Banner
Pilot Study: Fibromyalgia Fatigue Improved By TENS Therapy

Fibromyalgia is the term for a poorly-understood condition where people experience pain and fatigue...

High Meat Consumption Linked To Lower Dementia Risk

Older people who eat large amounts of meat have a lower risk of dementia and cognitive decline...

Long Before The Inca Colonized Peru, Natives Had A Thriving Trade Network

A new DNA analysis reveals that long before the Incan Empire took over Peru, animals were...

Mesolithic People Had Meals With More Tradition Than You Thought

The common imagery of prehistoric people is either rooting through dirt for grubs and picking berries...

User picture.
News StaffRSS Feed of this column.

News Releases From All Over The World, Right To You... Read More »

Blogroll

An international team of scientists today announced the results of a systematic effort to map the genetic changes underlying lung cancer, the world’s leading cause of cancer deaths.

The research provides a comprehensive view of the abnormal genetic landscape in lung cancer cells, revealing more than 50 genomic regions that are frequently gained or lost in human lung tumors. While one-third of these regions contain genes already known to play important roles in lung cancer, the majority harbor new genes yet to be discovered.

Inheriting two genetic mutations that can individually cause epilepsy might actually be “seizure-protective,” said Baylor College of Medicine researchers the journal Nature Neuroscience.

“In the genetics of the brain, two wrongs can make a right,” said Dr. Jeffrey L. Noebels, professor of neurology, neuroscience and molecular and human genetics at BCM. “We believe these findings have great significance to clinicians as we move toward relying upon genes to predict neurological disease.”

In addition, the finding might point the way to new ways of treating epilepsy using gene-directed therapy.

“If you have a potassium channel defect, then a drug blocking certain calcium channels might also benefit you,” said Noebels.

Recessive dystrophic epidermolysis bullosa (RDEB)is a disease where children lack a protein that anchors skin to the body, resulting in fragile skin that tears off with little movement or friction. They suffer painful wounds and must be bandaged at all times to protect their skin from further damage and infection.

University of Minnesota Children’s Hospital, Fairview physicians have performed the first bone marrow and cord blood transplant to treat RDEB.

The 18-month-old boy who was transplanted has the most severe form of RDEB, which also causes skin to slough off on the inside of the body, affecting the mouth, esophagus, and gastrointestinal tract. EB is genetic and severe forms are always fatal.

An age-related decline in heart function is a risk factor for heart disease in the elderly. While many factors contribute to a progressive age-related decline in heart function, alterations in the types of fuels the heart uses to produce energy also play important roles.

Jason Dyck and his research team at the University of Alberta have been studying the types of fuels used by the heart in young and aged mice. The young healthy heart normally used a balance of fat and sugar to generate energy to allow the heart to beat and pump blood efficiently. However, as the heart ages the ability to use fat as an energy source deteriorates. This compromises heart function in the elderly.

The universe’s clock has neither a start nor finish, yet time is still finite, according to a New Zealand theorist.

To understand that, we need to take a “cyclic” view of time similar to the one held by ancient thinkers like Plato, Aristotle and Leonardo da Vinci, rather than the Christian Calender and Bible-influenced belief in “linear” time so deeply imbedded in modern western thinking.

This theory, which tackles the age-old mystery of the origin of the universe, along with several other problems and paradoxes in cosmology, essentially calls for a new take on our concept of time.

The radar system on ESA’s Mars Express has uncovered new details about some of the most mysterious deposits on Mars: The Medusae Fossae Formation. It has given the first direct measurement of the depth and electrical properties of these materials, providing new clues about their origin.

The Medusae Fossae Formation (MFF) are unique deposits on Mars. They are also an enigma. Found near the equator, along the divide between the highlands and lowlands, they may represent some of the youngest deposits on the surface of the planet. This is inferred from the marked lack of impact craters dotting this terrain, unlike on older terrain. Mars Express has been collecting data from this region using its Mars Advanced Radar for Subsurface and Ionospheric Sounding (MARSIS).