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Carla A. Da Silva

Researcher at AstraZeneca

Publications -  29
Citations -  2678

Carla A. Da Silva is an academic researcher from AstraZeneca. The author has contributed to research in topics: Stem cell factor & Asthma. The author has an hindex of 17, co-authored 27 publications receiving 2392 citations. Previous affiliations of Carla A. Da Silva include French Institute of Health and Medical Research & Yale University.

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Role of chitin and chitinase/chitinase-like proteins in inflammation, tissue remodeling, and injury.

TL;DR: Levels of YKL-40 in the lung and serum are increased in asthma and other inflammatory and remodeling disorders and often correlate with disease severity, indicating understanding of the roles of C/CLPs in inflammation, tissue remodeling, and tissue injury in health and disease.
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Role of breast regression protein 39 (BRP-39)/chitinase 3-like-1 in Th2 and IL-13–induced tissue responses and apoptosis

TL;DR: These studies establish novel regulatory roles for BRP-39/YKL-40 in the initiation and effector phases of Th2 inflammation and remodeling and suggest that these proteins are therapeutic targets in Th2- and macrophage-mediated disorders.
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Chitin regulation of immune responses: an old molecule with new roles.

TL;DR: This work demonstrated that chitin has complex and size-dependent effects on innate and adaptive immune responses including the ability to recruit and activate innate immune cells and induce cytokine and chemokine production via a variety of cell surface receptors.
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Stem cell factor and its receptor c-Kit as targets for inflammatory diseases.

TL;DR: Data suggest that SCF/c-Kit may be a potential therapeutic target for the control of mast cell and eosinophil number and activation in inflammatory diseases.
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Chitin is a size-dependent regulator of macrophage TNF and IL-10 production.

TL;DR: Chitin contains size-dependent pathogen-associated molecular patterns that stimulate TLR2, dectin-1, and the mannose receptor, differentially activate NF-κB and spleen tyrosine kinase, and stimulate the production of pro- and anti-inflammatory cytokines.