reversible obstruction of airflow and to define reversibility as a greater than 12% increase in the patient’s forced expiratory volume in 1 second.
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Interferon γ induction of pulmonary emphysema in the adult murine lung

TL;DR: It is demonstrated that interferon γ (IFN-γ), a prominent product of CD8+ cells, causes emphysema with alveolar enlargement, enhanced lung volumes, enhanced pulmonary compliance, and macrophage- and neutrophil-rich inflammation when inducibly targeted to the adult murine lung.