| Progeroid syndrome (7) |  |
| Syndrome (115) | |
| Progeroid syndrome (7) | |
| Syndrome (115) | |
We investigated whether PTSD has genetic underpinnings that make some people more vulnerable to the syndrome than others."
& Biology identifies a drug candidate called DBIBB that increases the survival of mice suffering from radiation syndrome,
The findings suggest that DBIBB shows promise for becoming the first drug capable of treating acute radiation syndrome caused by the high levels of radiation released by nuclear explosions."
and porcine reproductive and respiratory syndrome. Plants have been used to produce pharmaceuticals in the past, but the crucial element at the heart of the three-year PLAPROVA project was a technique for doing this much more quickly than previously possible an advance
The syndrome occurs in up to 10 percent of premature infants and is fatal 25 to 35 percent of the time.
Clomid is prescribed often to women with polycystic ovary syndrome as a first step in their treatmentnd that population accounts for about a third of women who seek fertility treatment
Christman says. his study indicates that there is a safe and effective medical treatment to help infertility patients with polycystic ovarian syndrome,
one of a class of drugs shown in animal experiments to confer some protection from brain damage due to Fragile X syndrome,
#obbit skull points To down syndrome, not new species New analysis of a 15000-year-old skull and thigh bone shows the original descriptions of the remains may have been skewed.
Here the signs point rather clearly To down syndrome which occurs in more than one per thousand human births around the world. e
they seem to be a computational unit as well. is team plans to explore what this newly discovered dendritic role may play in brain circuitry and particularly in conditions like Timothy syndrome in
Researching the role of fragile X syndrome One heritable cause of intellectual disability and autism is fragile X syndrome,
which arises when a single gene on the X chromosome, called FMR1, is turned off during brain development.
Some of the 27 affected genes play a role in protein synthesis regulation, leading Bear and colleagues to wonder if 16p11.2 microdeletion syndrome and fragile X syndrome affect synapses in the same way.
#'Superspreading event'triggers MERS explosion in South korea SEOULUTHORITIES in South korea are scrambling to contain an outbreak of the deadly Middle Eastern respiratory syndrome (MERS.
whether viral infections can trigger diabetes or chronic fatigue syndrome. Elledge and colleagues used Virscan on more than 500 people from the United states
The worst-case scenario is the Kessler syndrome proposed by astrophysicist Donald Kessler in the 1970s.
Researching the role of fragile X syndrome One heritable cause of intellectual disability and autism is fragile X syndrome,
which arises when a single gene on the X chromosome, called FMR1, is turned off during brain development.
Some of the 27 affected genes play a role in protein synthesis regulation, leading Bear and colleagues to wonder if 16p11.2 microdeletion syndrome and fragile X syndrome affect synapses in the same way.
#Drug-infused nanoparticle is right for sore eyes For the millions of sufferers of dry eye syndrome their only recourse to easing the painful condition is to use drug-laced eye drops three times a day.
Now researchers from the University of Waterloo have developed a topical solution containing nanoparticles that will combat dry eye syndrome with only one application a week.
Dry eye syndrome is a more common ailment for people over the age of 50
What about the physical characteristics of Downs syndrome? Will the child still have mongoloid characteristics
#MERS Virus May be Able To Spread Through The Air Research strongly suggests that camels carry Middle east Respiratory Syndrome (MERS),
and locked-in syndrome to interact with the world around them by controlling a computer mouse with their mind.
but an individual with locked-in syndrome that is fully awake and conscious has no other means of producing speech move limbs
The syndrome is caused by a mutated protein called progerin which induces DNA damage, triggers premature cellular aging and slows down cell proliferation,
Sepsis is a whole-body inflammation syndrome set off when the immune system wildly overreacts to the presence of infectious pathogens.
when a patient has an outwardly similar but infection-free syndrome called sterile inflammation, an intense, systemic inflammatory response to traumatic injuries, surgery,
called The down Syndrome Biomarker Initiative (DSBI), involved twelve participants between the ages of 30 and 60 with Down syndrome,
Military applications include research on Gulf war syndrome, traumatic brain injury, and posttraumatic stress disorder. r
#Royal Navy could soon be using remote-controlled warships with'see-through'hulls Sleek and stealthy, it resembles something from Star wars. In fact,
In children with one of those conditions, autoimmune lymphoproliferative syndrome (ALPS), all the patients showed a durable, complete response, with normal blood cell counts and rapid improvements,
"These results suggest that inhibition of the enzyme cgas may be an effective therapy for autoimmune diseases such as Aicardi-Goutieres Syndrome (AGS) and systemic lupus erythematosus (SLE),
This treatment is particularly effective in children with autoimmune lymphoproliferative syndrome (ALPS), a chronic genetic disorder characterized by the buildup of white blood cells in the organs.
"In an intensive care setting, the technology has the potential to be used to make an early diagnosis of locked-in syndrome (LIS),
and Asperger syndrome, suggesting that the developmental effects of DISC1 could also be important for understanding these mental health conditions.
In an intensive care setting, the technology has the potential to be used to make an early diagnosis of locked-in syndrome (LIS),
of the disorder (fragile X syndrome and tuberous sclerosis 1 and 2). They discovered that a cellular calcium signaling process involving the inositol trisphosphate receptor was altered very much.
ranging from simple throat and skin infections to life-threatening invasive conditions such as necrotizing fasciitis (lesh-eating disease and toxic shock syndrome.
#New gene therapy success in a rare disease of the immune system Wiskott-Aldrich syndrome is a rare congenital immune and platelet deficiency
"Frdric Revah, CEO of Genethon, the laboratory of the AFM-Telethon and the trial sponsor, said"These first results of our clinical trial for the treatment of Wiskott Aldrich syndrome are very encouraging.
Mutations in this gene also cause a rare human disease called the Nail-patella syndrome (NPS
In an intensive care setting, the technology has the potential to be used to make an early diagnosis of locked-in syndrome (LIS),
#Research breakthrough in fight against muscle wasting diseases It is estimated that half of all cancer patients suffer from a muscle wasting syndrome called cachexia.
'Complex array of mutations found in rare, aggressive leukemia Sezary syndrome (SS), an aggressive leukemia of mature T cells, is complicated more at a molecular level than ever suspected, according to investigators from the Perelman School of medicine at the University of Pennsylvania.
Sezary syndrome is a rare condition: Its incidence is estimated to be about 0. 3-2 cases per 100,000 in the United states each year,
An identical effect was observed in flies with Leigh syndrome, a rare neurological disorder caused by a severe mitochondrial defect,
such as premature ovarian failure and polycystic ovarian syndrome, conditions that both result in hormone imbalances and infertility in women.
without any diagnosis other than udden infant death syndrome'says Karl Swärd and Catarina Rippe, researchers at Lund University.
phantom limb syndrome and other nervous systems disorders where the brain has overreacted to the loss of normal inputs.
of the disorder (fragile X syndrome and tuberous sclerosis 1 and 2). They discovered that a cellular calcium signaling process involving the inositol trisphosphate receptor was altered very much.
In tumor lysis syndrome, the body is overwhelmed by toxic substances released when many tumor cells die in rapid succession.
This provides an explanation for how cellular processes go awry in both Shwachman-Diamond syndrome and one in 10 cases of T-cell acute lymphoblastic leukaemia.
All patients who received the CTL019 hunter cells experienced a cytokine release syndrome (CRS) within a few days after receiving their infusions--a key indicator that the engineered cells have begun proliferating and killing tumor cells in the body.
In addition to short-term complications such as feeding intolerance intestinal obstruction and short-bowel syndrome surviving infants have poorer neurodevelopmental outcomes
#Cushings syndrome: Researchers characterize new tumor syndrome Scientists at the Luxembourg Centre for Systems Biomedicine (LCSB) of the University of Luxembourg have published their findings that mutations in a gene known as ARMC5 promote the growth of benign tumors in the adrenal glands
and on the meninges: ARMC5 appears to belong to the group of so-called tumor suppressor genes.
The results on this tumor syndrome obtained by the group of Dr. Patrick May and PD.
whether the gene and the metabolic pathways it influences offer new approaches for treating the tumor syndrome.
Changes in transcription factor 4 (TCF4) cause 18q21 deletion syndrome which is characterized by intellectual disability and psychiatric problems and mutations in euchromatic histone methyltransferase 1 (EHMT1) cause similar symptoms in a disease known as 9q34 deletion syndrome.
Interfering with the activity of TCF4 or EHMT1 produced similar molecular effects in the cells.
Luckily, experimental products that combat cute radiation syndrome (ARS) have already been tested in people and could be on the cusp of market approval, Nature Medicine reports.
Families affected by Phelan-Mcdermid syndrome, a rare condition in which a deletion on chromosome 22 causes problems such as learning and memory deficits, are building a database of information from genomic tests, clinical medical records, extensive family surveys and histories,
#Genome Editing to Reverse Bubble Boy Syndrome Researchers used an emerging technique to correct the gene behind a fatal immune system disorder in an infant.
researchers in Milan treated a condition known as Severe Combined Immunodeficiency Syndrome, or SCID (this condition is referred sometimes to as ubble boy diseasebecause children afflicted may live in protected environments
Among others, these include people with nonverbal autism, people with nonverbal learning disorders, people with ALS, people with Rett Syndrome,
In the most severe cases, bacterial poisoning causes severe disease and syndromes like sepsis, meningitis, pneumonia,
#South korea Reports its First 2 Deaths From MERS Virus South korea on Tuesday confirmed the country's first two deaths from Middle east Respiratory Syndrome as it fights to contain the spread of a virus that has killed hundreds
Authorities are scrambling to control the spread of the illness, known fully as the Middle east Respiratory Syndrome.
and it may provide patients the chance to perform early action treatment. t is important that women with the MEN1 syndrome now know that they have to be aware that they run the risk of developing breast cancer,
and Tourette syndrome. Dr Penny Whiting, from the University of Bristol, and her team evaluated the evidence for benefits and adverse events, related to medicinal cannabis use.
weight gain in HIV, sleep disorders and Tourette syndrome. And there was very-low quality evidence the drug eased anxiety.
and Tourette syndrome are required.''Further studies evaluating cannabis itself are required also because there is very little evidence on the effects and adverse effects of cannabis.'
#Rare case uncovers missing clue to Fragile X Fragile X syndrome may not only be a problem of receivers in the brain letting in too much information.
GENETIC ERROR Fragile X syndrome results from an inherited genetic error in a gene called FMR1.
so the syndrome affects males more often and more severely than females, who may be able to compensate for the genetic error
One of the mysteries of the syndrome is how loss of a single gene can lead to such a variety of effects in different patients.
the researchers genetic sequencing data from more than 900 males with intellectual disabilities but without classic fragile X syndrome.
his physical features are not typical of the syndrome, and he is not autistic. To see what effect this mutation might have,
who is also an associate professor of biomedical engineering. his patient presents a case of partial fragile X syndrome associated with mutated, rather than absent, FMRP.
an injection drug indicated for long-term treatment of adults with short bowel syndrome (SBS) who need parenteral support.
and ensure we continue to transform the lives of patients with short bowel syndrome, hypoparathyroidism,
#Scientists Devise Promising Strategy to Tackle MERS A Purdue University-led team of scientists studying the Middle east Respiratory Syndrome (MERS) reports that it found molecules that shut down the activity of an essential enzyme
chronic fatigue syndrome that researchers suspect may be caused by a virus but haven't proven for sure to have a viral origin.
This condition is the basis of some syndromes and neurological diseases.""If we can stimulate the remaining gene to work harder,
It could also be used to identify links between viral infections and mysterious diseases like chronic fatigue syndrome.
For example, Elledge's team will be collaborating with another group to test people with chronic fatigue syndrome,
and Afghanistan veterans with post-concussive syndrome and post-blast military brain injury. Estimates from the Centers for Disease Control and Prevention state about 2. 5 million U s. emergency department visits were associated with traumatic brain injury in 2010 with rates increasing by about 70 percent over the previous decade.
Oliver Mcfarlane Syndrome (OMS her unknown mutation sparked an international gene hunt. Comparing her genome to others with OMS and Leber congenital amaurosis (LCA),
Tissue-engineered small intestine (TESI) grows from stem cells contained in the intestine and offers a promising treatment for short bowel syndrome (SBS) a major cause of intestinal failure particularly in premature babies and newborns with congenital intestinal anomalies.
causing either advanced sleep syndrome or delayed sleep syndrome. There is also a growing body of evidence showing that environmental changes affecting circadian rhythms
In the most severe cases, bacterial poisoning causes severe disease and syndromes like sepsis, meningitis, pneumonia,
The researchers further found that the regulation of GLUT1 by PKC was impaired in some patients with a genetic disease called GLUT1 Deficiency Syndrome (G1d.
cancer Plants can undergo the same extreme'chromosome shattering'seen in some human cancers and developmental syndromes,
and Lesch-Nyhan syndrome. However studying mda neurons and neocortical neurons in isolation does not reveal much data about how these cells actually interact in these conditions.
In extreme cases, it leads to sepsis induced systemic inflammatory response syndrome, which can be fatal
and inadvertently triggered the biggest outbreak of Middle east Respiratory Syndrome (MERS) outside that region, and what is verging on national panic at home.
Many of the diseases affecting the commercial swine industry involve complex syndromes caused by multiple pathogens
and polymicrobial. hese multiple bacteria and viruses end up in a disease syndrome. Wee looking at a complex situation
tuberous sclerosis and Hirschsprung disease. hese observations may help to explain certain human disease syndromes in which abnormalities of the nervous system appear to be associated, for previously unclear reasons,
By comparing cells from CS patients and from patients with another, related syndrome causing only UV hypersensitivity,
and perhaps eating disorders, attention deficit-hyperactivity disorder, Tourette syndrome, and Lesch-Nyhan syndrome. However, studying mda neurons and neocortical neurons in isolation does not reveal much data about how these cells actually interact in these conditions.
This new capability to grow and interconnect two types of neurons in vitro now provides researchers with an excellent model for further study. his method,
#Risk of bowel cancer reduced by taking aspirin for Lynch syndrome patients An international study led by The University of Melbourne has confirmed that long-term regular taking of aspirin
or ibuprofen reduces the risk of bowel cancer by more than half for people with the genetic mutation causing Lynch syndrome.
At least 1 in 1000 people in the population have the genetic mutation that causes Lynch syndrome.
and Dr Aung Ko Win from the School of Population and Global Health confirmed that those with Lynch syndrome who took aspirin regularly were less likely to develop bowel cancer than Lynch syndrome patients who did not take aspirin.
The research team also uncovered a new finding that Lynch syndrome patients who took ibuprofen regularly,
Also, we were able to show the similar protective effect of ibuprofen such as Nurofen on bowel cancer for people with Lynch syndrome,
motor neurone disease or locked in syndrome the ability to control digital media by thought alone, according to Cyrus Saihan,
< Back - Next >
Overtext Web Module V3.0 Alpha
Copyright Semantic-Knowledge, 1994-2011