Genetics
'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.
Aug 31, 2011
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News tagged with genetic causes
Neuroscience
Researchers discover a new migraine-associated mechanism
A mutation in the gene that codes the ionic channel TRESK, involved in the control of neuron irritability, causes the dysfunction of some neurons that increase neuronal activity and induce migraine pain.
Mar 29, 2019
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Genetics
Scientists identify genetic cause of 'spongy' skin condition
Scientists have identified the genetic cause of a rare skin condition that causes the hands and feet to turn white and spongy when exposed to water.
Jul 3, 2013
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Oncology & Cancer
Researchers identify genetic mutation responsible for most cases of Waldenstrom's macroglobulinemia
Scientists at Dana-Farber Cancer Institute have identified a gene mutation that underlies the vast majority of cases of Waldenstrom's macroglobulinemia, a rare form of lymphoma that has eluded all previous efforts to find ...
Dec 12, 2011
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Inflammatory disorders
Researchers discover genetic basis for eczema, new avenue to therapies
(Medical Xpress)—Researchers at Oregon State University today announced the discovery of an underlying genetic cause of atopic dermatitis, a type of eczema most common in infancy that also affects millions of adults around ...
Dec 21, 2012
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Genetics
Medical mystery solved in record time
In a study published today in PLoS ONE, a team of researchers reports solving a medical mystery in a day's work. In record-time detective work, the scientists narrowed down the genetic cause of intellectual disability in ...
Apr 17, 2017
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Genetics
Mutated muscle protein causes deafness
(Medical Xpress) -- Excessive noise is not the only thing that causes damage to hearing. In many cases, genetic factors are responsible for the loss of hearing at a young age. Researchers at the Max Planck Institute for Molecular ...
May 30, 2011
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Medications
Thalidomide is an effective treatment for abnormal blood vessel formations
The same property of thalidomide that caused birth defects when it was given to pregnant women—the inhibition of blood vessel formation (anti-angiogenesis)—has led to an interest in thalidomide's therapeutic utility in ...
Jun 10, 2022
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Genetics
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. ...
Feb 15, 2012
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Oncology & Cancer
Research team discovers genes and disease mechanisms behind a common form of muscular dystrophy
Continuing a series of groundbreaking discoveries begun in 2010 about the genetic causes of the third most common form of inherited muscular dystrophy, an international team of researchers led by a scientist at Fred Hutchinson ...
Jan 12, 2012
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