Sentences with phrase «into human medicine»

Her love of animals was formed there, but she was discouraged from pursuing veterinary medicine and encouraged to go into human medicine.

Although I grew up with multiple kitties in the Chicago suburbs, I attended the University of Michigan undergrad because I planned to follow my dad into human medicine.

His findings frequently provide insight into human medicine.

He presides over Major Knox (Stephen Spinella), a drunken vet shanghaied into human medicine, pious and meek Private Toffler (Jeremy Davies), ever - stoned Private Cleaves (David Arquette) and gung - ho soldier Private Reich (Neal McDonough), whose enthusiasm is played at a pitch more worthy of Blackadder than even the light absurdity that settles over John Ford pictures with similar setups.

Not exact matches

David Agus, a professor of medicine and engineering at the University of Southern California, said at the Fortune Global Forum on Monday that he believes that with our current technology humans have the potential to regularly live into their ninth or tenth decade.

The argument from suffering reaches beyond medicine's responsibility and competence; it extends into metaphysical questions about the nature of human happiness and what constitutes a meaningful life.

Whereas medicine once aimed at human health, it has been transformed into the medical industry.

Because «the tacit goal of medicine» seemed to be «bodily immortality,» even the healthy human being was viewed as a defective model to be transformed into something better.

When old people rolled up on their Hovarounds to test their own blood pressure on the machine that I dominated for three plus hours, I shooed them away by throwing their medicine into the diarrhea aisle and telling them to register any complaints on the Health & Human Services website.

Just as in human medicine, Many status quo veterinary MUST DO items are now coming into question, including overvaccination, the growing cons of spaying / neutering dogs too young, the heavy pressure (but little real need) for certain «preventive» drugs.

An attempt to fill this gap was made by introducing a «Medicine and Human Rights» special study module into the undergraduate programme at Dundee.

A few years ago scientists at the Johns Hopkins School of Medicine inserted the gene for the human L - type photopigment into mice.

The drug - like compounds can be modified and developed into medicines that target a protein in the human body that is responsible for chemotherapy resistance in cancers, said biochemist Pia D. Vogel, lead author on the scientific paper reporting the discovery.

Diagnostic techniques common in human medicine, such as CT and MRI scanning and molecular studies, are now being used to improve insight into the causes.

«We wanted to investigate whether human adults had the ability to transform some white fat deposits into beige fat when they were exposed to cold,» said one of the study's authors, Philip A. Kern, MD, of the University of Kentucky School of Medicine in Lexington, KY. «Browning fat tissue would be an excellent defense against obesity.

A panel of small molecules that inhibit Zika virus infection, including one that stands out as a potent inhibitor of Zika viral entry into relevant human cell types, was discovered by researchers from the Perelman School of Medicine at the University of Pennsylvania.

The finding, reported in next month's issue of Nature Medicine, raises new questions about whether people could contract exotic diseases if animal organs become routinely transplanted into human patients.

X-rays are one of the most important diagnostic tools in medicine, biology and the material sciences, as they may penetrate deep into material which is opaque to the human eye.

Now, scientists at Boston University's Center for Regenerative Medicine (CReM) have announced two major findings that further our understanding of this process: the ability to grow and purify the earliest lung progenitors that emerge from human stem cells, and the ability to differentiate these cells into tiny «bronchospheres» that model cystic fibrosis.

By studying how these genes cause defects in fly and mouse models, we can improve our insights into the mechanisms related to human disease,» said corresponding author and Dr. Hugo J. Bellen, professor of neuroscience and molecular and human genetics at Baylor College of Medicine and an investigator at the Howard Hughes Medical Institute.

Dr. Funari's research interests include developing new approaches for obtaining mycobiome profiles in human disease and the translation of next generation sequencing applications into the clinic and personalized medicine.

«A genetic variant in cattle might tell us why some humans get into trouble at sea level and at altitude,» said first author John H. Newman, M.D., the Elsa S. Hanigan Professor of Pulmonary Medicine at Vanderbilt University Medical Center.

Less than a decade after a powerful gene - silencing method — RNA interference, or just RNAi — was discovered, the field's pioneers have not only won the 2006 Nobel Prize in Physiology or Medicine but have also helped launch an entirely new class of drugs into human clinical trials.

Human breast tumors transplanted into mice are excellent models of metastatic cancer and are providing insights into how to attack breast cancers that no longer respond to the drugs used to treat them, according to research from Washington University School of Medicine in St. Louis.

In a series of studies this year, molecular geneticists at the University of Pittsburgh School of Medicine used a harmless virus to ferry new genes through the bloodstream, across blood vessel walls, and into almost every muscle cell in the bodies of hamsters bred to have human genetic diseases.

For the animal experiments, Savio Woo of the Center for Gene Therapy at Baylor College of Medicine in Houston and his colleagues first isolated liver cells from transgenic mice that produce the human protein a1 - antitrypsin in their livers, from where it is secreted into the blood.

Although this human Gut Chip recreated the villus epithelium of normal intestine and enabled new insights into how flow and cyclic peristalsis affects intestinal differentiation and function, it could not be used to study processes that relied on normal intestinal cells from individual donors, which, for example, is crucial for studying patient - specific responses for personalized medicine.

Now advances such as machine learning are driving it into multiple fields of human endeavor, from transportation to medicine to finance.

And researchers at Stanford University School of Medicine report in Genome Research that they linked the evolution of a gene in the old platypus to a mutated version in humans responsible for moving the testes outside of the body and into an external pouch, or scrotum.

The ability of scientists to convert human skin cells into other cell types, such as neurons, has the potential to enhance understanding of disease and lead to finding new ways to heal damaged tissues and organs, a field called regenerative medicine.

Through his role in the UM Center for Genome Technology, part of the Miller School of Medicine, Dr. Hedges is actively involved in the incorporation of novel genomic technologies into the process of searching for the genetic variation underlying human disease risk.

Experiments conducted by lead author Fatima Syed - Picard, Ph.D., also of Pitt's Department of Ophthalmology, and the team showed that stem cells of the dental pulp, obtained from routine human third molar, or wisdom tooth, extractions performed at Pitt's School of Dental Medicine, could be turned into corneal stromal cells called keratocytes, which have the same embryonic origin.

Xiaowei «George» Xu, MD, PhD, associate professor of Pathology and Laboratory Medicine and Dermatology at the Perelman School of Medicine, University of Pennsylvania, and colleagues published in Nature Communications a method for converting adult cells into epithelial stem cells (EpSCs), the first time anyone has achieved this in either humans or mice.

His glimpses into the human body via these warriors» wounds, combined with much more systematic dissections of animals, became the basis of Islamic and European medicine for centuries.

Stem cells collected from human corneas restore transparency and don't trigger a rejection response when injected into eyes that are scarred and hazy, according to experiments conducted in mice by researchers at the University of Pittsburgh School of Medicine.

Human stem cells show much promise for regenerative medicine because they can transform into various specialized cell types, including bone and cartilage cells.

Coleen McNamara, MD, a Professor of Internal Medicine at the University of Virginia, recently discovered a B cell subset that produces natural antibodies to protect from diet - induced atherosclerosis in mice, and she hopes to gain insights into the equivalent mechanisms in humans.

Also speaking at the event are Dr. Ken Lacovara (Insights from the biggest dinosaur skeleton ever found), Dr. Roy Hamilton (Enhancing human mental performance with noninvasive brain stimulation), Dr. George Brainard (Better lighting for better sleep in space), Denise Wong (Tiny bio-robots for microscale medicine and engineering), Dr. Melinda Keefe (The chemistry of art conservation), and Dr. Michel Barsoum (Molding conductive «clay» into the next generation of batteries)

Articles and reports from the Life Sciences area deal with applied and basic research into modern biology, chemistry and human medicine.

The Sanford Consortium for Regenerative Medicine facility is intended to house biologists, chemists, technologists, bioengineers, computer scientists and clinicians in open laboratories and is designed to facilitate and encourage collaboration among them as required to translate the basic understanding of stem cell science into tools useful to diagnose and treat human disease.

Researchers at the University of North Carolina at Chapel Hill School of Medicine have transformed cells from human skin into cells that produce insulin, the hormone used to treat diabetes.

However, most previous attempts to transplant blood stem cells into a human fetus have been unsuccessful, prompting some researchers to lose interest in this promising field, according to MacKenzie, who also is an investigator with the Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research.

November 12, 2013 Kurt + Peter Foundation funds research into potential treatment for rare form of muscular dystrophy The Kurt + Peter Foundation has awarded a two - year grant to Elizabeth McNally, MD, PhD, professor of medicine and human genetics at the University of Chicago, to study a potential treatment for limb girdle muscular dystrophy, type 2C — a rare but severe form of muscular dystrophy.

Shinya Yamanaka MD, PhD, a senior investigator at the Gladstone Institutes has won the 2012 Nobel Prize in Physiology or Medicine for his discovery of how to transform ordinary adult skin cells into cells that, like embryonic stem cells, are capable of developing into any cell in the human body.

In a substudy, review outcomes were also compared across different types of clinical research, based in large part on the designations and definitions derived from a number of sources, including a report by Nathan, 14 the Institute of Medicine, 20 the NIH Director's Panel on Clinical Research, 9 the Association of American Medical Colleges and American Medical Association, 21 and the Agency for Healthcare Research and Quality.22 All 3599 R01 applications involving human subjects that were submitted to NIH for the October 2002 council were categorized into 1 of the following: (1) patient - oriented studies of mechanisms of human disease (bench to bedside); (2) clinical trials and other clinical interventions; (3) patient - oriented research focusing on development of new technologies; (4) epidemiological studies; (5) behavioral studies (including studies of normal human behavior); (6) health services research; and (7) use of deidentified human tissue.

For the first set of experiments, first author Trond Aasen, Ph.D., a postdoctoral researcher at the Center of Regenerative Medicine in Barcelona, used viral vectors to slip the genes for the master regulators Oct4, Sox2, as well as Klf4 and c - Myc into keratinocytes cultured from human skin explants.

Direct conversion or reprogramming of human postnatal cells into endothelial cells (ECs), bypassing stem or progenitor cell status, is crucial for regenerative medicine, cell therapy, and pathophysiological investigation but has remained largely unexplored.

November 5, 2015 Richard L. Landau, MD, 1916 - 2015 For more than half a century, Richard L. Landau was a demanding professor of medicine, performing path - breaking research into the effects of human hormones and treatment of hormone - related diseases while building a world - renowned endocrinology program at the University of Chicago.

In their Nature Medicine paper, Fu and colleagues point out that these initial studies relied on human tumors transplanted into mice.

Embryonic stem cells — «pluripotent» cells that can develop into any type of cell in the human body — hold tremendous promise for regenerative medicine, in which damaged organs and tissues can be replaced or repaired.