Not exact matches
It has been predicted already that
by 2020, we will be using gesture control on computers to stop us using our
mouse and keypad,
and that there will be a rise in robotics carrying out
human work in an office environment.
A study
by researchers at the University of Chicago Medicine shows that when
mice that are genetically susceptible to developing inflammatory bowel disease (IBD) were given antibiotics during late pregnancy
and the early nursing period, their offspring were more likely to develop an inflammatory condition of the colon that resembles
human IBD.
The
mice behaved just like others of their kind, as far as scientists could tell,
and they also looked the same — except for the
human mini brain that had been implanted into each rodent's own cortex, made visible
by a little clear cover replacing part of their skull.
«Our study shows that epigenetic drift, which is characterized
by gains
and losses in DNA methylation in the genome over time, occurs more rapidly in
mice than in monkeys
and more rapidly in monkeys than in
humans,» explains Jean - Pierre Issa, MD, Director of the Fels Institute for Cancer Research at LKSOM,
and senior investigator on the new study.
ARTIFICIAL sweeteners can cause glucose intolerance in
mice,
and perhaps in
humans,
by altering gut bacteria, a series of experiments suggests.
PDX models are created
by implanting cancerous tissue from a
human primary tumor directly into immunodeficient
mouse or rat models, enabling acceleration of oncology research or drug discovery
and development programs.
Duke scientists have shown that it's possible to pick out key changes in the genetic code between chimpanzees
and humans and then visualize their respective contributions to early brain development
by using
mouse embryos.
A joint work
by EPFL, ETH Zürich
and the CHUV has identified a pathological process that takes place in both
mice and humans towards one of the most common diseases that people face in the industrialized world: type 2 diabetes.
A study published
by Cell Press October 16th in Cell now reveals that gut microbes in
mice and humans have circadian rhythms that are controlled
by the biological clock of the host in which they reside.
A decade ago, he replicated the entire
human leukemia disease process
by introducing oncogenes into normal
human blood cells, transplanting them into xenografts (special immune - deficient
mice that accept
human grafts)
and watching leukemia develop — a motherlode discovery that has guided leukemia research ever since.
By combining the pieces in one way or another, we would obtain very different circuits (as happens between
mice and humans) although the basic mechanisms governing the operation are based on the same methods
and available resources.
Since then, he
and his colleagues have modified the sequences of influenza viruses to bind to a natural microRNA expressed in
humans and mice, in essence developing a virus that's knocked down
by the body's natural microRNA.
The method is relatively new, but far bacteria - based vaccines have proven effective: A seasonal flu vaccine produced
by VaxInnate successfully protected
humans in clinical trials,
and the company's recently tested swine flu vaccine immunized
mice against the virus.
An additional study, currently available at bioRxiv, led
by the researchers from the CRG
and Cold Spring Harbour Laboratory, highlights the fact that a substantial part of
human and mice genes have maintained an essentially constant expression throughout evolution, in tissues
and various organs.
Senior author Madhav Dhodapkar, M.D., the Arthur H.
and Isabel Bunker Professor of Medicine
and Immunobiology,
and chief of Hematology, said the study, using tissue
and blood samples from
humans and mice, shows that chronic stimulation of the immune system
by lipids made in the context of inflammation underlies the origins of at least a third of all myeloma cases.
This is the finding of a study in both
mice and human patients led
by researchers at NYU Langone Medical Center
and published online June 9 in the journal Cell.
He
and his colleagues are also attempting to make an animal model of stuttering
by inserting the
human mutation into
mice.
By promoting DNA demethylation, high - dose vitamin C treatment induced stem cells to mature,
and also suppressed the growth of leukemia cancer stem cells from
human patients implanted in
mice.
Kilian said his team's synthetic microenvironment lies somewhere in the middle of two extremes in the field of modeling biology: the hard plastic plate,
and expensive
mouse avatars that are created
by injecting
human tumor cells into
mice.
Scientists have assumed these tunes are hardwired in their tiny
mouse brains
and doubted that rodents modify their songs after hearing others — a cognitive feat similar to vocalizations
by birds
and some mammals, including dolphins, bats
and humans.
To see if they would suffice to make H5N1 infection less severe, Webby
and his co-workers injected
mice with DNA for the neuraminidase gene from
human H1N1, one of three flu subtypes covered
by this winter's flu shot.
They found that blocking ANGPTL3 activity with an investigative injectable antibody, known as evinacumab, reduced triglycerides
by up to 76 percent
and lowered LDL cholesterol 23 percent in
human study participants,
and largely reversed signs of atherosclerosis in a
mouse models.
«No matter whether
human being,
mouse, whale or bacterium, nature does not constantly invent proteins for various living organisms anew, but varies them
by evolutionary mutation
and selection,» Alexander Schug of the Steinbuch Centre for Computing (SCC) says.
Using a
mouse model of HSV - 1 as well as autopsied samples of
human adult
and fetal tissues, investigators from Dartmouth College's Geisel School of Medicine found that antibodies against HSV - 1 produced
by adult women or female
mice could travel to the nervous systems of their yet unborn babies, preventing the development
and spread of infection during birth.
Scientists have a promising new approach to combating deadly
human viruses thanks to an educated hunch
by University of California, Riverside microbiology professor Shou - Wei Ding,
and his 20 years of research on plants, fruit flies, nematodes
and mice to show the truth in his theory.
The authors said that this result suggests that the reason bacterial numbers are so high in these
mice,
and,
by extension,
human LAD patients, is not because of a defect in the immune system's surveillance mechanism but because of the inflammation caused
by the immune system's abnormal response to normal levels of bacteria in the gums.
By assessing the survival of the cells that engulf the particles
and measuring the levels of red or green light that they emitted, the researchers determined which formulation of particles performed best, then tested that formulation in
mice with
human brain cancer derived from their patients.
By comparing our genetic make - up to the genomes of
mice, chimps
and a menagerie of other species (rats, chickens, dogs, pufferfish, the microscopic worm Caenorhabditis elegans, the fruit fly Drosophila melanogaster
and many bacteria), scientists have learned a great deal about how genes evolve over time,
and gained insights into
human diseases.
Since the current work was done in
mice, O'Leary
and Zembrzycki want to confirm the link in
humans by using brain scans to measure the natural variation in the neocortical areas
and search for potential links to disease.
Joseph Castellano at Stanford University in California
and his colleagues discovered this
by collecting blood from people at three different life stages — babies, young people around the age of 22,
and older people around the age of 66 —
and injecting the plasma component into
mice that were the equivalent of around 50 years old in
human years.
However, cancer cells may instead be coaxed to turn back into normal tissue simply
by reactivating a single gene, according to a study that found that restoring normal levels of a
human colorectal cancer gene in
mice stopped tumor growth
and re-established normal intestinal function within only 4 days.
By pairing a receptor that targets neurons with a molecule that degrades the main component of Alzheimer's plaques, the biologists were able to substantially dissolve these plaques in
mice brains
and human brain tissue, offering a potential mechanism for treating the debilitating disease, as well as other conditions that involve either the brain or the eyes.
The results obtained
by Afsaneh Gaillard's team
and that Pierre Vanderhaeghen at the Institute of Interdisciplinary Research in
Human and Molecular Biology show, for the first time, using
mice, that pluripotent stem cells differentiated into cortical neurons make it possible to reestablish damaged adult cortical circuits, both neuroanatomically
and functionally.
One gene, which codes for a powerful growth - stimulating hormone in
mice and humans, is expressed only
by paternally derived genes.
Colonization
by the
human and animal parasite, Giardia, changed the species composition of the
mouse microbiome in a way that might be harmful.
They found evidence of Del - 1 in the same areas as osteoclast activity, then followed up
by generating
human and mouse osteoclasts in vitro
and found Del - 1 mRNA
and protein expressed at high levels.
Although that marker, called IL21, had not previously been associated with autoimmune diseases, the gene that produces it sits right in the stretch of DNA known to make these
mice vulnerable to diabetes, suggesting that IL21 might make a drug target, says Sarvetnick.Furthermore,
by giving the animals a shot of dead bacteria — similar to an immunization in
humans — when they were newborns, Sarvetnick
and her colleagues prevented a surfeit of CD4 +
and CD8 + cells.
They created inflammation in the temporomandibular joints of the
mice,
and then measured bite force exerted
by the
mice to assess jaw inflammation
and pain, similar to how TMJD pain is gauged in
human patients.
Gough Island might have been largely uninhabited
by humans, but 50 years later, residents of nearby islands raised questions about the unusually vicious
mice that now roam the island (50 per cent heavier than wild
mice anywhere in the world)
and devastate the bird population.
A 2007 study co-authored
by Small shows that exercise improves its function in both
mice and humans.
By studying how these genes cause defects in fly
and mouse models, we can improve our insights into the mechanisms related to
human disease,» said corresponding author
and Dr. Hugo J. Bellen, professor of neuroscience
and molecular
and human genetics at Baylor College of Medicine
and an investigator at the Howard Hughes Medical Institute.
The dosages used in
human executions are, in some cases, lower
by body weight than the dosages that would kill only 50 percent of
mice and from which monkeys have been able to successfully recover.
Researchers developed a new type of cell transplantation to treat
mice mimicking a rare lung disease that one day could be used to treat this
and other
human lung diseases caused
by dysfunctional immune cells.
«
By identifying the signals that instruct
mouse progenitor cells to become cells that make tubes
and later insulin - producing beta cells, we can transfer this knowledge to
human stem cells to more robustly make beta cells, says Professor
and Head of Department Henrik Semb from the Novo Nordisk Foundation Center for Stem Cell Biology at the Faculty of Health
and Medical Sciences.
By examining cell processes both in
mice and in
human cells, the researchers found out why: Re-esterification helps protect a key cell organelle called the endoplasmic reticulum (ER).
Mouse embryonic stem cells, reported in 1981
by Martin Evans, Matthew Kaufman,
and Gail Martin, have allowed scientists to generate genetically customized strains of
mice that have revolutionized studies of organismic development
and immunity
and have provided countless models of
human disease.
In addition, cohousing coprophagic
mice harboring transplanted microbiota from discordant pairs provides an opportunity to determine which bacterial taxa invade the gut communities of cage mates, how invasion correlates with host phenotypes,
and how invasion
and microbial niche are affected
by human diets.
The team led
by Dr Rubén López — of the UAB's Department of Cell Biology, Physiology
and Immunology
and Institute of Neuroscience,
and the Centre for Networked Biomedical Research in Neurodegenerative Diseases (CIBERNED)-- used a genetically modified
mouse that produces the
human form of IL - 37 to study the function of this protein.
By using molecular genetic tools to reduce the amount of PC in
human lung cancer cells, the team observed decreased cell growth, a compromised ability to form colonies in soft agar (a gelatinous material specifically used to grow bacteria
and other cells),
and a reduced rate of tumor growth in
mice.
A single gene appears to play a crucial role in coordinating the immune system
and metabolism,
and deleting the gene in
mice reduces body fat
and extends lifespan, according to new research
by scientists at the Jean Mayer USDA
Human Nutrition Research Center (USDA HNRCA) on Aging at Tufts University
and Yale University School of Medicine.