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Titlebook: Cell Fusion; Overviews and Method Kurt Pfannkuche Book 2015Latest edition Springer Science+Business Media New York 2015 cell fuse.cell orga

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楼主: 鸣叫大步走
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Chromosome Tracking in Fused Cells by Single Nucleotide Polymorphisms,g, inbred mouse strains can easily be distinguished by their typical SNPs. Therefore, if cell fusion partners are selected to originate from two different genotypes the detection of strain specific SNPs in the genome of fused cells can be utilized as a complimentary method to traditional karyotyping
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FISH Detection of X and Y Chromosomes in Combination with Immunofluorescence to Study Contribution rious tissues including skeletal muscle tissue. Studies in mice have demonstrated that regular physical activity is sufficient to induce contribution of BM derived cells to the skeletal muscle tissue, suggesting that this is part of the physiological remodeling of skeletal muscle. To analyze whether
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Using Phosphatidylserine Exposure on Apoptotic Cells to Stimulate Myoblast Fusion,tion of the phospholipid phosphatidylserine (PtdSer) exposed on certain myoblasts is required during fusion into multinuclear myofibers. Cell surface exposure of PtdSer is also a feature of cells dying through the process of apoptosis. Here, we describe the use of PtdSer exposing apoptotic cells as
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Analyzing Cell Fusion Events Within the Central Nervous System Using Bone Marrow Chimerism, to a range of neuronal cell types within the central nervous system. One such mechanism to account for this phenomenon is cellular fusion, occurring between migrating bone marrow-derived stem cells and neuronal cells in-situ. Biologically, the significance as to why cells from distinct lineages fus
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Cell Fusion Between Dendritic Cells and Whole Tumor Cells,approach allows DCs to be exposed to the entire repertoire of tumor-associated antigens (TAAs) originally expressed by the tumor cell, to process them endogenously, and to present antigenic epitopes thought the MHC class I and class II pathways to activate both CD8+ and CD4+ T cells, respectively. T
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Membrane Nanotube Formation in Osteoclastogenesis,ween cells present in a long distance. During osteoclastogenesis, mononuclear osteoclast precursors form abundant TNTs in prior to cell–cell fusion. Here we introduce a protocol for detecting TNTs during osteoclastogenesis by use of live cell imaging utilizing a confocal laser microscopy. We also de
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