scispace - formally typeset
G

Gerard J. Nuovo

Researcher at Ohio State University

Publications -  414
Citations -  32079

Gerard J. Nuovo is an academic researcher from Ohio State University. The author has contributed to research in topics: In situ hybridization & microRNA. The author has an hindex of 89, co-authored 395 publications receiving 29133 citations. Previous affiliations of Gerard J. Nuovo include Stony Brook University & Columbia University.

Papers
More filters
Journal ArticleDOI

Complement associated microvascular injury and thrombosis in the pathogenesis of severe COVID-19 infection: A report of five cases.

TL;DR: At least a subset of sustained, severe COVID-19 may define a type of catastrophic microvascular injury syndrome mediated by activation of complement pathways and an associated procoagulant state, and could suggest targets for specific intervention.
Journal ArticleDOI

MicroRNAs bind to Toll-like receptors to induce prometastatic inflammatory response

TL;DR: It is shown that tumor-secreted miR-21 andmiR-29a also can function by another mechanism, by binding as ligands to receptors of the Toll-like receptor (TLR) family, murine TLR7 and human TLR8, in immune cells, triggering a TLR-mediated prometastatic inflammatory response that ultimately may lead to tumor growth and metastasis.
Journal ArticleDOI

Expression profiling identifies microRNA signature in pancreatic cancer

TL;DR: A microRNA expression signature has been identified that is associated with pancreatic cancer and Aberrant microRNAs may offer new clues to pancreatic tumorigenesis and may provide diagnostic biomarkers for pancreatic adenocarcinoma.
Journal ArticleDOI

CD56bright natural killer cells are present in human lymph nodes and are activated by T cell–derived IL-2: a potential new link between adaptive and innate immunity

TL;DR: It is demonstrated that CD56(bright) NK cells are present in human lymph nodes and that endogenous T cell-derived IL-2, acting through the NK high-affinityIL-2 receptor, costimulates CD56 (bright)NK cells to secrete IFN-gamma.
Journal ArticleDOI

miR-221&222 regulate TRAIL resistance and enhance tumorigenicity through PTEN and TIMP3 downregulation.

TL;DR: It is reported that miR-221&222 are overexpressed in aggressive non-small cell lung cancer and hepatocarcinoma cells, as compared with less invasive and/or normal lung and liver cells, and it is demonstrated that the MET oncogene is involved in miR+222 activation through the c-Jun transcription factor.