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Short DNA Strands in Genome May Be Key to Understanding Human Cognition and Diseases
November 21, 2012 Previously discarded, human-specific “junk” DNA represents untapped resource in the study of diseases like Alzheimer’s and ... > full story -
Evolution of Human Intellect: Human-Specific Regulation of Neuronal Genes
November 20, 2012 A new study has identified hundreds of small regions of the genome that appear to be uniquely regulated in human neurons. These regulatory differences distinguish us from other primates, including ... > full story -
Sleep Disorder Research
Epigenetics
Insomnia Research
Children's Health
Infant's Health
Today's Healthcare
Adenotonsillectomy May Help Resolve Obstructive Sleep Apnea in Children With Prader-Willi Syndrome
November 20, 2012 Children with Prader-Willi syndrome may receive relief from sleep disorders after undergoing an adenotonsillectomy, suggests a new ... > full story -
A New Way of Looking at Prader-Willi Syndrome
November 15, 2012 An Australian study reveals that people with the rare genetic disorder known as Prader-Willi Syndrome may have an impaired autonomic nervous system. This discovery opens up a new way of looking at ... > full story -
Mutations in Genes That Modify DNA Packaging Result in Facioscapulohumeral Muscular Dystrophy (FSHD)
November 11, 2012 A worldwide group of collaborators has found that the way DNA is packaged in people with this form of muscular dystrophy may be responsible for their disease. A genetic error allows the DNA wrapping ... > full story -
Humans, Chimpanzees and Monkeys Share DNA but Not Gene Regulatory Mechanisms
November 6, 2012 Up to 40 percent of the differences in the expression or activity patterns of genes between humans, chimpanzees and rhesus monkeys can be explained by regulatory mechanisms that determine whether and ... > full story -
New Findings on Gene Regulation and Bone Development
November 5, 2012 The patients have single short fingers (metacarpals) and toes (metatarsals) and can be restricted in growth due to a shortened skeleton. This hereditary disease is called brachydactyly type E. Now, ... > full story -
How to Make Stem Cells: Nuclear Reprogramming Moves a Step Forward
October 29, 2012 The idea of taking a mature cell and removing its identity (nuclear reprogramming) so that it can then become any kind of cell, holds great promise for repairing damaged tissue or replacing bone ... > full story -
Deciphering the First Epigenomes of Chronic Lymphocytic Leukemia
October 19, 2012 Researchers have deciphered the first epigenomes of chronic lymphocytic ... > full story -
Genes and Immune System Shaped by Childhood Poverty, Stress
October 18, 2012 New research has revealed that childhood poverty, stress as an adult, and demographics such as age, sex and ethnicity, all leave an imprint on a person's genes. And, that this imprint could play a ... > full story
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