Human Molecular Genetics
Cells from skin create model of blinding eye disease
For the first time, Wisconsin researchers have taken skin from patients and, using induced pluripotent stem cell (iPSC) technology, turned them into a laboratory model for an inherited type of macular degeneration.
Genetics
Nov 08, 2012 |
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Common food supplement fights degenerative brain disorders
Widely available in pharmacies and health stores, phosphatidylserine is a natural food supplement produced from beef, oysters, and soy. Proven to improve cognition and slow memory loss, it's a popular treatment for older ...
Medical research
May 21, 2013 |
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Cancer drug prevents build-up of toxic brain protein
Researchers at Georgetown University Medical Center have used tiny doses of a leukemia drug to halt accumulation of toxic proteins linked to Parkinson's disease in the brains of mice. This finding provides the basis to plan ...
Genetics
May 10, 2013 |
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Researchers link facial structure to kidney disease
(Medical Xpress)—Researchers at King's College London's Dental Institute have shown that people with a certain kind of kidney disease have characteristic facial features that may reflect the genetic mutation ...
Diseases, Conditions, Syndromes
Apr 24, 2013 |
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Study uncovers key factor in Alzheimer's progression
(Medical Xpress)—A new study from researchers at the University of Florida may have uncovered a critical factor that drives the relentless progression of Alzheimer's disease ― a discovery that could eventually slow its ...
Alzheimer's disease & dementia
Apr 16, 2013 |
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Autism linked to increased genetic change in regions of genome instability
(Medical Xpress)—Children with autism have increased levels of genetic change in regions of the genome prone to DNA rearrangements, so called "hotspots," according to a research discovery to be published ...
Autism spectrum disorders
Apr 03, 2013 |
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Scientists provide insights into incurable brain disease
(Medical Xpress)—Queensland Institute of Medical Research, Griffith University and University of Queensland scientists researching a degenerative brain disease have developed a new way to understand its progression and ...
Genetics
Mar 22, 2013 |
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Team aids discovery of first dystonia gene found in African-Americans
A pair of studies tells the tale of how a neuroscientist at Mayo Clinic in Florida helped to discover the first African-American family to have inherited the rare movement disorder dystonia, which causes repetitive muscle ...
Genetics
Mar 07, 2013 |
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Genes that control nervous system development play a role in gum disease
(Medical Xpress)—By simultaneously investigating millions of gene variants in more than 5,000 individuals, researchers at the University of North Carolina at Chapel Hill reveal that genes that are responsible for nervous ...
Genetics
Mar 05, 2013 |
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Research uncovers a potential link between Parkinson's and visual problems
The most common genetic cause of Parkinson's is not only responsible for the condition's distinctive movement problems but may also affect vision, according to new research by scientists at the University of York.
Parkinson's & Movement disorders
Feb 15, 2013 |
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How deficiencies in two genes synergize to halt formation of gut nervous system
Mutations in single genes can cause catastrophic diseases, such as Huntington's Disease or sickle cell anemia. However, many conditions, including cancer, diabetes and birth defects are multigenic, arising ...
Genetics
Jan 31, 2013 |
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New research discovery provides therapeutic target for ALS
Research led by Dr. Udai Pandey, Assistant Professor of Genetics at LSU Health Sciences Center New Orleans, has found that the ability of a protein made by a gene called FUS to bind to RNA is essential to the development ...
Genetics
Dec 19, 2012 |
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New genes discovered for adult BMI levels
A large international study has identified three new gene variants associated with body mass index (BMI) levels in adults. The scientific consortium, numbering approximately 200 researchers, performed a meta-analysis of 46 ...
Genetics
Oct 25, 2012 |
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Early menopause in mice: A model of human POI
(Medical Xpress)—Scientists have established a genetic mouse model for primary ovarian insufficiency (POI), a human condition in which women experience irregular menstrual cycles and reduced fertility, ...
Genetics
Aug 30, 2012 |
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Low oxygen levels may decrease life-saving protein in spinal muscular atrophy
Investigators at Nationwide Children's Hospital may have discovered a biological explanation for why low levels of oxygen advance spinal muscular atrophy (SMA) symptoms and why breathing treatments help SMA patients live ...
Genetics
Aug 21, 2012 |
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