Oncology & Cancer
Study shows vitamin E may decrease cancer risk in Cowden syndrome patients
Cleveland Clinic researchers have discovered that vitamin E may prevent cancer in patients with an under-recognized genetic disorder.
Sep 17, 2012
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Page 27 - News tagged with mutant
Neuroscience
Toxic protein build-up in blood shines light on Huntington's disease
A new light-based technique for measuring levels of the toxic protein that causes Huntington's disease (HD) has been used to demonstrate that the protein builds up gradually in blood cells. Published today in the Journal ...
Sep 17, 2012
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Diseases, Conditions, Syndromes
New collaboration to develop treatments for liver disease
A new collaboration based at the University of Cambridge will aim to discover and develop new medicines to treat liver disease.
Sep 7, 2012
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Genetics
Researchers solve mystery surrounding the death of two sisters nearly 50 years ago
Researchers at Mount Sinai School of Medicine have identified the genetic cause of a rare and fatal bone disease by studying frozen skin cells that were taken from a child with the condition almost fifty years ago. Their ...
Aug 29, 2012
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Genetics
Enlisting the AIDS virus to fight cancer
(Medical Xpress)—Can HIV be transformed into a biotechnological tool for improving human health? According to a CNRS team at the Architecture et Réactivité de l'ARN (RNA Architecture and Reactivity) laboratory, the answer ...
Aug 29, 2012
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Genetics
Scientists identify new gene that influences survival in amyotrophic lateral sclerosis
A team of scientists, including faculty at the University of Massachusetts Medical School (UMMS), have discovered a gene that influences survival time in amyotrophic lateral sclerosis (ALS, also known as Lou Gehrig's disease). ...
Aug 26, 2012
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Medical research
Possible muscle disease therapeutic target found
The study of muscular system protein myostatin has been of great interest to researchers as a potential therapeutic target for people with muscular disorders. Although much is known about how myostatin affects muscle growth, ...
Aug 6, 2012
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Genetics
Study of zebra fish mouth formation may speak to Fraser syndrome hearing loss
Using mutant zebra fish, researchers studying the earliest formation of cartilage of the mouth believe they may have gotten a look at a mechanism involved in a genetic defect linked to Fraser syndrome deafness in humans.
Jul 31, 2012
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Oncology & Cancer
Uncommon BRAF mutation in melanoma sensitive to MEK inhibitor drug therapy
An uncommon mutation of the BRAF gene in melanoma patients has been found to respond to MEK inhibitor drugs, providing a rationale for routine screening and therapy in melanoma patients who harbor the BRAF L597 mutation.
Jul 16, 2012
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Oncology & Cancer
A new target in acute myeloid leukemia
Acute myeloid leukemia, a common leukemia in adults, is characterized by aberrant proliferation of cancerous bone marrow cells. Activating mutations in a protein receptor known as FLT3 receptor are among the most prevalent ...
Jul 16, 2012
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