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Monovar Drills Down Into Cancer Genome
Rice, MD Anderson develop program to ID mutations in single cancer cells.
Autism and Cancer Share a Remarkable Number of Risk Genes
Researchers with the UC Davis Comprehensive Cancer Center, MIND Institute identify more than 40 common genes.
Number Of Known Genetic Risk Factors For Endometrial Cancer Doubled
An international collaboration of researchers has identified five new gene regions that increase a woman’s risk of developing endometrial cancer, one of the most common cancers to affect women, taking the number of known gene regions associated with the disease to nine.
Genetic Variant May Help Explain Why Labradors Are Prone To Obesity
A genetic variation associated with obesity and appetite in Labrador retrievers – the UK and US’s favourite dog breed – has been identified by scientists at the University of Cambridge. The finding may explain why Labrador retrievers are more likely to become obese than dogs of other breeds.
How Scientists Use DNA to Track Disease Outbreaks
They’re the top questions on everyone’s mind when a new disease outbreak happens: where did the virus come from? When did this happen? How long has it been spreading in a particular country or group of people?
Genetic Risk Factors of Disparate Diseases Share Similar Biological Underpinnings
Penn Institute for Biomedical Informatics and colleagues identify "roadmap" of disease mechanisms to identify candidate drug targets.
Stem Cells Know How to Unwind
Research led by the Babraham Institute with collaborators in the UK, Canada and Japan has revealed a new understanding of how an open genome structure supports the long-term and unrestricted developmental potential in embryonic stem cells.
Childhood Asthma Research Receives $2M
Research into the impact of a child’s upbringing and social and physical environments on the development of asthma will receive $2 million to tackle the condition that affects as many as one in three Canadians.
Five New Breast Cancer Genes Found
Discovery of mutations paves the way for personalised treatment of breast cancer.
Cell Transplant Treats Parkinson’s in Mice
A University of Wisconsin—Madison neuroscientist has inserted a genetic switch into nerve cells so a patient can alter their activity by taking designer drugs that would not affect any other cell.

Chemical Restriction Length Polymorphism (CLFP) for Detection and Characterization of Bacterial Pathogens
Byron Brehm-Stecher, Iowa State University, speaking at Advances in Biosensors and Biotedection 2011.

Non-Coding RNAs and Genomic Imprinting: Insights From the Gnas Cluster
Professor Jo Peters, University of Oxford, speaking at Epigenetics 2011.

Applied Molecular Diagnostics in Solid Tumours: Past, Present and Future
Dr Brendan Pang, National University Health System, speaking at Molecular Diagnostics Asia 2011.

Genome-scale Analysis with Single Cells
Dr Honghua Li, UMDNJ Robert Wood Johnson Medical School, speaking at Single Cell Analysis Summit 2011.

Epigenetics of Renal Cell Carcinoma: The Path Towards New Diagnostics and Therapeutics
Professor Eamonn Maher, University of Birmingham, speaking at Epigenetics 2011.

Array CGH: Applications in the Clinical Setting
Lisa D. White, Associate Professor at Baylor College of Medicine, speaking at Advances in Microarray Technology 2011.

Punctuated Evolution of Breast Tumors Revealed by Single Cell Sequencing
Dr Nicholas Navin, MD Anderson Cancer Center, speaking at Single Cell Analysis Summit 2011.

Pharmacogenetics and Personalized Medicine: Reality vs. Hype
Professor Wayne W. Grody, UCLA School of Medicine, speaking at Molecular Diagnostics world Congress 2011.

Starting with the Right Stuff: The Challenge for Molecular Diagnostic Assays
Dr. Carolyn Compton, National Cancer Institute, speaking at Molecular Diagnostics World Congress 2011.

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