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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.

Next Generation X-Aptamers for Identification of Personalized Biomarkers in Cancer
David G. Gorenstein, Ph.D., University of Texas Health Sciences Center, speaking at Genomics Research 2012.

Genomic and Proteomic Biomarkers for Cardiac and Renal Transplantation: Computational Biomarker Pipeline from Discovery to Clinical Implementation
Dr. Robert McMaster, Professor, University of British Columbia, speaking at Genomics Research 2012.

LATE-PCR and Its Allied Technologies maximum Information from a Single Tube Application to Mitochondria
Professor Lawrence J. Wangh, Brandeis University, speaking at Genomics Research 2012.

LATE-PCR &Thermalight Probes: Single-Tube Solutions For Personalized Cancer Medicine
Dr. J. Aquiles Sanchez, Brandeis University, speaking at Genomics Research 2012.

Single Copy qPCR-Based Detection of BRAF and KRAS Mutations
Vladimir Makarov, Swift Biosciences Inc, speaking at Genomics Research 2012.

Rapid Diagnosis of Respiratory Viral Infections using an Integrated Sample Prep and qPCR Technology
Dr. Preveen Ramamoorthy, National Jewish Health, speaking at Genomics Research 2012.

Understanding Cell Transitions at Single-Cell Level
Dr Anders Ståhlberg, University of Gothenburg in Sweden, speaking at Single Cell Analysis Europe 2012.

Challenges of Analyzing Single Cell Gene Expression Data
Dr Kenneth Livak, Fluidigm, speaking at Single Cell Analysis Europe 2012.

Exploring the Global Genomic Landscape of Enteric Pathogens using DNA Microarray Technology
Dr Scott Jackson, Molecular Biologist, FDA, speaking at Advances in Microarray Technology 2012.

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