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UTSW Cancer Researchers Identify Irreversible Inhibitor for KRAS Gene Mutation
Irreversible inhibitor for KRAS gene mutation involved in lung, colon, and pancreatic cancers.
NIH Scientists Find Six New Genetic Risk Factors for Parkinson’s
Study shows power of combining big data analysis with cutting-edge genomic techniques.
Mount Sinai Scientists and International Team Shed New Light on Schizophrenia
Genes and pathways identified could inform new approaches to treatment and address acute need for drug development for this disorder.
Schizophrenia’s Genetic Skyline Rising
Suspect common variants soar from 30 to 108 - NIH-funded study.
Transplanting Gene into Injured Hearts Creates Biological Pacemakers
Researchers develop first minimally invasive gene therapy procedure to treat heart rhythm disorders by transforming ordinary heart muscle cells into specialized rhythm-keeping cells, potentially eliminating future need for electronic pacemakers.
Common Gene Variants Account for Most Genetic Risk for Autism
Roles of heritability, mutations, environment estimated - NIH-funded study.
Illumina's HiSeq X Ten Sequencing Technology for Population Studies
Next-generation sequencing technologies to be implemented at new High-Throughput Genomics Center for the MENA region.
Bowel Cancer Breakthrough May Benefit Thousands of Patients
Researchers at Queen’s University have discovered how two genes cause bowel cancer cells to become resistant to treatments used against the disease.
NIH Scientists Identify Gene Linked to Fatal Inflammatory Disease in Children
Repurposed drugs may offer first potential therapy.
Study Finds Low Oxygen Environment Helps Tumors Silence Critical Genes
The study led by Yale Cancer Center may provide clues to how some aggressive cancers turn off, or silence, genes critical to suppressing tumors.
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Proteomic Scale Generation and Validation of Recombinant Antibodies
John McCafferty, Senior Project Leader/Principal Investigator, Wellcome Trust Sanger Institute, speaking at Proteomics Europe 2007
Date Posted: Friday, March 14, 2008
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Punctuated Evolution in Cancer Genomes
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Tuesday, January 11, 2011
1000 Genomes Project Publishes Analysis Of Completed Pilot Phase
NIH-supported work produces tool for research into genetic contributors to human disease.
Friday, October 29, 2010
Sequence is Scaffold to Study Sleeping Sickness
Study probes Trypanosoma parasite genome for cause of human infectivity.
Thursday, April 15, 2010
Exploring Genetic Effects in Cells
A deep look into population variation in gene activity provides key insight to cell functions and disease susceptibility, researcher report.
Thursday, March 11, 2010
Broken Genomes Behind Breast Cancers
Scientists characterized the ways in which the human genome is broken and put back together in 24 breast cancers.
Thursday, December 24, 2009
Blood Counts Are Clues to Human Disease
Genome-wide meta-analysis identifies 22 regions associated with blood cell traits.
Monday, October 12, 2009
Malaria Study Points the Way Forward For Genetic Studies of Disease in Africa
A study carried out by MalariaGEN provides new insights into how to conduct genetic studies of common diseases in genetically-diverse African populations.
Wednesday, May 27, 2009
Genome Study Takes Targeted Approach to Cancer
An £8.5 million UK-US alliance funded by the Wellcome Trust will test the sensitivity of 1000 cancer cell samples to hundreds of molecular anticancer treatments.
Wednesday, December 31, 2008
Novel Method to Reveal Drug Targets
Scientists have developed a new large-scale method to identify the interactions between proteins that are a major target for therapeutic intervention.
Monday, March 03, 2008
International Consortium Announces the 1000 Genomes Project
Major sequencing effort will produce most detailed map of human genetic variation to support disease studies.
Wednesday, January 23, 2008
 
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