Genetic studies in
humans and mice with idiopathic epilepsy have revealed a number of causative genes for specific forms of epilepsy 31.
In
both humans and mice with lupus, groups of B lymphocytes (B cells) spontaneously arise in the absence of a pathogenic infection.
To make this discovery, the researchers stimulated isolated neutrophils from
humans and mice with nicotine and could measure a dose - dependent release of inflammatory molecules.
Not exact matches
Scientists know how to make fruit flies
and mice smarter,
and efforts to come up
with a treatment for Alzheimer's
and other neurological disorders are leading to drugs that enhance memory
and cognition in
humans.
Humans are not sterile
mice, after all,
and we all start
with our own unique mix of bacteria swirling around.
Researchers have injected
mice with human breast, ovary, colon, bladder, brain, liver
and prostate tumors,
and their new drug has killed the tumors every time.
In order to determine the lethal toxic level of capsaicinoids in animals,
and to extrapolate that level for
humans, researchers in 1980 performed a rather gruesome experiment
with mice, rats, guinea pigs
and rabbits.
The study found that
mice with peanut allergies developed similar symptoms as
humans, notably itchy skin
and breathing issues.
Hassles such as buying paper towels or searching for the perfect used car that used to require legwork,
human interaction,
and possibly even wearing pants can now be done
with a click of a
mouse from one's own living room.
The team found neonatal
mice with the mutations had normal - appearing skin,
and the dry itchy skin of dermatitis did not develop until the
mice were a few months old, the equivalent of a young adult in
human years.
Depending on results from further behavioural studies in
mice and humans, the abnormalities could then be treated in parallel
with seizures.
Much of their work focuses on the house
mouse (Mus musculus), which evolved to be commensal
with humans: The
mice are not domesticated like dogs or sheep, but they are dependent on living in
and around a
human settlement.
«Apart from
humans and some domestics that
humans brought
with them,
mice are the most globally distributed mammals,» he says.
Compared
with mice with cells from healthy people as well as non-chimera
mice, those whose brains had
human schizophrenia cells were more afraid to explore a maze, more anxious, more antisocial, less able to feel pleasure (from sipping sugar water), worse at remembering,
and more sleepless — all of which characterize people
with schizophrenia, too.
Now, a new study of wild
mice shows that they, too, can develop signs of domestication — white fur patches
and short snouts —
with hardly any
human influence.
To better understand their findings, the team examined the animal model for APS1 (i.e.
mice with the same genetic defect as
human patients
with the syndrome)
and found that male
mice spontaneously developed an inflammatory disease in their prostate glands — a so - called prostatitis —
and reacted to transglutaminase 4.
They seeded
mice with human pancreatic tumours
and then injected them daily
with the souped - up bacteria for a week, giving them a week off before four more days of injections.
First
mouse cells were turned into «totipotent» stem cells,
and now early work suggests the same might have been achieved
with human cells
Researchers at Weill Cornell Medical College recently identified a gene abnormality that is associated
with anxiety - related behaviors; it makes
humans and mice hypervigilant to cues that signal danger.
Shukla
and colleagues discovered that a small drug molecule called BX795, which is sold to labs for use in experiments, helped clear HSV - 1 infection in cultured
human corneal cells, in donated
human corneas,
and in the corneas of
mice infected
with HSV - 1.
What's more, an ointment containing the peptide effectively treated wounds infected
with methicillin - resistant Staphylococcus aureus (MRSA)
and the increasingly common hospital infection bacterium Acinetobacter baumannii in
mice and on laboratory samples of
human skin.
Recent collaborative work between UCR
and Cedars - Sinai Medical Center in Los Angeles demonstrated that in animal models of
human breast cancer,
mice treated
with 123B9 that was conjugated
with paclitaxel had significantly fewer circulating cancer cells in the blood compared to
mice that were not treated or even treated
with paclitaxel alone.
These four genes
and their proteins constitute the heart of the biological clock in flies,
and with some modifications they appear to form a mechanism governing circadian rhythms throughout the animal kingdom, from fish to frogs,
mice to
humans.
Fat
mice and humans have a less diverse milieu of gut bacteria,
with a greater proportion of Firmicutes to Bacteroidetes in their bowels.
Then the team injected the
mice with human liver cells
and withdrew the drug.
To see whether this also applies to
humans, the team engineered stem cells from people
with and without Down's syndrome
and injected them into
mice.
To investigate, Walker Jackson of the Whitehead Institute in Boston, Massachusetts,
and his colleagues created
mice with a mutation associated
with the
human prion disease Fatal Familial Insomnia
and injected some of their brain tissue into the brains of
mice without the mutation.
The «training data» were generated from 78
mice infected
with influenza or the cytomegalovirus (CMV)
and 32
humans infected
with flu, CMV or the Epstein - Barr virus.
This age period is associated
with a decline in reproductive function
and egg quality in both
humans and mice.
Like the Rosetta Stone that scholars used to decode hieroglyphics, researchers trained the algorithm
with more than 4,600 T cell receptors
and then used it to correctly assign 81 percent of the
human T cells
and 78 percent of
mouse T cells to one of 10 different viral epitopes.
«So far, the drug has only been tested in
mice,
and while some research in
human genetics suggests this approach could work in people too, we need more research before we know how relevant this could be for people
with type 2 diabetes.»
Shih, Wang
and their colleagues tested fostamatinib's power to reduce tumor size in
mice implanted
with human ovarian cancer cells that were resistant to paclitaxel.
An inflammatory protein that triggers a pregnant
mouse's immune response to an infection or other disease appears to cause brain injury in her fetus, but not the premature birth that was long believed to be linked
with such neurologic damage in both rodents
and humans, new Johns Hopkins - led research suggests.
Using the modified system,
human melanoma
and breast cancers as well as
mouse melanoma cells were diagnosed
with greater ease
and efficiency.
So he implanted various
human tumors — including ovarian, breast, colon, liver,
and brain — into
mice and then injected the animals
with antibodies that disable CD47.
Even the new studies clashed somewhat: Unlike the UCSF study, the German research found no major differences between the overall microbiomes of twins
with and without MS. Finally,
mouse models of MS are not perfect mimics of the
human disease,
and mouse immune systems aren't identical to people's.
Like the per gene, the new genes — dubbed RIGUI in
humans and m - rigui in
mice — are turned on
and off in a daily cycle
and may work
with other genes to generate the oscillating mechanism that runs the internal clock.
Although the researchers emphasized that laboratory results involving cell lines
and mice do not necessarily translate to
human treatment, they say their findings show that new mTOR inhibitors combined
with chemotherapy could become a new treatment strategy for T - ALL.
University of California, Irvine neurobiologists Leslie Thompson
and Joseph Ochaba
with the Departments of Neurobiology & Behavior
and Psychiatry &
Human Behavior
and their colleagues from UCI
and from Children's Hospital of Philadelphia have shown that reducing the aberrant accumulation of a particular form of the mutant Huntingtin protein corresponds to improvement in symptoms
and neuroinflammation in HD
mice.
An unknown component of breast milk appears to kill HIV particles
and virus - infected cells, as well as blocking HIV transmission in
mice with a
human immune system.
The investigators report that trapping virus - loaded stem cells in a gel
and applying them to tumors significantly improved survival in
mice with glioblastoma multiforme, the most common brain tumor in
human adults
and also the most difficult to treat.
In addition, they injected
mice with human cancer cells
and found that the tumors grown in
mice could be inhibited
with PD173074.
Géléoc
and colleagues at Boston Children's Hospital studied
mice with a mutation in Ush1c, the same mutation that causes Usher type 1c in
humans.
The scientists have detailed the functional parts of the
mouse genome
and have compared them
with those in
humans.
The research team also tried the GD2 CAR - T therapy in
mice with human spinal cord
and thalamic tumors implanted in their respective anatomical locations.
The
mouse telomerase RNA component was cloned
and contained only 65 percent sequence identity
with the
human telomerase RNA.
«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.
Part of the problem, he says, is that the incidence of many
human chronic diseases rises
with age, yet many researchers prefer using young
mice because of the pressures of being published
and getting funding.
Professor Chayama
and his research group used
mice with «humanized» livers,
and injected them
with human blood.
In the past, a drug's efficacy would often be measured
with one test in
mice and another in
humans.