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Monthly Archives: October 2014
tsunamaru – Orange Genome [gudbye] +DT – Video
Posted: October 15, 2014 at 9:45 am
tsunamaru - Orange Genome [gudbye] +DT
MAP : https://osu.ppy.sh/b/218944?m=0.
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What Is The Definition Of Human Genome Project – Video
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What Is The Definition Of Human Genome Project
Visit our website for text version of this Definition and app download. http://www.medicaldictionaryapps.com Subjects: medical terminology, medical dictionar...
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Fly Genome Could Help Us Improve Health And Our Environment
Posted: at 9:45 am
October 14, 2014
Provided by Alanna Orpen, BioMed Central
The house fly might be a worldwide pest, but its genome will provide information that could improve our lives. From insights into pathogen immunity, to pest control and decomposing waste, the 691 Mb genome has been sequenced and analyzed by a global consortium of scientists, and is published in the open access journal Genome Biology.
The genome highlights detoxification and immune system genes that are unique to the insect, and could be subjects of further study to help humans deal with toxic and disease causing environments.
The house fly (Musca domestica) lives on human and animal waste. They are an important species for scientific study because of their roles as waste decomposers and as carriers of over 100 human diseases, including typhoid, tuberculosis and worms. Fly transmitted trachoma alone causes 6 million cases of childhood blindness each year.
Because the house fly is so intimately involved in human processes, the researchers say sequencing its genome will have implications for human health, identifying the genes that allow the flies to live in toxic environments.
The lead author of the paper Jeff Scott, Cornell University, says: House flies are a fascinating insect for scientists in many areas, such as developmental biology, sex determination, immunity, toxicology and physiology. The completed genome will be a phenomenal tool for researchers in all of these fields and will facilitate rapid advancements
The consortium of scientists sequenced the genomes of six female houseflies, creating a 691 Mb long sequence. They compared it to the 123 Mb Drosophila melanogaster genome, to give an indication of the genes that were unique to house fly, and could be candidates for further study.
The comparison showed that the fly had many more immune genes, and that these were of a higher diversity than in the Drosophila genome. Understanding how this fly is immune to the human diseases it carries could help scientists to create treatments or vaccines for these diseases.
The fly genome also contained unique detoxification genes, which produce proteins that help the fly break down waste. Information about these genes could help us to handle human waste and improve the environment.
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Fly Genome Could Help Us Improve Health And Our Environment
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Fly genome could help improve health, environment
Posted: at 9:45 am
The house fly might be a worldwide pest, but its genome will provide information that could improve our lives. From insights into pathogen immunity, to pest control and decomposing waste, the 691 Mb genome has been sequenced and analyzed by a global consortium of scientists, and is published in the open access journal Genome Biology.
The genome highlights detoxification and immune system genes that are unique to the insect, and could be subjects of further study to help humans deal with toxic and disease causing environments.
The house fly (Musca domestica) lives on human and animal waste. They are an important species for scientific study because of their roles as waste decomposers and as carriers of over 100 human diseases, including typhoid, tuberculosis and worms. Fly transmitted trachoma alone causes 6 million cases of childhood blindness each year.
Because the house fly is so intimately involved in human processes, the researchers say sequencing its genome will have implications for human health, identifying the genes that allow the flies to live in toxic environments.
The lead author of the paper Jeff Scott, Cornell University, says: "House flies are a fascinating insect for scientists in many areas, such as developmental biology, sex determination, immunity, toxicology and physiology. The completed genome will be a phenomenal tool for researchers in all of these fields and will facilitate rapid advancements"
The consortium of scientists sequenced the genomes of six female houseflies, creating a 691 Mb long sequence. They compared it to the 123 Mb Drosophila melanogaster genome, to give an indication of the genes that were unique to house fly, and could be candidates for further study.
The comparison showed that the fly had many more immune genes, and that these were of a higher diversity than in the Drosophila genome. Understanding how this fly is immune to the human diseases it carries could help scientists to create treatments or vaccines for these diseases.
The fly genome also contained unique detoxification genes, which produce proteins that help the fly break down waste. Information about these genes could help us to handle human waste and improve the environment.
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The above story is based on materials provided by BioMed Central. Note: Materials may be edited for content and length.
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Fly genome could help improve health, environment
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Fly genome could help us improve our health and environment
Posted: at 9:45 am
The house fly might be a worldwide pest, but its genome will provide information that could improve our lives. From insights into pathogen immunity, to pest control and decomposing waste, the 691 Mb genome has been sequenced and analyzed by a global consortium of scientists, and is published in the open access journal Genome Biology.
The genome highlights detoxification and immune system genes that are unique to the insect, and could be subjects of further study to help humans deal with toxic and disease causing environments.
The house fly (Musca domestica) lives on human and animal waste. They are an important species for scientific study because of their roles as waste decomposers and as carriers of over 100 human diseases, including typhoid, tuberculosis and worms. Fly transmitted trachoma alone causes 6 million cases of childhood blindness each year.
Because the house fly is so intimately involved in human processes, the researchers say sequencing its genome will have implications for human health, identifying the genes that allow the flies to live in toxic environments.
The lead author of the paper Jeff Scott, Cornell University, says: "House flies are a fascinating insect for scientists in many areas, such as developmental biology, sex determination, immunity, toxicology and physiology. The completed genome will be a phenomenal tool for researchers in all of these fields and will facilitate rapid advancements".
The consortium of scientists sequenced the genomes of six female houseflies, creating a 691 Mb long sequence. They compared it to the 123 Mb Drosophila melanogaster genome, to give an indication of the genes that were unique to house fly, and could be candidates for further study.
The comparison showed that the fly had many more immune genes, and that these were of a higher diversity than in the Drosophila genome. Understanding how this fly is immune to the human diseases it carries could help scientists to create treatments or vaccines for these diseases.
The fly genome also contained unique detoxification genes, which produce proteins that help the fly break down waste. Information about these genes could help us to handle human waste and improve the environment.
See more at EurekAlert!
Read the study at GenomeBiology.
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Fly genome could help us improve our health and environment
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House fly genome reveals expanded immune system
Posted: at 9:45 am
PUBLIC RELEASE DATE:
14-Oct-2014
Contact: Syl Kacapyr vpk6@cornell.edu 607-255-7701 Cornell University @cornell
ITHACA, N.Y. Scientists have sequenced the house fly genome for the first time, revealing robust immune genes, as one might expect from an insect that thrives in pathogen-rich dung piles and garbage heaps.
The research, published Oct. 14 in the journal Genome Biology, will increase understanding of house fly genetics and biology and of how flies quickly adapt to resist insecticides, which could lead to novel control methods.
Adult house flies (Musca domestica) carry and transmit more than 100 human and animal diseases, including salmonellosis, anthrax, typhoid fever, tuberculosis, cholera and diarrhea as well as parasites such as pinworms, roundworms, hookworms and tapeworms. House fly larvae are important animal waste decomposers and live in close contact with many animal pathogens.
"Anything that comes out of an animal, such as bacteria and viruses, house flies can take from that waste and deposit on your sandwich," said Jeff Scott, the paper's lead author and a Cornell University professor of entomology. "House flies are the movers of any disgusting pathogenic microorganism you can think of," Scott added.
The genome, roughly twice the size of the fruit fly's genome, revealed an expanded number of immune response and defense genes. The researchers also discovered an expansion in the number of cytochrome P450s, which help the flies metabolize environmental toxins. "House flies have a lot more of these enzymes than would be expected based on other insects they are related to," said Scott, noting that the house fly's close relative, Glossina morsitans (tsetse fly), has half as many cytochrome P450s. These enzymes are more ancient than insecticides. "We don't have a clear handle on why house flies need so many," Scott said.
The M. domestica genome also revealed many genes for chemoreceptors, which detect certain chemical stimuli in the environment. These receptors are important in sensing food and moving in ways critical for survival, allowing house flies to detect a wide variety of different things, Scott said.
"If you think of the genome like a phone book, we now have the phone number of every gene," said Scott. "We now can study every gene. For any scientific question, we have a highway to get us there."
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House fly genome reveals expanded immune system
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Fly genome aids in hunt for vaccines
Posted: at 9:44 am
It's an almost unavoidable pest, but scientists are now saying the common house fly could hold the key to developing vaccines for a number of human diseases, including typhoid, tuberculosis and cholera.
Researchers at Cornell University sequenced the genomes of six female house flies, or Musca domestica, comparing them to those of the common fruit fly, or Drosophila melanogaster, which can carry bacteria but generally aren't associated with spreading human diseases.
The study, published in scientific journal Genome Biology, highlights detoxification and immune system genes apparently unique to the house fly.
Scientists believe further study could identify how those genes allow flies to break down waste and resist diseases that carry enormous consequences for humans.
"House flies are a fascinating insect for scientists in many areas, such as developmental biology, sex determination, immunity, toxicology and physiology," says lead author of the study, Dr Jeff Scott of Cornell University.
"The completed genome will be a phenomenal tool for researchers in all of these fields and will facilitate rapid advancements.
House flies carry more than 100 human diseases, as well as parasites such as worms and E. coli. Millions of children are infected with trachoma every year thanks to house flies, which have "shown a remarkable ability to rapidly evolve resistance", says Dr Scott.
This rapid evolution has given the house fly a much larger genome than its fruity cousin 691mb compared to 123mb. In comparison, the human genome is about 3000mb.
"The fly had many more immune genes, and that these were of a higher diversity than in the Drosophila genome. Understanding how this fly is immune to the human diseases it carries could help scientists to create treatments or vaccines for these diseases."
More than 90 percent of all flies that live around humans are Musca domestica, which are believed to owe their evolutionary success to their close proximity with humans.
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Fly genome aids in hunt for vaccines
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Common gene variants linked to delayed healing of bone fractures
Posted: at 9:43 am
PUBLIC RELEASE DATE:
14-Oct-2014
Contact: Matt Solovey msolovey@hmc.psu.edu 717-531-8606 Penn State @penn_state
Slow-healing or non-healing bone fractures in otherwise healthy people may be caused by gene variants that are common in the population, according to Penn State College of Medicine researchers.
"We found associations between certain gene polymorphisms and delayed fracture healing in a sample of patients," said J. Spence Reid, professor of orthopaedics and rehabilitation. "Our study was preliminary but it demonstrated the feasibility of a larger one, which we're now working to set up."
The identification of gene variants that delay fracture healing could lead to screening tests for patients with broken bones. Those patients deemed likely to experience slow healing could be given more aggressive treatment when they first reach the hospital, potentially avoiding months of debilitation.
The researchers reported their results in the Journal of Bone and Joint Surgery.
Of the eight million bone fractures in the U.S. every year, about 10 percent fail to heal normally. Smoking, diabetes, NSAID use, low vitamin D levels and old age are known risk factors, but in a significant subset of cases, unknown factors appear to be involved.
"Some fractures are slow-healing for no obvious reason, and we wondered if there is a genetic basis for those cases," said Reid.
He and his colleagues selected from their records 33 patients diagnosed with "atrophic nonunion" -- the failure of a fracture to knit together on its own within six months. As controls, they selected 29 patients whose fractures had healed normally.
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Common gene variants linked to delayed healing of bone fractures
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New Gene Therapy for "Bubble Boy" Disease Appears to be Safe, Effective
Posted: at 9:43 am
PHILADELPHIA A new form ofgene therapyfor boys with X-linked severe combined immunodeficiency syndrome (SCID-X1), a life-threatening condition also known as bubble boy disease, appears to be both effective and safe, according to an international clinical trial with sites inBoston, Cincinnati, Los Angeles, London, and Paris.
Early data published in theNew England Journal of Medicinesuggests that the therapy may avoid the late-developing leukemiaseen in a quarter of SCID-X1 patients in previous gene-therapy trials in Europe that took place more than a decade ago. Left untreated, boys with SCID-X1 usually die of infection before their first birthday.
The lab of coauthorFrederic Bushman, PhD, professor of Microbiology, from thePerelman School of Medicine at the University of Pennsylvania, carried out the deep DNA sequencing on patient specimens to track and verify distributions of integration sites of the vector.The vector used in the new trial was engineered to remove molecular signals implicated in cancers in the first trial.
Eight of nine boys recruited to date to the present trial are alive between 12 and 38 months after treatment, with no SCID-X1-associated infections. The gene therapy alone generated functioning immune systems in seven of eight boys. Genetic studies showed that the new viral vector did not lead to vector insertions near known cancer-causing genes, raising cautious hopes about the vector's long-term safety.
We showed that fewer cells accumulated with integration sites near cancer genes in the second trial, suggesting that the adverse properties had indeed been engineered out, explains Bushman So far there are no clinical adverse events in the present trial -- the integration site data has suggested improved safety.
The modified vector created for the current trial is a self-inactivating gammaretrovirus, designed to deliver its payload effectively while minimizing the chance of inadvertently turning on oncogenes that could lead to leukemia.
The core question of the trial was whether the new self-inactivating viral vector could safely and successfully shuttle a gene called theIL-2 receptor gamma(IL2RG) subunit into the patients' hematopoietic stem cells. In boys born with SCID-X1, mutations render theIL2RGgene inactive, robbing the children of the ability to produce a functional immune system.
For more information, see theDana-Farber/Boston Children's Cancer and Blood Disorders Centersnews release.
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Penn Medicine is one of the world's leading academic medical centers, dedicated to the related missions of medical education, biomedical research, and excellence in patient care. Penn Medicine consists of theRaymond and Ruth Perelman School of Medicine at the University of Pennsylvania(founded in 1765 as the nation's first medical school) and theUniversity of Pennsylvania Health System, which together form a $4.3 billion enterprise.
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New Gene Therapy for "Bubble Boy" Disease Appears to be Safe, Effective
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Gene variants implicated ADHD identify attention and language deficits general population
Posted: at 9:43 am
PUBLIC RELEASE DATE:
15-Oct-2014
Contact: Rhiannon Bugno Biol.Psych@utsouthwestern.edu 214-648-0880 Elsevier @ElsevierConnect
Philadelphia, PA, October 15, 2014 Are deficits in attention limited to those with attention-deficit/hyperactivity disorder (ADHD) or is there a spectrum of attention function in the general population? The answer to this question has implications for psychiatric diagnoses and perhaps for society, broadly.
A new study published in the current issue of Biological Psychiatry, by researchers at Cardiff University School of Medicine and the University of Bristol, suggests that there is a spectrum of attention, hyperactivity/impulsiveness and language function in society, with varying degrees of these impairments associated with clusters of genes linked with the risk for ADHD.
Viewing these functions as dimensions or spectrums contrasts with a traditional view of ADHD as a disease category.
To answer this question, researchers led by senior author Dr. Anita Thapar used genetic data from patients with ADHD as well as data from the Avon Longitudinal Study of Parents and Children (ALSPAC). The ALSPAC is based in England and is a large, ongoing study of parents and children followed since birth in the early '90s.
They created polygenic risk scores a 'composite' score of genetic effects that forms an index of genetic risk of ADHD for 8,229 ALSPAC participants.
They found that polygenic risk for ADHD was positively associated with higher levels of traits of hyperactivity/impulsiveness and attention at ages 7 and 10 in the general population. It was also negatively associated with pragmatic language abilities, e.g., the ability to appropriately use language in social settings.
"Our research finds that a set of genetic risks identified from UK patients with a clinical diagnosis of childhood ADHD also predicted higher levels of developmental difficulties in children from a UK population cohort, the ALSPAC," said Thapar.
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