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Aadel A. Chaudhuri

Researcher at Washington University in St. Louis

Publications -  110
Citations -  9792

Aadel A. Chaudhuri is an academic researcher from Washington University in St. Louis. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 23, co-authored 68 publications receiving 6903 citations. Previous affiliations of Aadel A. Chaudhuri include Barnes-Jewish Hospital & Massachusetts Institute of Technology.

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Determining cell type abundance and expression from bulk tissues with digital cytometry.

TL;DR: The utility of CIBERSORTx is evaluated in multiple tumor types, including melanoma, where single-cell reference profiles were used to dissect bulk clinical specimens, revealing cell-type-specific phenotypic states linked to distinct driver mutations and response to immune checkpoint blockade.
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Physiological and pathological roles for microRNAs in the immune system

TL;DR: Recent advances in understanding of both the intended functions of miRNAs in managing immune cell biology and their pathological roles when their expression is dysregulated are discussed.
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MicroRNA-155 Promotes Autoimmune Inflammation by Enhancing Inflammatory T Cell Development

TL;DR: It is shown that one aspect of miR-155 function is the promotion of T cell-dependent tissue inflammation, suggesting that miR -155 might be a promising therapeutic target for the treatment of autoimmune disorders.
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Inositol phosphatase SHIP1 is a primary target of miR-155.

TL;DR: This study unveils a molecular link between miR-155 and SHIP1 and provides evidence that repression ofSHIP1 is an important component of miR -155 biology.
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Sustained expression of microRNA-155 in hematopoietic stem cells causes a myeloproliferative disorder.

TL;DR: Evidence is presented of a strong but transient induction of miR-155 in mouse bone marrow after injection of bacterial lipopolysaccharide correlated with granulocyte/monocyte (GM) expansion, which implicate mi R-155 as a contributor to physiological GM expansion during inflammation and to certain pathological features associated with AML.