يعرض 1 - 10 نتائج من 122 نتيجة بحث عن '"Schmierer, Bernhard"', وقت الاستعلام: 1.41s تنقيح النتائج
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    دورية أكاديمية
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    دورية أكاديمية
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    دورية أكاديمية

    المساهمون: Institute of Biotechnology, Molecular Systems Biology, Research Programs Unit, STEMM - Stem Cells and Metabolism Research Program, Biosciences, Department of Pathology, Genome-Scale Biology (GSB) Research Program, Jussi Taipale / Principal Investigator

    وصف الملف: application/pdf

    العلاقة: Barncancerfonden Kornel Labun Emma Haapaniemi; Reint , G , Li , Z , Labun , K , Keskitalo , S , Soppa , I , Mamia , K , Tolo , E , Szymanska , M , Meza-Zepeda , L A , Lorenz , S , Cieslar-Pobuda , A , Hu , X , Bordin , D L , Staerk , J , Valen , E , Schmierer , B , Varjosalo , M , Taipale , J & Haapaniemi , E 2021 , ' Rapid genome editing by CRISPR-Cas9-POLD3 fusion ' , eLife , vol. 10 , 75415 . https://doi.org/10.7554/eLife.75415Test; ORCID: /0000-0002-1340-9732/work/108068909; ORCID: /0000-0001-5555-1975/work/108070990; f224ad0f-0c0e-42d9-baa4-dc8e4ce52d3a; http://hdl.handle.net/10138/339811Test; 000744007300001

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    دورية أكاديمية
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    كتاب

    المساهمون: Department of Pathology, Genome-Scale Biology (GSB) Research Program, Jussi Taipale / Principal Investigator, Research Programs Unit

    وصف الملف: application/pdf

    العلاقة: Haapaniemi , E , Botla , S , Persson , J , Schmierer , B & Taipale , J 2019 , ' Reply to "CRISPR screens are feasible in TP53 wild-type cells" ' , Molecular Systems Biology , vol. 15 , no. 8 , 9059 . https://doi.org/10.15252/msb.20199059Test; fc273e64-5518-41af-9fff-e31f59970974; http://hdl.handle.net/10138/305864Test; 000484419200007

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    دورية أكاديمية

    المساهمون: School of Physical and Mathematical Sciences

    مصطلحات موضوعية: Science::Chemistry, Genome-wide, Antisense Oligonucleotides

    وصف الملف: application/pdf

    العلاقة: Computational and Structural Biotechnology Journal; Iyer, V. S., Jiang, L., Shen, Y., Boddul, S. V., Panda, S. K., Kasza, Z., Schmierer, B. & Wermeling, F. (2020). Designing custom CRISPR libraries for hypothesis-driven drug target discovery. Computational and Structural Biotechnology Journal, 18, 2237-2246. https://dx.doi.org/10.1016/j.csbj.2020.08.009Test; orcid:0000-0002-8720-8992; orcid:0000-0002-9082-7022; orcid:0000-0001-9633-677X; https://hdl.handle.net/10356/149062Test; 2-s2.0-85090006870; 18; 2237; 2246

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    دورية أكاديمية

    المساهمون: Genome-Scale Biology (GSB) Research Program, University of Helsinki, Doctoral Programme in Integrative Life Science, Jussi Taipale / Principal Investigator, Medicum

    مصطلحات موضوعية: CELLS, INHIBITION, EFFICIENCY, REPAIR, GENES, 3111 Biomedicine

    وصف الملف: application/pdf

    العلاقة: Part of this work was carried out at the High Throughput Genome Engineering Facility and the Swedish National Genomics Infrastructure funded by Science for Life Laboratory (Scilifelab). The Knut and Alice Wallenberg Foundation, Cancerfonden, Barncancerfonden and the Academy of Finland supported this work. We thank H. Han and Y. Bryceson for providing equipment, the Protein Science Facility at Karolinska Institutet, as well as I. Sur and T. Kivioja for their comments on the manuscript.; Haapaniemi , E , Botla , S , Persson , J , Schmierer , B & Taipale , J 2018 , ' CRISPR-Cas9 genome editing induces a p53-mediated DNA damage response ' , Nature Medicine , vol. 24 , no. 7 , pp. 927-+ . https://doi.org/10.1038/s41591-018-0049-zTest; 85048349385; 8f67cc84-e64b-4e1c-84f3-f8fca5cc0ae0; http://hdl.handle.net/10138/303675Test; 000438187700019

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    دورية أكاديمية