نتایج جستجو برای: mir17hg

تعداد نتایج: 147  

2012
Andrius Serva Bettina Knapp Yueh-Tso Tsai Christoph Claas Tautvydas Lisauskas Petr Matula Nathalie Harder Lars Kaderali Karl Rohr Holger Erfle Roland Eils Vania Braga Vytaute Starkuviene

miRNA cluster miR-17-92 is known as oncomir-1 due to its potent oncogenic function. miR-17-92 is a polycistronic cluster that encodes 6 miRNAs, and can both facilitate and inhibit cell proliferation. Known targets of miRNAs encoded by this cluster are largely regulators of cell cycle progression and apoptosis. Here, we show that miRNAs encoded by this cluster and sharing the seed sequence of mi...

Journal: :Journal of immunology 2013
Dimitri de Kouchkovsky Jonathan H Esensten Wendy L Rosenthal Malika M Morar Jeffrey A Bluestone Lukas T Jeker

microRNAs (miRNA) are essential for regulatory T cell (Treg) function but little is known about the functional relevance of individual miRNA loci. We identified the miR-17-92 cluster as CD28 costimulation dependent, suggesting that it may be key for Treg development and function. Although overall immune homeostasis was maintained in mice with miR-17-92-deficient Tregs, expression of the miR-17-...

Journal: :Cell 2008
Joshua T. Mendell

MicroRNAs (miRNAs) encoded by the miR-17-92 cluster and its paralogs are known to act as oncogenes. Expression of these miRNAs promotes cell proliferation, suppresses apoptosis of cancer cells, and induces tumor angiogenesis. New work reveals essential functions for these miRNAs not only in tumor formation but also during normal development of the heart, lungs, and immune system.

2016
Cuong Khuu Tor Paaske Utheim Amer Sehic

MicroRNAs (miRNAs) form a class of noncoding RNA genes whose products are small single-stranded RNAs that are involved in the regulation of translation and degradation of mRNAs. There is a fine balance between deregulation of normal developmental programs and tumor genesis. An increasing body of evidence suggests that altered expression of miRNAs is entailed in the pathogenesis of human cancers...

2017
Stefan Nagel Claudia Pommerenke Corinna Meyer Maren Kaufmann Roderick A.F. MacLeod Hans G. Drexler

NKL homeobox gene MSX1 is physiologically expressed in lymphoid progenitors and subsequently downregulated in developing T- and B-cells. In contrast, elevated expression levels of MSX1 persist in mature natural killer (NK)-cells, indicating a functional role in this compartment. While T-cell acute lymphoblastic leukemia (T-ALL) subsets exhibit aberrant overexpression of MSX1, we show here that ...

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