The fragile X-related disorders (FXDs) are a group of clinical conditions that result primarily from an unusual mutation, the expansion of a CGG-repeat tract in exon 1 of the FMR1 gene. Mouse models are proving useful for understanding many aspects of disease pathology in these disorders. There is also reason to think that such models may be useful for understanding the molecular basis of the unusual mutation responsible for these disorders. This review will discuss what has been learnt to date about mechanisms of repeat instability from a knock-in FXD mouse model and what the implications of these findings may be for humans carrying expansion-prone FMR1 alleles.National Institute of Diabetes and Digestive and Kidney Diseases DK05780
Fragile X syndrome is one of 14 trinucleotide repeat diseases. It arises due to expansion of ...
Fragile X syndrome is one of 14 trinucleotide repeat diseases. It arises due to expansion of a CGG r...
The fragile X mental retardation (FMR1) gene contains an expansion-prone CGG repeat within its 5′ UT...
The fragile X-related disorders (FXDs) are a group of clinical conditions that result primarily from...
The fragile X-related disorders (FXDs) are a group of clinical conditions that result primarily from...
The fragile X-related disorders (FXDs) are a group of clinical conditions that result primarily from...
A dynamic mutation in exon 1 of the FMR1 gene causes Fragile X-related Disorders (FXDs), due to the ...
The Fragile X-related disorders (FXDs) are members of the Repeat Expansion Diseases, a group of huma...
The Fragile X-related disorders (FXDs) are members of the Repeat Expansion Diseases, a group of huma...
Repeat expansion diseases, including Fragile X Syndrome (FXS), Huntington’s Disease, and other disea...
The Fragile X-related disorders (FXDs), which include the intellectual disability fragile X syndrome...
textabstractThe human FMR1 gene contains a CGG repeat in its 5′ untranslated region. The repeat leng...
Carriers of the fragile X premutation (FPM) have CGG trinucleotide repeat expansions of between 55 a...
Author Summary: The repeat expansion diseases are a group of human genetic disorders that are caused...
Carriers of the fragile X premutation (FPM) have CGG trinucleotide repeat expansions of between 55 a...
Fragile X syndrome is one of 14 trinucleotide repeat diseases. It arises due to expansion of ...
Fragile X syndrome is one of 14 trinucleotide repeat diseases. It arises due to expansion of a CGG r...
The fragile X mental retardation (FMR1) gene contains an expansion-prone CGG repeat within its 5′ UT...
The fragile X-related disorders (FXDs) are a group of clinical conditions that result primarily from...
The fragile X-related disorders (FXDs) are a group of clinical conditions that result primarily from...
The fragile X-related disorders (FXDs) are a group of clinical conditions that result primarily from...
A dynamic mutation in exon 1 of the FMR1 gene causes Fragile X-related Disorders (FXDs), due to the ...
The Fragile X-related disorders (FXDs) are members of the Repeat Expansion Diseases, a group of huma...
The Fragile X-related disorders (FXDs) are members of the Repeat Expansion Diseases, a group of huma...
Repeat expansion diseases, including Fragile X Syndrome (FXS), Huntington’s Disease, and other disea...
The Fragile X-related disorders (FXDs), which include the intellectual disability fragile X syndrome...
textabstractThe human FMR1 gene contains a CGG repeat in its 5′ untranslated region. The repeat leng...
Carriers of the fragile X premutation (FPM) have CGG trinucleotide repeat expansions of between 55 a...
Author Summary: The repeat expansion diseases are a group of human genetic disorders that are caused...
Carriers of the fragile X premutation (FPM) have CGG trinucleotide repeat expansions of between 55 a...
Fragile X syndrome is one of 14 trinucleotide repeat diseases. It arises due to expansion of ...
Fragile X syndrome is one of 14 trinucleotide repeat diseases. It arises due to expansion of a CGG r...
The fragile X mental retardation (FMR1) gene contains an expansion-prone CGG repeat within its 5′ UT...