Mouse study indicates signaling molecules at play in cancer may also promote atherosclerosis
Not exact matches
While
study results
indicated that combining capsaicin with the chemicals «might promote cancer cell survival,» the report clearly stated that the control group of
mice treated only with capsaicin ``... did not induce any skin tumors...» In addition, the
study repeatedly cited other research
studies in which the anti-cancer properties of capsaicin were solidly demonstrated.
Osterhout
studied the
mouse embryos as they developed, tracking them to see when GFP glowed green,
indicating a retinal ganglion cell was born.
The new
study indicates that such infections in the
mice cause the number of tuft cells to increase by five - to tenfold, leading the norovirus to replicate more efficiently.
Further
studies indicated that social experience with a female seemed to be the key requirement for the
mice to develop separate, sex - specific populations of neurons, as well as aggressive behavior.
«Our results
indicate that the epigenetic modification we
studied makes both
mice and humans more susceptible to obesity and with increasing age increases their risk of developing a fatty liver,» said Anne Kammel, first author of the
study.
Studies in
mice indicated that drugs that activate the surface protein TRPA1 on pain - sensing nerve cells intensify postoperative pain.
Earlier
mouse studies by Li and his collaborators had
indicated that the expression of several imprinted genes changes as hematopoietic stem cells embark on their journey from quiescent reserve cells to multi-lineage progenitor cells, which form the many highly specialized cell types that circulate within the blood stream.
Although we did observe positive effects on some aging traits, such as memory impairments and reduced red blood cell counts, our
studies showed that similar drug effects are also seen in young
mice,
indicating that rapamycin did not influence these measures by slowing aging, but rather via other, aging - independent, mechanisms.»
Evolution has preserved the «neuropeptide Y (NPY) system», as it is known, in most species —
indicating its importance — and much of our understanding comes from
studying it in
mice.
Remarkably, although
mouse studies had
indicated that different transcription factors were differently important for generating pain and itch sensing neurons versus pressure and limb position neurons, in the dish these factors produced equal numbers of each of the three main subtypes.
«Previous
studies in
mice have
indicated that bacteria that are able to encroach upon the epithelium might be able to promote inflammation that drives metabolic diseases, and now we've shown that this is also a feature of metabolic disease in humans, specifically type 2 diabetics who are exhibiting microbiota encroachment.»
Previous research
indicated this was the case in
mice, but this is the first
study to document presymptomatic dysfunction in humans.
Their
study in aged
mice indicates that high folic acid intake causes lowered immune function because natural killer (NK) cells, a particular type of immune cell, are less effective.
Combined with previously published
studies, our data
indicate that infection with all three major North American T. gondii clonal lineages results in loss of innate, hard - wired aversion to feline predator urine in
mice.
In this regard, animal model
studies with FIPV in cats and RSV in
mice have
indicated that viral surface proteins may be the sensitizing protein of inactivated vaccines for immunopathology with infection [32], [45].
In addition to the reduction in total numbers of activated microglia in AFF 1 - treated TG
mice, it is of note that costaining
studies indicated that those activated microglia that did emerge in treated
mice were highly colocalized with recalcitrant (proteinase K - resistant) AS aggregate as compared to untreated PDGF - AS
mice.
Our mechanistic
studies, in both
mouse and human mammary cancer cells,
indicate that leptin and LepR are necessary for NANOG expression.
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 p
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 p
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.
«While past research
indicated that only
mice with compromised immune systems are susceptible to Zika virus infection, this
study shows that neonatal
mice with otherwise healthy immune systems are also susceptible,» according to the FDA news release.
For example, results of a
mouse study conducted by the National Institutes of Health (NIH) in collaboration with ChromaDex published in November 2014
indicated that NR was effective at restoring NAD + levels in mitochondria and rescuing phenotypes associated with a devastating accelerated aging disease known as Cockayne Syndrome (CS).
The
study results
indicated unfavorable atherosclerotic changes when
mice followed a low carb / high protein diet.