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 |
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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 |
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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 |
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Study offers new approach for spinal muscular atrophy
Spinal muscular atrophy is a debilitating neuromuscular disease that in its most severe form is the leading genetic cause of infant death. By experimenting with an ALS drug in two very different animal models, researchers ...
Neuroscience
Apr 09, 2013 |
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Researchers identify mutation that causes short-sightedness and hearing loss
(Medical Xpress)—Researchers have identified a new disorder caused by a genetic mutation that leads to short sightedness and deafness. They say the new link between the two sensory problems could lead to ...
Genetics
Apr 08, 2013 |
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New genetic evidence suggests continuum among neurodevelopmental and psychiatric disorders
A paper published this month in the prestigious medical journal The Lancet Neurology suggests that a broad spectrum of developmental and psychiatric disorders, ranging from autism and intellectual disability to schizophrenia, should ...
Genetics
Apr 05, 2013 |
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Acid reflux? It's in the genes
(Medical Xpress)—For many years it has been thought that acid reflux and a related condition called Barrett's Oesophagus were acquired conditions, via diet, smoking and other lifestyle activities. However, recent family ...
Diseases, Conditions, Syndromes
Apr 03, 2013 |
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'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 |
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Genetic risk strategies needed for young, black, female breast cancer patients, study shows
Researchers at Moffitt Cancer Center and colleagues in Canada have published study results focused on black women younger than 50, a population disproportionately afflicted with and dying from early-onset breast cancer compared ...
Cancer
Mar 21, 2013 |
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Faulty gene regulation triggers the kidney disease FSGS
The Clinical Institute of Pathology at the MedUni Vienna has discovered a previously unknown mechanism in the regulation of gene expression that leads to the development of a chronic renal condition known ...
Diseases, Conditions, Syndromes
Mar 20, 2013 |
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Family history of bowel cancer increases odds of survival
A new study that combines genetic information on bowel cancer with NHS patient outcome data has found a link between family history of the disease and a better chance of survival, published in the British Jo ...
Cancer
Mar 20, 2013 |
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New database to speed genetic discoveries
A new online database combining symptoms, family history and genetic sequencing information is speeding the search for diseases caused by a single rogue gene. As described in an article in the May issue of Human Mutation, the da ...
Genetics
Mar 18, 2013 |
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Network analysis sheds new light on the abnormal brain connectivity responsible for a common genetic cause of autism
Combining hospital MRIs with the mathematical tool known as network analysis, a group of researchers at UC San Francisco and UC Berkeley have mapped the three-dimensional global connections within the brains ...
Neuroscience
Feb 28, 2013 |
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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 |
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Discovery spurred by unique twist of fate
(Medical Xpress)—As people age, or as a result of poor nutrition, heart valves can become damaged by the accumulation of calcium deposits within the tissue. This calcification causes a thickening and hardening ...
Cardiology
Feb 21, 2013 |
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