By manipulating
a specific gene in a mouse blastocyst — the structure that develops from a fertilized egg but is not yet an actual embryo — scientists with the University of Florida's McKnight Brain Institute and the Harvard Stem Cell Institute caused cells destined to build an embryo to instead change direction and build the cell mass that leads to the placenta.
Not exact matches
Gene therapy delivered to a
specific part of the brain reverses symptoms of depression
in a
mouse model of the disease — potentially laying the groundwork for a new approach to treating severe cases of human depression
in which drugs are ineffective.
So far,
gene therapy attempts have only resulted
in partial improvements of hearing
in mouse models of
specific human deafness forms that did not include severe anomalies
in hair cell structure.
The team manipulated the genome of
mice such that they could initiate neuron death
in the hippocampus by turning on
specific genes.
Scientists had been searching
in vain for such a
gene since 1994 when Rockefeller University scientist Jeffery Friedman found that lab
mice with a
specific genetic mutation fail to produce leptin and as a result have uncontrollable appetites, and become huge.
Using a
mouse model, the team also demonstrated that two processes during neurodevelopment are regulated by the
gene: proliferation — the replication of neuronal stem cells that have the potential to become multiple different kinds of cells, including neurons — and migration — the movement of neurons to
specific locations
in the brain during development.
In their study, the researchers showed that already at the age of six weeks in the mice with a rapid weight gain, the DPP4 gene was less methylated at four specific loci, i.e. epigenetically altered, compared to the other mic
In their study, the researchers showed that already at the age of six weeks
in the mice with a rapid weight gain, the DPP4 gene was less methylated at four specific loci, i.e. epigenetically altered, compared to the other mic
in the
mice with a rapid weight gain, the DPP4
gene was less methylated at four
specific loci, i.e. epigenetically altered, compared to the other
mice.
«Understanding how
gene editing works
in human embryos will require research
in human embryos,» because
mouse embryos, for example, have species -
specific developmental differences, notes Dana Carroll, a biochemistry professor at the University of Utah who researches CRISPR.
Functional analyses indicate that MFSD12 encodes a lysosomal protein that affects melanogenesis
in zebrafish and
mice, and that mutations
in melanocyte -
specific regulatory regions near DDB1 / TMEM138 correlate with expression of ultraviolet response
genes under selection
in Eurasians.
We not only introduced the
gene into
specific brain regions of the
mouse, but we could also direct it to
specific cell types to test which ones played a role
in regulating sociability.»
Researchers find a full 12,000
genes that act differently
in male and female
mice, a finding that could lead to sex -
specific medicine.
The researchers used tools of epigenomic analysis to trace the
specific epigenetic switches controlling each of thousands of
genes in both
mouse and human retinal cells as the cells progressed through development.
The human -
specific gene ARHGAP11B is expressed only
in the right half of this embryonic
mouse cerebral cortex.
This allowed them to identify
specific genes that are turned on or off by co-regulators of
gene function called TAZ and YAP
in the nucleus of developing
mouse Schwann cells.
Gene editing using CRISPR / Cas9, also can introduce mutations into
specific organs or tissues
in postnatal
mice.
The researchers deliver a
specific gene, which hitches a ride on a harmless virus, into the livers of
mice, and once
in the liver that
gene codes for a protein called myelin oligodendrocyte glycoprotein.
In a scientific first, researchers at the Gladstone Institutes turned skin cells from mice into stem cells by activating a specific gene in the cells using CRISPR technolog
In a scientific first, researchers at the Gladstone Institutes turned skin cells from
mice into stem cells by activating a
specific gene in the cells using CRISPR technolog
in the cells using CRISPR technology.
A group of scientists have described their use of a
specific gene therapy to treat Alzheimer's disease
in a
mouse model.
Smithies was awarded the Nobel Prize
in 2007 alongside Mario Cappecchi and Martin Evans «for their discoveries of principles for introducing
specific gene modifications
in mice by the use of embryonic stem cells».
The creator of the BAC - HD
mice, William Yang at UCLA, cleverly modified the mutant HD
gene he put
in them, so that it could be turned off
in specific brain regions.
A purified inactivated virus vaccine derived from a Puerto Rican strain was shown to induce ZIKV -
specific neutralizing Abs and protect from virus challenge
in mice and NHP models (115), and DNA vaccines encoding the prM / E
genes of ZIKV elicited strong binding and neutralizing Abs
in rhesus monkeys (116, 117).
We use what are called conditional knockout
mice,
in which a
gene is deleted only
in a
specific organ or group of cells.
A
specific type of brain activity important for memory replay is disrupted
in mice with the E4 version of the apolipoprotein E (apoE4)
gene, which may interfere with memory formation.
The researchers looked at the dentate gyrus, a
specific area of the brain that is critical to memory and particularly vulnerable
in Alzheimer's disease, and compared the
genes that were turned on and off
in normal
mice and a
mouse model of Alzheimer's disease.
For example the researchers used the CRE - ERT2
mouse model validated at the ICS,
in which Cre function is controlled by the promoter of Atypical Notch ligand Delta - like homologue1 (Dlk1) under Tamoxifen activation, a skin fibroblast marker, to carry out temporal and tissue
specific inactivation of key
genes involved
in skin fibroblast diversity.
The lab has generated «floxed» alleles of GABAA receptor subunit
genes that allow us to ablate the respective subunit
in a subregion
specific manner — e.g.,
in hippocampal subregions or the amygdala — either via a cross with cre - transgenic
mice or via stereotaxic injection of cre - expressing viruses into defined brain regions.
In Aim 1, we generate cell
specific - knockout
mice and characterize deletion of expression of distinct
genes relevant to axon guidance.
We use the Cre - loxP recombination system to generate
mice with cell type -
specific inactivation of the IL - 10
gene in order to identify cellular sources of the cytokine that are relevant
in various situations of immune challenge.
In the double mutant
mice, the targeted
gene is biotinylated, allowing for its
specific immunoprecipitation and any bound proteins.
Besides information gathered to answer
specific experimental questions, as determined by the interests of individual partners [35]--[41], the collective data offered the opportunity to search for coordinated
gene expression patterns
in a systematic exploration of the
mouse ES transcriptome under a battery of different experimental settings, thus minimizing possible site -
specific artifacts.
Genetic studies
in humans and
mice with idiopathic epilepsy have revealed a number of causative
genes for
specific forms of epilepsy 31.