Hasil Pencarian - Schafiq Nabhani

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  1. 1
    The cell cycle regulator CCDC6 is a key target of RNA-binding protein EWS.

    The cell cycle regulator CCDC6 is a key target of RNA-binding protein EWS. oleh Sujitha Duggimpudi, Erik Larsson, Schafiq Nabhani, Arndt Borkhardt, Jessica I Hoell

    Diterbitkan 2015-01-01
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  2. 2
    Prostaglandin receptor EP4 expression by Th17 cells is associated with high disease activity in ankylosing spondylitis

    Prostaglandin receptor EP4 expression by Th17 cells is associated with high disease activity in ankylosing spondylitis oleh Charlotte Klasen, Anja Meyer, Paula S. Wittekind, Iris Waqué, Schafiq Nabhani, David M. Kofler

    Diterbitkan 2019-06-01
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  3. 3
    EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency

    EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency oleh Cyrill Schipp, David Schlütermann, Andrea Hönscheid, Schafiq Nabhani, Jessica Höll, Prasad T. Oommen, Sebastian Ginzel, Sebastian Ginzel, Bernhard Fleckenstein, Björn Stork, Arndt Borkhardt, Polina Stepensky, Ute Fischer

    Diterbitkan 2018-10-01
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  4. 4
    Deregulation of Fas ligand expression as a novel cause of autoimmune lymphoproliferative syndrome-like disease

    Deregulation of Fas ligand expression as a novel cause of autoimmune lymphoproliferative syndrome-like disease oleh Schafiq Nabhani, Sebastian Ginzel, Hagit Miskin, Shoshana Revel-Vilk, Dan Harlev, Bernhard Fleckenstein, Andrea Hönscheid, Prasad T. Oommen, Michaela Kuhlen, Ralf Thiele, Hans-Jürgen Laws, Arndt Borkhardt, Polina Stepensky, Ute Fischer

    Diterbitkan 2015-09-01
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  5. 5
    Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans

    Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans oleh Cyrill Schipp, Schafiq Nabhani, Kirsten Bienemann, Natalia Simanovsky, Shlomit Kfir-Erenfeld, Nathalie Assayag-Asherie, Prasad T. Oommen, Shoshana Revel-Vilk, Andrea Hönscheid, Michael Gombert, Sebastian Ginzel, Daniel Schäfer, Hans-Jürgen Laws, Eitan Yefenof, Bernhard Fleckenstein, Arndt Borkhardt, Polina Stepensky, Ute Fischer

    Diterbitkan 2016-10-01
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