Recent
genetic research shows that there were multiple interbreeding events.
Not exact matches
Research being done surrounding CRISPR Cas9 and
genetic engineering are also
showing numerous potential ways to increase human lifespan.
Research shows there's heritability in these traits, and some
genetic determinants of these personality characteristics.
Scientists, of which I am also one, have
researched everything from the parting of the sea to our own
genetic imprints
showing that we are all built with an instinct of faith and an afterlife.
If it could be
shown that
research into human cloning would contribute to the well - being of the children and adults who already (or may someday) suffer from tragic
genetic disorders (such as Down's syndrome or Huntington's disease) and that human cloning itself would benefit the children who are brought into the world through cloning.
Such studies
show that we are all walking
genetic junkyards: Recent U.S.
research suggests that every individual carries, on average, 313 disease - causing mutations.
It's all a work in progress and even though
research shows there are things you can do to help a kid be less picky (and
research also
shows there's
genetic component to it all) nothing replaces the work of exposing kids in a pleasant atmosphere over the years.
The
research also will investigate male / female athletes» willingness to have
genetic testing that may
show links to the repair and recovery of brain cells after concussion.
Longitudinal
research using these techniques
shows that although
genetic factors primarily account for developmental continuity, some evidence can be found for
genetic contributions to change, especially during the transition from early to middle childhood (Fulker, Cherny, & Cardon, 1993) and perhaps from middle childhood to late adolescence (Loehlin, Horn, & Willerman, 1989).
And new
research shows how
genetic alterations in this odd - colored blood have helped the octopus colonize the world's wide oceans — from the deep, freezing Antarctic to the warm equatorial tropics.The iron - based protein (hemoglobin) that carries oxygen in the blood for us red - blooded vertebrates becomes ineffective when faced with low - oxygen levels.
The
genetic studies provide greater context for archaeological evidence found in the Americas: The
research shows that the incredible diversity of cultures and languages among the native people of the Americas developed in place.
«
Genetic limits threaten chickpeas, a globally critical food: New
research shows promise in improving crops with use of wild relatives.»
New
research on HIV transmission
shows that viral fitness is an important basis of a «
genetic bottleneck» imposed every time a new person is infected.
Investigators at the Medical University of South Carolina (MUSC) report pre-clinical
research showing that a
genetic variant encoded in neutrophil cystolic factor 1 (NCF1) is associated with increased risk for autoimmune diseases, including systemic lupus erythematosus (SLE), rheumatoid arthritis, and Sjögren's syndrome, in the January 2017 issue of Nature Genetics.
However, new
research out of York University has now
shown that these drugs also reverse a number of potentially detrimental
genetic changes associated with heart disease.
The study involved participants of European descent exclusively, but co-author Roy Perlis, a researcher at Massachusetts General Hospital, notes it's standard method to focus on one group as a starting point, since previous
research shows genetic markers can vary by ethnicity.
Professor Peter Naredi, the ECCO scientific co-chair of the Congress, who was not involved in the
research, commented: «In my view Dr Brastianos and colleagues very elegantly
show what we mean with precision medicine, how
genetic profiling can support our understanding of the metastatic process and how it opens up different pathways for treatment.
Research has
shown that the activity level of HIV's
genetic material strongly influences whether the virus remains active or whether it becomes dormant.
Research presented today at the 117th Annual Meeting of the American Academy of Ophthalmology
shows promising data about a device that helps people who have lost their vision due to a blinding
genetic disease to recognize common objects.
Scientists at the Wellcome Trust Sanger Institute and the Institute for
Research on Cancer and Ageing of Nice in France,
show that high
genetic diversity can prime new mutations that cause drug resistance.
Multiple
research projects have
shown that about half of the variation in people's body mass index can be attributed to
genetic factors, while the rest is due to environmental factors, including diet and exercise.
Past behavior genetics
research using twin study survey data has
shown genetic influence on a wide range of communication behaviors.
Bru Cormand, head of the
Research Group on Neurogenetics at the Department of Genetics of the UB, affirms that «studies made with monozygotic (genetically identical) and dizygotic twins
show that
genetic factors play a major role in the aetiology of the disease.»
Research from Rutgers Cancer Institute of New Jersey
shows that the RUNX2 protein, which regulates the transcription of
genetic messages responsible for the different functions of cells, may play a role in melanoma cell growth and spread and could serve as a therapeutic target for the disease.
Using their new knowledge, the
research team
showed that the
genetic cause of LP is linked to whether people get scleroderma or not.
The
research team
showed that extra
genetic material on chromosome number 8 caused the condition in two families from Manchester.
However, they
show considerable
genetic overlap with present - day domesticated lines from the region,» explains Nils Stein, who directed the comparison of the ancient genome with modern genomes at the Leibniz Institute of Plant Genetics and Crop Plant
Research (IPK), Gatersleben, with the support of Robbie Waugh and colleagues at the James Hutton Institute, Dundee, Scotland, and Gary Muehlbauer, University of Minnesota, USA.
In fact, the
research showed that 62 % of the differences between individual students» GCSE scores were attributed to
genetic factors.
«Our
research shows that these fish have adapted to life at different depths, and that they segregate by depth as they mature, based on their
genetic makeup.»
New
research shows that the response to medical treatment depends on
genetic factors.
Some
research has
shown that the drug can cause
genetic changes in fish.
Last year, the plans ran into a last - minute hitch when the Medical
Research Council withdrew its support after research showed that tamoxifen can alter genetic material in rats» liver cells (This Week, 14 Marc
Research Council withdrew its support after
research showed that tamoxifen can alter genetic material in rats» liver cells (This Week, 14 Marc
research showed that tamoxifen can alter
genetic material in rats» liver cells (This Week, 14 March 1992).
The
research also
showed how
genetic mutations build up in the cancer as it develops over time, as the leftover cancer cells grow and spread.
Professor Jeremy Pearson, Associate Medical Director at the BHF, which part - funded the study, said: «By using the power of very large scale
genetic studies, this
research is the first to
show that the known association between increased height and a lower risk of coronary heart disease is at least in part due to genetics, rather than purely down to nutrition or lifestyle factors.
«We've also
shown that
genetic risk factors contribute to the most troublesome and long - lasting eczema, so these patients can be our focus for future
research to improve care.
For the public, the
research shows that paternal aging may exacerbate
genetic risks — this could explain why there is a rapid rise in the ratio of children with ASD or ADHD, due to men having children later in life.
Genetic research on black bears has
shown populations in southern Arizona are more closely related to bears in Mexico than those in northern Arizona.
Research at STRI has also
shown that, as with humans, microbes stimulate plants» ability to defend themselves and has demonstrated the magnitude and extent of endophyte effects on host
genetic expression.
Research on the geographically based
genetic differences in Helicobacter pylori
show that the stomach bacteria is intimately tied to man
But the work
shows that
research into complex
genetic traits is getting off the ground.
But preliminary
research has not
shown any evidence of
genetic changes, and the government of Saudi Arabia, where most of the new cases occur, says the sudden upswing is mostly the result of more widespread testing.
Subject areas, such as
genetic discrimination, patient (and
research participant) right to privacy, and ownership of
genetic material and data,
showed both the negative ways scientific information can be used and some of the gray areas that confront researchers every day.
The Neurogenomiks
research group, linked to the Achucarro Basque Centre for Neuroscience (EHUgroup) and the University of the Basque Country (UPV / EHU), has just had a
research article published in the scientific publication Journal of Immunology; it details how they have managed to
show that the gene known as ANKRD55 produces 3 different transcripts of the messenger RNA, and that the
genetic variant associated with MS greatly increases the production of these transcripts.
Last November, however, a team led by Mihael Polymeropoulos of the National Human Genome
Research Institute in Bethesda, Maryland, reported that the disease afflicting the Italian family, which develops at an unusually early age,
showed strong
genetic linkage to a region on chromosome 4.
For example, Ebers says, the new
research also
shows that the IL7R variant associated with increased MS risk is present in 70 % of people of European descent, suggesting that many other
genetic factors are involved because few of these people contract MS. «The most striking finding,» Ebers says, «is the degree of
genetic influence [on MS] that remains unexplained.»
But new
research shows the cuddly bird and the powerful feline share an unfortunate fate: Though their numbers have stabilized or are even rising, some populations are suffering from profound
genetic isolation or loss of
genetic diversity — enough in some cases to leave them deeply vulnerable to new diseases and other threats.
Dr Louise Wain, Associate Professor in
Genetic Epidemiology who led the team of analysts at the University of Leicester added: «The
research shows the value of the UK Biobank study and of «big data» for making discoveries that will improve health.
«Our society attributes the weight gain and lack of exercise at mid-life (approximately 30 - 60 years) primarily to poor lifestyle choices and lack of will power, but this study
shows that there is a
genetic program driven by an overactive enzyme that promotes weight gain and loss of exercise capacity at mid-life,» said lead study author Jay H. Chung, Ph.D., M.D., head of the Laboratory of Obesity and Aging
Research at the National Heart, Lung, and Blood Institute (NHLBI), part of NIH.
Even our own
research across a diverse group of young breast cancer survivors has
shown that blacks and Hispanics have much lower testing rates, which may be the result of lower awareness and access to
genetic testing among racial and ethnic minorities,» she said.
Of the 22 patients whose tumors successfully grafted, six died before data from the mice were available, but in 13 of the remaining 16 cases, there was a positive correlation between mouse and human results.2 In a second study, performed in collaboration with Manuel Hidalgo of the Spanish National Cancer
Research Center, the team found that 6 of 13 patients with advanced solid tumors who were treated based on results from personalized PDX mice had partial tumor remissions, even in cases where
genetic sequencing of the tumor
showed no actionable mutations.3