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Christoph A. Thaiss

Researcher at Weizmann Institute of Science

Publications -  72
Citations -  18747

Christoph A. Thaiss is an academic researcher from Weizmann Institute of Science. The author has contributed to research in topics: Microbiome & Medicine. The author has an hindex of 32, co-authored 53 publications receiving 13688 citations. Previous affiliations of Christoph A. Thaiss include Yale University & University of Bonn.

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Inflammasome-mediated dysbiosis regulates progression of NAFLD and obesity

TL;DR: Altered interactions between the gut microbiota and the host, produced by defective NLRP3 and NLRP6 inflammasome sensing, may govern the rate of progression of multiple metabolic syndrome-associated abnormalities, highlighting the central role of the microbiota in the pathogenesis of heretofore seemingly unrelated systemic auto-inflammatory and metabolic disorders.
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NLRP6 Inflammasome Regulates Colonic Microbial Ecology and Risk for Colitis

TL;DR: It is shown that deficiency of NLRP6 in mouse colonic epithelial cells results in reduced IL-18 levels and altered fecal microbiota characterized by expanded representation of the bacterial phyla Bacteroidetes (Prevotellaceae) and TM7.
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Artificial sweeteners induce glucose intolerance by altering the gut microbiota

TL;DR: It is demonstrated that consumption of commonly used NAS formulations drives the development of glucose intolerance through induction of compositional and functional alterations to the intestinal microbiota, thereby calling for a reassessment of massive NAS usage.
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Inflammation-induced cancer: crosstalk between tumours, immune cells and microorganisms.

TL;DR: It is proposed that understanding this microbial influence will be crucial for targeted therapy in modern cancer treatment and the recently suggested role of commensal microorganisms in inflammation-induced cancer is discussed.
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The microbiome and innate immunity

TL;DR: The intestinal microbiome is a signalling hub that integrates environmental inputs, such as diet, with genetic and immune signals to affect the host's metabolism, immunity and response to infection.