Titlebook: Glycoimmunology in Xenotransplantation; Cheorl-Ho Kim Book 2024 The Editor(s) (if applicable) and The Author(s), under exclusive license t

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Xenogeneic and Allogenic Cellular Rejection (CR),rates and proteins present in the pig vasculatures [1, 2]. During the last three decades, for the long-term solid organ survivals in xenotransplantation, vascular endothelial cells have been studied as a target for xenograft recipient immune system and grafted microvasculature has been received a gr

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Induction of Xenograft Tolerance and Chimerism as an Alternative Prevention of Xenograft Rejection,f human recipients is specifically not responsive to the xenografted organs of pigs [1–3], but the human immune system is normally with the responding ability to infectious pathogens. There are huge progresses in strategies to induce tolerance across xenoantigenic hurdles and rejection barriers. Als

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Genome Editing and Transgenes in Pigs,using damages in early embryo developments. The recent development of genome editing techniques is being evolved to the easier ZFN, TALEN, and CRISPR/Cas9 technologies than the conventional laborious one in various animals, giving generation of gene knock-out pigs. The pig genome is about 2.7 Gb siz

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,Allgemeines über Dampfkesselanlagen, mainly the organs rather than tissues and cells. As mentioned earlier, genetically edited and modified pig organs with multiple genes are attracted to solve the issues of donor organ supply and shortage. However, hurdles still include natural antibodies reactive to xenoantigens in human, and theref

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Lehrbuch der Bergwerksmaschinensmic reticulum (ER) and Golgi apparatus, the .-glycans not only stabilize the protein synthesis process in ER and Golgi apparatus but also relates to cell-to-cell communication in cell membranes. Furthermore, glycans are also important to immune responses due to their interaction with lectins. All a

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