Sentences with phrase «genetic study published»

A large - scale genetic study published in The Lancet in 2012 found no relationship between gene variants that increased HDL and the likelihood of heart attack (though this research did not evaluate the SCARB1 variants).

Not exact matches

Turns out, these flavor changes happen on a genetic level, according to a study published this month in the journal Proceedings of the National Academy of Science.

These genetic regulators may be the reason ho - mose - xuality persists in nature despite the fact that gay people are less likely to reproduce, suggests the new study published in the (Dec, 2012) journal ** The Quarterly Review of Biology **.

These genetic regulators may be the reason homosexuality persists in nature despite the fact that gay people are less likely to reproduce, suggests the new study published in the [Dec, 2012] journal The Quarterly Review of Biology.

His book The Evolution of Early Christianity a Genetic Study of First Century Christianity in Relation to its Religious Environment, published in 1914, was a manifesto of the socio - historical programme.

Blood pressure responses to high and low salt intakes may share similar genetic control mechanisms, according to a new study published in the Journal of Human Hypertension.

With co-authors John C. Besley (Michigan State University) and Joseph Steinhardt (Cornell), McComas will publish study results as «Factors influencing U.S. consumer support for genetic modification to prevent crop disease» in the July 2014 journal Appetite — right about the time airborne P. infestansspores are drifting through home - garden tomato crops.

Goebel is also co-author of a 2015 study published in Science that brings together genetic and archaeological data to end speculation.

The study, published in todays edition of the Proceedings of the National Academy of Sciences, tracked 308 subjects older than 90 in an attempt to find a genetic component to longevity.

Shortly after he published his gay brothers study, Hamer completed a similarly designed family study looking into a genetic cause for a certain kind of anxiety.

In this new study published in Nature, Alexandra Van Keymeulen and colleagues used state of the art genetic mouse models to identify the cellular origin of PIK3CA and p53 induced breast tumors.

Genetic alterations that can be modulated by stress have been identified in children at high risk for bipolar disorder, according to a recently published study by researchers at McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth).

In a new study published in The Quarterly Review of Biology, Dr. Karen Hardy and her team bring together archaeological, anthropological, genetic, physiological and anatomical data to argue that carbohydrate consumption, particularly in the form of starch, was critical for the accelerated expansion of the human brain over the last million years, and coevolved both with copy number variation of the salivary amylase genes and controlled fire use for cooking.

The results of the study, led by Postdoctoral Research Fellow Dr Laura Langan and Professor of Genetic Toxicology & Ecotoxicology Awadhesh Jha, are published in Biology Open.

In a new study now published in the latest edition of the scientific journal PNAS, Bárbara Parreira and Lounès Chikhi from Instituto Gulbenkian de Ciência (IGC; Portugal) show that social structure is important to maintain the genetic diversity within species.

The study, published in August in Nature Genetics, analyzed the genetic variations of 75,607 individuals who reported having depression, and 231,747 healthy controls.

An international study published in the Journal of the National Cancer Institute has identified a genetic connection to the aggressive form of prostate cancer.

Some scientists studying the genetic makeup of the West African Ebola strain were slow to share their data with others, perhaps fearful that they would lose their right to publish their findings in a major scientific journal.

While much research has highlighted the risk of genetic mutations passed along by older mothers, studies published this year flagged a similar risk for older fathers.

A study published in Nature Communications, led by the Max Delbrück Center for Molecular Medicine (MDC) and Charité — Universitätsmedizin Berlin, has found five genetic risk loci that point to the importance of skin and mucous membrane barriers and the immune system in the development of food allergies.

Genetic tests for mutations in the so - called breast cancer genes, BRCA1 and BRCA2, may not reveal as much about cancer risk as earlier reports have estimated, according to two studies published in tomorrow's New England Journal of Medicine.

The study, published in Nature, highlights the real complexity of the genetic interactions that lead to adult organisms» phenotypes (physical forms), helps to explain how natural selection influences body form and leads towards much more realistic virtual experiments on evolution.

The study, published in Cell Reports, shows that male and female flies live longer than average when given low doses of lithium during adulthood or later in life, regardless of their genetic make - up.

In their latest study, published today in the journal PLOS ONE, Scott Evans, a graduate student in the Department of Earth Sciences, and Mary Droser, a professor of paleontology, both in UCR's College of Natural and Agricultural Sciences, show that the Ediacaran - era fossil animal Dickinsonia developed in a complex, highly regulated way using a similar genetic toolkit to today's animals.

The new study, published today in Nature Genetics, largely explains the genetic knowledge gap.

That's the conclusion of a new study published in today's issue of Science, * which shows that worms with a metabolism - slowing genetic defect live 50 % longer lives than their bustling counterparts.

A new study in the journal Genetics in Medicine, published by Springer Nature, now shows that up to 40 percent of direct - to - consumer (DTC) genetic tests provide incorrect readings in the raw data.

The National Institutes of Health - funded study, published July 2 in the New England Journal of Medicine, also found that participants in Sweden had higher rates of celiac disease than participants in the United States, Finland and Germany, even with the same genetic risks.

ScienceExpress publishes the first detailed study of the new virus's genetic makeup, explaining the twisted histories of its closest relatives.

Publishing in Nature, the study reports that genetic alterations affecting a part of the PD - L1 gene increases the production of the protein, allowing cancer cells to escape detection by the immune system.

The St. Laurent Institute, a non-profit medical research institute focused on the systems biology of disease, today announced in a study published in the July edition of Genome Biology, that genetic matter, previously ignored by the scientific community, may play an important role in cancer.

Getting enough vitamin D during infancy and childhood is associated with a reduced risk of islet autoimmunity among children at increased genetic risk for type 1 diabetes, according to a study published this week in the journal Diabetes.

Publishing in Nature, a recent study reports that genetic alterations affecting a part of the PD - L1 gene increases the production of the protein, allowing cancer cells to escape detection by the immune system.

The study, published in Science and co-authored by University of Cambridge and King's College London, shows that the genetic variation of ribosomal DNA (rDNA) could be driving how the environment within the womb determines an offspring's attributes.

This milestone toward understanding the genetic control of human aging, and the results — together with a parallel study from colleagues at Stanford University — have now been published in the journal Cell.

Little has been known about the ways in which many diabetes genes work, but a study published in the journal Cell sheds light on a genetic risk component of type 1 diabetes and a new approach for keeping beta cells strong.

In a March 2009 study published in Genes and Immunity, researchers at the National Center for Computational Toxicology compared the genetic signatures of 16 people who experienced smallpox vaccine side effects, including fever, rashes and enlarged lymph nodes, to 45 people who did not.

The study, published this week in Science, is the first to simultaneously identify, date and characterise genetic mixing between populations.

In a study published online this week in the journal Scientific Reports, researchers from Rice University's Center for Theoretical Biological Physics (CTBP) and colleagues from Tel Aviv University and Harvard Medical School show how sophisticated genetic circuits allow an individual bacterium within a colony to act on its own while also ensuring that the colony pulls together in hard times.

University of Wyoming researchers studied inbred domestic ferrets and determined the mammals have low genetic diversity on a global scale, according to a paper recently published in Evolutionary Applications.

Published September 15 in Genome Biology, the study relied on new software for researchers that identifies connections between seemingly unrelated human diseases and traits through the tiny, risk - conferring genetic variations they have in common.

In a study led by Duke Health and published in the journal Alcoholism: Clinical and Experimental Research, scientists demonstrate in rats that a short duration of the drug donepezil can reverse both structural and genetic damage that bouts of alcohol use causes in neurons, or nerve cells, in the young brain.

Researchers conducted an analysis that included nearly 10,000 women with the BRCA1 or BRCA2 genetic mutations to estimate the age - specific risk of breast or ovarian cancer for women with these mutations, according to a study published by JAMA.

In a study published online in the journal Menopause, researchers from the Perelman School of Medicine at the University of Pennsylvania report the first evidence showing that smoking causes earlier signs of menopause — in the case of heavy smokers, up to nine years earlier than average — in white women with certain genetic variations.

Neanderthal genetic material is found in only small amounts in the genomes of modern humans because, after interbreeding, natural selection removed large numbers of weakly deleterious Neanderthal gene variants, according to a study by Ivan Juric and colleagues at the University of California, Davis, published November 8th, 2016 in PLOS Genetics.

Last November an international team of geneticists out of University College London and the University of Michigan at Ann Arbor published a key new study of genetic diversity among Native Americans.

The new study — published October 18, 2016 in the journal Molecular Psychiatry — combined genetic analysis of more than 9,000 human psychiatric patients with brain imaging, electrophysiology, and pharmacological experiments in mutant mice to suggest that mutations in the gene DIXDC1 may act as a general risk factor for psychiatric disease by interfering with the way the brain regulates connections between neurons.

The two Univerity of Washington studies, «Great ape genetic diversity and population history,» published in Nature, and «Evolution and diversity of copy number variation in the great ape lineage,» published in Genome Research, are funded by NIH grant HG002385 and support from the Howard Hughes Medical Institute.

This week, University of California, Davis, researchers reveal the discovery of a genetic mutation across breeds that is responsible for chondrodystrophy (the skeletal disorder leading to shorter legs and abnormal intervertebral discs) in a study published in the Proceedings of the National Academy of Sciences.

«This is by far the largest twin study of gene expression ever published, enabling us to make a roadmap of genes versus environment,» Sullivan says, adding that the study measured relationships with disease more precisely than had been previously possible, and uncovered important connections to recent human evolution and genetic influence in disease.