D
Dvir Netanely
Researcher at Tel Aviv University
Publications - 16
Citations - 906
Dvir Netanely is an academic researcher from Tel Aviv University. The author has contributed to research in topics: Gene & Cancer. The author has an hindex of 9, co-authored 14 publications receiving 790 citations. Previous affiliations of Dvir Netanely include Weizmann Institute of Science.
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Journal ArticleDOI
Network analysis of protein structures identifies functional residues.
Gil Amitai,Arye Shemesh,Einat Sitbon,Maxim Shklar,Dvir Netanely,Ilya Venger,Shmuel Pietrokovski +6 more
TL;DR: This work transformed protein structures into residue interaction graphs (RIGs), where amino acid residues are graph nodes and their interactions with each other are the graph edges, and found that active site, ligand-binding and evolutionary conserved residues, typically have high closeness values.
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Transcription factor/microRNA axis blocks melanoma invasion program by miR-211 targeting NUAK1.
Rachel E. Bell,Mehdi Khaled,Dvir Netanely,Steffen Schubert,Tamar Golan,Amir Buxbaum,Maja M. Janas,Benny Postolsky,Michael S. Goldberg,Ron Shamir,Carmit Levy +10 more
TL;DR: The MITF/miR-211 axis that inhibits the invasive program by blocking adhesion is defined and NUAK1 is identified as a potential target for the treatment of metastatic melanoma.
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Age-dependent spatial memory loss can be partially restored by immune activation.
Noga Ron-Harel,Yifat Segev,Gil M. Lewitus,Michal Cardon,Yaniv Ziv,Dvir Netanely,J. Jacob-Hirsch,J. Jacob-Hirsch,Ninette Amariglio,Ninette Amariglio,G. Rechavi,Eytan Domany,Michal Schwartz +12 more
TL;DR: It is shown that functional cell-mediated immunity is required for the maintenance of hippocampus-dependent spatial memory and that homeostatic-driven proliferation of lymphocytes, which expands the existing T cell repertoire, restored spatial memory deficits in aged mice.
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Expression and methylation patterns partition luminal-A breast tumors into distinct prognostic subgroups
TL;DR: The analysis of molecular classification of breast tumors using both expression and methylation data obtained from The Cancer Genome Atlas provides two prognostic gene sets that dissect and explain tumor variability within the luminal-A subgroup, thus, contributing to the advancement of subtype-specific diagnosis and treatment.
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The Effect of Simulated Microgravity on Human Mesenchymal Stem Cells Cultured in an Osteogenic Differentiation System: A Bioinformatics Study
TL;DR: Evaluation of human mesenchymal stem cells showed significant decreases in osteogenic and chondrogenic gene expression and an increase in adipogenic gene expression, indicating that ex vivo adipose tissue engineering may benefit from simulated microgravity.