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Titlebook: Sovereign Immunity Under Pressure; Norms, Values and In Régis Bismuth,Vera Rusinova,Geir Ulfstein Book 2022 The Editor(s) (if applicable) a

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31#
發(fā)表于 2025-3-27 00:25:04 | 只看該作者
32#
發(fā)表于 2025-3-27 02:57:51 | 只看該作者
33#
發(fā)表于 2025-3-27 05:49:35 | 只看該作者
Chimène I. Keitnerused scripting languages, and is written to be accessible to those new to electronics. After completing this book, and its fun example projects, you’ll be ready to ready to use MicroPython to develop your own IoT applications...?..What You Will Learn..Program in MicroPython.Understand sensors and ba
34#
發(fā)表于 2025-3-27 10:02:17 | 只看該作者
Stefan Oetere miRNAs target well-known melanoma-associated genes like the . oncogene, microphthalmia-associated transcription factor (.), receptor tyrosine kinase c-KIT or AP-2 transcription factors (.). Although we are still far from a complete understanding of the role of miRNA-target gene interactions in mal
35#
發(fā)表于 2025-3-27 17:04:15 | 只看該作者
Vladislav Starzhenetskiyally convened to consider the likelihood of miRNAs cooperativity in view of the targets, tissues and cell lines. We show that results from miRror2.0 can be further refined by an iterative procedure, calls Psi-miRror that gauges the robustness of the regulation. We illustrate the combinatorial regula
36#
發(fā)表于 2025-3-27 18:00:00 | 只看該作者
Apollin Koagne Zouapetcs into his work. Bioinformaticians and modellers are provided with a general perspective on microRNA biology in cancer, and the state-of-the-art in computational microRNA biology.978-94-024-0079-3978-94-007-5590-1Series ISSN 0065-2598 Series E-ISSN 2214-8019
37#
發(fā)表于 2025-3-27 22:39:55 | 只看該作者
Facundo Pérez-Aznarimaging detection techniques leads to multifunctional nanoprobe with specific-transfection, tracing, and regulation function in intracellular miRNA detection. ISH holds great promise for visualization of the spatial localization of RNA at the tissue, cellular, and even subcellular level.
38#
發(fā)表于 2025-3-28 02:20:15 | 只看該作者
Peng Wangeded to complete the entire experiment is shortened and the usage of lab consumables as well as RNA input per sample are low. Here, the methods of high-throughput RT-qPCR for the analysis of circulating microRNAs are described. Two distinctive qPCR chemistries (probe-based and intercalating dye-base
39#
發(fā)表于 2025-3-28 07:23:21 | 只看該作者
Giulia Bernabeisists of a fluorophore-labeled detecting strand and a quenching strand. The fluorophore-labeled LNA probe is designed to hybridize with the target microRNA (miRNA) specifically and displace from the quenching strand, allowing the fluorophore to fluorescence. Large-scale single-cell dynamic gene expr
40#
發(fā)表于 2025-3-28 10:44:56 | 只看該作者
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