Хайлтын үр дүнгүүд - Aleš Hnı́zda

  • 6-н 1 - 6 үр дүнгүүдийг харуулж байна
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  1. 1
    Conserved roles of C. elegans and human MANFs in sulfatide binding and cytoprotection

    Conserved roles of C. elegans and human MANFs in sulfatide binding and cytoprotection -н Meirong Bai, Roman Vozdek, Aleš Hnı́zda, Chenxiao Jiang, Bingying Wang, Ladislav Kuchař, Tiejun Li, Yuefan Zhang, Chase Wood, Liang Feng, Yongjun Dang, K. Dengke

    Хэвлэсэн 2018
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    Artigo
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  2. 2
    Dimers of DNA-PK create a stage for DNA double-strand break repair

    Dimers of DNA-PK create a stage for DNA double-strand break repair -н Amanda K. Chaplin, Steven W. Hardwick, Shikang Liang, Antonia Kefala Stavridi, Aleš Hnı́zda, Lee R. Cooper, Taianá Maia de Oliveira, Dimitri Y. Chirgadze, Tom L. Blundell

    Хэвлэсэн 2020
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    Artigo
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  3. 3
    PDGFRB mutation and tyrosine kinase inhibitor resistance in Ph-like acute lymphoblastic leukemia

    PDGFRB mutation and tyrosine kinase inhibitor resistance in Ph-like acute lymphoblastic leukemia -н Yingchi Zhang, Yufeng Gao, Hui Zhang, Jingliao Zhang, Fuhong He, Aleš Hnı́zda, Maoxiang Qian, Xiaoming Liu, Yoshihiro Gocho, Ching‐Hon Pui, Tao Cheng, Qianfei Wang, Jun J. Yang, Xiaofan Zhu, Xin Liu

    Хэвлэсэн 2018
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    Artigo
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  4. 4
    Mechanism of efficient double-strand break repair by a long non-coding RNA

    Mechanism of efficient double-strand break repair by a long non-coding RNA -н Roopa Thapar, Jinglong Wang, Michal Hammel, Ruiqiong Ye, Ke Liang, Cheng‐Cao Sun, Aleš Hnı́zda, Shikang Liang, Su S. Maw, Linda Lee, Heather Villarreal, Isaac Forrester, Shujuan Fang, Miaw-Sheue Tsai, Tom L. Blundell, Anthony J. Davis, Chunru Lin, Susan P. Lees‐Miller, Terence R. Strick, John A. Tainer

    Хэвлэсэн 2020
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    Errata/Corrigenda
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  5. 5
    Mechanism of efficient double-strand break repair by a long non-coding RNA

    Mechanism of efficient double-strand break repair by a long non-coding RNA -н Roopa Thapar, Jinglong Wang, Michal Hammel, Ruiqiong Ye, Ke Liang, Cheng‐Cao Sun, Aleš Hnı́zda, Shikang Liang, Su S. Maw, Linda Lee, Heather Villarreal, Isaac Forrester, Shujuan Fang, Miaw-Sheue Tsai, Tom L. Blundell, Anthony J. Davis, Chunru Lin, Susan P. Lees‐Miller, Terence R. Strick, John A. Tainer

    Хэвлэсэн 2020
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    Artigo
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  6. 6
    Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia

    Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia -н Nikhita Bolar, Christelle Golzio, Martina Živná, Gaëlle Hayot, Christine Van Hemelrijk, Dorien Schepers, Geert Vandeweyer, Alexander Hoischen, Jeroen R. Huyghe, Ann Raes, E Matthys, Emiel Sys, M Azou, Marie‐Claire Gubler, Marleen Praet, Guy Van Camp, Kelsey McFadden, Igor Pediaditakis, Anna Přistoupilová, Kateřina Hodaňová, Petr Vyleťal, Hana Hartmannová, Viktor Stránecký, Helena Hůlková, Veronika Barešová, Ivana Jedličková, Jana Sovová, Aleš Hnı́zda, Kendrah Kidd, Anthony J. Bleyer, Richard Spong, Johan Vande Walle, Geert Mortier, Han G. Brunner, Lut Van Laer, Stanislav Kmoch, Nicholas Katsanis, Bart Loeys

    Хэвлэсэн 2016
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    Artigo
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