Feature Channels: Genetics

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Released: 14-Nov-2013 10:00 AM EST
Genetic Signature Identified for RSV, the Leading Cause of Infant Hospitalizations Worldwide
Nationwide Children's Hospital

Scientists have identified the genetic signature of respiratory syncytial virus (RSV), the leading cause of infant hospitalizations around the world. The work is a key step toward a better understanding of the immune response to RSV, which will aid the development of a vaccine and a tool that could allow physicians to determine the severity of the infection when symptoms first develop.

13-Nov-2013 3:10 PM EST
Gut Microbes in Healthy Kids Carry Antibiotic Resistance Genes
Washington University in St. Louis

Friendly microbes in the intestinal tracts of healthy American children have numerous antibiotic resistance genes that could be passed to harmful microbes, according to a pilot study by scientists at Washington University School of Medicine in St. Louis.

Released: 13-Nov-2013 5:00 PM EST
Gene Linked to Common Intellectual Disability
University of Adelaide

University of Adelaide researchers have taken a step forward in unravelling the causes of a commonly inherited intellectual disability, finding that a genetic mutation leads to a reduction in certain proteins in the brain.

Released: 13-Nov-2013 4:45 PM EST
Deletion of Any Single Gene Provokes Mutations Elsewhere in the Genome
Johns Hopkins Medicine

The deletion of any single gene in yeast cells puts pressure on the organism’s genome to compensate, leading to a mutation in another gene. The discovery is likely applicable to human genetics and cancer, and could have significant consequences for the way genetic research is done.

   
11-Nov-2013 5:35 PM EST
Novel Gene Therapy Works to Reverse Heart Failure
Mount Sinai Health System

Researchers at the Cardiovascular Research Center at Icahn School of Medicine at Mount Sinai have successfully tested a powerful gene therapy, delivered directly into the heart, to reverse heart failure in large animal models.

5-Nov-2013 2:30 PM EST
New Compound Inhibits Cognitive Impairment in Animal Models of Alzheimer’s Disease
American Association of Pharmaceutical Scientists (AAPS)

The novel compound IRL-1620 may be useful in treating Alzheimer’s disease (AD) as it has been shown to prevent cognitive impairment and oxidative stress in animal models.

Released: 12-Nov-2013 6:00 PM EST
Single-Cell Genome Sequencing Gets Better
University of California San Diego

Researchers led by bioengineers at the University of California, San Diego have generated the most complete genome sequences from single E. coli cells and individual neurons from the human brain. The breakthrough comes from a new single-cell genome sequencing technique that confines genome amplification to fluid-filled wells with a volume of just 12 nanoliters.

Released: 11-Nov-2013 1:00 PM EST
Researchers Identify First Genetic Mutations Linked to Persistent Atopic Dermatitis in African-American Children
Perelman School of Medicine at the University of Pennsylvania

A new report by researchers in the Perelman School of Medicine at the University of Pennsylvania found that loss-of-function mutations to Filaggrin-2 (FLG2), a gene that creates a protein responsible for retaining moisture and protecting the skin from environmental irritants, were associated with atopic dermatitis in African American children.

8-Nov-2013 2:00 PM EST
Un-junking Junk DNA
UC San Diego Health

A study led by researchers at the University of California, San Diego School of Medicine shines a new light on molecular tools our cells use to govern regulated gene expression.

5-Nov-2013 5:00 PM EST
Genetic Variation Increases Risk of Kidney Disease Progression in African Americans
University of Maryland Medical Center

New research provides direct evidence that genetic variations in some African Americans with chronic kidney disease contribute to a more rapid decline in kidney function compared with white Americans.

6-Nov-2013 4:30 PM EST
Gene Puts African Americans At Higher Risk For Kidney Failure, Study Says
Johns Hopkins Bloomberg School of Public Health

Genetic factors in African Americans with chronic kidney disease (CKD) put them at a greater risk for end-stage renal disease (ESRD) compared to white Americans, according to a new study released today in the New England Journal of Medicine. Researchers at Johns Hopkins University and the University of Maryland contributed data from two separate studies: the African American Study of Kidney Disease and Hypertension (AASK) and the Chronic Renal Insufficiency Cohort Study (CRIC).

Released: 7-Nov-2013 3:10 PM EST
Improved Decoding of DNA for Custom Medical Treatments
American Technion Society

Technion scientists have moved a step closer to creating custom medical treatment plans based on a patient's DNA, pinpointing the root of a patient's illness and making sure treatment will not cause a fatal allergic reaction.

5-Nov-2013 5:00 PM EST
Mayo Clinic Researchers Identify Role of Cul4 Molecule in Genome Instability and Cancer
Mayo Clinic

Mayo Clinic researchers have shown that a molecule called Cul4 helps to deposit DNA-packaging histone proteins onto DNA, an integral step in cramming yards of genetic code into compact coils that can fit into each cell. When DNA isn’t packaged correctly, it can lead to the genomic instability characteristic of many forms of cancer.

5-Nov-2013 7:00 PM EST
Breakthrough Discoveries on Cellular Regeneration Seek to Turn Back the Body’s Clock
UT Southwestern Medical Center

Two groups of scientists at the Children’s Medical Center Research Institute at UT Southwestern (CRI) have made complementary discoveries that break new ground on efforts to turn back the body’s clock on cellular activity, paving the way for a better understanding of stem cells, tissue growth, and regeneration.

Released: 5-Nov-2013 5:00 PM EST
Researchers Discover New Path to Address Genetic Muscular Diseases
Arizona State University College of Liberal Arts and Sciences

For decades, scientists have searched for treatments for myopathies — genetic muscular diseases such as muscular dystrophy and ALS, also called Lou Gehrig’s disease. Now, an interdisciplinary team of researchers from Arizona State and Stanford Universities, and the University of Arizona, has discovered a new avenue to search for treatment possibilities.

Released: 5-Nov-2013 4:30 PM EST
Effects of Chronic Stress Can be Traced to Your Genes
Ohio State University

New study suggests “that if you’re working for a really bad boss over a long period of time, that experience may play out at the level of gene expression in your immune system," lead researcher says.

Released: 4-Nov-2013 3:00 PM EST
Brain Aging Is Conclusively Linked to Genes
Texas Biomedical Research Institute

For the first time in a large study sample, the decline in brain function in normal aging is conclusively shown to be influenced by genes, say researchers from the Texas Biomedical Research Institute in San Antonio and Yale University.

Released: 4-Nov-2013 11:00 AM EST
Gene Responsible for Hereditary Cancer Syndrome Found to Disrupt Critical Growth-Regulating Pathway
Whitehead Institute for Biomedical Research

Whitehead Institute scientists report that the gene mutated in the rare hereditary disorder known as Birt-Hogg-Dubé cancer syndrome prevents activation of mTORC1, a critical nutrient-sensing and growth-regulating cellular pathway.



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