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Titlebook: Genome Editing in Biomedical Sciences; Geraldo A. Passos Book 2023 The Editor(s) (if applicable) and The Author(s), under exclusive licens

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發(fā)表于 2025-3-21 16:53:09 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Genome Editing in Biomedical Sciences
編輯Geraldo A. Passos
視頻videohttp://file.papertrans.cn/383/382837/382837.mp4
概述Written by global experts in the evolving field of CRISPR genome editing.Provides timely overview of recent developments in the field, new technologies, and methodologies.Discusses ethical issues and
叢書名稱Advances in Experimental Medicine and Biology
圖書封面Titlebook: Genome Editing in Biomedical Sciences;  Geraldo A. Passos Book 2023 The Editor(s) (if applicable) and The Author(s), under exclusive licens
描述.This volume focuses on applying the Crispr system in editing the genome of human cells (.in vitro.?and?.in vivo.) and model organisms used in biomedical research. With the advent of Crispr technology, genome editing soon became a procedure of great interest to laboratories worldwide due to its relative ease and accuracy. In biomedical sciences, genome editing by Crispr has already enabled the development of new experimental model systems. In medicine, therapeutic alternatives for the genetic "correction" of diseases have already begun to appear. Therefore, the book‘s purpose is to bring in a single volume, chapters that show the scientific community in biomedicine, medicine, human genetics, oncology, virology, and parasitology, among others, the advances in genomic editing. In a chapter dedicated to the ethical aspects of human genomic editing, we also address what we can and should do with this (bio)technology. The book chapters were written by productive researchers specializing in Crispr genome editing. The chapters cover the concept of Crispr and genome editing and how to use this new methodology in biomedical research and medicine, among other aspects, including the ethical c
出版日期Book 2023
關(guān)鍵詞Crispr; Crispr-Cas9; gene therapy; human genome; gene regulation; biomedical research; biotechnology; oncol
版次1
doihttps://doi.org/10.1007/978-3-031-33325-5
isbn_ebook978-3-031-33325-5Series ISSN 0065-2598 Series E-ISSN 2214-8019
issn_series 0065-2598
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerl
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 21:11:38 | 只看該作者
https://doi.org/10.1007/978-3-531-90712-3We conclude that gene editing has been able to change quickly the scenario of these disorders, allowing the development of new therapies and improving the knowledge on disease pathogenesis. Should they confirm their hype, the first gene editing-based products for lysosomal disorders could be available in the next years.
板凳
發(fā)表于 2025-3-22 03:26:20 | 只看該作者
Genome Editing Tools for Lysosomal Storage Disorders,We conclude that gene editing has been able to change quickly the scenario of these disorders, allowing the development of new therapies and improving the knowledge on disease pathogenesis. Should they confirm their hype, the first gene editing-based products for lysosomal disorders could be available in the next years.
地板
發(fā)表于 2025-3-22 07:00:48 | 只看該作者
5#
發(fā)表于 2025-3-22 08:52:01 | 只看該作者
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發(fā)表于 2025-3-22 13:24:55 | 只看該作者
,Friendship in the Fathers’ Later Lives,icroRNAs and long noncoding RNAs. In this context, CRISPR/Cas9 emerges as a potential tool to modify gene sequence and modulate gene expression in thyroid cancer cell lines. In this chapter, we explore some of the current studies in which researchers have applied CRISPR/Cas9 in vitro to investigate thyroid cancer biology (Fig. .).
7#
發(fā)表于 2025-3-22 18:48:37 | 只看該作者
The CRISPR/Cas System in Human Cancer,llular and animal model generation, and new derivative tools applied to cancer research. CRISPR has opened new frontiers increasing the knowledge about cancer, pointing to new solutions to overcome several challenges to better understand the disease and design better treatments.
8#
發(fā)表于 2025-3-23 01:13:46 | 只看該作者
Using CRISPR/Cas9 to Edit a Thyroid Cancer Cell Line,icroRNAs and long noncoding RNAs. In this context, CRISPR/Cas9 emerges as a potential tool to modify gene sequence and modulate gene expression in thyroid cancer cell lines. In this chapter, we explore some of the current studies in which researchers have applied CRISPR/Cas9 in vitro to investigate thyroid cancer biology (Fig. .).
9#
發(fā)表于 2025-3-23 03:58:36 | 只看該作者
Joanne M. McKeown,Catherine G. FineNA targeting in tumorigenesis and drug resistance. Additionally, we highlighted the perspectives and potential applications of CRISPR approaches to treat cancer, as an emerging and promising target therapy.
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發(fā)表于 2025-3-23 06:06:38 | 只看該作者
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