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Genetic Cause Discovered for Rare Bleeding Disorder PDF Print E-mail
Wednesday, 10 March 2010 10:17

For some Canadians, any cut such as from dental work or surgery can cause days or more of bleeding. Although they are not hemophiliacs, for some an ordinary bruise can balloon into the size of an orange. For others, knees, elbows and ankles are crippled when bleeding seeps into joints. In very serious cases, hundreds of blood transfusions are required for recovery.

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Sonic Hedgehog Gene Found in an Unexpected Place During Limb Development PDF Print E-mail
Wednesday, 10 March 2010 10:09

Sonic hedgehog, a gene that plays a crucial rule in the positioning and growth of limbs, fingers and toes, has been confirmed in an unexpected place in the embryos of developing mice -- the layer of cells that creates the skin. Named for a video game character, Sonic hedgehog describes both a gene and the protein it produces in the body. Its study is important to increase understanding of human birth defects.

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'Death Messenger' Molecule Causes Inflammation After Spinal Cord Injury, Prevents Healing PDF Print E-mail
Monday, 08 March 2010 08:54

The signaling molecule CD95L, known as "death messenger," causes an inflammatory process in injured tissue after spinal cord injuries and prevents its healing, according to a new study published by scientists of the German Cancer Research Center in the journal Immunity. In mice, the researchers found out that if they switch off CD95L, the injured spinal cord heals and the animals regain better ability to move. Therefore, substances which block the death messenger might offer a new approach in the treatment of severe inflammatory diseases.

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Genetic Cause Discovered for Rare Bleeding Disorder PDF Print E-mail
Monday, 08 March 2010 08:48

For some Canadians, any cut such as from dental work or surgery can cause days or more of bleeding. Although they are not hemophiliacs, for some an ordinary bruise can balloon into the size of an orange. For others, knees, elbows and ankles are crippled when bleeding seeps into joints. In very serious cases, hundreds of blood transfusions are required for recovery.

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Age-Associated Defects in Schizophrenia: Gene Network-Based Analysis Reveals Unexpected Results PDF Print E-mail
Thursday, 04 March 2010 10:23

The underlying causes of the debilitating psychiatric disorder schizophrenia remain poorly understood. In a new study published online March 2, 2010 in Genome Research, however, scientists report that a powerful gene network analysis has revealed surprising new insights into how gene regulation and age play a role in schizophrenia.

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Gene Regulation: Can We Stomach It? New Technique Fights Against Cause of Peptic Ulcer Disease and Gastric Cancer PDF Print E-mail
Thursday, 04 March 2010 03:25

A breakthrough in decoding gene regulation of Helicobacter pylori has been made by an international research team led by Jörg Vogel of the Max Planck Institute for Infection Biology in Berlin. Using a newly developed sequencing technique, the researchers discovered 60 small ribonucleic acids (sRNAs) -- tiny RNA-particles which can regulate genes -- in the genome of this human pathogen. These findings could facilitate the development of new therapeutic strategies against this wide-spread pathogen.

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Genetic Link Between Misery and Death Discovered; Novel Strategy Probes 'Genetic Haystack' PDF Print E-mail
Monday, 01 March 2010 23:46

In ongoing work to identify how genes interact with social environments to impact human health, UCLA researchers have discovered what they describe as a biochemical link between misery and death. In addition, they found a specific genetic variation in some individuals that seems to disconnect that link, rendering them more biologically resilient in the face of adversity.

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Enzyme Deficiency Protects Hepatitis C Patients from Treatment-Related Anemia PDF Print E-mail
Monday, 01 March 2010 23:44

Many people who undergo treatment for hepatitis C develop hemolytic anemia, a disorder that destroys red blood cells. In some cases, it is so severe they have to reduce their medication or stop therapy altogether. But now, scientists in Duke University's Institute for Genome Sciences & Policy (IGSP) have discovered two genetic alterations linked to a benign enzyme condition that keep some patients anemia-free.

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UAB study shows African-Americans have highest stroke rate, southerners more likely to die PDF Print E-mail
Friday, 26 February 2010 22:39

BIRMINGHAM, Ala. African-Americans age 65 and younger are more than twice as likely to have a stroke compared with Caucasians in any region, and people who have a stroke are more likely to die in the South than elsewhere, according to researchers at the University of Alabama at Birmingham (UAB) School of Public Health.

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Transgenomic Licenses IntegraGen's Autism IP PDF Print E-mail
Friday, 26 February 2010 22:35
Transgenomic said today that it has licensed intellectual property from IntegraGen that it plans to use to develop a genetic test for autism risk in children who have older siblings who have already been diagnosed with an autism spectrum disorder.
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Genetic Variant Greatly Increases Lung Cancer Risk for Light Smokers PDF Print E-mail
Wednesday, 10 March 2010 10:15

Individuals with a certain type of genetic susceptibility to lung cancer face a greatly increased risk for the deadly disease with even a small exposure to cigarette smoke, a study team that includes researchers from the University of Cincinnati (UC) has concluded. For family members who carry this genetic variant, the risk of lung cancer is similar for both light and heavy smokers, the researchers say, adding that even non-smokers who are exposed to second-hand cigarette smoke and have a family history of lung cancer should be monitored for early detection.

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Institute for Systems Biology Gets $6M Donation PDF Print E-mail
Wednesday, 10 March 2010 10:03
An anonymous California venture capitalist and philanthropist has agreed to donate $6 million over five years to the Institute for Systems Biology toward a planned expansion and move, the hiring of additional faculty, and unrestricted research support.
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Offering Hope for Tissue Regeneration PDF Print E-mail
Monday, 08 March 2010 08:50

Researchers at Rhode Island Hospital have discovered how cells communicate with each other during times of cellular injury. The findings shed new light on how the body repairs itself when organs become diseased, through small particles known as microvesicles, and offers hope for tissue regeneration. The paper is published in the March 2010 edition of the journal Experimental Hematology and is now available online in advance of publication.

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Second Dose of Gene Therapy for Inherited Blindness Proves Safe in Animal Studies PDF Print E-mail
Monday, 08 March 2010 08:46

Gene therapy for a severe inherited blindness, which produced dramatic improvements last year in 12 children and young adults who received the treatment in a clinical trial, has cleared another hurdle. The same research team that conducted the human trial now reports that a study in animals has shown that a second injection of genes into the opposite, previously untreated eye is safe and effective, with no signs of interference from unwanted immune reactions following the earlier injection.

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Genome-Wide Study of Alcohol Dependence Points to Chromosome 11 PDF Print E-mail
Thursday, 04 March 2010 10:22

Alcohol dependence (AD) is a complex disease for which both genetic and environmental factors affect susceptibility. Previous research had identified several genes associated with AD through linkage analysis or candidate-gene approaches. Findings from a genome-wide association study (GWAS) support an association between AD and a cluster of genes on chromosome 11.

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Athena Licenses Genetic Test for Intellectual Disability PDF Print E-mail
Thursday, 04 March 2010 03:16
Athena Diagnostics, a subsidiary of Thermo Fisher Scientific, has licensed from Toronto's Centre for Addiction and Mental Health the rights to develop a test for intellectual disability based on CC2D2A gene mutations. The test was initially developed by a CAMH researcher in collaboration with an independent researcher and will be further developed by Athena. The partners hope to have a test available to physicians for clinical use in Canada, the US, and Japan by January 2011.
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Personalized Medicine in Warfarin Therapy PDF Print E-mail
Monday, 01 March 2010 23:45

Researchers from the Ohio State University have developed a rapid, multiplexed genotyping method to identify the single nucleotide polymorphisms (SNPs) that affect warfarin dose.

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Minor Variations in One Gene May Be Associated With Endurance Running PDF Print E-mail
Monday, 01 March 2010 23:33

A few minor variations in one gene may make a difference in athletic endurance, according to a new study from Physiological Genomics. The study found that elite endurance athletes were more likely to have variations of the NRF2 gene than elite sprinters. Non-elite endurance athletes were also more likely to have the genetic variations compared to sprinters, although the difference was not as pronounced.

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NIH, FDA Start $6.8M 'Microscope to Marketplace' Effort PDF Print E-mail
Friday, 26 February 2010 22:36
The National Institutes of Health and the US Food and Drug Administration today unveiled a new joint effort aimed at developing ways to translate new biomedical discoveries through regulation and into pharmacies and hospitals.
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GWAS Data Translating Into Improved Drug Safety, Researchers Say PDF Print E-mail
Friday, 26 February 2010 22:11
While genome-wide association studies have long been considered an avenue for improving diagnostics, prognostics, and treatment, their most immediate application appears to be for improving drug safety and decreasing adverse events, according to Lon Cardon, senior vice president of GlaxoSmithKline's genetics program.
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