Results 1 to 10 of about 17,978 (69)

Group II intron-anchored gene deletion in Clostridium. [PDF]

open access: yesPLoS ONE, 2011
Clostridium plays an important role in commercial and medical use, for which targeted gene deletion is difficult. We proposed an intron-anchored gene deletion approach for Clostridium, which combines the advantage of the group II intron "ClosTron" system
Kaizhi Jia   +3 more
doaj   +3 more sources

Detecting Photoactivatable Cre-mediated Gene Deletion Efficiency in Escherichia coli

open access: yesBio-Protocol, 2023
Gene deletion is one of the standard approaches in genetics to investigate the roles and functions of target genes. However, the influence of gene deletion on cellular phenotypes is usually analyzed sometime after the gene deletion was introduced.
Yuta Koganezawa   +3 more
doaj   +1 more source

Evaluation of Aeromonas hydrophila outer membrane protein deletion strains in response to environmental stresses

open access: yes浙江大学学报. 农业与生命科学版, 2022
In order to evaluate systematically the biological functions of outer membrane proteins (OMPs) under environmental stresses, we selected Aeromonas hydrophila ATCC 7966 as the research object, and constructed 33 OMP deletion strains to determine their ...
LI Zeqi   +4 more
doaj   +1 more source

Prognostic significance of copy number variation in B-cell acute lymphoblastic leukemia

open access: yesFrontiers in Oncology, 2022
Copy number variations (CNVs) are widespread in both pediatric and adult cases of B-cell acute lymphoblastic leukemia (B-ALL); however, their clinical significance remains unclear.
Yang Song, Qiuyun Fang, Yingchang Mi
doaj   +1 more source

Towards the Understanding of the Function of Lanthipeptide and TOMM-Related Genes in Haloferax mediterranei

open access: yesBiology, 2023
Research on secondary metabolites produced by Archaea such as ribosomally synthesized and post-translationally modified peptides (RiPPs) is limited. The genome of Haloferax mediterranei ATCC 33500 encodes lanthipeptide synthetases (medM1, medM2, and ...
Thales Costa   +4 more
doaj   +1 more source

Deletion of the Neuronal Transcription Factor Satb1 Induced Disturbance of the Kinome and Mechanisms of Hypoxic Preconditioning

open access: yesBiology, 2023
Genetic disorders affecting the functioning of the brain lead not only to the development of numerous hereditary diseases but also to the development of neurodegenerative and cognitive disorders.
Egor A. Turovsky   +2 more
doaj   +1 more source

Comprehensive evaluation of the safety and immunogenicity of a gene-deleted variant pseudorabies virus attenuated vaccine

open access: yesVeterinary Research, 2022
Pseudorabies virus (PRV) variant infections have caused a substantial economic impact on swine production in the absence of new powerful candidate vaccines.
Ling Li   +12 more
doaj   +1 more source

Establishment of High-Efficiency Screening System for Gene Deletion in Fusarium venenatum TB01

open access: yesJournal of Fungi, 2022
Genetic engineering is one of the most effective methods to obtain fungus strains with desirable traits. However, in some filamentous fungi, targeted gene deletion transformant screening on primary transformation plates is time-consuming and laborious ...
Sheng Tong   +6 more
doaj   +1 more source

Clinical Characteristics of Chronic Myeloid Leukemia Patients with Deletion and Non-deletion of ASS Gene on Derivative Chromosome 9

open access: yesZhongliu Fangzhi Yanjiu, 2023
Objective To investigate the clinical characteristics of patients with chronic myeloid leukemia (CML) in chronic phase with deletion and non-deletion of the argininosuccinate synthesis gene (ASS gene) on the derivative chromosome 9.
GAO Guanlun   +5 more
doaj   +1 more source

Gene Deletions and Prognostic Values in B-Linage Acute Lymphoblastic Leukemia

open access: yesFrontiers in Oncology, 2021
Although pediatric-like treatment regimen has remarkably improved the survival rates of adults with acute lymphoblastic leukemia (ALL), the outcome of some adult patients is still poor owing to adverse genetic features.
Qiuyun Fang   +20 more
doaj   +1 more source

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