News tagged with genetic cause
Related topics: genes , genetic mutations , gene mutation , neurodegenerative disorder
Four genes indentified that influence levels of 'bad' cholesterol
Scientists at the Texas Biomedical Research Institute in San Antonio have identified four genes in baboons that influence levels of "bad" cholesterol. This discovery could lead to the development of new drugs to reduce the ...
Medical research
May 15, 2013 |
4.5 / 5 (2) |
0
|
Genes and their regulatory 'tags' conspire to promote rheumatoid arthritis, study finds
In one of the first genome-wide studies to hunt for both genes and their regulatory "tags" in patients suffering from a common disease, researchers have found a clear role for the tags in mediating genetic ...
Genetics
Jan 20, 2013 |
4.6 / 5 (7) |
0
|
Genomic detectives crack the case of the missing heritability
(Medical Xpress)—Despite years of research, the genetic factors behind many human diseases and characteristics remain unknown. The inability to find the complete genetic causes of family traits such as ...
Genetics
Feb 22, 2013 |
4.8 / 5 (6) |
1
|
Team identifies two genes that combine to cause rare syndrome
Researchers from Massachusetts General Hospital (MGH) and Duke University have identified genetic mutations that appear to underlie a rare but devastating syndrome combining reproductive failure with cerebellar ataxia – ...
Genetics
May 08, 2013 |
5 / 5 (1) |
0
'Gene overdose' causes extreme thinness
Scientists have discovered a genetic cause of extreme thinness for the first time, in a study published today in the journal Nature.
Genetics
Aug 31, 2011 |
4.8 / 5 (4) |
0
|
Study links deletion of brain-derived neurotrophic factor to major depression, anxiety, and obesity
McGill researchers have identified a small region in the genome that conclusively plays a role in the development of psychiatric disease and obesity. The key lies in the genomic deletion of brain-derived neurotrophic factor, ...
Psychology & Psychiatry
Oct 08, 2012 |
5 / 5 (1) |
0
|
24 new genes for short-sightedness identified
An international team of scientists led by King's College London has discovered 24 new genes that cause refractive errors and myopia (short-sightedness).
Genetics
Feb 10, 2013 |
5 / 5 (3) |
1
|
Breast cancer risks acquired in pregnancy may pass to next three generations
Chemicals or foods that raise estrogen levels during pregnancy may increase cancer risk in daughters, granddaughters, and even great-granddaughters, according to scientists from Virginia Tech and Georgetown University.
Cancer
Sep 11, 2012 |
not rated yet |
0
|
Study links Fragile X Syndrome proteins and RNA editing mistakes at nerve-muscle junction
The most common form of heritable cognitive impairment is Fragile X Syndrome, caused by mutation or malfunction of the FMR1 gene. Loss of FMR1 function is also the most common genetic cause of autism. Understanding ...
Neuroscience
Oct 30, 2011 |
5 / 5 (1) |
0
|
Concert cacophony: Short-term hearing loss protective, not damaging
Contrary to conventional wisdom, short-term hearing loss after sustained exposure to loud noise does not reflect damage to our hearing: instead, it is the body's way to cope.
Medical research
Apr 15, 2013 |
3 / 5 (2) |
1
|
First evidence for genetic cause for Barrett's oesophagus found
Genetic variations that are linked with the onset of Barrett's oesophagus (BE), a pre-cancerous condition of the lower end of the gullet, have been identified for the first time. The discovery of variations in regions on ...
Genetics
Sep 09, 2012 |
not rated yet |
0
|
Genetic mutation implicated in 'broken' heart
For decades, researchers have sought a genetic explanation for idiopathic dilated cardiomyopathy (DCM), a weakening and enlargement of the heart that puts an estimated 1.6 million Americans at risk of heart failure each year. ...
Genetics
Feb 15, 2012 |
not rated yet |
0
|
'RNA sponge' mechanism may cause ALS/FTD neurodegeneration
The most common genetic cause of both ALS (amyotrophic lateral sclerosis) and FTD (frontotemporal dementia) was recently identified as an alteration in the gene C9orf72. But how the mutation causes neurodegenerative disease ...
Genetics
Apr 01, 2013 |
5 / 5 (2) |
0
|
A new light shed on genetic regulation's role in the predisposition to common diseases
An international team of researchers from King's College, Oxford University, Wellcome Trust Sanger Institute and Faculty of Medicine of University of Geneva, has discovered several thousands new genetic variants impacting ...
Genetics
Sep 02, 2012 |
5 / 5 (1) |
0
|
Translation error tracked in the brain of dementia patients
In certain dementias silent areas of the genetic code are translated into highly unusual proteins by mistake. An international team of scientists including researchers from the German Center for Neurodegenerative ...
Neuroscience
Feb 07, 2013 |
5 / 5 (1) |
0
|
