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Titlebook: DNA Repair; Methods and Protocol Lata Balakrishnan,Jason A. Stewart Book 2019 Springer Science+Business Media, LLC, part of Springer Nature

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https://doi.org/10.1007/978-1-349-00952-7 binding and hydrolysis, helicases behave as molecular motors capable of efficiently disrupting the many noncovalent hydrogen bonds that stabilize DNA molecules with secondary structure. In addition to their importance in DNA damage sensing and signaling, DNA helicases facilitate specific steps in D
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Creativity and Parkinson’s Disease was established by measuring the resistance capacity of .deficient mouse embryonic fibroblasts (MEFs) transfected with mammalian expression constructs. Here, we describe the methods used to assess colony survival following the treatment of transfected cells with genotoxic compounds. This approach p
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https://doi.org/10.1007/978-3-031-14724-1getable proteins beyond kinases and traditional enzymes. Many of the proteins involved in the DDR and repair impart their activity by making specific contacts with DNA. These protein–nucleic acid interactions represent a tractable target for perturbation with small molecules. We describe a high thro
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Lata Balakrishnan,Jason A. StewartIncludes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the experts
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Methods in Molecular Biologyhttp://image.papertrans.cn/d/image/260176.jpg
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Attention Deficit Hyperactivity Disorder,hat ALT telomeres are subjected to chronic replication stress. Here, we will review the features of telomeric DNA that challenge the replication machinery and also how the cell overcomes these challenges to maintain telomere stability and ensure the faithful duplication of the human genome.
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Scintillation and Apparent Motion, Together, we aim to provide robust visualization methods employing laser-microirradiation to detect and determine protein behavior, functions and dynamics in response to DNA damage in mammalian cells.
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Shared Reflections and Dialoguesve information about dNTP pools in different genetic and environmental contexts in vivo. Here we describe a high-throughput fluorescence-based assay that uses a qPCR-based approach to quantify dNTP levels for use with . extracts.
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