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Noam Shomron

Researcher at Tel Aviv University

Publications -  244
Citations -  8929

Noam Shomron is an academic researcher from Tel Aviv University. The author has contributed to research in topics: microRNA & Gene. The author has an hindex of 49, co-authored 212 publications receiving 7442 citations. Previous affiliations of Noam Shomron include International Computer Science Institute & Massachusetts Institute of Technology.

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MicroRNAs as predictors for CNS relapse of systemic diffuse large B-cell lymphoma

TL;DR: It is shown that the expression level of two miRNAs may have valuable information that may refine stratification for patients-at-risk for relapse with CNS involvement in DLBCL, and a number of putative mechanisms for these mi RNAs regulation of CNS relapse, including neuronal plasticity and WNT signaling pathway are revealed.
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Splicing factor hSlu7 contains a unique functional domain required to retain the protein within the nucleus.

TL;DR: Three functional domains of the hSlu7 protein are identified that have distinct roles in its subcellular localization: a nuclear localization signal, a zinc-knuckle motif, and a lysine-rich region, which indicates that zinc-dependent nucleocytoplasmic shuttling might be the possible molecular basis by which hSLU7 protein levels are regulated within the nucleus.
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A splice variant of ADAMTS13 is expressed in human hepatic stellate cells and cancerous tissues

TL;DR: Screening a panel of human tissues and cell lines revealed a spliced ADAMTS13 transcript in hepatic stellate cells and a hepatoma cell line that retains the 25th intron, suggesting its biological inaccessibility may prevent its participation in regulating haemostasis and other physiologic functions.
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Biomaterials for Abrogating Metastasis: Bridging the Gap between Basic and Translational Research

TL;DR: This work proposes to implement three possible strategies to treat cancer as a function of disease type and state, while leveraging the advancement in materials design and in particular nanotechnology: local primary tumor abrogation, primary tumor re‐programming to prevent metastasis, and combination therapy when metastasis has already transpired.
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Fluid consumption and taste novelty determines transcription temporal dynamics in the gustatory cortex

TL;DR: It is demonstrated that in taste learning, transcription programs were activated following the physiological responses and the specific information about a given taste, and the cortical differential prolonged kinetics of mRNA following novel versus familiar taste learning may represent additional novelty related molecular response.