Z
Zhuo Fang
Researcher at Max Delbrück Center for Molecular Medicine
Publications - 12
Citations - 4322
Zhuo Fang is an academic researcher from Max Delbrück Center for Molecular Medicine. The author has contributed to research in topics: Cytotoxic T cell & Gene. The author has an hindex of 8, co-authored 12 publications receiving 4024 citations. Previous affiliations of Zhuo Fang include Huazhong University of Science and Technology & Leibniz Association.
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Journal ArticleDOI
Widespread changes in protein synthesis induced by microRNAs
Matthias Selbach,Björn Schwanhäusser,Nadine Thierfelder,Zhuo Fang,Raya Khanin,Nikolaus Rajewsky +5 more
TL;DR: It is shown that a single miRNA can repress the production of hundreds of proteins, but that this repression is typically relatively mild, and the data suggest that a mi RNA can, by direct or indirect effects, tune protein synthesis from thousands of genes.
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The microRNA miR-182 is induced by IL-2 and promotes clonal expansion of activated helper T lymphocytes
Anna-Barbara Stittrich,Claudia Haftmann,Evridiki Sgouroudis,Anja A. Kühl,Ahmed N. Hegazy,Isabel Panse,René Riedel,Michael Flossdorf,Jun Dong,Franziska Fuhrmann,Gitta Anne Heinz,Zhuo Fang,Na Li,Ute Bissels,Farahnaz Hatam,Angelina Jahn,Ben Hammoud,Mareen Matz,Felix Michael Schulze,Ria Baumgrass,Andreas Bosio,Hans-Joachim Mollenkopf,Joachim R. Grün,Andreas Thiel,Wei Chen,Thomas Höfer,Christoph Loddenkemper,Max Löhning,Hyun-Dong Chang,Nikolaus Rajewsky,Andreas Radbruch,Mir-Farzin Mashreghi +31 more
TL;DR: A central role for miR-182 is demonstrated in the physiological regulation of IL-2-driven helper T cell–mediated immune responses and new therapeutic possibilities are opened.
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The Impact of miRNA Target Sites in Coding Sequences and in 3′UTRs
Zhuo Fang,Nikolaus Rajewsky +1 more
TL;DR: Using transcriptomics and proteomics data of ten miRNA mis-expression experiments as well as transcriptome-wide experimentally identified miRNA target sites, it is found that mRNA and protein expression of genes containing target Sites both in coding regions and 3′UTRs were in general mildly but significantly more regulated than those containing target sites in 3′utRs only.
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Human memory T cells from the bone marrow are resting and maintain long-lasting systemic memory
Anna Okhrimenko,Joachim R. Grün,Kerstin Westendorf,Zhuo Fang,Simon Reinke,Philipp von Roth,Georgi I. Wassilew,Anja A. Kühl,Robert Kudernatsch,Sonya Demski,Carmen Scheibenbogen,Koji Tokoyoda,Mairi McGrath,Martin Raftery,Günther Schönrich,Alessandro Serra,Hyun-Dong Chang,Andreas Radbruch,Jun Dong +18 more
TL;DR: It is shown that human bone marrow professional memory T cells are not activated but are resting in terms of proliferation, transcription, and mobility, and they are in the G0 phase of the cell cycle, and their transcriptome is that of resting T cells.
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Knowledge guided analysis of microarray data
TL;DR: A new algorithm capturing both expression pattern similarities and biological function similarities is developed, and it is shown that this method has advantages in both the quality of clusters and the precision of biological annotations.