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Common Cell Transformed into Master Heart Cell
By genetically reprogramming the most common type of cell in mammalian connective tissue, researchers at the University of Wisconsin—Madison have generated master heart cells — primitive progenitors that form the developing heart.
Genetic Mutation that Prevents Diabetes Complications
The most significant complications of diabetes include diabetic retinal disease, or retinopathy, and diabetic kidney disease, or nephropathy. Both involve damaged capillaries.
Could the Food we Eat Affect Our Genes?
Almost all of our genes may be influenced by the food we eat, according to new research.
Neanderthal DNA Influences Human Disease Risk
Large-scale, evolutionary analysis compares genetic data alongside electronic health records.
Improving Regenerative Medicine
Lab-created stem cells may lack key characteristics, UCLA research finds.
Tick Genome Reveals Secrets of a Successful Bloodsucker
NIH has announced that decipher the genome of the blacklegged tick which could lead to new tick control methods.
"Dark Side" of the Transcriptome
New approach to quantifying gene "read-outs" reveals important variations in protein synthesis and has implications for understanding neurodegenerative diseases.
Individuals' Medical Histories Predicted by their Noncoding Genomes
Researchers have found that analyzing mutations in regions of the genome that control genes can predict medical conditions such as hypertension, narcolepsy and heart problems.
New Source of Mutations in Cancer
Recently, a new mutation signature found in cancer cells was suspected to have been created by a family of enzymes found in human cells called the APOBEC3 family.
Advancing Synthetic Biology
Living systems rely on a dizzying variety of chemical reactions essential to development and survival. Most of these involve a specialized class of protein molecules — the enzymes.

The Effect of Early Life Nutrition on the Epigenome and Implications for Human Disease
Dr Karen Lillycrop, University of Southampton, speaking at Epigenetics 2011.

A Polycomb-Based Switch Underlying Quantitative Epigenetic Memory
Andrew Angel, John Innes Centre, UK, speaking at Epigenetics 2011.

Cancer Methylome Profiling using Methyl-DNA Capture
Dr Arjen Brinkman, Radboud University Nijmegen (NL), speaking at Next-Gen Sequencing Europe 2011.

A Systematic Investigation of Candidate Breast Cancer Progression-Associated Biomarkers Identified from Omic Screens: Leveraging Antibody-Based Proteomics
Prof. William Gallagher, Chief Scientific Officer at OncoMark, speaking at Advances in Microarray Technology 2011.

RNA-Seq for High Throughput Clinical Studies
Wenzhong Xiao, Assistant Professor of Bioinformatics, Massachusetts General Hospital, speaking at Next-Gen Sequencing Congress 2011.

Genome-scale Quantitative Tumour Proteomics for Cancer Biomarkers Discovery
Metodi Metodiev, Lecturer/Director of Proteomics Unit, University of Essex, speaking at European Biomarkers Summit 2011.

Single Cell Genomics: Accessing the Genomes of Uncultivated Microbes
Mary-Jane Lombardo, Research Scientist, J. Craig Venter Institute, speaking at Next-Gen Sequencing Congress 2011.

Genomics of Bacterial Pathogen Strain Variation
Timothy Read, Associate Professor, Emory University School of Medicine, speaking at Next-Gen Sequencing Congress 2011.

Using Next-Gen Sequencing to Uncover Patterns of Allele-Specific Expression
Sergio Baranzini, Associate Professor, University of California, San Francisco, speaking at Epigenetics World Congress 2011.

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