首页/数据集/Effective Lentiviral Gene Therapy for X-linked Chronic Granulomatous Disease

Effective Lentiviral Gene Therapy for X-linked Chronic Granulomatous Disease

NIAID Data Ecosystem2026-03-11 收录

慢病毒载体

X连锁慢性肉芽肿病

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA527850 数据链接链接失效反馈

官方服务：

资源简介：

Effective Lentiviral Gene Therapy for X-linked Chronic Granulomatous Disease

应用场景：

创建时间：

2019-03-18

造血干细胞表观遗传学

慢病毒载体

Human cord blood CD34+ cells respond to the infection with LV by modifying the methylation profile of a large number of CpG sites in their genome. Different vector preparations vary in their capacity

NIAID Data Ecosystem40

North America Lentiviral Vectors Market

慢病毒载体

市场分析

The North America Lentiviral Vectors report provides a detailed analysis of emerging investment pockets, highlighting current and future market trends. It offers strategic insights into capital flows

IMR REPORTS40

Lentiviral vector choice for CRISPR delivery affects the false-positive rate of genome-wide CRISPR screens

CRISPRi基因编辑

慢病毒载体

Lentivirus construct comparison for CRISPR screen

NIAID Data Ecosystem10

Ã-Globin Lentiviral Vectors Have Reduced Titers Due to Incomplete Vector RNA Genomes and Lowered Virion Production

慢病毒载体

细胞基因治疗

Lentiviral vectors (LV) commonly used for the treatment of hemoglobinopathies often have low titers and sub-optimal gene transfer efficiency for human hematopoietic stem and progenitor cells (HSPC), h

NIAID Data Ecosystem40

IRES sequences used for lentivirus library for Fig 3A and 3B.

基因表达调控

慢病毒载体

IRES sequences used for lentivirus library for Fig 3A and 3B.

NIAID Data Ecosystem20