Fragile X Syndrome News and Research

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Fragile X syndrome is the most common form of inherited mental retardation. A problem with a specific gene causes the disease. Normally, the gene makes a protein you need for brain development. But the mutation causes a person to make little or none of the protein, which results in the symptoms of Fragile X.

Protein called Elk-1appears to play role in neurodegeneration and schizophrenia

Pprotein called Elk-1 interacts with mitochondria, the energy storehouse of a cell, suggesting that this protein - typically active in the nucleus - could play a role in cell death and mitochondria-related diseases such as neurodegeneration and schizophrenia.

9 Jun 2006

No brain no gain

How do we process numbers? A new project from the Austrian Science Fund FWF hopes to find the complex answer to this seemingly simple question by building on the recent findings of a team from Innsbruck.

10 Apr 2006

New microRNA mechanism for regulating brain function

Non-coding regions of the genome - those that don't code for proteins - are now known to include important elements that regulate gene activity. Among those elements are microRNAs, tiny, recently discovered RNA molecules that suppress gene expression.

18 Jan 2006

Genetic cause of autism

The researchers at the U School of Medicine made the finding by tracing variations in the DNA of an extended Utah family that has a high occurrence of the disorder and whose members are descended from one couple.

18 Jan 2006

Researchers pinpoint specific cause of defects in motor learning in Fragile X patients

While researchers have long known the genetic defect underlying Fragile X syndrome, they are still tracing how that defect creates the complex mix of mental retardation, hyperactive behavior, attention deficits, and other problems in the disorder.

3 Aug 2005

Fragile X-associated tremor/ataxia syndrome difficult to diagnose

Fragile X-associated tremor/ataxia syndrome can be difficult to diagnose and should have guidelines for diagnostic testing, according to a study in the July 26 issue of Neurology, the scientific journal of the American Academy of Neurology. A second study found chemotherapy aggravated symptoms in one woman's case.

25 Jul 2005

Possible cure for Huntington's disease

Boosting levels of two critical proteins that normally shut down during Huntington's disease, researchers at the University of Wisconsin-Madison and the Cold Spring Harbor Laboratory have cured fruit flies of the genetic, neurodegenerative condition.

12 Jul 2005

Fragile-X-syndrome research

The fragile-X-syndrome is the most common hereditary form of mental retardation and occurs much more often in boys than in girls.

20 Jun 2005

Method shows how precisely gene expression signals are copied in DNA replication

Genetic information that determines hair color or whether an individual might develop a particular cancer is passed from one generation to the next through DNA. Genes encoded in the DNA contain information, but a process called methylation is one factor that often controls how that information is expressed.

19 Apr 2005

Possible treatment for Fragile X syndrome

The first evidence for a possible treatment for Fragile X syndrome, one of the leading inherited causes of mental retardation, has emerged from experiments with a mutant fruit fly that exhibits characteristics of the disorder.

2 Mar 2005

Entirely new approach to the treatment of aging

Dispelling the belief that the only way to treat such conditions is by fixing or replacing damaged genes, they instead focused on the field of epigenetics—the study of changes in gene silencing that occur without changes in the genes themselves.

3 Aug 2004