Furthermore,
gene disruption by gene editing techniques such as CRISPR - CAS resulted in the absence of growth of parasites carrying the mutated gene, indicating that the protein is required for parasite viability.
Not exact matches
By using engineered zinc - finger nucleases (ZFNs) designed to target an integrated reporter and two endogenous rat
genes, Immunoglobulin M (IgM) and Rab38, we demonstrate that a single injection of DNA or messenger RNA encoding ZFNs into the one - cell rat embryo leads to a high frequency of animals carrying 25 to 100 %
disruption at the target locus.
Through temporary
disruption of these interactions, the scientists were able to produce Drosophila epilines characterized
by different levels of PcG - dependent
gene repression or activation.
In the R5 - ZFN control group, with intact cxcr4
genes, 88 % of CD4 + T cells expressed CXCR4 protein at day 27 post engraftment, compared to 84 % of cells in the X4 - ZFN mice (∼ 24 % cxcr4
gene disruption) as determined
by a fluorescence minus - one (FMO) control.
Immune function and pathology dissected
by high - throughput analysis of mice with targeted
gene disruptions — an investigation
by the Infection and Immunity Immunophenotyping (3i) consortium.
To delineate the role of Emk in development and adult tissues, mice lacking Emk were generated
by targeted
gene disruption.
Genetic Alterations:
Disruption caused
by insertion of the retroviral
gene trap vector ROSAFARY.
As part of its efforts to develop and apply tools for large - scale functional analysis, the BDGP has undertaken a novel
gene disruption project based on mutagenesis
by transposable element insertion (Spradling et al., 1995).
In MMEJ pathway, we achieve efficient
gene disruption in human cell lines and animals
by developing a computer program that assists the choice of nuclease target sites based on microhomology prediction.
The frequent proximity of the insertions to the 5» portion of the transcription unit means that the
gene disruption in many lines could be molecularly identified
by comparing the DNA sequence flanking the insertion to genomic sequence data.
Following up on findings from genome - wide association studies, researchers identify two mechanisms
by which
disruptions in the
gene SLC16A11 may play a role in type 2 diabetes
We are currently testing the hypothesis that these transcription factors form a genomic regulatory network, and
disruption of that network
by mutation destabilizes
gene expression programs, contributing to malignancy.
Potential projects include identifying common pathways that modify retinal degenerative disease from a large collection of actively maintained mouse models; determining molecular networks implicated in pathological
disruption of the retinal pigment epithelium; identifying molecular pathways that regulate postnatal ocular growth; and using mouse models to assess the pathogenic role of
gene variants that increase the risk of age - related macular degeneration as identified
by human genome - wide association studies.
We have been searching for a mechanism that can explain the genetic cause of majority of BWS and that can provide better understanding of intragenic mutation of p57KIP2 and
disruption of KvLQT1
gene by balanced germline chromosomal rearrangements.
Gene disruption in cells and model organisms followed by phenotypic analysis has been a traditional approach to understand gene funct
Gene disruption in cells and model organisms followed
by phenotypic analysis has been a traditional approach to understand
gene funct
gene function.