Tuna oil alleviate D - galactose induced aging in mice accompanied by modulating gut microbiota and
brain protein expression — Dijun Zhang — Journal of Agricultural and Food Chemistry
Not exact matches
Alternately, The
brains of cesarean babies may have impaired
expression of the same
protein.
The activity of four transcription factors —
proteins that regulate the
expression of other genes — appears to distinguish the small proportion of glioblastoma cells responsible for the aggressiveness and treatment resistance of the deadly
brain tumor.
By deleting some of these «ultraconserved elements», researchers have found that these sequences guide
brain development by fine - tuning the
expression of
protein - coding genes.
«Those findings also suggest that FGF21 is regulated the same way in humans as in mice and that the process involves the
expression and activation of certain
proteins in the
brain.»
While previous investigations into the
protein's effects have used either mice in which gene
expression was knocked out or transgenic animals that expressed human gene variants throughout their lifetimes, the MGH - MIND - led study used a different approach to investigate the effects of introducing the variant forms of the
protein into
brains in which plaque formation had already begun.
Importantly, patients with mutations in a single copy of NKX2.1 often have
Brain - Lung - Thyroid Syndrome, which is characterized by respiratory distress after birth and accompanied by decreased surfactant
protein expression.
However, the team was able to show that so - called tight junction
proteins, which are known to be important for the blood -
brain barrier permeability, did undergo structural changes and had altered levels of
expression in the absence of bacteria.
Recent studies have found elevated levels of this
protein in post-mortem
brain samples of patients with MS.. In this latest work, investigators compared the frequencies of «more active» and «less active» variants of the DNA sequences that control
expression of the galanin gene between healthy controls and MS patients.
If a
brain is normal, each of those
proteins will have one level of
expression.
We have compared the transcriptome in blood leukocytes, liver, and
brain of humans, chimpanzees, orangutans, and macaques using microarrays, as well as
protein expression patterns of humans and chimpanzees using two - dimensional gel electrophoresis.
We identified species - specific gene
expression patterns indicating that changes in
protein and gene
expression have been particularly pronounced in the human
brain.
Notably, the
brains of treated fish showed increased
expression of genes involved in making ferritin, a
protein that stores and transports iron inside cells.
Synaptotrophic defects in mouse
brains lacking amyloid precursor
protein (APP)
expression can be selectively rescued by the non ‐ amyloidogenic APPsα fragment, for which α7 ‐ nAChRs may constitute a physiological receptor.
I am currently exploring functions of BIN1 by generating mouse models to modify the levels of BIN1
expression in the
brain, and investigating how altering the levels of this
protein can modify AD - related pathophysiology.
«This data allows classification of all human
protein - coding genes into those coding for house - hold functions (present in all cells) and those that are tissue - specific genes with highly specialized
expression in particular organs and tissues, such as kidney, liver,
brain, heart, pancreas.
In this context, Dr. Woo's work focuses on deepening the understanding of these mechanisms based on postmortem human
brains and animal studies using a variety of
protein and gene
expression techniques, in addition to the utilization of differentiated human neurons.
Expression of the familial PD - linked A53T or A30P mutant ASs in cell models results in an increased proportion of CTTAS being produced than is the case when expressing the WT
protein; consistent with this, a higher proportion of the total soluble AS in human
brain tissue with AS neuropathology is CTTAS, and a higher proportion yet of the total AS in insoluble AS deposits.
Evolutionary divergence of gene and
protein expression in the
brains of humans and chimpanzees.
The maturation of the
brain involves the coordinated
expression of thousands of genes,
proteins and regulatory elements over time.
A research team led by Fredrik Swartling (Uppsala University / SciLifeLab) has discovered that medulloblastoma, the most common type of malignant
brain tumor in children, can be effectively suppressed by combining two treatment strategies, disrupting both the
expression and stabilization of the
protein MYC.
A series of mouse
brain sections is explored for
protein expression and distribution in a large number of
brain regions.
Inhibition of pSTAT 1 Nuclear Translocation and Antiviral
Protein Expression in Human
Brain Vascular Adventitial Fibroblasts Infected with Varicella Zoster Virus J Virol.
Our biological studies suggest that a critically reduced amount of this
protein alters cell shape, migration, proliferation, and gene
expression to the detriment of
brain, heart, and kidney development.
However, recent evidence indicates that apoE4
expression compromises the blood -
brain barrier (as does apoE deficiency).40 Studies of
brain histology, neurodegenerative markers, cholinergic activity, and neuronal function in knockout mice have been equivocal.39 Failure of detailed neurocognitive and retinal studies to demonstrate defects in our patient suggests either that the functions of apoE in the
brain and eye are not critical or that they can be fulfilled by a surrogate
protein.
«Until quite recently, the
brain was considered to be an immunologically privileged organ due to the presence of the blood -
brain barrier (BBB), the low
expression of major histocompatibility complex class II (MHCII)
proteins, and the apparent lack of cerebral lymphatic vessels.
Robust changes in
expression of
brain - derived neurotrophic factor (BDNF) mRNA and
protein across the
brain do not translate to detectable changes in BDNF levels in CSF or plasma.