Sentences with phrase «human cancer genetics»

On Capitol Hill last week, Weinberg, an expert in the molecular biology of cancer, pointed out to the Congressional Biomedical Research Caucus that the major advances in understanding human cancer genetics had come, not from studying breast tissue, but from studying cow warts, worm vulvas, fruitfly retinas, and a chicken virus.

In addition, the researchers examined neuroligin - 3 data from The Cancer Genome Atlas, a large public database of human cancer genetics.

Not exact matches

The U.S. National Institutes of Health (NIH) has made major investments in network approaches in many areas, including cancer biology, cardiovascular and metabolic diseases, neurophysiology, and human genetics and genomics.

With an M.A. in human genetics and molecular biology from Johns Hopkins University School of Medicine and a B.S. in biochemistry from New Mexico State University, Cordova has held research internships at those institutions as well as at the Fred Hutchinson Cancer Research Center and at the University of Texas - Houston.

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.

Her research is both translational and clinical in nature and centers on the human genetics of healthy skin aging and diseases related to aging skin, including new treatments for advanced basal cell skin cancers.

The study was led by Guoping Fan, professor of human genetics and molecular biology and member of both the Jonsson Comprehensive Cancer Center and the Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research.

Physiological similarities between dogs and humans, and conserved genetics between some dog and human cancers, can allow pet dogs to serve as useful models for studying new cancer drugs, he said.

The MGH Research Institute conducts the largest hospital - based research program in the nation, with an annual research budget of more than $ 800 million and major research centers in HIV / AIDS, cardiovascular research, cancer, computational and integrative biology, cutaneous biology, human genetics, medical imaging, neurodegenerative disorders, regenerative medicine, reproductive biology, systems biology, photomedicine and transplantation biology.

Using mouse models that replicate the complexity of human hepatocellular carcinoma genetics, he is working on unravelling the mechanisms of regeneration and cancer development in the liver.

CSHL is a private, non-profit research and education institution dedicated to exploring molecular biology and genetics in order to advance the understanding and ability to diagnose and treat cancers, neurological diseases, and other causes of human suffering.

In addition to the inherited breast and ovarian cancer, her research interests include genetics of hearing loss, the genetic bases of schizophrenia, genetics of systemic lupus erythematosus, and human genetic diversity and evolution.

As Director of Cold Spring Harbor Laboratory (CSHL) from 1968 to 1994, he was a driving force behind creation of the Laboratory's cancer genetics and neuroscience programs and played a seminal role in organizing the Human Genome Project.

Reykjavik, ICELAND, September 14, 2008 — Scientists at deCODE genetics (Nasdaq: DCGN) and colleagues at Radboud University Medical Center in the Netherlands today report the discovery of two common single - letter variants in the human genome (SNPs) that confer increased risk of urinary bladder cancer.

Multimedia Resources include educational websites, videos, and apps, which cover basic heredity, genetic disorders, eugenics, the discovery of the structure of DNA, the human genome, cancer, neurobiology, plant genetics, RNA interference, epigenetics, and bioinformatics.

And we can also use what we know about the genetics of the human cancer to make mutations in normal cells, and see how different mutations drive invasion.»

December 17, 2013 Cancer genetics pioneer Janet Rowley, 1925 - 2013 A pioneer in connecting the development of cancer with genetic abnormalities, Janet D. Rowley, MD, the Blum - Riese Distinguished Service Professor of Medicine, Molecular Genetics & Cell Biology and Human Genetics at the University of Chicago, died from complications of ovarian cancer on December, 17, 2013, at herCancer genetics pioneer Janet Rowley, 1925 - 2013 A pioneer in connecting the development of cancer with genetic abnormalities, Janet D. Rowley, MD, the Blum - Riese Distinguished Service Professor of Medicine, Molecular Genetics & Cell Biology and Human Genetics at the University of Chicago, died from complications of ovarian cancer on December, 17, 2013, at hercancer with genetic abnormalities, Janet D. Rowley, MD, the Blum - Riese Distinguished Service Professor of Medicine, Molecular Genetics & Cell Biology and Human Genetics at the University of Chicago, died from complications of ovarian cancer on December, 17, 2013, at hercancer on December, 17, 2013, at her home.

According to Ophir Klein, MD, PhD, the Charles J. Epstein Professor of Human Genetics and chief of the Division of Medical Genetics at UCSF, «We are looking forward to a close interaction between Dr. Rajkovic and our clinical genetics faculty members in Pediatrics, Obstetrics, Internal Medicine and the Cancer Center, as well as with our colleagues working on genetic diseases in other departments.

I am applying principles from physical and computational sciences to the study of biology to find patterns in these interactions, to obtain insight into population genetics, human evolution, and diseases including cancer.

Dr. Chung directs NIH funded research programs in human genetics of obesity, breast cancer, pulmonary hypertension, and birth defects including congenital diaphragmatic hernia and congenital heart disease.

Recent advances in our knowledge of human genetics have enabled us to consider new approaches to how we treat cancer.

At the same time, we will integrate today's discovery into the prostate cancer module in our personal genome analysis service deCODEme ™, enabling our subscribers to stay abreast of how the latest discoveries in human genetics may relate to their genome,» said Kari Stefansson, CEO of deCODE.

Laboratory activities minimally include performing a lab - based patient - oriented research project applicable to cancer genomics, with an emphasis on mastering techniques commonly used within a human genetics laboratory, such as PCR, gene sequencing, mutation analysis, western blots, and functional protein studies.

COSMIC, the Catalogue of Somatic Mutations in Cancer (http://cancer.sanger.ac.uk) is a high - resolution resource for exploring targets and trends in the genetics of human cCancer (http://cancer.sanger.ac.uk) is a high - resolution resource for exploring targets and trends in the genetics of human ccancer.sanger.ac.uk) is a high - resolution resource for exploring targets and trends in the genetics of human cancercancer.

Massively parallel sequencing (next - generation sequencing) has revolutionized research in cancer genetics and genomics [1] and enhanced our understanding of natural human genetic variation [2], [3].

I encourage you to read the full CRUK Science Update Blog post «High - impact science: Hedgehogs, flies and skin cancer — the story of vismodegib», it's an excellent example of how research on flies, rodents and a range of other organisms combined with studies of cancer genetics in humans to enabled the development of an innovative therapy.

High - throughput sequencing has fundamentally changed the field of human genetics, particularly in how we study genetic diseases like cancer.

Jason H. Moore, PhD, Third Century Professor, a professor of genetics and of community and family medicine at Geisel, director of iQBS, and associate director of Norris Cotton Cancer Center, said that «bacterial cells outnumber human cells many-fold.

From our earliest research that established cancer as a genetic disease to today's work in precision medicine, our unswerving focus on genetics and genomics continues to generate advances that improve human health.

Reykjavik, ICELAND, January 19, 2009 — Scientists at deCODE genetics (Nasdaq: DCGN) and colleagues from the US and ten European countries today announced a long - awaited first in cancer research: the discovery of common single - letter variations in the human genome (SNPs) linked to susceptibility not of one, but several different types of cancer, including those of lung, bladder, prostate, skin and cervix.

How research on the genetics behind cancers common to dogs and humans became a commercial breed - test product is itself a unique story of technology transfer at the Center.

Ostrander, now chief of the cancer genetics branch of the National Human Genome Research Institute at the National Institutes of Health, said Wisdom Panel is a «very powerful tool for the millions of dog owners who buy their mixed - breed pets from a pound.

My primary research interests are human genetics and cancer genomics, and the content of my blog reflects that.

Articles cover the genetic basis of human disease including germline cancer genetics, the clinical manifestations of genetic disorders, applications of molecular genetics to medical practice.