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Jae Youn Cho

Researcher at University of California, San Diego

Publications -  45
Citations -  2916

Jae Youn Cho is an academic researcher from University of California, San Diego. The author has contributed to research in topics: Eosinophil & Fibrosis. The author has an hindex of 29, co-authored 44 publications receiving 2727 citations.

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Inhibition of airway remodeling in IL-5-deficient mice.

TL;DR: An important role for IL-5, eosinophils, alphaVbeta6, and TGF-beta in airway remodeling is suggested, and increased airway epithelial expression of alphaV beta6 integrin may contribute to the increased activation of latent T GF-beta.
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Defining the in vivo function of Siglec-F, a CD33-related Siglec expressed on mouse eosinophils.

TL;DR: The data support the proposed negative feedback role for Siglec-F, represent the first in vivo demonstration of biologic functions for any CD33rSiglec, and predict a role for human SigLec-8 (the isofunctional paralog of mouse SigleC-F) in regulating the pathogenesis of human eosinophil-mediated disorders.
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ORMDL3 is an inducible lung epithelial gene regulating metalloproteases, chemokines, OAS, and ATF6

TL;DR: Evidence of the inducible nature of ORMDL3 ER expression in particular in bronchial epithelial cells is provided and an ER UPR pathway through which OR MDL3 may be linked to asthma is suggested.
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Adiponectin and Functional Adiponectin Receptor 1 Are Expressed by Airway Epithelial Cells in Chronic Obstructive Pulmonary Disease

TL;DR: The novel observation that adiponectin and functional AdipoR1 are expressed by lung epithelial cells is demonstrated, suggesting a potential autocrine and/or paracrine pathway for adip onectin to activate epithelial Cells in COPD-E.
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The tumor necrosis factor family member LIGHT is a target for asthmatic airway remodeling

TL;DR: Pharmacological inhibition of LIGHT using a fusion protein between the IgG Fc domain and lymphotoxin β receptor reduces lung fibrosis, smooth muscle hyperplasia and airway hyperresponsiveness in mouse models of chronic asthma, despite having little effect on airway eosinophilia.