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Monthly Archives: June 2017
DNA Replication Filmed for First Time Shows How Awkward and Random Genetics Is – Newsweek
Posted: June 22, 2017 at 4:47 am
Researchers at the University of California, Davis, have just reported a small but significant accomplishment: catching the replication of a single DNA molecule on video for the first time. And the footage has revealed some surprising details about this structure on which all life depends.
DNA is composed of two strands bound together in a helical shape, like a twisting ladder. These strands are made of four basesadenine, guanine, cytosine and thymine, abbreviated as A, G, C and T, respectivelystrung together in various patterns and paired in specific ways across the rungs of the ladders. A always pairs with T, and C always pairs with G. Sugar and phosphate molecules help provide architectural support to the ladder-like structure. Human DNA contains about 3 billion bases. Discrete, repeated sequences of bases form the individual genes that encode the instructions for all our working parts. And every time a cell divides, which happens incredibly often, DNA replicates so that each new cell contains a complete copy of our entire genome, or genetic blueprint.
A digital representation of the human genome. Scientists at UC Davis have discovered that DNA replication is not as smooth as they thought. Mario Tama/Getty Images
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The process of DNA replication isa tremendous source of wonder and focus forresearch. The helix must unwind and have each strand copied smoothly and quickly. An enzyme called helicase triggers the unwinding and another called primase initiates the replication process. Athird, called polymerase, travels the length of a strand, adding the requisite base pairs along the way, leaving behind a new strand. Imagine splitting a ladder down the middle and assembling matching halves so that where there was once one ladder now there are two. That is DNA replication, only in place of saws, nails, wood and glue, there are enzymes and many microscopic and complex processes. Mysteries aboundwhen it comes to thishereditary material.
To better probe those mysteries, geneticist and microbiologist Stephen Kowalcyzkowski and colleagues watched DNA from bacteria replicate. They wanted to see exactly how fast the enzymes worked on each strand.
This first-ever view, shown in the video above, revealed a surprise: replication stopped unpredictably and moved at a varying pace. "The speed can vary about 10-fold," Kowalczykowski said in a statement. The two strands also replicated at different speeds.Sometimes the copying stalled on one strand while proceeding on the other. "We've shown that there is no coordination between the strands," said Kowalczykowski. "They are completely autonomous." The process, the researchers report in their study, published in Cell, is much more random than previously suspected.
The three enzymeshelicase, primase and polymeraseare also not alwys in sync. Even if polymerase stops its replication work, helicase can keep unzipping the helix. That lack of coordination leaves the half-helix of DNA exposed and vulnerable to damage. Such exposure is known to trigger repair mechanisms within the cell. Errors in replicating DNA, while often corrected, can also result ingenetic abnormalities that in turn lead to diseases.
This new look at DNA transforms the scientific understanding about replication. "It's a real paradigm shift," saidKowalcyzkowski, "and undermines a great deal of what's in the textbooks."
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A baby’s DNA may kick off mom’s preeclampsia – Science News Magazine
Posted: at 4:47 am
A protein made by the fetus may lead to preeclampsia in moms.
People born to mothers who had the prenatal disorder were more likely to have certain DNA variationsnear a gene known to influence blood vessels. The results, published online June 19 in Nature Genetics, point to that gene as a possible preeclampsia culprit, and may help scientists develop ways to stop or prevent the pregnancy complication. Preeclampsia, which is marked by a dangerous spike in blood pressure, affects about 5 percent of pregnancies and is estimated to kill over 70,000 women a year globally.
Scientists have known that preeclampsia can run in families, but the genetics of the fetus hadnt been scrutinized. Over the years, people have looked at mothers genes, says geneticist Linda Morgan of the University of Nottingham in England. This is the first large study to look at babies genes.
Morgan and colleagues compared DNA variations in 2,658 babies, children and adults born to mothers who had preeclampsia with those in more than 300,000 people. (This large group probably included some people born to mothers with the condition, but the vast majority were not.)
A genome-wide association study (GWAS), a technique used to comb through DNA looking for genetic variations that may be linked to a disorder, pinpointed a spot on chromosome 13, near a gene called FLT1. That gene is involved with blood vessel formation, an intricate process for the placenta as it grows into the inside wall of the uterus and merges the babys blood supply to the mothers. The same genetic hot spot turned up in tests of a second group of offspring from mothers who had preeclampsia, Morgan and colleagues report. Another DNA variation near the gene also showed a link to the disorder.
Identifying FLT1 makes a lot of sense, says Ananth Karumanchi, a vascular biologist at Beth Israel Deaconess Medical Center in Boston, who was not involved in the study. Earlier experiments by Karumanchi and others suggest that the gene plays a role in preeclampsia.
Preeclampsia is kicked off by the placenta, an organ grown mostly from fetal cells that helps provide nutrients to the fetus. And though the details are unclear, some scientists suspect that unhealthy placentas start to pump out too much Flt-1 protein. A version of the protein called sFlt-1 can then slip into a mothers bloodstream, where it may damage blood vessels in a way that leads to high blood pressure.
The GWAS results cant explain the bulk of preeclampsia cases. A fetus carrying a single copy of one of the troublesome variants near FLT1 raised a mothers risk of preeclampsia by about 20 percent, the analysis suggests. Other risk factors are known to be much stronger, Morgan says, including previous high blood pressure, former preeclampsia diagnoses or carrying twins.
Karumanchi says that the genetic results might not be strong enough on their own to make the case that the gene is involved. But other work points to FLT1. We feel its the right target, he says.
In Europe, a preliminary clinical trial is testing a filtration method that removes excess sFlt-1 protein from the blood of women with signs of preeclampsia. So far, about 20 women have undergone the procedure, says nephrologist Ravi Thadhani of Massachusetts General Hospital in Boston. Early results are quite encouraging, he says, and he hopes to expand the study soon.
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DNA study reveals cats traveled with humans centuries ago – New York Post
Posted: at 4:47 am
Long before cats became the darlings of Facebook and YouTube, they spread through the ancient human world.
A DNA study reached back thousands of years to track that conquest and found evidence of two major dispersals from the Middle East, in which people evidently took cats with them. Genetic signatures the felines had on those journeys are still seen in most modern-day breeds.
Researchers analyzed DNA from 209 ancient cats as old as 9,000 years from Europe, Africa and Asia, including some ancient Egyptian cat mummies.
They are direct witnesses of the situation in the past, said Eva-Maria Geigl of the Jacques Monod Institute in Paris. She and colleagues also looked at 28 modern feral cats from Bulgaria and east Africa.
Its the latest glimpse into the complicated story of domesticated cats. They are descendants of wild ancestors that learned to live with people and became relatively tame though some cat owners would say that nowadays, they dont always seem enthusiastic about our company.
The domestication process may have begun around 10,000 years ago when people settled in the Fertile Crescent, the arch-shaped region that includes the eastern shore of the Mediterranean Sea and land around the Tigris and Euphrates rivers. They stored grain, which drew rodents, which in turn attracted wild cats. Animal remains in trash heaps might have attracted them too. Over time, these wild felines adapted to this man-made environment and got used to hanging around people.
Previous study had found a cat buried alongside a human some 9,500 years ago in Cyprus, an island without any native population of felines. That indicates the cat was brought by boat and it had some special relationship to that person, researchers say.
Cats were clearly tame by about 3,500 years ago in Egypt, where paintings often placed them beneath chairs. That shows by that time, the cat makes its way to the household, said Geigl.
But the overall domestication process has been hard for scientists to track, in part because fossils skeletons dont reveal whether a cat was wild or domesticated.
Its easier to distinguish dogs, our first domesticated animal, from their wolf ancestors. Dogs evolved from wolves that had begun to associate with people even before farming began, perhaps drawn by the food the humans left behind.
The new study tracked the spread of specific cat DNA markers over long distances through time, a sign that people had taken cats with them. Results were released Monday by the journal Nature Ecology & Evolution.
The study strengthens and refines previous work, said Carlos Driscoll of the Wildlife Institute of India. The extensive sampling of cat DNA going back so far in time is unprecedented, he said.
Researchers also looked for a genetic variant that produces the blotchy coat pattern typical of modern-day domestic cats, rather than the tiger-like stripes seen in their wild cousins. It showed up more often in samples from after the year 1300 than earlier ones, which fits with other evidence that the tabby cat markings became common by the 1700s and that people started breeding cats for their appearance in the 1800s.
Thats late in the domestication of cats, in contrast to horses, which were bred for their appearance early on, Geigl said.
Most of the study focused on the ancient dispersals of cats. In the DNA samples analyzed, one genetic signature found first in the Asian portion of Turkey and perhaps once carried by some Fertile Crescent cats showed up more than 6,000 years ago in Bulgaria.
That indicates cats had been taken there by boat with the first farmers colonizing Europe, Geigl said. It also appeared more than 5,000 years ago in Romania, as well as around 3,000 years ago in Greece.
A second genetic signature, first seen in Egypt, had reached Europe between the first and fifth centuries, as shown by a sample from Bulgaria. It was found in a seventh-century sample from a Viking trading port in northern Europe, and an eighth-century sample from Iran.
The dispersal of the cats across the Mediterranean was probably encouraged by their usefulness in controlling rodents and other pests on ships, the researchers said.
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Alleged burglar identified through DNA – Muskogee Daily Phoenix
Posted: at 4:47 am
A lost hat while fleeing police led to a DNA match and an arrest in a burglary attempt at a local storage facility.
Matthew Kelly Carpenter, 34, was allegedly caught in the act by law enforcement at the storage facility on South Cherokee Street in Muskogee in late January, according to the probable cause affidavit filed in the case Wednesday.
Carpenter fled officers, losing his hat in the progress. DNA from the hat was sent to the Oklahoma State Bureau of Investigation for testing, and it came back as a match to Carpenter, the court documents state.
He has two prior convictions of second-degree burglary, according to supplemental information filed with the charges.
Carpenter was arrested Tuesday and is held without bond on four charges of second-degree burglary and two charges of attempted second-degree burglary, according to court documents.He returns to court June 26.
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Researchers find new mechanism for genome regulation – Phys.org – Phys.Org
Posted: at 4:46 am
June 21, 2017 Liquid-like fusion of heterochromatin protein 1a droplets in the embryo of a fruit fly. Credit: Amy Strom/Berkeley Lab
The same mechanisms that quickly separate mixtures of oil and water are at play when controlling the organization in an unusual part of our DNA called heterochromatin, according to a new study by researchers at the Department of Energy's Lawrence Berkeley National Laboratory (Berkeley Lab).
Researchers studying genome and cell biology provide evidence that heterochromatin organizes large parts of the genome into specific regions of the nucleus using liquid-liquid phase separation, a mechanism well known in physics but whose importance for biology has only recently been revealed.
They present their findings June 21 in the journal Nature, addressing a long-standing question about how DNA functions are organized in space and time, including how genes are regulated to be silenced or expressed.
"The importance of DNA sequences in health and disease has been clear for decades, but we only recently have come to realize that the organization of sections of DNA into different physical domains or compartments inside the nucleus is critical to promote distinct genome functions," said study corresponding author, Gary Karpen, senior scientist at Berkeley Lab's Biological Systems and Engineering Division.
The long stretches of DNA in heterochromatin contain sequences that, for the most part, need to be silenced for cells to work properly. Scientists once thought that compaction of the DNA was the primary mechanism for controlling which enzymes and molecules gain access to the sequences. It was reasoned that the more tightly wound the strands, the harder it would be to get to the genetic material inside.
That mechanism has been questioned in recent years by the discovery that some large protein complexes could get inside the heterochromatin domain, while smaller proteins can remain shut out.
In this new study of early Drosophila embryos, the researchers observed two non-mixing liquids in the cell nucleus: one that contained expressed genes, and one that contained silenced heterochromatin. They found that heterochromatic droplets fused together just like two drops of oil surrounded by water.
In lab experiments, researchers purified heterochromatin protein 1a (HP1a), a main component of heterochromatin, and saw that this single component was able to recreate what they saw in the nucleus by forming liquid droplets.
"We are excited about these findings because they explain a mystery that's existed in the field for a decade," said study lead author Amy Strom, a graduate student in Karpen's lab. "That is, if compaction controls access to silenced sequences, how are other large proteins still able to get in? Chromatin organization by phase separation means that proteins are targeted to one liquid or the other based not on size, but on other physical traits, like charge, flexibility, and interaction partners."
The Berkeley Lab study, which used fruit fly and mouse cells, will be published alongside a companion paper in Nature led by UC San Francisco researchers, who showed that the human version of the HP1a protein has the same liquid droplet properties, suggesting that similar principles hold for human heterochromatin.
Interestingly, this type of liquid-liquid phase separation is very sensitive to changes in temperature, protein concentration, and pH levels.
"It's an elegant way for the cell to be able to manipulate gene expression of many sequences at once," said Strom.
Other cellular structures, including some involved in disease, are also organized by phase separation.
"Problems with phase separation have been linked to diseases such as dementia and certain neurodegenerative disorders," said Karpen.
He noted that as we age, biological molecules lose their liquid state and become more solid, accumulating damage along the way. Karpen pointed to diseases like Alzheimer's and Huntington's, in which proteins misfold and aggregate, becoming less liquid and more solid over time.
"If we can better understand what causes aggregation, and how to keep things more liquid, we might have a chance to combat these types of disease," Strom added.
The work is a big step forward for understanding how DNA functions, but could also help researchers improve their ability to manipulate genes.
"Gene therapy, or any treatment that relies on tight regulation of gene expression, could be improved by precisely targeting molecules to the right place in the nucleus," says Karpen. "It is very difficult to target genes located in heterochromatin, but this understanding of the properties linked to phase separation and liquid behaviors could help change that and open up a third of the genome that we couldn't get to before."
This includes targeting gene-editing technologies like CRISPR, which has recently opened up new doors for precise genome manipulation and gene therapy.
Explore further: Discovery of a novel chromosome segregation mechanism during cell division
More information: Amy R. Strom et al, Phase separation drives heterochromatin domain formation, Nature (2017). DOI: 10.1038/nature22989
When cells divide, chromosomes need to be evenly segregated between daughter cells. This equal distribution of chromosomes is very important to accurately pass on genetic information to the next generation. Abnormal chromosomal ...
Scientists have found a new function of the nuclear membrane, the envelope that encases and protects DNA in the nucleus of a cell - it fixes potentially fatal breaks in DNA strands.
An organelle called the nucleolus resides deep within the cell nucleus and performs one of the cell's most critical functions: it manufactures ribosomes, the molecular machines that convert the genetic information carried ...
Scientists at The Scripps Research Institute (TSRI) have solved a cellular mystery that may have important implications for fundamental biology and diseases like ALS. Their new research suggests that RNA may be the secret ...
Research led by the Babraham Institute with collaborators in the UK, Canada and Japan has revealed a new understanding of how an open genome structure supports the long-term and unrestricted developmental potential in embryonic ...
Cell biologists believe that gene expression in eukaryotic cells is partly controlled by the uneven distribution of DNA in the nucleus. Colin Stewart and Audrey Wang at the A*STAR Institute of Medical Biology, Singapore, ...
Have you ever heard of biofilms? They are slimy, glue-like membranes that are produced by microbes, like bacteria and fungi, in order to colonize surfaces. They can grow on animal and plant tissues, and even inside the human ...
The absence of a single dominant bumblebee species from an ecosystem disrupts foraging patterns among a broad range of remaining pollinators in the systemfrom other bees to butterflies, beetles and more, field experiments ...
Humans possess many cognitive abilities not seen in other animals, such as a full-blown language capacity as well as reasoning and planning abilities. Despite these differences, however, it has been difficult to identify ...
The common understanding of evolution is that it is a battle for survival: one must either "scrunch or be scrunched," as Nicodemus Boffin, the Dickens' character, famously says.
The same mechanisms that quickly separate mixtures of oil and water are at play when controlling the organization in an unusual part of our DNA called heterochromatin, according to a new study by researchers at the Department ...
Gelada malesa close relative to baboonspay attention to the loud calls of a rival to gain information about his relative fighting ability compared to themselves, a new study indicated.
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Genes that affect diseases and other traits may be scattered across genome – Scope (blog)
Posted: at 4:46 am
Biomedical researchers tend to envision genes for traits from height to Alzheimers disease as being clustered in a limited number of pathways.
Two assumptions have guided this perspective: that specific traits or diseases are influenced by a few dozen genes andthat this limited menu of genes tends to be governed bymolecular pathways known to be associated with the disease.
For example, researchers might look for genes promoting diabetes in molecular pathways associated with sugar metabolism. Similarly, a hunt for genes that increase the risk for Alzheimers would focus on pathways active in the brain.
But while those assumptions make intuitive sense, Jonathan Pritchard, PhD, professor of genetics and of biology, said he has found that data dont always agree.
Recently, Pritchard and colleagues (shown above) published apaper in Cellsuggesting that the bulk of the inheritance of complex traits comes not from those few dozen core genes but from thousands of gene variants scattered across the genome. Graduate student Evan Boyle and postdoctoral scholar Yang Li, PhD, share lead authorship.
As Ireported in anews release:
The gene activity of cells is so broadly networked that virtually any gene can influence disease, the researchers found. As a result, most of the heritability of diseases is due not to a handful of core genes, but to tiny contributions from vast numbers of peripheral genes that function outside disease pathways.
Any given trait, it seems, is not controlled by a small set of genes. Instead, nearly every gene in the genome influences everything about us. The effects may be tiny, but they add up.
Its an interesting perspective, one that is sure to spur a host of inquiries.
Previously:New technique offers glimpse at human evolution in action,Genetics: A look back at the first 100 years,Computing our evolution Photo by Steve Fisch
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Human Longevity, Inc. Announces … – finance.yahoo.com
Posted: at 4:46 am
SAN DIEGO, June 15, 2017 /PRNewswire/ --Human Longevity, Inc. (HLI), the genomics-powered, health intelligence company, announced today that the company has signed an agreement with Merck KGaA, Darmstadt, Germany, which operates its biopharmaceutical business as EMD Serono in the U.S. and Canada, with the goal of pioneering the application of advanced genomics and expert analysis with machine learning to transform drug development and medical use of next generation therapeutics. As part of the agreement, the companies have started a joint pilot project to identify treatment response biomarker signatures in patients with advanced melanoma. Financial terms of the deal were not disclosed.
Human Longevity, Inc. (PRNewsFoto/Human Longevity, Inc.)
Cindy Collins, HLI CEO said, "Our agreement with Merck KGaA, Darmstadt, Germany will enable us to work together to discover novel insights that improve patient survival in melanoma, the deadliest form of skin cancer. With more than 230,000 new cases of melanoma diagnosed worldwide each year, and rates on the rise for the last 30 years, we believe our first pilot project is of great importance for society and look forward to working with Merck KGaA, Darmstadt, Germany to impact the treatment of melanoma."
In the pilot project, Merck KGaA, Darmstadt, Germany and HLI are working together to identify treatment response biomarkers in patients with locally advanced or metastatic NRAS mutated cutaneous melanoma that preferentially respond to Merck KGaA Darmstadt, Germany's MEK1/2 inhibitor, pimasertib. To enable this goal, HLI is generating genomic sequencing data from clinical trial participants' tumor and germline and utilizing its machine learning and analytical tools and expertise to interpret and analyze this data in the context of survival and other clinical data.
HLI is building the world's largest database of genomic, phenotypic, and clinical information. HLI has sequenced approximately 40,000 high-quality genomes and is building an unparalleled database of genomic and phenotypic integrated health records. HLI's customers include pharmaceutical and biotechnology companies, life insurance companies, large academic medical centers, physicians and individuals.
About Human Longevity, Inc
Human Longevity, Inc. (HLI) is the genomic-based, health intelligence company empowering proactive healthcare and enabling a life better lived. HLI combines the largest database of genomic and phenotypic data with machine learning to drive discoveries and revolutionize the practice of medicine. HLI's business areas include the HLI Health Nucleus, a genomic powered clinical research center which uses whole genome sequence analysis, advanced clinical imaging and innovative machine learning, along with curated personal health information, to deliver the most complete picture of individual health; HLIQ Whole Genome and HLIQ Oncology. For more information, please visit http://www.humanlongevity.com or http://www.healthnucleus.com.
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Men With This Genetic Mutation May Live 10 Years Longer – – Vital Updates
Posted: at 4:46 am
Males with a singular genetic mutation are likely to live about 10 years longer than their peers without the change, shows a new study appearing in the journal Science Advances.
Researchers have linked a mutation in the growth hormone receptor (GHR) gene to longer life in a number of populations, ranging from Ashkenazi Jews to Pennsylvania Amish.
Our study provides the first consistent evidence linking the GHR to human longevity, report the study authors from the Albert Einstein College of Medicine in New York City and other institutions.
The authors believe that their findings may support interventions on a genetic level that can impact the human lifespan.
These results may have implications in devising precision medicine strategies, such as GH-related interventional therapies in the elderly, the authors write.
The new findings come as one of the first clear associations between a populations genetic makeup and overall lifespan. Much previous work on population-level DNA has come up empty.
Its been a real disappointment, Nir Barzilai, a geneticist at Albert Einstein College of Medicine who led the current study, told the New York Times.
Yet researchers have begun to take cues from approachable physical evidence, rather than first burrowing deep into the genome to try to find the magical gene thats tied to a longer life.
Related:Running May Increase Life Expectancy
If you look at dogs, flies, mice, whatever it is, smaller lives longer, Gil Atzmon, a geneticist at the University of Haifa in Israel, explained to the New York Times.
That observation has led researchers to investigate growth hormone, a substance created in the brain that is directly tied to human growth and size. At a microscopic level, growth hormone attaches to cell molecules via the growth hormone receptor, and this connection guides the ability of the body to keep or stop growing.
The next step in comparing a persons size to longevity took the researchers on a course through history.
The researchers decided to investigate a specific population Ashkenazi Jews (AJ), whose history gave the researchers something of a clean slate from which to work.
To a large extent, this population exhibits both cultural and genetic homogeneity. For these reasons, the AJ population has been successfully used in the discovery of many disease-associated genes, report the study authors.
Among this population, most of whom were born or migrated to the United States in the years preceding World War II, the link between the GHR gene and longevity held true the genetic mutation was present in about 12 percent of men who were over the age of 100. Among those 70 years old, the rate of the GHR mutation was about three times less.
When observing data from an Amish population in Pennsylvania and a group of notably long-living people in France, the researchers found the same genetic trends the GHR mutation was again linked to longevity.
Although numerous genes have been shown to influence longevity, certain genes appear to affect life span across diverse organisms, conclude the researchers, who believe that plausible therapies are not too far off.
Richard Scott is a health care reporter focusing on health policy and public health. Richard keeps tabs on national health trends from his Philadelphia location and is an active member of the Association of Health Care Journalists.
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Cat Zingano on fighting Holly Holm next: ‘Hell yes’ – MMA Fighting
Posted: at 4:46 am
While Cat Zingano continues down the road to recovery, she cant help but think about whats next.
First, she expressed interest in fighting Cris Cyborg Justino at a later date. But after Holly Holms impressive win over Bethe Correia last Saturday in Singapore, the former UFC womens bantamweight contender said shed be interested in fighting Holm, too.
I'm excited to see Holly do as well as she did against Bethe, Zingano said. I'm always a fan of watching (Bethe) get humbled, in that case it was instant. You have to give it to Holly, she's amazing at implementing a gameplan.
Recently, I was asked about fighting her and for it to be in contention of possibly fighting the winner of Cyborg (Justino) vs. (Megan) Anderson. My answer is hell yes. As soon as my body is ready to safely go back in there, the heads will be rolling once again. The results and trials of the treatments Im focusing on are responding and that makes me happy to hear as an athlete, as well as a normal human. Longevity in health and sport are both my top priorities, as well as in the interest of the UFC, who is providing me huge support at this time.
Zingano declined to disclose whats ailing her right now and said shes unclear when she can return just yet because its dependent on these treatments.
The 34-year-old Zingano (9-2) hasnt fought since UFC 200 last July. She hasnt won since UFC 178 in September 2014 when she defeated Amanda Nunes, who is now the UFC womens bantamweight champion.
Justino vs. Anderson, for the now-vacant UFC womens featherweight title was officially booked earlier this week for UFC 214 on July 29.
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Cat Zingano on fighting Holly Holm next: 'Hell yes' - MMA Fighting
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eczema in children – ACAAI – ACAAI Public Website
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Eczema, also known as atopic dermatitis, is often associated with food allergy; approximately 37 percent of young children with moderate to severe eczema also have food allergies. However, scientists are still investigating the exact nature of this relationship do food allergies cause eczema or vice-versa?
Eczema is a non-contagious, inflammatory skin condition that is characterized by itching, redness, and scaly rashes. These symptoms can be painful, cause skin coloring changes, and blisters. Symptoms of eczema often appear on the arms, legs, hands, and face. The itch associated with eczema can be severe, often interrupting sleep. Scratching of the skin may lead to an infection. Infants who have eczema may rub against bedding or other things in an attempt to relieve the itch.
Eczema most commonly presents before the age of 5, but adolescents and adults can also develop this condition. About 60 percent of patients will experience symptoms of atopic dermatitis by age 1, and another 30 percent will experience symptoms by age 5. Children born into families that have a history of allergic diseases such as asthma or hay fever are at an increased risk for eczema developing.
Eczema is considered to be part of the atopic march. The atopic march involves the diagnosis of eczema, food allergy, allergic rhinitis, and asthma, typically in that sequential order.
There is documented association between food allergy and eczema among young children. It is recommended that children under the age of 5 who have moderate to severe eczema be evaluated for milk, egg, peanut, wheat, and soy allergies, if the child continues to have eczema even after treatment. Testing is also recommended when the child has a history of reaction after eating a specific food.4 An allergist can help identify which foods, if any, to eliminate from your childs diet.
Scientistshave found that people who have Filaggrin deficiency (Filaggrin is a protein found in the outermost layer of the skin; some people have a gene mutation that causes Filaggrin deficiency) are at risk for developing atopic eczema the presence of this gene defect is also believed to increase the risk of developing food allergy.
Children and adults diagnosed with eczema can manage this condition with the guidance of an allergist. In cases of moderate or severe eczema, an allergist may recommend prescription medication, including topical steroids and/or antihistamine. Milder cases may be treated with ointments and moisturizers. People with eczema should avoid harsh cleansers, drink water often, wear gloves in cold weather, and avoid wearing materials such as wool, which could irritate the skin.
Flare-ups of eczema can be caused by foods, cosmetics, soaps, wool, dust mites, mold, pollen, dog or cat dander, dry climate, and other variables.
Will the symptoms of eczema improve?
Eczema is a chronic condition, and the symptoms can come and go. The symptoms are treatable. Talk to your allergist about topical ointments or creams that can be applied to the skin. You can also help manage your eczema with regular moisturizing after baths and showers, avoiding things may that trigger a flare up (pollen or animal dander, for example), avoiding extremes in humidity levels, using non-perfumed soaps, and wearing loose-fitting, soft cotton clothing.
Is all eczema the same?
No. We have mainly discussed atopic dermatitis, also known as atopic eczema. Many other types of inflammatory skin conditions are also part of the eczema family. One such example is contact dermatitis, which is caused by direct contact with substances such as latex, detergents, perfumes, and a host of other allergens and substances to which an individual has developed sensitivities.
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