But the technology is already changing human health on another front, by allowing researchers to create genetically modified animals that can aid
in understanding human diseases.
Not exact matches
What it does: The role of this bacteria, which is most well - known for causing syphilis and Lyme
disease, is still not well -
understood in humans.
We must take a clear view of the medical realities of
disease and the spiritual realities of sin, but it makes a difference
in the pastor's
understanding of all
human ills that he sees every person as created for a life of love to God and his neighbor.
«These new insights into the complexities of epigenetic regulation are contributing to our basic
understanding of this process
in human health and
disease and gives us new vision for how to go about targeting errors
in DNA methylation with innovative drug therapies.»
Cloned primates could help researchers better
understand diseases in humans.
To better
understand their findings, the team examined the animal model for APS1 (i.e. mice with the same genetic defect as
human patients with the syndrome) and found that male mice spontaneously developed an inflammatory
disease in their prostate glands — a so - called prostatitis — and reacted to transglutaminase 4.
Human tissue grown
in the laboratory offers a critical model for
understanding the
disease process.
Therefore, it is essential that we learn how specific types of chemical modifications normally regulate RNA function
in our cells,
in order to
understand how dysregulation of this process contributes to
human disease, says Cristian Bellodi.
«It has profound implications for our
understanding of
human development and physiology, and gives us a remarkable wealth of resources to examine how disturbances of this system might result
in diseases such as cancer.»
Buttke is interested
in using public interest
in personal health as a way to increase support for public green space, and enhancing public
understanding of how
human actions can drive infectious
disease spread through a variety of avenues including school programs, websites, and smart phone apps.
One of the primary goals of genetics over the past decade has been to
understand human health and
disease in terms of differences
in DNA from person to person.
«Once we can build that sort of database for the
human organism, it helps us much better
understand disease, how to diagnose
disease, how better to treat
disease,» says Richard Wilson, the director of the Genome Sequencing Center at Washington University
in St. Louis.
«The next step
in understanding sleep apnea
in the future will be to dissect different subtypes of sleep apnea, likely defined by distinct pathophysiological mechanisms which may underlie different outcomes and predisposition to comorbidities,» Cavadas says, «As
human life expectancy increases, delaying the onset of age - related
diseases becomes critical to our society.»
Further studies of processes
in which GTPBP3 is involved will help towards the
understanding of
human diseases that are linked to mitochondrial DNA expression and to develop new therapies.
«
Understanding the evolution of malaria parasites in bats and other animals, and how they fit into the tree of life, is key to understanding this important human di
Understanding the evolution of malaria parasites
in bats and other animals, and how they fit into the tree of life, is key to
understanding this important human di
understanding this important
human disease.»
«
In many cases we're still learning how these bacteria influence our risk of disease, but understanding the human genetics component is a necessary step in unraveling the mystery,» Knights sai
In many cases we're still learning how these bacteria influence our risk of
disease, but
understanding the
human genetics component is a necessary step
in unraveling the mystery,» Knights sai
in unraveling the mystery,» Knights said.
Researches are now able to
understand for the first time the evolution of these parasites, causing
disease in humans and animals.
«Further work
in our lab will be aimed at
understanding the detailed mechanism of how these proteins regulate editing,
in turn providing an inroad to developing therapeutics that modulate editing for the treatment of
human diseases.»
«We hope that the results from this study will enable investigators to test the relevance of the maresin pathway
in human disease,» said Charles N. Serhan, Ph.D., a researcher involved
in the work from the Brigham & Women's Hospital and Harvard Medical School
in Boston, Mass. «Moreover, we hope to better
understand resolution biology and its potential pharmacology so that we can enhance our ability to control unwanted inflammation and improve the quality of life.»
«This research project is a prime example of how mouse models can help us to better
understand cancer
diseases in human beings,» says Sabine Harlander.
«Thus, it is clear that further studies must investigate an increasingly complex matrix of cell types and conditions to fully
understand the role of
human genetic variation
in disease.»
«
Understanding this previously ignored part of the
human genome, its role
in human development, and how it may be taken over by
disease, opens a new frontier
in science with important implications for medical advances,» said Philipp Kapranov, Ph.D., lead researcher at the St. Laurent Institute.
The findings, published
in the journal Nature, explain why the
human genome is so difficult to decipher — and contribute to the further
understanding of how genetic differences affect the risk of developing
diseases on an individual level.
In addition to shedding light on how major shifts in body design evolved, the new finding could help scientists better understand certain human diseases and deformitie
In addition to shedding light on how major shifts
in body design evolved, the new finding could help scientists better understand certain human diseases and deformitie
in body design evolved, the new finding could help scientists better
understand certain
human diseases and deformities.
NIH gets an extra $ 414 million for Alzheimer's
disease research, along with $ 400 million for the BRAIN Initiative, a research project announced by President Obama
in 2013 that aims to improve our
understanding of the
human brain.
To
understand why the long - spined urchins have not returned to the reef more than 30 years later, Scripps scientists Katie Cramer and Dick Norris analyzed the amount of fossilized urchin spines that accumulated
in reef sediment layers over the past 3,000 years to paint a picture of life on the reef before it was altered from the
disease outbreak and
human activities such as fishing and pollution.
These individual transcriptomes can be used to define cell types and to
understand the functions of healthy and
diseased cells
in the
human body.
«Gaining a better
understanding of the functions genes perform
in cells, whether plant or animal, is going to help us
understand how to diagnose and treat
diseases in humans,» says Richard K. Wilson of Washington University.
His research interests include the molecular underpinnings of cervical cancer (including developing genetic screens), the identification of the genetic determinants of quantitative traits
in humans, and the application of massively parallel sequencing technology for
understanding the genetics of complex
disease.
«We are only beginning to
understand the role that
human - made chemicals play
in causing
human disease,» said Regnier.
Because of the similarities
in ocular anatomy, canine models contribute significantly to the
understanding of retinal
disease mechanisms and the development of new therapies for
human patients.
Her research is at the interface between bioimaging and proteomics, and aims to define the spatiotemporal organization of the
human proteome at a subcellular level
in an effort to
understand how variations and deviations
in localization contribute to cellular function as well as
disease.
«It's a bit like
human disease but
in plants, to
understand the pathogen and its interaction with the plant allows to develop a functional cure to treat the affected plants» emphasizes the specialist
in plant genomics.
However, since the novel genes that were identified, are known to lead to aging - associated
diseases in humans, their further analysis seems to be promising for developing new approaches to
understand and possibly cure these
diseases and to contribute to a long life and healthy aging
in humans —
in a way, long - lived rodents do.
At the Rockefeller meeting, an important impetus behind the big ambitions — the quest to decipher the gamut of
human brain
diseases that are still incredibly poorly
understood — was evident
in the room.
«Now that we have a better
understanding of how an animal is built we can get some way closer to knowing how the
human body works
in health and
disease,» says John Sulston, director of the Sanger Centre at the Wellcome Trust Genome Campus, Cambridgeshire, England.
Conservation work to defeat the
disease has including removing infected individuals from the population and new research
in Evolutionary Applications explains how this gives us a unique opportunity to
understand how
human selection alters the evolution of cancerous cells.
Understanding how the
human immunodeficiency virus (HIV) reproduces itself is crucial
in the effort to fight the
disease.
«NGS technologies have vastly improved our
understanding of the
human genome and its variation
in diseases such as cancer,» said Ken Chen, Ph.D., assistant professor of Bioinformatics and Computational Biology and co-author of the Nature Methods article.
The Structural Genomics Consortium at the University of North Carolina at Chapel Hill (SGC - UNC),
in partnership with the DiscoverX Corporation, has reached the milestone halfway point
in its development of the Kinase Chemogenomic Set, a potent group of inhibitors which allow deeper exploration of the
human kinome, a family of enzymes critical to
understanding human disease and developing new therapies.
«
In the future, such efforts could allow us to much better understand human - microbiome interactions, model malnutrition disorders and inflammatory diseases of the gut, and perform personalized drug testing,» said co-first author Alessio Tovaglieri, a Graduate Student at the Department of Health Science and Technology at ETH Zurich in Switzerland, who performs his thesis work on Ingber's tea
In the future, such efforts could allow us to much better
understand human - microbiome interactions, model malnutrition disorders and inflammatory
diseases of the gut, and perform personalized drug testing,» said co-first author Alessio Tovaglieri, a Graduate Student at the Department of Health Science and Technology at ETH Zurich
in Switzerland, who performs his thesis work on Ingber's tea
in Switzerland, who performs his thesis work on Ingber's team.
By building this selective set of compounds and making it freely available, UNC - Chapel Hill and its partners are offering the scientific community a better
understanding of the roles the kinome plays
in human disease and the ability to collaborate on the discovery and advancement of new therapies.
«Aberrant splicing
in humans may lead to various complex
diseases and also underlies the development of some forms of cancer and the onset of neurodegenerative
diseases, so a better
understanding of the process can add important information for our fight against these
diseases.»
Overall, this work illustrates that better
understanding the basic biology of the immune system
in preclinical models may open up a window for the development of novel treatments for
human autoimmune
disease.
«Our findings also have important implications for mitochondrial
diseases in humans, because this research significantly advances our
understanding of how mitochondrial DNA mutations affect individuals and populations, and provides a potential mechanism to explain how different genetic variants may affect health,» Dr Rollins said.
Richard Lindsay, a PhD student who worked on the research team, added: «Our findings are of central importance
in understanding how microbial infections evolve, but also have wider significance for the treatment of cancer and the therapeutic control of
disease in humans, animals and plants.»
Because many rabbit genes are similar to their
human counterparts, manipulating
disease genes
in rabbits, like the one responsible for cystic fibrosis, may permit researchers to track the
disease's onset and better
understand what goes awry.
This discovery plays a primordial role
in understanding immune system
diseases in humans.
Knowing how cells exert force and sense mechanical feedback
in their microenvironment is crucial to
understanding how they activate a wide range of cellular functions, such as cell reproduction, differentiation and adhesion — basic physiological processes that underlie embryo development, tumor metastasis, wound healing and many other aspects of
human health and
disease.
Scientists are only beginning to
understand what role the billions of microbial cells colonizing the
human gut play
in diet and
disease.