Neuroscience

Researchers identify new genetic cause of epilepsy

A research team led by scientists at the Scripps Translational Science Institute (STSI) has used whole genome sequencing to identify a new genetic cause of a severe, rare and complex form of epilepsy that becomes evident ...

Diseases, Conditions, Syndromes

Genome sequenced of enterovirus D68 circulating in St. Louis

Researchers at Washington University School of Medicine in St. Louis have sequenced the genome of enterovirus D68 sampled from patients treated at St. Louis Children's Hospital. Nationwide, the virus has spread rapidly in ...

Diseases, Conditions, Syndromes

How the spread of Ebola is calculated

The number of reported Ebola cases is doubling roughly every five weeks in Sierra Leone, and in as little as two to three weeks in Liberia.

Neuroscience

New ALS associated gene identified using innovative strategy

Using an innovative exome sequencing strategy, a team of international scientists led by John Landers, PhD, at the University of Massachusetts Medical School has shown that TUBA4A, the gene encoding the Tubulin Alpha 4A protein, ...

Genetics

Conspicuous tRNA lookalikes riddle the human genome

Transfer RNAs (tRNAs) are ancient workhorse molecules and part of the cellular process that creates the proteins, critical building blocks of life that keep a cell running smoothly. A new discovery suggests that the number ...

Genetics

Infant's mysterious death leads to discovery of a family disease

(Medical Xpress)—Shortly after the death of his newborn son, 43-year-old Erik Drewniak was hospitalized with some of the same symptoms that killed the infant—high fever, severe respiratory distress, and hemorrhaging in ...

Genetics

Gene variant that dramatically reduces 'bad' lipids

In the first study to emerge from the UK10K Project's cohort of samples from the general public, scientists have identified a rare genetic variant that dramatically reduces levels of certain types of lipids in the blood. ...

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