Hasil Pencarian - Achim Dickmanns

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  1. 1
    Structural Basis of Targeting the Exportin CRM1 in Cancer

    Structural Basis of Targeting the Exportin CRM1 in Cancer oleh Achim Dickmanns, Thomas Monecke, Ralf Ficner

    Diterbitkan 2015-09-01
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  2. 2
    Bucky Ball Is a Novel Zebrafish Vasa ATPase Activator

    Bucky Ball Is a Novel Zebrafish Vasa ATPase Activator oleh Roshan Priyarangana Perera, Alaa Shaikhqasem, Nadia Rostam, Achim Dickmanns, Ralf Ficner, Kai Tittmann, Roland Dosch

    Diterbitkan 2021-10-01
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  3. 3
    Structural and Functional Characterization of CRM1-Nup214 Interactions Reveals Multiple FG-Binding Sites Involved in Nuclear Export

    Structural and Functional Characterization of CRM1-Nup214 Interactions Reveals Multiple FG-Binding Sites Involved in Nuclear Export oleh Sarah A. Port, Thomas Monecke, Achim Dickmanns, Christiane Spillner, Romina Hofele, Henning Urlaub, Ralf Ficner, Ralph H. Kehlenbach

    Diterbitkan 2015-10-01
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  4. 4
    A meet-up of two second messengers: the c-di-AMP receptor DarB controls (p)ppGpp synthesis in Bacillus subtilis

    A meet-up of two second messengers: the c-di-AMP receptor DarB controls (p)ppGpp synthesis in Bacillus subtilis oleh Larissa Krüger, Christina Herzberg, Dennis Wicke, Heike Bähre, Jana L. Heidemann, Achim Dickmanns, Kerstin Schmitt, Ralf Ficner, Jörg Stülke

    Diterbitkan 2021-02-01
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  5. 5
    The velvet family of fungal regulators contains a DNA-binding domain structurally similar to NF-κB.

    The velvet family of fungal regulators contains a DNA-binding domain structurally similar to NF-κB. oleh Yasar Luqman Ahmed, Jennifer Gerke, Hee-Soo Park, Özgür Bayram, Piotr Neumann, Min Ni, Achim Dickmanns, Sun Chang Kim, Jae-Hyuk Yu, Gerhard H Braus, Ralf Ficner

    Diterbitkan 2013-12-01
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  6. 6
    Case report: Compound heterozygous NUP85 variants cause autosomal recessive primary microcephaly

    Case report: Compound heterozygous NUP85 variants cause autosomal recessive primary microcephaly oleh Ethiraj Ravindran, Ethiraj Ravindran, Ethiraj Ravindran, Gaetan Lesca, Gaetan Lesca, Louis Januel, Linus Goldgruber, Achim Dickmanns, Henri Margot, Angela M. Kaindl, Angela M. Kaindl, Angela M. Kaindl

    Diterbitkan 2023-02-01
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  7. 7
    Monoallelic CRMP1 gene variants cause neurodevelopmental disorder

    Monoallelic CRMP1 gene variants cause neurodevelopmental disorder oleh Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander PA Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl

    Diterbitkan 2022-12-01
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  8. 8
    Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence.

    Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence. oleh Edith Bonnin, Pauline Cabochette, Alessandro Filosa, Ramona Jühlen, Shoko Komatsuzaki, Mohammed Hezwani, Achim Dickmanns, Valérie Martinelli, Marjorie Vermeersch, Lynn Supply, Nuno Martins, Laurence Pirenne, Gianina Ravenscroft, Marcus Lombard, Sarah Port, Christiane Spillner, Sandra Janssens, Ellen Roets, Jo Van Dorpe, Martin Lammens, Ralph H Kehlenbach, Ralf Ficner, Nigel G Laing, Katrin Hoffmann, Benoit Vanhollebeke, Birthe Fahrenkrog

    Diterbitkan 2018-12-01
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