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Peroxisome Biogenesis Disorder, Complementation Group G

Known as: CGG 
National Institutes of Health

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Broader (1)

Peroxisomal Disorders

Papers overview

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Highly Cited
2014
Highly Cited
2014
Promoter-Bound Trinucleotide Repeat mRNA Drives Epigenetic Silencing in Fragile X Syndrome
Repeat Silencing Fragile X syndrome, a genetic cause of many cases of autism and mental retardation, involves expansion of a… 
Highly Cited
2013
Highly Cited
2013
CGG Repeat-Associated Translation Mediates Neurodegeneration in Fragile X Tremor Ataxia Syndrome
Highly Cited
2010
Highly Cited
2010
A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome.
BACKGROUND Fragile X syndrome (FXS) is a trinucleotide-repeat disease caused by the expansion of CGG sequences in the 5… 
Highly Cited
2007
Highly Cited
2007
Pur α Binds to rCGG Repeats and Modulates Repeat-Mediated Neurodegeneration in a Drosophila Model of Fragile X Tremor/Ataxia Syndrome
Highly Cited
2006
Highly Cited
2006
Autism Spectrum Disorders and Attention-Deficit/Hyperactivity Disorder in Boys with the Fragile X Premutation
ABSTRACT. Fragile X syndrome (FXS) is caused by a full mutation expansion (>200 CGG repeats) in the FMR1 gene that results in a… 
Highly Cited
1995
Highly Cited
1995
Translational suppression by trinucleotide repeat expansion at FMR1
Fragile X syndrome is the result of the unstable expansion of a trinucleotide repeat in the 5'-untranslated region of the FMR1… 
Highly Cited
1995
Highly Cited
1995
CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro.
A large increase in the length of a CGG tandem array is associated with a number of triplet expansion diseases, including fragile… 
Highly Cited
1994
Highly Cited
1994
Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles
Highly Cited
1993
Highly Cited
1993
Characterization and localization of the FMR-1 gene product associated with fragile X syndrome
THE fragile X syndrome is the most frequent form of inherited mental retardation after Down's syndrome, having an incidence of… 
Highly Cited
1993
Highly Cited
1993
Association of fragile X syndrome with delayed replication of the FMR1 gene
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