検索結果 - Minhajuddin Sirajuddin

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  1. 1
    GTP-induced conformational changes in septins and implications for function

    GTP-induced conformational changes in septins and implications for function 著者: Minhajuddin Sirajuddin, Marián Farkašovský, Eldar Zent, Alfred Wittinghofer

    出版事項 2009
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    Artigo
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  2. 2
    Regulation of microtubule motors by tubulin isotypes and post-translational modifications

    Regulation of microtubule motors by tubulin isotypes and post-translational modifications 著者: Minhajuddin Sirajuddin, Luke M. Rice, Ronald D. Vale

    出版事項 2014
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    Artigo
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  3. 3
    Tyrosination of α‐tubulin controls the initiation of processive dynein–dynactin motility

    Tyrosination of α‐tubulin controls the initiation of processive dynein–dynactin motility 著者: Richard J. McKenney, Walter Huynh, Ronald D. Vale, Minhajuddin Sirajuddin

    出版事項 2016
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    Artigo
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  4. 4
    Structural insights into actin filament recognition by commonly used cellular actin markers

    Structural insights into actin filament recognition by commonly used cellular actin markers 著者: Archana Kumari, Shubham Kesarwani, Manjunath G. Javoor, Kutti R. Vinothkumar, Minhajuddin Sirajuddin

    出版事項 2020
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    Artigo
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  5. 5
    Sequence diversity of tubulin isotypes in regulation of the mitochondrial voltage-dependent anion channel

    Sequence diversity of tubulin isotypes in regulation of the mitochondrial voltage-dependent anion channel 著者: Tatiana K. Rostovtseva, Philip A. Gurnev, David P. Hoogerheide, Amandine Rovini, Minhajuddin Sirajuddin, Sergey M. Bezrukov

    出版事項 2018
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    Artigo
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  6. 6
    Lysate-based pipeline to characterize microtubule-associated proteins uncovers unique microtubule behaviours

    Lysate-based pipeline to characterize microtubule-associated proteins uncovers unique microtubule behaviours 著者: A. S. Jijumon, Satish Bodakuntla, Mariya Genova, Mamata Bangera, Violet I. Sackett, Laetitia Besse, Fatlinda Maksut, Véronique Henriot, Maria M. Magiera, Minhajuddin Sirajuddin, Carsten Janke

    出版事項 2022
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    Artigo
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  7. 7
    De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy

    De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy 著者: Sahar Esmaeeli Nieh, Maura R.Z. Madou, Minhajuddin Sirajuddin, Brieana Fregeau, Dianalee McKnight, Katrina W. Lexa, Jonathan B. Strober, Christine G. Spaeth, Barbara Hallinan, Nizar Smaoui, John Pappas, Thomas Andrew Burrow, Marie McDonald, Mariam Latibashvili, Esther Leshinsky‐Silver, Dorit Lev, Luba Blumkin, Ronald D. Vale, A. James Barkovich, Elliott H. Sherr

    出版事項 2015
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    Artigo
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