Evolving a novel AAV variant for efficient gene delivery to murine T lymphocytes

NIAID Data Ecosystem2026-03-14 收录

基因治疗载体

免疫细胞工程

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https://www.ncbi.nlm.nih.gov/sra/SRP404214 数据链接链接失效反馈

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Evolved an AAV6 capsid library on Murine T-cells. Overall design: High throughput sequencing of evolved AAV6 capsid libraries

创建时间：

2022-12-31

The genome-containing AAV11 capsid

病毒衣壳结构

基因治疗载体

The genome-containing AAV11 capsid Descriptor: 2'-DEOXYADENOSINE-5'-MONOPHOSPHATE, Capsid protein Authors: Mietzsch, M, Agbandje-McKenna, M. Deposit date: 2020-12-23 Release date: 2021-02-03 Last modi

Protein Data Bank Japan2025-06-04 更新30

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基因治疗载体

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Technological advancements in the North America Custom Adeno-associated Viral Vector Production Service industry are shaping the future market landscape. The report evaluates innovation-driven growth

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Novel Tat-Encoding Bicistronic Human Immunodeficiency Virus Type 1-Based Gene Transfer Vectors for High-Level Transgene Expression

基因治疗载体

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We describe bicistronic single-exon Tat (72-amino-acid Tat [Tat72])- and full-length Tat (Tat86)-encoding gene transfer vectors based on human immunodeficiency virus type 1 (HIV-1). We created version

PubMed Central00

Spatial Transcriptomics and Single Nucleus RNA Sequencing Reveal rAAV2- and rAAV9-Specific Transduction Signatures in the Mouse Liver: snRNA-seq FASTQ Male rAAV2-Treated Animal 203

基因治疗载体

单核RNA测序

You can find here the FASTQ files related to the datasets used in the publication: Amberg, B. et al. Spatial Transcriptomics and Single Nucleus RNA Sequencing Reveal rAAV2- and rAAV9-Specific Trans

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Identifying gene combinations for targeting innate immune cells to enhance T cells activation [DNA]. Identifying gene combinations for targeting innate immune cells to enhance T cells activation [DNA]

免疫细胞工程

CRISPRi筛选

Genetic engineering of hematopoietic cells ex-vivo opens new opportunities for programming immune cells and improving their functionality in response to illness and infections. Molecular methods for g

NIAID Data Ecosystem10

Evolving a novel AAV variant for efficient gene delivery to murine T lymphocytes

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