Hasil Pencarian - Martin Oti

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  1. 1
    Genome-wide p63-regulated gene expression in differentiating epidermal keratinocytes

    Genome-wide p63-regulated gene expression in differentiating epidermal keratinocytes oleh Martin Oti, Evelyn N. Kouwenhoven, Huiqing Zhou

    Diterbitkan 2015-09-01
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  2. 2
    Candidate disease gene prediction using Gentrepid: application to a genome‐wide association study on coronary artery disease

    Candidate disease gene prediction using Gentrepid: application to a genome‐wide association study on coronary artery disease oleh Sara Ballouz, Jason Y. Liu, Martin Oti, Bruno Gaeta, Diane Fatkin, Melanie Bahlo, Merridee A. Wouters

    Diterbitkan 2014-01-01
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  3. 3
    Prediction of human disease genes by human-mouse conserved coexpression analysis.

    Prediction of human disease genes by human-mouse conserved coexpression analysis. oleh Ugo Ala, Rosario Michael Piro, Elena Grassi, Christian Damasco, Lorenzo Silengo, Martin Oti, Paolo Provero, Ferdinando Di Cunto

    Diterbitkan 2008-03-01
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  4. 4
    An unbiased AAV-STARR-seq screen revealing the enhancer activity map of genomic regions in the mouse brain in vivo

    An unbiased AAV-STARR-seq screen revealing the enhancer activity map of genomic regions in the mouse brain in vivo oleh Ya-Chien Chan, Eike Kienle, Martin Oti, Antonella Di Liddo, Maria Mendez-Lago, Dominik F. Aschauer, Manuel Peter, Michaela Pagani, Cosmas Arnold, Andreas Vonderheit, Christian Schön, Sebastian Kreuz, Alexander Stark, Simon Rumpel

    Diterbitkan 2023-04-01
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  5. 5
    Mutant p63 Affects Epidermal Cell Identity through Rewiring the Enhancer Landscape

    Mutant p63 Affects Epidermal Cell Identity through Rewiring the Enhancer Landscape oleh Jieqiong Qu, Sabine E.J. Tanis, Jos P.H. Smits, Evelyn N. Kouwenhoven, Martin Oti, Ellen H. van den Bogaard, Colin Logie, Hendrik G. Stunnenberg, Hans van Bokhoven, Klaas W. Mulder, Huiqing Zhou

    Diterbitkan 2018-12-01
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  6. 6
    Human intellectual disability genes form conserved functional modules in Drosophila.

    Human intellectual disability genes form conserved functional modules in Drosophila. oleh Merel A W Oortveld, Shivakumar Keerthikumar, Martin Oti, Bonnie Nijhof, Ana Clara Fernandes, Korinna Kochinke, Anna Castells-Nobau, Eva van Engelen, Thijs Ellenkamp, Lilian Eshuis, Anne Galy, Hans van Bokhoven, Bianca Habermann, Han G Brunner, Christiane Zweier, Patrik Verstreken, Martijn A Huynen, Annette Schenck

    Diterbitkan 2013-10-01
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  7. 7
    Echocardiographic Measurements in a Preclinical Model of Chronic Chagasic Cardiomyopathy in Dogs: Validation and Reproducibility

    Echocardiographic Measurements in a Preclinical Model of Chronic Chagasic Cardiomyopathy in Dogs: Validation and Reproducibility oleh Eduardo B. Carvalho, Isalira P. R. Ramos, Alvaro F. S. Nascimento, Guilherme V. Brasil, Debora B. Mello, Martin Oti, Michael Sammeth, Maria T. Bahia, Antonio C. Campos de Carvalho, Antonio C. Campos de Carvalho, Antonio C. Campos de Carvalho, Adriana B. Carvalho, Adriana B. Carvalho, Adriana B. Carvalho

    Diterbitkan 2019-09-01
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  8. 8
    Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locus.

    Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locus. oleh Evelyn N Kouwenhoven, Simon J van Heeringen, Juan J Tena, Martin Oti, Bas E Dutilh, M Eva Alonso, Elisa de la Calle-Mustienes, Leonie Smeenk, Tuula Rinne, Lilian Parsaulian, Emine Bolat, Rasa Jurgelenaite, Martijn A Huynen, Alexander Hoischen, Joris A Veltman, Han G Brunner, Tony Roscioli, Emily Oates, Meredith Wilson, Miguel Manzanares, José Luis Gómez-Skarmeta, Hendrik G Stunnenberg, Marion Lohrum, Hans van Bokhoven, Huiqing Zhou

    Diterbitkan 2010-08-01
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  9. 9
    A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy

    A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy oleh Celia Zazo Seco, Anna Castells-Nobau, Seol-hee Joo, Margit Schraders, Jia Nee Foo, Monique van der Voet, S. Sendhil Velan, Bonnie Nijhof, Jaap Oostrik, Erik de Vrieze, Radoslaw Katana, Atika Mansoor, Martijn Huynen, Radek Szklarczyk, Martin Oti, Lisbeth Tranebjærg, Erwin van Wijk, Jolanda M. Scheffer-de Gooyert, Saadat Siddique, Jonathan Baets, Peter de Jonghe, Syed Ali Raza Kazmi, Suresh Anand Sadananthan, Bart P. van de Warrenburg, Chiea Chuen Khor, Martin C. Göpfert, Raheel Qamar, Annette Schenck, Hannie Kremer, Saima Siddiqi

    Diterbitkan 2017-02-01
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