FeaturedGenetics·July 5, 2013·6 min readUnique Epigenomic Code Identified During Human Brain DevelopmentA new study uncovers dynamic changes in the epigenome which occur during brain development.Read More
FeaturedGenetics·July 3, 2013·3 min readNew Mechanism for Human Gene Expression DiscoveredResearchers find a single gene which encodes two separate proteins from the same sequence of messenger RNA. The finding could provide new strategies for treating SCA6.Read More
FeaturedGenetics·July 2, 2013·3 min readResearchers Discover Gene’s Key Role in Building the Developing Brain’s ScaffoldingResearchers pinpoint the role of the Arl13b gene in the formation and proper placement of neurons during brain development.Read More
FeaturedNeurology·July 1, 2013·4 min readLack of Immune Cell Receptor Impairs Clearance of Amyloid Beta Protein from the BrainResearchers discover increased expression of the Scara1 protein could impede the progression of Alzheimer's disease as it plays an important role in the removal of amyloid beta from the brain.Read More
AutismFeaturedGeneticsOpen Neuroscience Articles·July 1, 2013·2 min readResearcher Discovers New Regulatory Autism GeneResearchers report RORA, a novel candidate gene for autism, regulates a large number of other genes associated with ASD.Read More
FeaturedNeuroscience·June 30, 2013·2 min readDifferent Neuronal Groups Govern Right-Left Alternation When WalkingResearchers identify neuronal circuits in the spinal cord of mice which control the ability to produce alternating movements of the legs during walking.Read More
FeaturedNeurologyNeuroscience Videos·June 28, 2013·5 min readScientists View ‘Protein Origami’ to Help Understand, Prevent Certain DiseasesUsing sophisticated imaging techniques, researchers observe a molecular protein folding process which could help better understand and treat neurodegenerative diseases and cancers.Read More
FeaturedGenetics·June 28, 2013·3 min readScientists Turn Muscular Dystrophy Defect On and Off in CellsResearchers have identified small molecules which allow for control over a genetic defect responsible for adult onset muscular dystrophy.Read More
FeaturedGenetics·June 26, 2013·3 min readSymptoms of Prader-Willi Syndrome Associated with Interference in Circadian, Metabolic GenesPrader-Willi syndrome, a genetic disorder characterized by an insatiable appetite, is associated with the loss of non-coding RNAs; resulting in dysregulation of the circadian and metabolic genes.Read More
FeaturedNeurology·June 25, 2013·1 min readResearchers Determine that Brain Reserve Independently Protects Against Cognitive Decline in MSResearchers suggest lifetime brain growth and early mental stimulation independently help protect against cognitive decline in multiple sclerosis.Read More
FeaturedOpen Neuroscience ArticlesPsychology·June 24, 2013·4 min readGenes Involved in Birth Defects Could Lead to Mental IllnessMutations of the Dact1 gene, which leads to major birth defects, may also cause subtle disruptions in the brain which contribute to the development of psychiatric disorders, according to new research.Read More
FeaturedGenetics·June 24, 2013·3 min readAbsence of Gene Leads to Earlier, More Severe Case of Multiple SclerosisA new study identifies a possible genetic mechanism that causes a quicker progression of multiple sclerosis. The absence of Tob1 in CD4+ T cells is key to early onset of a more aggressive form of MS.Read More
