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Titlebook: Design and Delivery of SiRNA Therapeutics; Henrik J. Ditzel,Martina Tuttolomondo,Sakari Kaupp Book 2021 Springer Science+Business Media, L

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51#
發(fā)表于 2025-3-30 11:57:23 | 只看該作者
52#
發(fā)表于 2025-3-30 14:48:33 | 只看該作者
,Gew?hnliche Differentialgleichungen,ived nanoparticles (NPs) are one of the best investigated systems for in vivo siRNA delivery. In the recent years, we have successfully redesigned the conventional cationic liposomes into Liposome/Protamine/hyaluronic acid (LPH) NPs and Lipid-Calcium-Phosphate (LCP) NPs in order to increase the in v
53#
發(fā)表于 2025-3-30 17:48:19 | 只看該作者
Abbildungen, reelle Funktionen,livery vector is imperative for clinical use. Since siRNA works in the cytoplasm, the ability of the carrier to escape destruction in the endosomes is a highly required characteristic for the induction of a high knockdown effect. Here, we describe the step-by-step procedure for the evaluation of hig
54#
發(fā)表于 2025-3-30 22:04:03 | 只看該作者
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發(fā)表于 2025-3-31 01:23:07 | 只看該作者
56#
發(fā)表于 2025-3-31 07:06:07 | 只看該作者
Wilfried Pla?mann,Detlef Schulzcovalent cationic dendrimers (CCDs) and self-assembled cationic dendrons (ACDs) for siRNA delivery in the presence and absence of their nucleic cargos. On the basis of the reported examples, a standard essential set of techniques is described for each step of a siRNA/nanovector (NV) complex characte
57#
發(fā)表于 2025-3-31 10:13:19 | 只看該作者
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發(fā)表于 2025-3-31 13:33:10 | 只看該作者
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發(fā)表于 2025-3-31 19:24:39 | 只看該作者
60#
發(fā)表于 2025-4-1 01:17:24 | 只看該作者
https://doi.org/10.1007/978-3-322-89910-1g RNAs (siRNA) are double-stranded RNA molecules capable of silencing the expression of a specific protein triggering the RNA interference (RNAi) pathway, but they are unable to cross the plasma membrane and have a short half-life in the bloodstream. In this overview, we assessed the many different
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