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Titlebook: Alpha-1 Antitrypsin; Methods and Protocol Cynthia L. Bristow Book 2024 The Editor(s) (if applicable) and The Author(s), under exclusive lic

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发表于 2025-3-21 16:25:37 | 显示全部楼层 |阅读模式
期刊全称Alpha-1 Antitrypsin
期刊简称Methods and Protocol
影响因子2023Cynthia L. Bristow
视频videohttp://file.papertrans.cn/154/153904/153904.mp4
发行地址Includes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the experts
学科分类Methods in Molecular Biology
图书封面Titlebook: Alpha-1 Antitrypsin; Methods and Protocol Cynthia L. Bristow Book 2024 The Editor(s) (if applicable) and The Author(s), under exclusive lic
影响因子.This volume provides a collection of protocols that will allow researchers to further explore the multiple, fascinating activities of  Alpha-1 Antitrypsin (AAT) isoforms in innate immunity, and gene therapy. Written in the highly successful .Methods in Molecular Biology .series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls... ..Authoritative and cutting-edge, .Alpha-1 Antitrypsin: Methods and Protocols .aims to ensure successful results in the further study of this vital field..
Pindex Book 2024
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书目名称Alpha-1 Antitrypsin影响因子(影响力)




书目名称Alpha-1 Antitrypsin影响因子(影响力)学科排名




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书目名称Alpha-1 Antitrypsin网络公开度学科排名




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书目名称Alpha-1 Antitrypsin被引频次学科排名




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书目名称Alpha-1 Antitrypsin年度引用学科排名




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书目名称Alpha-1 Antitrypsin读者反馈学科排名




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Approaches to Therapeutic Gene Editing in Alpha-1 Antitrypsin Deficiencyion of double-strand breaks (DSBs) and subsequent creation of insertions and deletions (indels) by DSB repair, homology-directed repair (HDR) targeted to the mutation site, base editing, prime editing, and alternatively targeted knock-in techniques. Each approach will be discussed and a brief summar
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Manipulation of Proteostasis Networks in Transgenic ZAAT Zebrafish via CRISPR–Cas9 Gene Editingfish α1-antitrypsin deficiency (AATD) model displays an unusual phenotype, in that it lacks the hepatic accumulation of the misfolding Z α1-antitrypsin (ZAAT) evident in human and mouse models. Here we describe the application of the CRISPR–Cas9 system to generate mutant zebrafish with defects in ke
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Alpha-1-Antitrypsin (A1AT) Proteotyping by LC-MS/MSrmination of specific allelic variants by phenotyping (isoelectric focusing (IEF) gel electrophoresis) and/or allele-specific genotyping. Various phenotyping and genotyping methodologies are available, and each has their own advantages and disadvantages. As an alternative, mass spectrometry is emerg
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