Search Results - Semplicio, Giuseppe

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  1. 1
    Multiple microRNAs Derived from Chemically Synthesized Precursors Regulate Thrombospondin 1 Expression

    Multiple microRNAs Derived from Chemically Synthesized Precursors Regulate Thrombospondin 1 Expression by Dogar, Afzal M., Semplicio, Giuseppe, Guennewig, Boris, Hall, Jonathan

    Published 2014
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  2. 2
    MAPCap allows high-resolution detection and differential expression analysis of transcription start sites

    MAPCap allows high-resolution detection and differential expression analysis of transcription start sites by Bhardwaj, Vivek, Semplicio, Giuseppe, Erdogdu, Niyazi Umut, Manke, Thomas, Akhtar, Asifa

    Published 2019
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  3. 3
    Facultative dosage compensation of developmental genes on autosomes in Drosophila and mouse embryonic stem cells

    Facultative dosage compensation of developmental genes on autosomes in Drosophila and mouse embryonic stem cells by Valsecchi, Claudia Isabelle Keller, Basilicata, M. Felicia, Semplicio, Giuseppe, Georgiev, Plamen, Gutierrez, Noel Marie, Akhtar, Asifa

    Published 2018
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  4. 4
    The NSL complex-mediated nucleosome landscape is required to maintain transcription fidelity and suppression of transcription noise

    The NSL complex-mediated nucleosome landscape is required to maintain transcription fidelity and suppression of transcription noise by Lam, Kin Chung, Chung, Ho-Ryun, Semplicio, Giuseppe, Iyer, Shantanu S., Gaub, Aline, Bhardwaj, Vivek, Holz, Herbert, Georgiev, Plamen, Akhtar, Asifa

    Published 2019
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  5. 5
    Binding of the Atg1/ULK1 kinase to the ubiquitin-like protein Atg8 regulates autophagy

    Binding of the Atg1/ULK1 kinase to the ubiquitin-like protein Atg8 regulates autophagy by Kraft, Claudine, Kijanska, Monika, Kalie, Eyal, Siergiejuk, Edyta, Lee, Sung Sik, Semplicio, Giuseppe, Stoffel, Ingrid, Brezovich, Andrea, Verma, Mayanka, Hansmann, Isabella, Ammerer, Gustav, Hofmann, Kay, Tooze, Sharon, Peter, Matthias

    Published 2012
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  6. 6
    De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation

    De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation by Basilicata, M. Felicia, Bruel, Ange-Line, Semplicio, Giuseppe, Keller Valsecchi, Claudia Isabelle, Aktaş, Tuğçe, Duffourd, Yannis, Rumpf, Tobias, Morton, Jenny, Bache, Iben, Szymanski, Witold G., Gilissen, Christian, Vanakker, Olivier, Õunap, Katrin, Mittler, Gerhard, van der Burgt, Ineke, Chehadeh-Djebbar, Salima El, Cho, Megan T, Pfundt, Rolph, Tan, Tiong Yang, Kirchhoff, Maria, Menten, Björn, Vergult, Sarah, Lindstrom, Kristin, Reis, André, Johnson, Diana S., Fryer, Alan, McKay, Victoria, Study, DDD, Fisher, Richard B., Thauvin-Robinet, Christel, Francis, David, Roscioli, Tony, Pajusalu, Sander, Radtke, Kelly, Ganesh, Jaya, Brunner, Han G., Wilson, Meredith, Faivre, Laurence, Kalscheuer, Vera M., Thevenon, Julien, Akhtar, Asifa

    Published 2018
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