Genomic 'hotspots' offer clues to causes of autism, other disorders
An international team, led by researchers from the University of California, San Diego School of Medicine, has discovered that "random" mutations in the genome are not quite so random after all. Their study, ...
Genetics
Dec 20, 2012 |
5 / 5 (1) |
0
|
High-throughput sequencing shows potentially hundreds of gene mutations related to autism
Genomic technology has revolutionized gene discovery and disease understanding in autism, according to an article published in the December 20 issue of the journal Neuron.
Genetics
Dec 19, 2012 |
5 / 5 (1) |
1
|
Researchers describe a key mechanism in muscle regeneration
Researchers at the Bellvitge Biomedical Research Institute (IDIBELL) have described a new selective target in muscle regeneration. This is the association of alpha-enolase protein and plasmin. The finding could be used to ...
Medical research
Dec 19, 2012 |
5 / 5 (1) |
0
Brain imaging identifies bipolar risk
(Medical Xpress)—Researchers from the Black Dog Institute and University of NSW have used brain imaging technology to show that young people with a known genetic risk of bipolar but no clinical signs of ...
Psychology & Psychiatry
Dec 17, 2012 |
not rated yet |
0
|
Uncovering a flaw in drug testing for chronic anxiety disorder
Pre-clinical trials—the stage at which medications or therapies are tested on animals like laboratory mice—is a crucial part of drug development. It's only then that scientists can assess benefits and side effects before ...
Medical research
Dec 13, 2012 |
5 / 5 (1) |
0
|
Psychology professor seeks clues to psychiatric disorders in DNA
Data, data everywhere. In genomics research, there is a data deluge, so innovative ways to analyze all that information will play a critical role in future breakthroughs.
Psychology & Psychiatry
Dec 12, 2012 |
not rated yet |
0
A better early blood test for autism: Genetic signatures point to disrupted neuro-immune pathways
(Medical Xpress)—Researchers at Boston Children's Hospital have developed a blood test for autism spectrum disorders (ASDs) that outperforms existing genetic tests, while presenting evidence that abnormal ...
Autism spectrum disorders
Dec 10, 2012 |
4 / 5 (3) |
1
|
Studies assess genetics, modified treatment to improve outcomes, reduce toxicity
Research identifying genetic factors that affect survival of patients with blood cancers and evaluating the effectiveness of modified treatment strategies to improve outcomes while reducing toxicity will be presented today ...
Cancer
Dec 09, 2012 |
5 / 5 (1) |
0
Scientists discovered genetic cause for rare disorder of motor neurones
(Medical Xpress)—Scientists have identified an underlying genetic cause for a rare disorder of motor neurones, and believe this may help find causes of other related diseases.
Genetics
Dec 07, 2012 |
5 / 5 (2) |
0
|
Combining two genome analysis approaches supports immune system contribution to autism
Researchers using novel approaches and methodologies of identifying genes that contribute to the development of autism have found evidence that disturbances in several immune-system-related pathways contribute to development ...
Autism spectrum disorders
Dec 06, 2012 |
5 / 5 (2) |
0
|
Neuroscientists prove ultrasound can be tweaked to stimulate different sensations
A century after the world's first ultrasonic detection device – invented in response to the sinking of the Titanic – Virginia Tech Carilion Research Institute scientists have provided the first neurophysiological evidence ...
Neuroscience
Dec 06, 2012 |
5 / 5 (1) |
0
|
Researchers find new genetic pathway behind neurodevelopmental disorders
Researchers at the Douglas Mental Health University Institute, have discovered a new genetic process that could one day provide a novel target for the treatment of neurodevelopmental disorders, such as intellectual disability ...
Genetics
Dec 06, 2012 |
5 / 5 (2) |
0
MECP2 duplication affects immune system as well as brain development
In 1999, Dr. Huda Zoghbi and colleagues at Baylor College of Medicine identified the genetic cause of Rett syndrome (a neurological disorder that begins after birth) – MECP2 mutation. Too little of the MeCP2 protein associated ...
Medical research
Dec 05, 2012 |
5 / 5 (2) |
0
|
Study of link between night eating and the peculiar internal clock of fat cells
When researchers at the University of Pennsylvania messed with the internal clocks of mouse fat cells, a surprising thing happened. The mice got fat.
Medical research
Dec 04, 2012 |
5 / 5 (2) |
0
Biologists achieve repair and read-through of stop mutations responsible for Usher syndrome
After years of basic research, scientists at Johannes Gutenberg University Mainz (JGU) are increasingly able to understand the mechanisms underlying the human Usher syndrome and are coming ever closer to ...
Genetics
Dec 04, 2012 |
3 / 5 (2) |
0
|