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Genomic Test Personalizes Breast Cancer Treatment A set of 50 genes can be used to reliably identify the four known types of breast cancer, according to research conducted at Washington University School of Medicine in St. topix.netPossible Treatment For Neurological Disorder Rett Syndrome -- Most Common Basis Of Autism In Girls Injecting the small protein insulin-like growth factor-1 into the bloodstream reduces Rett syndrome symptoms in mice, including lethargy, breathing and heart rhythm irregularities, reduced brain size, and stalled nerve cell development. Rett syndrome is an inherited neurological disease that affects one out of 10,000 girls born. Although some symptoms can be mediated with prescription drugs, the disease does not have a cure or treatment. MedicineNetFDA and International Serious Adverse Events Consortium Release First Data on Genetic Basis of Adverse Drug Events The first data offering health care professionals a better look into the genetic basis of certain types of adverse drug events was released today by the FDA and the International Serious Adverse Event Consortium (SAEC). news-medical.netSurgery makes artificial arms easier to control CHICAGO (Reuters) - A new type of surgery may give amputees better control over their artificial arms, allowing them to point a finger, grasp a baseball bat or even give someone a pinch, U.S. researchers said on Tuesday. ReutersChronic fatigue sufferers to welcome national expert Mary Carter says she has overcome Chronic Fatigue Syndrome through nutrition, exercise and a line of homeopathic supplements endorsed by Dr. topix.netWhat Is Behavioral Therapy? Behavioral therapy is a type of psychotherapy that focuses on changing and gaining control over unwanted behaviors. It is based upon the principles of classical conditioning developed by Ivan... About.comProzac Discontinuation Prozac and discontinuation syndrome; why is discontinuation syndrome less likely with Prozac? AboutA missense mutation, p.V132G, in the X-linked spermine synthase gene (SMS) causes Snyder-Robinson syndrome Snyder-Robinson syndrome (SRS, OMIM 309583) is a rare X-linked syndrome characterized by mental retardation, marfanoid habitus, skeletal defects, osteoporosis, and facial asymmetry. Linkage analysis localized the related gene to Xp21.3-p22.12, and a G-to-A transition at point +5 of intron 4 of the spermine synthase gene, which caused truncation of the SMS protein and loss of enzyme activity, was identified in the original family. Here we describe another family with Snyder-Robinson syndrome in two Mexican brothers and a novel mutation (c.496T>G) in the exon 5 of the SMS gene confirming its involvement in this rare X-linked mental retardation syndrome. © 2009 Wiley-Liss, Inc. (Source: American Journal of Medical Genetics Part A) MedWorm Message: Find out how you can get your message across here by sponsoring this MedWorm news feed. Med WormBreast Cancer Treatment Personalized By New Genomic Test A set of 50 genes can be used to reliably identify the four known types of breast cancer, according to research conducted at Washington University School of Medicine in St. Louis and collaborating institutions. Using this 50-gene set, oncologists can potentially predict the most effective therapy for each breast tumor type and thereby personalize breast cancer treatment for all patients. Medicalnewstoday.comResearchers Discover Molecular Causes For Pathologically Elevated Blood Fat Levels In Obesity Scientists at the German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ) have discovered a mechanism in liver metabolism that is responsible for pathologically elevated blood fat levels found in severe metabolic disorders. Mice suffering from metabolic syndrome or type 2 diabetes produce only small amounts of a molecule called LSR in the liver, as reported by researchers headed by Dr. Stephan Herzig of DKFZ in the specialist journal Diabetes. Medicalnewstoday.com1 2 3 |
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