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Lam Nhat Nguyen

Researcher at East Tennessee State University James H. Quillen College of Medicine

Publications -  31
Citations -  5346

Lam Nhat Nguyen is an academic researcher from East Tennessee State University James H. Quillen College of Medicine. The author has contributed to research in topics: Telomere & T cell. The author has an hindex of 10, co-authored 29 publications receiving 3798 citations. Previous affiliations of Lam Nhat Nguyen include Hallym University & St. Jude Children's Research Hospital.

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Journal Article

The Cancer Genome Atlas Pan-Cancer analysis project

Kyle Chang, +337 more
- 01 Sep 2013 - 
TL;DR: The Cancer Genome Atlas (TCGA) Research Network has profiled and analyzed large numbers of human tumors to discover molecular aberrations at the DNA, RNA, protein and epigenetic levels as mentioned in this paper.
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AIM2 forms a complex with pyrin and ZBP1 to drive PANoptosis and host defence

TL;DR: AIM2 regulates the innate immune sensors pyrin and ZBP1 to drive inflammatory signalling and a form of inflammatory cell death known as PANoptosis, and provide host protection during infections with herpes simplex virus 1 and Francisella novicida as discussed by the authors.
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ADAR1 restricts ZBP1-mediated immune response and PANoptosis to promote tumorigenesis.

TL;DR: In this article, the authors identify and characterize ADAR1's interaction with Z-DNA binding protein 1 (ZBP1), defining its role in cell death regulation and tumorigenesis.
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IL-10 induces an immune repressor pathway in sepsis by promoting S100A9 nuclear localization and MDSC development.

TL;DR: It is shown that the immunosuppressive cytokine IL-10 supports S100A9 expression and its nuclear localization in MDSCs to function as immune repressors, and that targeting this immune repressor path may improve sepsis survival in mice.
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Stearoyl Coenzyme A Desaturase 1 Is Associated with Hepatitis C Virus Replication Complex and Regulates Viral Replication

TL;DR: Manipulation of SCD1 activity may represent a novel host-targeted antiviral strategy for the treatment of HCV infection and provide novel mechanistic insights into the roles ofSCD1.