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          Genetics

          An image of fly spinal cord equivalent is shown.
          FeaturedNeuroscience
          ·October 11, 2012·6 min read

          Novel Mechanisms Underlying Major Childhood Neuromuscular Disease Identified

          A study suggests that spinal muscular atrophy (SMA), a genetic neuromuscular disease in infants and children, results primarily from motor circuit dysfunction, not motor neuron or muscle cell dysfunction, as is commonly thought. In a second study, the researchers identified the molecular pathway in SMA that leads to problems with motor function.
          Read More
          A portrait of Eugen Bleuler is shown.
          FeaturedGenetics
          ·October 9, 2012·2 min read

          Rare Genetic Disorder Points to Molecules that May Play Role in Schizophrenia

          Scientists studying a rare genetic disorder have identified a molecular pathway that may play a role in schizophrenia, according to new research. The findings may one day guide researchers to new treatment options for people with schizophrenia - a devastating disease that affects approximately 1 percent of the world's population.
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          A ketamine model is shown.
          FeaturedNeurology
          ·October 3, 2012·3 min read

          Drug Reverses Abnormal Brain Function in Rett Syndrome Mice

          in a mouse model of Rett syndrome, researchers were able to reverse abnormalities in brain activity and improve neurological function by treating animals with an FDA-approved anesthesia drug, ketamine.
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          Schizophrenia fMRI brain scans are shown.
          FeaturedGeneticsPsychology
          ·October 3, 2012·4 min read

          New de novo Genetic Mutations in Schizophrenia Identified

          Columbia University Medical Center (CUMC) researchers have identified dozens of new spontaneous genetic mutations that play a significant role in the development of schizophrenia, adding to the growing list of genetic variants that can contribute to the disease. The schizophrenia study was the largest and most comprehensive of its kind.
          Read More
          The location of the VCP gene.
          FeaturedNeurology
          ·October 2, 2012·2 min read

          New Research Model to Aid Search for Degenerative Disease Cures

          Efforts to treat disorders like Lou Gehrig’s disease, Paget’s disease, inclusion body myopathy and dementia will receive a considerable boost from a new research model created by UC Irvine scientists.
          Read More
          Drawing of a human head with gears and computer parts on it.
          FeaturedGeneticsPsychology
          ·October 2, 2012·2 min read

          Intelligence Is in the Genes, but Where?

          A new study reveals that most of the specific genes long thought to be linked to intelligence probably have no bearing on one’s IQ. And it may be some time before researchers can identify intelligence’s specific genetic roots.
          Read More
          A patient with Myasthenia Gravis is shown.
          FeaturedNeurology
          ·October 1, 2012·3 min read

          Researchers Halt Autoimmune Disease Myasthenia Gravis in Mice

          Working with mice, Johns Hopkins researchers say they have developed a gene-based therapy to stop the rodent equivalent of the autoimmune disease myasthenia gravis by specifically targeting the destructive immune response the disorder triggers in the body.
          Read More
          FeaturedNeuroscience
          ·September 21, 2012·4 min read

          Research Identifies Protein that Regulates Key Fate Decision in Cortical Progenitor Cells

          Researchers solved an important piece of one of neuroscience's outstanding puzzles: how progenitor cells in the developing mammalian brain reproduce themselves while also giving birth to neurons that will populate the emerging cerebral cortex, the seat of cognition and executive function in the mature brain.
          Read More
          FeaturedNeuroscience
          ·September 19, 2012·4 min read

          Human Brains Share a Consistent Genetic Blueprint and Possess Enormous Biochemical Complexity

          Scientists at the Allen Institute for Brain Science reported that human brains share a consistent genetic blueprint and possess enormous biochemical complexity. The findings stem from the first deep and large-scale analysis of the vast data set publicly available in the Allen Human Brain Atlas.
          Read More
          Genetics
          ·September 18, 2012·1 min read

          New Findings on Protein Misfolding

          Researchers identified 21 proteins that specifically bind to a protein called ataxin-1. Twelve of these proteins enhance the misfolding of ataxin-1 and thus promote the formation of harmful protein aggregate structures, whereas nine of them prevent the misfolding.
          Read More
          FeaturedNeurology
          ·September 17, 2012·3 min read

          Toxic Protein Build-up in Blood Shines Light on Fatal Brain 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.
          Read More
          AutismFeaturedNeurology
          ·September 14, 2012·2 min read

          Disorder of Neural Circuits in Autism Mouse Model is Reversible

          Scientists have now identified a specific dysfunction in neuronal circuits that is caused by autism. The scientists also report about their success in reversing these neuronal changes in mouse models.
          Read More
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          Mapping the Brain’s Resting Grid Through Menopause

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          Parental Infertility Biology, Not IVF, Linked to Child Autism Traits

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          Glucosamine Supplement Linked to Accelerated Alzheimer’s Progression

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