Hasil Pencarian - Leandros Boukas

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  1. 1
    Missense variants causing Wiedemann-Steiner syndrome preferentially occur in the KMT2A-CXXC domain and are accurately classified using AlphaFold2.

    Missense variants causing Wiedemann-Steiner syndrome preferentially occur in the KMT2A-CXXC domain and are accurately classified using AlphaFold2. oleh Tinna Reynisdottir, Kimberley Jade Anderson, Leandros Boukas, Hans Tomas Bjornsson

    Diterbitkan 2022-06-01
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  2. 2
    Pumping the brakes on RNA velocity by understanding and interpreting RNA velocity estimates

    Pumping the brakes on RNA velocity by understanding and interpreting RNA velocity estimates oleh Shijie C. Zheng, Genevieve Stein-O’Brien, Leandros Boukas, Loyal A. Goff, Kasper D. Hansen

    Diterbitkan 2023-10-01
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  3. 3
    Leveraging the Mendelian disorders of the epigenetic machinery to systematically map functional epigenetic variation

    Leveraging the Mendelian disorders of the epigenetic machinery to systematically map functional epigenetic variation oleh Teresa Romeo Luperchio, Leandros Boukas, Li Zhang, Genay Pilarowski, Jenny Jiang, Allison Kalinousky, Kasper D Hansen, Hans T Bjornsson

    Diterbitkan 2021-08-01
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  4. 4
    Growth deficiency in a mouse model of Kabuki syndrome 2 bears mechanistic similarities to Kabuki syndrome 1.

    Growth deficiency in a mouse model of Kabuki syndrome 2 bears mechanistic similarities to Kabuki syndrome 1. oleh Christine W Gao, WanYing Lin, Ryan C Riddle, Sheetal Chopra, Jiyoung Kim, Leandros Boukas, Kasper D Hansen, Hans T Björnsson, Jill A Fahrner

    Diterbitkan 2024-06-01
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  5. 5
    KMT2D regulates activation, localization, and integrin expression by T-cells

    KMT2D regulates activation, localization, and integrin expression by T-cells oleh Sarah J. Potter, Li Zhang, Michael Kotliar, Yuehong Wu, Caitlin Schafer, Kurtis Stefan, Leandros Boukas, Leandros Boukas, Dima Qu’d, Olaf Bodamer, Olaf Bodamer, Olaf Bodamer, Brittany N. Simpson, Brittany N. Simpson, Artem Barski, Artem Barski, Artem Barski, Andrew W. Lindsley, Andrew W. Lindsley, Hans T. Bjornsson, Hans T. Bjornsson, Hans T. Bjornsson

    Diterbitkan 2024-05-01
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  6. 6
    Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood

    Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood oleh Michael A. Levy, David B. Beck, Kay Metcalfe, Sofia Douzgou, Sivagamy Sithambaram, Trudie Cottrell, Muhammad Ansar, Jennifer Kerkhof, Cyril Mignot, Marie-Christine Nougues, Boris Keren, Hannah W. Moore, Renske Oegema, Jacques C. Giltay, Marleen Simon, Richard H. van Jaarsveld, Jessica Bos, Mieke van Haelst, M. Mahdi Motazacker, Elles M. J. Boon, Gijs W. E. Santen, Claudia A. L. Ruivenkamp, Marielle Alders, Teresa Romeo Luperchio, Leandros Boukas, Keri Ramsey, Vinodh Narayanan, G. Bradley Schaefer, Roberto Bonasio, Kimberly F. Doheny, Roger E. Stevenson, Siddharth Banka, Bekim Sadikovic, Jill A. Fahrner

    Diterbitkan 2021-11-01
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  7. 7
    Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood

    Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood oleh Michael A. Levy, David B. Beck, Kay Metcalfe, Sofia Douzgou, Sivagamy Sithambaram, Trudie Cottrell, Muhammad Ansar, Jennifer Kerkhof, Cyril Mignot, Marie-Christine Nougues, Boris Keren, Hannah W. Moore, Renske Oegema, Jacques C. Giltay, Marleen Simon, Richard H. van Jaarsveld, Jessica Bos, Mieke van Haelst, M. Mahdi Motazacker, Elles M. J. Boon, Gijs W. E. Santen, Claudia A. L. Ruivenkamp, Marielle Alders, Teresa Romeo Luperchio, Leandros Boukas, Keri Ramsey, Vinodh Narayanan, G. Bradley Schaefer, Roberto Bonasio, Kimberly F. Doheny, Roger E. Stevenson, Sidharth Banka, Bekim Sadikovic, Jill A. Fahrner

    Diterbitkan 2021-11-01
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