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Personalized Screening for Ovarian Cancer
With 60% of women diagnosed with ovarian cancer dying within five years of diagnosis there has been considerable efforts to try to detect the disease at an earlier stage.
Gene Therapy for Cystic Fibrosis Shows Encouraging Trial Results
A therapy that replaces the faulty gene responsible for cystic fibrosis in patients' lungs has produced encouraging results in a major UK trial.
In Blinding Eye Disease, Trash-Collecting Cells Go Awry, Accelerate Damage
NIH research points to microglia as potential therapeutic target in retinitis pigmentosa.
How the Mammoth Got its Wool
Evolutionary change in a gene reconstructed in the lab from the woolly mammoth was part of a suite of adaptations that allowed the mammoth to survive in harsh arctic environments, according to new research.
Brain Cells Switch Epigenetic Gears Throughout Life
Research finds that histone turnover regulates how genes in the brain are turned on and off in response to various stimuli, thereby allowing neurons to form new synaptic connections.
More Accurate Prediction on Prognosis in Multiple Myeloma (Bone Marrow Cancer)
Test of Dutch-based SkylineDx gives patients better insight in their chances and enables clinicians to adjust their treatment.
NuGEN Scientists Screen 400+ Genes for Fusion Events in Single Assay
Breakthrough proves efficacy of new sample preparation method that could accelerate cancer research and development of treatments and diagnostic tests.
Team Identifies Gene Responsible for Some Cases of Male Infertility
In the most severe form of male infertility, men do not make any measurable levels of sperm. This condition, called azoospermia, affects approximately 1 percent of the male population and is responsible for about a sixth of cases of male infertility.
Potential Therapeutic for Blinding Eye Disease
NIH research points to microglia as potential therapeutic target in retinitis pigmentosa.
Animals’ Genomic Buffers May Help Humans
Researchers at Duke University School of Medicine and Brigham and Women’s Hospital, Harvard Medical School have identified a mechanism that explains why some mutations can be disease-causing in one genome but benign in another.

Tumor Cell Heterogeneity: Achieving Single Cell Resolution
Robert Proulx, Silicon Biosystems, speaking at Exosomes and Circulating Biomarkers Summit 2013.

Monitoring Dynamic Interactions of Tumor Cells with Tissue and Immune Cells in a Lab-on-a-Chip
Peter Ertl, Austrian Institute of Technology, speaking at Lab-on-a-Chip European Congress 2014.

Detection and Expression Profiling of Tumor Initiating Cells (TIC) Among the Peripherally Circulating Epithelial Tumor Cells from Patients with Breast Cancer
Katharina Pachmann, University of Jena, speaking at Single Cell Analysis Europe 2014.

Improvements in Molecular Diagnosis of Pathogens and Diseases
Panagiotis Karanis, University of Cologne, speaking at Advnaces in Biodetection & Biosensors 2014.

Advances in Volatile Analyses for Disease Diagnosis
Norman Ratcliffe, University of the West of England, speaking at Advances in Biodetection & Biosensors 2014.

Alternative mRNA Cleavage and Polyadenylation in Genetic Diseases
Reuven Agami, The Netherlands Cancer Institute, speaking at Genomics Research Europe 2013.

Shaping the Epigenome by Histone Protein Exchange and Inheritance
Fred van Leeuwen, Netherlands Cancer Institute, speaking at Genomics Research Europe 2013.

Epigenetic Variation as a Driver of Breast Cancer Risk
James Flanagan, Imperial College London, speaking at Genomics Research Europe 2013.

Exosome Biogenesis: Role of Exosomal Cargo in the Production and Secretion of Exosomes
Professor Suraj Bhat, UCLA, speaking at Exosomes and Circulating Biomarkers 2013.

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