Not exact matches
[1] It is comprised of a network of
cells and organs working together to defend the body against infection and sickness by
producing secretions and
disease - fighting
cells.
Interestingly, those who suffer from narcolepsy, a
disease in which people are excessively tired and may spontaneously fall asleep during the day, also lack orexin due to a breakdown in the brain
cells that
produce it.
It's necessary, they argue, to protect the babies who would otherwise be born with mutated mitochondria - the power -
producing bits of
cells - which can lead to serious
diseases that currently affect around one in every 6,500 children.
Either approach could
produce enough HSCs to transplant and — pending further safety testing — potentially treat leukemia, sickle
cell disease and other severe blood disorders.
An engineered bone that has its own marrow can encourage donor stem
cells to
produce blood, a feat that could help people with anaemia and rare immune
diseases
Scientists use
cell reprogramming techniques to
produce cells in the lab so that they can study
diseases.
ORDINARY
cells from people with a genetic
disease can be «fixed» by gene therapy and then reprogrammed to be stem
cells that will
produce a limitless supply of defect - free
cells.
Characterized by tremors, rigidity, difficulty walking and other symptoms, Parkinson
disease is caused by the destruction of brain
cells that
produce the neurotransmitter dopamine.
Comparing his study to Surmeier's, Redmond noted: «One is an approach to try to minimize
disease progression or maybe even get some recovery, the other is more aimed at the other end, after (dopamine -
producing]
cells are already dead.»
In mice, the Runx2 knock - in myeloma
cells produced greater tumor growth and a wider spread of
disease compared with the original myeloma
cells; conversely, the Runx2 knock - down
cells had less tumor growth and
disease spread.
«If we take one of these modified
cells and treat it with a particular drug, if it doesn't
produce light anymore, then this means the drug is a potential treatment for this
disease,» Basu said.
Most importantly, these
cells protected mice from developing diabetes in a model of
disease, having the critical ability to
produce insulin in response to changes in glucose levels.
The
disease commonly starts in childhood and causes the body's own immune system to attack and destroy the insulin -
producing cells in the pancreas, leaving the patient dependent on life - long insulin injections.
Specific immune
cells have the ability to
produce a healing factor that can promote wound repair in the intestine, a finding that could lead to new, potential therapeutic treatments for inflammatory bowel
disease (IBD), according to a new research study.
«Only by understanding the complexities of what happens in specific
cell - types found in specific areas of the brain during this
disease can targeted treatments for Parkinson's
disease be
produced.»
By getting inside the
cell and getting the body to
produce intracellular proteins, we have the potential to address many
diseases that today aren't druggable with small molecule drugs or biologics.
Thus, the technique could
produce adult muscle
cells in a dish that carry genetic
diseases.
Research shows that in Parkinson's
disease a brainstem region called the pedunculopontine nucleus (PPN) develops changes in DNA found in mitochondria — the batteries of the
cell — as they
produce and store energy that
cells can use.
They believe a vaccine that stimulates the body to
produce more of these
cells could be effective at preventing flu viruses, including new strains that cross into humans from birds and pigs, from causing serious
disease.
The study, published in Nature Communications, shows that membralin regulates the
cell's machinery for
producing beta - amyloid (or amyloid beta, Aβ), the protein that causes neurons to die in Alzheimer's
disease.
Although some teams have managed to
produce nearly pure colonies of certain kinds of neural
cells from ES
cells, no one has managed to concoct a recipe that will direct the
cells to become, say, a pure population of dopamine -
producing neurons that could replace those missing in Parkinson's
disease.
Excessive or uncontrolled inflammation can actually make injuries worse and contribute to
disease in a couple of different ways — by activating
cell death processes, clogging and rupturing blood vessels and
producing toxic molecules like free radicals.
COUNTLESS research projects around the world into cancer and other major
diseases are
producing bogus or misleading results because investigators are studying the wrong type of
cell.
A few years ago, MS researchers were focused on a new type of immune
cell called the Th - 17
cell, which appeared to be a key player in driving the neuronal damage in MS. Because Th - 17
cells produce the cytokine IL - 17, researchers likewise thought this chemical was essential to the
disease.
Plus, hopes for therapeutic cloning rest on the ability to
produce embryonic stem
cells from
cells harvested from
diseased patients.
The new research shows that when the atheronals interact with various blood
cells, they
produce some of the effects known to lead to heart
disease, such as causing a malfunction in the
cells that line arterial walls.
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 continue to have the gene and they
produce VEGF - A, but it's like the patient's
cells don't realize they could be more protected or suffer from the
disease much less if the
cells produce more of this particular protective factor.»
In many cases, this procedure has
produced long - lived dopamine -
producing cells and reversed symptoms of the
disease, such as rigidity, slowness, and tremor.
Parkinson's
disease, which afflicts one million people in the United States, kills a class of brain
cells that
produce dopamine, one of the brain's chemical messengers.
«With a better understanding of how potential is regulated, it could be possible to broaden the development spectrum of aging stem
cells, allowing them to regain their capacity to
produce cell types from earlier development stages, which in the long - term perspective could be relevant to future treatment methods for neurodegenerative
disease.»
Among these: There can be no changes to his protocol; the
cells need to be
produced at one facility, under the supervision of a Stamina biologist; and the trial must include patients with three different
diseases.
Under pressure to name several possible future perspectives, Bente Vilsen mentions that the discovery of the electroneutral sodium - potassium pump also makes it possible to explore what an inability to
produce current means for the development of the
cells and the occurrence of
diseases in e.g. the brain and kidneys, where the sodium - potassium pump plays a crucial role.
After initial infection, HSV enters a latent state in sensory nerve
cells, periodically reactivating to
produce disease.
Researchers from the University's Institute of Ageing and Chronic
Disease, led by Senior Lecturer in Orthopaedic Sciences Dr Simon Tew, examined molecular messages
produced by cartilage
cells in both humans and rats.
In sickle
cell disease, individuals have two copies of a genetic mutation that
produces an abnormal change in hemoglobin, the primary molecule that carries oxygen in the blood.
The
disease is caused by a genetic mutation that prevents a protein required to keep muscle
cells intact from being
produced.
However, when mature blood
cells are lost, for example through severe bleeding or during infections, HSCs become activated to generate new «progenitor»
cells — the
cells that replenish the blood supply and
produce immune
cells to fight
disease.
At the same point in the
disease process, the scientists found no evidence of impairment in liver
cells, which also
produce the mutated huntingtin protein.
In previous studies, the same group along with others had demonstrated that microRNAs (miRNAs)
produced by eukaryotic
cells and viruses are present in human blood in highly stable,
cell - free forms and these so called circulating miRNAs can serve as non-invasive biomarkers for the early diagnosis of various
diseases, including viral
diseases.
In the tea drinkers» immune systems, gamma delta T
cells produced five times more infection - fighting interferon when exposed to
disease - causing bacteria than did the T
cells of the coffee drinkers.
The
disease begins when a person's own antibodies attack the insulin -
producing cells in the pancreas.
In principle, we hope to engineer T
cells or other
cell types to reside in the body long - term and
produce therapeutics if they recognize
disease or recurrence of
disease.
Parkinson's
disease occurs precisely because the group of nerve
cells in the brain that
produce dopamine stop working.
But scientists — who want to harness the potential of
cells as living computers that can respond to
disease, efficiently
produce biofuels or develop plant - based chemicals — don't want to wait for evolution to craft their desired cellular system.
Patients with Parkinson's
disease, cardiovascular
disease, and cystic fibrosis may have something in common:
cells in their
disease - affected tissues may
produce misfolded proteins that are incapable of functioning normally.
These damaged molecules trigger
cell death that
produces some human
diseases, according to the researchers.
THE DEMENTIA associated with Alzheimer's
disease may be caused by toxins that the body's own immune
cells produce.
«Bacteria can only cause
disease when virulence factors are appropriately
produced by the bacteria and transported (or secreted) onto the
cell surface where they become harmful,» says first author Matthew Doyle, PhD candidate in the School of Biological Sciences.
Through studies conducted in mice, Oliver M. Steinmetz, MD (University Hospital Hamburg Eppendorf, in Germany) and his colleagues have shown that the messenger protein IL - 6, which is rapidly
produced at high levels during an acute inflammatory form of kidney
disease, potently dampens activation of tissue - destructive immune
cells called macrophages.