Titlebook: Epidermal Cells; Methods and Protocol Kursad Turksen Book 2020Latest edition Springer Science+Business Media, LLC, part of Springer Nature

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https://doi.org/10.1007/978-1-0716-0251-5Keratinocytes; Regenerative medicine; Skin cells; Dermal cells; Cell culture

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https://doi.org/10.1007/978-3-642-50203-3eratinocytes. Here, we describe a method to quantify melanosome transfer using immunofluorescence microscopy coupled with automated image analysis of in vitro human melanocytes and keratinocytes in co-culture. In this method, the number of melanin capped keratinocyte nuclei is quantified.

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Information and Statistical Analysis Pipeline for High-Throughput RNA Sequencing Data,eline is indispensable to process raw RNA sequencing (RNA-seq) data generated by next-generation sequencers in order to extract biological implications. In this chapter, we introduce a common pipeline for RNA-seq data. A collection of notes on related advanced topics will be useful when conducting information and statistical analysis in practice.

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Allgemeine Topologie mit Anwendungen keratinocytes remains challenging. In this chapter, we introduce the simplest, at least to our knowledge, protocol that enables long-term expansion of p63. mouse epidermal keratinocytes in low Ca. media without the need of progenitor cell-purification steps or support by a feeder cell layer. Pharma

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https://doi.org/10.1007/978-3-662-39627-8tion) is an important basic investigation technique for pharmacology, toxicology, and biology. There are different systems of epidermal separation, including typical methods of chemical, enzyme, heat, etc. Each approach has advantages versus disadvantages, and thus the appropriate method should be c

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