Mycobacterium tuberculosis. Mycobacterium tuberculosis strain:H37Rv_delta_PonA1
收藏NIAID Data Ecosystem2026-03-08 收录
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资源简介：
Himar1 transposon library of knockout of PonA1 in M. tuberculosis H37Rv
应用场景：
创建时间：
2015-07-14
相关数据集
Supplementary Spreadsheet 2.xlsx
Camus Nimmo PhD Thesis 2020: Mycobacterium tuberculosis within-host genetic diversity and acquired drug resistance Supplementary spreadsheet 2: Accession details for samples included in analysis of
DataCite Commons2020-08-25 更新90
Whole ileal tissue from day 6 Dextran Sodium Sulfate (DSS) administered Il17rafl/fl;Atoh1-cre+/- mice. Whole ileal tissue from day 6 Dextran Sodium Sulfate (DSS) administered Il17rafl/fl;Atoh1-cre+/- mice
Total RNA sequencing (RNA-seq) of the terminal ileum of day 6 Dextran Sodium Sulfate (DSS) administered Il17rafl/fl;Atoh1-cre+ mice and littermate cre- mice was performed. Overall design: N = 3 Il17ra
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Impact of mutations in rv2887, putative transcriptional repressor, on gene expression in Mycobacterium tuberculosis.
Impact of mutations in rv2887, putative transcriptional repressor, on gene expression in Mycobacterium tuberculosis.
ChEBI2016-07-01 更新10
ATAC-seq analyses with knockout eHAP cells for effector genes. ATAC-seq analyses with knockout eHAP cells for effector genes
A genome-wide screening identified effector genes of chromatin accessibility. To investigate the functional consequences of the loss of each effector gene, we conducted ATAC-seq analysis with eHAP cel
NIAID Data Ecosystem70
Sequencing data of rv0191 insert in the pJET-0191 construct produced during the generation of the complementation of the ∆ rv 0191 M.tb mutant
The rv0191 gene that was cloned into the subcloning vector pJET for the purpose of generating the complementation construct.Many primers were used to sequence the insert, and the last two files are th
Figshare2024-02-16 更新10
