‘Genetics’ Articles
Gifts of the MAGI in Schizophrenia and Bipolar Disorder
These findings are not about the classic story of gift-giving, although the MAGI genes (officially named membrane associated guanylate kinase, WW and PDZ domain containing proteins) do influence brain function in important ways. [Read More]
Spontaneous gene glitches linked to autism risk with older dads
Researchers have turned up a new clue to the workings of a possible environmental factor in autism spectrum disorders (ASDs): fathers were four times more likely than mothers to transmit tiny, spontaneous mutations to their children with the disorders. Moreover, the number [Read More]
Genetic Clues To PTSD?
New research released today in PLoS ONE could help to find new treatment options for people suffering from high anxiety disorders such as PTSD. Using mice, researchers at Rutgers have identified genetic clues which pinpoint why some are more resilient to traumatic [Read More]
Gene Variant CYP2E1 Could Possibly Protect Against Alcoholism
Researchers have discovered a gene variant which is believed to possibly prevent against alcoholism. The gene variant, CYP2E1 appears to make people more sensitive to alcohol and can generate free radicals. Researchers consider a future application for drugs containing [Read More]
Treating Depression With Gene Therapy
A new study suggests gene therapy might be key to treating major depression in patients who do not respond to conventional drug treatments. Researchers have discovered that the p11 gene seems to play a major role in depression. By disabling the p11 protein in mice, [Read More]
PTCHD1 Gene Mutation Linked To Autism In Boys
Researchers have discovered a link between mutations in the PTCHD1 gene on the X-chromosome and an increased risk of developing autism in boys. As males inherit both X and Y chromosomes, the genetic mutation could explain why boys are four times more likely to develop ASD [Read More]
PIGV Gene Mutation Could Be Responsible For Mental Retardation In Mabry Syndrome
Researchers in Berlin have utilized a new process to analyse all of the genes in the human genome simultaneously. The researchers analysed the genetics of three children in one family who suffer from a rare form of mental retardation, Mabry Syndrome. [Read More]
